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Barbara C Paton

Showing results (1-10 of 7) with videos related to

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Human Mutation|August 9, 2005
PEX1 mutations in the Zellweger spectrum of the peroxisome biogenesis disordersDenis I Crane, Megan A Maxwell, Barbara C Paton
Journal of Cell Science|February 2, 2006
Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundanceTam Nguyen, Jonas Bjorkman, Barbara C Paton, et al.
Australian Journal of Primary Health|December 7, 2010
Implementing mental health peer support: a South Australian experienceCarmen C D Franke, Barbara C Paton, Lee-Anne J Gassner
Human Mutation|August 10, 2005
Novel PEX1 coding mutations and 5' UTR regulatory polymorphismsMegan A Maxwell, Pamela B Leane, Barbara C Paton, 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.
Molecular and Cellular Biology|August 5, 2003
Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotypeMegan Maxwell, Jonas Bjorkman, Tam Nguyen, et al.
American Journal of Medical Genetics. Part A|March 10, 2009
Prosaposin deficiency and saposin B deficiency (activator-deficient metachromatic leukodystrophy): report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutationsLadislav Kuchar, Jana Ledvinová, Martin Hrebícek, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Human Mutation|August 9, 2005
PEX1 mutations in the Zellweger spectrum of the peroxisome biogenesis disordersDenis I Crane, Megan A Maxwell, Barbara C Paton
Journal of Cell Science|February 2, 2006
Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundanceTam Nguyen, Jonas Bjorkman, Barbara C Paton, et al.
Australian Journal of Primary Health|December 7, 2010
Implementing mental health peer support: a South Australian experienceCarmen C D Franke, Barbara C Paton, Lee-Anne J Gassner
Human Mutation|August 10, 2005
Novel PEX1 coding mutations and 5' UTR regulatory polymorphismsMegan A Maxwell, Pamela B Leane, Barbara C Paton, 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.
Molecular and Cellular Biology|August 5, 2003
Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotypeMegan Maxwell, Jonas Bjorkman, Tam Nguyen, et al.
American Journal of Medical Genetics. Part A|March 10, 2009
Prosaposin deficiency and saposin B deficiency (activator-deficient metachromatic leukodystrophy): report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutationsLadislav Kuchar, Jana Ledvinová, Martin Hrebícek, et al.
Pageof 1