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Judith Fischer

Showing results (151-160 of 174) with videos related to

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The British Journal of Dermatology|March 28, 2025
A Proposal for a New Pathogenesis-guided Classification for Inherited Epidermal Differentiation DisordersÁngela Hernández-Martín, Amy S Paller, Eli Sprecher, et al.
The British Journal of Dermatology|April 4, 2025
Syndromic epidermal differentiation disorders: New classification towards pathogenesis-based therapyAmy S Paller, Joyce Teng, Juliette Mazereeuw-Hautier, et al.
The British Journal of Dermatology|March 19, 2025
Palmoplantar epidermal differentiation disorders: a new classification towards pathogenesis-based therapyEli Sprecher, Akemi Ishida-Yamamoto, Janice Schwartz, et al.
The British Journal of Dermatology|May 1, 2025
Nonsyndromic epidermal differentiation disorders: New classification and nomenclature based on disease-associated genes leading to targeted therapyMasashi Akiyama, Keith Choate, Angela Hernandez-Martin, et al.
Cell Stem Cell|August 13, 2013
The BAF complex interacts with Pax6 in adult neural progenitors to establish a neurogenic cross-regulatory transcriptional networkJovica Ninkovic, Andrea Steiner-Mezzadri, Melanie Jawerka, et al.
Genes|March 29, 2023
Mutational Spectrum of the <i>ABCA12</i> Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital IchthyosisAlrun Hotz, Julia Kopp, Emmanuelle Bourrat, et al.
The Journal of Investigative Dermatology|August 19, 2018
Epidermolysis Bullosa Simplex with KLHL24 Mutations Is Associated with Dilated CardiomyopathyAgnes Schwieger-Briel, Ignacia Fuentes, Daniele Castiglia, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Fine mapping of eight psoriasis susceptibility lociSayantan Das, Philip E Stuart, Jun Ding, et al.
Human Mutation|July 27, 2019
Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4Nadja Ballin, Alrun Hotz, Emmanuelle Bourrat, et al.
EMBO Molecular Medicine|April 4, 2022
Parkinson's disease motor symptoms rescue by CRISPRa-reprogramming astrocytes into GABAergic neuronsJessica Giehrl-Schwab, Florian Giesert, Benedict Rauser, et al.
Pageof 18

Showing results (151-160 of 174) with videos related to

Sort By:
Pageof 18
The British Journal of Dermatology|March 28, 2025
A Proposal for a New Pathogenesis-guided Classification for Inherited Epidermal Differentiation DisordersÁngela Hernández-Martín, Amy S Paller, Eli Sprecher, et al.
The British Journal of Dermatology|April 4, 2025
Syndromic epidermal differentiation disorders: New classification towards pathogenesis-based therapyAmy S Paller, Joyce Teng, Juliette Mazereeuw-Hautier, et al.
The British Journal of Dermatology|March 19, 2025
Palmoplantar epidermal differentiation disorders: a new classification towards pathogenesis-based therapyEli Sprecher, Akemi Ishida-Yamamoto, Janice Schwartz, et al.
The British Journal of Dermatology|May 1, 2025
Nonsyndromic epidermal differentiation disorders: New classification and nomenclature based on disease-associated genes leading to targeted therapyMasashi Akiyama, Keith Choate, Angela Hernandez-Martin, et al.
Cell Stem Cell|August 13, 2013
The BAF complex interacts with Pax6 in adult neural progenitors to establish a neurogenic cross-regulatory transcriptional networkJovica Ninkovic, Andrea Steiner-Mezzadri, Melanie Jawerka, et al.
Genes|March 29, 2023
Mutational Spectrum of the <i>ABCA12</i> Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital IchthyosisAlrun Hotz, Julia Kopp, Emmanuelle Bourrat, et al.
The Journal of Investigative Dermatology|August 19, 2018
Epidermolysis Bullosa Simplex with KLHL24 Mutations Is Associated with Dilated CardiomyopathyAgnes Schwieger-Briel, Ignacia Fuentes, Daniele Castiglia, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Fine mapping of eight psoriasis susceptibility lociSayantan Das, Philip E Stuart, Jun Ding, et al.
Human Mutation|July 27, 2019
Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4Nadja Ballin, Alrun Hotz, Emmanuelle Bourrat, et al.
EMBO Molecular Medicine|April 4, 2022
Parkinson's disease motor symptoms rescue by CRISPRa-reprogramming astrocytes into GABAergic neuronsJessica Giehrl-Schwab, Florian Giesert, Benedict Rauser, et al.
Pageof 18