Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

2,191 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Generation and characterization of a human induced pluripotent stem (iPS) cell line derived from an acute myeloid leukemia patient evolving from primary myelofibrosis carrying the CALR 52bp deletion and the ASXL1 p.R693X mutation.
Gomez Limia CE, Devalle S, Reis M, Sochacki J, Carneiro M, Madeiro da Costa R, D'Andrea M, Padilha T, Zalcberg IR, Solza C, Daumas A, Rehen S, Monte-Mór B, Bonamino MH. Gomez Limia CE, et al. Among authors: reis m. Stem Cell Res. 2017 Oct;24:16-20. doi: 10.1016/j.scr.2017.08.006. Epub 2017 Aug 8. Stem Cell Res. 2017. PMID: 29034885 Free article.
Generation of iPS cell lines from schizophrenia patients using a non-integrative method.
Sochacki J, Devalle S, Reis M, de Moraes Maciel R, da Silveira Paulsen B, Brentani H, Belmonte-de-Abreu PS, Rehen S. Sochacki J, et al. Among authors: reis m. Stem Cell Res. 2016 Jul;17(1):97-101. doi: 10.1016/j.scr.2016.05.017. Epub 2016 May 25. Stem Cell Res. 2016. PMID: 27558610 Free article. No abstract available.
Characterization of a human induced Pluripotent Stem (iPS) cell line (INCABRi002-A) derived from a primary myelofibrosis patient harboring the 5-bp insertion in CALR and the p.W146X mutation in TP53.
Gomez Limia CE, Devalle S, Reis M, Sochacki J, Madeiro da Costa R, D'Andrea M, Padilha T, Zalcberg IR, Solza C, Daumas A, Rehen S, Bonamino MH, Monte-Mór B. Gomez Limia CE, et al. Among authors: reis m. Stem Cell Res. 2018 Dec;33:130-134. doi: 10.1016/j.scr.2018.09.012. Epub 2018 Sep 20. Stem Cell Res. 2018. PMID: 30343103 Free article.
Perinatal stress and methylation of the NR3C1 gene in newborns: systematic review.
Chalfun G, Reis MM, de Oliveira MBG, de Araújo Brasil A, Dos Santos Salú M, da Cunha AJLA, Prata-Barbosa A, de Magalhães-Barbosa MC. Chalfun G, et al. Among authors: reis mm. Epigenetics. 2022 Sep;17(9):1003-1019. doi: 10.1080/15592294.2021.1980691. Epub 2021 Oct 1. Epigenetics. 2022. PMID: 34519616 Free PMC article.
NR3C1 gene methylation and cortisol levels in preterm and healthy full-term infants in the first 3 months of life.
Chalfun G, Araújo Brasil A, Paravidino VB, Soares-Lima SC, Souza Almeida Lopes M, Santos Salú MD, Barbosa E Dos Santos PV, P da Cunha Trompiere AC, Vieira Milone LT, Rodrigues-Santos G, Genuíno de Oliveira MB, Robaina JR, Lima-Setta F, Reis MM, Ledo Alves da Cunha AJ, Prata-Barbosa A, de Magalhães-Barbosa MC. Chalfun G, et al. Among authors: reis mm. Epigenomics. 2022 Dec;14(24):1545-1561. doi: 10.2217/epi-2022-0444. Epub 2023 Mar 2. Epigenomics. 2022. PMID: 36861354 Free article.
EGFR Mutation Detection in Brazilian Patients With Non-Small-Cell Lung Cancer: Lessons From Real-World Data Scenario of Molecular Testing.
Montella T, Zalis M, Zukin M, Cordeiro de Lima VC, Baldotto C, De Marchi P, Salles P, Mathias C, Barrios C, Kawamura C, Calabrich A, Araújo LH, Castro G, Bustamante C, Santa Maria A, Reis M, Ferreira CG. Montella T, et al. Among authors: reis m. JCO Glob Oncol. 2023 Sep;9:e2200426. doi: 10.1200/GO.22.00426. JCO Glob Oncol. 2023. PMID: 37769218 Free PMC article.
2,191 results