نتایج جستجو برای: y polymorphisms

تعداد نتایج: 560033  

Journal: :iranian journal of basic medical sciences 0
liou cao department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china shan mou department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china wei fang department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china chaojun qi department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china xinbei chang department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china leyi gu department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china

objective(s):the aim of the study was to investigate the relationship between insulin resistance (ir) and leptin (lep) gene polymorphisms in peritoneal dialysis (pd) patients. materials and methods: from july 1, 2011 to august 1, 2011, patients who received chronic pd were chosen and divided into three groups (dm, high homr-ir, and low homr-ir). two pcr products of lep were sequenced and aligne...

Journal: :international journal of reproductive biomedicine 0
robab davar nasim tabibnejad seyed mehdi kalantar mohammad hasan sheikhha

background: despite extensive progress in ivf techniques, one of the most difficult problems is the variability in the response to controlled ovarian hyperstimulation (coh). recent studies show the effects of individual genetic variability on coh outcome. objective: to evaluate the correlation between lhβ g1502a polymorphisms in exon 3 of the lh gene and ovarian response to coh. materials and m...

Journal: :Revista medica de Chile 2008
Hugo Jorquera G Mónica Acuña P Lucía Cifuentes L

BACKGROUND Autosomal and Y chromosome short tandem repeats (STRs) and mitochondrial DNA polymorphisms are the most commonly used molecular tools for determination of kinship. AIM To report a revision of 1,120 kinship cases (paternity and others) analyzed in our laboratory. MATERIAL AND METHODS Revision of all kinship cases analyzed between years 2001-2006. Autosomal and Y chromosome STRs an...

2013
Chuan-Chao Wang Hui Li

Current Y chromosome research is limited in the poor resolution of Y chromosome phylogenetic tree. Entirely sequenced Y chromosomes in numerous human individuals have only recently become available by the advent of next-generation sequencing technology. The 1000 Genomes Project has sequenced Y chromosomes from more than 1000 males. Here, we analyzed 1000 Genomes Project Y chromosome data of 126...

Journal: :PLoS ONE 2007
Raymond K. Auerbach Apichai Tuanyok William S. Probert Leo Kenefic Amy J. Vogler David C. Bruce Christine Munk Thomas S. Brettin Mark Eppinger Jacques Ravel David M. Wagner Paul Keim

BACKGROUND Yersinia pestis, the etiologic agent of plague, was responsible for several devastating epidemics throughout history and is currently of global importance to current public heath and biodefense efforts. Y. pestis is widespread in the Western United States. Because Y. pestis was first introduced to this region just over 100 years ago, there has been little time for genetic diversity t...

Journal: :American journal of human genetics 2009
Steve Rozen Janet D Marszalek Raaji K Alagappan Helen Skaletsky David C Page

Y-linked single-nucleotide polymorphisms (SNPs) have served as powerful tools for reconstructing the worldwide genealogy of human Y chromosomes and for illuminating patrilineal relationships among modern human populations. However, there has been no systematic, worldwide survey of sequence variation within the protein-coding genes of the Y chromosome. Here we report and analyze coding sequence ...

Journal: :Peer Reviewed Journal of Forensic & Genetic Sciences 2018

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2013
Lisa D S Bloomer Christopher P Nelson James Eales Matthew Denniff Paraskevi Christofidou Radoslaw Debiec Jasbir Moore Ewa Zukowska-Szczechowska Alison H Goodall John Thompson Nilesh J Samani Fadi J Charchar Maciej Tomaszewski

OBJECTIVE Haplogroup I of male-specific region of the human Y chromosome is associated with 50% increased risk of coronary artery disease. It is not clear to what extent conventional cardiovascular risk factors and genes of the male-specific region may explain this association. APPROACH AND RESULTS A total of 1988 biologically unrelated men from 4 white European populations were genotyped usi...

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