檢索結果 - Maciej Pronicki
- Showing 1 - 7 results of 7
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Oxidative stress-dependent p66Shc phosphorylation in skin fibroblasts of children with mitochondrial disorders 由 Magdalena Lebiedzińska, Agnieszka Karkucińska‐Więckowska, Carlotta Giorgi, Elżbieta Karczmarewicz, Ewa Pronicka, Paolo Pinton, Jerzy Duszyński, Maciej Pronicki, Mariusz R. Więckowski
出版 2010Artigo -
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Retrospective, Multicentric Study of 180 Children with Cytochrome c Oxidase Deficiency 由 Marek Böhm, Ewa Pronicka, Elżbieta Karczmarewicz, Maciej Pronicki, Dorota Piekutowska‐Abramczuk, Jolanta Sykut‐Cegielska, Hanna Mierzewska, Hana Hansı́ková, Kateřina Veselá, Markéta Tesařová, H Houst'ková, J Houštěk, J Zeman
出版 2005Artigo -
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Western Diet Causes Obesity-Induced Nonalcoholic Fatty Liver Disease Development by Differentially Compromising the Autophagic Response 由 Inês C. M. Simões, Agnieszka Karkucińska‐Więckowska, Justyna Janikiewicz, Sylwia Szymańska, Maciej Pronicki, Paweł Dobrzyń, Michał Dąbrowski, Agnieszka Dobrzyń, Paulo J. Oliveira, Hans Zischka, Yaiza Potes, Mariusz R. Więckowski
出版 2020Artigo -
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Oxidative stress in metabolic dysfunction‐associated steatotic liver disease (<scp>MASLD</scp>): How does the animal model resemble human disease? 由 Patrycja Jakubek, Piotr Kalinowski, Agnieszka Karkucińska‐Więckowska, Aakruti Kaikini, Inês C. M. Simões, Yaiza Potes, Beata Kruk, Wiesława Grajkowska, Paolo Pinton, Piotr Milkiewicz, Michał Grąt, Maciej Pronicki, Magdalena Lebiedzińska, Marcin Krawczyk, Mariusz R. Więckowski
出版 2024Artigo -
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New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre 由 Ewa Pronicka, Dorota Piekutowska‐Abramczuk, Elżbieta Ciara, Joanna Trubicka, Dariusz Rokicki, Agnieszka Karkucińska‐Więckowska, Magdalena Pajdowska, Elżbieta Jurkiewicz, Paulina Halat, Joanna Kosińska, Agnieszka Pollak, Małgorzata Rydzanicz, Piotr Stawiński, Maciej Pronicki, Małgorzata Krajewska‐Walasek, Rafał Płoski
出版 2016Artigo -
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Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy 由 Katharina Danhauser, Bader Alhaddad, Christine Makowski, Dorota Piekutowska‐Abramczuk, Steffen Syrbe, Natalia Gomez‐Ospina, Melanie A. Manning, Anna Kostera‐Pruszczyk, Claudia Krahn-Peper, Riccardo Berutti, Réka Kovács-Nagy, Mirjana Gušić, Elisabeth Graf, Lucia Laugwitz, Michaela Röblitz, Andreas Wroblewski, Hans Hartmann, Anibh M. Das, Eva Bültmann, Fang Fang, Manting Xu, Ulrich A. Schatz, Daniela Karall, Herta Zellner, Edda Haberlandt, René G. Feichtinger, Johannes A. Mayr, Thomas Meitinger, Holger Prokisch, Tim M. Strom, Rafał Płoski, Georg F. Hoffmann, Maciej Pronicki, Penelope E. Bonnen, Susanne Morlot, Tobias B. Haack
出版 2018Artigo
相關主題
Biology
Medicine
Gene
Internal medicine
Disease
Biochemistry
Fatty liver
Genetics
Mitochondrial DNA
Mitochondrion
Oxidative phosphorylation
Oxidative stress
Allele
Endocrinology
Exome
Exome sequencing
Lipid peroxidation
Mitochondrial disease
Mutation
Nonalcoholic fatty liver disease
Pathology
Steatosis
Anatomy
Antioxidant
Artificial intelligence
Ataxia
Bioinformatics
Biopsy
Cell biology
Chemistry