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Relevant bibliographies by topics / Gen Beta

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Academic literature on the topic 'Gen Beta'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Gen Beta"

1

Fitria, Murni, Anggi Saputra, Rahmat Hidayat, and Niken Feladita. "Analisis Protein Gen LCYB pada Mikroalga Laut Phaeodactylum tricornutum menggunakan Pendekatan Bioinformatika." IJCA (Indonesian Journal of Chemical Analysis) 5, no. 2 (2022): 138–44. http://dx.doi.org/10.20885/ijca.vol5.iss2.art8.

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LCYB merupakan gen yang memproduksi enzim Lycopene Beta Cyclase. Enzim Lycopene Beta Cyclase beperan dalam mengubah likopen menjadi ß-karoten. Gen LCYB terdapat pada diatom maupun mikroalga hijau. Berbeda dengan mikroalga hijau, penelitian mengenai struktur protein Lycopene Beta Cyclase selaku produk gen LCYB pada diatom masih minim publikasi. Dalam penelitian ini dilakukan prediksi struktur produk gen LCYB pada diatom P. tricornutum secara bioinformatika. Untuk menganalisis perbedaan produk gen LCYB pada diatom dan mikroalga hijau, produk gen LCYB pada diatom P. tricornutum dibandingkan denga

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Widyawati, Keri Ayu, Suliati, Anita Dwi Anggraini, and Wisnu Istanto. "Deteksi Gen blaTEM Dari Bakteri Klebsiella Pneumoniae Penghasil Extended Spectrum Beta-Lactamase (ESBL) Pada Pasien Infeksi Saluran Kemih." Jurnal Media Analis Kesehatan 15, no. 2 (2024): 158–66. https://doi.org/10.32382/jmak.v15i2.814.

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Infeksi saluran kemih merupakan infeksi yang terjadi pada saluran uretra dan kandung kemih yang disebabkan oleh bakteri Klebsiella pneumoniae salah satunya. Pengobatan atau terapi yang sering digunakan untuk penderita infeksi saluran kemih yakni dengan pemberian antibiotik golongan beta-laktam. Namun, terdapat beberapa bakteri yang memiliki enzim beta-laktamase yang merupakan salah satu penyebab bakteri resisten terhadap antibiotik. Enzim tersebut dikodekan oleh gen salah satunya gen TEM yang dapat menghidrolisis antibiotik golongan beta-laktam. Tujuan studi ini untuk mendeteksi gen blaTEM ter

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Pujianto, Dwi Ari, Andika Setyoadi, and Asmarinah ,. "Study of Expression and Regulation of Mouse Beta-Defensin 2 as a Model for Understanding Its Role in the Process of Sperm Maturation." Jurnal Biotek Medisiana Indonesia 9, no. 2 (2021): 128–38. http://dx.doi.org/10.22435/jbmi.v9i2.4417.

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Abstrak Beberapa gen yang terekspresi spesfik di epididimis diduga terlibat dalam proses pematangan sperma. Ekspresi gen spesifik di epididimis dipengaruhi oleh androgen, faktor testikuler, dan terekspresi pada masa pubertas. Famili gen yang cukup banyak ditemukan terekspresi di epididimis adalah beta-defensin, salah satunya yaitu beta-defensin 2 (Defb2). Penelitian ini bertujuan untuk mengkarakterisasi gen Defb2 terkait dengan perannya pada proses pematangan sperma. Analisis bioinformatika digunakan pada penelitian ini untuk mendapatkan informasi mengenai struktur gen, signal peptide, d

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Dr.A.Shaji, George. "The Beta Generation: How AI, Climate Change, and Technology Will Shape the Next Wave of Humans." Partners Universal International Innovation Journal (PUIIJ) 02, no. 06 (2024): 1–8. https://doi.org/10.5281/zenodo.14626033.

