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J LOCKHART

Showing results (171-180 of 454) with videos related to

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Human Molecular Genetics|May 20, 1999
Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutantsS La Fontaine, S D Firth, P J Lockhart, et al.
American Journal of Human Genetics|December 4, 2018
Detecting Expansions of Tandem Repeats in Cohorts Sequenced with Short-Read Sequencing DataRick M Tankard, Mark F Bennett, Peter Degorski, et al.
Discovery Medicine|January 14, 2014
Beyond loss of frataxin: the complex molecular pathology of Friedreich ataxiaMarguerite V Evans-Galea, Paul J Lockhart, Charles A Galea, et al.
Cell|June 10, 2000
Functional and genomic analyses reveal an essential coordination between the unfolded protein response and ER-associated degradationK J Travers, C K Patil, L Wodicka, et al.
Molecular Ecology|November 11, 2008
Transcriptional and biochemical signatures of divergence in natural populations of two species of New Zealand alpine PachycladonC Voelckel, P B Heenan, B Janssen, et al.
Applied and Environmental Microbiology|September 30, 2008
Cellulose degradation by micromonosporas recovered from freshwater lakes and classification of these actinomycetes by DNA gyrase B gene sequencingAlexandre B de Menezes, Robert J Lockhart, Michael J Cox, et al.
Neurology|August 29, 2018
Teaching NeuroImages: Imaging features of <i>DCC</i>-mediated mirror movements and isolated agenesis of the corpus callosumTimothy J Edwards, Ashley P L Marsh, Paul J Lockhart, et al.
Genome Research|August 15, 2002
Parallel identification of new genes in Saccharomyces cerevisiaeGuy Oshiro, Lisa M Wodicka, Michael P Washburn, et al.
Parkinsonism & Related Disorders|April 1, 2019
Familial early onset Parkinson's disease caused by a homozygous frameshift variant in PARK7: Clinical features and literature updateSarah Em Stephenson, Ruth Djaldetti, Haloom Rafehi, et al.
International Journal of Molecular Sciences|February 15, 2022
Cortical Dysplasia and the mTOR Pathway: How the Study of Human Brain Tissue Has Led to Insights into EpileptogenesisWei Shern Lee, Sara Baldassari, Sarah E M Stephenson, et al.
Pageof 46

Showing results (171-180 of 454) with videos related to

Sort By:
Pageof 46
Human Molecular Genetics|May 20, 1999
Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutantsS La Fontaine, S D Firth, P J Lockhart, et al.
American Journal of Human Genetics|December 4, 2018
Detecting Expansions of Tandem Repeats in Cohorts Sequenced with Short-Read Sequencing DataRick M Tankard, Mark F Bennett, Peter Degorski, et al.
Discovery Medicine|January 14, 2014
Beyond loss of frataxin: the complex molecular pathology of Friedreich ataxiaMarguerite V Evans-Galea, Paul J Lockhart, Charles A Galea, et al.
Cell|June 10, 2000
Functional and genomic analyses reveal an essential coordination between the unfolded protein response and ER-associated degradationK J Travers, C K Patil, L Wodicka, et al.
Molecular Ecology|November 11, 2008
Transcriptional and biochemical signatures of divergence in natural populations of two species of New Zealand alpine PachycladonC Voelckel, P B Heenan, B Janssen, et al.
Applied and Environmental Microbiology|September 30, 2008
Cellulose degradation by micromonosporas recovered from freshwater lakes and classification of these actinomycetes by DNA gyrase B gene sequencingAlexandre B de Menezes, Robert J Lockhart, Michael J Cox, et al.
Neurology|August 29, 2018
Teaching NeuroImages: Imaging features of <i>DCC</i>-mediated mirror movements and isolated agenesis of the corpus callosumTimothy J Edwards, Ashley P L Marsh, Paul J Lockhart, et al.
Genome Research|August 15, 2002
Parallel identification of new genes in Saccharomyces cerevisiaeGuy Oshiro, Lisa M Wodicka, Michael P Washburn, et al.
Parkinsonism & Related Disorders|April 1, 2019
Familial early onset Parkinson's disease caused by a homozygous frameshift variant in PARK7: Clinical features and literature updateSarah Em Stephenson, Ruth Djaldetti, Haloom Rafehi, et al.
International Journal of Molecular Sciences|February 15, 2022
Cortical Dysplasia and the mTOR Pathway: How the Study of Human Brain Tissue Has Led to Insights into EpileptogenesisWei Shern Lee, Sara Baldassari, Sarah E M Stephenson, et al.
Pageof 46