about
PRDM16 controls a brown fat/skeletal muscle switchMeat Science and Muscle Biology Symposium: stem cell niche and postnatal muscle growthNotch signaling as a novel regulator of metabolismPark7 expression influences myotube size and myosin expression in muscleLkb1 controls brown adipose tissue growth and thermogenesis by regulating the intracellular localization of CRTC3Canonical Wnt signaling induces BMP-4 to specify slow myofibrogenesis of fetal myoblastsNotch activation drives adipocyte dedifferentiation and tumorigenic transformation in micemiR-133a regulates adipocyte browning in vivoMammalian target of rapamycin is essential for cardiomyocyte survival and heart development in miceTRIM32 regulates skeletal muscle stem cell differentiation and is necessary for normal adult muscle regenerationAsymmetric self-renewal and commitment of satellite stem cells in muscle.Plk1 phosphorylates Sgt1 at the kinetochores to promote timely kinetochore-microtubule attachment.Long-term culture of decapsulated gastropod embryos: a transplantation study.p38-{gamma}-dependent gene silencing restricts entry into the myogenic differentiation program.Dlk1 is necessary for proper skeletal muscle development and regeneration.Loss of MyoD Promotes Fate Transdifferentiation of Myoblasts Into Brown Adipocytes.Notch signaling deficiency underlies age-dependent depletion of satellite cells in muscular dystrophy.Inhibition of polo-like kinase 1 (Plk1) enhances the antineoplastic activity of metformin in prostate cancer.Inhibition of Notch signaling promotes browning of white adipose tissue and ameliorates obesityElevated levels of active matrix metalloproteinase-9 cause hypertrophy in skeletal muscle of normal and dystrophin-deficient mdx mice.Heterogeneous activation of a slow myosin gene in proliferating myoblasts and differentiated single myofibersmTOR is necessary for proper satellite cell activity and skeletal muscle regenerationIntramuscular adipose is derived from a non-Pax3 lineage and required for efficient regeneration of skeletal musclesAMP-Activated Protein Kinase Directly Phosphorylates and Destabilizes Hedgehog Pathway Transcription Factor GLI1 in Medulloblastoma.Fighting obesity: When muscle meets fat.Hypoxia promotes satellite cell self-renewal and enhances the efficiency of myoblast transplantationDistinct roles for Pax7 and Pax3 in adult regenerative myogenesis.Myostatin facilitates slow and inhibits fast myosin heavy chain expression during myogenic differentiation.Hypoxia Inhibits Myogenic Differentiation through p53 Protein-dependent Induction of Bhlhe40 Protein.Fatty acid binding protein 4 expression marks a population of adipocyte progenitors in white and brown adipose tissuesDistinct populations of adipogenic and myogenic Myf5-lineage progenitors in white adipose tissues.Plk1 phosphorylation of orc2 and hbo1 contributes to gemcitabine resistance in pancreatic cancer.Stilbenoids remodel the DNA methylation patterns in breast cancer cells and inhibit oncogenic NOTCH signaling through epigenetic regulation of MAML2 transcriptional activity.A heterogeneous lineage origin underlies the phenotypic and molecular differences of white and beige adipocytes.Integrative biology of an embryonic respiratory behaviour in pond snails: the 'embryo stir-bar hypothesis'.Stage-specific effects of Notch activation during skeletal myogenesis.Proinflammatory cytokine tumor necrosis factor (TNF)-like weak inducer of apoptosis (TWEAK) suppresses satellite cell self-renewal through inversely modulating Notch and NF-κB signaling pathways.The molecular regulation of muscle stem cell function.miR-133 links to energy balance through targeting Prdm16.Conditional Loss of Pten in Myogenic Progenitors Leads to Postnatal Skeletal Muscle Hypertrophy but Age-Dependent Exhaustion of Satellite Cells.
