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Gert C Scheper

Showing results (21-30 of 52) with videos related to

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Clinical Neurology and Neurosurgery|August 6, 2008
The ovarioleukodystrophyStéphane Mathis, Gert C Scheper, Nicole Baumann, et al.
The Biochemical Journal|December 3, 2010
A human pathology-related mutation prevents import of an aminoacyl-tRNA synthetase into mitochondriaMarie Messmer, Catherine Florentz, Hagen Schwenzer, et al.
Journal of Child Neurology|June 10, 2008
Vanishing white matter disease: the first reported chinese patientSheila S N Wong, David C K Luk, Virginia C N Wong, et al.
Journal of Child Neurology|December 1, 2010
Vanishing white matter disease associated with ptosis and myoclonic seizuresSuvasini Sharma, Ravindra Arya, K N Vykunta Raju, et al.
The Biochemical Journal|October 26, 2011
Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation is associated with cell-type-dependent splicing of mtAspRS mRNALaura van Berge, Stephanie Dooves, Carola G M van Berkel, et al.
The Turkish Journal of Pediatrics|June 22, 2010
Two cases with megalencephalic leukoencephalopathy with subcortical cysts and MLC1 mutations in the Turkish populationUluç Yiş, Gert C Scheper, Nedret Uran, et al.
Molecular and Cellular Biology|August 5, 2003
The N and C termini of the splice variants of the human mitogen-activated protein kinase-interacting kinase Mnk2 determine activity and localizationGert C Scheper, Josep L Parra, Mary Wilson, et al.
The Biochemical Journal|December 11, 2012
Pathogenic mutations causing LBSL affect mitochondrial aspartyl-tRNA synthetase in diverse waysLaura van Berge, Josta Kevenaar, Emiel Polder, et al.
Biochimie|October 15, 2013
Released selective pressure on a structural domain gives new insights on the functional relaxation of mitochondrial aspartyl-tRNA synthetaseHagen Schwenzer, Gert C Scheper, Nathalie Zorn, et al.
Human Mutation|May 3, 2006
Megalencephalic leukoencephalopathy with subcortical cysts: an update and extended mutation analysis of MLC1P K Ilja Boor, Koen de Groot, Vlatka Mejaski-Bosnjak, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Clinical Neurology and Neurosurgery|August 6, 2008
The ovarioleukodystrophyStéphane Mathis, Gert C Scheper, Nicole Baumann, et al.
The Biochemical Journal|December 3, 2010
A human pathology-related mutation prevents import of an aminoacyl-tRNA synthetase into mitochondriaMarie Messmer, Catherine Florentz, Hagen Schwenzer, et al.
Journal of Child Neurology|June 10, 2008
Vanishing white matter disease: the first reported chinese patientSheila S N Wong, David C K Luk, Virginia C N Wong, et al.
Journal of Child Neurology|December 1, 2010
Vanishing white matter disease associated with ptosis and myoclonic seizuresSuvasini Sharma, Ravindra Arya, K N Vykunta Raju, et al.
The Biochemical Journal|October 26, 2011
Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation is associated with cell-type-dependent splicing of mtAspRS mRNALaura van Berge, Stephanie Dooves, Carola G M van Berkel, et al.
The Turkish Journal of Pediatrics|June 22, 2010
Two cases with megalencephalic leukoencephalopathy with subcortical cysts and MLC1 mutations in the Turkish populationUluç Yiş, Gert C Scheper, Nedret Uran, et al.
Molecular and Cellular Biology|August 5, 2003
The N and C termini of the splice variants of the human mitogen-activated protein kinase-interacting kinase Mnk2 determine activity and localizationGert C Scheper, Josep L Parra, Mary Wilson, et al.
The Biochemical Journal|December 11, 2012
Pathogenic mutations causing LBSL affect mitochondrial aspartyl-tRNA synthetase in diverse waysLaura van Berge, Josta Kevenaar, Emiel Polder, et al.
Biochimie|October 15, 2013
Released selective pressure on a structural domain gives new insights on the functional relaxation of mitochondrial aspartyl-tRNA synthetaseHagen Schwenzer, Gert C Scheper, Nathalie Zorn, et al.
Human Mutation|May 3, 2006
Megalencephalic leukoencephalopathy with subcortical cysts: an update and extended mutation analysis of MLC1P K Ilja Boor, Koen de Groot, Vlatka Mejaski-Bosnjak, et al.
Pageof 6