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Nicole Cesarato

Showing results (11-20 of 17) with videos related to

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Clinical and Experimental Dermatology|February 7, 2023
A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani familyXing Xiong, Syed Ashraf Uddin, Sobia Munir, et al.
Acta Dermato-Venereologica|September 14, 2020
Apparent Missense Variant in COL7A1 Causes a Severe Form of Recessive Dystrophic Epidermolysis Bullosa via Effects on SplicingSyed Ashraf Uddin, Nicole Cesarato, Aytaj Humbatova, et al.
The Journal of Dermatology|June 26, 2024
Novel pathogenic variants in HR underlie atrichia with papular lesions in a cohort of 10 familiesKifayat Ullah, Sohail Ahmed, Nicole Cesarato, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2020
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosisLiron Malki, Ofer Sarig, Nicole Cesarato, et al.
The British Journal of Dermatology|September 6, 2023
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair lossNicole Cesarato, Agnes Schwieger-Briel, Yasmina Gossmann, et al.
American Journal of Human Genetics|June 5, 2020
Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP SyndromeHuijun Wang, Aytaj Humbatova, Yuanxiang Liu, et al.
JAMA Dermatology|August 31, 2022
Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 IndividualsF Buket Basmanav, Nicole Cesarato, Sheetal Kumar, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Clinical and Experimental Dermatology|February 7, 2023
A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani familyXing Xiong, Syed Ashraf Uddin, Sobia Munir, et al.
Acta Dermato-Venereologica|September 14, 2020
Apparent Missense Variant in COL7A1 Causes a Severe Form of Recessive Dystrophic Epidermolysis Bullosa via Effects on SplicingSyed Ashraf Uddin, Nicole Cesarato, Aytaj Humbatova, et al.
The Journal of Dermatology|June 26, 2024
Novel pathogenic variants in HR underlie atrichia with papular lesions in a cohort of 10 familiesKifayat Ullah, Sohail Ahmed, Nicole Cesarato, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2020
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosisLiron Malki, Ofer Sarig, Nicole Cesarato, et al.
The British Journal of Dermatology|September 6, 2023
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair lossNicole Cesarato, Agnes Schwieger-Briel, Yasmina Gossmann, et al.
American Journal of Human Genetics|June 5, 2020
Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP SyndromeHuijun Wang, Aytaj Humbatova, Yuanxiang Liu, et al.
JAMA Dermatology|August 31, 2022
Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 IndividualsF Buket Basmanav, Nicole Cesarato, Sheetal Kumar, et al.
Pageof 2