about
Cis-Natural Antisense Transcripts Are Mainly Co-expressed with Their Sense Transcripts and Primarily Related to Energy Metabolic Pathways during Muscle Development.FoxO1: a novel insight into its molecular mechanisms in the regulation of skeletal muscle differentiation and fiber type specificationIdentification and Expression Profiling of miRNAome in Goat longissimus dorsi Muscle from Prenatal Stages to a Neonatal StageThe Longissimus and Semimembranosus muscles display marked differences in their gene expression profiles in pigMaternal and paternal genomes differentially affect myofibre characteristics and muscle weights of bovine fetuses at midgestationQTL for microstructural and biophysical muscle properties and body composition in pigs.Target genes of myostatin loss-of-function in muscles of late bovine fetuses.Gene expression studies of developing bovine longissimus muscle from two different beef cattle breeds.Specific fibre composition and metabolism of the rectus abdominis muscle of bovine Charolais cattle.A gene network switch enhances the oxidative capacity of ovine skeletal muscle during late fetal developmentOntogenetic changes in skeletal muscle fiber type, fiber diameter and myoglobin concentration in the Northern elephant seal (Mirounga angustirostris)An integrated analysis revealed different microRNA-mRNA profiles during skeletal muscle development between Landrace and Lantang pigs.Genome-wide association study identifies candidate genes for piglet splay leg syndrome in different populations.Comparative analyses by sequencing of transcriptomes during skeletal muscle development between pig breeds differing in muscle growth rate and fatness.Genetic variability of transcript abundance in pig peri-mortem skeletal muscle: eQTL localized genes involved in stress response, cell death, muscle disorders and metabolism.Co-expression analysis of fetal weight-related genes in ovine skeletal muscle during mid and late fetal development stages.Genome-wide association study for intramuscular fat deposition and composition in Nellore cattle.Muscle transcriptomic investigation of late fetal development identifies candidate genes for piglet maturity.Integrative analysis of porcine microRNAome during skeletal muscle development.Skeletal muscle characterization of Japanese quail line selectively bred for lower body weight as an avian model of delayed muscle growth with hypoplasia.Wnt antagonist, secreted frizzled-related protein 1, is involved in prenatal skeletal muscle development and is a target of miRNA-1/206 in pigs.Transcriptome analysis of cattle muscle identifies potential markers for skeletal muscle growth rate and major cell types.Dynamic transcriptome profiles of skeletal muscle tissue across 11 developmental stages for both Tongcheng and Yorkshire pigs.Effects of Dietary Energy Sources on Post Mortem Glycolysis, Meat Quality and Muscle Fibre Type Transformation of Finishing Pigs.Double Muscling in Cattle: Genes, Husbandry, Carcasses and Meat.Transcriptional Profiling Identifies Location-Specific and Breed-Specific Differentially Expressed Genes in Embryonic Myogenesis in Anas Platyrhynchos.iTRAQ-based quantitative proteomic analysis reveals the distinct early embryo myofiber type characteristics involved in landrace and miniature pigComparative Analyses between Skeletal Muscle miRNAomes from Large White and Min Pigs Revealed MicroRNAs Associated with Postnatal Muscle Hypertrophy.Integrative analysis of transcriptomics and proteomics of skeletal muscles of the Chinese indigenous Shaziling pig compared with the Yorkshire breed.Are fish fed with cyanobacteria safe, nutritious and delicious? A laboratory study.Developmental Stage, Muscle and Genetic Type Modify Muscle Transcriptome in Pigs: Effects on Gene Expression and Regulatory Factors Involved in Growth and Metabolism.Effects of SNPs and alternative splicing within HGF gene on its expression patterns in Qinchuan cattle.Transcriptome analysis revealed chimeric RNAs, single nucleotide polymorphisms and allele-specific expression in porcine prenatal skeletal muscle.Identification and profiling of microRNAs in the embryonic breast muscle of pekin duck.The effects of Capn1 gene inactivation on skeletal muscle growth, development, and atrophy, and the compensatory role of other proteolytic systemsCNN3 is regulated by microRNA-1 during muscle development in pigs.Molecular and functional heterogeneity of early postnatal porcine satellite cell populations is associated with bioenergetic profile.Deep RNA sequencing of pectoralis muscle transcriptomes during late-term embryonic to neonatal development in indigenous Chinese duck breeds.Systematic analysis of transcription start sites in avian developmentMyostatin preferentially down-regulates the expression of fast 2x myosin heavy chain in cattle.
