(Q47933557)

6 February 2018

title

Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb. (English)

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6 February 2018

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Akiko Kashiwagi

1

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6 February 2018

Makiko Meguro

2

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6 February 2018

Hidetoshi Hoshiya

3

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6 February 2018

Masayuki Haruta

4

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6 February 2018

Fumitoshi Ishino

5

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6 February 2018

Toshiyuki Shibahara

6

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6 February 2018

Mitsuo Oshimura

7

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6 February 2018

publication date

12 March 2003

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6 February 2018

Journal of Human Genetics

published in

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6 February 2018

volume

48

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6 February 2018

issue

4

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6 February 2018

page(s)

194-198

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6 February 2018

https://scigraph.springernature.com/pub.10.1007/s10038-003-0009-3

exact match

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cites work

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

1 reference

12 December 2020

Multiple members of a third subfamily of P-type ATPases identified by genomic sequences and ESTs

1 reference

12 December 2020

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

1 reference

12 December 2020

Mutation screening and transmission disequilibrium study of ATP10C in autism.

1 reference

12 December 2020

Differential expression of putative transbilayer amphipath transporters

1 reference

12 December 2020

A novel ATPase on mouse chromosome 7 is a candidate gene for increased body fat

1 reference

12 December 2020

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

1 reference

12 December 2020

A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.

1 reference

12 December 2020

Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11- q13 duplications

1 reference

12 December 2020

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

1 reference

12 December 2020

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain.

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12 December 2020

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

1 reference

12 December 2020

Copper transport and its alterations in Menkes and Wilson diseases.

1 reference

12 December 2020

Genomic imprinting and the differential roles of parental genomes in brain development.

1 reference

12 December 2020

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons.

1 reference

12 December 2020

Prader-Willi and Angelman syndromes: sister imprinted disorders

1 reference

12 December 2020

1 reference

12 December 2020

The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a.

1 reference

12 December 2020

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

1 reference

12 December 2020

The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression

1 reference

12 December 2020

Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).

1 reference

12 December 2020

The role of tissue-specific imprinting as a source of phenotypic heterogeneity in human disease.

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12 December 2020

10.1007/S10038-003-0009-3

Identifiers

DOI

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6 February 2018

release_eit4xog57bhntk3vanhkjdmree

Fatcat ID

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PubMed ID

12730723

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6 February 2018