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Items: 1 to 20 of 39

1.

Abnormal adherence junctions in the heart and reduced angiogenesis in transgenic mice overexpressing mutant type XIII collagen.

Sund M, Ylönen R, Tuomisto A, Sormunen R, Tahkola J, Kvist AP, Kontusaari S, Autio-Harmainen H, Pihlajaniemi T.

EMBO J. 2001 Sep 17;20(18):5153-64.

2.

Distinct expression of type XIII collagen in neuronal structures and other tissues during mouse development.

Sund M, Väisänen T, Kaukinen S, Ilves M, Tu H, Autio-Harmainen H, Rauvala H, Pihlajaniemi T.

Matrix Biol. 2001 Jul;20(4):215-31.

PMID:
11470398
3.

Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease.

Mann DM, Pickering-Brown SM, Takeuchi A, Iwatsubo T; Members of the Familial Alzheimer's Disease Pathology Study Group.

Am J Pathol. 2001 Jun;158(6):2165-75.

4.

Alzheimer's disease: genes, proteins, and therapy.

Selkoe DJ.

Physiol Rev. 2001 Apr;81(2):741-66. Review.

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6.

Apolipoprotein E isoform-dependent amyloid deposition and neuritic degeneration in a mouse model of Alzheimer's disease.

Holtzman DM, Bales KR, Tenkova T, Fagan AM, Parsadanian M, Sartorius LJ, Mackey B, Olney J, McKeel D, Wozniak D, Paul SM.

Proc Natl Acad Sci U S A. 2000 Mar 14;97(6):2892-7.

7.

Primary cultures of neuronal and non-neuronal rat brain cells secrete similar proportions of amyloid beta peptides ending at A beta40 and A beta42.

Fukumoto H, Tomita T, Matsunaga H, Ishibashi Y, Saido TC, Iwatsubo T.

Neuroreport. 1999 Sep 29;10(14):2965-9.

PMID:
10549806
8.

Furin mediates enhanced production of fibrillogenic ABri peptides in familial British dementia.

Kim SH, Wang R, Gordon DJ, Bass J, Steiner DF, Lynn DG, Thinakaran G, Meredith SC, Sisodia SS.

Nat Neurosci. 1999 Nov;2(11):984-8.

PMID:
10526337
9.
10.

A stop-codon mutation in the BRI gene associated with familial British dementia.

Vidal R, Frangione B, Rostagno A, Mead S, Révész T, Plant G, Ghiso J.

Nature. 1999 Jun 24;399(6738):776-81.

PMID:
10391242
11.

Type XIII collagen is identified as a plasma membrane protein.

Hägg P, Rehn M, Huhtala P, Väisänen T, Tamminen M, Pihlajaniemi T.

J Biol Chem. 1998 Jun 19;273(25):15590-7.

13.

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
14.

Abeta deposition is associated with neuropil changes, but not with overt neuronal loss in the human amyloid precursor protein V717F (PDAPP) transgenic mouse.

Irizarry MC, Soriano F, McNamara M, Page KJ, Schenk D, Games D, Hyman BT.

J Neurosci. 1997 Sep 15;17(18):7053-9.

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17.

Charge-based binding of complement component C1q to the Alzheimer amyloid beta-peptide.

Webster S, Bonnell B, Rogers J.

Am J Pathol. 1997 May;150(5):1531-6.

18.

The pathogenesis of senile plaques.

Dickson DW.

J Neuropathol Exp Neurol. 1997 Apr;56(4):321-39. Review.

19.

The presenilin 2 mutation (N141I) linked to familial Alzheimer disease (Volga German families) increases the secretion of amyloid beta protein ending at the 42nd (or 43rd) residue.

Tomita T, Maruyama K, Saido TC, Kume H, Shinozaki K, Tokuhiro S, Capell A, Walter J, Grünberg J, Haass C, Iwatsubo T, Obata K.

Proc Natl Acad Sci U S A. 1997 Mar 4;94(5):2025-30.

20.

The catenin/cadherin adhesion system is localized in synaptic junctions bordering transmitter release zones.

Uchida N, Honjo Y, Johnson KR, Wheelock MJ, Takeichi M.

J Cell Biol. 1996 Nov;135(3):767-79.

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