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Monkol Lek

Showing results (11-20 of 153) with videos related to

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Human Gene Therapy|January 15, 2021
Nuclease-Deficient Clustered Regularly Interspaced Short Palindromic Repeat-Based Approaches for <i>In Vitro</i> and <i>In Vivo</i> Gene ActivationAngela Lek, Kaiyue Ma, Keryn G Woodman, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|December 8, 2009
The evolution of skeletal muscle performance: gene duplication and divergence of human sarcomeric alpha-actininsMonkol Lek, Kate G R Quinlan, Kathryn N North
Bioinformatics (Oxford, England)|May 13, 2022
MitoVisualize: a resource for analysis of variants in human mitochondrial RNAs and DNANicole J Lake, Lily Zhou, Jenny Xu, et al.
BMC Evolutionary Biology|July 30, 2010
Phylogenetic analysis of ferlin genes reveals ancient eukaryotic originsAngela Lek, Monkol Lek, Kathryn N North, et al.
Molecular Biology and Evolution|November 10, 2009
Phylogenetic analysis of gene structure and alternative splicing in alpha-actininsMonkol Lek, Daniel G MacArthur, Nan Yang, et al.
Disease Models & Mechanisms|June 28, 2024
High-throughput assays to assess variant effects on diseaseKaiyue Ma, Logan O Gauthier, Frances Cheung, et al.
Trends in Genetics : TIG|July 31, 2022
Neuromuscular disorders: finding the missing genetic diagnosesKatherine E Koczwara, Nicole J Lake, Alec M DeSimone, et al.
Neurology. Genetics|March 22, 2018
Whole-exome sequencing identifies mutations in <i>MYMK</i> in a mild form of Carey-Fineman-Ziter syndromeHadil Alrohaif, Ana Töpf, Teresinha Evangelista, et al.
Journal of Neuromuscular Diseases|April 3, 2023
Estimating the Prevalence of LAMA2 Congenital Muscular Dystrophy using Population Genetic DatabasesNicole J Lake, Joel Phua, Wei Liu, et al.
Disease Models & Mechanisms|July 10, 2024
Translating multiscale research in rare diseaseKirsty M Hooper, Monica J Justice, Monkol Lek, et al.
Pageof 16

Showing results (11-20 of 153) with videos related to

Sort By:
Pageof 16
Human Gene Therapy|January 15, 2021
Nuclease-Deficient Clustered Regularly Interspaced Short Palindromic Repeat-Based Approaches for <i>In Vitro</i> and <i>In Vivo</i> Gene ActivationAngela Lek, Kaiyue Ma, Keryn G Woodman, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|December 8, 2009
The evolution of skeletal muscle performance: gene duplication and divergence of human sarcomeric alpha-actininsMonkol Lek, Kate G R Quinlan, Kathryn N North
Bioinformatics (Oxford, England)|May 13, 2022
MitoVisualize: a resource for analysis of variants in human mitochondrial RNAs and DNANicole J Lake, Lily Zhou, Jenny Xu, et al.
BMC Evolutionary Biology|July 30, 2010
Phylogenetic analysis of ferlin genes reveals ancient eukaryotic originsAngela Lek, Monkol Lek, Kathryn N North, et al.
Molecular Biology and Evolution|November 10, 2009
Phylogenetic analysis of gene structure and alternative splicing in alpha-actininsMonkol Lek, Daniel G MacArthur, Nan Yang, et al.
Disease Models & Mechanisms|June 28, 2024
High-throughput assays to assess variant effects on diseaseKaiyue Ma, Logan O Gauthier, Frances Cheung, et al.
Trends in Genetics : TIG|July 31, 2022
Neuromuscular disorders: finding the missing genetic diagnosesKatherine E Koczwara, Nicole J Lake, Alec M DeSimone, et al.
Neurology. Genetics|March 22, 2018
Whole-exome sequencing identifies mutations in <i>MYMK</i> in a mild form of Carey-Fineman-Ziter syndromeHadil Alrohaif, Ana Töpf, Teresinha Evangelista, et al.
Journal of Neuromuscular Diseases|April 3, 2023
Estimating the Prevalence of LAMA2 Congenital Muscular Dystrophy using Population Genetic DatabasesNicole J Lake, Joel Phua, Wei Liu, et al.
Disease Models & Mechanisms|July 10, 2024
Translating multiscale research in rare diseaseKirsty M Hooper, Monica J Justice, Monkol Lek, et al.
Pageof 16