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Journal articles on the topic "F10"

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Wenas, Adrina Syulie, Ponirin Ponirin, and Wiri Wirastuti. "FAKTOR-FAKTOR YANG DIPERTIMBANGKAN MAHASISWA FAKULTAS EKONOMI UNIVERSITAS TADULAKO MENGGUNAKAN MEDIA SOSIAL INSTAGRAM SEBAGAI SARANA JUAL BELI ONLINE." Jurnal Ilmu Manajemen Universitas Tadulako (JIMUT) 1, no. 2 (May 31, 2015): 165–80. http://dx.doi.org/10.22487/jimut.v1i2.18.

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The study determines some factors considered by the students of the Economic Faculties University Tadulako using social media Instagram as a means of buying & selling online. The sampling technique is accidental side, with 105 samples taken. Based on the analysis factors using 21 indicators, the study finds 3 factors that are considered by students in using social media Instagram as a means of buying and selling online. These factors are: 1) Online Marketing consists of F3 (Ease in business), F12 (Facilitate the search for products), F14 (There are lots of goods imported or local), F15 (to hunt many gifts), F17 (can develop the business). 2) lifestyle, includes: F2 (following the trend of lifestyle), F6 (Instagram is already a lot of users), F10 (the event to seek friendship), F11 (as the entertainment media), F21 (the advice of friends); and 3) Sales Promotion factors such as: F1 (Promotion convincing), F16 (As an advertising medium offers products or services), F19 (price offered various kinds), F20 (For media information). Tujuan dari penelitian ini adalah untuk mengetahui faktor-faktor yang harus diperhatikan mahasiswa fakultas ekonomi Universitas Tadulako menggunakan media sosial Instagram sebagai alat untuk membeli & menjual secara online. Teknik yang digunakan untuk menentukan sampel adalah metode yang digunakan untuk menentukan sampel Sampling Sampling yang disela. Jumlah sampel yang diambil sebanyak 105 orang. Berdasarkan analisis faktor-faktor yang telah dilakukan melalui tahap pengujian dengan menggunakan 21 indikator ditemukan bahwa hanya 3 faktor yang dianggap mahasiswa, dengan menggunakan media sosial Instagram sebagai alat untuk jual-beli secara online merupakan faktor Pemasaran Online: F3 (Kemudahan dalam berbisnis), F12 (Memfasilitasi pencarian produk), F14 (Ada banyak barang impor atau lokal), F15 (untuk memburu banyak hadiah), F17 (bisa mengembangkan bisnis), maka faktor faktor kedua gaya hidup: F2 (mengikuti tren gaya hidup), F6 (Instagram sudah banyak pengguna), F10 (acara untuk mencari pertemanan), F11 (sebagai media hiburan), F21 (saran dari teman). Selanjutnya, faktor ketiga, yaitu faktor Promosi Penjualan: F1 (Promotion meyakinkan), F16 (Sebagai media periklanan menawarkan produk atau jasa), F19 (harga yang ditawarkan bermacam macam), F20 (Untuk informasi media).
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Mahyudin, Mahyudin, and Yusrizal Yusrizal. "Analisis Faktor-Faktor yang Mempengaruhi Keputusan Mahasiswa dalam Memilih Studi Online Program Sarjana dan Diploma di UPBJJ Ut Jambi." Jurnal Ilmiah Universitas Batanghari Jambi 21, no. 2 (July 4, 2021): 481. http://dx.doi.org/10.33087/jiubj.v21i2.1482.

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The purpose of this study was to determine (1) the description of student decisions in choosing online studies at UPBJJ UT Jambi, and (2) the factors that influence student decisions in choosing online studies at UPBJJ UT Jambi. The results showed that (1) the student's decision variable in choosing online studies was in the high category with an average of 4.29 and the Respondent Achievement Level (TCR) of 85.81, (2) There were 6 (six) dominant factors that influenced the decision. students in choosing online studies, namely (a) Factor 1 which is given the identity of the Motivation, which consists of statement items F8, F9, F10, F11, and F12, (b) Factor 2 which is given the identity of the Reference Group, which consists of statement items F19 , F20, and F21, (c) Factor 3 which is given the identity of Belief and Attitude, which consists of statement items F4, F16, F17, and F18, (d) Factor 4 which is given the identity of Economic State, which consists of statement items F3, F5, and F6, (e) Factor 5 which is given the identity of Perception, which consists of statement items F14, F15, and F26, and (f) Factor 6 which is assigned the identity of Role and Status, which consists of statement items F23, F24, and F25.
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SINGH, RAVINDRA, SUNIL KUMAR, AVINASH K. KONDALKAR, and MURAREE LAL. "FORMULATION AND EVALUATON OF FLOATING TABLET OF CEFPODOXIME PROXETIL." Current Research in Pharmaceutical Sciences 10, no. 3 (October 8, 2020): 47–57. http://dx.doi.org/10.24092/crps.2020.100303.

