Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice
about
Separate necdin domains bind ARNT2 and HIF1alpha and repress transcriptionDevelopmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdinLoss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice.Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint regionPostnatal changes in the expression pattern of the imprinted signalling protein XLαs underlie the changing phenotype of deficient mice.The Necdin-Wnt pathway causes epigenetic peroxisome proliferator-activated receptor gamma repression in hepatic stellate cells.The role of serotonin in respiratory function and dysfunction.Interactions between imprinting effects in the mouseImpaired hypothalamic regulation of endocrine function and delayed counterregulatory response to hypoglycemia in Magel2-null mice.Biological functions of melanoma-associated antigensNeurotoxicity of prenatal alcohol exposure on medullary pre-Bötzinger complex neurons in neonatal rats.Necdin, a p53 target gene, regulates the quiescence and response to genotoxic stress of hematopoietic stem/progenitor cells.Preparing for the first breath: prenatal maturation of respiratory neural control.Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development.Leptin signaling defects in a mouse model of Prader-Willi syndrome: An orphan genetic obesity syndrome no more?Natural breaking of the maternal silence at the mouse and human imprinted Prader-Willi locus: A whisper with functional consequences.Isolated in vitro brainstem-spinal cord preparations remain important tools in respiratory neurobiology.Distinct transcriptomes define rostral and caudal serotonin neurons.A Comprehensive Guide to the MAGE Family of Ubiquitin Ligases.Epigenetic cell fate regulation of hepatic stellate cells.Necdin shapes serotonergic development and SERT activity modulating breathing in a mouse model for Prader-Willi syndrome.Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome.
P2860
Q24674557-3F533C9D-0049-4DE4-B23E-4BBDE39A0B6FQ28585818-BB486583-52A3-4CEA-80C2-E62D774E0335Q30440358-B61630C6-F783-4369-A948-B3671A912D5EQ31138426-B41D3397-A0EA-42CB-A5F4-64FEAA6DE9D8Q33316874-4E4BBD92-16E4-4B74-AF19-190011F74EF1Q34130616-32ED93C6-9224-463B-90FD-CE1A2C550EC0Q34155250-2727E07B-F2B2-422D-A308-48C990B66D31Q34357201-905ED2A3-FA2B-437D-B889-B3901DA81FC2Q34567123-BA3486C7-52EF-4049-852D-3CBEF6D8385BQ35416510-683906B6-8EFB-47F4-82B8-D3D66A9C133BQ35819901-BCD948FD-10F5-4F7B-A985-8864DF54C2D1Q35969689-223C3D9F-1107-4724-8921-66CC9E8A7E20Q36194229-0C3B2463-1B9A-49C7-984E-00F0C11E7AA9Q36311721-7190E49E-F62C-447C-99CE-D3C049C3D959Q37089973-A1FF3095-95B9-48A9-8E3F-7ADB4EBC22C0Q37590281-E3170AA0-C936-4767-B444-FF0FCBB8A50CQ37690666-C4DEA983-2A81-46AE-9BD5-5736CEF3E39CQ37947957-0D663231-CE90-4A72-AA9C-B9F71F6E89BCQ38507715-29B0169A-ADA1-4BF2-AFA6-4012DB25E789Q39181769-05ED370A-FDCE-4C60-9D1F-C305CCFD7705Q41866516-925AB02A-25C3-4D12-8896-C8B995BA5965Q47230157-DA884593-F99E-4840-A3BD-43ECC6A5DDFCQ54566126-2B2872C1-4812-473F-B775-4D5E23787A79
P2860
Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice
description
2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2003
@ast
im März 2003 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2003/03/01)
@sk
vědecký článek publikovaný v roce 2003
@cs
wetenschappelijk artikel (gepubliceerd op 2003/03/01)
@nl
наукова стаття, опублікована в березні 2003
@uk
مقالة علمية (نشرت في مارس 2003)
@ar
name
Absence of Ndn, encoding the P ...... iratory drive in neonatal mice
@ast
Absence of Ndn, encoding the P ...... iratory drive in neonatal mice
@en
Absence of Ndn, encoding the P ...... iratory drive in neonatal mice
@nl
type
label
Absence of Ndn, encoding the P ...... iratory drive in neonatal mice
@ast
Absence of Ndn, encoding the P ...... iratory drive in neonatal mice
@en
Absence of Ndn, encoding the P ...... iratory drive in neonatal mice
@nl
prefLabel
Absence of Ndn, encoding the P ...... iratory drive in neonatal mice
@ast
Absence of Ndn, encoding the P ...... iratory drive in neonatal mice
@en
Absence of Ndn, encoding the P ...... iratory drive in neonatal mice
@nl
P2093
P1476
Absence of Ndn, encoding the P ...... iratory drive in neonatal mice
@en
P2093
Colin L Stewart
John J Greer
Matthieu Gérard
Rachel Wevrick
Silvia Pagliardini
P304
P356
10.1523/JNEUROSCI.23-05-01569.2003
P407
P577
2003-03-01T00:00:00Z