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Дисертації з теми "COMMON INHIBITOR"

Автор: Grafiati

Опубліковано: 11 вересня 2023

Оновлено: 31 липня 2025

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1

Hay, Marshall Mark. "Control of Palmer amaranth (Amaranthus palmeri) and common waterhemp (Amaranthus rudis) in double crop soybean and with very long chain fatty acid inhibitor herbicides." Thesis, Kansas State University, 2017. http://hdl.handle.net/2097/35489.

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Master of Science<br>Department of Agronomy<br>Dallas E. Peterson<br>During 2015 and 2016, five site years of research were implemented in double crop soybean after winter wheat at experiment fields in Kansas near Manhattan, Hutchinson, and Ottawa to assess various non-glyphosate herbicide treatments at three different application timings for control of Palmer amaranth (Amaranthus palmeri S. Wats.) and common waterhemp (Amaranthus rudis Sauer). Spring-post (SP) treatments with residual control of Palmer amaranth and waterhemp were applied in the winter wheat at Feekes 4 and resulted in less t

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2

Rothmayr, Christoph. "Common and distinct neural networks for theory of mind reasoning and inhibitory control." Diss., lmu, 2009. http://nbn-resolving.de/urn:nbn:de:bvb:19-124976.

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3

Pei, Fen, Susanne DiSalvo, Suzanne S. Sindi, and Tricia R. Serio. "A dominant-negative mutant inhibits multiple prion variants through a common mechanism." PUBLIC LIBRARY SCIENCE, 2017. http://hdl.handle.net/10150/626074.

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Prions adopt alternative, self-replicating protein conformations and thereby determine novel phenotypes that are often irreversible. Nevertheless, dominant-negative prion mutants can revert phenotypes associated with some conformations. These observations suggest that, while intervention is possible, distinct inhibitors must be developed to overcome the conformational plasticity of prions. To understand the basis of this specificity, we determined the impact of the G58D mutant of the Sup35 prion on three of its conformational variants, which form amyloids in S. cerevisiae. G58D had been previo

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4

Isaacs, Mark Allen. "Investigations on the Interations of Acetolactate Synthase (ALS)-Inhibiting Herbicides with Growth Regulator and non ALS-Inhibiting Herbicides in Corn (Zea mays) and Selected Weeds." Diss., Virginia Tech, 2000. http://hdl.handle.net/10919/77970.

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Herbicide combinations are common in corn production in the United States to control broadleaf and grass weed species. Studies were conducted in 1995 and 1996 to: (1) investigate the interactions of 2,4-D and dicamba with halosulfuron-methyl on common lambsquarters and common ragweed control in corn, (2) determine the effect of 2,4-D on the foliar absorption, translocation, and metabolism of 14C halosulfuron-methyl in common lambsquarters, (3) examine the interactions of 2,4-D, dicamba, and ALS-inhibitor herbicides with rimsulfuron plus thifensulfuron-methyl (RT) and with sethoxydim on giant

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5

Maire, Marie-Aline Vasseur Paule. "Inhibition de l'apoptose comme facteur de la transformation morphologique des cellules embryonnaires de hamster Syrien." Metz : Université Metz, 2008. ftp://ftp.scd.univ-metz.fr/pub/Theses/2004/Maire.Marie_Aline.SMZ0434.pdf.

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6

Lang, Jean. "Calcium et actions pharmacologiques sur les tissus spécialisé et commun auriculaires." Lyon 1, 1987. http://www.theses.fr/1987LYO1H069.

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7

Zaffarano, Jennifer I. "MINIMUM INHIBITORY CONCENTRATIONS OF TWO COMMON FOOD PHENOLIC COMPOUNDS AND THEIR EFFECT ON THE MICROBIAL ECOLOGY OF SWINE FECES IN VITRO." UKnowledge, 2003. http://uknowledge.uky.edu/gradschool_theses/182.

