Rosset C - Search Results

1

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.

2

Vitamin D Status and VDR Genotype in NF1 Patients: A Case-Control Study from Southern Brazil.

Souza Mario Bueno L, Rosset C, Aguiar E, Pereira Fde S, Izetti Ribeiro P, Scalco R, Matzenbacher Bittar C, Brinckmann Oliveira Netto C, Gischkow Rucatti G, Chies JA, Camey SA, Ashton-Prolla P. Souza Mario Bueno L, et al. Among authors: rosset c. Int J Endocrinol. 2015;2015:402838. doi: 10.1155/2015/402838. Epub 2015 Jun 16. Int J Endocrinol. 2015. PMID: 26161090 Free PMC article.

3

TSC1 and TSC2 gene mutations and their implications for treatment in Tuberous Sclerosis Complex: a review.

Rosset C, Netto CBO, Ashton-Prolla P. Rosset C, et al. Genet Mol Biol. 2017 Jan-Mar;40(1):69-79. doi: 10.1590/1678-4685-GMB-2015-0321. Epub 2017 Feb 20. Genet Mol Biol. 2017. PMID: 28222202 Free PMC article.

4

Molecular analysis of TSC1 and TSC2 genes and phenotypic correlations in Brazilian families with tuberous sclerosis.

Rosset C, Vairo F, Bandeira IC, Correia RL, de Goes FV, da Silva RTB, Bueno LSM, de Miranda Gomes MCS, Galvão HCR, Neri JICF, Achatz MI, Netto CBO, Ashton-Prolla P. Rosset C, et al. PLoS One. 2017 Oct 2;12(10):e0185713. doi: 10.1371/journal.pone.0185713. eCollection 2017. PLoS One. 2017. PMID: 28968464 Free PMC article.

5

Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome.

Schneider NB, Pastor T, Paula AE, Achatz MI, Santos ÂRD, Vianna FSL, Rosset C, Pinheiro M, Ashton-Prolla P, Moreira MÂM, Palmero EI; Brazilian Lynch Syndrome Study Group. Schneider NB, et al. Among authors: rosset c. Cancer Med. 2018 May;7(5):2078-2088. doi: 10.1002/cam4.1316. Epub 2018 Mar 25. Cancer Med. 2018. PMID: 29575718 Free PMC article.

6

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.

7

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.

8

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.

9

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.

10

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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