(Q48415183)

11 February 2018

title

Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC. (English)

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11 February 2018

author name string

Amanda J DuBose

1

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11 February 2018

Karen A Johnstone

2

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11 February 2018

Emily Y Smith

3

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11 February 2018

Ryan A E Hallett

4

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11 February 2018

James L Resnick

5

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11 February 2018

publication date

6 November 2009

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11 February 2018

published in

Neurogenetics

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11 February 2018

volume

11

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11 February 2018

issue

2

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11 February 2018

page(s)

145-151

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11 February 2018

On the conflicting reports of imprinting status of mouse ATP10a in the adult brain: strain-background-dependent imprinting?

cites work

1 reference

12 December 2020

Mice heterozygous for Atp10c, a putative amphipath, represent a novel model of obesity and type 2 diabetes

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12 December 2020

High sensitivity mapping of methylated cytosines

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12 December 2020

Prader-Willi syndrome: consensus diagnostic criteria.

1 reference

12 December 2020

Imprinting-mutation mechanisms in Prader-Willi syndrome

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

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12 December 2020

Mechanisms of genomic imprinting

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12 December 2020

Distinct phenotypes distinguish the molecular classes of Angelman syndrome

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12 December 2020

Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb

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12 December 2020

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

1 reference

12 December 2020

A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects

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12 December 2020

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

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12 December 2020

UBE3A/E6-AP mutations cause Angelman syndrome

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

A targeted deletion upstream of Snrpn does not result in an imprinting defect

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12 December 2020

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

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12 December 2020

The Angelman ("happy puppet") syndrome

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12 December 2020

Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans

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12 December 2020

Atp10a, the mouse ortholog of the human imprinted ATP10A gene, escapes genomic imprinting

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12 December 2020

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

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12 December 2020

Gender influences monoallelic expression of ATP10A in human brain

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12 December 2020

The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion

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12 December 2020

10.1007/S10048-009-0226-9

Identifiers

DOI

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11 February 2018

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11 February 2018