Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Familial glioma"'
Autor:
Robert Hüneburg, Helge Martens, Martin Stangel, Andreas Erbersdobler, Wiebke Ewert, Matthias Preller, Stephan Wolf, Ruthild G. Weber, Bettina Wiese, Amir Samii, Natalie Elyan, Christopher Previti, Joachim K. Krauss, Stefan Aretz, Rouzbeh Banan, Ulrike Beyer, Bujung Hong, Christine A. M. Weber, Jan Hinrich Bräsen, Frank Brand, Alisa Förster, Jessica Kronenberg, Christian Hartmann
Publikováno v:
Acta Neuropathologica
Acta Neuropathol (2021) 142:191–210
Acta Neuropathol (2021) 142:191–210
The genetic basis of brain tumor development is poorly understood. Here, leukocyte DNA of 21 patients from 15 families with ≥ 2 glioma cases each was analyzed by whole-genome or targeted sequencing. As a result, we identified two families with rare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f362899dd7954c1947571837da807f8
https://doi.org/10.1007/s00401-021-02307-1
https://doi.org/10.1007/s00401-021-02307-1
Akademický článek
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Autor:
Matthew L. Kosel, Georgina Armstrong, Beatrice Melin, Melissa L. Bondy, Thomas M. Kollmeyer, Corinne Praska, Matthew N. Bainbridge, Paul A. Decker, Jeanette E. Eckel-Passow, Vanessa Y Ruiz, Robert B. Jenkins, Daniel H. Lachance, Seiji Yamada
Publikováno v:
Neuro-Oncology. 20:810-817
BACKGROUND: Single-gene mutation syndromes account for some familial glioma (FG); however, they make up only a small fraction of glioma families. Gliomas can be classified into 3 major molecular subtypes based on isocitrate dehydrogenase (IDH) mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e2034744c8939e17f88391a5d5382b
https://doi.org/10.1093/neuonc/nox192
https://doi.org/10.1093/neuonc/nox192
Autor:
Riccardo Bazzoni, Angela Bentivegna
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Glioma is the most common brain tumor, characterized by several histological and malignancy grade. The majority of gliomas are sporadic, but some familial cases have been reported ( < 5%). Despite hereditary predisposition to gliomas has been associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be2cd533c088bdb3a58d0b26ea7a84d2
https://doi.org/10.4267/2042/70461
https://doi.org/10.4267/2042/70461
Akademický článek
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Autor:
Jeanette E. Eckel-Passow, Christopher I. Amos, Richard S. Houlston, Jonine L. Bernstein, Robert B. Jenkins, Jill S. Barnholtz-Sloan, Joellen M. Schildkraut, Daniel H. Lachance, Georgina Armstrong, Rose Lai, Elizabeth B. Claus, Quinn T. Ostrom, Dora Il'yasova, Melissa L. Bondy, Sanjay Shete, Sara H. Olson, Beatrice Melin, Christoffer Johansen, Ryan Merrell, Margaret Wrensch
Publikováno v:
Neuro-Oncology. 20:vi108-vi108
BACKGROUND: Approximately 5% of gliomas occur in individuals with a family history of glioma, and first-degree relatives of brain tumor cases have a two-fold increase in risk of brain tumor. Family-based studies have had little success in identifying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06d1e5dabafe9c223c93345227f052e3
https://doi.org/10.1093/neuonc/noy148.449
https://doi.org/10.1093/neuonc/noy148.449
Autor:
Georgina Armstrong, Jason T. Huse, Donna M. Muzny, Daniel I. Jacobs, Melissa L. Bondy, Kazutaka Fukumura, Beatrice Melin, Matthew N. Bainbridge
Publikováno v:
Cancer Research. 78:1243-1243
INTRODUCTION: In recent years, the molecular characterization of sporadically arising diffuse gliomas has identified recurrent driving alterations and delineated molecularly and clinically distinct subclasses of disease. However, less is known about
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2cc075c6c2a2fe2edd0f03005ce8c66
https://doi.org/10.1158/1538-7445.am2018-1243
https://doi.org/10.1158/1538-7445.am2018-1243
Akademický článek
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Autor:
Matthew L. Kosel, Corinne Praska, Georgina Armstrong, Melissa L. Bondy, Matthew N. Bainbridge, Jeanette E. Eckel-Passow, Beatrice Melin, Vanessa Y Ruiz, Seiji Yamada, Daniel H. Lachance, Thomas M. Kollmeyer, Paul A. Decker, Robert B. Jenkins
Publikováno v:
Neuro-Oncology. 18:vi76-vi76
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ffc2a27d5c7e02517de8e7316412b8e
https://doi.org/10.1093/neuonc/now212.318
https://doi.org/10.1093/neuonc/now212.318
Publikováno v:
JOURNAL OF NEURO-ONCOLOGY. 24(3):251-258
The familial occurrence of gliomas, in the absence of well-defined neurological tumor syndromes such as the neurofibromatoses, is uncommon, We present a family of ten children in which the four eldest suffered from gliomas. Three of these siblings ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dris___01423::1a4ef90348f03d7b0f01a2bc86cd4337
https://research.rug.nl/en/publications/60f11415-fe50-4943-b447-35fd9f2dac56
https://research.rug.nl/en/publications/60f11415-fe50-4943-b447-35fd9f2dac56