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Ideal once daily floating drug delivery system should release the drug for 24 hours and float up to 24 hrs. Once daily floating matrix tablet of Cefpodoxime proxetil should be release the drug for 24 hours to maintain the effective plasma level. All the formulations were prepared by using two different grades of HPMC (K100 and K4), cross povidone and MCC pH 101. HPMC is a matrix forming agent. All the formulations showed buoyancy lag time of less than 5 seconds regardless of concentration of HPMC K100 M, K4 and cross povidone. It may be due to the low density of tablet. The swelling index of HPMC K100 M was found to be higher than that of HPMC K4 M. This may be due to high molecular weight and high viscosity of HPMC K100 M. The formulation F1 containing low level of HPMC K100 M (75 mg) and low level of cross povidone (75 mg) showed higher burst release and maintained drug release up to 24 hours. The tablet was remained floated for 24 hours. High level of HPMC K100 M (F2, F3, F5,F6,) results in greater amount of gel being formed. This gel increases diffusion path length of the drug and hence release rate decreases. On the same line it formulation F5 and F8 should show relatively less drug release as high level of HPMC K100 M(100 mg & 125 mg respectively) is used in these formulations. But both the formulations released more than 97% drug within 24 hours. the formulations F10,F13,F14,F16,F17 released the drug within 20 hours. The formulation F11 which contains high amount of HPMC K4 M than F10 (100mg) and low level of cross povidone (75 mg) shows drug release up to 24 hours with sufficient floating duration. The formulation F15 and F18 contains high level of HPMC K4 M (125mg) and high level of cross povidone (100mg and 125mg) respectively. Both the formulations showed sustained drug release up to 24 hrs. EYWORDS: formulation, floating tablet, cefpodoxime proxetil
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Gunandini, Dwi Jayanti, and P. B. Wicaksana. "Peningkatan dan aktivitas enzim asetilkolinesterase pada nyamuk Aedes aegypti yang diseleksi dengan malation." Jurnal Entomologi Indonesia 2, no. 2 (February 23, 2017): 24. http://dx.doi.org/10.5994/jei.2.2.24.

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The Elevated and Activity of Acetilcholinesterase Enzyme on Aedes aegypti Selected by Malathion. The aim of this research was to study the effect of selection by malathion on the activity level Acetilcholinesterase enzyme on Aedes aegypti mosquitoes. Selection of Aedes aegypti larval by mean of malathion have been conducted for 20 generations. During the selection process time has been increased of concentration applied and exposure. For generation 0-5 (F0-F5), a concentration of 25 µl/l (24 ppm) was used to expose the larvae to malathion for five minutes. In generation 6-10 (F6-F10) the concentration has increased to 50 µl/l (48 ppm); in F11-F15 the concentration used was 100 µl/l (96 ppm) whereas in F16-F20 200µl/l (192 ppm) was used. Mosquito generations that would be regarded as representative and reference groups were F0, F5, F10, F15 and F20. The LC50 of F0, F5, F10, F15 and F20 was 0,025; 0,032; 0,042; 0,062 and 0,071 ppm respectively. Increases LT50 values was also observed in Aedes aegypti selected by malathion. The LT50 of F0, F5, F10, F15 and F20 generations was 7,9; 11,3; 18; 30,6 and 33,1 minutes respectively. The low levels of malathion resistance could be conferred by the elevated of α-esterase. The values of the α-esterase in F0, F5, F10, F15 and F20 were 0,155; 0,174; 0,203; 0,209 and 0,215 µmol/min/mg protein respectively. The acetilcholinesterase activities were also raised in F0, F5, F10, F15 and F20, the value of acetilcholinesterase activities were 20,35; 20,26; 23,14; 23,18 and 24,9%.
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Omphemetse S. Sibanda, Sr. "The Advent of the African Continental Free Trade Agreement as a Tool for Development." Foreign Trade Review 56, no. 2 (April 23, 2021): 216–24. http://dx.doi.org/10.1177/0015732521995171.

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Modelled on the North American Free Trade Agreement (NAFTA), the African Continental Free Trade Agreement (AfCFTA), signed at the Extraordinary Summit of the African Union, which convened in Kigali, Rwanda, on 21 March 2018, is designed to facilitate a single continental trade regulation and integration framework for trade disciplines and intentioned to boost intra-Africa trade. AfCFTA came on the backdrop of not less than eight regional economic communities (RECs), which are loosely regulated. The study finds that AfCFTA can become a beacon of development in the African continent, provided an array of issues including addressing the multiplicity of RECs, putting in place a Development-focused migration and labour policy or developing a side labour agreement similar to that of NAFTA to address other issues like harmonisation of treatment and conditions of workforce and pursuing industrialisation that will help manage the negative spillovers of the Fourth Industrial Revolution (4IR). JEL Codes: C23, F10, F13, F14, F15, F17, F19, K33, K41
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Nurdiana, Dadi, and Rahmi Fatima. "PENGARUH BERBAGAI JENIS FUNGISIDA TERHADAP PERKEMBANGAN JAMUR Fusarium Oxysporum." Jagros : Jurnal Agroteknologi dan Sains (Journal of Agrotechnology Science) 1, no. 1 (April 1, 2018): 22. http://dx.doi.org/10.52434/jagros.v1i1.304.

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Penelitian ini dilakukan untuk mempelajari pengaruh dari berbagai jenis fungisida alami terhadap resiko fusarium penyakit layu (Fusarium oxysporum) in vitro. Percobaan dilakukan di Laboratorium Pertanian, Fakultas Pertanian Universitas Garut September-Oktober 2015. Perlakuan sebanyak 16 yang diulang sebanyak dua kali yang disusun dalam Rancangan Acak Lengkap (RAL). Semua data yang diamati dianalisis dengan uji scott knott. Perlakuannya yaitu: F0 = (Tanpa fungisida), F1 = Chitosan 1%, F2 = Chitosan 2%, F3 = Ekstrak Bayam duri 5%, F4 = Ekstrak Bayam duri 10%, F5 = Ekstrak Bawang putih 5%, F6 = Ekstrak Bawang putih 10%, F7 = Ekstrak Jawer kotok 5%, F8 = Ekstrak Jawer kotok 10%, F9 = Ekstrak kangkung 5%, F10 = Ekstrak kangkung 10%, F11 = Ekstrak Sirih 5%, F12 = Ekstrak Sirih 10%, F13 = Ekstrak serai wangi 5%, F14 = Ekstrak wangi 10%, F15 = fungisida sintetis 3g/liter. Hasil menunjukkan bahwa ekstrak bawang putih dengan konsentrasi 10% (F6) memberi efek terbaik pada penghambatanpertumbuhan hifaF. oxysporumyang ditunjukkan nilai terendah dalam panjang hifa dan diameter penghambatan. Kata kunci: Fungisida alami, Penyakit layu Fusarium, In vitro
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OLIVEIRA, VALTER RODRIGUES, VICENTE WAGNER DIAS CASALI, COSME DAMIÃO CRUZ, PAULO ROBERTO GOMES PEREIRA, and CARLOS ALBERTO SCAPIM. "CAPACIDADE DE COMBINAÇÃO ENTRE LINHAGENS DE PIMENTÃO DIFERINDO NA TOLERÂNCIA AO BAIXO TEOR DE FÓSFORO NO SOLO." Bragantia 57, no. 2 (1998): 203–14. http://dx.doi.org/10.1590/s0006-87051998000200002.