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The arrival of Generation Beta, which includes people born between 2025 and 2039, marks a significant transition in the course of human history. As the first generation to mature in a world where technology and artificial intelligence are intricately connected with daily life, Gen Beta will be influenced by an unprecedented number of influences. Climate change, economic uncertainty, and social pressures will all be very hard to deal with, but this generation is ready to rise to the task with a unique mix of creativity, resilience, and AI-driven innovation. According to a report from the Pew Re

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Quỳnh, Bạch Thị Như, Nguyễn Hải Bằng, Hà Thị Thu, Nguyễn Văn Thảnh та Dương Quốc Chính. "Tạo thư viện chứng dương cho xét nghiệm sinh học phân tử chẩn đoán bệnh Beta Thalassemia". Tạp chí Nghiên cứu Y học 151, № 3 (2022): 9–17. http://dx.doi.org/10.52852/tcncyh.v151i3.641.

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Beta Thalassemia là bệnh thiếu máu tan máu bẩm sinh gây ra bởi sự bất thường về di truyền trên gen beta-globin (HBB) để lại hậu quả nghiêm trọng về sức khỏe, ảnh hưởng tới giống nòi và là gánh nặng cho gia đình và xã hội. Xét nghiệm phát hiện sớm người mang gen bệnh bằng kỹ thuật sinh học phân tử hiện nay sử dụng chứng dương tách chiết từ máu của người mang đột biến, dẫn tới sự không đồng nhất về chất lượng, sự thiếu hụt nguồn chứng dương đặc biệt là những đột biến hiếm. Mục tiêu: tạo thư viện chứng dương cho 8 đột biến trên gen HBB. Đối tượng và phương pháp: 1456 bệnh nhân tiến hành sàng lọc

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Febrianto, Yahya, Ana Indrayati, and Elfahmi . "Deteksi Molekuler Ekson 2 Gen Beta Globin pada Pasien Beta Talasemia Mayor di RSUD DR. Soeroto Ngawi menggunakan Metode Polymerase Chain Reaction- Single Strand Conformation Polimorfism." Jurnal Farmasi Indonesia 15, no. 1 (2019): 1–12. http://dx.doi.org/10.31001/jfi.v15i1.350.

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Beta talasemia adalah kelainan darah herediter akibat kelainan genetik pada genglobin.Hal ini menyebabkan kerusakan pada sel darah merah sehingga harus dilakukantransfusi darah secara teratur.Penelitian ini bertujuan mengetahui adanya mutasi pada ekson 2 gen beta globin daripasien talasemia menggunakan metode PCR-SSCP.Sebanyak 5 sampel diisolasi DNA dandiamplifikasi dengan metode PCR.Selanjutnya hasil amplifikasi dikarakterisasi dengan metodeelektroforesis. Region 2 gen beta globin merupakan hasil amplifikasi dari primer forward 4 danprimer reverse 5 dengan ukuran target 350 bp. Produk PCR dar

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Huda, Choirul, Ana Indrayati, and Elfahmi Elfahmi. "Deteksi Molekuler Ekson 3 Gen Beta Globin pada Pasien Beta Talasemia Mayor di RSUD DR. Soeroto Ngawi menggunakan Metode Polymerase Chain Reaction- Single Strand Conformation Polimorfism." Jurnal Farmasi Indonesia 16, no. 1 (2019): 24–33. http://dx.doi.org/10.31001/jfi.v16i1.484.

