Cooper DN - Search Results

1

Vogt G, Vogt B, Chuzhanova N, Julenius K, Cooper DN, Casanova JL. Vogt G, et al. Among authors: cooper dn. Curr Opin Genet Dev. 2007 Jun;17(3):245-51. doi: 10.1016/j.gde.2007.04.008. Epub 2007 Apr 30. Curr Opin Genet Dev. 2007. PMID: 17467977 Review.

2

Evolution of the proximal promoter region of the mammalian growth hormone gene.

Krawczak M, Chuzhanova NA, Cooper DN. Krawczak M, et al. Among authors: cooper dn. Gene. 1999 Sep 3;237(1):143-51. doi: 10.1016/s0378-1119(99)00313-3. Gene. 1999. PMID: 10524245

3

Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regions.

Krawczak M, Chuzhanova NA, Stenson PD, Johansen BN, Ball EV, Cooper DN. Krawczak M, et al. Among authors: cooper dn. Hum Genet. 2000 Oct;107(4):362-5. doi: 10.1007/s004390000393. Hum Genet. 2000. PMID: 11129336

4

Identification of an intronic regulatory element in the human protein C (PROC) gene.

Shamsher MK, Chuzhanova NA, Friedman B, Scopes DA, Alhaq A, Millar DS, Cooper DN, Berg LP. Shamsher MK, et al. Among authors: cooper dn. Hum Genet. 2000 Nov;107(5):458-65. doi: 10.1007/s004390000391. Hum Genet. 2000. PMID: 11140943

5

Meta-analysis of indels causing human genetic disease: mechanisms of mutagenesis and the role of local DNA sequence complexity.

Chuzhanova NA, Anassis EJ, Ball EV, Krawczak M, Cooper DN. Chuzhanova NA, et al. Among authors: cooper dn. Hum Mutat. 2003 Jan;21(1):28-44. doi: 10.1002/humu.10146. Hum Mutat. 2003. PMID: 12497629

6

Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer.

Turner C, Killoran C, Thomas NS, Rosenberg M, Chuzhanova NA, Johnston J, Kemel Y, Cooper DN, Biesecker LG. Turner C, et al. Among authors: cooper dn. Hum Genet. 2003 Mar;112(3):303-9. doi: 10.1007/s00439-002-0892-2. Epub 2003 Jan 25. Hum Genet. 2003. PMID: 12545275

7

A rare complex DNA rearrangement in the murine Steel gene results in exon duplication and a lethal phenotype.

Chandra S, Kapur R, Chuzhanova N, Summey V, Prentice D, Barker J, Cooper DN, Williams DA. Chandra S, et al. Among authors: cooper dn. Blood. 2003 Nov 15;102(10):3548-55. doi: 10.1182/blood-2003-05-1468. Epub 2003 Jul 24. Blood. 2003. PMID: 12881302 Free article.

8

Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs.

Abeysinghe SS, Chuzhanova N, Krawczak M, Ball EV, Cooper DN. Abeysinghe SS, et al. Among authors: cooper dn. Hum Mutat. 2003 Sep;22(3):229-44. doi: 10.1002/humu.10254. Hum Mutat. 2003. PMID: 12938088

9

Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends.

Chuzhanova N, Abeysinghe SS, Krawczak M, Cooper DN. Chuzhanova N, et al. Among authors: cooper dn. Hum Mutat. 2003 Sep;22(3):245-51. doi: 10.1002/humu.10253. Hum Mutat. 2003. PMID: 12938089

10

Genomic rearrangements in the CFTR gene: extensive allelic heterogeneity and diverse mutational mechanisms.

Audrézet MP, Chen JM, Raguénès O, Chuzhanova N, Giteau K, Le Maréchal C, Quéré I, Cooper DN, Férec C. Audrézet MP, et al. Among authors: cooper dn. Hum Mutat. 2004 Apr;23(4):343-57. doi: 10.1002/humu.20009. Hum Mutat. 2004. PMID: 15024729

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