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Seis linhagens de pimentão (Capsicum annuum L.) diferindo na tolerância ao baixo teor de fósforo (P) no solo, os híbridos F1 e seus recíprocos, obtidos de um cruzamento dialélico completo, foram avaliados em casa de vegetação, para estimar as capacidades combinatórias em relação à acumulação de matéria seca total, matéria seca da parte aérea, matéria seca das raízes, razão raiz:parte aérea, área foliar, altura da planta, conteúdo de P total na planta e coeficiente de translocação de P. Ambas as capacidades, geral (CGC) e específica de combinação (CEC), foram estatisticamente significativas, com o componente quadrático associado à CEC superior ao relativo à CGC em todas as características avaliadas, evidenciando predominância de efeitos gênicos não aditivos nos cruzamentos. Linhagens tolerantes à baixa disponibilidade de P exibiram elevadas estimativas positivas da CGC, foram as mais divergentes e seus híbridos revelaram médias elevadas para a maioria das características avaliadas, enquanto comportamento inverso foi apresentado pelas linhagens intolerantes. Levando-se em consideração o desempenho das linhagens, as heteroses e o efeito da CEC, destacaram-se as combinações P-141-190-F16 x P-142-403-F11, P-142-215-F15 x P-142-270-F12, P-141-152-F14 x P-142-215-F15, P-141-152-F14 x P-142-403-F11 e P-141-150-F10 x P-141-152-F14. Não houve ocorrência de diferenças entre cruzamentos recíprocos, em relação às características avaliadas
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Al-Akkam, Entidhar Jasim, and Laila Abdulhussein Alwan. "Formulation and In vitro Evaluation of Piroxicam Conventional and Hollow Suppositories." International Journal of Drug Delivery Technology 10, no. 02 (June 25, 2020): 200–209. http://dx.doi.org/10.25258/ijddt.10.2.3.

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Objective: The objective of this study was to develop higher and rapid release of piroxicam from suppositories of different types (conventional and hollow) using different bases. Methods: Thirteen formulas (F1–F13) were prepared (five were conventional, and the rest were hollow type suppositories) by using different bases, such as, witepsol H35, polyethylene glycols (PEGs) with different ratio and glycerinated gelatin. The prepared suppositories were evaluated for physical properties, such as, hardness, melting time, softening time, and for dissolution profile. Results: All of the prepared suppositories had acceptable physical properties. The maximum percent release of piroxicam was 98, 97, 95, and 91% within 50 minutes were obtained from hollow type suppositories containing piroxicam in a solution form and utilizing witepsol H35 base (F10), glycerinated gelatin base (F13), PEGs 400:4000 (70:30) (F12), and PEGs 200:6000 (70:30) (F11), respectively. Also, they exhibited rapid release of piroxicam, however, F10 and F12 released 65 and 50% of piroxicam within 5 minutes, while, F11 released 57% within 10 minutes. Conclusion: Hollow type suppositories containing piroxicam in a solution form can be considered as the most suitable formulas (F10–F13). So, hollow-type suppository is useful as a promising approach for enhancing the release of piroxicam to be administered rectally. Also, the study revealed that in addition to the type of suppositories, the type of the base, the grade, and the ratio of PEGs bases are other important factors affecting the physical properties of suppositories and the dissolution profile of piroxicam.
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Al-Akkam, Entidhar J., and Laila Abdulhussein Alwan. "Formulation and In vitro Evaluation of Piroxicam Conventional and Hollow Suppositories." International Journal of Drug Delivery Technology 10, no. 03 (September 25, 2020): 477–86. http://dx.doi.org/10.25258/ijddt.10.3.31.

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Objective: The objective of this study was to develop a higher and rapid release of piroxicam from suppositories of different types (conventional and hallow) using different bases. Methods: Thirteen formulas (F1–F13) were prepared (five were conventional and the rest were hollow-type suppositories (HTS)] by using different bases, such as, witepsol H35, polyethylene glycols (PEGs) with a different ratio, and glycerinated gelatin. The prepared suppositories were evaluated for physical properties, such as, hardness, melting time, softening time, and dissolution profile. Results: All of the prepared suppositories had acceptable physical properties. The maximum percent release of piroxicam was 98, 97, 95, and 91% within 50 minutes were obtained from hollow-type suppositories containing piroxicam in a solution form and utilizing witepsol H35 base (F10), glycerinated gelatin base (F13), PEGs 400:4000 (70:30) (F12), and PEGs 200:6000 (70:30) (F11), respectively. Also, they exhibited rapid release of piroxicam however, F10 and F12 released 65 and 50% of piroxicam within 5 minutes, while, F11 released 57% within 10 minutes. Conclusion: Hollow type suppositories containing piroxicam in a solution form can be considered as the most suitable formulas (F10–F13). So, a hollow-type suppository is useful as a promising approach for enhancing the release of piroxicam to be administered rectally. Also, the study revealed that in addition to the type of suppositories, the type of the base, the grade, and the ratio of PEGs bases are other important factors affecting the physical properties of suppositories and the dissolution profile of piroxicam.
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Ernoviya, Ernoviya, Masfria Masfria, and Kasmirul Ramlan Sinaga. "OPTIMIZATION AND EVALUATION OF TOPICAL KETOCONAZOLE NANOEMULSION." Asian Journal of Pharmaceutical and Clinical Research 11, no. 5 (May 1, 2018): 143. http://dx.doi.org/10.22159/ajpcr.2018.v11i5.23540.