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Talasemia merupakan penyakit genetik yang menyebabkan gangguan sintesis rantai globin, komponen utama molekul hemoglobin. dengan adanya sintesis rantai globin yang tidak seimbang maka akan menurunkan produksi sel darah merah. Penelitian ini bertujuan mengetahui adanya mutasi pada ekson 3 gen beta globin pasien talasemia menggunakan metode PCR, dimana 5 sampel di isolasi DNA dan dilanjutkan amplifikasi PCR, hasil amplifikasi dielektroforesis region IV gen beta globin Region IV merupakan hasil amplifikasi dari primer forward 8 dan primer reverse 9 dengan target yaitu 214 bp, pada PCR terja

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Supriadi, Agus, Ana Indrayati, and Elfahmi Elfahmi. "DETEKSI MOLEKULER EKSON 1 GEN BETA GLOBIN PADA PASIEN TALASEMIA BETA MAYOR DI RSUD DR. SOEROTO NGAWI DENGAN METODE POLYMERASE CHAIN REACTION (PCR)." Jurnal Farmasi Indonesia 14, no. 2 (2019): 191–200. http://dx.doi.org/10.31001/jfi.v14i2.372.

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Talasemia merupakan kelainan akibat mutasi gen yang bersifat autosumal resesif yang disebabkan kekurangan sintesis rantai globin pembentuk hemoglobin darah dengan gejala mirip anemia maka akan menurunkan produksi sel darah merah, dan harus dilakukan penanganan dengan dilakukan transfusi darah secara teratur.Penelitian ini bertujuan mengetahui adanya mutasi pada ekson 1 gen beta globin pasien talasemia menggunakan metode PCR, dimana 5 sampel di isolasi DNA dan dilanjutkan amplifikasi PCR, hasil amplifikasi dielektroforesis region 1 gen beta globin Region I merupakan hasil amplifikasi dari prime

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Yuwono, Yuwono. "Identifikasi Gen SHV pada Enterobacteriaceae Produsen Extended-Spectrum Beta-Lactamases (ESBLs)." Syifa' MEDIKA: Jurnal Kedokteran dan Kesehatan 4, no. 1 (2013): 9. http://dx.doi.org/10.32502/sm.v4i1.1413.

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Salah satu problem resistensi terhadap antimikroba terutama di rumah sakit adalah kelompokEnterobacteriaceae yang memproduksi Extended-Spectrum Beta-Lactamases (ESBLs). Tujuanpenelitian ini adalah untuk mengidentifikasi gen SHV pada Enterobacteriaceae produsen ESBLs padapasien yang dirawat di RSUP Mohammad Hoesin Palembang. Didapatkan 75 sampelEnterobacteriaceae berdasarkan uji Double Disk Approximation dan PCR. Spesies yang ditemukanadalah Klebsiella pneumoniae 30 (40,00%), Escherichia coli 17 (22,66%), Enterobacter sp 14(18,67%), Proteus Sp 12 (16,00%), dan Acinetobacter calcoaceticus 2 (2,6

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Lestari, Ida, Pestariati Pestariati, and Sri Sulami Endah Astuti. "Deteksi Gen Tem (Temoneira) dari Isolat Klinis Escherichia Coli Penghasil Extended Spectrum Beta Lactamases (ESBL) Pasien Penderita Infeksi Saluran Kemih." Malahayati Nursing Journal 5, no. 1 (2023): 173–83. http://dx.doi.org/10.33024/mnj.v5i1.7832.

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ABSTRACT Urinary tract infection (UTI) is a most common infectious disease. The prevalence of UTIs in Indonesia is estimated at 180.000 per year and can affect people of all ages. In East Java, the number of cases of Urinary Tract Infection reaches 3-4 cases per 100,000 population per year. The most dominant urinary tract infection is caused by Escherichia coli bacteria from the multidrug-resistant Gram-negative group, such as producing of Extended Spectrum Beta Lactamases (ESBL). Extended Spectrum Beta-Lactamases (ESBLs) are Beta- Lactamase enzymes which ability can cause bacteria resistant t

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Dissertations / Theses on the topic "Gen Beta"

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Heydenreich, Monika. "Phänotypische Charakterisierung von Patienten mit hypertropher Kardiomyopathie und Varianten im [beta]-MHC-Gen [beta-MHC-Gen] und [alpha]-Tropomyosin-Gen [alpha-Tropomyosin-Gen]." [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=965437485.

