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Items: 1 to 20 of 98

1.

Evidence for an ancestral alphoid domain on the long arm of human chromosome 2.

Avarello R, Pedicini A, Caiulo A, Zuffardi O, Fraccaro M.

Hum Genet. 1992 May;89(2):247-9.

PMID:
1587535
3.
4.

Isolation and comparative mapping of a human chromosome 20-specific alpha-satellite DNA clone.

Baldini A, Archidiacono N, Carbone R, Bolino A, Shridhar V, Miller OJ, Miller DA, Ward DC, Rocchi M.

Cytogenet Cell Genet. 1992;59(1):12-6.

PMID:
1733665
5.

Absence of satellite III DNA in the centromere and the proximal long-arm region of human chromosome 14: analysis of a 14p- variant.

Earle E, Voullaire LE, Hills L, Slater H, Choo KH.

Cytogenet Cell Genet. 1992;61(1):78-80.

PMID:
1505236
6.

Comparative mapping of human alphoid sequences in great apes using fluorescence in situ hybridization.

Archidiacono N, Antonacci R, Marzella R, Finelli P, Lonoce A, Rocchi M.

Genomics. 1995 Jan 20;25(2):477-84.

PMID:
7789981
7.
8.

p82H identifies sequences at every human centromere.

Aleixandre C, Miller DA, Mitchell AR, Warburton DA, Gersen SL, Disteche C, Miller OJ.

Hum Genet. 1987 Sep;77(1):46-50.

PMID:
3476456
9.
10.
11.

Structural rearrangements and insertions of dispersed elements in pericentromeric alpha satellites occur preferably at kinkable DNA sites.

Mashkova TD, Oparina NY, Lacroix MH, Fedorova LI, G Tumeneva I, Zinovieva OL, Kisselev LL.

J Mol Biol. 2001 Jan 5;305(1):33-48.

PMID:
11114245
12.
13.

Identification of a whole-arm translocation by in situ hybridization with directly fluorochrome-labeled probes in a myelodysplastic syndrome.

Bajalica S, Brøndum-Nielsen K, Sørensen AG, Pedersen NT, Heim S.

Genes Chromosomes Cancer. 1992 Sep;5(2):128-31.

PMID:
1381948
14.

Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.

Tharapel AT, Qumsiyeh MB, Martens PR, Tharapel SA, Dalton JD, Ward JC, Wilroy RS Jr.

Am J Med Genet. 1991 Jul 1;40(1):117-20.

PMID:
1887840
15.
16.

CENP-B box is required for de novo centromere chromatin assembly on human alphoid DNA.

Ohzeki J, Nakano M, Okada T, Masumoto H.

J Cell Biol. 2002 Dec 9;159(5):765-75. Epub 2002 Dec 2.

17.

Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10.

Devilee P, Kievits T, Waye JS, Pearson PL, Willard HF.

Genomics. 1988 Jul;3(1):1-7.

PMID:
3220475
18.

Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probe.

Delattre O, Bernard A, Malfoy B, Marlhens F, Viegas-Pequignot E, Brossard C, Haguenauer O, Creau-Goldberg N, N'guyen VC, Dutrillaux B, et al.

Hum Hered. 1988;38(3):156-67.

PMID:
2899543
19.

A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma.

Haaf T, Sumner AT, Köhler J, Willard HF, Schmid M.

Cytogenet Cell Genet. 1992;60(1):12-7. Erratum in: Cytogenet Cell Genet 1992;61(3):following 223. Summer AT [corrected to Sumner AT].

PMID:
1582251
20.

[Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization].

Solov'ev IV, Iurov IuB, Vorsanova SG, Marcais B, Rogaev EI, Kapanadze BI, Brodianskiĭ VM, Iankovskiĭ NK, Roizes G.

Genetika. 1998 Nov;34(11):1470-9. Russian.

PMID:
10096024

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