Dutra A - Search Results

1

Telomere-to-telomere assembly of a complete human X chromosome.

Miga KH, Koren S, Rhie A, Vollger MR, Gershman A, Bzikadze A, Brooks S, Howe E, Porubsky D, Logsdon GA, Schneider VA, Potapova T, Wood J, Chow W, Armstrong J, Fredrickson J, Pak E, Tigyi K, Kremitzki M, Markovic C, Maduro V, Dutra A, Bouffard GG, Chang AM, Hansen NF, Wilfert AB, Thibaud-Nissen F, Schmitt AD, Belton JM, Selvaraj S, Dennis MY, Soto DC, Sahasrabudhe R, Kaya G, Quick J, Loman NJ, Holmes N, Loose M, Surti U, Risques RA, Graves Lindsay TA, Fulton R, Hall I, Paten B, Howe K, Timp W, Young A, Mullikin JC, Pevzner PA, Gerton JL, Sullivan BA, Eichler EE, Phillippy AM. Miga KH, et al. Among authors: dutra a. Nature. 2020 Sep;585(7823):79-84. doi: 10.1038/s41586-020-2547-7. Epub 2020 Jul 14. Nature. 2020. PMID: 32663838 Free PMC article.

2

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.

Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS. Eriksson M, et al. Among authors: dutra a. Nature. 2003 May 15;423(6937):293-8. doi: 10.1038/nature01629. Epub 2003 Apr 25. Nature. 2003. PMID: 12714972 Free PMC article.

3

A female with complete lack of Müllerian fusion, postaxial polydactyly, and tetralogy of fallot: genetic heterogeneity of McKusick-Kaufman syndrome or a unique syndrome?

Slavotinek AM, Dutra A, Kpodzo D, Pak E, Nakane T, Turner J, Whiteford M, Biesecker LG, Stratton P. Slavotinek AM, et al. Among authors: dutra a. Am J Med Genet A. 2004 Aug 15;129A(1):69-72. doi: 10.1002/ajmg.a.30071. Am J Med Genet A. 2004. PMID: 15266619

4

Chromosome 8 BAC array comparative genomic hybridization and expression analysis identify amplification and overexpression of TRMT12 in breast cancer.

Rodriguez V, Chen Y, Elkahloun A, Dutra A, Pak E, Chandrasekharappa S. Rodriguez V, et al. Among authors: dutra a. Genes Chromosomes Cancer. 2007 Jul;46(7):694-707. doi: 10.1002/gcc.20454. Genes Chromosomes Cancer. 2007. PMID: 17440925

5

Advantages of q-PCR as a method of screening for gene targeting in mammalian cells using conventional and whole BAC-based constructs.

Gómez-Rodríguez J, Washington V, Cheng J, Dutra A, Pak E, Liu P, McVicar DW, Schwartzberg PL. Gómez-Rodríguez J, et al. Among authors: dutra a. Nucleic Acids Res. 2008 Oct;36(18):e117. doi: 10.1093/nar/gkn523. Epub 2008 Aug 18. Nucleic Acids Res. 2008. PMID: 18710883 Free PMC article.

6

Comparative sequence analyses reveal sites of ancestral chromosomal fusions in the Indian muntjac genome.

Tsipouri V, Schueler MG, Hu S; NISC Comparative Sequencing Program; Dutra A, Pak E, Riethman H, Green ED. Tsipouri V, et al. Among authors: dutra a. Genome Biol. 2008 Oct 28;9(10):R155. doi: 10.1186/gb-2008-9-10-r155. Genome Biol. 2008. PMID: 18957082 Free PMC article.

7

DNA damage responses by human ELG1 in S phase are important to maintain genomic integrity.

Sikdar N, Banerjee S, Lee KY, Wincovitch S, Pak E, Nakanishi K, Jasin M, Dutra A, Myung K. Sikdar N, et al. Among authors: dutra a. Cell Cycle. 2009 Oct 1;8(19):3199-207. doi: 10.4161/cc.8.19.9752. Epub 2009 Oct 7. Cell Cycle. 2009. PMID: 19755857 Free PMC article.

8

Nuclear bud formation: a novel manifestation of Zidovudine genotoxicity.

Dutra A, Pak E, Wincovitch S, John K, Poirier MC, Olivero OA. Dutra A, et al. Cytogenet Genome Res. 2010;128(1-3):105-10. doi: 10.1159/000298794. Epub 2010 Apr 20. Cytogenet Genome Res. 2010. PMID: 20407220 Free PMC article.

9

Minimal evidence for a direct involvement of twisted gastrulation homolog 1 (TWSG1) gene in human holoprosencephaly.

Kauvar EF, Hu P, Pineda-Alvarez DE, Solomon BD, Dutra A, Pak E, Blessing B, Proud V, Shanske AL, Stevens CA, Rosenfeld JA, Shaffer LG, Roessler E, Muenke M. Kauvar EF, et al. Among authors: dutra a. Mol Genet Metab. 2011 Apr;102(4):470-80. doi: 10.1016/j.ymgme.2010.12.008. Epub 2010 Dec 21. Mol Genet Metab. 2011. PMID: 21227728 Free PMC article.

10

Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type 1-associated glomus tumors.

Stewart DR, Pemov A, Van Loo P, Beert E, Brems H, Sciot R, Claes K, Pak E, Dutra A, Lee CC, Legius E. Stewart DR, et al. Among authors: dutra a. Genes Chromosomes Cancer. 2012 May;51(5):429-37. doi: 10.1002/gcc.21928. Epub 2012 Jan 17. Genes Chromosomes Cancer. 2012. PMID: 22250039 Free PMC article.

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