about
myKaryoView: a light-weight client for visualization of genomic dataRecombinant growth hormone in Prader-Willi syndromeHigh-resolution analysis of parent-of-origin allelic expression in the mouse brainGenomic imprinting disorders in humans: a mini-reviewCopy number variants in obesity-related syndromes: review and perspectives on novel molecular approachesGenetics of Prader-Willi syndrome and Prader-Will-Like syndromePrader-Willi syndrome mental health research strategy workshop proceedings: the state of the science and future directionsMagel2 is required for leptin-mediated depolarization of POMC neurons in the hypothalamic arcuate nucleus in miceMagel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cellsThe motivating operations concept: current status and critical responseWhole genome sequencing of one complex pedigree illustrates challenges with genomic medicineA novel mutation in the maternally imprinted PEG3 domain results in a loss of MIMT1 expression and causes abortions and stillbirths in cattle (Bos taurus).Postural adaptations to long-term training in Prader-Willi patients.Circulating angiopoietin-like 8 (ANGPTL8) is a marker of liver steatosis and is negatively regulated by Prader-Willi Syndrome.Severe Short Stature in an Adolescent Male with Prader-Willi Syndrome and Congenital Adrenal Hyperplasia: A Therapeutic ConundrumColloquium papers: Transfers and transitions: parent-offspring conflict, genomic imprinting, and the evolution of human life history.A reduced-energy intake, well-balanced diet improves weight control in children with Prader-Willi syndrome.Necdin protects embryonic motoneurons from programmed cell death.Prader-Willi syndrome: a single center's experience in KoreaLower brain-derived neurotrophic factor in patients with prader-willi syndrome compared to obese and lean control subjectsEffects of growth hormone treatment in adults with Prader-Willi syndromeInduced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes.Genotype-phenotype associations and human eye color.Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology.Prader-Willi Syndrome: Obesity due to Genomic Imprinting.A homozygous missense mutation in HERC2 associated with global developmental delay and autism spectrum disorder.Different distribution of the genetic subtypes of the Prader-Willi syndrome in the elderly.A descriptive study of colorectal function in adults with Prader-Willi Syndrome: high prevalence of constipationRegulation of alternative splicing by the core spliceosomal machinery.An atypical case of hypomethylation at multiple imprinted loci.Growth standards of infants with Prader-Willi syndrome.Systematic review of the clinical and genetic aspects of Prader-Willi syndrome.Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome.Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes.Ube3a imprinting impairs circadian robustness in Angelman syndrome modelsBirth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion.Prader-Willi syndrome: A primer for clinicians.The neurobiology of mouse models syntenic to human chromosome 15q.Irisin and the Metabolic Phenotype of Adults with Prader-Willi SyndromeUnique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Prader-Willi syndrome.
@en
type
label
Prader-Willi syndrome.
@en
prefLabel
Prader-Willi syndrome.
@en
P2860
P356
P1476
Prader-Willi syndrome.
@en
P2093
Daniel J Driscoll
Suzanne B Cassidy
P2860
P2888
P356
10.1038/EJHG.2008.165
P577
2008-09-10T00:00:00Z