P50
Q24657178-076D24BD-2E7F-41E7-A04A-4F396344C957Q26824418-0AFFCD8C-2AC7-47E4-9781-6200E0693C4DQ27014152-41567D9A-B618-447A-B301-82A10126D5CFQ27314984-33E2C086-F4CD-4115-B9FD-3F35939FB8A0Q27335445-67ADA735-5DAA-4849-84EB-DA82896292A5Q27499254-67DEA626-E5EB-4954-9441-C3F398241C9DQ28389770-A2FE8417-7C97-466F-B338-F1EAEB7AF77DQ28534612-6C2BB861-116E-47FE-9223-0D98C849FC2DQ28593301-F6C7FB57-E823-4DB8-8368-0F8E2A06F2F9Q28593851-19856A7F-3B30-4CD3-AA60-D743848ACA42Q30489194-5E5F039B-387F-49B0-AA4D-69DD4FF1187BQ30525261-C4626F0A-11FA-462D-BD87-4C8E92A7BC91Q31121294-CC4AC521-7911-4EE2-8A95-B4A842B3FC9FQ33589771-07A3E96D-DA17-4C7C-A6C7-3DE87F0236FDQ33760580-16384A2B-A318-4E8E-B588-1566AC7AE0DCQ33809481-B66C3FA4-05CE-44B8-ADC9-79071160202AQ33935640-6808BF94-520B-4347-A369-1714FC704300Q34042731-FC294E02-985F-4675-B2CB-2C837D39DF61Q34275062-AA9DAE4E-ACDA-490D-929C-FE3D7460C374Q35389391-2324487C-BD56-4D9A-BE0A-ECB514E5FE36Q35618657-17D3ACEB-5812-4620-9098-FB59DF3D2713Q35795172-6BDD9353-FEB3-4D57-B1F1-99CAFFF27317Q35875354-98D30CB9-838B-4E4D-A357-ACB11DF85517Q35906944-EB4061EF-EA00-42F4-BA76-14148F2486D0Q35998806-06000A14-3760-4B85-9F90-D931FCF695E0Q36110979-50BB8FD2-3D6E-4A59-B803-3A88BD659459Q36116761-4AB4F2A7-C335-41B9-BD34-BC9E6AEC0E79Q36353084-664D0D00-5782-4533-8DE8-0CF5C4F53832Q36444267-64CFD05D-C96C-481E-A63E-59A58CB76BA1Q36482896-D6FFE592-9ED4-4712-A39C-4653C6AF349EQ37002690-9E3A6B8D-C51F-49B7-9EC6-F7411EFAC7CDQ37066064-D1C90C8A-AC24-44FB-B26D-AB7845481E31Q37074064-01571F40-AEEB-4971-B38C-09643AEA02E1Q37096483-A1B9C8F8-F03C-4BC2-9482-131A87C2B921Q37167970-1E3F43E3-7E97-4182-AAFF-A4987A9656AFQ37351564-4CB5A23A-D60C-45BC-8287-498F585E7D46Q37368645-A78FA4BC-EFD0-41FA-BE55-27137826FA8BQ37426152-B9E09541-4039-4EE0-8209-4905B8BA8F26Q37511399-FEC34D66-2D55-40F5-8260-64A011E9A570Q37530309-1D7C2F62-1DF6-4B6D-9D72-F98E382B2F5B
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Shihuan Kuang
@ast
Shihuan Kuang
@en
Shihuan Kuang
@es
Shihuan Kuang
@nl
Shihuan Kuang
@sl
type
label
Shihuan Kuang
@ast
Shihuan Kuang
@en
Shihuan Kuang
@es
Shihuan Kuang
@nl
Shihuan Kuang
@sl
prefLabel
Shihuan Kuang
@ast
Shihuan Kuang
@en
Shihuan Kuang
@es
Shihuan Kuang
@nl
Shihuan Kuang
@sl
P106
P1153
55680946000
P31
P496
0000-0001-9180-3180