Prader-Willi syndrome, Snord115, and Htr2c editing (Q48494823)

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scientific article published on 4 August 2009

Language	Label	Description	Also known as
English	Prader-Willi syndrome, Snord115, and Htr2c editing	scientific article published on 4 August 2009

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

Prader-Willi syndrome, Snord115, and Htr2c editing (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

Prader–Willi syndrome

1 reference

based on heuristic

inferred from title

author name string

Heather Glatt-Deeley

1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

Daria L Bancescu

2

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

Marc Lalande

3

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

publication date

4 August 2009

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

11

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

143-144

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour

1 reference

https://pubmed.ncbi.nlm.nih.gov/19653017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered G protein-coupling functions of RNA editing isoform and splicing variant serotonin2C receptors

1 reference

https://pubmed.ncbi.nlm.nih.gov/19653017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of serotonin-2C receptor G-protein coupling by RNA editing

1 reference

https://pubmed.ncbi.nlm.nih.gov/19653017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19653017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19653017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19653017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large-scale mRNA sequencing determines global regulation of RNA editing during brain development.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19653017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-009-0209-X

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/19653017

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