(Q37349747)

English

Mutation in Mpzl3, a novel [corrected] gene encoding a predicted [corrected] adhesion protein, in the rough coat (rc) mice with severe skin and hair abnormalities

scientific article published on February 2007

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Mutation in Mpzl3, a novel [corrected] gene encoding a predicted [corrected] adhesion protein, in the rough coat (rc) mice with severe skin and hair abnormalities (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

author name string

Tongyu Cao

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Peter Racz

2

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Kornelia M Szauter

3

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Gergely Groma

4

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Garrett Y Nakamatsu

5

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Benjamin Fogelgren

6

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Eszter Pankotai

7

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Qing-Ping He

8

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Katalin Csiszar

9

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

language of work or name

0 references

publication date

1 February 2007

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Journal of Investigative Dermatology

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

127

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

1375-1386

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

https://scigraph.springernature.com/pub.10.1038/sj.jid.5700706

0 references

Progressive hair loss and myocardial degeneration in rough coat mice: reduced lysyl oxidase-like (LOXL) in the skin and heart

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

6 September 2017

Purkinje cell degeneration (pcd) phenotypes caused by mutations in the axotomy-induced gene, Nna1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

6 September 2017

Map Manager QTX, cross-platform software for genetic mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

6 September 2017

Desmosomes: structure and function in normal and diseased epidermis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

6 September 2017

c-Myc activation in transgenic mouse epidermis results in mobilization of stem cells and differentiation of their progeny

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

6 September 2017

An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

6 September 2017

Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

6 September 2017

Epithelial V-like antigen (EVA), a novel member of the immunoglobulin superfamily, expressed in embryonic epithelia with a potential role as homotypic adhesion molecule in thymus histogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

6 September 2017

Overexpression of Smad7 results in severe pathological alterations in multiple epithelial tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

14 September 2017

Evidence that Myc activation depletes the epidermal stem cell compartment by modulating adhesive interactions with the local microenvironment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

26 June 2018

Deregulated expression of c-Myc depletes epidermal stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

26 June 2018

The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

26 June 2018

Genetics analysis of mouse mutations Abnormal feet and tail and rough coat, which cause developmental abnormalities and alopecia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2745225

2 September 2018

Histological characteristics of the pelage skin of rough fur mice (C3H/HeJ- ruf/ruf)

1 reference

https://pubmed.ncbi.nlm.nih.gov/17273165

12 December 2020

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Identifiers

10.1038/SJ.JID.5700706

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

ResearchGate publication ID

0 references

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