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P Cras

Showing results (91-100 of 119) with videos related to

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American Journal of Medical Genetics|May 20, 1999
Postmortem examination of two fragile X brothers with an FMR1 full mutationE Reyniers, J J Martin, P Cras, et al.
Brain Research|September 24, 1993
Degeneration of vascular muscle cells in cerebral amyloid angiopathy of Alzheimer diseaseM Kawai, R N Kalaria, P Cras, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 26, 2002
Phosphorylated tau in cerebrospinal fluid as a marker for Creutzfeldt-Jakob diseaseB Van Everbroeck, A J E Green, E Vanmechelen, et al.
Journal of Cancer Research and Clinical Oncology|September 28, 1998
Determination of growth fraction and cell density to evaluate the potential growth of human oligodendroglial and astrocytic tumoursL Gordower, C Decaestecker, M B Lopes, et al.
Molecular Pharmacology|July 1, 1999
Humanization of mouse 5-hydroxytryptamine1B receptor gene by homologous recombination: in vitro and in vivo characterizationP Bonaventure, L Umans, M H Bakker, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 1, 1991
Association of heparan sulfate proteoglycan with the neurofibrillary tangles of Alzheimer's diseaseG Perry, S L Siedlak, P Richey, et al.
Journal of Neuropathology and Experimental Neurology|August 28, 1998
Characterization of astroglial versus oligodendroglial phenotypes in glioblastomas by means of quantitative morphonuclear variables generated by computer-assisted microscopyC Decaestecker, I Camby, L Gordower, et al.
Public Health in Practice (Oxford, England)|September 14, 2022
HIV sero-positivity and risk factors for ischaemic and haemorrhagic stroke in hospitalised patients in Uganda: A prospective-case-control studyG Namale, O Kamacooko, A Makhoba, et al.
Neuroscience Letters|October 31, 2001
Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotypeB Van Everbroeck, E A Croes, P Pals, et al.
Human Molecular Genetics|December 1, 1995
Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3M Cruts, H Backhovens, S Y Wang, et al.
Pageof 12

Showing results (91-100 of 119) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics|May 20, 1999
Postmortem examination of two fragile X brothers with an FMR1 full mutationE Reyniers, J J Martin, P Cras, et al.
Brain Research|September 24, 1993
Degeneration of vascular muscle cells in cerebral amyloid angiopathy of Alzheimer diseaseM Kawai, R N Kalaria, P Cras, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 26, 2002
Phosphorylated tau in cerebrospinal fluid as a marker for Creutzfeldt-Jakob diseaseB Van Everbroeck, A J E Green, E Vanmechelen, et al.
Journal of Cancer Research and Clinical Oncology|September 28, 1998
Determination of growth fraction and cell density to evaluate the potential growth of human oligodendroglial and astrocytic tumoursL Gordower, C Decaestecker, M B Lopes, et al.
Molecular Pharmacology|July 1, 1999
Humanization of mouse 5-hydroxytryptamine1B receptor gene by homologous recombination: in vitro and in vivo characterizationP Bonaventure, L Umans, M H Bakker, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 1, 1991
Association of heparan sulfate proteoglycan with the neurofibrillary tangles of Alzheimer's diseaseG Perry, S L Siedlak, P Richey, et al.
Journal of Neuropathology and Experimental Neurology|August 28, 1998
Characterization of astroglial versus oligodendroglial phenotypes in glioblastomas by means of quantitative morphonuclear variables generated by computer-assisted microscopyC Decaestecker, I Camby, L Gordower, et al.
Public Health in Practice (Oxford, England)|September 14, 2022
HIV sero-positivity and risk factors for ischaemic and haemorrhagic stroke in hospitalised patients in Uganda: A prospective-case-control studyG Namale, O Kamacooko, A Makhoba, et al.
Neuroscience Letters|October 31, 2001
Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotypeB Van Everbroeck, E A Croes, P Pals, et al.
Human Molecular Genetics|December 1, 1995
Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3M Cruts, H Backhovens, S Y Wang, et al.
Pageof 12