نتایج جستجو برای: gene defect

تعداد نتایج: 1219432  

Anbiaee, Najme , Ebrahimi, Saeede , Sahebnasagh, Zoha , Ebrahimnejad, Hamed , Mohammadzade Rezaie, Maryam ,

Parotid Stafne bone defect is a very rare and infrequent variant, which is located on the buccal or lingual surface of the mandibular ascending ramus. In this paper, a case of parotid Stafne defect, which was incidentally discovered during dental radiographic examination, is reported. This bone defect was observed as a lucent oval-shaped defect on the lingual aspect of the right mandibu...

Journal: :journal of applied research in water and wastewater 2014
matthieu dufresne jose vazquez

venturi flumes are measurement structures commonly used in water systems to measure the flow discharge. some of them are not well installed or present some geometrical defects. the objective of this study is to investigate the hydraulic influence of a number of typical wrong installations and geometrical defects of long-throated venturi flumes: significant positive or adverse slopes, humps and ...

Journal: :physical chemistry research 2015
salimeh kimiagar ali rajabpour fatemeh tavazoee

graphene sheet including single vacancy, double vacancy and stone-wales with armchair and zigzag structure was simulated using molecular dynamics simulation. the effect of defects on shear’s modulus, shear strength and fracture  strain was investigated. results showed that these shear properties reduce when the degrees of all kinds of defects increase. the dangling bond in sv and dv defected gr...

Journal: :Genes & development 1995
V Steimle B Durand E Barras M Zufferey M R Hadam B Mach W Reith

Regulation of MHC class II gene expression is an essential aspect of the control of the immune response. Primary MHC class II deficiency is a genetically heterogeneous disease of gene regulation that offers the unique opportunity of a genetic approach for the identification of the functionally relevant regulatory genes and factors. Most patients exhibit a characteristic defect in the binding of...

زوار رضا, جواد , صالحی پور, مسعود, منصوری, رضا, نهنگی, حسین,

Introduction: Defect in the cholesterol homeostasis in macrophage as well as converting them to foam cells is one of the most important factors in the initiation and progression of atherosclerosis. Many genes and transcription factors like Peroxisome Proliferators Activated Receptors are involved in cholesterol homeostasis in these cells. N-3 fatty acids are one of the most important factors re...

Journal: :Atherosclerosis 2000
S Mott L Yu M Marcil B Boucher C Rondeau J Genest

BACKGROUND High density lipoproteins (HDL) are complex lipoprotein particles involved in reverse cholesterol (C) transport and are negatively associated with the risk for coronary artery disease (CAD). We have described a disorder of familial HDL deficiency (FHD) due to abnormal cellular cholesterol efflux. In the present study, we investigated cellular cholesterol efflux on skin fibroblast fro...

Journal: :The Journal of Clinical Endocrinology & Metabolism 1999

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تبریز - دانشکده کشاورزی 1390

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