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J A Mayr

Showing results (1-10 of 15) with videos related to

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FEBS Letters|September 16, 1996
Identification of a novel, Ca(2+)-dependent phospholipase D with preference for phosphatidylserine and phosphatidylethanolamine in Saccharomyces cerevisiaeJ A Mayr, S D Kohlwein, F Paltauf
British Journal of Cancer|January 13, 2006
Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolismD Meierhofer, J A Mayr, K Fink, et al.
Leukemia|December 17, 2005
Platelet transfusion can mimic somatic mtDNA mutationsD Meierhofer, S Ebner, J A Mayr, et al.
Neuropediatrics|August 26, 2004
Mitochondrial DNA depletion in Alpers syndromeM Tesarova, J A Mayr, L Wenchich, et al.
The Journal of Biological Chemistry|September 25, 1999
Characterization and function in vivo of two novel phospholipases B/lysophospholipases from Saccharomyces cerevisiaeO Merkel, M Fido, J A Mayr, et al.
British Journal of Cancer|April 9, 2009
Lack of complex I is associated with oncocytic thyroid tumoursF A Zimmermann, J A Mayr, D Neureiter, et al.
Orphanet Journal of Rare Diseases|July 19, 2022
A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathyIngrid Bader, M Freilinger, F Landauer, et al.
Neuropediatrics|June 24, 2010
Leigh disease with brainstem involvement in complex I deficiency due to assembly factor NDUFAF2 defectM Herzer, J Koch, H Prokisch, et al.
European Journal of Medical Genetics|July 6, 2016
MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosumIngrid Bader, E Decker, J A Mayr, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolismR Horváth, P Freisinger, R Rubio, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
FEBS Letters|September 16, 1996
Identification of a novel, Ca(2+)-dependent phospholipase D with preference for phosphatidylserine and phosphatidylethanolamine in Saccharomyces cerevisiaeJ A Mayr, S D Kohlwein, F Paltauf
British Journal of Cancer|January 13, 2006
Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolismD Meierhofer, J A Mayr, K Fink, et al.
Leukemia|December 17, 2005
Platelet transfusion can mimic somatic mtDNA mutationsD Meierhofer, S Ebner, J A Mayr, et al.
Neuropediatrics|August 26, 2004
Mitochondrial DNA depletion in Alpers syndromeM Tesarova, J A Mayr, L Wenchich, et al.
The Journal of Biological Chemistry|September 25, 1999
Characterization and function in vivo of two novel phospholipases B/lysophospholipases from Saccharomyces cerevisiaeO Merkel, M Fido, J A Mayr, et al.
British Journal of Cancer|April 9, 2009
Lack of complex I is associated with oncocytic thyroid tumoursF A Zimmermann, J A Mayr, D Neureiter, et al.
Orphanet Journal of Rare Diseases|July 19, 2022
A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathyIngrid Bader, M Freilinger, F Landauer, et al.
Neuropediatrics|June 24, 2010
Leigh disease with brainstem involvement in complex I deficiency due to assembly factor NDUFAF2 defectM Herzer, J Koch, H Prokisch, et al.
European Journal of Medical Genetics|July 6, 2016
MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosumIngrid Bader, E Decker, J A Mayr, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolismR Horváth, P Freisinger, R Rubio, et al.
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