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Heydenreich, Monika. "Phänotypische Charakterisierung von Patienten mit hypertropher Kardiomyopathie und Varianten im Beta-MHC-Gen und Alpha-Tropomyosin-Gen." Doctoral thesis, Humboldt-Universität zu Berlin, Medizinische Fakultät - Universitätsklinikum Charité, 2002. http://dx.doi.org/10.18452/14777.

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Die hypertrophe Kardiomyopathie ist eine autosomal dominant vererbte Herzmuskelerkrankung. Es kommt zu einer asymmetrischen Hypertrophie insbesondere des Herzmuskels. Symptome sind unspezifisch und reichen von Dyspnoe bis hin zu Synkopen. Gelegentlich ist der plötzliche Herztod die erste Manifestation der Erkrankung. Molekulargenetische Untersuchung des Genomes dieser Patienten zeigten, dass diese Patienten Mutationen im Proteinen des Sarkomers aufwiesen. Hierunter fällt das beta-MHC-Gen und alpha-Tropomysin-Gen. Wir untersuchten 45 nicht miteinanderverwandte Patienten auf Mutationen im beta

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Reinisch, Veronika. "Einfluss genetischer Polymorphismen im Interleukin-1 beta Gen auf kognitive Phänotypen." Diss., lmu, 2007. http://nbn-resolving.de/urn:nbn:de:bvb:19-71766.

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Götz, Thomas. "Charakterisierung von Tabaktransformanten mit einem bakteriellen beta-Carotin-Hydroxylase-Gen (crtZ) /." [S.l. : s.n.], 2001. http://www.bsz-bw.de/cgi-bin/xvms.cgi?SWB9423827.

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Biele, Janita. "Untersuchung der Assoziation von Einzelnukleotidpolymorphismen im Fibrinogen-alpha- und -beta-Gen mit dem Myokardinfarkt." kostenfrei, 2009. http://mediatum2.ub.tum.de/node?id=683771.

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Heydenreich, Monika Verfasser], and Vera [Gutachter] [Regitz-Zagrosek. "Phänotypische Charakterisierung von Patienten mit hypertropher Kardiomyopathie und Varianten im Beta-MHC-Gen und Alpha-Tropomyosin-Gen / Monika Heydenreich ; Gutachter: V. Regitz-Zagrosek." Berlin : Humboldt-Universität zu Berlin, 2002. http://d-nb.info/1207663522/34.

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Dähmlow, Steffen. "Mutationen und Polymorphismen im Beta-MHC- und Troponin T-Gen bei Patienten mit dilatativer Kardiomyopathie." Doctoral thesis, Humboldt-Universität zu Berlin, Medizinische Fakultät - Universitätsklinikum Charité, 2006. http://dx.doi.org/10.18452/15456.

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Die ersten identifizierten Krankheitsgene der dilatativen Kardiomyopathie (DCM) kodierten alle für Proteine des Zytoskeletts. Deshalb wurde DCM als Erkrankung des Zytoskeletts bezeichnet. Bei der hypertrophen Kardiomyopathie (HCM) wurden bisher mehr als 250 Mutationen in neun Sarkomerprotein-Genen beschrieben. Deshalb wurde HCM als Erkrankung des Sarkomers bezeichnet. In den letzten Jahren wurde dieses Konzept durch Entdeckung von Mutationen in Sarkomerprotein-Genen bei DCM jedoch in Frage gestellt. Vor diesem Hintergrund haben wir die Sarkomerprotein-Gene beta-MHC und Troponin T bei 46 nicht

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Drees, Nathalie. "Untersuchung auf antimikrobielle Resistenzen und Vorkommen von Extended‐Spectrum‐Beta‐Lactamasen bei Shigatoxin‐Gen tragenden Escherichia coli." Diss., lmu, 2012. http://nbn-resolving.de/urn:nbn:de:bvb:19-148880.

