Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J C Lambert

Showing results (81-90 of 112) with videos related to

Pageof 12
Sort By:
Neuroscience Letters|May 4, 2002
A polymorphism within intron 11 of the tau gene is not increased in frequency in patients with sporadic Alzheimer's disease, nor does it influence the extent of tau pathology in the brainE K Green, U Thaker, A M McDonagh, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosisP Guicheney, N Vignier, A Helbling-Leclerc, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 1997
[Fragile X syndrome is still unrecognized: efficacy of molecular diagnosis in mentally retarded probands]M Cossée, C Moutou, V Biancalana, et al.
Neurology|February 28, 2007
Variations in the APP gene promoter region and risk of Alzheimer diseaseL Guyant-Maréchal, A Rovelet-Lecrux, L Goumidi, et al.
Human Genetics|July 8, 1999
Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's diseaseF Wavrant-DeVrièze, J C Lambert, L Stas, et al.
The Journal of Prevention of Alzheimer'S Disease|January 31, 2022
Association between 9p21-23 Locus and Frailty in a Community-Dwelling Greek Population: Results from the Hellenic Longitudinal Investigation of Ageing and DietN Mourtzi, A Hatzimanolis, G Xiromerisiou, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Tetrasomy 18p de novo: parental origin and different mechanisms of formationM Bugge, E Blennow, U Friedrich, et al.
Human Molecular Genetics|August 13, 1998
Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's diseaseJ C Lambert, C Berr, F Pasquier, et al.
Molecular Psychiatry|March 16, 2011
Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sitesN Brouwers, C Van Cauwenberghe, S Engelborghs, et al.
Molecular Psychiatry|June 21, 2007
Evidence for the association of the S100beta gene with low cognitive performance and dementia in the elderlyJ-C Lambert, S Ferreira, J Gussekloo, et al.
Pageof 12

Showing results (81-90 of 112) with videos related to

Sort By:
Pageof 12
Neuroscience Letters|May 4, 2002
A polymorphism within intron 11 of the tau gene is not increased in frequency in patients with sporadic Alzheimer's disease, nor does it influence the extent of tau pathology in the brainE K Green, U Thaker, A M McDonagh, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosisP Guicheney, N Vignier, A Helbling-Leclerc, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 1997
[Fragile X syndrome is still unrecognized: efficacy of molecular diagnosis in mentally retarded probands]M Cossée, C Moutou, V Biancalana, et al.
Neurology|February 28, 2007
Variations in the APP gene promoter region and risk of Alzheimer diseaseL Guyant-Maréchal, A Rovelet-Lecrux, L Goumidi, et al.
Human Genetics|July 8, 1999
Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's diseaseF Wavrant-DeVrièze, J C Lambert, L Stas, et al.
The Journal of Prevention of Alzheimer'S Disease|January 31, 2022
Association between 9p21-23 Locus and Frailty in a Community-Dwelling Greek Population: Results from the Hellenic Longitudinal Investigation of Ageing and DietN Mourtzi, A Hatzimanolis, G Xiromerisiou, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Tetrasomy 18p de novo: parental origin and different mechanisms of formationM Bugge, E Blennow, U Friedrich, et al.
Human Molecular Genetics|August 13, 1998
Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's diseaseJ C Lambert, C Berr, F Pasquier, et al.
Molecular Psychiatry|March 16, 2011
Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sitesN Brouwers, C Van Cauwenberghe, S Engelborghs, et al.
Molecular Psychiatry|June 21, 2007
Evidence for the association of the S100beta gene with low cognitive performance and dementia in the elderlyJ-C Lambert, S Ferreira, J Gussekloo, et al.
Pageof 12