نتایج جستجو برای: respectively three different genotypic variants including aa

تعداد نتایج: 3886708  

2016
Touraj Mahmoudi Hamid Farahani Hossein Nobakht Reza Dabiri Mohammad Reza Zali

BACKGROUND Colorectal cancer (CRC) is the second most commonly diagnosed cancer and the fourth leading cause of cancer-related mortality around the world. OBJECTIVES With regard to the role of obesity in colorectal cancer (CRC) and the role of leptin in obesity, we investigated whether leptin (LEP) and leptin receptor (LEPR) gene variants are associated with CRC risk. PATIENTS AND METHODS W...

Journal: :international journal of molecular and cellular medicine 0
fakhraddin naghibalhossaini department of biochemistry, shiraz university of medical sciences, school of medicine, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)سازمان های دیگر: autoimmune research center, shiraz university of medical sciences, school of medicine,shiraz,iran . hesam ehyakonandeh department of biochemistry, shiraz university of medical sciences, school of medicine, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences) alireza nikseresht autoimmune research center, shiraz university of medical sciences, school of medicine, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences) eskandar kamali autoimmune research center, shiraz university of medical sciences, school of medicine, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)

multiple sclerosis (ms) is a demyelinating neuro- inflammatory autoimmune disease of the central nervous system. genetic predisposition has long been suspected in the etiology of this disease. the association between mthfr polymorphisms and ms has been ivestigated in different ethnic groups. we investigated the association between mthfr c677t and a1298c missense variants and ms in 180 patients ...

Journal: :Genetics 1966
E Pollak

N most of the existing theory of selection the genotypes present in a population I are assumed to have constant selective advantages or disadvantages in relation to each other. But a different case was considered by HALDANE (1 961 ) . He assumed that generations do not overlap and that in each generation a proportion C of the males and a proportion c of the females are removed from the populati...

Journal: :Genes 2023

Catechol-O-methyl transferase (COMT) gene variants are involved in different neuropsychiatric disorders and cognitive impairments, associated with altered dopamine function. This study investigated the genotypic haplotypic association of COMT rs4680 rs4618 polymorphisms severity other clinical symptoms 544 male 385 female subjects schizophrenia. rs4818 G carriers were more frequent patients mil...

Journal: :JIIS (Jurnal Ilmiah Ibnu Sina): ilmu farmasi dan kesehatan 2022

Potassium-azeloyl-diglycinate is an active ingredient as a sebum normalizer and skin lightening-agent to moisturize treat hyperpigmentation. Anti-aging (AA) cream cosmetic used prevent premature aging. The use of emulsifying agent necessary produce stable cream. One the commonly emulsifying-agents triethanolamine. This study aims formulate AA-cream potassium-azeloyl-diglycinate preparation vari...

2015
Enas Osman Fatme Al Anouti Gehad El ghazali Afrozul Haq Rajaa Mirgani Habiba Al Safar

Vitamin D is getting more attention everyday due to its importance in maintaining bone and calcium homeostasis, cellular proliferation, differentiation and immune response. Vitamin D is derived from diet or elicited in the skin by the activation of 7-dehydrocholesterol, which is an inert molecule that must be activated by ultraviolet light to form pre-vitamin D3. Recent studies connected the ge...

Journal: :thrita 0
zahra salehi department of medical biotechnology, school of allied medicine, iran university of medical sciences, tehran, ir iran arshad hosseini department of medical biotechnology, school of allied medicine, iran university of medical sciences, tehran, ir iran; department of medical biotechnology, school of allied medicine, iran university of medical sciences, tehran, ir iran. tel: +98-2186704604, fax: +98-2188622533 mohammad najafi department of biochemistry, school of medicine, iran university of medical sciences, tehran, ir iran hussain ahmad department of medical biotechnology, school of advanced technologies in medicine, international campus, tehran university of medical sciences, tehran, ir iran mohammad reza fayazi department of medical biotechnology, school of advanced technologies in medicine, tehran university of medical sciences, tehran, ir iran

results no significant correlation was seen in rs3743527 and rs129081 polymorphism’s allelic and genotypic frequencies between the patient group and control individuals (p value > 0.05). the average frequencies of rs129081 g and c alleles was 40 (58%) and 29 (42%), respectively. in our sample the average frequencies of rs3743527 c and t alleles, were 41 (61%) and 28 (39%), respectively. the res...

2011
Jian Zhao Hui Wu Melanie Khosravi Huijuan Cui Xiaoxia Qian Jennifer A. Kelly Kenneth M. Kaufman Carl D. Langefeld Adrienne H. Williams Mary E. Comeau Julie T. Ziegler Miranda C. Marion Adam Adler Stuart B. Glenn Marta E. Alarcón-Riquelme Bernardo A. Pons-Estel John B. Harley Sang-Cheol Bae So-Young Bang Soo-Kyung Cho Chaim O. Jacob Timothy J. Vyse Timothy B. Niewold Patrick M. Gaffney Kathy L. Moser Robert P. Kimberly Jeffrey C. Edberg Elizabeth E. Brown Graciela S. Alarcon Michelle A. Petri Rosalind Ramsey-Goldman Luis M. Vilá John D. Reveille Judith A. James Gary S. Gilkeson Diane L. Kamen Barry I. Freedman Juan-Manuel Anaya Joan T. Merrill Lindsey A. Criswell R. Hal Scofield Anne M. Stevens Joel M. Guthridge Deh-Ming Chang Yeong Wook Song Ji Ah Park Eun Young Lee Susan A. Boackle Jennifer M. Grossman Bevra H. Hahn Timothy H. J. Goodship Rita M. Cantor Chack-Yung Yu Nan Shen Betty P. Tsao

Systemic lupus erythematosus (SLE), a complex polygenic autoimmune disease, is associated with increased complement activation. Variants of genes encoding complement regulator factor H (CFH) and five CFH-related proteins (CFHR1-CFHR5) within the chromosome 1q32 locus linked to SLE, have been associated with multiple human diseases and may contribute to dysregulated complement activation predisp...

2008
Satyanarayana Rachagani Ishwar Dayal Gupta

Point mutations in exon IV of the bovine κ-casein (CSN3) gene determine two allelic variants, A and B. These variants were distinguished by polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) analysis in the indigenous Sahiwal and Tharparkar cattle breeds. DNA samples (252 Sahiwal and 56 Tharparkar) were analyzed for allelic variants of the CSN3 gene. Polymorphism ...

2013
Wen-Ping Lin Xue-Jin Wang Cong-Ren Wang Li-Qun Zhang Neng Li Fa-Sheng Wang Jian-Hua Lin

OBJECTIVE This study aimed to investigate whether or not hypoxia-inducible factor-1α (HIF-1α) gene variants are associated with the susceptibility and clinical characteristics of lumbar disc degeneration (LDD). METHODS We examined 320 patients with LDD and 447 gender- and age-matched control subjects. We also determined the HIF-1α gene variants, including C1772T (P582S) and G1790A (A588T) pol...

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