about
Differences in muscle transcriptome among pigs phenotypically extreme for fatty acid compositionInformation compression exploits patterns of genome composition to discriminate populations and highlight regions of evolutionary interestInferring the in vivo cellular program of developing bovine skeletal muscle from expression data.Validation of alternative methods of data normalization in gene co-expression studies.A gene coexpression network for bovine skeletal muscle inferred from microarray data.Porcine tissue-specific regulatory networks derived from meta-analysis of the transcriptome.Gene expression studies of developing bovine longissimus muscle from two different beef cattle breeds.A differential wiring analysis of expression data correctly identifies the gene containing the causal mutation.Regulatory impact factors: unraveling the transcriptional regulation of complex traits from expression data.A Pathway-Centered Analysis of Pig Domestication and Breeding in Eurasia.RNF14 is a regulator of mitochondrial and immune function in muscle.Chicken muscle mitochondrial content appears co-ordinately regulated and is associated with performance phenotypes.Compression distance can discriminate animals by genetic profile, build relationship matrices and estimate breeding values.Effect of aestivation on long bone mechanical properties in the green-striped burrowing frog, Cyclorana alboguttata.Surviving the drought: burrowing frogs save energy by increasing mitochondrial coupling.Role of calcium and vesicle-docking proteins in remobilising dormant neuromuscular junctions in desert frogs.Obese humans as economically designed feed converters: symmorphosis and low oxidative capacity skeletal muscle.Disorder of endoplasmic reticulum calcium channel components is associated with the increased apoptotic potential in pale, soft, exudative pork.Molecular regulation of high muscle mass in developing Blonde d'Aquitaine cattle foetuses.Chronic exposure to anabolic steroids induces the muscle expression of oxytocin and a more than fiftyfold increase in circulating oxytocin in cattle.Skeletal muscle extracellular matrix remodelling after aestivation in the green striped burrowing frog, Cyclorana alboguttata.Effect of prolonged inactivity on skeletal motor nerve terminals during aestivation in the burrowing frog, Cyclorana alboguttata.Skeletal muscle atrophy occurs slowly and selectively during prolonged aestivation in Cyclorana alboguttata (Gunther 1867).A marker-derived gene network reveals the regulatory role of PPARGC1A, HNF4G, and FOXP3 in intramuscular fat deposition of beef cattle1The effects of saltwater acclimation on neurotransmitters in the lingual salt glands of the estuarine crocodile, Crocodylus porosusGene expression profiling of bovine skeletal muscle in response to and during recovery from chronic and severe undernutritionSymmorphosis and livestock bioenergetics: production animal muscle has low mitochondrial volume fractionsLongitudinal muscle gene expression patterns associated with differential intramuscular fat in cattleGene expression identifies metabolic and functional differences between intramuscular and subcutaneous adipocytes in cattle
P50
Q27323691-AE14F63A-ADB5-4AB3-B70B-ED1084BE91ADQ28657673-2991973E-E29B-47B9-9256-B53A72B30AA0Q30590381-3B08AFAA-897D-4516-A735-8150311117FFQ30977172-58EC6DC8-40C6-47C2-9E21-EB5710E7B45AQ31061577-9649519B-6FE0-4DB5-94A2-F5840804DB8FQ31104325-3367AC04-7C1C-4D60-BBBF-1E1EB4F289DCQ33294143-D87B6D24-25E2-4F8A-BB65-AD2628173529Q33438450-4D2519FB-7291-40F9-A1B4-EA2EEAAD2D84Q33530433-169988F2-11EE-4B2A-8E22-F0CD16C84D64Q33877320-B84333CF-820A-4C75-93A2-5E53AD868349Q37531752-87BBB9DA-E287-4769-A5E6-0F86966FE762Q37612449-CEC92C34-9F13-4075-B205-C0AAA5CC09BFQ39085336-42920E93-A9FF-481D-8152-B8AC235D2DBCQ39085347-4C104378-DEFD-42EC-88FE-4161EAD0AD18Q39125444-FD26D979-EF1E-4EDD-994C-C15D23D38B83Q39162790-C3771198-E12A-47C7-B9D4-45DD5BFD15FBQ39273298-077319B5-C909-4FC5-920A-F932F1A1689DQ40070179-61BE25A2-C538-438F-996A-6CD1BFBC7F17Q45693870-8BB24B89-EB4E-48FC-BF52-1F4D990BFF79Q48286148-42EE47E5-1E59-4B6C-8B2E-B8D5237C5C2AQ50699911-FCE6F4BD-187F-4362-A7A8-A36E259C80A4Q50781005-B12875D3-B9C8-415B-8E75-69BE04FBF793Q51413148-37AEB779-A209-4582-8543-85345D884EE5Q57278736-1C3DE931-4A04-453C-91EA-A2537FA057E3Q60302737-8D354214-1460-45F4-9604-0FAE858F07C8Q79341075-4EEED12F-1FEE-4129-AE97-8D2760659ED4Q83703748-1BACA354-586C-4A73-AB11-5261154D8E6AQ85951888-F4668199-C885-4A04-9088-24FAFB2D6855Q93009243-D2E24354-B289-45A7-82E6-5012E8F9E9C2
P50
description
researcher ORCID ID = 0000-0002-3549-9396
@en
wetenschapper
@nl
name
Nick Hudson
@ast
Nick Hudson
@en
Nick Hudson
@es
Nick Hudson
@nl
type
label
Nick Hudson
@ast
Nick Hudson
@en
Nick Hudson
@es
Nick Hudson
@nl
prefLabel
Nick Hudson
@ast
Nick Hudson
@en
Nick Hudson
@es
Nick Hudson
@nl
P31
P496
0000-0002-3549-9396