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Bradley Peter

Showing results (1-10 of 20) with videos related to

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Genes|April 15, 2020
TWINKLE and Other Human Mitochondrial DNA Helicases: Structure, Function and DiseaseBradley Peter, Maria Falkenberg
European Biophysics Journal : EBJ|June 14, 2014
A conserved cationic motif enhances membrane binding and insertion of the chloride intracellular channel protein 1 transmembrane domainBradley Peter, Sylvia Fanucchi, Heini W Dirr
Biochemistry|December 17, 2013
A Lys-Trp cation-π interaction mediates the dimerization and function of the chloride intracellular channel protein 1 transmembrane domainBradley Peter, Anton A Polyansky, Sylvia Fanucchi, et al.
Human Molecular Genetics|November 30, 2018
Structural basis for adPEO-causing mutations in the mitochondrial TWINKLE helicaseBradley Peter, Geraldine Farge, Carlos Pardo-Hernandez, et al.
Nucleic Acids Research|January 12, 2022
Ribonucleotides embedded in template DNA impair mitochondrial RNA polymerase progressionMeenakshi Singh, Viktor Posse, Bradley Peter, et al.
Biochemistry|April 4, 2013
Membrane mimetics induce helix formation and oligomerization of the chloride intracellular channel protein 1 transmembrane domainBradley Peter, Nomxolisi Chloë Mina-Liz Ngubane, Sylvia Fanucchi, et al.
Plos One|May 14, 2020
Democratizing water monitoring: Implementation of a community-based qPCR monitoring program for recreational water hazardsSydney P Rudko, Ronald L Reimink, Bradley Peter, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|June 11, 2023
The disease-causing mutation p.F907I reveals a novel pathogenic mechanism for POLγ-related diseasesDirenis Erdinc, Bertil Macao, Sebastian Valenzuela, et al.
Nucleic Acids Research|August 14, 2018
A two-nuclease pathway involving RNase H1 is required for primer removal at human mitochondrial OriLAli Al-Behadili, Jay P Uhler, Anna-Karin Berglund, et al.
Neurology. Genetics|February 12, 2020
Deep sequencing of mitochondrial DNA and characterization of a novel <i>POLG</i> mutation in a patient with arPEOCarola Hedberg-Oldfors, Bertil Macao, Swaraj Basu, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Genes|April 15, 2020
TWINKLE and Other Human Mitochondrial DNA Helicases: Structure, Function and DiseaseBradley Peter, Maria Falkenberg
European Biophysics Journal : EBJ|June 14, 2014
A conserved cationic motif enhances membrane binding and insertion of the chloride intracellular channel protein 1 transmembrane domainBradley Peter, Sylvia Fanucchi, Heini W Dirr
Biochemistry|December 17, 2013
A Lys-Trp cation-π interaction mediates the dimerization and function of the chloride intracellular channel protein 1 transmembrane domainBradley Peter, Anton A Polyansky, Sylvia Fanucchi, et al.
Human Molecular Genetics|November 30, 2018
Structural basis for adPEO-causing mutations in the mitochondrial TWINKLE helicaseBradley Peter, Geraldine Farge, Carlos Pardo-Hernandez, et al.
Nucleic Acids Research|January 12, 2022
Ribonucleotides embedded in template DNA impair mitochondrial RNA polymerase progressionMeenakshi Singh, Viktor Posse, Bradley Peter, et al.
Biochemistry|April 4, 2013
Membrane mimetics induce helix formation and oligomerization of the chloride intracellular channel protein 1 transmembrane domainBradley Peter, Nomxolisi Chloë Mina-Liz Ngubane, Sylvia Fanucchi, et al.
Plos One|May 14, 2020
Democratizing water monitoring: Implementation of a community-based qPCR monitoring program for recreational water hazardsSydney P Rudko, Ronald L Reimink, Bradley Peter, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|June 11, 2023
The disease-causing mutation p.F907I reveals a novel pathogenic mechanism for POLγ-related diseasesDirenis Erdinc, Bertil Macao, Sebastian Valenzuela, et al.
Nucleic Acids Research|August 14, 2018
A two-nuclease pathway involving RNase H1 is required for primer removal at human mitochondrial OriLAli Al-Behadili, Jay P Uhler, Anna-Karin Berglund, et al.
Neurology. Genetics|February 12, 2020
Deep sequencing of mitochondrial DNA and characterization of a novel <i>POLG</i> mutation in a patient with arPEOCarola Hedberg-Oldfors, Bertil Macao, Swaraj Basu, et al.
Pageof 2