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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
August 1, 1991
Anomalous gene expression in Alzheimer disease: cause or effect
D R McLachlan, W J Lukiw, C Mizzen, et al.
Journal of Cellular Biochemistry
|
December 1, 1992
Methylation of the 5' flanking sequences of the ribosomal DNA in human cell lines and in a human-hamster hybrid cell line
R Dante, M E Percy, A Baldini, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
October 1, 1991
A family with multiple instances of definite, probable and possible early-onset Alzheimer's disease
H Karlinsky, E Madrick, J Ridgley, et al.
American Journal of Medical Genetics
|
April 1, 1990
Red cell superoxide dismutase, glutathione peroxidase and catalase in Down syndrome patients with and without manifestations of Alzheimer disease
M E Percy, A J Dalton, V D Markovic, et al.
American Journal of Medical Genetics
|
October 1, 1986
DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy
D F Andrews, P M Brasher, K E Manchester, et al.
The Analyst
|
May 15, 1998
Iron metabolism and human ferritin heavy chain cDNA from adult brain with an elongated untranslated region: new findings and insights
M E Percy, S Wong, S Bauer, et al.
Journal of Inorganic Biochemistry
|
November 11, 2019
Aluminum-induced generation of lipopolysaccharide (LPS) from the human gastrointestinal (GI)-tract microbiome-resident Bacteroides fragilis
P N Alexandrov, J M Hill, Y Zhao, et al.
American Journal of Medical Genetics
|
June 22, 2000
Are hereditary hemochromatosis mutations involved in Alzheimer disease?
S Moalem, M E Percy, D F Andrews, et al.
Neuron
|
September 1, 1994
Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosis
T Tsuda, S Munthasser, P E Fraser, et al.
Neurology
|
August 1, 1992
Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene
H Karlinsky, G Vaula, J L Haines, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
August 1, 1991
Anomalous gene expression in Alzheimer disease: cause or effect
D R McLachlan, W J Lukiw, C Mizzen, et al.
Journal of Cellular Biochemistry
|
December 1, 1992
Methylation of the 5' flanking sequences of the ribosomal DNA in human cell lines and in a human-hamster hybrid cell line
R Dante, M E Percy, A Baldini, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
October 1, 1991
A family with multiple instances of definite, probable and possible early-onset Alzheimer's disease
H Karlinsky, E Madrick, J Ridgley, et al.
American Journal of Medical Genetics
|
April 1, 1990
Red cell superoxide dismutase, glutathione peroxidase and catalase in Down syndrome patients with and without manifestations of Alzheimer disease
M E Percy, A J Dalton, V D Markovic, et al.
American Journal of Medical Genetics
|
October 1, 1986
DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy
D F Andrews, P M Brasher, K E Manchester, et al.
The Analyst
|
May 15, 1998
Iron metabolism and human ferritin heavy chain cDNA from adult brain with an elongated untranslated region: new findings and insights
M E Percy, S Wong, S Bauer, et al.
Journal of Inorganic Biochemistry
|
November 11, 2019
Aluminum-induced generation of lipopolysaccharide (LPS) from the human gastrointestinal (GI)-tract microbiome-resident Bacteroides fragilis
P N Alexandrov, J M Hill, Y Zhao, et al.
American Journal of Medical Genetics
|
June 22, 2000
Are hereditary hemochromatosis mutations involved in Alzheimer disease?
S Moalem, M E Percy, D F Andrews, et al.
Neuron
|
September 1, 1994
Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosis
T Tsuda, S Munthasser, P E Fraser, et al.
Neurology
|
August 1, 1992
Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene
H Karlinsky, G Vaula, J L Haines, et al.
Page
of 6