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D Campion

Showing results (91-100 of 146) with videos related to

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Psychiatric Genetics|January 1, 1994
No major role for the dopamine D2 receptor Ser-->Cys311 mutation in schizophreniaC Laurent, S Bodeau-Péan, D Campion, et al.
Human Molecular Genetics|June 17, 1999
Presenilins interact with Rab11, a small GTPase involved in the regulation of vesicular transportC Dumanchin, C Czech, D Campion, et al.
American Journal of Medical Genetics|April 24, 1995
Allelic association at the D14S43 locus in early onset Alzheimer's disease. French Alzheimer's Disease Collaborative Study GroupA Brice, S Tardieu, D Campion, et al.
Human Molecular Genetics|December 1, 1995
Mutations of the presenilin I gene in families with early-onset Alzheimer's diseaseD Campion, J M Flaman, A Brice, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's diseaseA Brice, A L Boch, G Stevanin, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|August 25, 2009
Family history and obstetric complications in deficit and non-deficit schizophrenia: preliminary resultsS Dollfus, S Germain-Robin, B Chabot, et al.
Journal of Medical Genetics|August 27, 1998
De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study GroupC Dumanchin, A Brice, D Campion, et al.
Psychiatry Research|December 1, 1992
Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 familiesD Campion, T d'Amato, H Laklou, et al.
Nature Genetics|December 1, 1992
More missense in amyloid geneD A Carter, E Desmarais, M Bellis, et al.
The American Journal of Psychiatry|January 1, 1994
Failure to find evidence for linkage or association between the dopamine D3 receptor gene and schizophreniaO Sabaté, D Campion, T d'Amato, et al.
Pageof 15

Showing results (91-100 of 146) with videos related to

Sort By:
Pageof 15
Psychiatric Genetics|January 1, 1994
No major role for the dopamine D2 receptor Ser-->Cys311 mutation in schizophreniaC Laurent, S Bodeau-Péan, D Campion, et al.
Human Molecular Genetics|June 17, 1999
Presenilins interact with Rab11, a small GTPase involved in the regulation of vesicular transportC Dumanchin, C Czech, D Campion, et al.
American Journal of Medical Genetics|April 24, 1995
Allelic association at the D14S43 locus in early onset Alzheimer's disease. French Alzheimer's Disease Collaborative Study GroupA Brice, S Tardieu, D Campion, et al.
Human Molecular Genetics|December 1, 1995
Mutations of the presenilin I gene in families with early-onset Alzheimer's diseaseD Campion, J M Flaman, A Brice, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's diseaseA Brice, A L Boch, G Stevanin, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|August 25, 2009
Family history and obstetric complications in deficit and non-deficit schizophrenia: preliminary resultsS Dollfus, S Germain-Robin, B Chabot, et al.
Journal of Medical Genetics|August 27, 1998
De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study GroupC Dumanchin, A Brice, D Campion, et al.
Psychiatry Research|December 1, 1992
Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 familiesD Campion, T d'Amato, H Laklou, et al.
Nature Genetics|December 1, 1992
More missense in amyloid geneD A Carter, E Desmarais, M Bellis, et al.
The American Journal of Psychiatry|January 1, 1994
Failure to find evidence for linkage or association between the dopamine D3 receptor gene and schizophreniaO Sabaté, D Campion, T d'Amato, et al.
Pageof 15