A hypomorphic mutation in Lpin1 induces progressively improving neuropathy and lipodystrophy in the rat (Q30425836)

19 October 2017

A hypomorphic mutation in Lpin1 induces progressively improving neuropathy and lipodystrophy in the rat (English)

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Jean-Sébastien Saulnier-Blache

19 October 2017

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Isaac J Nijman

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Joram D Mul

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19 October 2017

Noorjahan B Jagalur

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19 October 2017

Pim W Toonen

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19 October 2017

Gil-Soo Han

1 reference

19 October 2017

Jos F Brouwers

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19 October 2017

George M Carman

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19 October 2017

Dies Meijer

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19 October 2017

language of work or name

English

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publication date

1 June 2011

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Journal of Biological Chemistry

19 October 2017

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19 October 2017

286

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19 October 2017

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19 October 2017

26781-26793

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describes a project that uses

19 October 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3143639/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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The Transcription Factors SCIP and Krox-20 Mark Distinct Stages and Cell Fates in Schwann Cell Differentiation

20 June 2018

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Pmch expression during early development is critical for normal energy homeostasis

21 January 2018

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LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood

21 January 2018

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21 January 2018

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21 January 2018

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Expression of phosphatidylethanolamine N-methyltransferase-2 is markedly enhanced in long term choline-deficient rats

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21715287

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1074/JBC.M110.197947

1 reference

19 October 2017

1 reference

19 October 2017

PubMed publication ID

21715287

1 reference