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Sara Shanske

Showing results (1-10 of 45) with videos related to

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Methods in Cell Biology|April 21, 2007
Detection of mutations in mtDNAAli Naini, Sara Shanske
Mitochondrion|August 27, 2005
Molecular analysis for mitochondrial DNA disordersSara Shanske, Lee-Jun C Wong
Methods in Molecular Biology (Clifton, N.J.)|May 17, 2002
Identification of mutations in mtDNA from patients suffering mitochondrial diseasesEric A Schon, Ali Naini, Sara Shanske
Methods in Cell Biology|March 19, 2020
Detection of mitochondrial DNA (mtDNA) mutationsAli Naini, Robert Gilkerson, Sara Shanske, et al.
Archives of Neurology|June 24, 2004
Association of mutations in SCO2, a cytochrome c oxidase assembly gene, with early fetal lethalityStacey K H Tay, Sara Shanske, Paige Kaplan, et al.
Archives of Neurology|June 12, 2002
Complex neurologic syndrome associated with the G1606A mutation of mitochondrial DNASabrina Sacconi, Leonardo Salviati, Clifton Gooch, et al.
Journal of the Neurological Sciences|January 26, 2002
A new stop codon mutation (Y52X) in the myophosphorylase gene in a Greek patient with McArdle's diseaseGeorgios M Hadjigeorgiou, Alexandros Papadimitriou, Olimpia Musumeci, et al.
Archives of Neurology|July 23, 2003
Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 geneMichelangelo Mancuso, Massimiliano Filosto, Eduardo Bonilla, et al.
American Journal of Medical Genetics. Part A|March 16, 2007
Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairmentJoy Samanich, Christina Lowes, Robert Burk, et al.
Journal of the Neurological Sciences|April 11, 2003
Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b geneMichelangelo Mancuso, Massimiliano Filosto, J Clarke Stevens, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Methods in Cell Biology|April 21, 2007
Detection of mutations in mtDNAAli Naini, Sara Shanske
Mitochondrion|August 27, 2005
Molecular analysis for mitochondrial DNA disordersSara Shanske, Lee-Jun C Wong
Methods in Molecular Biology (Clifton, N.J.)|May 17, 2002
Identification of mutations in mtDNA from patients suffering mitochondrial diseasesEric A Schon, Ali Naini, Sara Shanske
Methods in Cell Biology|March 19, 2020
Detection of mitochondrial DNA (mtDNA) mutationsAli Naini, Robert Gilkerson, Sara Shanske, et al.
Archives of Neurology|June 24, 2004
Association of mutations in SCO2, a cytochrome c oxidase assembly gene, with early fetal lethalityStacey K H Tay, Sara Shanske, Paige Kaplan, et al.
Archives of Neurology|June 12, 2002
Complex neurologic syndrome associated with the G1606A mutation of mitochondrial DNASabrina Sacconi, Leonardo Salviati, Clifton Gooch, et al.
Journal of the Neurological Sciences|January 26, 2002
A new stop codon mutation (Y52X) in the myophosphorylase gene in a Greek patient with McArdle's diseaseGeorgios M Hadjigeorgiou, Alexandros Papadimitriou, Olimpia Musumeci, et al.
Archives of Neurology|July 23, 2003
Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 geneMichelangelo Mancuso, Massimiliano Filosto, Eduardo Bonilla, et al.
American Journal of Medical Genetics. Part A|March 16, 2007
Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairmentJoy Samanich, Christina Lowes, Robert Burk, et al.
Journal of the Neurological Sciences|April 11, 2003
Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b geneMichelangelo Mancuso, Massimiliano Filosto, J Clarke Stevens, et al.
Pageof 5