175 related articles for article (PubMed ID: 15006697)
1. The presenilin 2 M239I mutation associated with familial Alzheimer's disease reduces Ca2+ release from intracellular stores.
Zatti G; Ghidoni R; Barbiero L; Binetti G; Pozzan T; Fasolato C; Pizzo P
Neurobiol Dis; 2004 Mar; 15(2):269-78. PubMed ID: 15006697
[TBL] [Abstract][Full Text] [Related]
2. Reduction of Ca2+ stores and capacitative Ca2+ entry is associated with the familial Alzheimer's disease presenilin-2 T122R mutation and anticipates the onset of dementia.
Giacomello M; Barbiero L; Zatti G; Squitti R; Binetti G; Pozzan T; Fasolato C; Ghidoni R; Pizzo P
Neurobiol Dis; 2005 Apr; 18(3):638-48. PubMed ID: 15755689
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 16620965
[TBL] [Abstract][Full Text] [Related]
4. Familial Alzheimer's disease-linked presenilin mutants and intracellular Ca
Greotti E; Capitanio P; Wong A; Pozzan T; Pizzo P; Pendin D
Cell Calcium; 2019 May; 79():44-56. PubMed ID: 30822648
[TBL] [Abstract][Full Text] [Related]
5. Interactions of endoplasmic reticulum and mitochondria Ca(2+) stores with capacitative calcium entry.
Huang HM; Chen HL; Gibson GE
Metab Brain Dis; 2014 Dec; 29(4):1083-93. PubMed ID: 24748364
[TBL] [Abstract][Full Text] [Related]
6. Familial Alzheimer's disease-associated presenilin 1 mutants promote γ-secretase cleavage of STIM1 to impair store-operated Ca2+ entry.
Tong BC; Lee CS; Cheng WH; Lai KO; Foskett JK; Cheung KH
Sci Signal; 2016 Sep; 9(444):ra89. PubMed ID: 27601731
[TBL] [Abstract][Full Text] [Related]
7. Presenilin 1 regulates the processing of beta-amyloid precursor protein C-terminal fragments and the generation of amyloid beta-protein in endoplasmic reticulum and Golgi.
Xia W; Zhang J; Ostaszewski BL; Kimberly WT; Seubert P; Koo EH; Shen J; Selkoe DJ
Biochemistry; 1998 Nov; 37(47):16465-71. PubMed ID: 9843412
[TBL] [Abstract][Full Text] [Related]
8. Presenilin-mediated modulation of capacitative calcium entry.
Yoo AS; Cheng I; Chung S; Grenfell TZ; Lee H; Pack-Chung E; Handler M; Shen J; Xia W; Tesco G; Saunders AJ; Ding K; Frosch MP; Tanzi RE; Kim TW
Neuron; 2000 Sep; 27(3):561-72. PubMed ID: 11055438
[TBL] [Abstract][Full Text] [Related]
9. Lack of evidence for presenilins as endoplasmic reticulum Ca2+ leak channels.
Shilling D; Mak DO; Kang DE; Foskett JK
J Biol Chem; 2012 Mar; 287(14):10933-44. PubMed ID: 22311977
[TBL] [Abstract][Full Text] [Related]
10. Calcium Signaling and Mitochondrial Function in Presenilin 2 Knock-Out Mice: Looking for Any Loss-of-Function Phenotype Related to Alzheimer's Disease.
Rossi A; Galla L; Gomiero C; Zentilin L; Giacca M; Giorgio V; Calì T; Pozzan T; Greotti E; Pizzo P
Cells; 2021 Jan; 10(2):. PubMed ID: 33494218
[TBL] [Abstract][Full Text] [Related]
11. Capacitative calcium entry deficits and elevated luminal calcium content in mutant presenilin-1 knockin mice.
Leissring MA; Akbari Y; Fanger CM; Cahalan MD; Mattson MP; LaFerla FM
J Cell Biol; 2000 May; 149(4):793-8. PubMed ID: 10811821
[TBL] [Abstract][Full Text] [Related]
12. The overexpression of presenilin2 and Alzheimer's-disease-linked presenilin2 variants influences TRPC6-enhanced Ca2+ entry into HEK293 cells.
Lessard CB; Lussier MP; Cayouette S; Bourque G; Boulay G
Cell Signal; 2005 Apr; 17(4):437-45. PubMed ID: 15601622
[TBL] [Abstract][Full Text] [Related]
13. 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; 949(1-2):105-11. PubMed ID: 12213305
[TBL] [Abstract][Full Text] [Related]
14. Presenilin-dependent expression of STIM proteins and dysregulation of capacitative Ca2+ entry in familial Alzheimer's disease.
Bojarski L; Pomorski P; Szybinska A; Drab M; Skibinska-Kijek A; Gruszczynska-Biegala J; Kuznicki J
Biochim Biophys Acta; 2009 Jun; 1793(6):1050-7. PubMed ID: 19111578
[TBL] [Abstract][Full Text] [Related]
15. Molecular dissection of domains in mutant presenilin 2 that mediate overproduction of amyloidogenic forms of amyloid beta peptides. Inability of truncated forms of PS2 with familial Alzheimer's disease mutation to increase secretion of Abeta42.
Tomita T; Tokuhiro S; Hashimoto T; Aiba K; Saido TC; Maruyama K; Iwatsubo T
J Biol Chem; 1998 Aug; 273(33):21153-60. PubMed ID: 9694871
[TBL] [Abstract][Full Text] [Related]
16. Presenilins form ER Ca2+ leak channels, a function disrupted by familial Alzheimer's disease-linked mutations.
Tu H; Nelson O; Bezprozvanny A; Wang Z; Lee SF; Hao YH; Serneels L; De Strooper B; Yu G; Bezprozvanny I
Cell; 2006 Sep; 126(5):981-93. PubMed ID: 16959576
[TBL] [Abstract][Full Text] [Related]
17. Subcellular compartment and molecular subdomain of beta-amyloid precursor protein relevant to the Abeta 42-promoting effects of Alzheimer mutant presenilin 2.
Iwata H; Tomita T; Maruyama K; Iwatsubo T
J Biol Chem; 2001 Jun; 276(24):21678-85. PubMed ID: 11283011
[TBL] [Abstract][Full Text] [Related]
18. Involvement of presenilin holoprotein upregulation in calcium dyshomeostasis of Alzheimer's disease.
Honarnejad K; Jung CK; Lammich S; Arzberger T; Kretzschmar H; Herms J
J Cell Mol Med; 2013 Feb; 17(2):293-302. PubMed ID: 23379308
[TBL] [Abstract][Full Text] [Related]
19. Familial Alzheimer disease-linked mutations specifically disrupt Ca2+ leak function of presenilin 1.
Nelson O; Tu H; Lei T; Bentahir M; de Strooper B; Bezprozvanny I
J Clin Invest; 2007 May; 117(5):1230-9. PubMed ID: 17431506
[TBL] [Abstract][Full Text] [Related]
20. Familial Alzheimer's disease mutations in presenilins: effects on endoplasmic reticulum calcium homeostasis and correlation with clinical phenotypes.
Nelson O; Supnet C; Liu H; Bezprozvanny I
J Alzheimers Dis; 2010; 21(3):781-93. PubMed ID: 20634584
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
