De Jonghe C - Search Results

1

Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation.

Dermaut B, Kumar-Singh S, De Jonghe C, Cruts M, Löfgren A, Lübke U, Cras P, Dom R, De Deyn PP, Martin JJ, Van Broeckhoven C. Dermaut B, et al. Among authors: de jonghe c. Brain. 2001 Dec;124(Pt 12):2383-92. doi: 10.1093/brain/124.12.2383. Brain. 2001. PMID: 11701593

2

Processing of presenilin 1 in brains of patients with Alzheimer's disease and controls.

Hendriks L, Thinakaran G, Harris CL, De Jonghe C, Martin JJ, Sisodia SS, Van Broeckhoven C. Hendriks L, et al. Among authors: de jonghe c. Neuroreport. 1997 May 6;8(7):1717-21. doi: 10.1097/00001756-199705060-00030. Neuroreport. 1997. PMID: 9189920

3

Immunoreactivity of presenilin-1 and tau in Alzheimer's disease brain.

Hendriks L, De Jonghe C, Lübke U, Woodrow S, Vanderhoeven I, Boons J, Cras P, Martin JJ, Van Broeckhoven C. Hendriks L, et al. Among authors: de jonghe c. Exp Neurol. 1998 Feb;149(2):341-8. doi: 10.1006/exnr.1997.6739. Exp Neurol. 1998. PMID: 9500965

4

Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion.

De Jonghe C, Cruts M, Rogaeva EA, Tysoe C, Singleton A, Vanderstichele H, Meschino W, Dermaut B, Vanderhoeven I, Backhovens H, Vanmechelen E, Morris CM, Hardy J, Rubinsztein DC, St George-Hyslop PH, Van Broeckhoven C. De Jonghe C, et al. Hum Mol Genet. 1999 Aug;8(8):1529-40. doi: 10.1093/hmg/8.8.1529. Hum Mol Genet. 1999. PMID: 10401002

5

Evidence that Abeta42 plasma levels in presenilin-1 mutation carriers do not allow for prediction of their clinical phenotype.

De Jonghe C, Cras P, Vanderstichele H, Cruts M, Vanderhoeven I, Smouts I, Vanmechelen E, Martin JJ, Hendriks L, Van Broeckhoven C. De Jonghe C, et al. Neurobiol Dis. 1999 Aug;6(4):280-7. doi: 10.1006/nbdi.1999.0247. Neurobiol Dis. 1999. PMID: 10448055

6

Proteolytic processing of presenilin-1 in human lymphoblasts is not affected by the presence of the I143T and G384A mutations.

Vanderhoeven I, Cras P, Martin JJ, Van Broeckhoven C, De Jonghe C. Vanderhoeven I, et al. Among authors: de jonghe c. Neurosci Lett. 1999 Oct 29;274(3):183-6. doi: 10.1016/s0304-3940(99)00722-3. Neurosci Lett. 1999. PMID: 10548420

7

Behavioral disturbances without amyloid deposits in mice overexpressing human amyloid precursor protein with Flemish (A692G) or Dutch (E693Q) mutation.

Kumar-Singh S, Dewachter I, Moechars D, Lübke U, De Jonghe C, Ceuterick C, Checler F, Naidu A, Cordell B, Cras P, Van Broeckhoven C, Van Leuven F. Kumar-Singh S, et al. Among authors: de jonghe c. Neurobiol Dis. 2000 Feb;7(1):9-22. doi: 10.1006/nbdi.1999.0272. Neurobiol Dis. 2000. PMID: 10671319

8

Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692).

Roks G, Van Harskamp F, De Koning I, Cruts M, De Jonghe C, Kumar-Singh S, Tibben A, Tanghe H, Niermeijer MF, Hofman A, Van Swieten JC, Van Broeckhoven C, Van Duijn CM. Roks G, et al. Among authors: de jonghe c. Brain. 2000 Oct;123 ( Pt 10):2130-40. doi: 10.1093/brain/123.10.2130. Brain. 2000. PMID: 11004129 Free article.

9

Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's disease.

Kumar-Singh S, De Jonghe C, Cruts M, Kleinert R, Wang R, Mercken M, De Strooper B, Vanderstichele H, Löfgren A, Vanderhoeven I, Backhovens H, Vanmechelen E, Kroisel PM, Van Broeckhoven C. Kumar-Singh S, et al. Among authors: de jonghe c. Hum Mol Genet. 2000 Nov 1;9(18):2589-98. doi: 10.1093/hmg/9.18.2589. Hum Mol Genet. 2000. PMID: 11063718

10

Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutation.

Singleton AB, Hall R, Ballard CG, Perry RH, Xuereb JH, Rubinsztein DC, Tysoe C, Matthews P, Cordell B, Kumar-Singh S, De Jonghe C, Cruts M, van Broeckhoven C, Morris CM. Singleton AB, et al. Among authors: de jonghe c. Brain. 2000 Dec;123 Pt 12:2467-74. doi: 10.1093/brain/123.12.2467. Brain. 2000. PMID: 11099448

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