Хайлтын үр дүнгүүд - Holger Prokisch
- 172-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
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ncRNAs: New Players in Mitochondrial Health and Disease? -н Mirjana Gušić, Holger Prokisch
Хэвлэсэн 2020Revisão -
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The Dimensions of Primary Mitochondrial Disorders -н Lea D. Schlieben, Holger Prokisch
Хэвлэсэн 2020Revisão -
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Mitochondrial disorders -н Thomas Klopstock, Claudia Priglinger, Ali Yılmaz, Cornelia Kornblum, Felix Distelmaier, Holger Prokisch
Хэвлэсэн 2021Revisão -
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Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress a... -н Paola Venco, Massimo Bonora, Carlotta Giorgi, Elena Papaleo, Arcangela Iuso, Holger Prokisch, Paolo Pinton, Valeria Tiranti
Хэвлэсэн 2015Artigo -
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A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1 -н Eva Lattka, Stefanie Eggers, Gabriele Moeller, Katharina Heim, Malory Weber, Divya Mehta, Holger Prokisch, Thomas Illig, Jerzy Adamski
Хэвлэсэн 2009Artigo -
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The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity -н Christian Johannes Gloeckner, Norbert Kinkl, Annette Schumacher, Ralf J. Braun, Eric O’Neill, Thomas Meitinger, Walter Kölch, Holger Prokisch, Marius Ueffing
Хэвлэсэн 2005Artigo -
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OCR-Stats: Robust estimation and statistical testing of mitochondrial respiration activities using Seahorse XF Analyzer -н Vicente A. Yépez, Laura S. Kremer, Arcangela Iuso, Mirjana Gušić, Robert Kopajtich, Eliška Koňaříková, Agnieszka Nadel, Leonhard Wachutka, Holger Prokisch, Julien Gagneur
Хэвлэсэн 2018Artigo -
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Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9 -н Katharina Danhauser, Diran Herebıan, Tobias B. Haack, Richard J. Rodenburg, Tim M. Strom, Thomas Meitinger, Dirk Klee, Ertan Mayatepek, Holger Prokisch, Felix Distelmaier
Хэвлэсэн 2015Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Gene
Genetics
Medicine
Internal medicine
Mutation
Computational biology
Disease
Mitochondrial DNA
Mitochondrion
Phenotype
Endocrinology
Bioinformatics
Gene expression
Exome sequencing
Biochemistry
Genotype
Pathology
Mitochondrial disease
Single-nucleotide polymorphism
Genome-wide association study
Neuroscience
Cell biology
DNA methylation
Allele
Population
Environmental health
RNA
Respiratory chain
Exome