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Objective: The present study is to formulate and optimization of surfactant, cosurfactant, and oil of ketoconazole nanoemulsion.Methods: Ketoconazole was dissolved in surfactant, cosurfactant, and oil until saturated, clear solution extracted with methanol, its absorbance was measured using a UV spectrophotometer at 243 nm. Comparisons of surfactants, cosurfactants, and oils are variously varied. Formulation method was performed using spontaneous nanoemulsion method.Results: Surfactants, cosurfactants, and oils used for the nanoemulsion formula are tween 80, ethanol, and isopropyl myristate (IPM). Formulation of ketoconazole nanoemulsion with comparison of tween 80 concentration with ethanol (smix) 4:1 and smix with oil 9:1 was found that the formulae F1, F2, F3, F4, F5, F6, and F7 are unstable and the formulae F8, F9, F10, F11, and F12 are stable at the period of manufacture. The best physical stability tests from F8, F9, F10, F11, and F12 are F10.Conclusions: Optimization of ketoconazole nanoemulsion formula was obtained at Tween 80, 36% concentration, 9% ethanol, and IPM 5%.
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Dissertations / Theses on the topic "F10"

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Badinger, Harald, and Fritz Breuss. "Do small countries of a trade bloc gain more of its enlargement? An empirical test of the Casella effect for the case of the European Community." Forschungsinstitut für Europafragen, WU Vienna University of Economics and Business, 2002. http://epub.wu.ac.at/1732/1/document.pdf.

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Casella (1996) derives theoretically the result that the gains from enlarging a trade bloc fall disproportionately on its small member states. Testing this hypothesis for the Member States of the European Community and its enlargements since 1973, we find mixed results, indicating that such a small country bonus may well exists, but that it is partly neutralized or dominated by economic forces that tend to favour large countries.
Series: EI Working Papers / Europainstitut
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Ferreira, Marianna Boia. "Avaliação do papel da proteína TCTP em melanoma murino (B16-F1 e B16-F10)." reponame:Repositório Institucional da UFPR, 2014. http://hdl.handle.net/1884/49141.

