Forsell C - Search Results

1

The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Abeta protofibril formation.

Nilsberth C, Westlind-Danielsson A, Eckman CB, Condron MM, Axelman K, Forsell C, Stenh C, Luthman J, Teplow DB, Younkin SG, Näslund J, Lannfelt L. Nilsberth C, et al. Among authors: forsell c. Nat Neurosci. 2001 Sep;4(9):887-93. doi: 10.1038/nn0901-887. Nat Neurosci. 2001. PMID: 11528419

2

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. Forsell C, et al. Neurosci Lett. 1995 Jan 23;184(2):90-3. doi: 10.1016/0304-3940(94)11176-j. Neurosci Lett. 1995. PMID: 7724053

3

No association between polymorphisms in the neprilysin promoter region and Swedish Alzheimer's disease patients.

Lilius L, Forsell C, Axelman K, Winblad B, Graff C, Tjernberg L. Lilius L, et al. Among authors: forsell c. Neurosci Lett. 2003 Feb 6;337(2):111-3. doi: 10.1016/s0304-3940(02)01300-9. Neurosci Lett. 2003. PMID: 12527400

4

A novel pathogenic mutation (Leu262Phe) found in the presenilin 1 gene in early-onset Alzheimer's disease.

Forsell C, Froelich S, Axelman K, Vestling M, Cowburn RF, Lilius L, Johnston JA, Engvall B, Johansson K, Dahlkild A, Ingelson M, St George-Hyslop PH, Lannfelt L. Forsell C, et al. Neurosci Lett. 1997 Sep 26;234(1):3-6. doi: 10.1016/s0304-3940(97)00603-4. Neurosci Lett. 1997. PMID: 9347932

5

The Glu318Gly mutation of the presenilin-1 gene does not necessarily cause Alzheimer's disease.

Mattila KM, Forsell C, Pirttilä T, Rinne JO, Lehtimäki T, Röyttä M, Lilius L, Eerola A, St George-Hyslop PH, Frey H, Lannfelt L. Mattila KM, et al. Among authors: forsell c. Ann Neurol. 1998 Dec;44(6):965-7. doi: 10.1002/ana.410440617. Ann Neurol. 1998. PMID: 9851443

6

Tau gene polymorphisms and apolipoprotein E epsilon4 may interact to increase risk for Alzheimer's disease.

Lilius L, Froelich Fabre S, Basun H, Forsell C, Axelman K, Mattila K, Andreadis A, Viitanen M, Winblad B, Fratiglioni L, Lannfelt L. Lilius L, et al. Among authors: forsell c. Neurosci Lett. 1999 Dec 17;277(1):29-32. doi: 10.1016/s0304-3940(99)00833-2. Neurosci Lett. 1999. PMID: 10643890

7

Investigations of a CA repeat in the oestrogen receptor beta gene in patients with Alzheimer's disease.

Forsell C, Enmark E, Axelman K, Blomberg M, Wahlund LO, Gustafsson JA, Lannfelt L. Forsell C, et al. Eur J Hum Genet. 2001 Oct;9(10):802-4. doi: 10.1038/sj.ejhg.5200714. Eur J Hum Genet. 2001. PMID: 11781694

8

Allelic association but only weak evidence for linkage to the apolipoprotein E locus in late-onset Swedish Alzheimer families.

Liu L, Forsell C, Lilius L, Axelman K, Corder EH, Lannfelt L. Liu L, et al. Among authors: forsell c. Am J Med Genet. 1996 May 31;67(3):306-11. doi: 10.1002/(SICI)1096-8628(19960531)67:3<306::AID-AJMG7>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8725748

9

Genome scan on Swedish Alzheimer's disease families.

Sillén A, Forsell C, Lilius L, Axelman K, Björk BF, Onkamo P, Kere J, Winblad B, Graff C. Sillén A, et al. Among authors: forsell c. Mol Psychiatry. 2006 Feb;11(2):182-6. doi: 10.1038/sj.mp.4001772. Mol Psychiatry. 2006. PMID: 16288313 Clinical Trial.

10

No linkage to chromosome 14 in Swedish Alzheimer's disease families.

Lannfelt L, Lilius L, Appelgren H, Axelman K, Forsell C, Liu L, Johansson K, Graff C. Lannfelt L, et al. Among authors: forsell c. Nat Genet. 1993 Jul;4(3):218-9. doi: 10.1038/ng0793-218. Nat Genet. 1993. PMID: 8358427 No abstract available.

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