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Denis I Crane

Showing results (11-20 of 27) with videos related to

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Journal of Neuroscience Methods|May 9, 2009
Quantitative genotyping of mouse brain-specific PEX13 gene disruption by real-time PCRC Catharina Müller, Jamie P Nourse, Tam H Nguyen, et al.
Journal of Neuroscience Methods|August 11, 2007
Segmentation of cultured neurons using logical analysis of grey and distance differenceDonggang Yu, Tuan D Pham, Hong Yan, et al.
Human Mutation|August 10, 2005
Novel PEX1 coding mutations and 5' UTR regulatory polymorphismsMegan A Maxwell, Pamela B Leane, Barbara C Paton, et al.
Forensic Science International|April 2, 2015
A new disaster victim identification management strategy targeting "near identification-threshold" cases: Experiences from the Boxing Day tsunamiKirsty Wright, Amy Mundorff, Janet Chaseling, et al.
Molecular and Cellular Neurosciences|December 1, 2017
Impaired neurogenesis and associated gliosis in mouse brain with PEX13 deficiencyRani Sadia Rahim, James A St John, Denis I Crane, et al.
Neuroscience|August 13, 2016
Mitochondrial changes and oxidative stress in a mouse model of Zellweger syndrome neuropathogenesisRani Sadia Rahim, Mo Chen, C Cathrin Nourse, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|June 23, 2020
Hepatocyte-specific deletion of peroxisomal protein PEX13 results in disrupted iron homeostasisGautam Rishi, Maneet Bhatia, Eriza S Secondes, et al.
Human Mutation|October 29, 2002
Novel PEX1 mutations and genotype-phenotype correlations in Australasian peroxisome biogenesis disorder patientsMegan A Maxwell, Tamara Allen, Pamela B Solly, et al.
Journal of Neuroscience Research|October 16, 2009
alpha-Synuclein abnormalities in mouse models of peroxisome biogenesis disordersEugenia Yakunin, Ann Moser, Virginie Loeb, et al.
Biology Open|May 27, 2014
Low dose tubulin-binding drugs rescue peroxisome trafficking deficit in patient-derived stem cells in Hereditary Spastic ParaplegiaYongjun Fan, Gautam Wali, Ratneswary Sutharsan, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Journal of Neuroscience Methods|May 9, 2009
Quantitative genotyping of mouse brain-specific PEX13 gene disruption by real-time PCRC Catharina Müller, Jamie P Nourse, Tam H Nguyen, et al.
Journal of Neuroscience Methods|August 11, 2007
Segmentation of cultured neurons using logical analysis of grey and distance differenceDonggang Yu, Tuan D Pham, Hong Yan, et al.
Human Mutation|August 10, 2005
Novel PEX1 coding mutations and 5' UTR regulatory polymorphismsMegan A Maxwell, Pamela B Leane, Barbara C Paton, et al.
Forensic Science International|April 2, 2015
A new disaster victim identification management strategy targeting "near identification-threshold" cases: Experiences from the Boxing Day tsunamiKirsty Wright, Amy Mundorff, Janet Chaseling, et al.
Molecular and Cellular Neurosciences|December 1, 2017
Impaired neurogenesis and associated gliosis in mouse brain with PEX13 deficiencyRani Sadia Rahim, James A St John, Denis I Crane, et al.
Neuroscience|August 13, 2016
Mitochondrial changes and oxidative stress in a mouse model of Zellweger syndrome neuropathogenesisRani Sadia Rahim, Mo Chen, C Cathrin Nourse, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|June 23, 2020
Hepatocyte-specific deletion of peroxisomal protein PEX13 results in disrupted iron homeostasisGautam Rishi, Maneet Bhatia, Eriza S Secondes, et al.
Human Mutation|October 29, 2002
Novel PEX1 mutations and genotype-phenotype correlations in Australasian peroxisome biogenesis disorder patientsMegan A Maxwell, Tamara Allen, Pamela B Solly, et al.
Journal of Neuroscience Research|October 16, 2009
alpha-Synuclein abnormalities in mouse models of peroxisome biogenesis disordersEugenia Yakunin, Ann Moser, Virginie Loeb, et al.
Biology Open|May 27, 2014
Low dose tubulin-binding drugs rescue peroxisome trafficking deficit in patient-derived stem cells in Hereditary Spastic ParaplegiaYongjun Fan, Gautam Wali, Ratneswary Sutharsan, et al.
Pageof 3