Similar articles for PMID: 11239002

Year	Number of Results
1985	1
1991	1
1992	3
1994	1
1996	4
1997	2
1998	8
1999	21
2000	18
2001	11
2002	10
2003	6
2004	3
2005	5
2006	1
2008	3
2009	1
2010	1
2011	2
2012	1
2013	1
2024	0

1

Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5.

Wilson MD, Riemer C, Martindale DW, Schnupf P, Boright AP, Cheung TL, Hardy DM, Schwartz S, Scherer SW, Tsui LC, Miller W, Koop BF. Wilson MD, et al. Nucleic Acids Res. 2001 Mar 15;29(6):1352-65. doi: 10.1093/nar/29.6.1352. Nucleic Acids Res. 2001. PMID: 11239002 Free PMC article.

2

Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.

DeSilva U, Elnitski L, Idol JR, Doyle JL, Gan W, Thomas JW, Schwartz S, Dietrich NL, Beckstrom-Sternberg SM, McDowell JC, Blakesley RW, Bouffard GG, Thomas PJ, Touchman JW, Miller W, Green ED. DeSilva U, et al. Genome Res. 2002 Jan;12(1):3-15. doi: 10.1101/gr.214802. Genome Res. 2002. PMID: 11779826 Free PMC article.

3

Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).

Valero MC, de Luis O, Cruces J, Pérez Jurado LA. Valero MC, et al. Genomics. 2000 Oct 1;69(1):1-13. doi: 10.1006/geno.2000.6312. Genomics. 2000. PMID: 11013070

4

Comparative genomic sequencing reveals a strikingly similar architecture of a conserved syntenic region on human chromosome 11p15.3 (including gene ST5) and mouse chromosome 7.

Amid C, Bahr A, Mujica A, Sampson N, Bikar SE, Winterpacht A, Zabel B, Hankeln T, Schmidt ER. Amid C, et al. Cytogenet Cell Genet. 2001;93(3-4):284-90. doi: 10.1159/000056999. Cytogenet Cell Genet. 2001. PMID: 11528127

5

ERCC1: a comparative genomic perspective.

Wilson MD, Ruttan CC, Koop BF, Glickman BW. Wilson MD, et al. Environ Mol Mutagen. 2001;38(2-3):209-15. doi: 10.1002/em.1073. Environ Mol Mutagen. 2001. PMID: 11746756

6

Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21.

Pletcher MT, Wiltshire T, Cabin DE, Villanueva M, Reeves RH. Pletcher MT, et al. Genomics. 2001 May 15;74(1):45-54. doi: 10.1006/geno.2001.6533. Genomics. 2001. PMID: 11374901

7

Mapping the human acetylcholinesterase gene to chromosome 7q22 by fluorescent in situ hybridization coupled with selective PCR amplification from a somatic hybrid cell panel and chromosome-sorted DNA libraries.

Ehrlich G, Viegas-Pequignot E, Ginzberg D, Sindel L, Soreq H, Zakut H. Ehrlich G, et al. Genomics. 1992 Aug;13(4):1192-7. doi: 10.1016/0888-7543(92)90037-s. Genomics. 1992. PMID: 1380483

8

Juxta-centromeric region of human chromosome 21 is enriched for pseudogenes and gene fragments.

Ruault M, Trichet V, Gimenez S, Boyle S, Gardiner K, Rolland M, Roizès G, De Sario A. Ruault M, et al. Gene. 1999 Oct 18;239(1):55-64. doi: 10.1016/s0378-1119(99)00381-9. Gene. 1999. PMID: 10571034

9

Genetic, physical, and comparative map of the subtelomeric region of mouse Chromosome 4.

Li X, Bachmanov AA, Li S, Chen Z, Tordoff MG, Beauchamp GK, de Jong PJ, Wu C, Chen L, West DB, Ross DA, Ohmen JD, Reed DR. Li X, et al. Mamm Genome. 2002 Jan;13(1):5-19. doi: 10.1007/s0033501-2109-8. Mamm Genome. 2002. PMID: 11773963 Free PMC article. Review.

10

Candidate gene isolation and comparative analysis of a commonly deleted segment of 7q22 implicated in myeloid malignancies.

Kratz CP, Emerling BM, Donovan S, Laig-Webster M, Taylor BR, Thompson P, Jensen S, Banerjee A, Bonifas J, Makalowski W, Green ED, Le Beau MM, Shannon KM. Kratz CP, et al. Genomics. 2001 Oct;77(3):171-80. doi: 10.1006/geno.2001.6636. Genomics. 2001. PMID: 11597142

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