about
P688
Necdin-related MAGE proteins differentially interact with the E2F1 transcription factor and the p75 neurotrophin receptorThe Prader-Willi syndrome protein necdin interacts with the E1A-like inhibitor of differentiation EID-1 and promotes myoblast differentiationCellular and subcellular localization of necdin in fetal and adult mouse brainNecdin interacts with the Msx2 homeodomain protein via MAGE-D1 to promote myogenic differentiation of C2C12 cellsAbsence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal miceEssential role for the Prader-Willi syndrome protein necdin in axonal outgrowthDisruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survivalDevelopmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdinDisruption of the mouse necdin gene results in early post-natal lethalityThe ciliary protein cystin forms a regulatory complex with necdin to modulate Myc expression
P921
Q24298935-3EB92E85-4E13-471F-B92C-DC7C9AC73E47Q24321957-DC5CC9F6-1BB0-4752-A948-B6A2AAEA0EB6Q28144941-645B9BD8-6F2D-4542-AB02-429750567E6BQ28505040-1736DD07-5720-44D0-9A96-B6C3092A1EEAQ28505055-21B5454A-87C4-429D-B192-1263AA5D2AE1Q28508700-10E85940-25C1-42B7-A8AA-7EA76FED2453Q28508839-A5255ABF-F838-4F10-8607-8AF4BB893D84Q28585818-9E60315E-6177-4B85-9943-36471CA49578Q28587922-B6F8D32F-D648-4E34-8C69-7A8562B10096Q28591172-37A18D0B-3C0C-44A7-91B6-BBA99A004824
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
proteinë
@sq
proteïne in Necdin
@nl
protèin
@ace
بروتين في فأر المنازل
@ar
name
Necdin
@en
Necdin
@nl
type
label
Necdin
@en
Necdin
@nl
altLabel
Ndn
@en
necdin
@en
prefLabel
Necdin
@en
Necdin
@nl