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The paradox of autophagy in Tuberous Sclerosis Complex.

Reis LB, Filippi-Chiela EC, Ashton-Prolla P, Visioli F, Rosset C. Reis LB, et al. Among authors: rosset c. Genet Mol Biol. 2021 Apr 5;44(2):e20200014. doi: 10.1590/1678-4685-GMB-2020-0014. eCollection 2021. Genet Mol Biol. 2021. PMID: 33821877 Free PMC article.

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Impact of photobiomodulation in a patient-derived xenograft model of oral squamous cell carcinoma.

Silveira FM, Schmidt TR, Neumann B, Rosset C, Zanella VG, Maahs GS, Martins MAT, Arany P, Wagner VP, Lopes MA, Santos-Silva AR, Martins MD. Silveira FM, et al. Among authors: rosset c. Oral Dis. 2021 Jul 17. doi: 10.1111/odi.13967. Online ahead of print. Oral Dis. 2021. PMID: 34273227

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Primary cells derived from Tuberous Sclerosis Complex patients show autophagy alteration in the haploinsufficiency state.

Rosset C, Jaeger MDC, Filippi-Chiela E, Reis LB, Sartor ITS, Oliveira Netto CB, Farias CB, Roesler R, Ashton-Prolla P. Rosset C, et al. Genet Mol Biol. 2021 Oct 1;44(4):e20200475. doi: 10.1590/1678-4685-GMB-2020-0475. eCollection 2021. Genet Mol Biol. 2021. PMID: 34609442 Free PMC article.

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Clinical and molecular characterization of patients fulfilling Chompret criteria for Li-Fraumeni syndrome in Southern Brazil.

Matzenbacher Bittar C, de Araújo Rocha YM, Vieira IA, Rosset C, Andreis TF, Sartor ITS, Artigalás O, Netto CBO, Alemar B, Macedo GS, Ashton-Prolla P. Matzenbacher Bittar C, et al. Among authors: rosset c. PLoS One. 2021 Sep 16;16(9):e0251639. doi: 10.1371/journal.pone.0251639. eCollection 2021. PLoS One. 2021. PMID: 34529667 Free PMC article.

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Clinical and molecular characterization of neurofibromatosis in southern Brazil.

Rosset C, Vairo F, Cristina Bandeira I, Fonini M, Netto CBO, Ashton-Prolla P. Rosset C, et al. Expert Rev Mol Diagn. 2018 Jun;18(6):577-586. doi: 10.1080/14737159.2018.1468256. Epub 2018 Apr 27. Expert Rev Mol Diagn. 2018. PMID: 29685074 Clinical Trial.

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Detection of SARS-CoV-2 lineage P.1 in patients from a region with exponentially increasing hospitalisation rate, February 2021, Rio Grande do Sul, Southern Brazil.

Martins AF, Zavascki AP, Wink PL, Volpato FCZ, Monteiro FL, Rosset C, De-Paris F, Ramos ÁK, Barth AL. Martins AF, et al. Among authors: rosset c. Euro Surveill. 2021 Mar;26(12):2100276. doi: 10.2807/1560-7917.ES.2021.26.12.2100276. Euro Surveill. 2021. PMID: 33769251 Free PMC article.

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Systems Biology Approaches Reveal Potential Phenotype-Modifier Genes in Neurofibromatosis Type 1.

Woycinck Kowalski T, Brussa Reis L, Finger Andreis T, Ashton-Prolla P, Rosset C. Woycinck Kowalski T, et al. Among authors: rosset c. Cancers (Basel). 2020 Aug 26;12(9):2416. doi: 10.3390/cancers12092416. Cancers (Basel). 2020. PMID: 32858845 Free PMC article.

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Synchronous Periampullary Tumors in a Patient With Pancreas Divisum and Neurofibromatosis Type 1.

Gregório C, Rosset C, Alves LDS, Netto CBO, Machado SMDS, Bersch VP, Osvaldt AB, Ashton-Prolla P. Gregório C, et al. Among authors: rosset c. Front Genet. 2020 Apr 28;11:395. doi: 10.3389/fgene.2020.00395. eCollection 2020. Front Genet. 2020. PMID: 32425982 Free PMC article.

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The Role of Co-Deleted Genes in Neurofibromatosis Type 1 Microdeletions: An Evolutive Approach.

Brussa Reis L, Turchetto-Zolet AC, Fonini M, Ashton-Prolla P, Rosset C. Brussa Reis L, et al. Among authors: rosset c. Genes (Basel). 2019 Oct 24;10(11):839. doi: 10.3390/genes10110839. Genes (Basel). 2019. PMID: 31652930 Free PMC article.

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Factor VIII mutations and inhibitor formation in a southern Brazilian population.

Rosset C, Gorziza RP, Botton MR, Salzano FM, Bandinelli E. Rosset C, et al. Blood Coagul Fibrinolysis. 2014 Mar;25(2):125-7. doi: 10.1097/MBC.0b013e328364cc83. Blood Coagul Fibrinolysis. 2014. PMID: 23963097

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