Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies.

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FOXN1 deficient nude severe combined immunodeficiency.

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Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies.

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2015 nî lūn-bûn

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Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies.

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Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies.

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Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies.

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P1476

Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies

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Anna Fusco

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Roberta D'Assante

http://www.w3.org/2001/XMLSchema#string

Vera Gallo

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P2860

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

Combined immunodeficiency associated with DOCK8 mutations

EDA signaling and skin appendage development

Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium

T-box genes in human disorders

Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

An organized and functional thymus generated from FOXN1-reprogrammed fibroblasts

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25-38

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scholarly article

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10.3109/08830185.2015.1010724

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2015-03-16T00:00:00Z

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273638053

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25774666

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Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies.

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P2860

P2860

Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies.

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P2093

P2860

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P5875

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P1476

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P31

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P577

P5875

P698