Marie Unna Congenital Hypotrichosis Latest Advances

Identification of a novel sporadic U2HR pathogenic variant in a patient with Marie Unna hereditary hypotrichosis.

Journal: Pediatric dermatology

Published: December 09, 2022

A novel loci of the HR gene in Marie - Unna hereditary hypotrichosis using whole-exome sequencing.

Journal: Indian journal of dermatology, venereology and leprology

Published: April 03, 2020

Two females with hair loss.

Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

Published: July 16, 2019

Marie Unna hereditary hypotrichosis accompanied by multiple familial trichoepithelioma in a Chinese family.

Journal: The Journal of dermatology

Published: September 18, 2018

Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report.

Journal: European journal of dermatology : EJD

Published: June 29, 2018

Novel heterozygous mutation, c.74C>G (p.Pro25Arg), in the U2HR gene underlies Marie Unna hereditary hypotrichosis in a Japanese family.

Journal: The Journal of dermatology

Published: April 14, 2017

Identification of mutations in U2HR in two Chinese families with Marie Unna hereditary hypotrichosis.

Journal: Clinical and experimental dermatology

Published: December 11, 2014

Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis.

Journal: International journal of dermatology

Published: June 26, 2014

Marie Unna hereditary hypotrichosis: a recurrent c.74C>T mutation in the U2HR gene and literature review.

Journal: International journal of dermatology

Published: November 23, 2013

Increased expression of Dkk1 by HR is associated with alteration of hair cycle in hairpoor mice.

Journal: Journal of dermatological science

Published: October 07, 2013

Nucleic acid-based non-invasive prenatal diagnosis of genetic skin diseases: are we ready?

Journal: Experimental dermatology

Published: April 17, 2013

Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis.

Journal: The Journal of dermatology

Published: January 09, 2013

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Identification of a novel sporadic U2HR pathogenic variant in a patient with Marie Unna hereditary hypotrichosis.

Identification of a novel sporadic U2HR pathogenic variant in a patient with Marie Unna hereditary hypotrichosis.

A novel loci of the HR gene in Marie - Unna hereditary hypotrichosis using whole-exome sequencing.

A novel loci of the HR gene in Marie - Unna hereditary hypotrichosis using whole-exome sequencing.

Two females with hair loss.

Two females with hair loss.

Marie Unna hereditary hypotrichosis accompanied by multiple familial trichoepithelioma in a Chinese family.

Marie Unna hereditary hypotrichosis accompanied by multiple familial trichoepithelioma in a Chinese family.

Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report.

Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report.

Novel heterozygous mutation, c.74C>G (p.Pro25Arg), in the U2HR gene underlies Marie Unna hereditary hypotrichosis in a Japanese family.

Novel heterozygous mutation, c.74C>G (p.Pro25Arg), in the U2HR gene underlies Marie Unna hereditary hypotrichosis in a Japanese family.

Identification of mutations in U2HR in two Chinese families with Marie Unna hereditary hypotrichosis.

Identification of mutations in U2HR in two Chinese families with Marie Unna hereditary hypotrichosis.

Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis.

Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis.

Marie Unna hereditary hypotrichosis: a recurrent c.74C>T mutation in the U2HR gene and literature review.

Marie Unna hereditary hypotrichosis: a recurrent c.74C>T mutation in the U2HR gene and literature review.

Increased expression of Dkk1 by HR is associated with alteration of hair cycle in hairpoor mice.

Increased expression of Dkk1 by HR is associated with alteration of hair cycle in hairpoor mice.

Nucleic acid-based non-invasive prenatal diagnosis of genetic skin diseases: are we ready?

Nucleic acid-based non-invasive prenatal diagnosis of genetic skin diseases: are we ready?

Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis.

Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis.