Krepischi ACV - Search Results

1

TET Upregulation Leads to 5-Hydroxymethylation Enrichment in Hepatoblastoma.

Rivas MP, Aguiar TFM, Fernandes GR, Caires-Júnior LC, Goulart E, Telles-Silva KA, Cypriano M, de Toledo SRC, Rosenberg C, Carraro DM, da Costa CML, da Cunha IW, Krepischi ACV. Rivas MP, et al. Among authors: krepischi acv. Front Genet. 2019 Jun 12;10:553. doi: 10.3389/fgene.2019.00553. eCollection 2019. Front Genet. 2019. PMID: 31249594 Free PMC article.

2

Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy.

Krepischi AC, Knijnenburg J, Bertola DR, Kim CA, Pearson PL, Bijlsma E, Szuhai K, Kok F, Vianna-Morgante AM, Rosenberg C. Krepischi AC, et al. Epilepsia. 2010 Dec;51(12):2457-60. doi: 10.1111/j.1528-1167.2010.02742.x. Epub 2010 Sep 30. Epilepsia. 2010. PMID: 21204806 Free article.

3

Down-regulation of ANAPC13 and CLTCL1: Early Events in the Progression of Preinvasive Ductal Carcinoma of the Breast.

Sens-Abuázar C, Napolitano E Ferreira E, Osório CA, Krepischi AC, Ricca TI, Castro NP, da Cunha IW, Maciel Mdo S, Rosenberg C, Brentani MM, Soares FA, Rocha RM, Carraro DM. Sens-Abuázar C, et al. Transl Oncol. 2012 Apr;5(2):113-23. doi: 10.1593/tlo.11280. Epub 2012 Apr 1. Transl Oncol. 2012. PMID: 22496928 Free PMC article.

4

Germline copy number variations and cancer predisposition.

Krepischi AC, Pearson PL, Rosenberg C. Krepischi AC, et al. Future Oncol. 2012 Apr;8(4):441-50. doi: 10.2217/fon.12.34. Future Oncol. 2012. PMID: 22515447 Free article. Review.

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. 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. 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

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. BMC Med Genet. 2014 May 15;15:55. doi: 10.1186/1471-2350-15-55. BMC Med Genet. 2014. PMID: 24884479 Free PMC article.

8

Association of melanoma with intraepithelial neoplasia of the pancreas in three patients.

Fidalgo F, Gomes EE, Moredo Facure L, Da Silva FC, Carraro DM, de Sá BC, Duprat Neto JP, Krepischi AC. Fidalgo F, et al. Exp Mol Pathol. 2014 Aug;97(1):144-7. doi: 10.1016/j.yexmp.2014.06.013. Epub 2014 Jun 28. Exp Mol Pathol. 2014. PMID: 24984283 Free article.

9

Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma.

de Ávila AL, Krepischi AC, Moredo LF, Aguiar TF, da Silva FC, de Sá BC, de Nóbrega AF, Achatz MI, Duprat JP, Landman G, Carraro DM. de Ávila AL, et al. Fam Cancer. 2014 Dec;13(4):645-9. doi: 10.1007/s10689-014-9736-1. Fam Cancer. 2014. PMID: 25023876

10

Large germline copy number variations as predisposing factor in childhood neoplasms.

Krepischi AC, Capelli LP, Silva AG, de Araújo ÉS, Pearson PL, Heck B, da Costa CM, de Camargo B, Rosenberg C. Krepischi AC, et al. Future Oncol. 2014;10(9):1627-33. doi: 10.2217/fon.14.41. Future Oncol. 2014. PMID: 25145432 Free article.

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