نتایج جستجو برای: nucleotide polymorphism

تعداد نتایج: 201089  

Journal: :iranian journal of basic medical sciences 0
tausif ahmed rajput department of biochemistry and molecular biology, centre for research in experimental and applied medicine (cream), army medical college, national university of sciences & technology (nust), islamabad, pakistan abdul khaliq naveed department of biochemistry and molecular biology, centre for research in experimental and applied medicine (cream), army medical college, national university of sciences & technology (nust), islamabad, pakistan shakir khan department of biochemistry and molecular biology, centre for research in experimental and applied medicine (cream), army medical college, national university of sciences & technology (nust), islamabad, pakistan zia-ur rehman farooqi department of biochemistry and molecular biology, centre for research in experimental and applied medicine (cream), army medical college, national university of sciences & technology (nust), islamabad, pakistan

objective(s):organic anion transporter polypeptide 1b1 (oatp1b1) encoded by solute carrier organic transporter 1b1 (slco1b1) gene; a transporter involved in the uptake of drugs and endogenous compounds is present in hepatocyte sinusoidal membrane. aim of this study was to investigate the frequencies of functionally significant snps (388a>g and 521t>c) and their haplotypes in 6 ethnic groups of ...

ژورنال: :thrita 0
bahareh moradi najafabad branch, islamic azad university, najafabad, isfahan, iran hossein tabatabaeian genetics division, biology department, faculty of sciences, university of isfahan, isfahan, iran samira sadeghi genetics division, biology department, faculty of sciences, university of isfahan, isfahan, iran mansoureh azadeh najafabad branch, islamic azad university, najafabad, isfahan, iran kamran ghaedi cellular and molecular biology division, biology department, faculty of sciences, university of isfahan, isfahan, iran; cellular and molecular biology division, biology department, faculty of sciences, university of isfahan, isfahan, iran. tel: +98-3137932479, fax: +98-3137932456

conclusions rs1595065 could be recommended as a risk factor in regulating her4 expression and affecting her2 positivity incidence among bc patients. methods overall, 156 patients and controls were genotyped using rflp-pcr. armitage test for trend was utilized to investigate the association between rs1595065 and susceptibility to bc. the possible change in the interaction between rs1595065 and m...

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...

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...

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: :iranian journal of public health 0
n parvaneh dept. of pediatrics, infectious disease research center, children's medical center, tehran universit b pourakbari dept. of pediatrics, infectious disease research center, children's medical center, tehran universit kh daneshjoo dept. of pediatrics, imam khomeini hospital, tehran university of medical sciences, iran h ashraf dept. of pediatrics, infectious disease research center, children's medical center, tehran universit a salavati dept. of pediatrics, infectious disease research center, children's medical center, tehran universit s mamishi dept. of pediatrics, infectious disease research center, children’s medical center, tehran universit

background: cytokines and specially interferon-gamma (ifn-g) are largely responsible for the regulation of the protective im­mune response against mycobacterial infections. several studies have clarified the importance of common variants of ifn- g gene regarding the susceptibility to tuberculosis. bacille calmette-guérin (bcg) vaccine that is used to prevent se­vere forms of tuberculosis could ...

Azita Shafighian, Hadi Mirzapour, Zahra Shahidi,

  Purpose: Estrogen as a crucial hormone during pregnancy acts by two types of receptors.   Estrogen receptor alpha, expressed by estrogen receptor 1 (ESR1) gene, is more abundant and   exists in all human reproductive systems. Association of ESR1 gene polymorphism has been   shown in some reproductive fields such as spontaneous abortion, endometriosis-related infertility   and in vitro fertili...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید