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Journal of Neurology, Neurosurgery, and Psychiatry
|
April 20, 2007
APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage
A Rovelet-Lecrux, T Frebourg, H Tuominen, et al.
Human Mutation
|
June 30, 2000
A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease
G Raux, R Gantier, C Martin, et al.
Oncogene
|
June 29, 2001
Amifostine (WR2721) restores transcriptional activity of specific p53 mutant proteins in a yeast functional assay
D Maurici, P Monti, P Campomenosi, et al.
Biotechniques
|
September 1, 1995
Simple protocol for rapid, direct sequencing of immunoglobulin variable-region genes
F Jovelin, D Gilbert, F Brard, et al.
European Journal of Human Genetics : EJHG
|
August 31, 2001
TP63 gene mutation in ADULT syndrome
J Amiel, G Bougeard, C Francannet, et al.
Journal of Medical Genetics
|
February 12, 2002
Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's disease
M L Jacquemont, D Campion, V Hahn, et al.
Molecular and Cellular Biology
|
May 1, 1995
An Sp1 binding site and the minimal promoter contribute to overexpression of the cytokeratin 18 gene in tumorigenic clones relative to that in nontumorigenic clones of a human carcinoma cell line
M Gunther, T Frebourg, M Laithier, et al.
La Revue De Medecine Interne
|
January 1, 1996
[Genetics of Alzheimer's disease]
D Hannequin, D Campion, A Brice, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis
|
August 2, 2015
A new genotoxicity assay based on p53 target gene induction
Y Zerdoumi, E Kasper, F Soubigou, et al.
British Journal of Haematology
|
March 1, 1995
Co-segregation of thrombosis with the factor V Q506 mutation in an extended family with resistance to activated protein C
S Beufé, J Y Borg, M Vasse, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 103) with videos related to
Sort By:
Page
of 11
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 20, 2007
APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage
A Rovelet-Lecrux, T Frebourg, H Tuominen, et al.
Human Mutation
|
June 30, 2000
A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease
G Raux, R Gantier, C Martin, et al.
Oncogene
|
June 29, 2001
Amifostine (WR2721) restores transcriptional activity of specific p53 mutant proteins in a yeast functional assay
D Maurici, P Monti, P Campomenosi, et al.
Biotechniques
|
September 1, 1995
Simple protocol for rapid, direct sequencing of immunoglobulin variable-region genes
F Jovelin, D Gilbert, F Brard, et al.
European Journal of Human Genetics : EJHG
|
August 31, 2001
TP63 gene mutation in ADULT syndrome
J Amiel, G Bougeard, C Francannet, et al.
Journal of Medical Genetics
|
February 12, 2002
Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's disease
M L Jacquemont, D Campion, V Hahn, et al.
Molecular and Cellular Biology
|
May 1, 1995
An Sp1 binding site and the minimal promoter contribute to overexpression of the cytokeratin 18 gene in tumorigenic clones relative to that in nontumorigenic clones of a human carcinoma cell line
M Gunther, T Frebourg, M Laithier, et al.
La Revue De Medecine Interne
|
January 1, 1996
[Genetics of Alzheimer's disease]
D Hannequin, D Campion, A Brice, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis
|
August 2, 2015
A new genotoxicity assay based on p53 target gene induction
Y Zerdoumi, E Kasper, F Soubigou, et al.
British Journal of Haematology
|
March 1, 1995
Co-segregation of thrombosis with the factor V Q506 mutation in an extended family with resistance to activated protein C
S Beufé, J Y Borg, M Vasse, et al.
Page
of 11