Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation (Q21092489)

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scientific article published on 28 December 2007

Deletion of the MBII-85 snoRNA Gene Cluster in Mice Results in Postnatal Growth Retardation

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English	Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation	scientific article published on 28 December 2007	Deletion of the MBII-85 snoRNA Gene Cluster in Mice Results in Postnatal Growth Retardation

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scholarly article

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Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation (English)

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Timofey S Rozhdestvensky

object named as

Timofey S Rozhdestvensky

8

author given names

Timofey S

author last names

Rozhdestvensky

1 reference

PubMed publication ID

15 August 2022

Jürgen Brosius

9

object named as

Jürgen Brosius

author given names

Jürgen

author last names

Brosius

1 reference

PubMed publication ID

15 August 2022

Boris V Skryabin

1

author given names

Boris V

author last names

Skryabin

object named as

Boris V Skryabin

1 reference

PubMed publication ID

15 August 2022

2

author given names

Leonid V

author last names

Gubar

object named as

Leonid V Gubar

1 reference

PubMed publication ID

15 August 2022

3

author given names

Birte

author last names

Seeger

object named as

Birte Seeger

1 reference

PubMed publication ID

15 August 2022

5

author given names

Sergej

author last names

Handel

object named as

Sergej Handel

1 reference

PubMed publication ID

15 August 2022

6

author given names

Thomas

author last names

Robeck

object named as

Thomas Robeck

1 reference

PubMed publication ID

15 August 2022

author name string

Jana Pfeiffer

4

author given names

Jana

author last names

Pfeiffer

1 reference

PubMed publication ID

15 August 2022

Elena Karpova

7

author given names

Elena

author last names

Karpova

1 reference

PubMed publication ID

15 August 2022

language of work or name

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publication date

28 December 2007

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3

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12

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e235

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copyright license

Creative Commons Attribution 4.0 International

28 December 2007

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April 2022 Public Data File from Crossref

copyright status

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

Small nucleolar RNAs: an abundant group of noncoding RNAs with diverse cellular functions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

A mammalian gene with introns instead of exons generating stable RNA products

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

Disruption of the mouse necdin gene results in early post-natal lethality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

19 March 2017

Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

7 April 2017

The Prader-Willi/Angelman imprinted domain and its control center

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

ADAR2-mediated editing of RNA substrates in the nucleolus is inhibited by C/D small nucleolar RNAs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

Neuronal untranslated BC1 RNA: targeted gene elimination in mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

Small Nucleolar RNAs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

Chromosome engineering in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

Superpolylinkers in cloning and expression vectors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

12 September 2017

Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

27 September 2017

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

27 September 2017

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

30 May 2018

A candidate model for Angelman syndrome in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

30 May 2018

An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

30 May 2018

Prevalence study of Prader-Willi syndrome in North Dakota

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

30 May 2018

The imprinted gene Magel2 regulates normal circadian output.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

29 November 2018

Hormonal and metabolic defects in a prader-willi syndrome mouse model with neonatal failure to thrive

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

29 November 2018

The paradox of Prader-Willi syndrome: a genetic model of starvation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

29 November 2018

Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

29 November 2018

The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

29 November 2018

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

29 November 2018

Standard growth curves for Japanese patients with Prader-Willi syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

29 November 2018

Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2323313

29 November 2018

Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18166085

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhythm is not enough

1 reference

https://pubmed.ncbi.nlm.nih.gov/18166085

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/18166085

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incriminating gene suspects, Prader-Willi style

1 reference

https://pubmed.ncbi.nlm.nih.gov/18166085

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PGEN.0030235

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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