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Joseph G Gleeson

Showing results (161-170 of 325) with videos related to

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Biorxiv : the Preprint Server for Biology|October 10, 2024
Genomic mosaicism reveals developmental organization of trunk neural crest-derived gangliaKeng Ioi Vong, Yanina D Alvarez, Geoffroy Noel, et al.
Nature Biotechnology|January 2, 2023
Control-independent mosaic single nucleotide variant detection with DeepMosaicXiaoxu Yang, Xin Xu, Martin W Breuss, et al.
Human Molecular Genetics|December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stabilityMartin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.
American Journal of Human Genetics|August 22, 2017
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar HypoplasiaIsaac Marin-Valencia, Andreas Gerondopoulos, Maha S Zaki, et al.
Human Genetics|October 4, 2024
Biallelic variants in ERLIN1: a series of 13 individuals with spastic paraparesisGuillaume Cogan, Maha S Zaki, Mahmoud Issa, et al.
Journal of Medical Genetics|March 11, 2017
Homozygous mutation in <i>NUP107</i> leads to microcephaly with steroid-resistant nephrotic condition similar to Galloway-Mowat syndromeRasim Ozgur Rosti, Bethany N Sotak, Stephanie L Bielas, et al.
Nature|April 10, 2024
Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrainChanguk Chung, Xiaoxu Yang, Robert F Hevner, et al.
American Journal of Human Genetics|July 24, 2018
Mutations in LNPK, Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental SyndromeMartin W Breuss, An Nguyen, Qiong Song, et al.
JAMA Network Open|February 9, 2023
Reclassification of the Etiology of Infant Mortality With Whole-Genome SequencingMallory J Owen, Meredith S Wright, Sergey Batalov, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 25, 2006
Coupling of cell migration with neurogenesis by proneural bHLH factorsWeihong Ge, Fei He, Kevin J Kim, et al.
Pageof 33

Showing results (161-170 of 325) with videos related to

Sort By:
Pageof 33
Biorxiv : the Preprint Server for Biology|October 10, 2024
Genomic mosaicism reveals developmental organization of trunk neural crest-derived gangliaKeng Ioi Vong, Yanina D Alvarez, Geoffroy Noel, et al.
Nature Biotechnology|January 2, 2023
Control-independent mosaic single nucleotide variant detection with DeepMosaicXiaoxu Yang, Xin Xu, Martin W Breuss, et al.
Human Molecular Genetics|December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stabilityMartin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.
American Journal of Human Genetics|August 22, 2017
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar HypoplasiaIsaac Marin-Valencia, Andreas Gerondopoulos, Maha S Zaki, et al.
Human Genetics|October 4, 2024
Biallelic variants in ERLIN1: a series of 13 individuals with spastic paraparesisGuillaume Cogan, Maha S Zaki, Mahmoud Issa, et al.
Journal of Medical Genetics|March 11, 2017
Homozygous mutation in <i>NUP107</i> leads to microcephaly with steroid-resistant nephrotic condition similar to Galloway-Mowat syndromeRasim Ozgur Rosti, Bethany N Sotak, Stephanie L Bielas, et al.
Nature|April 10, 2024
Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrainChanguk Chung, Xiaoxu Yang, Robert F Hevner, et al.
American Journal of Human Genetics|July 24, 2018
Mutations in LNPK, Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental SyndromeMartin W Breuss, An Nguyen, Qiong Song, et al.
JAMA Network Open|February 9, 2023
Reclassification of the Etiology of Infant Mortality With Whole-Genome SequencingMallory J Owen, Meredith S Wright, Sergey Batalov, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 25, 2006
Coupling of cell migration with neurogenesis by proneural bHLH factorsWeihong Ge, Fei He, Kevin J Kim, et al.
Pageof 33