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Janan Mohamad

Showing results (1-10 of 24) with videos related to

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Pediatric Dermatology|February 8, 2021
Epidermolytic epidermal nevus caused by a somatic mutation in KRT2Janan Mohamad, Liat Samuelov, Sari Assaf, et al.
Harefuah|January 14, 2020
[LINEAR MYCOSIS FUNGOIDES IN A BLASCHKOID DISTRIBUTION]Yehonatan Kaplan, Ofer Sarig, Tom Rabinowitz, et al.
Pediatric Dermatology|May 19, 2025
Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two PatientsFiona Haxho, Richard M Haber, Janan Mohamad, et al.
Scientific Reports|April 9, 2022
Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expressionSari Assaf, Dan Vodo, Kiril Malovitski, et al.
The British Journal of Dermatology|May 20, 2023
Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratodermaKiril Malovitski, Ofer Sarig, Yarden Feller, et al.
Experimental Dermatology|April 1, 2018
SAM syndrome is characterized by extensive phenotypic heterogeneityShahar Taiber, Liat Samuelov, Janan Mohamad, et al.
Biomedicines|December 23, 2022
Cutaneous and Developmental Effects of <i>CARD14</i> Overexpression in ZebrafishAvital Baniel, Limor Ziv, Zohar Ben-Moshe, et al.
The British Journal of Dermatology|July 13, 2022
A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genesJanan Mohamad, Ofer Sarig, Paula Beattie, et al.
American Journal of Medical Genetics. Part A|August 3, 2022
Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1Janan Mohamad, Liat Samuelov, Sari Assaf, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 16, 2022
Loss-of-function variants in KLF4 underlie autosomal dominant palmoplantar keratodermaKiril Malovitski, Ofer Sarig, Sari Assaf, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Pediatric Dermatology|February 8, 2021
Epidermolytic epidermal nevus caused by a somatic mutation in KRT2Janan Mohamad, Liat Samuelov, Sari Assaf, et al.
Harefuah|January 14, 2020
[LINEAR MYCOSIS FUNGOIDES IN A BLASCHKOID DISTRIBUTION]Yehonatan Kaplan, Ofer Sarig, Tom Rabinowitz, et al.
Pediatric Dermatology|May 19, 2025
Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two PatientsFiona Haxho, Richard M Haber, Janan Mohamad, et al.
Scientific Reports|April 9, 2022
Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expressionSari Assaf, Dan Vodo, Kiril Malovitski, et al.
The British Journal of Dermatology|May 20, 2023
Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratodermaKiril Malovitski, Ofer Sarig, Yarden Feller, et al.
Experimental Dermatology|April 1, 2018
SAM syndrome is characterized by extensive phenotypic heterogeneityShahar Taiber, Liat Samuelov, Janan Mohamad, et al.
Biomedicines|December 23, 2022
Cutaneous and Developmental Effects of <i>CARD14</i> Overexpression in ZebrafishAvital Baniel, Limor Ziv, Zohar Ben-Moshe, et al.
The British Journal of Dermatology|July 13, 2022
A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genesJanan Mohamad, Ofer Sarig, Paula Beattie, et al.
American Journal of Medical Genetics. Part A|August 3, 2022
Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1Janan Mohamad, Liat Samuelov, Sari Assaf, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 16, 2022
Loss-of-function variants in KLF4 underlie autosomal dominant palmoplantar keratodermaKiril Malovitski, Ofer Sarig, Sari Assaf, et al.
Pageof 3