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Feeding sub-therapeutic levels of antibiotics to livestock has been associated withdevelopment and spread of antibiotic resistant bacteria. The present experiment was conductedto investigate the effect of antibiotic alternatives (caffeic acid, chlorogenic acid, and carbadox)on the microbial ecology of swine feces in vitro.Minimum inhibitory concentrations of caffeic and chlorogenic acids were determined forseveral pathogens using macrobroth and agar dilution techniques. Gram-negative bacteria werenot inhibited. Caffeic acid inhibited four Staphylococcus aureus strains at 200 ppm or less, andtw

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8

Zaffarano, Jennifer I. "Minimum inhibitory concentration of two common food phenolic compounds and their effects on the microbial ecology of swine feces in vitro." Lexington, Ky. : [University of Kentucky Libraries], 2003. http://lib.uky.edu/ETD/ukyansc2003t00099/JZThesis.pdf.

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Thesis--University of Kentucky (M.S.), 2003.<br>Title from document title page. Document formatted into pages; contains ix, 127 p. : ill. Includes abstract and vita. Includes bibliographical references (p. 110-126).

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9

Sekhon, Jaspreet. "Antisense inhibition of methylenetetrahydrofolate reductase as a cancer treatment and a pharmacogenetic study to examine the effects of a common polymorphism." Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=33029.

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Methylenetetrahydrofolate reductase (MTHFR) is an important enzyme in the metabolism of folate and methionine. MTHFR catalyzes the conversion of 5,10 methylenetetrahydrofolate (5,10-methyleneTHF) to 5-methyltetrahydrofolate (5-methylTHF). 5-MethylTHF is a co-substrate for homocysteine remethylation to methionine catalyzed by the vitamin B12-dependent enzyme methionine synthase. A common MTHFR variant, 677C → T substitution resulting in the conversion of an alanine to a valine residue, has been shown to be a thermolabile form of MTHFR and to have reduced activity (Frosst et al., 1995). Sin

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10

Sköld, Anna-Carin. "Teratogenicity as a consequence of drug-induced embryonic cardiac arrhythmia : Common mechanism for almokalant, sotalol, cisapride, and phenytoin via inhibition of IKr." Doctoral thesis, Uppsala University, Department of Pharmaceutical Biosciences, 2000. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-515.

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<p>During the last years, drugs that prolong the repolarisation phase of the myocardial action potential, due to inhibition of the rapid component of the delayed-rectifying potassium channel (I<sub>Kr</sub>) have been in focus. In addition to arrhythmogenic potential, selective Ikr-blockers have also been shown to be embryotoxic and teratogenic in animal studies. The aim of this thesis was to investigate a theory that these developmental toxic results from pharmacologically induced episodes of embryonic cardiac arrhythmias leading to hypoxia related damage in the embryo. Almokalant (ALM) was u

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11

Djuv, Ane. "Co-Use of Drugs and Herbal Remedies in General Practice and In Vitro Inhibition of CYP3A4, CYP2D6 and P-Glycoprotein by the Common Herb Aloe Vera." Doctoral thesis, Norges teknisk-naturvitenskapelige universitet, Institutt for kreftforskning og molekylær medisin, 2013. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-23578.

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There is a widespread use of complementary and alternative medicine (CAM) and herbal remedies in particular in different patients groups, but very few are published about co-use among patients in general practice (GP) and herb-drug combinations at risk. Co-use of herbal remedies and drugs can result in none or server adverse effects. Of this reason, knowledge about the GP patients co-use and research on mechanisms of such interactions is needed. The aims of this thesis were divided; 1) To register the co-use of drugs and herbs among GP patients in Norway and the patients communication of such

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12

Maire, Marie-Aline. "Inhibition de l'apoptose comme facteur de la transformation morphologique des cellules embryonnaires de hamster Syrien." Metz, 2004. http://docnum.univ-lorraine.fr/public/UPV-M/Theses/2004/Maire.Marie_Aline.SMZ0434.pdf.

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Le but de ce travail consistait d'une part, à étudier l'hypothèse qu'une défaillance des processus apoptotiques favoriserait la transformation cellulaire, et d'autre part, à élucider certains des mécanismes moléculaires de substances inhibitrices de l'apoptose. Ce travail a été réalisé sur les cellules embryonnaires de hamster Syrien, des cellules normales, diploïdes et capables de métaboliser un grand nombre de substances chimiques. Cette étude a été appliquée à trois substances, le zinc, inhibiteur de l'apoptose, le DEHP (di-2-ethylhexyl phtalate), transformant in vitro, le 2,4-D (acide 2,4-

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13

Pagé-Veillette, Hélène. "Caractérisation moléculaire d'un mutant d'arabidopsis thaliana résistant à la thaxtomine A." Mémoire, Université de Sherbrooke, 2012. http://hdl.handle.net/11143/5747.