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Izquierdo, García Ana Cristina. "Caracterización del gen CRIO4 y su implicación en tolerancia a estrés por frío." Doctoral thesis, Universitat Politècnica de València, 2016. http://hdl.handle.net/10251/62826.

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[EN] Cold is one of the most important abiotic stresses, severely affects the growth and development of plants, and limits their geographical distribution. Given that cold, salinity and drought stresses overlap some of their molecular mechanisms of response, a cDNA library of sugar beet (Beta vulgaris), generated from leaves of plants subjected to saline stress, was used to try to identify genes for tolerance to cold stress by its overexpression in yeast. In this way it was identified, among others, the CRIO4 gene whose characterization has been the work of this thesis. CRIO4 encodes a SEC14-l

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Matas, Martín Elisabet. "Expresión del gen de la proteína MxA como biomarcador de respuesta al interferón beta en pacientes con esclerosis múltiple." Doctoral thesis, Universitat de Barcelona, 2016. http://hdl.handle.net/10803/401755.

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El Interferón beta (IFN-β) es uno de los tratamientos más ampliamente utilizados para la Esclerosis múltiple (EM). Se trata de una citoquina que actúa a través de su unión a un receptor de elevada afinidad en la superficie celular. Esto provoca la transcripción de factores que modifican la expresión génica, dando lugar a proteínas responsables del efecto antiviral, antiproliferativo y antiinflamatorio, tales como la proteína Mixovirus resistance A (MxA). Desafortunadamente, no todos los pacientes responden adecuadamente al tratamiento. Disponer de biomarcadores que faciliten la selección del t

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Books on the topic "Gen Beta"

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Mönke, Enrico. Etablierung und Anwendung des [beta]-Glucuronidase Gen-Systems im phytopathogenen Pilz Cochliobolus heterostrophus. [s.n.], 1991.

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Malik, Punam, and John Tisdale, eds. Gene and Cell Therapies for Beta-Globinopathies. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7299-9.

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Łukasiak, Jan. Mazowiecka Szkoła Podchorążych Rezerwy Artylerii im. gen. Józefa Bema. Ajaks, 1999.

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Żychowska, Maria. Harcerskie miejsca pamięci Tarnowskiej Chorągwi ZHP im. gen. Józefa Bema. Muzeum Okręgowe w Tarnowie, 1987.

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Foster, Leslie John Ray. The degradation of gel-spun poly(beta-hydroxybutyrate) fibrous matrix. Aston University. Department of Chemical Engineering and Applied Chemistry, 1992.

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Foster, Leslie John Ray. The degradation of gel-spun poly(beta-hydroxybutyrate) fibrous matrix. Aston University. Department of Chemical Engineering and Applied Chemistry, 1992.

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Chen, Weiguan, Haoyue Guan, Weisheng Huang, and Jianfeng Chen. Xue jing chu geng: On the first beat. Tai sheng yu le gong si, 2010.

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Afshari, Jalil Tavakol. Analysis of T cell antigen receptor [beta]-chain gene repertoires in alloreactive T lymphocytes. University of Manchester, 1996.

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Khan, Wasif Noor. The carcinoembryonic antigen gene family: Molecular analysis of the pregnancy-specific [beta]1 glycoprotein subgroup. University of Umeaa, 1990.

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Aggarwal, Anil. The development and application of retroviral-mediated gene transfer technology within the lysosomal beta-hexosaminidase system. National Library of Canada = Bibliothèque nationale du Canada, 1995.

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Book chapters on the topic "Gen Beta"

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Kagawa, Yasuo, and Shigeo Ohta. "Gene Structure of Human ATP Synthase Beta Subunit." In Bioenergetics. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-5835-0_31.

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Reitzig, Markus. "When Can Flat Structures Beat More Centralized Structures?" In Get Better at Flatter. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-89254-8_7.

