SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice (Q21562297)

26 August 2022

Sally A Camper

Sally A

Camper

1 reference

26 August 2022

Feng Ding

Feng

Ding

1 reference

26 August 2022

Hong Hua Li

Hong Hua

1 reference

26 August 2022

Shengwen Zhang

series ordinal

author given names

Shengwen

author last names

Zhang

1 reference

26 August 2022

Nicola M Solomon

series ordinal

author given names

Nicola M

author last names

Solomon

1 reference

26 August 2022

Uta Francke

series ordinal

author given names

Uta

author last names

Francke

1 reference

Creative Commons Attribution 4.0 International

26 August 2022

language of work or name

English

0 references

publication date

2008

0 references

0 references

0 references

0 references

e1709

0 references

start time

5 March 2008

1 reference

April 2022 Public Data File from Crossref

copyrighted

0 references

cites work

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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

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Targeted disruption of the melanocortin-4 receptor results in obesity in mice

19 March 2017

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7 April 2017

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7 April 2017

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12 September 2017

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12 September 2017

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12 September 2017

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Eating behavior in Prader-Willi syndrome, normal weight, and obese control groups

12 September 2017

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12 September 2017

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Comparison of leptin protein levels in Prader-Willi syndrome and control individuals.

12 September 2017

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12 September 2017

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Growth hormone binding proteins and various forms of growth hormone: implications for measurements

12 September 2017

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Double-reciprocal crossover mediated by FLP-recombinase: a concept and an assay

12 September 2017

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Characteristics of abnormal food-intake patterns in children with Prader-Willi syndrome and study of effects of naloxone

27 September 2017

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Ube3a expression is not altered in Mecp2 mutant mice

27 September 2017

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Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?

30 May 2018

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Somatostatin infusion lowers plasma ghrelin without reducing appetite in adults with Prader-Willi syndrome

30 May 2018

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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

30 May 2018

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Prader-Willi syndrome and the hypothalamus

30 May 2018

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The response of "obese" (ob-ob) and "diabetic" (db-db) mice to treatments that influence body temperature

30 May 2018

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Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes.

30 May 2018

1 reference

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

21 January 2018

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Hypothalamic growth hormone-releasing hormone (GHRH) cell number is increased in human illness, but is not reduced in Prader-Willi syndrome or obesity

21 January 2018

1 reference

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Neural representations of hunger and satiety in Prader-Willi syndrome

21 January 2018

1 reference

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Elevated plasma ghrelin levels in Prader–Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001709

Serum ghrelin levels are inversely correlated with body mass index, age, and insulin concentrations in normal children and are markedly increased in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001709

Increased density of ghrelin-expressing cells in the gastric fundus and body in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001709

Extent and direction of ghrelin transport across the blood-brain barrier is determined by its unique primary structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001709

Efficient FLP recombination in mouse ES cells and oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001709

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001709

Increased adrenal androgen levels in patients with Prader-Willi syndrome are associated with insulin, IGF-I, and leptin, but not with measures of obesity.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248623

Assessment of growth parameters and life span of GHR/BP gene-disrupted mice.

29 November 2018

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Thermogenic defect in pre-obese ob/ob mice

29 November 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001709

Growth hormone improves body composition and motor development in infants with Prader-Willi syndrome after six months

21 January 2018

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12 December 2020

Measurement of excessive appetite and metabolic changes in Prader-Willi syndrome

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12 December 2020

Food intake in Prader-Willi syndrome and controls with obesity after administration of a benzodiazepine receptor agonist

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12 December 2020

Final adult height in children with Prader-Willi syndrome with and without human growth hormone treatment

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12 December 2020

Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice

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12 December 2020

10.1371/JOURNAL.PONE.0001709

Identifiers

DOI

1 reference

ADS bibcode

2008PLoSO...3.1709D

0 references

1 reference

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