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J LOCKHART

Showing results (351-360 of 454) with videos related to

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Nanoscale|July 13, 2021
A chemisorbed interfacial layer for seeding atomic layer deposition on graphiteAnton Brown, John Greenwood, César J Lockhart de la Rosa, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
Microdissected tumor cuboids: a microscale cancer model for large-scale testing that retains a complex tumor microenvironmentLisa F Horowitz, Ricard A Rodríguez-Mias, Marina Chang, et al.
Human Mutation|October 29, 2009
The pharmacological chaperone 1-deoxynojirimycin increases the activity and lysosomal trafficking of multiple mutant forms of acid alpha-glucosidaseJohn J Flanagan, Barbara Rossi, Katherine Tang, et al.
Annals of Clinical and Translational Neurology|July 30, 2019
Second-hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIAWei Shern Lee, Sarah E M Stephenson, Katherine B Howell, et al.
Iscience|August 28, 2023
Emerging advances in biosecurity to underpin human, animal, plant, and ecosystem healthPhilip E Hulme, Jacqueline R Beggs, Rachelle N Binny, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 5, 2012
Co-administration with the pharmacological chaperone AT1001 increases recombinant human α-galactosidase A tissue uptake and improves substrate reduction in Fabry miceElfrida R Benjamin, Richie Khanna, Adriane Schilling, et al.
European Journal of Human Genetics : EJHG|October 10, 2013
Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndromeGabrielle R Wilson, Jasmine Sunley, Katherine R Smith, et al.
Microvascular Research|April 10, 2021
Assessment of the conjunctival microcirculation in adult patients with cyanotic congenital heart disease compared to healthy controlsPaul F Brennan, Min Jing, Andrew J McNeil, et al.
Brain Communications|February 10, 2025
The genetic landscape and classification of infantile epileptic spasms syndrome requiring surgery due to suspected focal brain malformationsMatthew Coleman, Min Wang, Penny Snell, et al.
Human Molecular Genetics|September 8, 2021
Pathogenic variants in nucleoporin TPR (translocated promoter region, nuclear basket protein) cause severe intellectual disability in humansNicole J Van Bergen, Katrina M Bell, Kirsty Carey, et al.
Pageof 46

Showing results (351-360 of 454) with videos related to

Sort By:
Pageof 46
Nanoscale|July 13, 2021
A chemisorbed interfacial layer for seeding atomic layer deposition on graphiteAnton Brown, John Greenwood, César J Lockhart de la Rosa, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
Microdissected tumor cuboids: a microscale cancer model for large-scale testing that retains a complex tumor microenvironmentLisa F Horowitz, Ricard A Rodríguez-Mias, Marina Chang, et al.
Human Mutation|October 29, 2009
The pharmacological chaperone 1-deoxynojirimycin increases the activity and lysosomal trafficking of multiple mutant forms of acid alpha-glucosidaseJohn J Flanagan, Barbara Rossi, Katherine Tang, et al.
Annals of Clinical and Translational Neurology|July 30, 2019
Second-hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIAWei Shern Lee, Sarah E M Stephenson, Katherine B Howell, et al.
Iscience|August 28, 2023
Emerging advances in biosecurity to underpin human, animal, plant, and ecosystem healthPhilip E Hulme, Jacqueline R Beggs, Rachelle N Binny, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 5, 2012
Co-administration with the pharmacological chaperone AT1001 increases recombinant human α-galactosidase A tissue uptake and improves substrate reduction in Fabry miceElfrida R Benjamin, Richie Khanna, Adriane Schilling, et al.
European Journal of Human Genetics : EJHG|October 10, 2013
Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndromeGabrielle R Wilson, Jasmine Sunley, Katherine R Smith, et al.
Microvascular Research|April 10, 2021
Assessment of the conjunctival microcirculation in adult patients with cyanotic congenital heart disease compared to healthy controlsPaul F Brennan, Min Jing, Andrew J McNeil, et al.
Brain Communications|February 10, 2025
The genetic landscape and classification of infantile epileptic spasms syndrome requiring surgery due to suspected focal brain malformationsMatthew Coleman, Min Wang, Penny Snell, et al.
Human Molecular Genetics|September 8, 2021
Pathogenic variants in nucleoporin TPR (translocated promoter region, nuclear basket protein) cause severe intellectual disability in humansNicole J Van Bergen, Katrina M Bell, Kirsty Carey, et al.
Pageof 46