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necdin

Known as: Necdin Homolog (Mouse), Necdin (Mouse) Homolog, Prader-Willi Syndrome Chromosome Region 
Necdin (321 aa, ~36 kDa) is encoded by the human NDN gene. This protein plays a role in suppression of cell growth in postmitotic neurons.
National Institutes of Health

Papers overview

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Highly Cited
2006
Highly Cited
2006
Necdin, a member of the MAGE (melanoma antigen) protein family, is expressed predominantly in terminally differentiated neurons… 
Highly Cited
2005
Highly Cited
2005
Necdin and Magel2 are related proteins inactivated in Prader-Willi syndrome (PWS), a sporadic chromosomal deletion disorder. We… 
Highly Cited
2004
Highly Cited
2004
Necdin is a growth suppressor expressed predominantly in postmitotic neurons and implicated in their terminal differentiation… 
Highly Cited
2003
Highly Cited
2003
necdin (Ndn) is one of a cluster of genes deleted in the neurodevelopmental disorder Prader-Willi syndrome. necdin is upregulated… 
Review
2002
Review
2002
Since the identification of the first MAGE gene in 1991, the MAGE family has expanded dramatically, and over 25 MAGE genes have… 
Highly Cited
1999
Highly Cited
1999
Necdin is expressed in virtually all postmitotic neurons, and ectopic expression of this protein suppresses cell proliferation… 
Highly Cited
1998
Highly Cited
1998
Necdin is a nuclear protein expressed in virtually all postmitotic neurons, and ectopic expression of this protein strongly… 
Highly Cited
1996
Highly Cited
1996
Necdin is a 325 amino acid residue protein encoded by a cDNA clone isolated from neurally differentiated embryonal carcinoma… 
Highly Cited
1995
Highly Cited
1995
Necdin is a 325 amino acid residue protein localized to the nuclei of postmitotic neurons, which withdraw permanently from the…