(Q37462762)

English

Establishment of an improved mouse model for infantile neuroaxonal dystrophy that shows early disease onset and bears a point mutation in Pla2g6.

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Establishment of an improved mouse model for infantile neuroaxonal dystrophy that shows early disease onset and bears a point mutation in Pla2g6. (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Infantile neuroaxonal dystrophy

1 reference

based on heuristic

inferred from title

Masaru Taniguchi

8

object named as

Masaru Taniguchi

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

author name string

Haruka Wada

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Takuwa Yasuda

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Ikuo Miura

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Kazuhiko Watabe

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Chika Sawa

5

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Hajime Kamijuku

6

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Satoshi Kojo

7

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Ichizo Nishino

9

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Shigeharu Wakana

10

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Hisahiro Yoshida

11

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Ken-ichiro Seino

12

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

0 references

publication date

5 November 2009

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

The American Journal of Pathology

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

175

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

2257-2263

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Current hypotheses for the underlying biology of amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

Phospholipase A2 structure/function, mechanism, and signaling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

Age-related changes in bone morphology are accelerated in group VIA phospholipase A2 (iPLA2beta)-null mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

PLA2G6 mutation underlies infantile neuroaxonal dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

ENU-mutagenesis: insight into immune function and pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

Insulin secretory responses and phospholipid composition of pancreatic islets from mice that do not express Group VIA phospholipase A2 and effects of metabolic stress on glucose homeostasis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

Male mice that do not express group VIA phospholipase A2 produce spermatozoa with impaired motility and have greatly reduced fertility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

The molecular biology of the group VIA Ca2+-independent phospholipase A2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

Multiple splice variants of the human calcium-independent phospholipase A2 and their effect on enzyme activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

23 August 2017

Regulation of group VIA phospholipase A2 expression by sterol availability.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

14 September 2017

Establishment and characterization of immortalized Schwann cells from murine model of Niemann-Pick disease type C (spm/spm).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

26 June 2018

Expression, purification, and kinetic characterization of a recombinant 80-kDa intracellular calcium-independent phospholipase A2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

26 June 2018

Infantile neuroaxonal dystrophy--immunohistochemical and ultrastructural studies on the central and peripheral nervous systems in infantile neuroaxonal dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

26 June 2018

Infantile neuroaxonal dystrophy. Histological and electron microscopical study of two cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

26 June 2018

Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

26 June 2018

Neuroaxonal dystrophy caused by group VIA phospholipase A2 deficiency in mice: a model of human neurodegenerative disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

2 September 2018

Development and implementation of a database system to manage a large-scale mouse ENU-mutagenesis program

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

2 September 2018

A series of maturity onset diabetes of the young, type 2 (MODY2) mouse models generated by a large-scale ENU mutagenesis program

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

2 September 2018

Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2789634

2 September 2018

The Hallervorden-Spatz Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19893029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metachromatic leukodystrophy: molecular genetics and an animal model

1 reference

https://pubmed.ncbi.nlm.nih.gov/19893029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.2353/AJPATH.2009.090343

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q37462762&oldid=1508256663"