Dutra A - Search Results

1

Macrophage models of Gaucher disease for evaluating disease pathogenesis and candidate drugs.

Aflaki E, Stubblefield BK, Maniwang E, Lopez G, Moaven N, Goldin E, Marugan J, Patnaik S, Dutra A, Southall N, Zheng W, Tayebi N, Sidransky E. Aflaki E, et al. Among authors: dutra a. Sci Transl Med. 2014 Jun 11;6(240):240ra73. doi: 10.1126/scitranslmed.3008659. Sci Transl Med. 2014. PMID: 24920659 Free PMC article.

2

A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease.

Westbroek W, Nguyen M, Siebert M, Lindstrom T, Burnett RA, Aflaki E, Jung O, Tamargo R, Rodriguez-Gil JL, Acosta W, Hendrix A, Behre B, Tayebi N, Fujiwara H, Sidhu R, Renvoise B, Ginns EI, Dutra A, Pak E, Cramer C, Ory DS, Pavan WJ, Sidransky E. Westbroek W, et al. Among authors: dutra a. Dis Model Mech. 2016 Jul 1;9(7):769-78. doi: 10.1242/dmm.024588. Epub 2016 May 19. Dis Model Mech. 2016. PMID: 27482815 Free PMC article.

3

Generation and characterization of four Chediak-Higashi Syndrome (CHS) induced pluripotent stem cell (iPSC) lines.

Serra-Vinardell J, Sandler MB, Pak E, Zheng W, Dutra A, Introne W, Gahl WA, Malicdan MC. Serra-Vinardell J, et al. Among authors: dutra a. Stem Cell Res. 2020 Jun 22;47:101883. doi: 10.1016/j.scr.2020.101883. Online ahead of print. Stem Cell Res. 2020. PMID: 32619719 Free article.

4

Genome-Edited Coincidence and PMP22-HiBiT Fusion Reporter Cell Lines Enable an Artifact-Suppressive Quantitative High-Throughput Screening Strategy for PMP22 Gene-Dosage Disorder Drug Discovery.

Martinez NJ, Braisted JC, Dranchak PK, Moran JJ, Larson H, Queme B, Pak E, Dutra A, Rai G, Cheng KC, Svaren J, Inglese J. Martinez NJ, et al. Among authors: dutra a. ACS Pharmacol Transl Sci. 2021 Jun 10;4(4):1422-1436. doi: 10.1021/acsptsci.1c00110. eCollection 2021 Aug 13. ACS Pharmacol Transl Sci. 2021. PMID: 34423274 Free PMC article.

5

Long term maintenance of myeloid leukemic stem cells cultured with unrelated human mesenchymal stromal cells.

Ito S, Barrett AJ, Dutra A, Pak E, Miner S, Keyvanfar K, Hensel NF, Rezvani K, Muranski P, Liu P, Larochelle A, Melenhorst JJ. Ito S, et al. Among authors: dutra a. Stem Cell Res. 2015 Jan;14(1):95-104. doi: 10.1016/j.scr.2014.11.007. Epub 2014 Dec 6. Stem Cell Res. 2015. PMID: 25535865 Free PMC article.

6

The genomic structure, chromosome location, and analysis of the human DKK1 head inducer gene as a candidate for holoprosencephaly.

Roessler E, Du Y, Glinka A, Dutra A, Niehrs C, Muenke M. Roessler E, et al. Among authors: dutra a. Cytogenet Cell Genet. 2000;89(3-4):220-4. doi: 10.1159/000015618. Cytogenet Cell Genet. 2000. PMID: 10965128

7

The genomic structure, chromosomal localization, and analysis of SIL as a candidate gene for holoprosencephaly.

Karkera JD, Izraeli S, Roessler E, Dutra A, Kirsch I, Muenke M. Karkera JD, et al. Among authors: dutra a. Cytogenet Genome Res. 2002;97(1-2):62-7. doi: 10.1159/000064057. Cytogenet Genome Res. 2002. PMID: 12438740

8

A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes.

Rozenblum E, Vahteristo P, Sandberg T, Bergthorsson JT, Syrjakoski K, Weaver D, Haraldsson K, Johannsdottir HK, Vehmanen P, Nigam S, Golberger N, Robbins C, Pak E, Dutra A, Gillander E, Stephan DA, Bailey-Wilson J, Juo SH, Kainu T, Arason A, Barkardottir RB, Nevanlinna H, Borg A, Kallioniemi OP. Rozenblum E, et al. Among authors: dutra a. Hum Genet. 2002 Feb;110(2):111-21. doi: 10.1007/s00439-001-0646-6. Epub 2001 Dec 14. Hum Genet. 2002. PMID: 11935316

9

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

10

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

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