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La thaxtomine A (TA) est la principale toxine produite par l'agent pathogène causant la gale commune Streptomyces scabies.La TA est nécessaire et suffisante à l'induction des symptômes de la maladie.La TA a un rôle d'inhibiteur de la synthèse de la cellulose et cause une inhibition importante de la croissance racinaire chez Arabidopsis thaliana. Ce projet avait pour objectif de caractériser un mutant d'Arabidopsis plus résistant à la TA, 9F32, dans le but de mieux comprendre le mécanisme d'action de la TA. 9F32 a démontré une résistance trois fois plus importante à la TA que Col 0, autant au n

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14

Messaadia, Hocine. "Les facteurs d'inhibition de la régénération naturelle du hêtre (fagus sylvatica L. ) dans la forêt domaniale de Lyons (Haute-Normandie), influence de l'allélopathie et du mode de recyclage des litières forestières." Rouen, 1987. http://www.theses.fr/1987ROUES041.

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Cette étude consacrée aux facteurs d'inhibition de la régénération du hêtre (fagus sylvica L) dans les stations à moder mulleux met en évidence l'action allélopathique de composés phénoliques (acides benzoïque, salicylique, cinnamique) qui proviennent des litières fraîches et des feuilles de hêtre et de ronce (Rubus sp)

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15

Wang, Hsi-Hua, та 王晞華. "Purification and activity of α-amylase inhibitor 1 from NaN3-induced common bean mutants". Thesis, 2010. http://ndltd.ncl.edu.tw/handle/87146006711412832532.

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碩士<br>國立中興大學<br>農藝學系所<br>98<br>Common bean (Phaseolus vulgaris L.) contain α-amylase inhibitor 1 (α-AI1), which would bind α-amylase and subsequently reduce starch digestion. Thus, α-AI1 can be used to control the deterioration of type II diabetes and obesity. In this study, a three-phase partitioning (TPP) technique was used to extract and purify α-AI1 from common bean. The crud extracts were adjusted to pH 5.25, and 30% ammonium sulfate was added. Then the tert-butanol was added to the mixing solution for obtaining three phases. The results indicated that the α-AI1 proteins were mainly reco

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16

PATEL, KUNAL. "PARALLEL VIRTUAL SCREENING TO DISCOVER PHYTOCOMPOUNDS TO COUNTER THE RESISTANCE INDUCING EFFECT OF DOUBLE MUTATIONS IN MDR TUBERCULOSIS." Thesis, 2014. http://dspace.dtu.ac.in:8080/jspui/handle/repository/15469.

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Drug resistant tuberculosis has threaten all the advances made in tuberculosis control at the global stage in the last few decades. Resistance to quinolone class of drug like Ofloxacin which are being used as a main drug for multiple drug resistant tuberculosis treatment have given rise to cases of extensive drug resistant tuberculosis. DNA gyrase enzyme, essential for DNA replication, translation, and transcription are targeted by quinolones for their bactericidal effect and can be an excellent target for antibacterial drug discovery. Mutations in quinolone resistance determining region

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17

Van, der Walt Lydia. "Reproductive inhibition in female common and highveld mole-rats: neuroanatomical and neuroendocrine perspectives." Thesis, 2004. http://hdl.handle.net/2263/24996.

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The social reproductive inhibition evident in female common (Cryptomys hottentotus hottentotus) and highveld (Cryptomys hottentotus pretoriae) mole-rats was investigated, focussing on intra- and inter-subspecies differences in gonadotropin¬releasing hormone (GnRH) neuroanatomy and neuroendocrinology and potential mechanisms mediating social infertility through the suppression of luteinizing hormone (LH) and/or GnRH synthesis or release. The molecular structure of the GnRH peptide present in highveld mole-rat tissue was determined. Messenger ribonucleic acid (mRNA) coding for GnRH was isolated

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18

Rothmayr, Christoph [Verfasser]. "Common and distinct neural networks for theory of mind reasoning and inhibitory control / vorgelegt von Christoph Rothmayr." 2009. http://d-nb.info/1009712195/34.

