Zobrazeno 1 - 10
of 349
pro vyhledávání: '"Gert C"'
Autor:
Kai Dun Tang, Lilian Menezes, Kurt Baeten, Laurence J. Walsh, Bernard C. S. Whitfield, Martin D. Batstone, Liz Kenny, Ian H. Frazer, Gert C. Scheper, Chamindie Punyadeera
Publikováno v:
Biomolecules, Vol 10, Iss 2, p 223 (2020)
The role of human papillomavirus type 16 (HPV16) in oral potentially malignant disorders (OPMD) and oral cavity carcinoma (OC) is still under debate. We investigated HPV16 prevalence in unstimulated saliva, oral rinse samples, oral swabs and tumour b
Externí odkaz:
https://doaj.org/article/8f7742d605bf4a3583c12904228b7b04
Autor:
Anna Duarri, Miguel Lopez de Heredia, Xavier Capdevila-Nortes, Margreet C. Ridder, Marisol Montolio, Tania López-Hernández, Ilja Boor, Chun-Fu Lien, Tracy Hagemann, Albee Messing, Dariusz C. Gorecki, Gert C. Scheper, Albert Martínez, Virginia Nunes, Marjo S. van der Knaap, Raúl Estévez
Publikováno v:
Neurobiology of Disease, Vol 43, Iss 1, Pp 228-238 (2011)
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a rare type of leukodystrophy, in the majority of cases caused by mutations in the MLC1 gene. MRI from MLC patients shows diffuse cerebral white matter signal abnormality and swellin
Externí odkaz:
https://doaj.org/article/ab7e770a271145778d5dd3d5e8bc9908
Autor:
Barbara van Kollenburg, Adri A.M. Thomas, Gerre Vermeulen, Gesina A.M. Bertrand, Carola G.M. van Berkel, Jan C. Pronk, Christopher G. Proud, Marjo S. van der Knaap, Gert C. Scheper
Publikováno v:
Neurobiology of Disease, Vol 21, Iss 3, Pp 496-504 (2006)
Leukoencephalopathy with vanishing white matter (VWM) is an inherited childhood white matter disorder, caused by mutations in the genes encoding eukaryotic initiation factor 2B (eIF2B). The present study showed that, while the eIF2B activity was redu
Externí odkaz:
https://doaj.org/article/8159bc0d1f464732aa20f85a8cf2c051
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 66, Iss 3a, Pp 549-551 (2008)
Externí odkaz:
https://doaj.org/article/3f4e5a5e50e44c83a06a22d9ff1026ba
Autor:
Rogerio A de Almeida, Anne Fogli, Marina Gaillard, Gert C Scheper, Odile Boesflug-Tanguy, Graham D Pavitt
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e53958 (2013)
Recessive inherited mutations in any of five subunits of the general protein synthesis factor eIF2B are responsible for a white mater neurodegenerative disease with a large clinical spectrum. The classical form is called Childhood Ataxia with CNS hyp
Externí odkaz:
https://doaj.org/article/ae292ce4100b43458a091927160c0aa8
Autor:
Greenbaum, Noam, Schwartz, Uri, Benito, Gerardo, Porat, Naomi, Cloete, Gert C., Enzel, Yehouda
Publikováno v:
In Quaternary Science Reviews 1 November 2014 103:153-169
Publikováno v:
Biologist. Winter2021, Vol. 68 Issue 4, p44-46. 3p.
Autor:
Arnold, Klaus Jochen, Lübbers, Gert C.
Publikováno v:
Journal of Contemporary History, 2007 Oct 01. 42(4), 613-626.
Externí odkaz:
https://www.jstor.org/stable/30036472
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2007 Jul . 104(31), 12902-12906.
Externí odkaz:
https://www.jstor.org/stable/25436402
Autor:
Lübbers, Gert C.
Publikováno v:
Vierteljahrshefte für Zeitgeschichte, 2006 Jan 01. 54(1), 87-123.
Externí odkaz:
http://dx.doi.org/10.1524/vfzg.2006.54.1.87