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La Revue De Medecine Interne
|
January 1, 1996
[Genetics of Alzheimer's disease]
D Hannequin, D Campion, A Brice, et al.
Human Molecular Genetics
|
March 1, 1993
No mutation in codon 713 of the amyloid precursor gene in schizophrenic patients
D Carter, D Campion, T d'Amato, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
July 1, 1992
Evidence for a pseudoautosomal locus for schizophrenia. I: A replication study using phenotype analysis
P Gorwood, M Leboyer, T d'Amato, et al.
American Journal of Medical Genetics
|
September 22, 1999
Linkage disequilibrium on the COMT gene in French schizophrenics and controls
M de Chaldée, C Laurent, F Thibaut, et al.
Revue Neurologique
|
December 3, 1998
[Genetics of Alzheimer's disease]
D Hannequin, D Campion, C Dumanchin, et al.
Biochemical and Biophysical Research Communications
|
September 7, 2000
Overexpression of Rab11 or constitutively active Rab11 does not affect sAPPalpha and Abeta secretions by wild-type and Swedish mutated betaAPP-expressing HEK293 cells
E Lopez-Perez, C Dumanchin, C Czech, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 31, 1999
Unusual phenotypic alteration of beta amyloid precursor protein (betaAPP) maturation by a new Val-715 --> Met betaAPP-770 mutation responsible for probable early-onset Alzheimer's disease
K Ancolio, C Dumanchin, H Barelli, et al.
Biological Psychiatry
|
September 1, 1996
Association study between dopamine D1, D2, D3, and D4 receptor genes and schizophrenia defined by several diagnostic systems
S Dollfus, D Campion, T Vasse, et al.
Psychiatric Genetics
|
November 5, 1997
Detection of two new polymorphic sites in the human interleukin-1 beta gene: lack of association with schizophrenia in a French population
C Laurent, F Thibaut, P Ravassard, et al.
Neuroreport
|
November 5, 1999
The L392V mutation of presenilin 1 associated with autosomal dominant early-onset Alzheimer's disease alters the secondary structure of the hydrophilic loop
R Gantier, C Dumanchin, D Campion, et al.
Page
of 15
Search research articles
Search
Showing results (61-70 of 146) with videos related to
Sort By:
Page
of 15
La Revue De Medecine Interne
|
January 1, 1996
[Genetics of Alzheimer's disease]
D Hannequin, D Campion, A Brice, et al.
Human Molecular Genetics
|
March 1, 1993
No mutation in codon 713 of the amyloid precursor gene in schizophrenic patients
D Carter, D Campion, T d'Amato, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
July 1, 1992
Evidence for a pseudoautosomal locus for schizophrenia. I: A replication study using phenotype analysis
P Gorwood, M Leboyer, T d'Amato, et al.
American Journal of Medical Genetics
|
September 22, 1999
Linkage disequilibrium on the COMT gene in French schizophrenics and controls
M de Chaldée, C Laurent, F Thibaut, et al.
Revue Neurologique
|
December 3, 1998
[Genetics of Alzheimer's disease]
D Hannequin, D Campion, C Dumanchin, et al.
Biochemical and Biophysical Research Communications
|
September 7, 2000
Overexpression of Rab11 or constitutively active Rab11 does not affect sAPPalpha and Abeta secretions by wild-type and Swedish mutated betaAPP-expressing HEK293 cells
E Lopez-Perez, C Dumanchin, C Czech, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 31, 1999
Unusual phenotypic alteration of beta amyloid precursor protein (betaAPP) maturation by a new Val-715 --> Met betaAPP-770 mutation responsible for probable early-onset Alzheimer's disease
K Ancolio, C Dumanchin, H Barelli, et al.
Biological Psychiatry
|
September 1, 1996
Association study between dopamine D1, D2, D3, and D4 receptor genes and schizophrenia defined by several diagnostic systems
S Dollfus, D Campion, T Vasse, et al.
Psychiatric Genetics
|
November 5, 1997
Detection of two new polymorphic sites in the human interleukin-1 beta gene: lack of association with schizophrenia in a French population
C Laurent, F Thibaut, P Ravassard, et al.
Neuroreport
|
November 5, 1999
The L392V mutation of presenilin 1 associated with autosomal dominant early-onset Alzheimer's disease alters the secondary structure of the hydrophilic loop
R Gantier, C Dumanchin, D Campion, et al.
Page
of 15