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19

Biegler, Kelly Ann. "Competition and inhibition in lexical retrieval: Are common mechanisms used in language and memory tasks?" Thesis, 2007. http://hdl.handle.net/1911/20578.

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The following series of experiments examined whether common mechanisms are involved in word retrieval within language and memory domains. Four patients with short-term memory (STM) deficits were examined; however, two of the patients showed a consistent impairment in inhibiting irrelevant verbal information as well. To the extent that repeatedly retrieving verbal items from the same category would require the capacity to suppress competing items to select the target, we investigated whether patients with a verbal inhibitory deficit, in addition to a reduced STM capacity, would be impaired in r

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20

Chiang, Yi-Chen, та 江怡晨. "Characteristics of common bean seed extracts and their inhibitory activities against aldose reductase, α-amylase, and α-glucosidase in vitro". Thesis, 2013. http://ndltd.ncl.edu.tw/handle/umvjeh.

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碩士<br>國立中興大學<br>農藝學系所<br>101<br>Common bean (Phaseolus vulgaris L.) contain many polyphenolics compounds and and α-amylase inhibitor 1 (α-AI1). These bioactive compounds can be used to regulate the carbohydrate metabolism, slow down the intake of sugars and thus reduce the risks of diabetes mellitus and related diabetic complications. In this study, the polyphenolics andα-AI1s were extracted from the seeds of NaN3-induced mutant SA-05 and its wild type Hwachia by using various solvents. The chemical contents and the inhibitory activities of prepared extracts against α-amylase, α-glucosidase a

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21

Liu, Yueh-Sung, and 劉岳松. "Study on the inhibitory effects of immobilized antibacterial substrata coated with quaternary ammonium salt or silver ion against common waterborne pathogens." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/52146364516901914484.

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碩士<br>國立海洋大學<br>食品科學系<br>87<br>Immobilized antibacterial substrata are carrying the antibacterial component via binding or coating to the surface of solid material, and make the solid material have antibacterial activities. The inhibitory effect of this coating substratum is mainly progressing by contacting or releasing gradually the antibacterial compound. This study takes honeycombs ceramic and carborundum coating with quaternary ammonium salt or silver ions were produced by Cargico Engineering Corp. to study the influence of antimicrobes substratum to the usual seen pathogens in water.

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22

Hsueh, Shu-Ping, and 薛淑萍. "SV40 T/t-common polypeptide inhibits angiogenesis and enhances the cytotoxic activity of chemotherapeutic agents in human HER2-overexpressing tumors." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/57959984650785599184.

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博士<br>國立臺灣大學<br>微生物學研究所<br>100<br>Overexpression of HER2 has been frequently detected in many types of human cancer, most notably breast and ovarian cancers. HER2 overexpression is associated with increased angiogenesis, increased metastasis, increased chemoresistance and reduced survival. Inhibition of HER2 in HER2-overexpressing cancers can lead to reduced angiogenesis, reduced chemoresistance and improved survival. Previously, we reported that Simian Virus 40 T/t-common polypeptide can inhibit HER2, suppress the tumorigenic potential of HER2-overexpressing cancer cells and specifically indu

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23

Mera, Mario Felix. "Recurrent selection for nodule mass and identification of tolerance to nitrate-induced inhibition of dinitrogen fixaton in common bean (Phaseolus vulgaris L.)." 1993. http://catalog.hathitrust.org/api/volumes/oclc/31128198.html.

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24

Bayat, Mokhtari Reza. "Dietary Chemoprevention Agent Sulforaphane Inhibits Growth, Survival and Tumorigenic Activity in Human Neuroblastoma." Thesis, 2010. http://hdl.handle.net/1807/25424.

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Objective: To evaluate the anti-tumor and histone deacetylase (HDAC) inhibitory activity of the dietary isothiocyanate, sulforaphane (SFN) in the paediatric cancer,neuroblastoma (NB). Materials and Methods: NB cell line (NUB-7), fibroblasts (FLF; negative control) and MCF-7 (positive control), were treated with SFN for up to 7 days and effects on growth, cytotoxicity, differentiation and tumorigenicity assessed. HDAC inhibition was determined by histone (H3/ H4) acetylation. Results: 10 μM SFN significantly decreased in vitro growth and survival of NUB-7 to 10.22 ± 0.71% (p < 0.001) with no si

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