P2860
Q27301016-5FD61936-02F0-4E85-BE7D-D478E0CE91D7Q28080095-DE644A80-C805-4DB2-BAC4-B3355E230329Q28109674-BBA8A100-B68B-4CA7-8CCB-0B81AB4CFFB1Q28385436-2C9ADD03-EC91-4BE9-B772-F9CB966B86FEQ28709986-8E6F8000-8B62-4559-A8AE-B81186A2FA1BQ33235949-1B86151E-4B67-40E1-8999-9F3E5F188E5BQ33276244-9AF19F9A-1A88-423D-8FBE-E08A2B603A40Q33294143-8F23FBF3-83DE-4C5A-BA49-9B68A220DD61Q33537384-9C83E19E-21D2-403E-9415-6DD7324490EDQ33603782-7B8B11A9-CBE8-4768-8BF2-FD1B3CD0D95DQ33729455-7A24DC27-37D9-426F-A191-ED11E648EAF2Q33747250-75FAAB9A-6264-4068-83A6-1E5365A18938Q33876945-DC602F1D-6E92-4809-93E7-0E2813DF2ECCQ33921312-529DCA3C-FB41-437D-81EA-F7D852FCD8B6Q34067233-30660CB3-9DAD-4E0F-8051-D5563E4FD497Q34284046-B53CC529-EF2E-4C3E-ABF7-1E2D8975EC6DQ34504380-1735726E-B105-4D38-8C70-E17BBFCD497DQ34869247-CE540C7A-2D4B-45B7-B1A1-D9DC090A6871Q34988387-58C4EE47-EB66-4097-821B-5A75746742F1Q35157246-EC71E7BE-4C92-4F9C-AB92-A20FB6B6AE7CQ35177245-B771F705-5440-40E4-8D16-318BEC367584Q35607754-EB1F6A0E-3330-4416-B551-EBC4EE6C746FQ35623815-C65E698F-4991-4256-A25C-7F9E64C4BFC2Q35678742-5B465F8C-A6FA-4D99-986C-E1B7BDCFA567Q35826856-F177FFC6-A1B2-43B9-834F-0FB735C4CAF9Q35858762-5A39C075-8731-4467-8815-9E5566EAAFBAQ35934436-7F4CFFFF-D4FD-49C4-A2B6-25283F7A8D06Q36038035-57B0A782-39E4-457C-815C-D3C3FEEF9D09Q36050937-505EFB98-8A05-4E7F-9278-D2234A40F35DQ36168460-7A38B5D6-A7F1-4395-9189-C8EC5101644BQ36218606-D4DD4494-76CE-40FF-804F-98EB70963DAEQ36398090-FA4A2E6C-FD73-436B-9CD1-EB182E365257Q37050183-36CFBAAD-306D-4531-828E-307569884A23Q37509912-F6A482AA-2652-4720-A260-0DD65B11A8D4Q37656447-0AD800A5-51FA-4478-91EE-528E5F611900Q37692725-75E811DE-CF21-4313-A93F-48DDD3E7F465Q37721483-ED4CDA00-985C-435E-A1F9-C9687B3E0D9AQ38403227-2EECAD40-5D56-4EC3-9911-C00CFE0DC520Q41702214-CA35F7F4-A52A-4E3B-B0B9-701F4F14538DQ43076554-69520FBD-0594-411A-A171-243B7801B043
P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Muscle fibre ontogenesis in farm animal species.
@ast
Muscle fibre ontogenesis in farm animal species.
@en
type
label
Muscle fibre ontogenesis in farm animal species.
@ast
Muscle fibre ontogenesis in farm animal species.
@en
prefLabel
Muscle fibre ontogenesis in farm animal species.
@ast
Muscle fibre ontogenesis in farm animal species.
@en
P2093
P356
P1476
Muscle fibre ontogenesis in farm animal species
@en
P2093
Brigitte Picard
Cécile Berri
Louis Lefaucheur
P304
P356
10.1051/RND:2002035
P577
2002-09-01T00:00:00Z