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W Schulz-Schaeffer

Showing results (11-20 of 29) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 11, 2000
Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targetsJ Bieschke, A Giese, W Schulz-Schaeffer, et al.
Oncogene|May 24, 2011
Uncommitted precursor cells might contribute to increased incidence of embryonal rhabdomyosarcoma in heterozygous Patched1-mutant miceF Nitzki, A Zibat, A Frommhold, et al.
Journal of Medical Primatology|November 3, 2007
Leucoencephalopathy with cerebral calcinosis in a young chimpanzee (Pan troglodytes) - a case reportM Zöller, A Grevot, K Mätz-Rensing, et al.
Genomics|June 1, 1994
Human brain factor 1, a new member of the fork head gene familyD B Murphy, S Wiese, P Burfeind, et al.
Genomics|December 28, 1999
SALL3, a new member of the human spalt-like gene family, maps to 18q23J Kohlhase, S Hausmann, G Stojmenovic, et al.
British Journal of Haematology|April 12, 2000
Differential constitutive and activation-dependent expression of prion protein in human peripheral blood leucocytesJ Dürig, A Giese, W Schulz-Schaeffer, et al.
Annals of Neurology|October 17, 2001
Pick's disease associated with the novel Tau gene mutation K369IM Neumann, W Schulz-Schaeffer, R A Crowther, et al.
Neuroscience|June 16, 2010
Cellular prion protein overexpression disturbs cellular homeostasis in SH-SY5Y neuroblastoma cells but does not alter p53 expression: a proteomic studyE Weiss, S Ramljak, A R Asif, et al.
Human Genetics|September 15, 2000
Molecular genetics of human prion diseases in GermanyO Windl, A Giese, W Schulz-Schaeffer, et al.
Neuropediatrics|March 6, 2004
CNS disease as the main manifestation of hemophagocytic lymphohistiocytosis in two childrenK Rostasy, R Kolb, D Pohl, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2000
Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targetsJ Bieschke, A Giese, W Schulz-Schaeffer, et al.
Oncogene|May 24, 2011
Uncommitted precursor cells might contribute to increased incidence of embryonal rhabdomyosarcoma in heterozygous Patched1-mutant miceF Nitzki, A Zibat, A Frommhold, et al.
Journal of Medical Primatology|November 3, 2007
Leucoencephalopathy with cerebral calcinosis in a young chimpanzee (Pan troglodytes) - a case reportM Zöller, A Grevot, K Mätz-Rensing, et al.
Genomics|June 1, 1994
Human brain factor 1, a new member of the fork head gene familyD B Murphy, S Wiese, P Burfeind, et al.
Genomics|December 28, 1999
SALL3, a new member of the human spalt-like gene family, maps to 18q23J Kohlhase, S Hausmann, G Stojmenovic, et al.
British Journal of Haematology|April 12, 2000
Differential constitutive and activation-dependent expression of prion protein in human peripheral blood leucocytesJ Dürig, A Giese, W Schulz-Schaeffer, et al.
Annals of Neurology|October 17, 2001
Pick's disease associated with the novel Tau gene mutation K369IM Neumann, W Schulz-Schaeffer, R A Crowther, et al.
Neuroscience|June 16, 2010
Cellular prion protein overexpression disturbs cellular homeostasis in SH-SY5Y neuroblastoma cells but does not alter p53 expression: a proteomic studyE Weiss, S Ramljak, A R Asif, et al.
Human Genetics|September 15, 2000
Molecular genetics of human prion diseases in GermanyO Windl, A Giese, W Schulz-Schaeffer, et al.
Neuropediatrics|March 6, 2004
CNS disease as the main manifestation of hemophagocytic lymphohistiocytosis in two childrenK Rostasy, R Kolb, D Pohl, et al.
Pageof 3