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Brain : a Journal of Neurology|September 26, 2001
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22S M Rosso, W Kamphorst, B de Graaf, et al.Pediatric Research|October 1, 1990
Rat heart perfusion as model system for enzyme replacement therapy in glycogenosis type IIA T van der Ploeg, A M van der Kraaij, R Willemsen, et al.Human Molecular Genetics|April 10, 1999
Different targets for the fragile X-related proteins revealed by their distinct nuclear localizationsF Tamanini, C Bontekoe, C E Bakker, et al.Brain : a Journal of Neurology|July 15, 2005
Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathologyI F Bronner, B C ter Meulen, A Azmani, et al.Journal of Inherited Metabolic Disease|January 1, 1985
Sucrase-isomaltase and cystic fibrosisH J Sips, A H Claass, J M van Dongen, et al.The Biochemical Journal|December 1, 1990
Expression and routeing of human lysosomal alpha-glucosidase in transiently transfected mammalian cellsL H Hoefsloot, R Willemsen, M A Kroos, et al.Molecular and Chemical Neuropathology|February 1, 1995
A biochemical and ultrastructural evaluation of the type 2 Gaucher mouseR Willemsen, V Tybulewicz, E Sidransky, et al.Human Genetics|March 1, 1997
Rapid antibody test for diagnosing fragile X syndrome: a validation of the techniqueR Willemsen, A Smits, S Mohkamsing, et al.Nature|June 24, 1993
Characterization and localization of the FMR-1 gene product associated with fragile X syndromeC Verheij, C E Bakker, E de Graaff, et al.Human Molecular Genetics|May 1, 1995
Characterization of FMR1 proteins isolated from different tissuesC Verheij, E de Graaff, C E Bakker, et al.Pageof 11