نتایج جستجو برای: single nucleotide polymorphism

تعداد نتایج: 1014701  

Journal: :iranian journal of applied animal science 2015
b. hemati s. gharaie-fathabad m.h. fazeli z. namvar m. ranji

in the present research, molecular detection of bovine leukocyte adhesion deficiency (blad) and complex vertebral malformation (cvm)in a population of iranian holstein cows has been carried outusing milk somatic cells by polymerase chain reaction-restriction fragment length polymorphism(pcr-rflp). the blad and cvm are monogenic and autosomal recessive heredity lethal syndrome in holstein-friesi...

ژورنال: :iranian red crescent medical journal 0
xin liu department of epidemiology and biostatistics, school of public health, jilin university, changchun, china shuang li department of epidemiology and biostatistics, school of public health, jilin university, changchun, china xuejun lin department of epidemiology and biostatistics, school of public health, jilin university, changchun, china kangkang yan department of epidemiology and biostatistics, school of public health, jilin university, changchun, china longyu zhao department of epidemiology and biostatistics, school of public health, jilin university, changchun, china qiong yu department of epidemiology and biostatistics, school of public health, jilin university, changchun, china; qiong yu, department of epidemiology and biostatistics, school of public health, jilin university, changchun, china. tel: +86-43185619451, fax: +86-43185619163

objectives the aim of this study was to explore the association between axin2 gene polymorphism and papillary thyroid carcinoma (ptc). patients and methods 106 blood samples (56 ptc patients and 50 healthy controls) were drawn from china-japan :union: hospital in jilin province, china, during october 2010 to march 2011. a case-control study was designed to examine the association between axin2 ...

Journal: :avicenna journal of medical biochemistry 0
iraj khodadadi department of biochemistry, faculty of medicine, hamadan university of medical sciences, hamadan, ir iran; department of biochemistry, faculty of medicine, hamadan university of medical sciences, hamadan, ir iran. tel: +98-8138380572

Journal: :health scope 0
hooshang rafighdoost cellular and molecular research center, zahedan university of medical sciences, zahedan, ir iran; department of anatomy, school of medicine, zahedan university of medical sciences, zahedan, ir iran zahra rafighdoost department of anatomy, school of medicine, zahedan university of medical sciences, zahedan, ir iran mohsen taheri genetics of non communicable disease research center, zahedan university of medical science, zahedan, ir iran; corresponding author: mohsen taheri, corresponding author: mohsen taheri, genetics of non communicable disease research center, zahedan university of medical science, zahedan, ir iran, tel: +54-13416703, fax: +54-13416708

results no significant difference was found between the groups regarding bmht rs3797546 gene polymorphism. the c allele was not associated with ns-cl/p (or = 1.27, 95% ci = 0.85-2.79, p = 0.690). conclusions our data suggested that bmht rs3797546 gene polymorphism was not associated with risk/ protection for ns-cl/p in a sample of iranian population. larger studies are required to validate our ...

Journal: :journal of family and reproductive health 0
mohammad karimian gametogenesis research center, kashan university of medical sciences, kashan, iran hossein nikzad gametogenesis research center, kashan university of medical sciences, kashan, iran abolfazl azami-tameh anatomical sciences research center, kashan university of medical sciences, kashan, iran aliakbar taherian gametogenesis research center, kashan university of medical sciences, kashan, iran fatemeh zahra darvishi department of biology, division of biochemistry, cell and molecular biology, university of isfahan, isfahan, iran mohammad javad haghighatnia gametogenesis research center, kashan university of medical sciences, kashan, iran

objective: to investigate the association of c631t single nucleotide polymorphisms in spo11 gene with male infertilityfollowed by an in silico approach. spo11 is a gene involved in meiosis and spermatogenesis process, which in humans, this gene is located on chromosome 20 (20q13.2-13.3) with 13 exons. materials and methods: in a case-control study, 200 blood samples were collected from the ivf ...

Journal: :hepatitis monthly 0
lizhen chen department of gastroenterology, qingdao municipal hospital, school of medicine, qingdao university, qingdao, china zhonghua lin department of gastroenterology, qingdao municipal hospital, school of medicine, qingdao university, qingdao, china man jiang department of gastroenterology, qingdao municipal hospital, school of medicine, qingdao university, qingdao, china linlin lu central laboratories, qingdao municipal hospital, qingdao, china haiying zhang department of gastroenterology, qingdao central hospital, qingdao, china yongning xin department of gastroenterology, qingdao municipal hospital, school of medicine, qingdao university, qingdao, china; department of gastroenterology, qingdao municipal hospital, school of medicine, qingdao university, p. o. box: 266021, qingdao, china. tel: +86-53282789463, fax: +86-53285968434, e-mail:; shiying xuan, department of gastroenterology, qingdao municipal hospital, school of medicine, qingdao university, p. o. box: 266021, qingdao, china. tel: +86-53288905508, fax: +86-53282031522

background genome-wide association studies have shown that rs738491, rs2143571, and rs3761472 in the sorting and assembly machinery component 50 homolog (samm50) gene are significantly associated with susceptibility to nonalcoholic fatty liver disease (nafld). conclusions we first demonstrated that the rs738491 t allele, rs2143571 a allele, and rs3761472 g allele in the samm50 gene created susc...

Journal: :iranian journal of applied animal science 2015
s. behzadi s.r. miraei-ashtiani m. sadeghi p. zamani r. abdoli

molecular genetics selection on individual genes is a promising method to genetically improve economically important traits in livestock. the insulin like growth factor-i (igf-i) gene may play important roles in growth of multiple tissues, including muscle cells, cartilage and bone. the objectives of the present study were the estimate the haplotype frequencies of the igf-i gene polymorphisms i...

B.R. Yadav D.S. Kale, J. Prasad

DNA polymorphism within diacylglycerol transferase 2 (DGAT2) / monoacyl glycerol transferases 2 (MOGAT2), leptin and butyrophilin genes were analysed using PCR-SSCP in Murrah buffalo. The single strand conformation polymorphism (SSCP) analysis of amplified gene fragment in exon 5 of MOGAT2, exon 3 of leptin and intron 1 of butyrophilin gene revealed different patterns. A, B and C showed the fol...

Journal: :iranian journal of applied animal science 2014
d.s. kale b.r. yadav j. prasad

dna polymorphism within diacylglycerol transferase 2 (dgat2) / monoacyl glycerol transferases 2 (mogat2), leptin and butyrophilin genes were analysed using pcr-sscp in murrah buffalo. the single strand conformation polymorphism (sscp) analysis of amplified gene fragment in exon 5 of mogat2, exon 3 of leptin and intron 1 of butyrophilin gene revealed different patterns. a, b and c showed the fol...

Apurva Srivastava, Balraj Mittal, Jai Prakash, Neena Srivastava, Pranjal Srivastava, Shally Awasthi,

Background: Obesity is a very common disorder resulting from an imbalance between food intake and energy expenditure, and it has a substantial impact on the development of chronic diseases.  The aim of this study was to examine the association of INSIG2 (rs7566605) gene polymorphism with obesity and obesity associated phenotypes in North Indian subjects. Methods: The variants were investig...

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