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F Morel

Showing results (421-430 of 444) with videos related to

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Pediatric Neurology|June 13, 2009
Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutationsKlaus G E Werner, Chantal F Morel, Adam Kirton, et al.
Natural Product Research|May 22, 2018
A phytochemical study of the <i>Cuphea glutinosa</i> from Southern Brazil: Na<sup>+</sup>,K<sup>+</sup>-ATPase activity inhibition and antioxidant propertiesAdriana M Zago, Fabiano B Carvalho, Jessié Martins Gutierres, et al.
Human Mutation|April 17, 2009
Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlationsJordan P Lerner-Ellis, Natascia Anastasio, Junhui Liu, et al.
American Journal of Human Genetics|November 9, 2010
A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromesAdam Shlien, Berivan Baskin, Maria Isabel W Achatz, et al.
Molecular Therapy. Methods & Clinical Development|February 23, 2023
Persistent hematopoietic polyclonality after lentivirus-mediated gene therapy for Fabry diseaseAmr H Saleh, Michael Rothe, Dwayne L Barber, et al.
Circulation|July 1, 2018
Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada SyndromeS Mohsen Hosseini, Raymond Kim, Sharmila Udupa, et al.
Nature Genetics|November 29, 2005
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC typeJordan P Lerner-Ellis, Jamie C Tirone, Peter D Pawelek, et al.
Nature Communications|February 26, 2021
Lentivirus-mediated gene therapy for Fabry diseaseAneal Khan, Dwayne L Barber, Ju Huang, et al.
Journal of Medical Genetics|May 22, 2023
A model for the return and referral of all clinically significant secondary findings of genomic sequencingRita Kodida, Emma Reble, Marc Clausen, et al.
Brain : a Journal of Neurology|March 20, 2014
Epilepsy due to PNPO mutations: genotype, environment and treatment affect presentation and outcomePhilippa B Mills, Stephane S M Camuzeaux, Emma J Footitt, et al.
Pageof 45

Showing results (421-430 of 444) with videos related to

Sort By:
Pageof 45
Pediatric Neurology|June 13, 2009
Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutationsKlaus G E Werner, Chantal F Morel, Adam Kirton, et al.
Natural Product Research|May 22, 2018
A phytochemical study of the <i>Cuphea glutinosa</i> from Southern Brazil: Na<sup>+</sup>,K<sup>+</sup>-ATPase activity inhibition and antioxidant propertiesAdriana M Zago, Fabiano B Carvalho, Jessié Martins Gutierres, et al.
Human Mutation|April 17, 2009
Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlationsJordan P Lerner-Ellis, Natascia Anastasio, Junhui Liu, et al.
American Journal of Human Genetics|November 9, 2010
A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromesAdam Shlien, Berivan Baskin, Maria Isabel W Achatz, et al.
Molecular Therapy. Methods & Clinical Development|February 23, 2023
Persistent hematopoietic polyclonality after lentivirus-mediated gene therapy for Fabry diseaseAmr H Saleh, Michael Rothe, Dwayne L Barber, et al.
Circulation|July 1, 2018
Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada SyndromeS Mohsen Hosseini, Raymond Kim, Sharmila Udupa, et al.
Nature Genetics|November 29, 2005
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC typeJordan P Lerner-Ellis, Jamie C Tirone, Peter D Pawelek, et al.
Nature Communications|February 26, 2021
Lentivirus-mediated gene therapy for Fabry diseaseAneal Khan, Dwayne L Barber, Ju Huang, et al.
Journal of Medical Genetics|May 22, 2023
A model for the return and referral of all clinically significant secondary findings of genomic sequencingRita Kodida, Emma Reble, Marc Clausen, et al.
Brain : a Journal of Neurology|March 20, 2014
Epilepsy due to PNPO mutations: genotype, environment and treatment affect presentation and outcomePhilippa B Mills, Stephane S M Camuzeaux, Emma J Footitt, et al.
Pageof 45