Zobrazeno 1 - 10
of 595
pro vyhledávání: '"H. Koeppen"'
Autor:
Arpita Chatterjee, Saikat Saha, Anirban Chakraborty, Anabela Silva-Fernandes, Santi M Mandal, Andreia Neves-Carvalho, Yongping Liu, Raj K Pandita, Muralidhar L Hegde, Pavana M Hegde, Istvan Boldogh, Tetsuo Ashizawa, Arnulf H Koeppen, Tej K Pandita, Patricia Maciel, Partha S Sarkar, Tapas K Hazra
Publikováno v:
PLoS Genetics, Vol 20, Iss 1, p e1011124 (2024)
[This corrects the article DOI: 10.1371/journal.pgen.1004749.].
Externí odkaz:
https://doaj.org/article/35d8c4e7cc8048d1a6e35ea051295bfe
Autor:
Arnulf H Koeppen
Publikováno v:
Journal of Integrative Neuroscience, Vol 23, Iss 1, p 4 (2024)
Heart, dentate nucleus, and dorsal root ganglia (DRG) are targets of tissue damage in Friedreich ataxia (FA). This report summarizes the histology and histopathology of iron in the main tissues affected by FA. None of the affected anatomical sites re
Externí odkaz:
https://doaj.org/article/ca9ef51067b649fcb6262b62a01cfc97
Autor:
Arnulf H. Koeppen
Publikováno v:
Free Neuropathology, Vol 2 (2021)
Externí odkaz:
https://doaj.org/article/254977b5c1ad46f6a6da741dd4ca45ed
Autor:
Arnulf H. Koeppen
Publikováno v:
Myelin ISBN: 9780203746141
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a517085dc3eaa6d9aeb20030d820b4e
https://doi.org/10.1201/9780203746141-28
https://doi.org/10.1201/9780203746141-28
Akademický článek
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Autor:
Ashlee Long, Jill S Napierala, Urszula Polak, Lauren Hauser, Arnulf H Koeppen, David R Lynch, Marek Napierala
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189990 (2017)
Friedreich's ataxia (FRDA) is a genetic neurodegenerative disorder caused by transcriptional silencing of the frataxin gene (FXN) due to expansions of GAA repeats in intron 1. FRDA manifests with multiple symptoms, which may include ataxia, cardiomyo
Externí odkaz:
https://doaj.org/article/df6afd54e6fb4223aed6fa368d898031
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Arnulf H Koeppen, R Liane Ramirez, Alyssa B Becker, Sarah T Bjork, Sonia Levi, Paolo Santambrogio, Patrick J Parsons, Pamela C Kruger, Karl X Yang, Paul J Feustel, Joseph E Mazurkiewicz
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0116396 (2015)
Friedreich ataxia (FA) is an autosomal recessive disease with a complex neurological phenotype, but the most common cause of death is heart failure. This study presents a systematic analysis of 15 fixed and 13 frozen archival autopsy tissues of FA he
Externí odkaz:
https://doaj.org/article/b701158d15db466b802bee797fea0330
Autor:
Rui Gao, Yongping Liu, Anabela Silva-Fernandes, Xiang Fang, Adriana Paulucci-Holthauzen, Arpita Chatterjee, Hang L Zhang, Tohru Matsuura, Sanjeev Choudhary, Tetsuo Ashizawa, Arnulf H Koeppen, Patricia Maciel, Tapas K Hazra, Partha S Sarkar
Publikováno v:
PLoS Genetics, Vol 11, Iss 1, p e1004834 (2015)
Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is an untreatable autosomal dominant neurodegenerative disease, and the most common such inherited ataxia worldwide. The mutation in SCA3 is the expansion of a polymorp
Externí odkaz:
https://doaj.org/article/1887acc43953446592da2d9b8dcea9d3
Autor:
Arpita Chatterjee, Saikat Saha, Anirban Chakraborty, Anabela Silva-Fernandes, Santi M Mandal, Andreia Neves-Carvalho, Yongping Liu, Raj K Pandita, Muralidhar L Hegde, Pavana M Hegde, Istvan Boldogh, Tetsuo Ashizawa, Arnulf H Koeppen, Tej K Pandita, Patricia Maciel, Partha S Sarkar, Tapas K Hazra
Publikováno v:
PLoS Genetics, Vol 11, Iss 1, p e1004749 (2015)
DNA strand-breaks (SBs) with non-ligatable ends are generated by ionizing radiation, oxidative stress, various chemotherapeutic agents, and also as base excision repair (BER) intermediates. Several neurological diseases have already been identified a
Externí odkaz:
https://doaj.org/article/816f1319fae448229cf3154cfe1d4f34