Disruption of the mouse necdin gene results in early post-natal lethality

Prader-Willi Syndrome: Consensus Diagnostic Criteria

1993 • 1,279 citations

Know Your Neighbors: Three Phenotypes in Null Mutants of the Myogenic bHLH Gene MRF4

1996 • 572 citations

Cre-mediated gene deletion in the mammary gland

1997 • 504 citations

A mouse model for Prader-Willi syndrome imprinting-centre mutations

1998 • 298 citations

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region

1992 • 265 citations

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

1997 • 247 citations

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region

1992 • 243 citations

Identification of a novel paternally expressed gene in the Prader - Willi syndrome region

1994 • 243 citations

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

Modification of 15q11 — q13 DNA methylation imprints in unique Angelman and Prader — Willi patients

1993 • 142 citations

Deletion of a HoxD enhancer induces transcriptional heterochrony leading to transposition of the sacrum

1997 • 112 citations

Imprinting of a RING Zinc-Finger Encoding Gene in the Mouse Chromosome Region Homologous to the Prader-Willi Syndrome Genetic Region

1999 • 110 citations

Structure and Expression of the Mouse Necdin Gene

1996 • 107 citations

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

1995 • 90 citations

Expression of necdin, an embryonal carcinoma-derived nuclear protein, in developing mouse brain

1992 • 88 citations

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

1998 • 70 citations

NEONATAL RESPIRATORY DEPRESSION AND DELAY IN DIAGNOSIS IN PRADER‐WILLI SYNDROME

1989 • 38 citations

The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region.

1997 • 38 citations

The Mouse Necdin Gene Is Expressed from the Paternal Allele Only and Lies in the 7C Region of the Mouse Chromosome 7, a Region of Conserved Synteny to the Human Prader-Willi Syndrome Region

1997 • 31 citations

Structure and function of the human chromosome 15 imprinting center

1997 • 22 citations