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Potts, Philip J. "New Detection Techniques for Locating Precious Metal Minerals by Beta Autoradiography: Preliminary Results for Rhodium and Silver Grains." In Geo-Platinum 87. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1353-0_7.

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Trucco, Massimo, Edward Ball, Carlo Carcassi, et al. "RFLP Analysis of DQ-Beta Chain Gene: Workshop Report." In Immunobiology of HLA. Springer New York, 1989. http://dx.doi.org/10.1007/978-1-4612-3552-1_253.

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Whitfield, G. Kerr, Robin E. Powers, James A. Gurr, Ofra Wolf, and Ione A. Kourides. "Isolation of a Gene Encoding Human Thyrotropin Beta Subunit." In Frontiers in Thyroidology. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5260-0_26.

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Leibiger, B., P. O. Berggren, and I. B. Leibiger. "Regulation of β-Cell GK Gene Transcription by Insulin." In Frontiers in Diabetes. KARGER, 2004. http://dx.doi.org/10.1159/000079021.

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Octave, J. N., F. de Sauvage, A. F. Macq, et al. "Cloning of the Beta Amyloid Peptide Gene in Alzheimer’s Disease." In Genetics and Alzheimer’s Disease. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73647-6_15.

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Falqui, Luca. "Beta-Cell Function Replacement by Islet Transplantation and Gene Therapy." In Diabetes in Childhood and Adolescence. KARGER, 2005. http://dx.doi.org/10.1159/000085808.

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Dufva, Martin, and Lena Poulsen. "Genotyping of Mutation in the Beta-Globin Gene Using DNA Microarrays." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-59745-372-1_4.

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Yucel, Zeliha, and E. Berrin Yuksel. "The Genetics of Diabetic Neuropathy." In Current Perspective on Diabetes Mellitus in Clinical Sciences. Nobel Tip Kitabevleri, 2023. http://dx.doi.org/10.69860/nobel.9786053359111.39.

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Diabetic neuropathy, a common complication of diabetes mellitus (DM), involves nerve damage resulting from prolonged exposure to high blood sugar levels. Genetic factors play a crucial role in influencing susceptibility to this condition. Variations in genes related to nerve structure and function, inflammatory responses, and metabolic processes have been implicated in diabetic neuropathy. For instance, polymorphisms in the gene encoding protein kinase C beta (PKC-β) contribute to increased vulnerability by promoting oxidative stress and inflammation in nerve tissues. Similarly, genetic variat

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Conference papers on the topic "Gen Beta"

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"Identifikasi Keragaman Gen Follicle Stimulating Hormone Sub-Unit Beta (FSH-β) pada Tiga Sumber Daya Genetik Sapi Lokal Indonesia". У Teknologi Peternakan dan Veteriner Mendukung Kemandirian Pangan di Era Industri 4.0. Pusat Penelitian dan Pengembangan Peternakan, 2019. http://dx.doi.org/10.14334/pros.semnas.tpv-2019-p.171-179.

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Fischer, J., S. Long, E. Koukoulioti, et al. "Assoziation von rs16944 im Interleukin-1-beta-Gen mit der Entwicklung eines hepatozellulären Karzinoms in kaukasischen Patienten mit chronischer Virushepatitis." In DGVS Digital: BEST OF DGVS. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1716159.

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Vasconcelos, Matheus Felipe de Souza, Francisco Tomaz Meneses de Oliveira, Rafael Zini Moreira da Silva, and Alex Michel Daoud. "Neurological and adrenal insufficiency symptons in adult x-linked adrenoleukodystrophy: case report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.347.

