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Mark Pierson

Showing results (11-20 of 54) with videos related to

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Molecular Brain|October 26, 2019
Pathogenic Cav3.2 channel mutation in a child with primary generalized epilepsyIvana A Souza, Maria A Gandini, Fang-Xiong Zhang, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 19, 2023
Natural Microbial Exposure from the Earliest Natural Time Point Enhances Immune Development by Expanding Immune Cell Progenitors and Mature Immune CellsSarah Burger, Terran Stenger, Mark Pierson, et al.
Neuromuscular Disorders : NMD|November 4, 2015
Acid ceramidase deficiency associated with spinal muscular atrophy with progressive myoclonic epilepsyJoanna J Gan, Virginie Garcia, Jane Tian, et al.
Nature Aging|April 30, 2024
PD1 blockade improves survival and CD8<sup>+</sup> cytotoxic capacity, without increasing inflammation, during normal microbial experience in old miceKorbyn J V Dahlquist, Matthew A Huggins, Matthew J Yousefzadeh, et al.
American Journal of Medical Genetics. Part A|September 30, 2022
Familial Bainbridge-Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotypeSchaida Schirwani, Emily Woods, David A Koolen, et al.
Biorxiv : the Preprint Server for Biology|February 12, 2026
Diverse Microbial Exposure Enhances CD8 <sup>+</sup> T Cell Effector Memory Output and FunctionClaire E Thefaine, Erin D Lucas, Katharine E Block, et al.
Molecular Genetics and Metabolism|November 20, 2012
Juvenile-onset motor neuron disease caused by novel mutations in β-hexosaminidaseTyler Mark Pierson, Paola A Torres, Bei-Jin Zeng, et al.
Journal of Human Genetics|February 24, 2017
GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and functionWenjuan Chen, Christine Shieh, Sharon A Swanger, et al.
Translational Psychiatry|January 18, 2024
Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterningClemer Abad, Maria C Robayo, Maria Del Mar Muñiz-Moreno, et al.
Annals of Clinical and Translational Neurology|July 8, 2014
Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11Benoît Renvoisé, Jaerak Chang, Rajat Singh, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Molecular Brain|October 26, 2019
Pathogenic Cav3.2 channel mutation in a child with primary generalized epilepsyIvana A Souza, Maria A Gandini, Fang-Xiong Zhang, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 19, 2023
Natural Microbial Exposure from the Earliest Natural Time Point Enhances Immune Development by Expanding Immune Cell Progenitors and Mature Immune CellsSarah Burger, Terran Stenger, Mark Pierson, et al.
Neuromuscular Disorders : NMD|November 4, 2015
Acid ceramidase deficiency associated with spinal muscular atrophy with progressive myoclonic epilepsyJoanna J Gan, Virginie Garcia, Jane Tian, et al.
Nature Aging|April 30, 2024
PD1 blockade improves survival and CD8<sup>+</sup> cytotoxic capacity, without increasing inflammation, during normal microbial experience in old miceKorbyn J V Dahlquist, Matthew A Huggins, Matthew J Yousefzadeh, et al.
American Journal of Medical Genetics. Part A|September 30, 2022
Familial Bainbridge-Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotypeSchaida Schirwani, Emily Woods, David A Koolen, et al.
Biorxiv : the Preprint Server for Biology|February 12, 2026
Diverse Microbial Exposure Enhances CD8 <sup>+</sup> T Cell Effector Memory Output and FunctionClaire E Thefaine, Erin D Lucas, Katharine E Block, et al.
Molecular Genetics and Metabolism|November 20, 2012
Juvenile-onset motor neuron disease caused by novel mutations in β-hexosaminidaseTyler Mark Pierson, Paola A Torres, Bei-Jin Zeng, et al.
Journal of Human Genetics|February 24, 2017
GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and functionWenjuan Chen, Christine Shieh, Sharon A Swanger, et al.
Translational Psychiatry|January 18, 2024
Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterningClemer Abad, Maria C Robayo, Maria Del Mar Muñiz-Moreno, et al.
Annals of Clinical and Translational Neurology|July 8, 2014
Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11Benoît Renvoisé, Jaerak Chang, Rajat Singh, et al.
Pageof 6