Concurrent Lpin1 and Nrcam mouse mutations result in severe peripheral neuropathy with transitory hindlimb paralysis (Q30491463)

20 August 2017

Concurrent Lpin1 and Nrcam mouse mutations result in severe peripheral neuropathy with transitory hindlimb paralysis (English)

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20 August 2017

peripheral neuropathy

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Brian Popko

8

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Jennifer L. Moran

object named as

Jennifer L Moran

2

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author name string

Darlene S Douglas

1

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20 August 2017

John R Bermingham

3

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20 August 2017

Xiang-Jun Chen

4

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20 August 2017

David N Brindley

5

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20 August 2017

Betty Soliven

6

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20 August 2017

David R Beier

7

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20 August 2017

language of work or name

English

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publication date

1 September 2009

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20 August 2017

Journal of Neuroscience

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20 August 2017

29

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20 August 2017

39

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20 August 2017

12089-12100

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describes a project that uses

20 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2773685/fullTextXML

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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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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Characterization of the peripheral neuropathy in neonatal and adult mice that are homozygous for the fatty liver dystrophy (fld) mutation

20 June 2018

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20 June 2018

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Bravo/Nr-CAM is closely related to the cell adhesion molecules L1 and Ng-CAM and has a similar heterodimer structure

20 June 2018

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TORC2 regulates hepatic insulin signaling via a mammalian phosphatidic acid phosphatase, LIPIN1.

20 June 2018

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Association of lipin 1 gene polymorphisms with measures of energy and glucose metabolism

26 November 2018

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Human subcutaneous adipose tissue LPIN1 expression in obesity, type 2 diabetes mellitus, and human immunodeficiency virus--associated lipodystrophy syndrome

26 November 2018

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Genetic variants within the LPIN1 gene, encoding lipin, are influencing phenotypes of the metabolic syndrome in humans

26 November 2018

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Dual functional activity of semaphorin 3B is required for positioning the anterior commissure

26 November 2018

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Disruption of the mouse Large gene in the enr and myd mutants results in nerve, muscle, and neuromuscular junction defects.

26 November 2018

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Myelin galactolipids are essential for proper node of Ranvier formation in the CNS.

26 November 2018

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Pathological and genetic analysis of the degenerating muscle (dmu) mouse: a new allele of Scn8a

26 November 2018

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12 December 2020

Nr-CAM and neurofascin interactions regulate ankyrin G and sodium channel clustering at the node of Ranvier

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12 December 2020

Peripheral neuropathy: a picture is worth a thousand words

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12 December 2020

Characterization of acetylcholine release and the compensatory contribution of non-Ca(v)2.1 channels at motor nerve terminals of leaner Ca(v)2.1-mutant mice

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12 December 2020

Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a-mutant mouse rolling Nagoya

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12 December 2020

10.1523/JNEUROSCI.2029-09.2009

Identifiers

DOI

1 reference

20 August 2017

1 reference

20 August 2017

PubMed publication ID

19793967

1 reference