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Context: X-linked adrenoleukodystrophy (X-ALD) is a rare genetic demyelinating disease caused by mutations in ABC1 gen associated with an impairment of beta- oxidation of very long chain fatty acids (VLCFA) in peroxisomes. It causes accumulation of VCLFA in tissues affecting majoritary the central nervous system, testicles and the adrenal córtex resulting in symptoms which provides restricted neurological prognosis and sequels. Methods: Specific data related of a clinical case through prontuary and complementary exams in a patient attended at Santa Casa de Misericórdia de São Paulo hospital. C

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Chang, Ilhan, and Gye-Chun Cho. "Elastic Wave Behaviors of Beta-Glucan Biopolymer-Treated Residual Soil." In Geo-Congress 2014. American Society of Civil Engineers, 2014. http://dx.doi.org/10.1061/9780784413272.153.

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Kim, Donghyun, Jaehoon Yu, Yujie Chi, and Mingwu Jin. "Position Resolved Beta Particle Detection Using GEM." In 2020 IEEE Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC). IEEE, 2020. http://dx.doi.org/10.1109/nss/mic42677.2020.9507946.

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Likins, Garland, and Frank Rausche. "Pile Damage Prevention and Assessment Using Dynamic Monitoring and the Beta Method." In Geo-Congress 2014. American Society of Civil Engineers, 2014. http://dx.doi.org/10.1061/9780784413265.034.

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"Prevalence of beta-thalassemia gene mutations in Iran." In International Conference on Medicine, Public Health and Biological Sciences. CASRP Publishing Company, Ltd. Uk, 2016. http://dx.doi.org/10.18869/mphbs.2016.201.

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Sato, Takeshi, and Kiyoshi Furukawa. "REGULATION OF HUMAN BETA-1,4-GALACTOSYLTRANSFERASE (BETA-1,4-Galt) V GENE EXPRESSION IN CANCER CELLS." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.677.

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Brandt, O., B. Yang, H. Yang, J. R. Mullhauser, and K. H. Ploog. "Growth and doping of /spl beta/-GaN and /spl beta/-(In,Ga)N films and heterostructures." In Compound Semiconductors 1997. Proceedings of the IEEE Twenty-Fourth International Symposium on Compound Semiconductors. IEEE, 1997. http://dx.doi.org/10.1109/iscs.1998.711530.

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Wang, Qin. "Analysis of Luteinizing Hormone Beta-Subunit Gene in Mammal." In 2012 International Conference on Biomedical Engineering and Biotechnology (iCBEB). IEEE, 2012. http://dx.doi.org/10.1109/icbeb.2012.68.

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Reports on the topic "Gen Beta"

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Ren, Weiju, and Claire Luttrell. Gen IV Materials Handbook Beta Release for Structural and Functional Evaluation. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/1136738.

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Rimphanitchayakit, Vichien, and Raevadee Siritunyanont. Mutagenesis of cyclodextrin glucanotransferase gene that affects themostability of the enzyme. Chulalongkorn University, 2006. https://doi.org/10.58837/chula.res.2006.34.

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Cyclodextrins are cyclic oligosaccharides of 6, 7 andf 8 glucose units, called [alpha]-, [beta]- and [gamma]- cyclodextrins (CDs)s, respectively. CDs are the products of enzymatic conversation of starch and related substrates by cyclodextrin glucanotransferases (CGTases), and are useful carrier molecules for applications in industries. The CGTase consists of 5 domains, A, B, C, D, and E. Domains A/B are the central catalytic domains while others perform accessory functions. The commercial production of CDs required that the starch be liquefied at high temperature before the CGTase reaction at

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ตัณฑะพานิชกุล, วิวัฒน์. การศึกษาผลการเตรียมที่มีต่อสมบัติของ RF gel/RF carbon gel และการนำ RF gel/carbon gel ไปใช้ประโยชน์ : รายงานวิจัยฉบับสมบูรณ์. จุฬาลงกรณ์มหาวิทยาลัย, 2004. https://doi.org/10.58837/chula.res.2004.62.

