Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects.
about
Pseudohypoparathyroidism: one gene, several syndromes.A novel deletion involving GNAS exon 1 causes PHP1A and further refines the region required for normal methylation at exon A/B.A Large Inversion Involving GNAS Exon A/B and All Exons Encoding Gsα Is Associated With Autosomal Dominant Pseudohypoparathyroidism Type Ib (PHP1B).Early-Onset Obesity: Unrecognized First Evidence for GNAS Mutations and Methylation Changes.Pseudohypoparathyroidism type 1B - a rare cause of tetany: case report.Maternal 5mCpG Imprints at the PARD6G-AS1 and GCSAML Differentially Methylated Regions Are Decoupled From Parent-of-Origin Expression Effects in Multiple Human Tissues.Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans
P2860
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P2860
Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Genome-wide DNA methylation an ...... with GNAS imprinting defects.
@ast
Genome-wide DNA methylation an ...... with GNAS imprinting defects.
@en
type
label
Genome-wide DNA methylation an ...... with GNAS imprinting defects.
@ast
Genome-wide DNA methylation an ...... with GNAS imprinting defects.
@en
prefLabel
Genome-wide DNA methylation an ...... with GNAS imprinting defects.
@ast
Genome-wide DNA methylation an ...... with GNAS imprinting defects.
@en
P2093
P2860
P50
P1433
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Genome-wide DNA methylation an ...... s with GNAS imprinting defects
@en
P2093
Alejandro Martin-Trujillo
Anne Rochtus
Brigitte Decallonne
Chris Van Geet
David Monk
Giovanna Mantovani
Intza Garin
Suzanne Thiele
P2860
P2888
P356
10.1186/S13148-016-0175-8
P577
2016-01-26T00:00:00Z
P5875
P6179
1025009600
1029140069