Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6) (Q24675845)

GOA release 2020-03-11

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2

Akira Kinoshita

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author name string

Christopher R Ingraham

1

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Shinji Kondo

3

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Baoli Yang

4

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Samin Sajan

5

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Kurt J Trout

6

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Margaret I Malik

7

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Martine Dunnwald

8

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Stephen L Goudy

9

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Michael Lovett

10

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Jeffrey C Murray

11

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Brian C Schutte

Mammary serine protease inhibitor (Maspin) binds directly to interferon regulatory factor 6: identification of a novel serpin partnership

12

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language of work or name

English

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publication date

November 2006

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published in

Nature Genetics

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volume

38

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page(s)

1335-40

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issue

11

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cites work

1 reference

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Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population

7 April 2017

1 reference

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Interferon regulatory factor 1 binding to p300 stimulates DNA-dependent acetylation of p53

7 April 2017

1 reference

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Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

7 April 2017

1 reference

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Immunodeficiency and chronic myelogenous leukemia-like syndrome in mice with a targeted mutation of the ICSBP gene

7 April 2017

1 reference

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Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Variation in IRF6 contributes to nonsyndromic cleft lip and palate

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

IRF-7 is the master regulator of type-I interferon-dependent immune responses

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Integral role of IRF-5 in the gene induction programme activated by Toll-like receptors

7 April 2017

1 reference

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Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

The POU domain factor Skin-1a represses the keratin 14 promoter independent of DNA binding. A possible role for interactions between Skn-1a and CREB-binding protein/p300

7 April 2017

1 reference

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Identification of 14-3-3sigma mutation causing cutaneous abnormality in repeated-epilation mutant mouse

7 April 2017

1 reference

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Interferon regulatory factor-7 synergizes with other transcription factors through multiple interactions with p300/CBP coactivators

7 April 2017

1 reference

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Distinct and essential roles of transcription factors IRF-3 and IRF-7 in response to viruses for IFN-alpha/beta gene induction

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population

7 April 2017

1 reference

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Stem cell depletion through epidermal deletion of Rac1.

28 September 2017

1 reference

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Significant association between IRF6 820G->A and non-syndromic cleft lip with or without cleft palate in the Thai population

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

p300 regulates p63 transcriptional activity

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Novel IRF6 mutations in Japanese patients with Van der Woude Syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Essential and non-redundant roles of p48 (ISGF3 gamma) and IRF-1 in both type I and type II interferon responses, as revealed by gene targeting studies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Targeted disruption of IRF-1 or IRF-2 results in abnormal type I IFN gene induction and aberrant lymphocyte development

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Abnormal expression and processing of keratins in pupoid fetus (pf/pf) and repeated epilation (Er/Er) mutant mice

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

A mutation in stratifin is responsible for the repeated epilation (Er) phenotype in mice.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Crystal structure of IRF-3 in complex with CBP.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

IkappaB kinase-alpha acts in the epidermis to control skeletal and craniofacial morphogenesis

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Abnormal morphogenesis but intact IKK activation in mice lacking the IKKalpha subunit of IkappaB kinase

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082114

Developmental expression analysis of the mouse and chick orthologues of IRF6: the gene mutated in Van der Woude syndrome.

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG1903

Novel mutations in the IRF6 gene for Van der Woude syndrome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17041601

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Requirement for the transcription factor LSIRF/IRF4 for mature B and T lymphocyte function

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17041601

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG1903

1 reference

Dimensions Publication ID

2938292

1003571215

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2938292

1 reference

1 reference

1 reference