(Q28253418)

1

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author name string

C Rougeulle

2

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A Massacrier

3

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A Moncla

4

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M G Mattei

5

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P Malzac

6

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N Roëckel

7

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S Taviaux

8

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J L Lefranc

9

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P Cau

10

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P Berta

11

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M Lalande

https://scigraph.springernature.com/pub.10.1038/ng1197-357

12

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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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page(s)

357-61

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issue

3

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exact match

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cites work

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

1 reference

https://api.crossref.org/works/10.1038/NG1197-357

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG1197-357

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG1197-357

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

Parental imprinting and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

Biochemical characterization of mouse brain necdin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

Arrest of cell growth by necdin, a nuclear protein expressed in postmitotic neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

Characterization of the human jumonji gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-357

7 January 2021

Identifiers

DOI

10.1038/NG1197-357

1 reference

Consolidated OpenCitations Corpus – April 2017

4858274

4858274

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference