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Items: 5

1.

A novel presenilin-1 mutation: increased beta-amyloid and neurofibrillary changes.

Gómez-Isla T, Wasco W, Pettingell WP, Gurubhagavatula S, Schmidt SD, Jondro PD, McNamara M, Rodes LA, DiBlasi T, Growdon WB, Seubert P, Schenk D, Growdon JH, Hyman BT, Tanzi RE.

Ann Neurol. 1997 Jun;41(6):809-13.

PMID:
9189043
2.

Association of a novel human FE65-like protein with the cytoplasmic domain of the beta-amyloid precursor protein.

Guénette SY, Chen J, Jondro PD, Tanzi RE.

Proc Natl Acad Sci U S A. 1996 Oct 1;93(20):10832-7.

3.

Familial Alzheimer's chromosome 14 mutations.

Wasco W, Pettingell WP, Jondro PD, Schmidt SD, Gurubhagavatula S, Rodes L, DiBlasi T, Romano DM, Guenette SY, Kovacs DM, et al.

Nat Med. 1995 Sep;1(9):848. No abstract available.

PMID:
7585193
4.

Candidate gene for the chromosome 1 familial Alzheimer's disease locus.

Levy-Lahad E, Wasco W, Poorkaj P, Romano DM, Oshima J, Pettingell WH, Yu CE, Jondro PD, Schmidt SD, Wang K, et al.

Science. 1995 Aug 18;269(5226):973-7.

PMID:
7638622
5.

Genome-wide search for CLN2, the gene causing late-infantile neuronal ceroid-lipofuscinosis (LNCL).

Haines JL, Boustany RM, Worster T, Ter-Minassian M, Jondro P, Lerner TJ.

Am J Med Genet. 1995 Jun 5;57(2):344-7.

PMID:
7668360

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