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รีโซซินอล-ฟอร์มัลดีไฮด์ เจล เป็นวัสดุตั้งต้นที่มีความเหมาะสมในการเตรียมเป็นคาร์บอนที่มีรูพรุนในช่วงไมโครพอร์และมีโซพอร์ได้ โดยปรกติแล้ว รีโซซินอล-ฟอร์มัลดีไฮด์เจล เตรียมขึ้นด้วยวิธี โซล-เจล พอลีคอนเดนเซซัน ของ รีโซซินอล กับ ฟอร์มัลดีไฮด์ ภายใต้สารละลายที่เป็นด่าง ในงานวิจัยนี้แบ่งศึกษาเป็น 3 ส่วน ได้แก่ ส่วนที่ 1 ศึกษาความเป็นไปได้ในการใช้กระบวนการอบแห้งด้วยคลื่นไมโครเวฟเพื่อใช้ในการอบแห้ง RF Gel ที่เตรียมด้วยการใช้คลื่นเหนือเสียงระหว่างกระบวนการโซล เจล พอลีคอนเดนเซซัน พบว่าเมื่อใช้คลื่นไมโครเวฟในการอบแห้ง ปริมาณตัวเร่งปฏิกิริยาชนิดด่างหรือค่า C/W ต้องมีค่าน้อยกว่า 40 โมลต่อลูกบาศก์เมตรเพื่อรั

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Suriyaphol, Gunnaporn. Study the gene expression of E-cadherin, syndecan1, matrix metalloproteinases-2, -7, -9, -14 and tissue inhibitors of metalloproteinases-1 and -2 in canine oral melanoma. Chulalongkorn University, 2015. https://doi.org/10.58837/chula.res.2015.80.

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The objectives of this study were to 1.) select the suitable reference genes for quantitative real-time polymerse chain reaction in the most common canine oral cancers: oral melanoma (OM) and oral squamous cell carcinoma (OSCC), 2.) study the gene expression of E-cadherin (CDH1), syndecan 1 (SDC1), matrix metalloproteinases-2, -7, -9, -14 (MMP2, MMP7, MMP9, MMP14) and tissue inhibitors of metalloproteinases-1 and -2 (TIMP1, TIMP2) in canine OM at the mRNA level and study the CDH1, SDC1 and Ki-67 protein expression by immunohistochemistry, and 3.) study the association of gene expression and th

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Jarrett, Christy R. A New APC-Like Gene Involved in Regulation of Beta-Catenin/LEF Signaling. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada409414.

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Broide, David, and Seema Aceves. TGF-Beta Gene Polymorphisms in Food Allergic versus Non-Food Allergic Eosinophilic Esophagitis. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada612768.

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Chirthaworn, Chintana, Kanitha Patarakul, Duangporn Phulsuksombati, and Yong Pooworawan. Study of pathology and pathogenesis of leptospirosis in an animal model inoculated with various in vivo passages of leptospires : implications for vaccine development and diagnosis. Chulalongkorn University, 2006. https://doi.org/10.58837/chula.res.2006.26.

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Leptospirosis is a worldwide zoonosis caused by bacteria from the genus leptospira. Several reports have suggested the roles of cytokines in pathogenesis of this infectious disease. In this study, cytokine gene expression in kidneys livers and lung was investigated. In addition to host cytokine gene expression, the expression of leptospira genes at target organs was also studied. Golden Syrian hamsters were injected with virulent or avirulent leptospira interrogans serovar pyrogenes. Kidney liver and lung tissues were collected for pathological examination and gene expression. RNA was extracte

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Grimm, Sandra L., and Jeffrey M. Rosen. Gene Targets of C/EBP/Beta Involved in Mammary Gland Development and Breast Cancer. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada396636.

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Chaney, William G. Control of Metastasis-Associated Gene Expression by Cell-Surface Beta-1,6 Branched Oligosaccharide Levels. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada420126.

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Belldegrun, Arie S. Prostate-Specific Gene Therapy Using a Gutless" Adeno-Vector Expressing Antisense TGF-Beta and PSA Promoter-Controlled TNF-Alpha Gene". Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada406173.

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