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The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader–Willi syndrome deletion region

Data up to Jan 2025

Published1998
Citations70
References16

Total Citations Per Year

Abstract

References (16)

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The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

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The Necdin Gene is Deleted in Prader-Willi Syndrome and is Imprinted in Human and Mouse

1997 • 230 citations

Necdin, A Postmitotic Neuron-specific Growth Suppressor, Interacts with Viral Transforming Proteins and Cellular Transcription Factor E2F1

1998 • 163 citations

A novel brain-specific mRNA encoding nuclear protein (necdin) expressed in neurally differentiated embryonal carcinoma cells

1991 • 150 citations

High-Resolution Cytogenetic Mapping of 342 New Cosmid Markers Including 43 RFLP Markers on Human Chromosome 17 by Fluorescence in Situ Hybridization

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Structure and Expression of the Mouse Necdin Gene

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Arrest of Cell Growth by Necdin, a Nuclear-Protein Expressed in Postmitotic Neurons

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The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader–Willi… (1998) – Gene | Metascience Observatory Explorer