Janna Nousbeck

6, Weizmann Street
Tel Aviv, TA 64239, Israel

Last Updated: 09/26/2026

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Found 15 publications

Effect of Topical Corticosteroid Treatment on microRNA Expression in Infants with Atopic Dermatitis.

Effect of Topical Corticosteroid Treatment on microRNA Expression in Infants with Atopic Dermatitis.

Journal: JID innovations : skin science from molecules to population health

Published: January 14, 2025

Peripheral Blood Gene Expression Profile of Infants with Atopic Dermatitis.

Peripheral Blood Gene Expression Profile of Infants with Atopic Dermatitis.

Journal: JID innovations : skin science from molecules to population health

Published: September 22, 2021

Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasis.

Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasis.

Journal: Experimental dermatology

Published: May 22, 2021

MicroRNA analysis of childhood atopic dermatitis reveals a role for miR-451a.

MicroRNA analysis of childhood atopic dermatitis reveals a role for miR-451a.

Journal: The British journal of dermatology

Published: May 25, 2020

Atopic Dermatitis According to GARP: New Mechanistic Insights in Disease Pathogenesis.

Atopic Dermatitis According to GARP: New Mechanistic Insights in Disease Pathogenesis.

Journal: The Journal of investigative dermatology

Published: August 24, 2016

RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63.

RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63.

Journal: Experimental dermatology

Published: April 24, 2015

Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes.

Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes.

Journal: The British journal of dermatology

Published: June 03, 2014

A mutation in TP63 causing a mild ectodermal dysplasia phenotype.

A mutation in TP63 causing a mild ectodermal dysplasia phenotype.

Journal: The Journal of investigative dermatology

Published: March 29, 2014

Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris.

Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris.

Journal: The British journal of dermatology

Published: December 24, 2013

New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndrome.

New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndrome.

Journal: Clinical and experimental dermatology

Published: May 09, 2013

Semidominant inheritance in epidermolytic ichthyosis.

Semidominant inheritance in epidermolytic ichthyosis.

Journal: The Journal of investigative dermatology

Published: April 23, 2013

The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12.

The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12.

Journal: Experimental dermatology

Published: February 07, 2013

Showing 1-12 of 15

Last Updated: 09/26/2026