Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 95

1.
2.
3.

Implications of presenilin 1 mutations in Alzheimer's disease.

Komano H, Sudoh S, Kawamura Y, Wang R, Yanagisawa K.

Mech Ageing Dev. 1999 Mar 15;107(3):281-98.

PMID:
10360683
4.

Developmental expression of wild-type and mutant presenilin-1 in hippocampal neurons from transgenic mice: evidence for novel species-specific properties of human presenilin-1.

Lévesque L, Annaert W, Craessaerts K, Mathews PM, Seeger M, Nixon RA, Van Leuven F, Gandy S, Westaway D, St George-Hyslop P, De Strooper B, Fraser PE.

Mol Med. 1999 Aug;5(8):542-54.

5.

Ca(2+) stores and capacitative Ca(2+) entry in human neuroblastoma (SH-SY5Y) cells expressing a familial Alzheimer's disease presenilin-1 mutation.

Smith IF, Boyle JP, Vaughan PF, Pearson HA, Cowburn RF, Peers CS.

Brain Res. 2002 Sep 13;949(1-2):105-11.

PMID:
12213305
6.

Neurons overexpressing mutant presenilin-1 are more sensitive to apoptosis induced by endoplasmic reticulum-Golgi stress.

Terro F, Czech C, Esclaire F, Elyaman W, Yardin C, Baclet MC, Touchet N, Tremp G, Pradier L, Hugon J.

J Neurosci Res. 2002 Aug 15;69(4):530-9.

PMID:
12210846
7.

Presenilin expression during induced differentiation of the human neuroblastoma SH-SY5Y cell line.

Flood F, Sundström E, Samuelsson EB, Wiehager B, Seiger A, Johnston JA, Cowburn RF.

Neurochem Int. 2004 Jun;44(7):487-96.

PMID:
15209417
8.

Presenilin 2 expression in neuronal cells: induction during differentiation of embryonic carcinoma cells.

Culvenor JG, Evin G, Cooney MA, Wardan H, Sharples RA, Maher F, Reed G, Diehlmann A, Weidemann A, Beyreuther K, Masters CL.

Exp Cell Res. 2000 Mar 15;255(2):192-206.

PMID:
10694435
10.

Morphological change by overexpression of D385A dominant negative presenilin 1 in human neuroblastoma SH-SY5Y cells.

Tsuchiya D, Kitamura Y, Takata K, Taniguchi T, Uemura K, Miki H, Takenawa T, Shimohama S.

J Pharmacol Sci. 2006 Nov;102(3):354-8. Epub 2006 Nov 10.

11.

The presenilin-1 familial Alzheimer disease mutant P117L impairs neurogenesis in the hippocampus of adult mice.

Wen PH, Hof PR, Chen X, Gluck K, Austin G, Younkin SG, Younkin LH, DeGasperi R, Gama Sosa MA, Robakis NK, Haroutunian V, Elder GA.

Exp Neurol. 2004 Aug;188(2):224-37.

PMID:
15246822
12.

Enhanced generation of intracellular Abeta42 amyloid peptide by mutation of presenilins PS1 and PS2.

Takeda K, Araki W, Tabira T.

Eur J Neurosci. 2004 Jan;19(2):258-264.

PMID:
14725619
13.

Abnormal intracellular trafficking of high affinity nerve growth factor receptor, Trk, in stable transfectants expressing presenilin 1 protein.

Hamano T, Mutoh T, Tabira T, Araki W, Kuriyama M, Mihara T, Yano S, Yamamoto H.

Brain Res Mol Brain Res. 2005 Jun 13;137(1-2):70-6. Epub 2005 Mar 19.

PMID:
15950763
14.

Chinese Presenilin-1 V97L mutation enhanced Abeta42 levels in SH-SY5Y neuroblastoma cells.

Fang B, Jia L, Jia J.

Neurosci Lett. 2006 Oct 2;406(1-2):33-7. Epub 2006 Aug 17.

PMID:
16916581
15.

The presenilin 1 deltaE9 mutation gives enhanced basal phospholipase C activity and a resultant increase in intracellular calcium concentrations.

Cedazo-Minguez A, Popescu BO, Ankarcrona M, Nishimura T, Cowburn RF.

J Biol Chem. 2002 Sep 27;277(39):36646-55. Epub 2002 Jul 16.

16.
17.

Presenilin mutations linked to familial Alzheimer's disease reduce endoplasmic reticulum and Golgi apparatus calcium levels.

Zatti G, Burgo A, Giacomello M, Barbiero L, Ghidoni R, Sinigaglia G, Florean C, Bagnoli S, Binetti G, Sorbi S, Pizzo P, Fasolato C.

Cell Calcium. 2006 Jun;39(6):539-50. Epub 2006 Apr 18.

PMID:
16620965
18.

Subcellular localization of presenilin 2 endoproteolytic C-terminal fragments.

Tekirian TL, Merriam DE, Marshansky V, Miller J, Crowley AC, Chan H, Ausiello D, Brown D, Buxbaum JD, Xia W, Wasco W.

Brain Res Mol Brain Res. 2001 Nov 30;96(1-2):14-20.

PMID:
11731004
19.

Enhanced accumulation of phosphorylated alpha-synuclein and elevated beta-amyloid 42/40 ratio caused by expression of the presenilin-1 deltaT440 mutant associated with familial Lewy body disease and variant Alzheimer's disease.

Kaneko H, Kakita A, Kasuga K, Nozaki H, Ishikawa A, Miyashita A, Kuwano R, Ito G, Iwatsubo T, Takahashi H, Nishizawa M, Onodera O, Sisodia SS, Ikeuchi T.

J Neurosci. 2007 Nov 28;27(48):13092-7.

20.

The presenilin 1 mutation (M146V) linked to familial Alzheimer's disease attenuates the neuronal differentiation of NTera 2 cells.

Tokuhiro S, Tomita T, Iwata H, Kosaka T, Saido TC, Maruyama K, Iwatsubo T.

Biochem Biophys Res Commun. 1998 Mar 27;244(3):751-5.

PMID:
9535737

Supplemental Content

Support Center