The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region
about
Necdin-related MAGE proteins differentially interact with the E2F1 transcription factor and the p75 neurotrophin receptorThe postmitotic growth suppressor necdin interacts with a calcium-binding protein (NEFA) in neuronal cytoplasmPhysical and functional interactions of neuronal growth suppressor necdin with p53Ectopic expression of necdin induces differentiation of mouse neuroblastoma cellsNecdin promotes ubiquitin-dependent degradation of PIAS1 SUMO E3 ligaseCancer/testis antigens: structural and immunobiological properties.Biological functions of melanoma-associated antigensNeural control of breathing: insights from genetic mouse models.Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.EBNA3C can modulate the activities of the transcription factor Necdin in association with metastasis suppressor protein Nm23-H1.Identification of candidate genes involved in the radiosensitivity of esophageal cancer cells by microarray analysis.cDNA cloning and tissue expression analyses of the encoding regions for three novel porcine genes- MJD1, CDC42 and NECD.On the origin of sensory impairment and altered pain perception in Prader-Willi syndrome: a neurophysiological study.Novel NTRK1 Frameshift Mutation in Congenital Insensitivity to Pain With Anhidrosis.Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation
P2860
Q24298935-F68DFC14-74CE-41D7-828E-FE5F8EB9E180Q28142122-DB415A9A-8619-4A51-B523-84E7A28A41CAQ28144785-798629B8-2A12-41AD-9F21-1B6AD4A9C89DQ28219184-5BC5BD73-1026-44C1-9F66-BEB1EACEF15EQ33727985-19552EF6-0AE2-45A2-9982-139AFF4D5A9DQ34568997-4DF3CF76-1E93-4FBC-B096-017A292F7D89Q35819901-5F20732F-0EE8-4BBF-A805-E9233A86F7ABQ37064742-09B35119-808F-45D8-AEEE-9268A884DAABQ38110760-9238297C-0E20-4DFB-98F3-DAFFF82E9931Q39900063-F062C99F-2265-4AB4-8CD7-2EF9770028F2Q39982783-DB9EE6EA-3578-4203-A51E-A6158CAD3930Q45905392-8D08C9F2-6325-4B41-88BC-FA060CF53552Q46262537-21A83A67-AF81-4596-937A-08231F1A7674Q51107047-E707DDDE-1DC3-4022-B95B-D03EF97BEECAQ53640716-105A27DC-3EBD-4ADB-A9A8-B01830B7C9F2Q57338204-56079C9F-89E0-44D0-8691-D281F42B86FF
P2860
The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
The human chromosomal gene for ...... Willi syndrome deletion region
@ast
The human chromosomal gene for ...... Willi syndrome deletion region
@en
The human chromosomal gene for ...... Willi syndrome deletion region
@en-gb
The human chromosomal gene for ...... Willi syndrome deletion region
@nl
type
label
The human chromosomal gene for ...... Willi syndrome deletion region
@ast
The human chromosomal gene for ...... Willi syndrome deletion region
@en
The human chromosomal gene for ...... Willi syndrome deletion region
@en-gb
The human chromosomal gene for ...... Willi syndrome deletion region
@nl
prefLabel
The human chromosomal gene for ...... Willi syndrome deletion region
@ast
The human chromosomal gene for ...... Willi syndrome deletion region
@en
The human chromosomal gene for ...... Willi syndrome deletion region
@en-gb
The human chromosomal gene for ...... Willi syndrome deletion region
@nl
P2093
P1433
P1476
The human chromosomal gene for ...... Willi syndrome deletion region
@en
P2093
P356
10.1016/S0378-1119(98)00206-6
P407
P577
1998-06-15T00:00:00Z