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Sara E Mole

Showing results (1-10 of 92) with videos related to

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The Lancet. Neurology|July 7, 2014
Development of new treatments for Batten diseaseSara E Mole
Brain Pathology (Zurich, Switzerland)|March 5, 2004
The genetic spectrum of human neuronal ceroid-lipofuscinosesSara E Mole
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2006
Neuronal ceroid lipofuscinoses (NCL)Sara E Mole
Developmental Medicine and Child Neurology|May 31, 2017
The value of a comprehensive natural history in late infantile CLN5 diseaseSara E Mole
Journal of Cell Science|March 21, 2009
S. pombe btn1, the orthologue of the Batten disease gene CLN3, is required for vacuole protein sorting of Cpy1p and Golgi exit of Vps10pSandra Codlin, Sara E Mole
Frontiers in Neurology|November 4, 2021
The Genetic Basis of Phenotypic Heterogeneity in the Neuronal Ceroid LipofuscinosesEmily Gardner, Sara E Mole
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 15, 2022
Sex bias and omission exists in Batten disease research: Systematic review of the use of animal disease modelsAnnie McShane, Sara E Mole
Biochimica Et Biophysica Acta|June 1, 2015
Genetics of the neuronal ceroid lipofuscinoses (Batten disease)Sara E Mole, Susan L Cotman
Biochimica Et Biophysica Acta. Molecular Basis of Disease|January 12, 2020
Future perspectives: What lies ahead for Neuronal Ceroid Lipofuscinosis research?Jonathan D Cooper, Sara E Mole
Neurology|July 11, 2012
New nomenclature and classification scheme for the neuronal ceroid lipofuscinosesRuth E Williams, Sara E Mole
Pageof 10

Showing results (1-10 of 92) with videos related to

Sort By:
Pageof 10
The Lancet. Neurology|July 7, 2014
Development of new treatments for Batten diseaseSara E Mole
Brain Pathology (Zurich, Switzerland)|March 5, 2004
The genetic spectrum of human neuronal ceroid-lipofuscinosesSara E Mole
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2006
Neuronal ceroid lipofuscinoses (NCL)Sara E Mole
Developmental Medicine and Child Neurology|May 31, 2017
The value of a comprehensive natural history in late infantile CLN5 diseaseSara E Mole
Journal of Cell Science|March 21, 2009
S. pombe btn1, the orthologue of the Batten disease gene CLN3, is required for vacuole protein sorting of Cpy1p and Golgi exit of Vps10pSandra Codlin, Sara E Mole
Frontiers in Neurology|November 4, 2021
The Genetic Basis of Phenotypic Heterogeneity in the Neuronal Ceroid LipofuscinosesEmily Gardner, Sara E Mole
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 15, 2022
Sex bias and omission exists in Batten disease research: Systematic review of the use of animal disease modelsAnnie McShane, Sara E Mole
Biochimica Et Biophysica Acta|June 1, 2015
Genetics of the neuronal ceroid lipofuscinoses (Batten disease)Sara E Mole, Susan L Cotman
Biochimica Et Biophysica Acta. Molecular Basis of Disease|January 12, 2020
Future perspectives: What lies ahead for Neuronal Ceroid Lipofuscinosis research?Jonathan D Cooper, Sara E Mole
Neurology|July 11, 2012
New nomenclature and classification scheme for the neuronal ceroid lipofuscinosesRuth E Williams, Sara E Mole
Pageof 10