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Khriezhanuo Nakhro

Showing results (1-10 of 6) with videos related to

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Molecular Medicine Reports|November 20, 2013
Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutationBum Chun Suh, Young Bin Hong, Khriezhanuo Nakhro, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 13, 2017
Haploid selection within a single ejaculate increases offspring fitnessGhazal Alavioon, Cosima Hotzy, Khriezhanuo Nakhro, et al.
Neuromuscular Disorders : NMD|June 26, 2013
A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot-Marie-Tooth disease type 2LKhriezhanuo Nakhro, Jin-Mo Park, Ye Jin Kim, et al.
Human Mutation|June 26, 2012
Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth diseaseByung-Ok Choi, Soo Kyung Koo, Mi-Hyun Park, et al.
Neurology|June 11, 2013
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3Khriezhanuo Nakhro, Jin-Mo Park, Young Bin Hong, et al.
DNA Repair|August 14, 2021
Large-scale generation and phenotypic characterization of zebrafish CRISPR mutants of DNA repair genesUnbeom Shin, Khriezhanuo Nakhro, Chang-Kyu Oh, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Molecular Medicine Reports|November 20, 2013
Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutationBum Chun Suh, Young Bin Hong, Khriezhanuo Nakhro, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 13, 2017
Haploid selection within a single ejaculate increases offspring fitnessGhazal Alavioon, Cosima Hotzy, Khriezhanuo Nakhro, et al.
Neuromuscular Disorders : NMD|June 26, 2013
A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot-Marie-Tooth disease type 2LKhriezhanuo Nakhro, Jin-Mo Park, Ye Jin Kim, et al.
Human Mutation|June 26, 2012
Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth diseaseByung-Ok Choi, Soo Kyung Koo, Mi-Hyun Park, et al.
Neurology|June 11, 2013
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3Khriezhanuo Nakhro, Jin-Mo Park, Young Bin Hong, et al.
DNA Repair|August 14, 2021
Large-scale generation and phenotypic characterization of zebrafish CRISPR mutants of DNA repair genesUnbeom Shin, Khriezhanuo Nakhro, Chang-Kyu Oh, et al.
Pageof 1