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F Arwert

Showing results (51-60 of 73) with videos related to

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Neurology|December 1, 1996
Presynaptic nigrostriatal function in genetically tested asymptomatic relatives from the pallido-ponto-nigral degeneration familyA Kishore, Z K Wszolek, B J Snow, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|December 1, 1979
Erythrocyte superoxide dismutase deficiency in Fanconi's anaemia established by two independent methods of assayH Joenje, R R Frants, F Arwert, et al.
American Journal of Human Genetics|August 11, 2000
Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group AH Joenje, M Levitus, Q Waisfisz, et al.
Human Molecular Genetics|August 1, 2000
Mice with a targeted disruption of the Fanconi anemia homolog FancaN C Cheng, H J van de Vrugt, M A van der Valk, et al.
British Journal of Haematology|February 13, 2001
Aberrant Fanconi anaemia protein profiles in acute myeloid leukaemia cellsY Xie, J P de Winter, Q Waisfisz, et al.
Human Genetics|December 1, 1986
Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cellsF Arwert, H J Porck, M Fràter-Schröder, et al.
Human Molecular Genetics|January 1, 1996
Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21M Wijker, Z K Wszolek, E C Wolters, et al.
Annals of Neurology|September 1, 1992
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degenerationZ K Wszolek, R F Pfeiffer, M H Bhatt, et al.
Human Molecular Genetics|November 7, 2000
The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCGJ P de Winter, L van der Weel, J de Groot, et al.
Human Genetics|January 1, 1985
Assignment of human pepsinogen A locus to the q12-pter region of chromosome 11B Zelle, A Geurts van Kessel, J de Wit, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
Neurology|December 1, 1996
Presynaptic nigrostriatal function in genetically tested asymptomatic relatives from the pallido-ponto-nigral degeneration familyA Kishore, Z K Wszolek, B J Snow, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|December 1, 1979
Erythrocyte superoxide dismutase deficiency in Fanconi's anaemia established by two independent methods of assayH Joenje, R R Frants, F Arwert, et al.
American Journal of Human Genetics|August 11, 2000
Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group AH Joenje, M Levitus, Q Waisfisz, et al.
Human Molecular Genetics|August 1, 2000
Mice with a targeted disruption of the Fanconi anemia homolog FancaN C Cheng, H J van de Vrugt, M A van der Valk, et al.
British Journal of Haematology|February 13, 2001
Aberrant Fanconi anaemia protein profiles in acute myeloid leukaemia cellsY Xie, J P de Winter, Q Waisfisz, et al.
Human Genetics|December 1, 1986
Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cellsF Arwert, H J Porck, M Fràter-Schröder, et al.
Human Molecular Genetics|January 1, 1996
Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21M Wijker, Z K Wszolek, E C Wolters, et al.
Annals of Neurology|September 1, 1992
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degenerationZ K Wszolek, R F Pfeiffer, M H Bhatt, et al.
Human Molecular Genetics|November 7, 2000
The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCGJ P de Winter, L van der Weel, J de Groot, et al.
Human Genetics|January 1, 1985
Assignment of human pepsinogen A locus to the q12-pter region of chromosome 11B Zelle, A Geurts van Kessel, J de Wit, et al.
Pageof 8