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Items: 1 to 20 of 84

1.

Molecular biology. Chromosome capture brings it all together.

Kleckner N, Zickler D, Witz G.

Science. 2013 Nov 22;342(6161):940-1. doi: 10.1126/science.1247514. No abstract available.

2.

Organization of the mitotic chromosome.

Naumova N, Imakaev M, Fudenberg G, Zhan Y, Lajoie BR, Mirny LA, Dekker J.

Science. 2013 Nov 22;342(6161):948-53. doi: 10.1126/science.1236083. Epub 2013 Nov 7.

3.

Physical mapping of the long arm of chromosome 21.

Gardiner K.

Prog Clin Biol Res. 1990;360:1-14. No abstract available.

PMID:
2247504
4.

Tertiary structures of the Escherichia coli and human chromosome 21 molecules of DNA.

Hanzálek P, Kypr J.

Biochem Biophys Res Commun. 2001 Apr 27;283(1):219-23.

PMID:
11322791
5.

Translocation (11;14)(q13;q32) and preferential involvement of chromosomes 1, 2, 9, 13, and 17 in mantle cell lymphoma.

Espinet B, Solé F, Woessner S, Bosch F, Florensa L, Campo E, Costa D, Lloveras E, Vilà RM, Besses C, Montserrat E, Sans-Sabrafen J.

Cancer Genet Cytogenet. 1999 May;111(1):92-8.

PMID:
10326598
6.

[Stereospecific DNA anomalies in the human chromosome 21].

Lukina NI, Soĭdla TR.

Tsitologiia. 2002;44(6):585-91. Russian.

PMID:
12236103
7.

Isolation of human chromosome 21-specific cosmids and their uses in mapping of cosmid contigs on chromosomal subregions.

Hou DX, Kishida H, Shimokawa T, Soeda E.

Jpn J Hum Genet. 1994 Dec;39(4):411-20.

PMID:
7873753
8.

Identification of DNA sequences flanking the breakpoint of human t(14q21q) Robertsonian translocations.

Earle E, Shaffer LG, Kalitsis P, McQuillan C, Dale S, Choo KH.

Am J Hum Genet. 1992 Apr;50(4):717-24.

9.

Mitotic chromosome structure.

Heermann DW.

Exp Cell Res. 2012 Jul 15;318(12):1381-5. doi: 10.1016/j.yexcr.2012.03.027. Epub 2012 Apr 4. Review.

PMID:
22507271
10.

Large-scale oscillation of structure-related DNA sequence features in human chromosome 21.

Li W, Miramontes P.

Phys Rev E Stat Nonlin Soft Matter Phys. 2006 Aug;74(2 Pt 1):021912. Epub 2006 Aug 9.

PMID:
17025477
11.

Identification of two highly polymorphic CA-repeats (D21S1224 and D21S1261) on human chromosome 21q22.3.

Bosch A, Guimerà J, Wiemann S, Ansorge W, Patterson D, Estivill X.

Hum Genet. 1995 Mar;95(3):367-9.

PMID:
7868138
12.

Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age.

Antonarakis SE, Avramopoulos D, Blouin JL, Talbot CC Jr, Schinzel AA.

Nat Genet. 1993 Feb;3(2):146-50.

PMID:
8499948
13.
14.

Mitotic and salivary gland chromosome analyses in the Musca domestica L. (house fly) (Diptera: Muscidae).

el Agoze M, Lemeunier F, Periquet G.

Heredity (Edinb). 1992 Jul;69 ( Pt 1):57-64.

PMID:
1487427
16.

Chromosome missegregation and trisomy 21 mosaicism in Alzheimer's disease.

Geller LN, Potter H.

Neurobiol Dis. 1999 Jun;6(3):167-79.

PMID:
10408806
17.

Human chromosome 21/Down syndrome gene function and pathway database.

Nikolaienko O, Nguyen C, Crinc LS, Cios KJ, Gardiner K.

Gene. 2005 Dec 30;364:90-8. Epub 2005 Nov 28.

PMID:
16310977
18.

Mitotic errors in chromosome 21 of human preimplantation embryos are associated with non-viability.

Katz-Jaffe MG, Trounson AO, Cram DS.

Mol Hum Reprod. 2004 Feb;10(2):143-7.

PMID:
14742700
19.

Release of chromosomes from the nuclear envelope: a universal mechanism for eukaryotic mitosis?

Kanoh J.

Nucleus. 2013 Mar-Apr;4(2):100-4. doi: 10.4161/nucl.23984. Epub 2013 Feb 14.

20.

The spatial localization of homologous chromosomes in human fibroblasts at mitosis.

Leitch AR, Brown JK, Mosgöller W, Schwarzacher T, Heslop-Harrison JS.

Hum Genet. 1994 Mar;93(3):275-80.

PMID:
8125477

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