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Orientadora : Profª. Drª. Andrea Senff Ribeiro
Coorientador : Prof. Dr. Silvio Sanches Veiga
Dissertação (mestrado) - Universidade Federal do Paraná, Setor de Ciências Biológicas, Programa de Pós-Graduação em Biologia Celular e Molecular. Defesa: Curitiba, 27/02/2017
Inclui referências : f. 73-83
Resumo: O tumor do tipo melanoma da pele apresenta baixa incidência contudo, sua letalidade é extremamente elevada. As linhagens B16 constituem um modelo de melanoma murino muito útil na oncologia experimental. A linhagem B16F10 apresenta alta capacidade de invasão e metastização enquanto que a linhagem B16-F1 apresenta menor motilidade in vitro e, portanto, baixo potencial metastático. A TCTP (Translationally Controlled Tumor Protein) é expressa em diversos organismos e tecidos, o que aponta um papel biológico fundamental. Diferentes estudos já estabeleceram seu envolvimento na regulação do ciclo e proliferação celular, bem como na malignidade e como fator protetor contra estresse e apoptose. Dessa forma, o objetivo desse trabalho foi avaliar o papel da TCTP em melanoma murino (B16F1 e B16F10). O perfil proteico bidimensional apresentado pelas linhagens foi diferente: a linhagem B16-F10 apresentou 201 spots e a linhagem B16-F1 126 spots. Essa diferença pode estar relacionada à complexidade celular da B16-F10, mais maligna e metastática. Em ambos os extratos foi identificada uma proteína com mobilidade eletroforética de 20 kDa e pI de 4,8 (valores esperados para TCTP). Além disso, a TCTP foi imunodetectada por western blotting. A linhagem B16- F1 apresentou um menor sinal de detecção quando comparada à B16-F10., Essa diferença poderia estar associada a uma maior expressão de TCTP em células tumorais mais metastáticas e invasivas e, consequentemente, a B16F10 apresentaria níveis superiores de TCTP. Esta hipótese foi confirmada por PCR em tempo real: B16-F10 apresentou níveis de RNAm para TCTP superiores aos encontrados para B16-F1. Esses dados corroboram com os resultados do western blotting e com dados da literatura que relacionam a TCTP à linhagens malignas, devido ao seu papel anti-apoptótico e seu antagonismo com a p53. A fim de avaliar o papel biológico da TCTP no melanoma, esta foi silenciada na linhagem B16-F10, utilizando a técnica de RNAi. O silenciamento diminuiu os níveis de TCTP em 50 a 70% quando utilizado 50 nM e 60 a 80% quando utilizado 100 nM do duplex após 24, 48 e 72 horas de transfecção. As linhagens transfectadas com RNAi para TCTP apresentaram menor proliferação, menor migração e maior adesão celular às moléculas da matriz extracelular quando comparadas às linhagens transfectadas com o controle negativo. Porém, não houve qualquer alteração significativa da viabilidade celular. O aumento da proliferação celular e do potencial migratório são dois eventos muito importantes para a tumorigênese, e estão intimamente relacionados à malignidade. Portanto, o silenciamento foi capaz de regredir o fenótipo de malignidade da linhagem B16-F10, deixando esse mais próximo da B16-F1. Dessa forma, nosso estudo caracterizou os perfis celulares das duas linhagens e demonstrou uma diferença no número de proteínas e parceiros moleculares entre ambas linhagens. Além disso, nossos dados sugerem que o silenciamento da TCTP tornou a linhagem B16-F10 menos metastática e maligna, com um fenótipo mais próximo ao de uma célula normal. Mais estudos são necessários com o intuito de identificar possíveis parceiros e melhor entender o papel dessa proteína multifuncional no melanoma murino. Palavras-chave: TCTP, melanoma, B16-10, B16-F1, câncer
Abstract: Skin melanoma tumor displays low incidence, however, its lethality is extremely high. B16 cell lines typify a murine melanoma model very useful on the experimental oncology field. B16-F10 cell line exhibits high invasion and metastization capacities while B16-F1 cell line depicts lower in vitro motility and, therefore, low metastasis potential. TCTP (translationally controlled tumor protein) is expressed in several organisms and tissues, which suggests a fundamental biological role. Different studies have already settled its participation in cell cycle regulation and cell proliferation, as well as in malignancy and as a protective factor against stress and apoptosis. Thus, this study aimed to assess the TCTP role in in murine melanoma (B16-F1 and B16- F10). Two-dimensional electrophoresis profiles of proteins from the two cell lines were different: B16-F10 cells presented 201 electrophoresis spots while B16-F1 originated 126 spots. This difference may be related to the B16-F10 cell complexity, since this cell line is more malignant and metastatic. In both cell extracts was identified a protein with electrophoretic mobility about 20 kDa and deduced pI of 4.8 (expected parameters for TCTP). Furthermore, TCTP was immunodetected by western blotting analysis. B16-F1 cells produced low detection signals when compared to the B16-F10 cells. This difference may be associated to the higher TCTP expression in more metastatic and invasive tumoral cells and, consequently, B16-F10 would present higher TCTP levels. This hypothesis was confirmed by Real-Time PCR, since B16-F10 revealed RNAm levels for TCTP higher than the B16-F1. These data corroborate with western blotting results and the specific literature, which connect TCTP and malignant cell lines due to the anti-apoptotic function and its p53 antagonism. In order to evaluate the biological role of TCTP in melanoma, it was performed the TCTP silencing in B16-F10 cell line by using RNA interference (RNAi) method. The gene silencing reduced TCTP levels in 50% to 70% when used 50 nM and 60% to 80% when used 100 nm of the duplex after 24, 48 and 72 hours of transfection. The transfected cell lines with RNAi for TCTP presented lower proliferation, lower migration and higher cell adhesion to extracellular matrix molecules when compared to the cell lines transfected with negative control. However, there was no significant change in cell viability. Increasing cell proliferation and migration potential are two events very important for the tumorigenesis process and they are closely related to the malignancy. Therefore, gene silencing was able to recede the malignant phenotype of B16- F10 cell line, resulting in a similar aspect to the B16-F1 cells. Thus, this study characterized the profile of two cell lines and it demonstrated differences in protein number and molecular partners between these two cell lines. Moreover, the generated data suggest that TCTP gene silencing became B16-F10 cells less metastatic and malignant, resembling the normal cell phenotype. Further studies are necessary in order to identify possible partners and to better understand the TCTP role in the murine melanoma. Key-words: TCTP, melanoma, B16-10, B16-F1, cancer.
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Badinger, Harald, and Kemal Türkcan. "Currency unions, export margins, and product differentiation: an empirical assessment for European Monetary Union." Wiley, 2014. http://dx.doi.org/10.1111/roie.12094.

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This paper reconsiders the trade effects of the euro, providing a decomposition into its effects on the extensive margin and intensive margin. Furthermore, it relates the more disaggregated estimates for 93 two-digit HS product groups to the elasticity of substitution, thereby testing a key hypothesis of recent trade theory. The estimates for the period 1996-2011 suggest a trade effect of the euro of some 28 percent, which has mainly materialized through the intensive margin. For several product groups, we find a negative net effect of the euro on the extensive margin, supporting anecdotal evidence that firms have consolidated their product varieties in response to the elimination of exchange rate variability. Finally, the disaggregated estimates are in line with recent trade theory, suggesting that a large elasticity of substitution dampens the effect of a trade cost reduction on the extensive margin and amplifies its effect on the intensive margin.
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Dawid, Herbert. "Learning to trade and mediate." SFB Adaptive Information Systems and Modelling in Economics and Management Science, WU Vienna University of Economics and Business, 1997. http://epub.wu.ac.at/952/1/document.pdf.

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In this paper we study the behavior of boundedly rational agents in a two good economy where trading is costly with respect to time. All individuals have a fixed time budget and may spend time for the production of good one, the production of good two and trading. They update their strategies, which determine their time allocation, according to a simple imitation type learning rule with noise. In a setup with two different type of agents with different production technologies we show by the means of simulations that both direct trade and trade via mediators who specialize in trading can emerge. We can also observe the transition from a pure production economy via direct trade to an economy with mediated trade. (author's abstract)
Series: Report Series SFB "Adaptive Information Systems and Modelling in Economics and Management Science"
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Bellak, Christian. "Gaining and losing competitive advantage." Inst. für Volkswirtschaftstheorie und -politik, WU Vienna University of Economics and Business, 2003. http://epub.wu.ac.at/1414/1/document.pdf.

