about
Variation in FTO contributes to childhood obesity and severe adult obesityGrowth hormone stimulates interferon regulatory factor-1 gene expression in the liverEndocrine manifestations of the rapid-onset obesity with hypoventilation, hypothalamic, autonomic dysregulation, and neural tumor syndrome in childhood.Functional Characterization of PRKAR1A Mutations Reveals a Unique Molecular Mechanism Causing Acrodysostosis but Multiple Mechanisms Causing Carney Complex.Acrodysostosis syndromes.Methylation and transcripts expression at the imprinted GNAS locus in human embryonic and induced pluripotent stem cells and their derivatives.Knock-In of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP-Dependent Protein Kinase A Activation: A Model of Type 1 Acrodysostosis.Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3.INS VNTR is a QTL for the insulin response to oral glucose in obese children.The common -866 G/A polymorphism in the promoter of uncoupling protein 2 is associated with increased carbohydrate and decreased lipid oxidation in juvenile obesity.A homozygous null mutation delineates the role of the melanocortin-4 receptor in humans.The human MC4R promoter: characterization and role in obesity.Association analysis indicates that a variant GATA-binding site in the PIK3CB promoter is a Cis-acting expression quantitative trait locus for this gene and attenuates insulin resistance in obese children.A single-nucleotide polymorphism in the p110beta gene promoter is associated with partial protection from insulin resistance in severely obese adolescents.Modulation of signaling through GPCR-cAMP-PKA pathways by PDE4 depends on stimulus intensity: Possible implications for the pathogenesis of acrodysostosis without hormone resistance.Heterogeneity of class I INS VNTR allele association with insulin secretion in obese children.Fetal growth is associated with the CpG methylation of the P2 promoter of the IGF1 gene.Correction to: Fetal growth is associated with CpG methylation in the P2 promoter of the IGF1 gene.Common nonsynonymous variants in PCSK1 confer risk of obesityGenetic Study of the Melanin-Concentrating Hormone Receptor 2 in Childhood and Adulthood Severe ObesityIn obese and non-obese adults, the cis-regulatory rs361072 promoter variant of PIK3CB is associated with insulin resistance not with type 2 diabetesAcute nuclear actions of growth hormone (GH): cycloheximide inhibits inducible activator protein-1 activity, but does not block GH-regulated signal transducer and activator of transcription activation or gene expressionContrasting acute in vivo nuclear actions of growth hormone and prolactinPaternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesityAkt phosphorylation in lymphocytes provides an index of in vitro insulin-like growth factor I sensitivity associated with growth hormone-induced growth
P50
Q28301922-7879B6A3-4D86-49DC-9504-277C29F49338Q28566393-B48F8CF0-5A69-4E69-B5FE-41801D32769EQ34796391-D3F006D9-88B1-4E56-93EB-3A63275EA64BQ36282925-01576099-6B81-4749-8717-64349F33920BQ37405329-C1E311BB-7AAE-47E2-A019-26F63D3DFC1EQ38954631-4395DA1C-AC0D-40FB-9098-72F3B47D5C7BQ42498492-13E5077B-8A53-47E0-8D87-F8EA17125B42Q42516625-F507DA30-2EC4-4DCD-9972-E12B6F457E4BQ44681233-C34F7769-AFFB-4098-9099-2CFCADBDECCFQ44705013-BC442F24-69CC-4A17-8184-182882E11176Q45973449-F860194F-A34A-4AAD-9281-5682ECA1A7D0Q46527935-BEEA5134-5E73-4CA5-9037-B7B628B646E1Q46918386-E0E12171-0ADA-4EDB-9DBE-46C14D91696FQ46923113-21C98ADA-2397-47FC-A029-1AA43F575683Q50472798-E16D998C-D6CF-4361-BC23-2A8993B2FF83Q51501014-1728C7D9-3FC6-45AC-9003-A747664E9500Q55260698-7191BD56-8044-4356-BF3E-DA274DF481BDQ55489825-3BF2150A-4D6C-41D4-AC7B-7E0A96128264Q57249730-C0E1C24C-30AB-4F99-9EBE-247028B07F2BQ57249760-11A64030-EF3D-41D1-B9CC-C2869C03015CQ57605783-B17942E5-242E-4628-ABD4-D204CB465ED6Q70824088-1830E4BC-A24C-4DDB-8501-4837F07C79FFQ71727314-56F837D3-C323-4C86-AD12-BD03DBD7C862Q74441641-6EBEF695-2368-4669-9983-9C819DE275C0Q80640344-A47785CE-0AD5-4B27-B41C-F6F132E2EC1C
P50
description
researcher ORCID ID = 0000-0001-8419-0451
@en
wetenschapper
@nl
name
Catherine Le Stunff
@ast
Catherine Le Stunff
@en
Catherine Le Stunff
@nl
type
label
Catherine Le Stunff
@ast
Catherine Le Stunff
@en
Catherine Le Stunff
@nl
prefLabel
Catherine Le Stunff
@ast
Catherine Le Stunff
@en
Catherine Le Stunff
@nl
P21
P31
P496
0000-0001-8419-0451