Carraro DM - Search Results

1

Enhanced type I interferon gene signature in primary antiphospholipid syndrome: Association with earlier disease onset and preeclampsia.

Ugolini-Lopes MR, Torrezan GT, Gândara APR, Olivieri EHR, Nascimento IS, Okazaki E, Bonfá E, Carraro DM, de Andrade DCO. Ugolini-Lopes MR, et al. Among authors: carraro dm. Autoimmun Rev. 2019 Apr;18(4):393-398. doi: 10.1016/j.autrev.2018.11.004. Epub 2019 Feb 14. Autoimmun Rev. 2019. PMID: 30772492

2

Evaluation of O6-methylguanine-DNA methyltransferase by immunohistochemistry: best clinical and research practices.

Neto JC, Carvalho K, Olivieri E, Carraro D, Cunha I, Vassallo J, Kagohara L, Soares F, Rocha R. Neto JC, et al. Pathol Res Pract. 2011 Aug 15;207(8):492-7. doi: 10.1016/j.prp.2011.06.003. Epub 2011 Jul 20. Pathol Res Pract. 2011. PMID: 21767920

3

Breakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: case report.

Torrezan GT, da Silva FC, Krepischi AC, Santos ÉM, Ferreira Fde O, Rossi BM, Carraro DM. Torrezan GT, et al. Among authors: carraro dm. BMC Med Genet. 2011 Sep 30;12:128. doi: 10.1186/1471-2350-12-128. BMC Med Genet. 2011. PMID: 21962078 Free PMC article.

4

Hyaluronidase splice variants are associated with histology and outcome in adenocarcinoma and squamous cell carcinoma of the lung.

de Sá VK, Olivieri E, Parra ER, Ab'Saber AM, Takagaki T, Soares FA, Carraro D, Carvalho L, Capelozzi VL. de Sá VK, et al. Hum Pathol. 2012 May;43(5):675-83. doi: 10.1016/j.humpath.2011.06.010. Epub 2011 Oct 10. Hum Pathol. 2012. PMID: 21992818

5

A novel SYBR-based duplex qPCR for the detection of gene dosage: detection of an APC large deletion in a familial adenomatous polyposis patient with an unusual phenotype.

Torrezan GT, da Silva FC, Krepischi AC, dos Santos EM, Rossi BM, Carraro DM. Torrezan GT, et al. Among authors: carraro dm. BMC Med Genet. 2012 Jul 16;13:55. doi: 10.1186/1471-2350-13-55. BMC Med Genet. 2012. PMID: 22799487 Free PMC article.

6

Mutational spectrum of the APC and MUTYH genes and genotype-phenotype correlations in Brazilian FAP, AFAP, and MAP patients.

Torrezan GT, da Silva FC, Santos EM, Krepischi AC, Achatz MI, Aguiar S Jr, Rossi BM, Carraro DM. Torrezan GT, et al. Among authors: carraro dm. Orphanet J Rare Dis. 2013 Apr 5;8:54. doi: 10.1186/1750-1172-8-54. Orphanet J Rare Dis. 2013. PMID: 23561487 Free PMC article.

7

Does germ-line deletion of the PIP gene constitute a widespread risk for cancer?

Silva AG, Krepischi AC, Torrezan GT, Capelli LP, Carraro DM, D'Angelo CS, Koiffmann CP, Zatz M, Naslavsky MS, Masotti C, Otto PA, Achatz MI, Mills RE, Lee C, Pearson PL, Rosenberg C. Silva AG, et al. Among authors: carraro dm. Eur J Hum Genet. 2014 Mar;22(3):307-9. doi: 10.1038/ejhg.2013.134. Epub 2013 Jun 19. Eur J Hum Genet. 2014. PMID: 23778870 Free PMC article. No abstract available.

8

Biobanking practice: RNA storage at low concentration affects integrity.

Olivieri EH, Franco Lde A, Pereira RG, Mota LD, Campos AH, Carraro DM. Olivieri EH, et al. Among authors: carraro dm. Biopreserv Biobank. 2014 Feb;12(1):46-52. doi: 10.1089/bio.2013.0056. Biopreserv Biobank. 2014. PMID: 24620769

9

Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients.

Silva FC, Lisboa BC, Figueiredo MC, Torrezan GT, Santos EM, Krepischi AC, Rossi BM, Achatz MI, Carraro DM. Silva FC, et al. Among authors: carraro dm. BMC Med Genet. 2014 May 15;15:55. doi: 10.1186/1471-2350-15-55. BMC Med Genet. 2014. PMID: 24884479 Free PMC article.

10

Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumour.

Torrezan GT, Ferreira EN, Nakahata AM, Barros BD, Castro MT, Correa BR, Krepischi AC, Olivieri EH, Cunha IW, Tabori U, Grundy PE, Costa CM, de Camargo B, Galante PA, Carraro DM. Torrezan GT, et al. Among authors: carraro dm. Nat Commun. 2014 Jun 9;5:4039. doi: 10.1038/ncomms5039. Nat Commun. 2014. PMID: 24909261 Free PMC article.

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