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Efficient policies to stimulate the competitiveness of firms require knowledge of future firm-strategies and a proper assessment of the location advantages of a country or region. Therefore, industry comparative advantage analysis needs to be complemented by firm competitive advantage analysis. This yields four hypotheses of firm strategies on the basis of the existing advantage combination. Detailed empirical analysis of a representative sample of Austrian manufacturing firms during 1990- 2000 shows that changes in employment, value-added and exports are in line with the suggested development. Three of the 3-digit industries lost their advantages while seven industries gained advantages, yet overall industry distribution has been remarkable stable over the four advantage combinations. In terms of number of firms, however, a large share (30%) of the total population shifts between advantage combinations even during short periods of time. The firm strategies outlined suggest a differentiated policy approach, yet the short-term dynamics revealed empirically imply a high potential for policy failure.
Series: Working Papers Series "Growth and Employment in Europe: Sustainability and Competitiveness"
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Gong, Xuan Verfasser], Jürgen [Akademischer Betreuer] Schrader, and Wolfgang Arthur [Akademischer Betreuer] [Schulz. "Rolle der CD73 bei B16-F10-induzierter Tumorprogression / Xuan Gong. Gutachter: Jürgen Schrader ; Wolfgang A. Schulz." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2014. http://d-nb.info/1062696778/34.

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Gong, Xuan [Verfasser], Jürgen Akademischer Betreuer] Schrader, and Wolfgang Arthur [Akademischer Betreuer] [Schulz. "Rolle der CD73 bei B16-F10-induzierter Tumorprogression / Xuan Gong. Gutachter: Jürgen Schrader ; Wolfgang A. Schulz." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2014. http://d-nb.info/1062696778/34.

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Roser, Max, and Cuaresma Jesus Crespo. "Why is Income Inequality Increasing in the Developed World?" Wiley, 2016. http://dx.doi.org/10.1111/roiw.12153.

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We address empirically the factors affecting the dynamics of income inequality among industrialized economies. Using a panel for 32 developed countries spanning the last four decades, our results indicate that the predictions of the Stolper-Samuelson theorem concerning the effects of international trade on income inequality find support in the data if we concentrate on imports from developing countries as a trade measure, as theory would imply. We find that democratization, the interaction of technology and education and changes in the relative power of labour unions affect inequality dynamics robustly.
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Tuchman, Jolante [Verfasser]. "Die Effekte der Implementierung von Behandlungspfaden in der stationären Behandlung der Alkoholabhängigkeit (CD-10:F10) / Jolante Tuchman." Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2018. http://d-nb.info/1160514755/34.

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Marrero, Bernadette. "Evaluation of Immunogene Therapy Using a Plasmid Encoding IL-15 Delivered by Electroporation in a 3D Tumor Model and a Mouse Melanoma Model." Scholar Commons, 2010. http://scholarcommons.usf.edu/etd/3520.

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Melanoma is an aggressive disease with few effective treatment options. Non-toxic, anti-tumor therapies and prophylactic approaches are currently being investigated to identify treatment options that will control and remove late-stage melanoma. The overall goal of this project was to establish an effective delivery method for a plasmid encoding human interleukin (phIL-15) into mouse melanoma cells (B16.F10) using the gene transfer technique electroporation (EP)1. The EP delivery phIL-15 was optimized using an in vitro 3D tumor model. The purpose was to translate these IL-15 delivery conditions into an in vivo mouse melanoma model to study IL-15 signal transduction and stimulate immune cells to destroy tumor antigens as well as promote an anti-tumor immune memory response. The in vitro 3D tumor model and the mouse model demonstrated similar expression patterns when delivering phIL-15 with different EP conditions. Intra-tumoral delivery using 500V/cm 20ms enhanced gene delivery and increased IL-15 protein expression compared to 1300V/cm 100μs. There was also a visible increase in transfection efficacy between tumor cells compared to skin cells when delivering pmIL-12 and phIL-15 plasmid constructs in vivo. The plasmid+EP groups 1300V/cm and 500V/cm stimulated increased expression of cytokines IL-1β, IL-6, INFγ, MIP-1β and TNFα. These EP groups also promoted tumor regression by up-regulating CD8+ T cells and CD4+ T cells which targeted melanoma. Regression and survival studies demonstrated that 73.3% of mice cleared B16.F10 cells when treated with phIL-xi15+1300V/cm and pVax+500V/cm. In addition, 53% of the mice responded to the phIL-15+500V/cm treatment group. Furthermore, 75% of the mice from group phIL-15+500V/cm survived secondary inoculation and tumor challenge. In conclusion, plasmid with encoding gene insert phIL-15 delivered by EP has the potential to act as an anti-tumor therapy because it promotes melanoma regression and enhances mouse survival through innate and adaptive cell-mediated immune responses.
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Books on the topic "F10"

1

Auteur, Bouchon Benjamin, ed. Mathématiques: Premières F (F1, F2, F3, F4, F5, F6, F9, F10) : nouveaux programmes. [Paris]: Nathan Technique, 1986.

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Pennington, Nancy J. FASINEX moored current meter array data report including WHOI meteorologically instrumented surface moorings (F2-845, F4-846, F6-847. F8-848. F10-849) and WHOI long term subsurface moorings (F1-829, F12-830). Woods Hole, Mass: Woods Hole Oceanographic Institution, 1988.

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Foster, Peter R. Century series fighters: F100 Super Sabre--F106 Delta Dart. Osceola, WI, USA: Motorbooks Internatoinal, 1992.

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Nikon F90. Rochester, NY: Saunders Group, 1993.

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Günter, Richter. Nikon N50, F50. Rochester, NY: Silver Pixel Press, 1994.

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Nikon N50/F50. Rochester, N.Y: Silver Pixel, 1994.

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Nikon N70, F70. Rochester, NY: Silver Pixel Press, 1995.

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Günter, Richter. Nikon N70, F70. Rochester, NY: Silver Pixel Press, 1995.

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Clements, John. Nikon F90, N90. Jersey, Channel Islands: Hove Foto Books, 1993.

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Camm, Frank A. The development of the F100-PW-220 and F110-GE-100 engines: A case study of risk assessment and risk management. Santa Monica, CA (P.O. Box 2138, Santa Monica 90407-2138): Rand, 1993.

