نتایج جستجو برای: gdf8

تعداد نتایج: 96  

Journal: :Genome research 1997
R Kambadur M Sharma T P Smith J J Bass

A visibly distinct muscular hypertrophy (mh), commonly known as double muscling, occurs with high frequency in the Belgian Blue and Piedmontese cattle breeds. The autosomal recessive mh locus causing double-muscling condition in these cattle maps to bovine chromosome 2 within the same interval as myostatin, a member of the TGF-beta superfamily of genes. Because targeted disruption of myostatin ...

Journal: :Journal of animal science 2009
P L Johnson K G Dodds W E Bain G J Greer N J McLean R J McLaren S M Galloway T C van Stijn J C McEwan

This work investigated effects of carrying 0, 1, or 2 copies of the A allele resulting from the g+6723G-A transition in growth differentiation factor gene (GDF8) in New Zealand Texel-cross sheep at different lamb ages and carcass weights. Two Texel-cross sires carrying 1 copy of the A allele were mated to approximately 200 ewes carrying 0, 1, or 2 copies of the A allele. A total of 187 progeny ...

ژورنال: :تولیدات دامی 2011
یونس میار عبدالرضا صالحی سید احمد آل یاسین سمیه رئوف زاده

میوستاتین (mstn) که عامل رشد و تمایز شماره 8 (gdf8) نیز نامیده می شود از گروه عوامل تغییر رشد بتا (tgf?) می باشد که در کاهش رشد در پستانداران نقش دارد. یک چند شکلی تـک نوکلئوتیدی (snp) در ناحیه ترجمه نشده َ3 (3'utr) ژن میوستاتین به عنوان عامل هایپرتروفی عضله در کروموزوم شماره 2 (oar2) نژادهای گوسفند اروپایی تشخیص داده شده است. در این تحقیق، برای شناسایی چندشکلی تک نوکلئوتیدی (snp) ژن میوستاتین د...

ژورنال: تولیدات دامی 2011
سمیه رئوف زاده سید احمد آل یاسین عبدالرضا صالحی, یونس میار

میوستاتین (MSTN) که عامل رشد و تمایز شماره 8 (GDF8) نیز نامیده می شود از گروه عوامل تغییر رشد بتا (TGF?) می باشد که در کاهش رشد در پستانداران نقش دارد. یک چند شکلی تـک نوکلئوتیدی (SNP) در ناحیه ترجمه نشده َ3 (3'UTR) ژن میوستاتین به عنوان عامل هایپرتروفی عضله در کروموزوم شماره 2 (OAR2) نژادهای گوسفند اروپایی تشخیص داده شده است. در این تحقیق، برای شناسایی چندشکلی تک نوکلئوتیدی (SNP) ژن میوستاتین د...

Journal: :Physiological genomics 2008
Richard A Dennis Beata Przybyla Cathy Gurley Patrick M Kortebein Pippa Simpson Dennis H Sullivan Charlotte A Peterson

The purpose of this investigation was to compare expression of genes that function in inflammation and stress, cell structure and signaling, or remodeling and growth in skeletal muscle of young (32 +/- 7 yr, n = 15) and elderly (72 +/- 5 yr, n = 16) healthy subjects before and after a bout of resistance leg exercises. A real-time RT-PCR method was used to screen 100 transcripts in v. lateralis ...

Journal: :Molecular reproduction and development 2008
Michael K Skinner Michelle Schmidt Marina I Savenkova Ingrid Sadler-Riggleman Eric E Nilsson

Coordinated interactions between ovarian granulosa and theca cells are required for female endocrine function and fertility. To elucidate these interactions the regulation of the granulosa and theca cell transcriptomes during bovine antral follicle development were investigated. Granulosa cells and theca cells were isolated from small (<5 mm), medium (5-10 mm), and large (>10 mm) antral bovine ...

Journal: :Genetics and molecular research : GMR 2016
X C Song C Xu Z G Yue L Wang G W Wang F H Yang

Myostatin, encoded by the MSTN gene (previously GDF8), is a member of the transforming growth factor-β superfamily, which normally acts to limit skeletal muscle mass by regulating the number and growth of muscle fibers. In this study, a total of 84 myostatin gene sequences with known complete coding regions (CDS) and corresponding amino acid sequences were analyzed from 17 species, and differen...

Journal: :Biochimica et biophysica acta 2000
K Sakuma K Watanabe M Sano I Uramoto T Totsuka

Mice genetically deficient in growth and differentiation factor 8 (GDF8/myostatin) had markedly increased muscle fiber numbers and fiber hypertrophy. In the regenerating muscle of mice possessing FGF6 mutation, fiber remodeling was delayed. Although myostatin and FGF6 may be important for the maintenance, regeneration and/or hypertrophy of muscle, little work has been done on the possible role ...

2009
Jane Palsgaard Charlotte Brøns Martin Friedrichsen Helena Dominguez Maja Jensen Heidi Storgaard Camilla Spohr Christian Torp-Pedersen Rehannah Borup Pierre De Meyts Allan Vaag

BACKGROUND Gene expression alterations have previously been associated with type 2 diabetes, however whether these changes are primary causes or secondary effects of type 2 diabetes is not known. As healthy first degree relatives of people with type 2 diabetes have an increased risk of developing type 2 diabetes, they provide a good model in the search for primary causes of the disease. METHO...

Journal: :Development 2004
Xiuqian Mu Phillip D Beremand Sheng Zhao Rashmi Pershad Hongxia Sun Ann Scarpa Shuguang Liang Terry L Thomas William H Klein

Brn3b/Brn-3.2/POU4f2 is a POU domain transcription factor that is essential for retinal ganglion cell (RGC) differentiation, axonal outgrowth and survival. Our goal was to establish a link between Brn3b and the downstream events leading to RGC differentiation. We sought to determine both the number and types of genes that depend on Brn3b for their expression. RNA probes from wild-type and Brn3b...

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