Tìm thấy 19+ kết quả cho từ khóa "Fat deposition"
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Our study also provides an idea for investigating the molecular mechanism of abdominal fat deposition across multiple broiler lines.. Keywords: WGCNA, Broiler, Abdominal fat deposition, Lipid metabolism, Autophagy. abdominal fat deposition [3]. Excessive abdominal fat deposition not only wastes feed to producers but also in- creases risk to human health [4, 5].
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Crossing of sheep breeds with different patterns of fat deposition is one of the agronomical strategies for improving the meat qual- ity. To investigate the genetic profiles of fat tissues and to understand the differences in the genetic mechanisms determining fat deposition between distinct breeds, we characterized the transcriptome of PEF, SUF, and TAF from GLT and STH sheep breeds..
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Decreased testosterone levels after caponization leads to abdominal fat deposition in chickens. 0.05) and serum and AF testosterone levels decreased significantly ( P <. 0.01) after caponization. In AF tissue, 90 differentially expressed genes related to lipid metabolism were screened by gene expression profiling in caponized and sham-treated chickens. In vitro, Fat content was significantly lower in cells treated with testosterone compared with control cells ( P <.
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The discovery of QTL associated with fat deposition in the carcass allows the identification of positional candidate genes (PCGs) that might regulate fat deposition and be useful for selection against excess fat content in chicken ’ s carcass. Among these, four QTL were novel, while five have been previously reported in the literature.. We used sequence information from founder animals to detect 4843 SNPs in the 13 PCGs..
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Differentially expressed mRNAs during intramuscular fat deposition. Fig 1 The dynamics in the live weight (a) and the intramuscular fat (IMF) content (b) across and 7.5-year-old of age.. Similarly, after comparison of the data between the 0.5- and 2.5-year-old AA tissues, 72 DEGs were obtained, of which 39 were upregulated and 33 were downregulated (Fig. These results indicated that these 16 DEGs may have a role in the regulation of IMF- deposition development..
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The fat deposition is a consequence of the balance between energy intake and expenditure.
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More- over, the results showed that IRLnc and NR4A3 were. 6 Fold changes of Sec61B and NR4A3 . b Expression of Sec61B and NR4A3 in IRLnc silent cells and normal cells. 7 In situ colocalization of IRLnc and NR4A3 mRNA in myoblast and the potential effect pathway of IRLnc on fat deposition ( n =3). f Potential effect pathway of IRLnc on lipolysis. mechanism of the candidate LincRNA and its down- stream gene..
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Genomic scan of selective sweeps in thin and fat tail sheep breeds for identifying of candidate regions associated with fat deposition. Genome-wide analysis of the world's sheep breeds reveals high levels of historic mixture and strong recent selection
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A: Oil red O staining using frozen LD samples from each of the 6 pigs, HF: high-fat deposition group, LF: low-fat deposition group. B: Statistical analysis of the ratio of Oil red O-stained regions using students ’ T test. B: Heat map of the DEGs in the different lipid deposition groups. Validation of the transcriptome via qRT-PCR. The expression trends for all 14 genes in the LD tissues were consistent with the results of the transcriptome analysis.
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Pathways related to fat deposition, including fatty acid biosynthesis, steroid bio- synthesis, biosynthesis of unsaturated fatty acid and adipo- cytokine signalling pathways, were revealed in the comparison between 120 d and 240 d. The fatty acid bio- synthesis pathway was also significantly enriched in 400 d, but most of the DEGs were down-regulated..
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DEcircRNA host genes were concentrated predominately in TGF- β , MAPK, FoxO, and other signaling pathways related to skeletal muscle growth and fat deposition. The constructed ceRNA network plays a vital role in skeletal muscle growth and development, and fat deposition. miR-23b and SESN3 were found to participate in skeletal muscle growth regulation, also playing an important role in fat deposition.
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As mentioned above, we found that genes/proteins related to lipid transport and energy metabolism were differentially expressed in the embryonic liver between the fat and lean lines. Molecular differences related to lipid transport, lipid clearance and energy metabolism exist for hepatic lipid metabolism at embryonic stages between the fat and lean chicken lines, which might contribute to the striking differences of abdominal fat deposition at post-hatch stages..
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A better understanding of the genetic regulation network of subcutaneous fat tissue is necessary for the rational selection of Chinese domestic pig breeds. In the present study, subcutaneous adipocytes were isolated from Jiaxing Black pigs a Chinese indigenous pig breed with redundant subcutaneous fat deposition and Large White pigs a lean-type pig breed with relatively low subcutaneous fat deposition.
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In response to fasting, transgenic mice overexpressing SIRT6 gene attenuated excess fat deposition due to the reduction of PPARγ gene [9]. These results re- vealed that SIRT6 gene acted as a critical enzyme for the maintaining of lipid metabolism, which may be closely re- lated to fat deposition in mammals..
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Glucose metabolism and inflammation processes were the main pathways found in silico to influence intramuscular fat deposition in beef cattle in the integrative mRNA-miRNA co-expression analysis.. How- ever, little attention has been paid to the role of microRNAs in the regulation of IMF deposition in cattle..
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Patients with ectopic ACTH syndrome generally exhibit less marked weight gain and centripetal fat redistribution, probably because the exposure to excess glucocorticoids is relatively short and because cachexia reduces the propensity for weight gain and fat deposition. The ectopic ACTH syndrome is associated with several clinical features that distinguish it from other causes of Cushing's syndrome (e.g., pituitary adenomas, adrenal adenomas, iatrogenic glucocorticoid excess).
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These results expand the number of miRNAs expressed in abdominal adipose tissue and pro- vide a valuable resource for the selective breeding of ab- dominal fat traits in chickens.. The dy- namic change in abdominal fat deposition in Gushi chicken is largely consistent with the cellular basis of ab- dominal adipose tissue development described in.
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The gene STK3 (known in humans as MST2) acts as a repressor of genes involved in the fat deposition of Han- woo bovines. The genes MAPK11 and MAPK12 are part of the metabolic pathway p38 MAPK, which is a preserved mechanism of cellular response to a broad variety of extracellular signals, and is proposed as a regulator of cellular differentiation, proliferation and development [48].
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In obese patients, there is increased fat deposition in the chest wall, espe- cially in the back, which consequently increases the antero-posterior chest diameter.
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Fat deposition in the broiler chicken: a review. Neuronal atlas of the dorsal horn defines its architecture and links sensory input to transcriptional cell types. Evaluation of the effect of static magnetic fields combined with human hepatocyte growth factor on human satellite cell cultures. Single-Cell Analysis of the Muscle Stem Cell Hierarchy Identifies Heterotypic Communication Signals Involved in Skeletal Muscle Regeneration.