نتایج جستجو برای: ژن loc387715

تعداد نتایج: 15841  

Journal: :PLoS ONE 2008
Jeffrey A. Canter Lana M. Olson Kylee Spencer Nathalie Schnetz-Boutaud Brent Anderson Michael A. Hauser Silke Schmidt Eric A. Postel Anita Agarwal Margaret A. Pericak-Vance Paul Sternberg Jonathan L. Haines

The objective of this study was to determine if MTND2*LHON4917G (4917G), a specific non-synonymous polymorphism in the mitochondrial genome previously associated with neurodegenerative phenotypes, is associated with increased risk for age-related macular degeneration (AMD). A preliminary study of 393 individuals (293 cases and 100 controls) ascertained at Vanderbilt revealed an increased occurr...

Journal: :PLoS ONE 2008
Albert O. Edwards Brooke L. Fridley Katherine M. James Anil S. Sharma Julie M. Cunningham Nirubol Tosakulwong

Genome-wide association studies (GWASs) assess correlation between traits and DNA sequence variation using large numbers of genetic variants such as single nucleotide polymorphisms (SNPs) distributed across the genome. A GWAS produces many trait-SNP associations with low p-values, but few are replicated in subsequent studies. We sought to determine if characteristics of the genomic loci associa...

2009
Paul P. Connell Pearse A. Keane Evelyn C. O'Neill Rasha W. Altaie Edward Loane Kumari Neelam John M. Nolan Stephen Beatty

Age-related maculopathy (ARM) is the leading cause of blindness in the elderly. Although beneficial therapeutic strategies have recently begun to emerge, much remains unclear regarding the etiopathogenesis of this disorder. Epidemiologic studies have enhanced our understanding of ARM, but the data, often conflicting, has led to difficulties with drawing firm conclusions with respect to risk for...

Journal: :Archives of ophthalmology 2008
Daniela C Ferrara Joanna E Merriam K Bailey Freund Richard F Spaide Beatriz S Takahashi Inna Zhitomirsky Howard F Fine Lawrence A Yannuzzi Rando Allikmets

OBJECTIVE To analyze the frequency of major age-related macular degeneration (AMD)-associated alleles in patients with multifocal choroiditis (MFC). METHODS A cohort of 48 patients with MFC was compared with previously characterized cohorts of patients with advanced AMD (368 samples) and matched unaffected controls (368 samples). Allele and genotype frequencies of single nucleotide polymorphi...

Journal: :Ophthalmology 2010
Dominique C Baas Lintje Ho Sarah Ennis Joanna E Merriam Michael W T Tanck André G Uitterlinden Paulus T V M de Jong Angela J Cree Helen L Griffiths Fernando Rivadeneira Albert Hofman Cornelia van Duijn R Theodore Smith Gaetano R Barile Theo G M F Gorgels Johannes R Vingerling Caroline C W Klaver Andrew J Lotery Rando Allikmets Arthur A B Bergen

OBJECTIVE To investigate the association between variants in the complement component 5 (C5) gene and age-related macular degeneration (AMD). DESIGN Separate and combined data from 3 large AMD case-control studies and a prospective population-based study (The Rotterdam Study). PARTICIPANTS A total of 2599 AMD cases and 3458 ethnically matched controls. METHODS Fifteen single nucleotide po...

Journal: :Human molecular genetics 2007
Anand Swaroop Kari Eh Branham Wei Chen Goncalo Abecasis

Age-related macular degeneration (AMD) is a progressive neurodegenerative disease, which affects quality of life for millions of elderly individuals worldwide. AMD is associated with a diverse spectrum of clinical phenotypes, all of which include the death of photoreceptors in the central part of the human retina (called the macula). Tremendous progress has been made in identifying genetic susc...

Journal: :Molecular Vision 2009
Kyu Hyung Park Euijung Ryu Nirubol Tosakulwong Yanhong Wu Albert O. Edwards

PURPOSE Common genetic variation in the complement component 1 inhibitor gene (SERPING1) was recently reported to increase the risk of developing age-related macular degeneration (AMD). This study was performed to replicate the association between SERPING1 and AMD. METHODS Seven single nucleotide polymorphisms (SNPs) tagging common haplotypes across SERPING1 were genotyped on 786 (The Mayo Cl...

Journal: : 2023

زمینه و هدف: کم‌تحرکی در مقابل آن تمرین جزء عوامل مرتبط با شاخص‌های آسیب کبدی به‌شمار می‌روند. وجود این هنوز نقش بسیاری از تمرین‌های ورزشی به‌ویژه تمرینات تناوبی مقاومتی مصرف برخی مکمل‌های غذایی جمله اسپیرولینا بر ایمنی التهابی کاملاٌ شناخته نشده است؛ بنابراین هدف پژوهش تعیین اثر هشت هفته مکمل‌دهی هوازی فعالیت بافت کبد بیان ژن CXCL1 عضلة موش‌های صحرایی نر بود.مواد روش‌ها: نیمه‌تجربی، 60 سر موش ن...

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