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Book chapters on the topic "F10"

1

Ulatowski, Heike. "Störungen durch psychotrope Substanzen (F10–F19)." In Pflegeplanung in der Psychiatrie, 31–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48546-0_6.

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Bradnock, Tim J., and Graham Haddock. "F10 Open Orchidopexy." In Basic Techniques in Pediatric Surgery, 404–6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-20641-2_123.

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Schöpf, Josef. "F10–F19: Psychische und Verhaltensstörungen durch psychotrope Substanzen." In Psychiatrie für die Praxis, 82–128. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-97592-9_9.

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Rothenhäusler, Hans-Bernd, and Karl-Ludwig Täschner. "Psychische und Verhaltensstörungen durch psychotrope Substanzen (F10–F19)." In Kompendium Praktische Psychiatrie, 233–76. Vienna: Springer Vienna, 2012. http://dx.doi.org/10.1007/978-3-7091-1237-3_5.

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Phull, Jaspreet. "Mental and behavioural disorders due to psychoactive substance use (F10–F19)." In ICD-10 in Psychiatry, 41–45. London: CRC Press, 2021. http://dx.doi.org/10.4324/9781846198618-3.

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Pena, S. D. J., P. C. Santos, M. C. B. N. Campos, and A. M. Macedo. "Paternity testing with the F10 multilocus DNA fingerprinting probe." In DNA Fingerprinting: State of the Science, 237–47. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-8583-6_20.

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Ulatowski, Heike. "Gerontopsychiatrische Störungen (F00–F01)." In Pflegeplanung in der Psychiatrie, 265–85. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48546-0_12.

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Poljak-Blazi, M., A. Ferle Vidovic, V. Rapic, and D. Škare. "Antiproliferative Ability of Ferric-Sorbitol-Citrate and Ferrocenes for Malignant Cell Line, Hep2 and F10." In Trace Elements in Man and Animals 10, 135–36. New York, NY: Springer US, 2002. http://dx.doi.org/10.1007/0-306-47466-2_29.

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Sick, Henri, and Francis Veillon. "Frontal Sections F1–F30." In Atlas of Slices of the Temporal Bone and Adjacent Region, 45–105. Munich: J.F. Bergmann-Verlag, 1988. http://dx.doi.org/10.1007/978-3-642-80516-5_4.

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Sick, Henri, and Jean-Louis Burguet. "Frontal Slices F1–F13." In Imaging Anatomy of the Knee Region, 5–31. Munich: J.F. Bergmann-Verlag, 1988. http://dx.doi.org/10.1007/978-3-642-80519-6_3.

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Conference papers on the topic "F10"

1

González Espinoza, Jorge. "PATOLOGIA DUAL FORENSE." In 23° Congreso de la Sociedad Española de Patología Dual (SEPD) 2021. SEPD, 2021. http://dx.doi.org/10.17579/sepd2021o008.

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El año 2005, se promulga la Reforma Procesal Penal en Chile, pasando a ser un sistema acusatorio oral; en este contexto, están los Peritos Psiquiátricos, con el rol de diagnosticar y entregar conclusiones; junto con ello dar cumplimiento de garantías de accesibilidad, oportunidad y tratamiento en duales - forenses. Objetivos: Diagnosticar y Cuantificar Patología Dual en imputados del sistema judicial. Material: Fichas Institucionalizadas(2014-2016) computarizadas Método Revisión de contenidos bio sicosociales, diagnostico CE10y conclusiones forenses Resultados 121 imputados; hombres 104 , mujeres 17 Edad: 21 a 40 a = 56,4% ; de 51 y más 9% EstadoCivil Sin pareja 101 Escolaridad: Básica (60%) Media (32%), Superior (8.%) Actividad Laboral Con trabajo (63.6%), sin trabajo (36.4%). Etnia: Indígena (3.3%), Blanca (96.7%) Credo: Católicos (31.4%), Evangélicos (49.5%), Sin credo (19%) Red Familiar: Con (27.3%), Sin (72,7%). Patologías no adictivas (F0) =9 , (F20)=20 (F30) =17, (F40)=1, (F6, F65.2) =35, (F70)=7, (F90)=14 .Sin consignar 3. Patologías Adictivas (F10)6, (F14)5, (F18)2, (F13)1, (F 19)55. Dualidad más habitual: F-10 / T. Orgánicos F-11 -F-12/Esquizofrenia F-14 /T. Afectivos /T. Personalidad, Diagnósticos: No adicto (25.6%) , Adicto (14%) , Duales (54.5%), Sin Diagnóstico (5.7%). Conclusiones Delitos: Robos 44, Abuso Sexual 19, Homicidio10, 1, Violencia Intrafamiliar15, Desacato 17,sin delito 4. Forenses: Responsables 54.5%) Disminuida (14%), No Responsables (23.9%) Los Imputados Duales (66) , presentan importantes diferencias con otros pacientes Duales, mayoritariamente están en la edad media de la vida, con importante incidencia de alcoholismo y Cluster B (23) Hombre /Mujer (6 a 1) mayormente bajo nivel de escolaridad, sin pareja/apoyo familiar, relevante cantidad de Evangélicos, mayoritariamente sin oficio, Responsabilidad Penal (54.5%). Se hace necesario implementar programas, para imputados Duales con el fin de lograr una inserción real a la sociedad.
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Thaker, Shrey, William H. Gmeiner, Ping Ji, Jovanny Zabaleta, Tiana Reyes, Matthew DiGiovanni, Xuefeng Wang, and Jennie L. Williams. "Abstract 1842: F10 and 5-fluorouracil: Chemotherapeutic potential of F10 in alleviating colon cancer racial health disparity." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-1842.

