Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models (Q28265327)

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5 January 2020

title

Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models (English)

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5 January 2020

main subject

Prader–Willi syndrome

1 reference

5

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5 January 2020

author name string

Feng Ding

1

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5 January 2020

Yelena Prints

2

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5 January 2020

Madhu S Dhar

3

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5 January 2020

Dabney K Johnson

4

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5 January 2020

Robert D Nicholls

6

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5 January 2020

Uta Francke

7

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language of work or name

English

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publication date

1 June 2005

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5 January 2020

number of pages

8

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inferred from page(s)

published in

Mammalian Genome

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volume

16

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issue

6

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5 January 2020

page(s)

424-431

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https://scigraph.springernature.com/pub.10.1007/s00335-005-2460-2

5 January 2020

exact match

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cites work

The human beta-globin locus control region

1 reference

12 December 2020

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

1 reference

12 December 2020

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

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

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

1 reference

12 December 2020

Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome

1 reference

12 December 2020

Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus

1 reference

12 December 2020

The expanding snoRNA world

1 reference

12 December 2020

Complementation analyses for 45 mutations encompassing the pink-eyed dilution (p) locus of the mouse

1 reference

12 December 2020

A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes

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

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

1 reference

12 December 2020

Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome

1 reference

12 December 2020

Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome

1 reference

12 December 2020

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

1 reference

12 December 2020

Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain

1 reference

12 December 2020

A microsatellite map of the pink-eyed dilution (p) deletion complex in mouse chromosome 7

1 reference

12 December 2020

10.1007/S00335-005-2460-2

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

3340240

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16075369%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

3340240

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

3340240