Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
about
Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardationSnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in miceTen putative contributors to the obesity epidemicA deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadismThe Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin geneDBS for ObesityQuantitative analysis of 5HT(2C) receptor RNA editing patterns in psychiatric disordersPsychosis and autism as diametrical disorders of the social brainDevelopmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdinGrowth hormone treatment and adverse events in Prader-Willi syndrome: data from KIGS (the Pfizer International Growth Database).Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death.Unraveling the genetics of human obesity.Central nervous system regulation of energy metabolism: ghrelin versus leptin.Editing of neurotransmitter receptor and ion channel RNAs in the nervous systemMice with altered serotonin 2C receptor RNA editing display characteristics of Prader-Willi syndrome.The role of GNAS and other imprinted genes in the development of obesity.Translational neuroscience approaches to hyperphagia.Obesity and leptin resistance: distinguishing cause from effect.The role of serotonin in respiratory function and dysfunction.Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome.The serotonergic anatomy of the developing human medulla oblongata: implications for pediatric disorders of homeostasisEpigenetic regulation of mesenchymal stem cells: a focus on osteogenic and adipogenic differentiation.Congenital imprinting disorders: EUCID.net - a network to decipher their aetiology and to improve the diagnostic and clinical careMutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism.Prader-Willi syndrome: A primer for clinicians.Genomic imprinting and the social brain.Neural and hormonal control of food hoardingInduced pluripotent stem cells to model and treat neurogenetic disordersEnhanced activation of reward mediating prefrontal regions in response to food stimuli in Prader-Willi syndrome.Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.Identification of Candidate Genes for Reactivity in Guzerat (Bos indicus) Cattle: A Genome-Wide Association Study.Modes of imprinted gene action in learning disability.Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS featuresSerotonin and the regulation of mammalian energy balance.Epigenetic regulation of neural gene expression and neuronal function.Ghrelin, the peripheral hunger hormone.Klinefelter's syndrome and Prader-Willi syndrome: a rare combination.Rare variants in single-minded 1 (SIM1) are associated with severe obesity.Ghrelin concentrations in Prader-Willi syndrome (PWS) infants and children: changes during developmentNecdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development.
P2860
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P2860
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
@ast
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
@en
type
label
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
@ast
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
@en
prefLabel
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
@ast
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
@en
P1476
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
@en
P356
10.1016/J.TEM.2003.11.003
P577
2004-01-01T00:00:00Z