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E Harley

Showing results (91-100 of 102) with videos related to

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American Journal of Medical Genetics. Part A|August 16, 2022
Clinical insights from Wolman disease: Evaluating infantile hepatosplenomegalyWilliam B Hannah, Katherine Ryan, Surekha Pendyal, et al.
Pharmaceutics|October 26, 2024
Electrospun PCL Nerve Wrap Coated with Graphene Oxide Supports Axonal Growth in a Rat Sciatic Nerve Injury ModelMeaghan E Harley-Troxell, Richard Steiner, Steven D Newby, et al.
American Journal of Medical Genetics. Part A|July 24, 2012
Growth in individuals with Majewski osteodysplastic primordial dwarfism type II caused by pericentrin mutationsMichael B Bober, Tim Niiler, Angela L Duker, et al.
Microbiology Resource Announcements|February 13, 2023
Severe Acute Respiratory Syndrome Coronavirus-2 Lambda Variant Collected from a Child from Arkansas and SequencedLori Wong, Christopher Randolph, Emily Kanwischer, et al.
Hormone Research in Paediatrics|June 5, 2024
Genetic Findings in Short Turkish Children Born to Consanguineous ParentsSjoerd D Joustra, Emregul Isik, Jan M Wit, et al.
Genes & Development|April 10, 2025
<i>CDK4</i> loss-of-function mutations cause microcephaly and short statureAitana Verdu Schlie, Andrea Leitch, Maria Izabel Arismendi, et al.
Nature Genetics|November 24, 2015
TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfismMargaret E Harley, Olga Murina, Andrea Leitch, et al.
Nature Genetics|March 2, 2011
Mutations in the pre-replication complex cause Meier-Gorlin syndromeLouise S Bicknell, Ernie M H F Bongers, Andrea Leitch, et al.
Nature Genetics|October 27, 2014
Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathyCarol-Anne Martin, Ilyas Ahmad, Anna Klingseisen, et al.
Biological Reviews of the Cambridge Philosophical Society|November 28, 2014
Acoustic sequences in non-human animals: a tutorial review and prospectusArik Kershenbaum, Daniel T Blumstein, Marie A Roch, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics. Part A|August 16, 2022
Clinical insights from Wolman disease: Evaluating infantile hepatosplenomegalyWilliam B Hannah, Katherine Ryan, Surekha Pendyal, et al.
Pharmaceutics|October 26, 2024
Electrospun PCL Nerve Wrap Coated with Graphene Oxide Supports Axonal Growth in a Rat Sciatic Nerve Injury ModelMeaghan E Harley-Troxell, Richard Steiner, Steven D Newby, et al.
American Journal of Medical Genetics. Part A|July 24, 2012
Growth in individuals with Majewski osteodysplastic primordial dwarfism type II caused by pericentrin mutationsMichael B Bober, Tim Niiler, Angela L Duker, et al.
Microbiology Resource Announcements|February 13, 2023
Severe Acute Respiratory Syndrome Coronavirus-2 Lambda Variant Collected from a Child from Arkansas and SequencedLori Wong, Christopher Randolph, Emily Kanwischer, et al.
Hormone Research in Paediatrics|June 5, 2024
Genetic Findings in Short Turkish Children Born to Consanguineous ParentsSjoerd D Joustra, Emregul Isik, Jan M Wit, et al.
Genes & Development|April 10, 2025
<i>CDK4</i> loss-of-function mutations cause microcephaly and short statureAitana Verdu Schlie, Andrea Leitch, Maria Izabel Arismendi, et al.
Nature Genetics|November 24, 2015
TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfismMargaret E Harley, Olga Murina, Andrea Leitch, et al.
Nature Genetics|March 2, 2011
Mutations in the pre-replication complex cause Meier-Gorlin syndromeLouise S Bicknell, Ernie M H F Bongers, Andrea Leitch, et al.
Nature Genetics|October 27, 2014
Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathyCarol-Anne Martin, Ilyas Ahmad, Anna Klingseisen, et al.
Biological Reviews of the Cambridge Philosophical Society|November 28, 2014
Acoustic sequences in non-human animals: a tutorial review and prospectusArik Kershenbaum, Daniel T Blumstein, Marie A Roch, et al.
Pageof 11