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Mark Davis

Showing results (291-300 of 318) with videos related to

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Neuromuscular Disorders : NMD|December 24, 2023
A recurrent ACTA1 amino acid change in mosaic form causes milder asymmetric myopathyVilma-Lotta Lehtokari, Lydia Sagath, Mark Davis, et al.
Annals of Neurology|May 10, 2016
Diagnosis and etiology of congenital muscular dystrophy: We are halfway thereGina L O'Grady, Monkol Lek, Shireen R Lamande, et al.
Biotechnology for Biofuels|May 9, 2013
Enhanced characteristics of genetically modified switchgrass (Panicum virgatum L.) for high biofuel productionHui Shen, Charleson R Poovaiah, Angela Ziebell, et al.
Tree Physiology|June 19, 2019
Involvement of CesA4, CesA7-A/B and CesA8-A/B in secondary wall formation in Populus trichocarpa woodManzar Abbas, Ilona Peszlen, Rui Shi, et al.
JAMA Neurology|October 6, 2015
Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy: Outcomes and Lessons LearnedRoula Ghaoui, Sandra T Cooper, Monkol Lek, et al.
Neurology|June 29, 2018
A Roma founder <i>BIN1</i> mutation causes a novel phenotype of centronuclear myopathy with rigid spineMacarena Cabrera-Serrano, Fabiola Mavillard, Valerie Biancalana, et al.
BMC Bioinformatics|October 9, 2009
Comparative genome analysis of lignin biosynthesis gene families across the plant kingdomZhanyou Xu, Dandan Zhang, Jun Hu, et al.
Environment International|October 8, 2024
Towards integrated cross-sectoral surveillance of pathogens and antimicrobial resistance: Needs, approaches, and considerations for linking surveillance to actionRachael Lappan, Steven L Chown, Matthew French, et al.
Orphanet Journal of Rare Diseases|June 12, 2016
The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical serviceGareth Baynam, Nicholas Pachter, Fiona McKenzie, et al.
Cell|June 26, 2021
The single-cell epigenomic and transcriptional landscape of immunity to influenza vaccinationFlorian Wimmers, Michele Donato, Alex Kuo, et al.
Pageof 32

Showing results (291-300 of 318) with videos related to

Sort By:
Pageof 32
Neuromuscular Disorders : NMD|December 24, 2023
A recurrent ACTA1 amino acid change in mosaic form causes milder asymmetric myopathyVilma-Lotta Lehtokari, Lydia Sagath, Mark Davis, et al.
Annals of Neurology|May 10, 2016
Diagnosis and etiology of congenital muscular dystrophy: We are halfway thereGina L O'Grady, Monkol Lek, Shireen R Lamande, et al.
Biotechnology for Biofuels|May 9, 2013
Enhanced characteristics of genetically modified switchgrass (Panicum virgatum L.) for high biofuel productionHui Shen, Charleson R Poovaiah, Angela Ziebell, et al.
Tree Physiology|June 19, 2019
Involvement of CesA4, CesA7-A/B and CesA8-A/B in secondary wall formation in Populus trichocarpa woodManzar Abbas, Ilona Peszlen, Rui Shi, et al.
JAMA Neurology|October 6, 2015
Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy: Outcomes and Lessons LearnedRoula Ghaoui, Sandra T Cooper, Monkol Lek, et al.
Neurology|June 29, 2018
A Roma founder <i>BIN1</i> mutation causes a novel phenotype of centronuclear myopathy with rigid spineMacarena Cabrera-Serrano, Fabiola Mavillard, Valerie Biancalana, et al.
BMC Bioinformatics|October 9, 2009
Comparative genome analysis of lignin biosynthesis gene families across the plant kingdomZhanyou Xu, Dandan Zhang, Jun Hu, et al.
Environment International|October 8, 2024
Towards integrated cross-sectoral surveillance of pathogens and antimicrobial resistance: Needs, approaches, and considerations for linking surveillance to actionRachael Lappan, Steven L Chown, Matthew French, et al.
Orphanet Journal of Rare Diseases|June 12, 2016
The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical serviceGareth Baynam, Nicholas Pachter, Fiona McKenzie, et al.
Cell|June 26, 2021
The single-cell epigenomic and transcriptional landscape of immunity to influenza vaccinationFlorian Wimmers, Michele Donato, Alex Kuo, et al.
Pageof 32