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Items: 1 to 20 of 83

1.

Is mammalian chromosomal evolution driven by regions of genome fragility?

Ruiz-Herrera A, Castresana J, Robinson TJ.

Genome Biol. 2006;7(12):R115.

2.

Gene synteny comparisons between different vertebrates provide new insights into breakage and fusion events during mammalian karyotype evolution.

Kemkemer C, Kohn M, Cooper DN, Froenicke L, Högel J, Hameister H, Kehrer-Sawatzki H.

BMC Evol Biol. 2009 Apr 24;9:84. doi: 10.1186/1471-2148-9-84.

3.

Assessing the role of tandem repeats in shaping the genomic architecture of great apes.

Farré M, Bosch M, López-Giráldez F, Ponsà M, Ruiz-Herrera A.

PLoS One. 2011;6(11):e27239. doi: 10.1371/journal.pone.0027239. Epub 2011 Nov 4.

4.

Comparative analysis of chicken chromosome 28 provides new clues to the evolutionary fragility of gene-rich vertebrate regions.

Gordon L, Yang S, Tran-Gyamfi M, Baggott D, Christensen M, Hamilton A, Crooijmans R, Groenen M, Lucas S, Ovcharenko I, Stubbs L.

Genome Res. 2007 Nov;17(11):1603-13. Epub 2007 Oct 5.

5.

Evolutionary conserved chromosomal segments in the human karyotype are bounded by unstable chromosome bands.

Ruiz-Herrera A, García F, Mora L, Egozcue J, Ponsà M, Garcia M.

Cytogenet Genome Res. 2005;108(1-3):161-74.

PMID:
15545726
7.

Comparative genomics reveals birth and death of fragile regions in mammalian evolution.

Alekseyev MA, Pevzner PA.

Genome Biol. 2010;11(11):R117. doi: 10.1186/gb-2010-11-11-r117. Epub 2010 Nov 30.

8.

High-resolution comparative mapping among man, cattle and mouse suggests a role for repeat sequences in mammalian genome evolution.

Schibler L, Roig A, Mahe MF, Laurent P, Hayes H, Rodolphe F, Cribiu EP.

BMC Genomics. 2006 Aug 1;7:194.

9.
10.

[Divergence of the polytene chromosome banding sequences as a reflection of evolutionary rearrangements of the genome linear structure].

Gunderina LI, Kiknadze II, Istomina AG, Gusev VD, Miroshnichenko LA.

Genetika. 2005 Feb;41(2):187-95. Russian.

PMID:
15810608
11.

Fragile regions and not functional constraints predominate in shaping gene organization in the genus Drosophila.

von Grotthuss M, Ashburner M, Ranz JM.

Genome Res. 2010 Aug;20(8):1084-96. doi: 10.1101/gr.103713.109. Epub 2010 Jul 2.

12.

Characterization of FRA7B, a human common fragile site mapped at the 7p chromosome terminal region.

Bosco N, Pelliccia F, Rocchi A.

Cancer Genet Cytogenet. 2010 Oct 1;202(1):47-52. doi: 10.1016/j.cancergencyto.2010.06.008.

PMID:
20804921
13.

A high resolution map of mammalian X chromosome fragile regions assessed by large-scale comparative genomics.

Prada CF, Laissue P.

Mamm Genome. 2014 Dec;25(11-12):618-35. doi: 10.1007/s00335-014-9537-8. Epub 2014 Aug 3.

PMID:
25086724
14.

Human and mouse genomic sequences reveal extensive breakpoint reuse in mammalian evolution.

Pevzner P, Tesler G.

Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7672-7. Epub 2003 Jun 16.

15.

Analysis of fine-scale mammalian evolutionary breakpoints provides new insight into their relation to genome organisation.

Lemaitre C, Zaghloul L, Sagot MF, Gautier C, Arneodo A, Tannier E, Audit B.

BMC Genomics. 2009 Jul 24;10:335. doi: 10.1186/1471-2164-10-335.

16.

Common fragile sites in man and three closely related primate species.

Smeets DF, van de Klundert FA.

Cytogenet Cell Genet. 1990;53(1):8-14.

PMID:
2323227
17.

Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites.

Burrow AA, Williams LE, Pierce LC, Wang YH.

BMC Genomics. 2009 Jan 30;10:59. doi: 10.1186/1471-2164-10-59.

18.
19.

No statistical association between common fragile sites and nonrandom chromosome breakpoints in cancer cells.

Sutherland GR, Simmers RN.

Cancer Genet Cytogenet. 1988 Mar;31(1):9-15.

PMID:
3162194
20.

Cartographic study: breakpoints in 1574 families carrying human reciprocal translocations.

Cohen O, Cans C, Cuillel M, Gilardi JL, Roth H, Mermet MA, Jalbert P, Demongeot J.

Hum Genet. 1996 May;97(5):659-67.

PMID:
8655149

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