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European Journal of Human Genetics : EJHG
|
October 16, 2014
Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma
Jean-Benoît Courcet, Siham Chafai Elalaoui, Laurence Duplomb, et al.
Frontiers in Genetics
|
February 3, 2022
XPC and POLH/XPV Genes Mutated in a Genetic Cluster of Xeroderma Pigmentosum Patients in Northeast Brazil
Ligia Pereira Castro, Danilo Batista-Vieira, Tiago Antonio de Souza, et al.
Carcinogenesis
|
May 17, 2023
Mutational signatures and increased retrotransposon insertions in xeroderma pigmentosum variant skin tumors
Camila Corradi, Juliana B Vilar, Vanessa C Buzatto, et al.
American Journal of Human Genetics
|
August 3, 2019
Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype
Arjan F Theil, Elena Botta, Anja Raams, et al.
Nature Communications
|
June 18, 2021
BRN2 is a non-canonical melanoma tumor-suppressor
Michael Hamm, Pierre Sohier, Valérie Petit, et al.
The British Journal of Dermatology
|
September 25, 2016
A genetic cluster of patients with variant xeroderma pigmentosum with two different founder mutations
V Munford, L P Castro, R Souto, et al.
The Journal of Clinical Investigation
|
February 16, 2018
DNA repair deficiency sensitizes lung cancer cells to NAD+ biosynthesis blockade
Mehdi Touat, Tony Sourisseau, Nicolas Dorvault, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis
|
April 9, 2020
The Iberian legacy into a young genetic xeroderma pigmentosum cluster in central Brazil
L P Castro, M Sahbatou, F S G Kehdy, et al.
Journal of the American Heart Association
|
February 10, 2018
Prohormones in the Early Diagnosis of Cardiac Syncope
Patrick Badertscher, Thomas Nestelberger, Jeanne du Fay de Lavallaz, et al.
Human Mutation
|
November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome
V Laugel, C Dalloz, M Durand, et al.
Page
of 48
Search research articles
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Showing results (471-480 of 480) with videos related to
Sort By:
Page
of 48
You have reached the last page of results.
This site can display upto 480 results.
European Journal of Human Genetics : EJHG
|
October 16, 2014
Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma
Jean-Benoît Courcet, Siham Chafai Elalaoui, Laurence Duplomb, et al.
Frontiers in Genetics
|
February 3, 2022
XPC and POLH/XPV Genes Mutated in a Genetic Cluster of Xeroderma Pigmentosum Patients in Northeast Brazil
Ligia Pereira Castro, Danilo Batista-Vieira, Tiago Antonio de Souza, et al.
Carcinogenesis
|
May 17, 2023
Mutational signatures and increased retrotransposon insertions in xeroderma pigmentosum variant skin tumors
Camila Corradi, Juliana B Vilar, Vanessa C Buzatto, et al.
American Journal of Human Genetics
|
August 3, 2019
Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype
Arjan F Theil, Elena Botta, Anja Raams, et al.
Nature Communications
|
June 18, 2021
BRN2 is a non-canonical melanoma tumor-suppressor
Michael Hamm, Pierre Sohier, Valérie Petit, et al.
The British Journal of Dermatology
|
September 25, 2016
A genetic cluster of patients with variant xeroderma pigmentosum with two different founder mutations
V Munford, L P Castro, R Souto, et al.
The Journal of Clinical Investigation
|
February 16, 2018
DNA repair deficiency sensitizes lung cancer cells to NAD+ biosynthesis blockade
Mehdi Touat, Tony Sourisseau, Nicolas Dorvault, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis
|
April 9, 2020
The Iberian legacy into a young genetic xeroderma pigmentosum cluster in central Brazil
L P Castro, M Sahbatou, F S G Kehdy, et al.
Journal of the American Heart Association
|
February 10, 2018
Prohormones in the Early Diagnosis of Cardiac Syncope
Patrick Badertscher, Thomas Nestelberger, Jeanne du Fay de Lavallaz, et al.
Human Mutation
|
November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome
V Laugel, C Dalloz, M Durand, et al.
Page
of 48