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O Jensson

Showing results (41-50 of 102) with videos related to

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Journal of the Neurological Sciences|April 1, 1992
On the role of monocytes/macrophages in the pathogenesis of central nervous system lesions in hereditary cystatin C amyloid angiopathyL Thorsteinsson, G Georgsson, B Asgeirsson, et al.
The Biochemical Journal|June 1, 1990
Structure and expression of the human cystatin C geneM Abrahamson, I Olafsson, A Palsdottir, et al.
Development (Cambridge, England)|January 1, 1988
The application of molecular genetics to detection of craniofacial abnormalityG Moore, A Ivens, J Chambers, et al.
Acta Neurologica Scandinavica|June 1, 1989
Absence of the cystatin C amyloid in the cerebral amyloid angiopathy, senile plaque, and extra-CNS amyloid deposits of aged JapaneseM Yamada, H Tsukagoshi, Y Wada, et al.
Progress in Clinical and Biological Research|January 1, 1989
Mutation in the cystatin C gene causes hereditary brain hemorrhageA Palsdottir, M Abrahamson, L Thorsteinsson, et al.
Tissue Antigens|February 1, 1978
On the mapping of PGM3, GLO and HLAL U Lamm, L R Weitkamp, O Jensson, et al.
Biological Chemistry Hoppe-Seyler|May 1, 1990
Cystatin C mutation causing amyloid angiopathy and brain hemorrhageO Jensson, A Pálsdóttir, L Thorsteinsson, et al.
Human Genetics|July 1, 1993
Icelandic families with autosomal dominant polycystic kidney disease: families unlinked to chromosome 16p13.3 revealed by linkage analysisR Fossdal, M Böthvarsson, P Asmundsson, et al.
The Cleft Palate Journal|April 1, 1990
X chromosome genes involved in the regulation of facial clefting and spina bifidaG E Moore, A Ivens, R Newton, et al.
Human Genetics|April 1, 1988
X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17A Ivens, G E Moore, J Chambers, et al.
Pageof 11

Showing results (41-50 of 102) with videos related to

Sort By:
Pageof 11
Journal of the Neurological Sciences|April 1, 1992
On the role of monocytes/macrophages in the pathogenesis of central nervous system lesions in hereditary cystatin C amyloid angiopathyL Thorsteinsson, G Georgsson, B Asgeirsson, et al.
The Biochemical Journal|June 1, 1990
Structure and expression of the human cystatin C geneM Abrahamson, I Olafsson, A Palsdottir, et al.
Development (Cambridge, England)|January 1, 1988
The application of molecular genetics to detection of craniofacial abnormalityG Moore, A Ivens, J Chambers, et al.
Acta Neurologica Scandinavica|June 1, 1989
Absence of the cystatin C amyloid in the cerebral amyloid angiopathy, senile plaque, and extra-CNS amyloid deposits of aged JapaneseM Yamada, H Tsukagoshi, Y Wada, et al.
Progress in Clinical and Biological Research|January 1, 1989
Mutation in the cystatin C gene causes hereditary brain hemorrhageA Palsdottir, M Abrahamson, L Thorsteinsson, et al.
Tissue Antigens|February 1, 1978
On the mapping of PGM3, GLO and HLAL U Lamm, L R Weitkamp, O Jensson, et al.
Biological Chemistry Hoppe-Seyler|May 1, 1990
Cystatin C mutation causing amyloid angiopathy and brain hemorrhageO Jensson, A Pálsdóttir, L Thorsteinsson, et al.
Human Genetics|July 1, 1993
Icelandic families with autosomal dominant polycystic kidney disease: families unlinked to chromosome 16p13.3 revealed by linkage analysisR Fossdal, M Böthvarsson, P Asmundsson, et al.
The Cleft Palate Journal|April 1, 1990
X chromosome genes involved in the regulation of facial clefting and spina bifidaG E Moore, A Ivens, R Newton, et al.
Human Genetics|April 1, 1988
X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17A Ivens, G E Moore, J Chambers, et al.
Pageof 11