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J Lockhart

Showing results (301-310 of 454) with videos related to

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Neurology. Genetics|March 18, 2024
Ectopic HCN4 Provides a Target Biomarker for the Genetic Spectrum of mTORopathiesMatthew Coleman, Paulo Pinares-Garcia, Sarah E Stephenson, et al.
Nature Biotechnology|December 1, 1996
Expression monitoring by hybridization to high-density oligonucleotide arraysD J Lockhart, H Dong, M C Byrne, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 7, 2014
HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxiaMartin B Delatycki, Geneieve Tai, Louise Corben, et al.
Neurology. Genetics|October 30, 2016
Heterozygous mutations in <i>HSD17B4</i> cause juvenile peroxisomal D-bifunctional protein deficiencyDavid J Amor, Ashley P L Marsh, Elsdon Storey, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 26, 2021
Clinical seizure manifestations in the absence of synaptic connectionsEmma Macdonald-Laurs, Catherine A Bailey, Sarah Barton, et al.
Human Mutation|May 21, 2011
A pharmacogenetic approach to identify mutant forms of α-galactosidase A that respond to a pharmacological chaperone for Fabry diseaseXiaoyang Wu, Evan Katz, Maria Cecilia Della Valle, et al.
Emerging Infectious Diseases|October 21, 2021
Genomic Profiling of Mycobacterium tuberculosis Strains, MyanmarHtin Lin Aung, Wint Wint Nyunt, Yang Fong, et al.
Science Advances|May 14, 2025
Low-cost robotic manipulation of live microtissues for cancer drug testingIvan Stepanov, Noah R Gottshall, Alireza Ahmadianyazdi, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
Low-Cost Robotic Manipulation of Live Microtissues for Cancer Drug TestingIvan Stepanov, Noah R Gottshall, Alireza Ahmadianyazdi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2008
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive ParkinsonismMing-Jen Lee, Ignacio F Mata, Chin-Hsien Lin, et al.
Pageof 46

Showing results (301-310 of 454) with videos related to

Sort By:
Pageof 46
Neurology. Genetics|March 18, 2024
Ectopic HCN4 Provides a Target Biomarker for the Genetic Spectrum of mTORopathiesMatthew Coleman, Paulo Pinares-Garcia, Sarah E Stephenson, et al.
Nature Biotechnology|December 1, 1996
Expression monitoring by hybridization to high-density oligonucleotide arraysD J Lockhart, H Dong, M C Byrne, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 7, 2014
HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxiaMartin B Delatycki, Geneieve Tai, Louise Corben, et al.
Neurology. Genetics|October 30, 2016
Heterozygous mutations in <i>HSD17B4</i> cause juvenile peroxisomal D-bifunctional protein deficiencyDavid J Amor, Ashley P L Marsh, Elsdon Storey, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 26, 2021
Clinical seizure manifestations in the absence of synaptic connectionsEmma Macdonald-Laurs, Catherine A Bailey, Sarah Barton, et al.
Human Mutation|May 21, 2011
A pharmacogenetic approach to identify mutant forms of α-galactosidase A that respond to a pharmacological chaperone for Fabry diseaseXiaoyang Wu, Evan Katz, Maria Cecilia Della Valle, et al.
Emerging Infectious Diseases|October 21, 2021
Genomic Profiling of Mycobacterium tuberculosis Strains, MyanmarHtin Lin Aung, Wint Wint Nyunt, Yang Fong, et al.
Science Advances|May 14, 2025
Low-cost robotic manipulation of live microtissues for cancer drug testingIvan Stepanov, Noah R Gottshall, Alireza Ahmadianyazdi, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
Low-Cost Robotic Manipulation of Live Microtissues for Cancer Drug TestingIvan Stepanov, Noah R Gottshall, Alireza Ahmadianyazdi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2008
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive ParkinsonismMing-Jen Lee, Ignacio F Mata, Chin-Hsien Lin, et al.
Pageof 46