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Cialla, D., K. Weber, J. Popp, S. Pahlow, and A. März. "F10 - Nanoflower-based SERS active particles for chemosensing." In 11. Dresdner Sensor-Symposium 2013. AMA Service GmbH, Von-Münchhausen-Str. 49, 31515 Wunstorf, Germany, 2013. http://dx.doi.org/10.5162/11dss2013/f10.

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Besztercei, Balázs, Enikő Major, Anett Benedek, Zoltán Benyó, and Andrea Balogh. "Abstract 196: The effect of modulated electro-hyperthermia on B16-F10 melanoma tumor growth." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-196.

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Mwita, W. M., and E. T. Akinlabi. "Numerical Investigation on Strain Properties of Ti6Al4V Alloy Processed by Constrained Bending and Straightening Severe Plastic Deformation." In ASME 2019 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/imece2019-11163.

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Abstract This paper presents a numerical investigation on strain properties of Ti6Al4V alloy processed by constrained bending and straightening (CBS) severe plastic deformation (SPD) technique. CBS is a new SPD method that has been proposed to enhance continuous processing of metal sheets and improve magnitude and homogeneity of induced properties such as strain. The model considers a rectangular sheet of Ti6Al4V alloy processed with CBS at 2, 4 passes denoted as N2, N4 each combined with 10, 5, 3 mm feed length denoted as F10, F5, F3 respectively. ABAQUS Standard FEA Software was used to simulate and investigate the magnitude and homogeneity of equivalent plastic (EP) strain induced in material. Results show that for all feeds, magnitude values of EP strain at N4 passes were higher than those at N2 passes. The magnitude of EP strain increased with the number of passes. Values of both magnitude and homogeneity of EP strain were highest at F3 feed followed by those at F5 and F10 feeds respectively. The study has promised that CBS is the potential process for continuous production of metal sheets with improved EP strain magnitude and homogeneity.
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Gmeiner, William H., Chinnadurai Mani, and Komaraiah Palle. "Abstract 2828: MMR status affects efficiency of homologous recombination repair of F10-induced DNA DSBs." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-2828.

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"Moving window analysis links landscape-scale resource utilization to habitat suitability models of feral pigs in northern Australia." In 21st International Congress on Modelling and Simulation (MODSIM2015). Modelling and Simulation Society of Australia and New Zealand, 2015. http://dx.doi.org/10.36334/modsim.2015.f10.froese.

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"A GIS tool for land and water use planning in mining regions." In 21st International Congress on Modelling and Simulation (MODSIM2015). Modelling and Simulation Society of Australia and New Zealand, 2015. http://dx.doi.org/10.36334/modsim.2015.f10.lechner.

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"Modelling structures of terrain surface using GIS in Loess Plateau." In 21st International Congress on Modelling and Simulation (MODSIM2015). Modelling and Simulation Society of Australia and New Zealand, 2015. http://dx.doi.org/10.36334/modsim.2015.f10.wang.

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"Land use decisions under uncertainty: optimal strategies to switch between agriculture and afforestation." In 20th International Congress on Modelling and Simulation (MODSIM2013). Modelling and Simulation Society of Australia and New Zealand, 2013. http://dx.doi.org/10.36334/modsim.2013.f10.bao.

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Reports on the topic "F10"

1

Chiang I. H., R. DiFranco, C. B. Eld, J. Funaro, J. W. Glenn, R. Lockey, and A. McNerney. Contribution of F5, F10 Extraction Magnets to Slow Spill. Office of Scientific and Technical Information (OSTI), June 1986. http://dx.doi.org/10.2172/1130918.

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Gill E., J. W. Glenn, J. Funaro, C. Gardner, and W. van Asselt. Study of the Effect on Injection of D.C. Powering F10 Extraction Septum Magnet. Office of Scientific and Technical Information (OSTI), June 1987. http://dx.doi.org/10.2172/1131557.

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Bailey, David, and Sean Morefield. Investigation of Natural Cementation to Mitigate Corrosion-Promoting Characteristics of Unsurfaced Roadways : Final Report on Project F10-AR06. Construction Engineering Research Laboratory (U.S.), August 2018. http://dx.doi.org/10.21079/11681/28183.

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McInerney, Michael, Christopher Athmer, and Lawrence Clark. Demonstration and validation of single-well electro-osmotic dewatering systems for corrosion mitigation : final report on Project F10-AR07. Construction Engineering Research Laboratory (U.S.), June 2018. http://dx.doi.org/10.21079/11681/27271.

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Wilson, Rebekah, and Lawrence Clark. Demonstration of antimicrobial corrosion-resisting interior coating systems for military facilities in warm, humid locations : final report on Project F10-AR04. Construction Engineering Research Laboratory (U.S.), June 2017. http://dx.doi.org/10.21079/11681/22647.

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Ooi, Phillip, and Michelle Coskey. Laboratory investigation of natural cementation road surfacing for corrosion control of aluminum on Army vehicles : contractor’s supplemental report for Project F10-AR06. Construction Engineering Research Laboratory (U.S.), May 2018. http://dx.doi.org/10.21079/11681/26824.

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Richard Metcalf. Safeguards Envelope Progress FY10. Office of Scientific and Technical Information (OSTI), October 2010. http://dx.doi.org/10.2172/1004253.

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Tommasini, R. FY10 LLNL OMEGA Experimental Programs. Office of Scientific and Technical Information (OSTI), September 2010. http://dx.doi.org/10.2172/1124919.

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Ethington, P. R. Concentrator E-F11 water test. Office of Scientific and Technical Information (OSTI), February 1994. http://dx.doi.org/10.2172/10153902.

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Lane, M., S. Aceves, C. Paulson, J. Candy, C. Bennett, K. Carlisle, D. Chen, et al. FY10 Engineering Innovations, Research and Technology Report. Office of Scientific and Technical Information (OSTI), January 2011. http://dx.doi.org/10.2172/1018760.

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