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Handbook of Clinical Neurology
|
February 22, 2023
Genetics of mitochondrial diseases: Current approaches for the molecular diagnosis
Lea D Schlieben, Holger Prokisch
Clinics in Laboratory Medicine
|
May 23, 2020
The Clinical Application of RNA Sequencing in Genetic Diagnosis of Mendelian Disorders
Sarah L Stenton, Holger Prokisch
Essays in Biochemistry
|
June 29, 2018
Advancing genomic approaches to the molecular diagnosis of mitochondrial disease
Sarah Louise Stenton, Holger Prokisch
International Journal of Molecular Sciences
|
May 11, 2024
Digenic Inheritance in Rare Disorders and Mitochondrial Disease-Crossing the Frontier to a More Comprehensive Understanding of Etiology
Christiane M Neuhofer, Holger Prokisch
Fungal Genetics and Biology : FG & B
|
June 26, 2002
Protein import into mitochondria of Neurospora crassa
Holger Prokisch, Stephan Nussberger, Benedikt Westermann
Genome Medicine
|
November 27, 2016
Mitochondrial replacement approaches: challenges for clinical implementation
Thomas Klopstock, Barbara Klopstock, Holger Prokisch
Human Molecular Genetics
|
January 30, 2003
An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria
Konstanze Hörtnagel, Holger Prokisch, Thomas Meitinger
Pediatric Investigation
|
April 6, 2022
RNA sequencing role and application in clinical diagnostic
Fatemeh Peymani, Aiman Farzeen, Holger Prokisch
Journal of Inherited Metabolic Disease
|
August 9, 2023
Integrative omics approaches to advance rare disease diagnostics
Dmitrii Smirnov, Nikita Konstantinovskiy, Holger Prokisch
Methods in Molecular Biology (Clifton, N.J.)
|
March 10, 2017
Analysis of Mitochondrial RNA-Processing Defects in Patient-Derived Tissues by qRT-PCR and RNAseq
Robert Kopajtich, Johannes A Mayr, Holger Prokisch
Page
of 40
Search research articles
Search
Showing results (11-20 of 394) with videos related to
Sort By:
Page
of 40
Handbook of Clinical Neurology
|
February 22, 2023
Genetics of mitochondrial diseases: Current approaches for the molecular diagnosis
Lea D Schlieben, Holger Prokisch
Clinics in Laboratory Medicine
|
May 23, 2020
The Clinical Application of RNA Sequencing in Genetic Diagnosis of Mendelian Disorders
Sarah L Stenton, Holger Prokisch
Essays in Biochemistry
|
June 29, 2018
Advancing genomic approaches to the molecular diagnosis of mitochondrial disease
Sarah Louise Stenton, Holger Prokisch
International Journal of Molecular Sciences
|
May 11, 2024
Digenic Inheritance in Rare Disorders and Mitochondrial Disease-Crossing the Frontier to a More Comprehensive Understanding of Etiology
Christiane M Neuhofer, Holger Prokisch
Fungal Genetics and Biology : FG & B
|
June 26, 2002
Protein import into mitochondria of Neurospora crassa
Holger Prokisch, Stephan Nussberger, Benedikt Westermann
Genome Medicine
|
November 27, 2016
Mitochondrial replacement approaches: challenges for clinical implementation
Thomas Klopstock, Barbara Klopstock, Holger Prokisch
Human Molecular Genetics
|
January 30, 2003
An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria
Konstanze Hörtnagel, Holger Prokisch, Thomas Meitinger
Pediatric Investigation
|
April 6, 2022
RNA sequencing role and application in clinical diagnostic
Fatemeh Peymani, Aiman Farzeen, Holger Prokisch
Journal of Inherited Metabolic Disease
|
August 9, 2023
Integrative omics approaches to advance rare disease diagnostics
Dmitrii Smirnov, Nikita Konstantinovskiy, Holger Prokisch
Methods in Molecular Biology (Clifton, N.J.)
|
March 10, 2017
Analysis of Mitochondrial RNA-Processing Defects in Patient-Derived Tissues by qRT-PCR and RNAseq
Robert Kopajtich, Johannes A Mayr, Holger Prokisch
Page
of 40