نتایج جستجو برای: y polymorphisms

تعداد نتایج: 560033  

Journal: :American journal of human biology : the official journal of the Human Biology Council 2009
Stéphane Mazières André Sevin Sidia M Callegari-Jacques Eric Crubézy Georges Larrouy Jean-Michel Dugoujon Francisco M Salzano

Three sets of genetic markers (blood group plus protein polymorphisms, mitochondrial DNA, and Y-chromosome) were compared in four French Guiana and one Brazilian Amerindian populations. Spearman's rank correlation coefficient between five gene diversity statistics and historical or present-day population sizes showed significant values, indicating loss of diversity due to population bottlenecks...

Journal: :Journal of bacteriology 1998
S S Ingavale R Kaur P Aggarwal A K Bachhawat

We describe the presence of a minisatellite sequence that displays length polymorphisms in the fission yeast Schizosaccharomyces pombe. The minisatellite sequence was found to reside within the propeptide region of the vacuolar carboxypeptidase Y gene. The minisatellite sequence, which was found only at a single locus, was mitotically stable and displayed length polymorphisms between the two va...

Journal: :iranian biomedical journal 0
ایرج سعادت iraj saadat شاهپور امیدواری shahpour omidvari مصطفی سعادت mostafa saadat

glutathione s-transferases (gsts) are encoded by a superfamily of genes and play a role in the detoxification of potential carcinogens. the human gsts are divided into four classes: alpha, mu, pi and theta. previous studies indicated that the absence of the glutathione s-transferase m1 (gstm1) protein correlated with an increased risk of developing some types of cancers. association between spe...

Journal: :Genetics and Molecular Research 2015

Journal: :iranian red crescent medical journal 0
milad gholami department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran hossein darvish behavioral sciences research center, shahid beheshti university of medical sciences, tehran, ir iran habib ahmadi department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran simin rahimi-aliabadi department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran babak emamalizadeh department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran mohammad reza eslami amirabadi behavioral sciences research center, shahid beheshti university of medical sciences, tehran, ir iran

background multiple sclerosis (ms) is an autoimmune disease that affects the central nervous system (cns). ms is one of the most common cause of neurological impairment at a young age with a complex etiology. the forkhead/winged helix (foxp3) gene encodes a transcription factor that plays an important role in the working and progress of regulatory t cells. loss of the foxp3 function impairs the...

Journal: :jundishapur journal of microbiology 0
bahman mirzaei department of bacteriology, pasteur institute of iran, tehran, ir iran zakaria bameri department of bacteriology, pasteur institute of iran, tehran, ir iran ryhane babaei department of bacteriology, pasteur institute of iran, tehran, ir iran fereshteh shahcheraghi department of bacteriology, pasteur institute of iran, tehran, ir iran; department of bacteriology, pasteur institute of iran, tehran, ir iran. tel: +98-2166953311, fax: +98-2166953331

conclusions although previous studies have shown that a-g transition mutations in 23 srrna gene (domain v) are the main reason for the occurrence of high level macrolides resistance in b. pertussis, however, the mentioned single nucleotide polymorphisms (snps) have not been detected in our resistant strain. this is the first report of high level macrolide resistant b. pertussis, without snps in...

Journal: :anatomical sciences journal 0
hajar dahim falavarjan azad university kahin shahani falavarjan azad university ahmad sabanizadeh rafsanjan university of medical sciences mohsen mohsen mohsen سید مسعود ذوالحواریه

introduction: endometriosis is a prevalent gynecological disorder among women which is diagnosed by the growth of endometrial tissue outside of uterus and is mainly accompanied by severe pelvic pain and infertility. p53 also known as cellular tumor antigen p53 inside codons 11, 72 and 248 are contained with single nucleotide changes in which tends to be nearly rampant.this will probably be incr...

Journal: :hepatitis monthly 0
haiying zhang department of gastroenterology, the second affiliated hospital of qingdao university medical college, qingdao, china; department of gastroenterology, qingdao central hospital, qingdao, china; medical college of qingdao university, qingdao, china lizhen chen medical college of qingdao university, qingdao, china yongning xin department of gastroenterology, qingdao municipal hospital, qingdao, china; department of gastroenterology, qingdao municipal hospital, qingdao 266021, shandong province, china. tel: +86-53288905289, fax: +86-53288905293, e-mail:; shiying xuan, department of gastroenterology, qingdao municipal hospital, qingdao 266021, shandong province, china yuangui lou department of gastroenterology, the second affiliated hospital of qingdao university medical college, qingdao, china; department of gastroenterology, qingdao central hospital, qingdao, china yang liu medical college of qingdao university, qingdao, china shiying xuan department of gastroenterology, qingdao municipal hospital, qingdao, china; department of gastroenterology, qingdao municipal hospital, qingdao 266021, shandong province, china. tel: +86-53288905289, fax: +86-53288905293, e-mail:; shiying xuan, department of gastroenterology, qingdao municipal hospital, qingdao 266021, shandong province, china

conclusions our meta-analysis, while not ruling out possible publication bias, showed no association between gene polymorphisms of apoc3 and the risk of nafld development in different populations in the world. evidence acquisition we performed a meta-analysis of all relevant studies published in the literature. a total of 115 clinical trials or reports were identified, but only seven trials met...

Journal: :Genetics 2013
Suo Qiu Roberta Bergero Deborah Charlesworth

The existence of sexually antagonistic (SA) polymorphism is widely considered the most likely explanation for the evolution of suppressed recombination of sex chromosome pairs. This explanation is largely untested empirically, and no such polymorphisms have been identified, other than in fish, where no evidence directly implicates these genes in events causing loss of recombination. We tested f...

2008
Paolo Francalacci Laura Morelli Antonella Useli Daria Sanna

The knowledge of the evolution of the human genome is strictly dependent on the availability of appropriate genetic markers and their relative coverage of genetic variation which refine the phylogenetic reconstruction. While autosomal markers are particularly valuable for recognizing correspondence between genetic and geographic distances, markers on mitochondrial DNA (mtDNA) or Non Recombining...

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