106 related articles for article (PubMed ID: 1307241)
21. Schizophrenia and APP gene mutations.
Jönsson E; Forsell C; Lannfelt L; Sedvall G
Biol Psychiatry; 1995 Jan; 37(2):135-6. PubMed ID: 7718679
[No Abstract] [Full Text] [Related]
22. Missense mutations associated with familial Alzheimer's disease in Sweden lead to the production of the amyloid peptide without internalization of its precursor.
Essalmani R; Macq AF; Mercken L; Octave JN
Biochem Biophys Res Commun; 1996 Jan; 218(1):89-96. PubMed ID: 8573182
[TBL] [Abstract][Full Text] [Related]
23. The amyloid peptide precursor in Alzheimer's disease.
Octave JN
Acta Neurol Belg; 1995 Dec; 95(4):197-209. PubMed ID: 8553793
[TBL] [Abstract][Full Text] [Related]
24. A system for studying the effect(s) of familial Alzheimer disease mutations on the processing of the beta-amyloid peptide precursor.
Denman RB; Rosenzcwaig R; Miller DL
Biochem Biophys Res Commun; 1993 Apr; 192(1):96-103. PubMed ID: 8476439
[TBL] [Abstract][Full Text] [Related]
25. Split verdict on schizophrenia.
Nat Genet; 1992 Jul; 1(4):231-2. PubMed ID: 1302017
[No Abstract] [Full Text] [Related]
26. Amyloid precursor protein mutation at codon 713 (Ala-->Val) does not cause schizophrenia: non-pathogenic variant found at codon 705 (silent).
Forsell C; Lannfelt L
Neurosci Lett; 1995 Jan; 184(2):90-3. PubMed ID: 7724053
[TBL] [Abstract][Full Text] [Related]
27. [The search for a mutation in the gene coding the beta-amyloid protein precursor gene in patients with Alzheimer-type dementias].
Golimbet VE; Ovchinnikov IV; Voskresenskaia NI; Iurov IuB; Rogaev EI; Doronina OA; Maksunova IV
Zh Nevrol Psikhiatr Im S S Korsakova; 1996; 96(1):75-8. PubMed ID: 8677726
[TBL] [Abstract][Full Text] [Related]
28. A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) gene.
Vaula G; Mortilla M; Tupler R; Lukiw W; Tanzi R; Nee L; Polinsky R; Foncin JF; Bruni AC; Montesi MP
Neurosci Lett; 1992 Sep; 144(1-2):46-8. PubMed ID: 1436713
[TBL] [Abstract][Full Text] [Related]
29. Amyloid precursor protein gene analysis in familial Alzheimer's disease cases: a lack of mutations in exons 16 and 17.
Kowalska A; Pruchnik-Wolińska D; Florczak J; Szczech J; Kozubski W; Rossa G; Wender M
Folia Neuropathol; 2004; 42(1):1-7. PubMed ID: 15119738
[TBL] [Abstract][Full Text] [Related]
30. Screening for the APP codon 670/671 mutations in Alzheimer's disease.
Houlden H; Crawford F; Rossor M; Mullan M
Neurosci Lett; 1993 May; 154(1-2):161-2. PubMed ID: 8395665
[TBL] [Abstract][Full Text] [Related]
31. Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the beta-amyloid sequence.
Crawford F; Hardy J; Mullan M; Goate A; Hughes D; Fidani L; Roques P; Rossor M; Chartier-Harlin MC
Neurosci Lett; 1991 Nov; 133(1):1-2. PubMed ID: 1791986
[TBL] [Abstract][Full Text] [Related]
32. 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.
Karlinsky H; Vaula G; Haines JL; Ridgley J; Bergeron C; Mortilla M; Tupler RG; Percy ME; Robitaille Y; Noldy NE
Neurology; 1992 Aug; 42(8):1445-53. PubMed ID: 1520398
[TBL] [Abstract][Full Text] [Related]
33. Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->Ile.
Fidani L; Rooke K; Chartier-Harlin MC; Hughes D; Tanzi R; Mullan M; Roques P; Rossor M; Hardy J; Goate A
Hum Mol Genet; 1992 Jun; 1(3):165-8. PubMed ID: 1303172
[TBL] [Abstract][Full Text] [Related]
34. A novel silent variant at codon 711 and a variant at codon 708 of the APP sequence detected in Spanish Alzheimer and control cases.
Adroer R; Lopez-Acedo C; Oliva R; Hardy J; Fidani L
Neurosci Lett; 1993 Feb; 150(1):33-4. PubMed ID: 8469399
[TBL] [Abstract][Full Text] [Related]
35. RFLP analysis for APP 717 mutations associated with Alzheimer's disease.
Zeldenrust SR; Murrell J; Farlow M; Ghetti B; Roses AD; Benson MD
J Med Genet; 1993 Jun; 30(6):476-8. PubMed ID: 7686976
[TBL] [Abstract][Full Text] [Related]
36. Screening for mutations at codon 717 of the amyloid precursor protein gene in Alzheimer's disease.
Dai XY; Hattori M; Hirasawa H; Isse K; Ueki A; Nanko S
Psychiatry Clin Neurosci; 1995 Jun; 49(3):175-8. PubMed ID: 8612192
[TBL] [Abstract][Full Text] [Related]
37. Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region.
Kamino K; Orr HT; Payami H; Wijsman EM; Alonso ME; Pulst SM; Anderson L; O'dahl S; Nemens E; White JA
Am J Hum Genet; 1992 Nov; 51(5):998-1014. PubMed ID: 1415269
[TBL] [Abstract][Full Text] [Related]
38. Clinical comparison of Alzheimer's disease in pedigrees with the codon 717 Val-->Ile mutation in the amyloid precursor protein gene.
Mullan M; Tsuji S; Miki T; Katsuya T; Naruse S; Kaneko K; Shimizu T; Kojima T; Nakano I; Ogihara T
Neurobiol Aging; 1993; 14(5):407-19. PubMed ID: 8247223
[TBL] [Abstract][Full Text] [Related]
39. No mutation in codon 713 of the amyloid precursor gene in schizophrenic patients.
Carter D; Campion D; d'Amato T; Jay M; Brice A; Bellis M; Mallet J; Agid Y
Hum Mol Genet; 1993 Mar; 2(3):321. PubMed ID: 8499923
[No Abstract] [Full Text] [Related]
40. Amyloid precursor protein gene mutation at codon 670/671 in familial Alzheimer's disease in Sweden.
Lannfelt L; Johnston J; Bogdanovich N; Cowburn R
Biochem Soc Trans; 1994 Feb; 22(1):176-9. PubMed ID: 8206219
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
