The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region (Q28253418)

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author name string

C Rougeulle

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A Massacrier

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A Moncla

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M G Mattei

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P Malzac

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N Roëckel

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S Taviaux

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J L Lefranc

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P Cau

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P Berta

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M Lalande

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

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language of work or name

English

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publication date

November 1997

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published in

Nature Genetics

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volume

17

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issue

3

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page(s)

357-61

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cites work

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Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient

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Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint

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Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

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Parental imprinting and human disease

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Isolation and regional mapping of cDNAs expressed during early human development.

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Biochemical characterization of mouse brain necdin

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Structure and expression of the mouse necdin gene. Identification of a postmitotic neuron-restrictive core promoter

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

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The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain

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Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

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The Human γ-Aminobutyric Acid Receptor Subunit β3 and α5 Gene Cluster in Chromosome 15q11-q13 Is Rich in Highly Polymorphic (CA)n Repeats

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The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

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7 January 2021

Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region

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7 January 2021

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

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A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene.

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7 January 2021

Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution

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The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence

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Mice lacking Snrpn expression show normal regulation of neuronal alternative splicing events

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7 January 2021

Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndrome

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Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15

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7 January 2021

A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes

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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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Characterization of the human jumonji gene

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Identifiers

DOI

10.1038/NG1197-357

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

9354807

1 reference

Consolidated OpenCitations Corpus – April 2017