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Results: 1 to 20 of 21

1.

Recent Perspectives on APP, Secretases, Endosomal Pathways and How they Influence Alzheimer's Related Pathological Changes in Down Syndrome.

Decourt B, Mobley W, Reiman E, Shah RJ, Sabbagh MN.

J Alzheimers Dis Parkinsonism. 2013 Mar 20;Suppl 7:002.

PMID:
24782952
[PubMed]
Free PMC Article
2.

Turnover of amyloid precursor protein family members determines their nuclear signaling capability.

Gersbacher MT, Goodger ZV, Trutzel A, Bundschuh D, Nitsch RM, Konietzko U.

PLoS One. 2013 Jul 18;8(7):e69363. doi: 10.1371/journal.pone.0069363. Print 2013.

PMID:
23874953
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Random-breakage mapping method applied to human DNA sequences.

Löbrich M, Rydberg B, Cooper PK.

Nucleic Acids Res. 1996 May 15;24(10):1802-8.

PMID:
8657558
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.

Bonné-Tamir B, DeStefano AL, Briggs CE, Adair R, Franklyn B, Weiss S, Korostishevsky M, Frydman M, Baldwin CT, Farrer LA.

Am J Hum Genet. 1996 Jun;58(6):1254-9.

PMID:
8651303
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Exclusion of familial dysautonomia from more than 60% of the genome.

Blumenfeld A, Axelrod FB, Trofatter JA, Maayan C, Lucente DE, Slaugenhaupt SA, Liebert CB, Ozelius LJ, Haines JL, Breakefield XO, et al.

J Med Genet. 1993 Jan;30(1):47-52.

PMID:
8093738
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Human ETS2 gene on chromosome 21 is not rearranged in Alzheimer disease.

Sacchi N, Nalbantoglu J, Sergovich FR, Papas TS.

Proc Natl Acad Sci U S A. 1988 Oct;85(20):7675-9.

PMID:
2902635
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Clustering of multiallele DNA markers near the Huntington's disease gene.

MacDonald ME, Cheng SV, Zimmer M, Haines JL, Poustka A, Allitto B, Smith B, Whaley WL, Romano DM, Jagadeesh J, et al.

J Clin Invest. 1989 Sep;84(3):1013-6.

PMID:
2569477
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Isolation and characterization of a human telomere.

Cheng JF, Smith CL, Cantor CR.

Nucleic Acids Res. 1989 Aug 11;17(15):6109-27.

PMID:
2549507
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

Rahmani Z, Blouin JL, Creau-Goldberg N, Watkins PC, Mattei JF, Poissonnier M, Prieur M, Chettouh Z, Nicole A, Aurias A, et al.

Proc Natl Acad Sci U S A. 1989 Aug;86(15):5958-62.

PMID:
2527368
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Long-range restriction map of the terminal part of the short arm of the human X chromosome.

Petit C, Levilliers J, Weissenbach J.

Proc Natl Acad Sci U S A. 1990 May;87(10):3680-4.

PMID:
2339111
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Five polymorphic microsatellite VNTRs on the human X chromosome.

Luty JA, Guo Z, Willard HF, Ledbetter DH, Ledbetter S, Litt M.

Am J Hum Genet. 1990 Apr;46(4):776-83.

PMID:
2316523
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

An interspersed repeated sequence specific for human subtelomeric regions.

Rouyer F, de la Chapelle A, Andersson M, Weissenbach J.

EMBO J. 1990 Feb;9(2):505-14.

PMID:
2303040
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21.

Owen MJ, James LA, Hardy JA, Williamson R, Goate AM.

Am J Hum Genet. 1990 Feb;46(2):316-22.

PMID:
2301399
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions.

Gardiner K, Horisberger M, Kraus J, Tantravahi U, Korenberg J, Rao V, Reddy S, Patterson D.

EMBO J. 1990 Jan;9(1):25-34.

PMID:
2295313
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

Rouleau GA, Seizinger BR, Wertelecki W, Haines JL, Superneau DW, Martuza RL, Gusella JF.

Am J Hum Genet. 1990 Feb;46(2):323-8.

PMID:
2105641
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.

Pericak-Vance MA, Bebout JL, Gaskell PC Jr, Yamaoka LH, Hung WY, Alberts MJ, Walker AP, Bartlett RJ, Haynes CA, Welsh KA, et al.

Am J Hum Genet. 1991 Jun;48(6):1034-50.

PMID:
2035524
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.

Schellenberg GD, Pericak-Vance MA, Wijsman EM, Moore DK, Gaskell PC Jr, Yamaoka LA, Bebout JL, Anderson L, Welsh KA, Clark CM, et al.

Am J Hum Genet. 1991 Mar;48(3):563-83.

PMID:
1998342
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Trisomy 21: association between reduced recombination and nondisjunction.

Sherman SL, Takaesu N, Freeman SB, Grantham M, Phillips C, Blackston RD, Jacobs PA, Cockwell AE, Freeman V, Uchida I, et al.

Am J Hum Genet. 1991 Sep;49(3):608-20.

PMID:
1831960
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Protocols to establish genotype-phenotype correlations in Down syndrome.

Epstein CJ, Korenberg JR, Annerén G, Antonarakis SE, Aymé S, Courchesne E, Epstein LB, Fowler A, Groner Y, Huret JL, et al.

Am J Hum Genet. 1991 Jul;49(1):207-35. No abstract available.

PMID:
1829580
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

A contiguous Not I restriction map of band q22.3 of human chromosome 21.

Wang D, Fang H, Cantor CR, Smith CL.

Proc Natl Acad Sci U S A. 1992 Apr 15;89(8):3222-6.

PMID:
1565613
[PubMed - indexed for MEDLINE]
Free PMC Article

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