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Experimental Gerontology
|
January 1, 1996
Differential effects of transforming growth factor-beta 1 on the expression of matrix metalloproteinases and tissue inhibitors of metalloproteinases in young and old human fibroblasts
D R Edwards, K J Leco, P P Beaudry, et al.
Dementia and Geriatric Cognitive Disorders
|
March 6, 1999
14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
P Beaudry, P Cohen, J P Brandel, et al.
Neurology
|
December 1, 1994
Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies
J L Laplanche, N Delasnerie-Lauprêtre, J P Brandel, et al.
Human Mutation
|
May 2, 2000
Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype
K Peoc'h, P Manivet, P Beaudry, et al.
Neurology
|
May 1, 1997
Creutzfeldt-Jakob disease after extracranial dura mater embolization for a nasopharyngeal angiofibroma
J C Antoine, D Michel, P Bertholon, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity
|
March 1, 1996
The roles of tissue inhibitors of metalloproteinases in tissue remodelling and cell growth
D R Edwards, P P Beaudry, T D Laing, et al.
The American Journal of Cardiology
|
August 1, 1982
Myocardial metabolic alterations after contrast angiography
J A Wisneski, E W Gertz, R Neese, et al.
Neurology
|
October 1, 1993
A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease
L Ripoll, J L Laplanche, M Salzmann, et al.
Journal of Psychiatry & Neuroscience : JPN
|
October 1, 1992
A dose-finding study with remoxipride in the acute treatment of schizophrenic patients
Y D Lapierre, R Ancill, G Awad, et al.
FEBS Letters
|
February 15, 2003
Prion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt-Jakob disease
K Peoc'h, H Volland, A De Gassart, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 69) with videos related to
Sort By:
Page
of 7
Experimental Gerontology
|
January 1, 1996
Differential effects of transforming growth factor-beta 1 on the expression of matrix metalloproteinases and tissue inhibitors of metalloproteinases in young and old human fibroblasts
D R Edwards, K J Leco, P P Beaudry, et al.
Dementia and Geriatric Cognitive Disorders
|
March 6, 1999
14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
P Beaudry, P Cohen, J P Brandel, et al.
Neurology
|
December 1, 1994
Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies
J L Laplanche, N Delasnerie-Lauprêtre, J P Brandel, et al.
Human Mutation
|
May 2, 2000
Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype
K Peoc'h, P Manivet, P Beaudry, et al.
Neurology
|
May 1, 1997
Creutzfeldt-Jakob disease after extracranial dura mater embolization for a nasopharyngeal angiofibroma
J C Antoine, D Michel, P Bertholon, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity
|
March 1, 1996
The roles of tissue inhibitors of metalloproteinases in tissue remodelling and cell growth
D R Edwards, P P Beaudry, T D Laing, et al.
The American Journal of Cardiology
|
August 1, 1982
Myocardial metabolic alterations after contrast angiography
J A Wisneski, E W Gertz, R Neese, et al.
Neurology
|
October 1, 1993
A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease
L Ripoll, J L Laplanche, M Salzmann, et al.
Journal of Psychiatry & Neuroscience : JPN
|
October 1, 1992
A dose-finding study with remoxipride in the acute treatment of schizophrenic patients
Y D Lapierre, R Ancill, G Awad, et al.
FEBS Letters
|
February 15, 2003
Prion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt-Jakob disease
K Peoc'h, H Volland, A De Gassart, et al.
Page
of 7