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Showing results (741-750 of 835) with videos related to

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Annals of Clinical and Translational Neurology|October 15, 2020
Novel NUDT2 variant causes intellectual disability and polyneuropathyFrank Diaz, Shaweta Khosa, Dmitriy Niyazov, et al.
American Journal of Human Genetics|April 2, 2002
A genomewide scan for loci involved in attention-deficit/hyperactivity disorderSimon E Fisher, Clyde Francks, James T McCracken, et al.
Neurosurgery|December 10, 2015
Facial Nerve Outcome and Tumor Control Rate as a Function of Degree of Resection in Treatment of Large Acoustic Neuromas: Preliminary Report of the Acoustic Neuroma Subtotal Resection Study (ANSRS)Ashkan Monfared, Carlton E Corrales, Philip V Theodosopoulos, et al.
Scientific Reports|May 14, 2014
High-throughput profiling of influenza A virus hemagglutinin gene at single-nucleotide resolutionNicholas C Wu, Arthur P Young, Laith Q Al-Mawsawi, et al.
Neurology|October 14, 2022
Evaluating Genetic Modifiers of Duchenne Muscular Dystrophy Disease Progression Using Modeling and MRIAlison M Barnard, David W Hammers, William T Triplett, et al.
American Journal of Human Genetics|March 3, 2015
De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delayValerie A Arboleda, Hane Lee, Naghmeh Dorrani, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentationsShilpa Nadimpalli Kobren, Mikhail A Moldovan, Rebecca Reimers, et al.
The Journal of Cell Biology|August 3, 2005
Maternal embryonic leucine zipper kinase (MELK) regulates multipotent neural progenitor proliferationIchiro Nakano, Andres A Paucar, Ruchi Bajpai, et al.
The Journal of Clinical Investigation|July 17, 2025
Endocochlear potential contributes to hair cell death in TMPRSS3 hearing lossA Eliot Shearer, Yuan-Siao Chen, Stephanie L Rouse, et al.
Nature Genetics|July 1, 2008
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmiaMatthew J Rock, Jean Prenen, Vincent A Funari, et al.
Pageof 84

Showing results (741-750 of 835) with videos related to

Sort By:
Pageof 84
Annals of Clinical and Translational Neurology|October 15, 2020
Novel NUDT2 variant causes intellectual disability and polyneuropathyFrank Diaz, Shaweta Khosa, Dmitriy Niyazov, et al.
American Journal of Human Genetics|April 2, 2002
A genomewide scan for loci involved in attention-deficit/hyperactivity disorderSimon E Fisher, Clyde Francks, James T McCracken, et al.
Neurosurgery|December 10, 2015
Facial Nerve Outcome and Tumor Control Rate as a Function of Degree of Resection in Treatment of Large Acoustic Neuromas: Preliminary Report of the Acoustic Neuroma Subtotal Resection Study (ANSRS)Ashkan Monfared, Carlton E Corrales, Philip V Theodosopoulos, et al.
Scientific Reports|May 14, 2014
High-throughput profiling of influenza A virus hemagglutinin gene at single-nucleotide resolutionNicholas C Wu, Arthur P Young, Laith Q Al-Mawsawi, et al.
Neurology|October 14, 2022
Evaluating Genetic Modifiers of Duchenne Muscular Dystrophy Disease Progression Using Modeling and MRIAlison M Barnard, David W Hammers, William T Triplett, et al.
American Journal of Human Genetics|March 3, 2015
De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delayValerie A Arboleda, Hane Lee, Naghmeh Dorrani, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentationsShilpa Nadimpalli Kobren, Mikhail A Moldovan, Rebecca Reimers, et al.
The Journal of Cell Biology|August 3, 2005
Maternal embryonic leucine zipper kinase (MELK) regulates multipotent neural progenitor proliferationIchiro Nakano, Andres A Paucar, Ruchi Bajpai, et al.
The Journal of Clinical Investigation|July 17, 2025
Endocochlear potential contributes to hair cell death in TMPRSS3 hearing lossA Eliot Shearer, Yuan-Siao Chen, Stephanie L Rouse, et al.
Nature Genetics|July 1, 2008
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmiaMatthew J Rock, Jean Prenen, Vincent A Funari, et al.
Pageof 84