Ron Bochner

6 Weizmann Street
Tel Aviv, TA 64239, Israel

Last Updated: 09/26/2026

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Found 12 publications

Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.

Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.

Journal: American journal of medical genetics. Part A

Published: June 02, 2023

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

Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin.

Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin.

Journal: The British journal of dermatology

Published: November 15, 2019

The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM Syndrome.

The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM Syndrome.

Journal: The Journal of investigative dermatology

Published: March 12, 2019

Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A.

Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A.

Journal: The Journal of investigative dermatology

Published: September 19, 2017

A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENEN.

A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENEN.

Journal: The British journal of dermatology

Published: July 27, 2017

SVEP1 plays a crucial role in epidermal differentiation.

SVEP1 plays a crucial role in epidermal differentiation.

Journal: Experimental dermatology

Published: October 31, 2016

Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.

Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.

Journal: PLoS genetics

Published: June 27, 2016

Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis.

Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis.

Journal: The Journal of investigative dermatology

Published: March 28, 2016

Segmental basal cell naevus syndrome caused by an activating mutation in smoothened.

Segmental basal cell naevus syndrome caused by an activating mutation in smoothened.

Journal: The British journal of dermatology

Published: January 19, 2016

Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene.

Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene.

Journal: PLoS genetics

Published: October 31, 2015

Phosphatidylserine increases IKBKAP levels in a humanized knock-in IKBKAP mouse model.

Phosphatidylserine increases IKBKAP levels in a humanized knock-in IKBKAP mouse model.

Journal: Human molecular genetics

Published: March 22, 2013

Showing 1-12 of 12

Last Updated: 09/26/2026