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Biblio
Found 7 results
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Keyword
is
Polymorphism, Single Nucleotide
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2018
Cheng-Hathaway PJ, Reed-Geaghan EG, Jay TR, Casali BT, Bemiller SM, Puntambekar SS, von Saucken VE, Williams RY, J Karlo C, Moutinho M et al.
. 2018.
The Trem2 R47H variant confers loss-of-function-like phenotypes in Alzheimer's disease.
.
Mol Neurodegener. 13(1):29.
2017
Dincheva I, Yang J, Li A, Marinic T, Freilingsdorf H, Huang C, Casey BJ, Hempstead B, Glatt CE, Lee FS et al.
. 2017.
Effect of Early-Life Fluoxetine on Anxiety-Like Behaviors in BDNF Val66Met Mice.
.
Am J Psychiatry. 174(12):1203-1213.
Bonham LW, Sirkis DW, Fan J, Aparicio RE, Tse M, Ramos EMarisa, Wang Q, Coppola G, Rosen HJ, Miller BL et al.
. 2017.
Identification of a rare coding variant in TREM2 in a Chinese individual with Alzheimer's disease.
.
Neurocase. 23(1):65-69.
Hosono N, Makishima H, Mahfouz R, Przychodzen B, Yoshida K, Jerez A, LaFramboise T, Polprasert C, Clemente MJ, Shiraishi Y et al.
. 2017.
Recurrent genetic defects on chromosome 5q in myeloid neoplasms.
.
Oncotarget. 8(4):6483-6495.
2016
Puckett EE, Park J, Combs M, Blum MJ, Bryant JE, Caccone A, Costa F, Deinum EE, Esther A, Himsworth CG et al.
. 2016.
Global population divergence and admixture of the brown rat (Rattus norvegicus).
.
Proc Biol Sci. 283(1841)
Sirkis DW, Bonham LW, Aparicio RE, Geier EG, Ramos EMarisa, Wang Q, Karydas A, Miller ZA, Miller BL, Coppola G et al.
. 2016.
Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression.
.
Acta Neuropathol Commun. 4(1):98.
2001
Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, Lavery T, Kouyoumjian R, Farhadian SF, Ward R et al.
. 2001.
Linkage disequilibrium in the human genome.
.
Nature. 411(6834):199-204.