(Q34396280)

English

Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l) gene

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l) gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Joseph Toonen

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Lina Liang

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Duska J Sidjanin

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

publication date

28 August 2012

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

13

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

76

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

https://scigraph.springernature.com/pub.10.1186/1471-2156-13-76

0 references

Inhibitor of apoptosis-stimulating protein of p53 (iASPP) prevents senescence and is required for epithelial stratification

1 reference

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6 July 2018

iASPP/p63 autoregulatory feedback loop is required for the homeostasis of stratified epithelia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

The international workshop on meibomian gland dysfunction: report of the definition and classification subcommittee

1 reference

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6 July 2018

Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice

1 reference

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6 July 2018

ΔNp63 is an ectodermal gatekeeper of epidermal morphogenesis

1 reference

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6 July 2018

The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

The Meibomian puzzle: combining pieces together

1 reference

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6 July 2018

Deletion of G protein-coupled receptor 48 leads to ocular anterior segment dysgenesis (ASD) through down-regulation of Pitx2.

1 reference

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6 July 2018

Biochemical and structural studies of ASPP proteins reveal differential binding to p53, p63, and p73

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

Genetic basis of skin appendage development

1 reference

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6 July 2018

ASPP: a new family of oncogenes and tumour suppressor genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 mice

1 reference

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6 July 2018

Anterior eye development and ocular mesenchyme: new insights from mouse models and human diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

Velvet, a dominant Egfr mutation that causes wavy hair and defective eyelid development in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

c-Jun is essential for organization of the epidermal leading edge

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

iASPP oncoprotein is a key inhibitor of p53 conserved from worm to human.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

Identification of a novel inhibitor of nuclear factor-kappaB, RelA-associated inhibitor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

TGF alpha deficiency results in hair follicle and eye abnormalities in targeted and waved-1 mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

Mice with a null mutation of the TGF alpha gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

Eyelid development, fusion and subsequent reopening in the mouse.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

Targeted disruption of mouse EGF receptor: effect of genetic background on mutant phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

6 July 2018

The mouse waved-2 phenotype results from a point mutation in the EGF receptor tyrosine kinase

1 reference

https://api.crossref.org/works/10.1186%2F1471-2156-13-76

21 January 2018

Epithelial immaturity and multiorgan failure in mice lacking epidermal growth factor receptor

1 reference

https://api.crossref.org/works/10.1186%2F1471-2156-13-76

21 January 2018

A mutation in NFkappaB interacting protein 1 causes cardiomyopathy and woolly haircoat syndrome of Poll Hereford cattle.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2156-13-76

21 January 2018

Ectodermal dysplasias: clinical and molecular review.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2156-13-76

21 January 2018

Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

27 October 2018

Electron-microscopic and immunohistochemical studies of eyelid reopening in the mouse.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469352

27 October 2018

Ocular symptoms and signs in patients with ectodermal dysplasia syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22928477

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An essential role for ectodomain shedding in mammalian development

1 reference

https://pubmed.ncbi.nlm.nih.gov/22928477

12 December 2020

based on heuristic

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HB-EGF promotes epithelial cell migration in eyelid development

1 reference

https://pubmed.ncbi.nlm.nih.gov/22928477

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cutting edge: TNF-alpha-converting enzyme (TACE/ADAM17) inactivation in mouse myeloid cells prevents lethality from endotoxin shock

1 reference

https://pubmed.ncbi.nlm.nih.gov/22928477

12 December 2020

based on heuristic

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10.1186/1471-2156-13-76

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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0 references

release_y4cnjpuc6fcvfk5xc53ugjx4lm

1 reference

https://api.fatcat.wiki/v0/release/y4cnjpuc6fcvfk5xc53ugjx4lm

24 November 2022

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

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1 August 2017

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