Ashton-Prolla P - Search Results

1

Screening and characterization of BRCA2 c.156_157insAlu in Brazil: Results from 1380 individuals from the South and Southeast.

Felicio PS, Alemar B, Coelho AS, Berardinelli GN, Melendez ME, Lengert AVH, Miche Lli RD, Reis RM, Fernandes GC, Ewald IP, Bittar CM, Netto CBO, Artigalas O, Peixoto A, Pinheiro M, Teixeira MR, Vargas FR, Dos Santos ACE, Moreira MAM, Ashton-Prolla P, Palmero EI. Felicio PS, et al. Cancer Genet. 2018 Dec;228-229:93-97. doi: 10.1016/j.cancergen.2018.09.001. Epub 2018 Oct 6. Cancer Genet. 2018. PMID: 30553478

2

The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families.

Achatz MI, Olivier M, Le Calvez F, Martel-Planche G, Lopes A, Rossi BM, Ashton-Prolla P, Giugliani R, Palmero EI, Vargas FR, Da Rocha JC, Vettore AL, Hainaut P. Achatz MI, et al. Cancer Lett. 2007 Jan 8;245(1-2):96-102. doi: 10.1016/j.canlet.2005.12.039. Epub 2006 Feb 21. Cancer Lett. 2007. PMID: 16494995

3

Clinical characterization and risk profile of individuals seeking genetic counseling for hereditary breast cancer in Brazil.

Palmero EI, Ashton-Prolla P, da Rocha JC, Vargas FR, Kalakun L, Blom MB, Azevedo SJ, Caleffi M, Giugliani R, Schüler-Faccini L. Palmero EI, et al. J Genet Couns. 2007 Jun;16(3):363-71. doi: 10.1007/s10897-006-9073-0. Epub 2007 Feb 23. J Genet Couns. 2007. PMID: 17318454

4

Cancer genetic counseling in public health care hospitals: the experience of three Brazilian services.

Palmero EI, Kalakun L, Schüler-Faccini L, Giugliani R, Regla Vargas F, Rocha JC, Ashton-Prolla P. Palmero EI, et al. Community Genet. 2007;10(2):110-9. doi: 10.1159/000099089. Community Genet. 2007. PMID: 17380061

5

Clinical and molecular characterization of patients at risk for hereditary melanoma in southern Brazil.

Ashton-Prolla P, Bakos L, Junqueira G Jr, Giugliani R, Azevedo SJ, Hogg D. Ashton-Prolla P, et al. J Invest Dermatol. 2008 Feb;128(2):421-5. doi: 10.1038/sj.jid.5701030. Epub 2007 Aug 23. J Invest Dermatol. 2008. PMID: 17713569 Free article.

6

Detection of R337H, a germline TP53 mutation predisposing to multiple cancers, in asymptomatic women participating in a breast cancer screening program in Southern Brazil.

Palmero EI, Schüler-Faccini L, Caleffi M, Achatz MI, Olivier M, Martel-Planche G, Marcel V, Aguiar E, Giacomazzi J, Ewald IP, Giugliani R, Hainaut P, Ashton-Prolla P. Palmero EI, et al. Cancer Lett. 2008 Mar 8;261(1):21-5. doi: 10.1016/j.canlet.2007.10.044. Epub 2008 Jan 11. Cancer Lett. 2008. PMID: 18248785

7

Founder effect of the BRCA1 5382insC mutation in Brazilian patients with hereditary breast ovary cancer syndrome.

da Costa EC, Vargas FR, Moreira AS, Lourenço JJ, Caleffi M, Ashton-Prolla P, Martins Moreira MA. da Costa EC, et al. Cancer Genet Cytogenet. 2008 Jul;184(1):62-6. doi: 10.1016/j.cancergencyto.2008.03.011. Cancer Genet Cytogenet. 2008. PMID: 18558292

8

Consistency of self-reported first-degree family history of cancer in a population-based study.

Roth FL, Camey SA, Caleffi M, Schuler-Faccini L, Palmero EI, Bochi C, Moreira SM, Kalakun L, Giugliani R, Ashton-Prolla P. Roth FL, et al. Fam Cancer. 2009;8(3):195-202. doi: 10.1007/s10689-008-9228-2. Epub 2009 Jan 20. Fam Cancer. 2009. PMID: 19153822

9

TP53 PIN3 and MDM2 SNP309 polymorphisms as genetic modifiers in the Li-Fraumeni syndrome: impact on age at first diagnosis.

Marcel V, Palmero EI, Falagan-Lotsch P, Martel-Planche G, Ashton-Prolla P, Olivier M, Brentani RR, Hainaut P, Achatz MI. Marcel V, et al. J Med Genet. 2009 Nov;46(11):766-72. doi: 10.1136/jmg.2009.066704. Epub 2009 Jun 18. J Med Genet. 2009. PMID: 19542078

10

Association between myeloperoxidase polymorphisms and its plasma levels with severity of coronary artery disease.

Wainstein RV, Wainstein MV, Ribeiro JP, Dornelles LV, Tozzati P, Ashton-Prolla P, Ewald IP, Vietta G, Polanczyk CA. Wainstein RV, et al. Clin Biochem. 2010 Jan;43(1-2):57-62. doi: 10.1016/j.clinbiochem.2009.07.022. Epub 2009 Aug 3. Clin Biochem. 2010. PMID: 19651119

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