-
genetic variant. It is a
single nucleotide polymorphism (SNP) in the COMT
gene that
codes catechol-O-Methyltransferase. The
single nucleotide substitution...
- 2007-10-08.
Retrieved 2009-03-12. "
Gene overview of all
published AD-****ociation
studies for PTEN". Alzforum:
AlzGene.
Alzheimer Research Forum. Archived...
-
Biotechnology Information, U.S.
National Library of Medicine. "Alzforum:
AlzGene".
Archived from the
original on 2004-12-27.
Zahran A, El-Husseini A, Shoker...
- a
genetic variation—a
single nucleotide polymorphism (SNP)—in the
MTHFR gene.
Among Americans the
frequency of T-homozygosity
ranges from 1% or less among...
-
widely used
gene databases:
AlzGene,
PDGene and SZGene. 2008: Emplo**** family-based GWAS to
discover the AD
gene, CD33, the
first AD
gene controlling...
- Rs6265, also
called Val66Met or G196A, is a
gene variation, a
single nucleotide polymorphism (SNP) in the BDNF
gene that
codes for brain-derived neurotrophic...
- rs6313 also
called T102C or C102T is a
gene variation—a
single nucleotide polymorphism (SNP)—in the
human HTR2A
gene that
codes for the 5-HT2A receptor....
- "Systematic meta-analyses of
Alzheimer disease genetic ****ociation studies: the
AlzGene database".
Nature Genetics. 39 (1): 17–23. doi:10.1038/ng1934. ISSN 1061-4036...
-
nucleotide polymorphism (SNP), in the HTR6
gene. It is one of the few
investigated polymorphisms of its
gene. C267T is a
synonymous polymorphism. As of...
-
protocols and
antecedent biomarker studies. Of
particular note are the
AlzGene database of
genetic studies of Alzheimer's disease,
which has been cited...
