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Year | Number of Results |
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2019 | 2 |
2020 | 3 |
2021 | 2 |
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Page 1
The paradox of autophagy in Tuberous Sclerosis Complex.
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.
Tuberous Sclerosis Complex with rare associated findings in the gastrointestinal system: a case report and review of the literature.
Reis LB, Konzen D, Netto CBO, Braghini PMB, Prolla G, Ashton-Prolla P.
Reis LB, et al.
BMC Gastroenterol. 2020 Nov 23;20(1):394. doi: 10.1186/s12876-020-01481-y.
BMC Gastroenterol. 2020.
PMID: 33225890
Free PMC article.
Review.
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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: brussa reis l.
Cancers (Basel). 2020 Aug 26;12(9):2416. doi: 10.3390/cancers12092416.
Cancers (Basel). 2020.
PMID: 32858845
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.
Genes (Basel). 2019 Oct 24;10(11):839. doi: 10.3390/genes10110839.
Genes (Basel). 2019.
PMID: 31652930
Free PMC article.
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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. Among authors: reis lb.
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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MIR605 rs2043556 is associated with the occurrence of multiple primary tumors in TP53 p.(Arg337His) mutation carriers.
Bandeira IC, Vieira IA, Andreis TF, Brussa Reis L, Macedo GS, Vianna FSL, Santos-Silva P, Palmero EI, Galvão HCR, Ramos CRN, Santiago KM, Achatz MI, da Costa AABA, Ashton-Prolla P.
Bandeira IC, et al. Among authors: brussa reis l.
Cancer Genet. 2020 Jan;240:54-58. doi: 10.1016/j.cancergen.2019.11.005. Epub 2019 Nov 20.
Cancer Genet. 2020.
PMID: 31778928
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Functional pri-miR-34b/c rs4938723 and KRAS 3'UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?
Vieira IA, Pezzi EH, Bandeira IC, Reis LB, de Araújo Rocha YM, Fernandes BV, Siebert M, Miyamoto KN, Siqueira MB, Achatz MI, Galvão HCR, Garcia FAO, Campacci N, Carraro DM, Formiga MN, Vianna FSL, Palmero EI, Macedo GS, Ashton-Prolla P.
Vieira IA, et al. Among authors: reis lb.
Gene. 2024 Mar 10;898:148069. doi: 10.1016/j.gene.2023.148069. Epub 2023 Dec 7.
Gene. 2024.
PMID: 38070788
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