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Methods in Molecular Biology (Clifton, N.J.)
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March 10, 2017
Identification of Disease-Causing Mutations by Functional Complementation of Patient-Derived Fibroblast Cell Lines
Laura S Kremer, Holger Prokisch
Human Molecular Genetics
|
May 23, 2024
Coordinating mitochondrial translation with assembly of the OXPHOS complexes
Laura S Kremer, Peter Rehling
Journal of Inherited Metabolic Disease
|
January 27, 2018
"Transcriptomics": molecular diagnosis of inborn errors of metabolism via RNA-sequencing
Laura S Kremer, Saskia B Wortmann, Holger Prokisch
Journal of Inherited Metabolic Disease
|
May 24, 2019
The diagnosis of inborn errors of metabolism by an integrative "multi-omics" approach: A perspective encompassing genomics, transcriptomics, and proteomics
Sarah L Stenton, Laura S Kremer, Robert Kopajtich, et al.
Life Science Alliance
|
November 20, 2023
Mitochondrial phosphoproteomes are functionally specialized across tissues
Fynn M Hansen, Laura S Kremer, Ozge Karayel, et al.
Science Advances
|
November 12, 2025
The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagy
Laura S Kremer, Zoe Golder, Tom Barton-Owen, et al.
Plos Genetics
|
January 6, 2023
A role for BCL2L13 and autophagy in germline purifying selection of mtDNA
Laura S Kremer, Lyuba V Bozhilova, Diana Rubalcava-Gracia, et al.
Nature Communications
|
January 23, 2021
Detection of aberrant splicing events in RNA-seq data using FRASER
Christian Mertes, Ines F Scheller, Vicente A Yépez, et al.
Nature Communications
|
June 17, 2022
Author Correction: Detection of aberrant splicing events in RNA-seq data using FRASER
Christian Mertes, Ines F Scheller, Vicente A Yépez, et al.
Plos One
|
July 12, 2018
OCR-Stats: Robust estimation and statistical testing of mitochondrial respiration activities using Seahorse XF Analyzer
Vicente A Yépez, Laura S Kremer, Arcangela Iuso, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
Methods in Molecular Biology (Clifton, N.J.)
|
March 10, 2017
Identification of Disease-Causing Mutations by Functional Complementation of Patient-Derived Fibroblast Cell Lines
Laura S Kremer, Holger Prokisch
Human Molecular Genetics
|
May 23, 2024
Coordinating mitochondrial translation with assembly of the OXPHOS complexes
Laura S Kremer, Peter Rehling
Journal of Inherited Metabolic Disease
|
January 27, 2018
"Transcriptomics": molecular diagnosis of inborn errors of metabolism via RNA-sequencing
Laura S Kremer, Saskia B Wortmann, Holger Prokisch
Journal of Inherited Metabolic Disease
|
May 24, 2019
The diagnosis of inborn errors of metabolism by an integrative "multi-omics" approach: A perspective encompassing genomics, transcriptomics, and proteomics
Sarah L Stenton, Laura S Kremer, Robert Kopajtich, et al.
Life Science Alliance
|
November 20, 2023
Mitochondrial phosphoproteomes are functionally specialized across tissues
Fynn M Hansen, Laura S Kremer, Ozge Karayel, et al.
Science Advances
|
November 12, 2025
The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagy
Laura S Kremer, Zoe Golder, Tom Barton-Owen, et al.
Plos Genetics
|
January 6, 2023
A role for BCL2L13 and autophagy in germline purifying selection of mtDNA
Laura S Kremer, Lyuba V Bozhilova, Diana Rubalcava-Gracia, et al.
Nature Communications
|
January 23, 2021
Detection of aberrant splicing events in RNA-seq data using FRASER
Christian Mertes, Ines F Scheller, Vicente A Yépez, et al.
Nature Communications
|
June 17, 2022
Author Correction: Detection of aberrant splicing events in RNA-seq data using FRASER
Christian Mertes, Ines F Scheller, Vicente A Yépez, et al.
Plos One
|
July 12, 2018
OCR-Stats: Robust estimation and statistical testing of mitochondrial respiration activities using Seahorse XF Analyzer
Vicente A Yépez, Laura S Kremer, Arcangela Iuso, et al.
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of 3