نتایج جستجو برای: caprine gh gene

تعداد نتایج: 1151879  

Journal: :Molecular endocrinology 2008
Valerie Wauthier David J Waxman

Pituitary GH-secretory profiles are sex dependent and regulate the sexually dimorphic expression of a large number of genes in the liver. The slow response of many sex-specific liver genes to changes in plasma GH status suggests that GH acts in the liver via both direct and indirect mechanisms organized in a hierarchical regulatory network. Presently, genome-wide liver transcription profiling w...

2014
Sonika Ahlawat Rekha Sharma A. Maitra Manoranjan Roy M.S. Tantia

New, quick, and inexpensive methods for genotyping novel caprine Fec gene polymorphisms through tetra-primer ARMS PCR were developed in the present investigation. Single nucleotide polymorphism (SNP) genotyping needs to be attempted to establish association between the identified mutations and traits of economic importance. In the current study, we have successfully genotyped three new SNPs ide...

2016
Justyna Jarczak Jarosław Kaba Daria Reczyńska Emilia Bagnicka

Knowing about the genes involved in immunity, and being able to identify the factors influencing their expressions, helps in gaining awareness of the immune processes. The qPCR method is a useful gene expression analysis tool, but studies on immune system genes are still limited, especially on the caprine immune system. Caprine arthritis encephalitis, a disease caused by small ruminant lentivir...

2013
Alejandra Soberano Martínez José Herrera Camacho José Candelario Segura Correa

The objective of this study was to test the use of a commercial extender (Triladyl) as a diluent in caprine semen refrigerated at 15 ̊C, using caffeine (CF), heparin (HP), synthetic oviductal fluid (SOF) andtriladyl (TRY) as capacitating chemical agents at different times. Twenty ejaculates of caprine semen were collected using an artificial vagina. The ejaculates were diluted and refrigerated b...

Journal: :General and comparative endocrinology 2006
Hiroshi Kawauchi Stacia A Sower

The adenohypophysial hormones have been believed to have evolved from several ancestral genes by duplication followed by evolutionary divergence. To understand the origin and evolution of the endocrine systems in vertebrates, we have characterized adenohypophysial hormones in an agnathan, the sea lamprey Petromyzon marinus. In gnathostomes, adrenocorticotropin (ACTH) and melanotropin (MSH) toge...

Journal: :Molecular endocrinology 2009
Rosana D Meyer Ekaterina V Laz Ting Su David J Waxman

The transcriptional repressor Bcl6 is a male-specific rat liver gene product and one of 24 early GH-response genes encoding DNA-binding proteins. Presently, the sex specificity of Bcl6 was shown to emerge at puberty, when hepatic Bcl6 mRNA was induced in males and repressed in females by the female plasma GH profile. Hepatic Bcl6 mRNA was increased to near-normal male levels in hypophysectomize...

Journal: :Endocrinology 2000
H K Choi D J Waxman

The intracellular signaling molecule STAT5 is activated in rat liver by the intermittent male plasma GH pattern to a 10-fold higher level than by the more continuous pattern of plasma GH stimulation seen in females. Individual adult male rats are presently shown to exhibit large differences in liver STAT5 DNA-binding activity, which correlates with the presence of significant levels of GH in pl...

Journal: :American journal of physiology. Endocrinology and metabolism 2004
Joachim Woelfle Peter Rotwein

The long-term effects of growth hormone (GH) are mediated through coordinated changes in gene expression that are the outcome of interactions between hormone-activated signal transduction pathways and specific feedback loops. Recent studies in mice have implicated the transcription factor STAT5b as part of the GH-regulated somatic growth pathway, because mice lacking this protein showed diminis...

2014
Lina Merjaneh John S Parks Andrew B Muir Doris Fadoju

The role of growth hormone (GH) and its therapeutic supplementation in the trichorhinophalangeal syndrome type I (TRPS I) is not well delineated. TRPS I is a rare congenital syndrome, characterized by craniofacial and skeletal malformations including short stature, sparse, thin scalp hair and lateral eyebrows, pear-shaped nose, cone shaped epiphyses and hip dysplasia. It is inherited in an auto...

Journal: :Endocrine journal 1998
M Sato T Ohyama J Takahara

SECRETION and gene expression of GH are controlled by hypothalamic GH-releasing hormone (GRH) which acts through a G protein-coupled receptor, GRH receptor, resulting in activation of cyclic AMP and A-kinase systems in the somatotropes [1]. Many humoral factors affect GH responses to GRH [1] and some of their effects may be caused by qualitative and quantitative changes in GRH receptors. Glucoc...

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