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Year Number of Results
2013 1
2014 1
2015 2
2017 1
2018 2
2019 3
2020 3
2021 2
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2023 2
2024 1

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Page 1
Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico.
Leal-Anaya P, Kimball TN, Yanez-Felix AL, Fiesco-Roa MÓ, García-de Teresa B, Monsiváis A, Juárez-Velázquez R, Lieberman E, Villarroel C, Yokoyama E, Fernández-Hernández L, Rivera-Osorio A, Sosa D, Ortiz Sandoval MM, López-Santiago N, Frías S, Del Castillo V, Rodríguez A. Leal-Anaya P, et al. Among authors: garcia de teresa b. Front Genet. 2024 Jan 24;14:1293929. doi: 10.3389/fgene.2023.1293929. eCollection 2023. Front Genet. 2024. PMID: 38327701 Free PMC article.
A Boolean network model of the double-strand break repair pathway choice.
Ayala-Zambrano C, Yuste M, Frias S, Garcia-de-Teresa B, Mendoza L, Azpeitia E, Rodríguez A, Torres L. Ayala-Zambrano C, et al. Among authors: garcia de teresa b. J Theor Biol. 2023 Sep 21;573:111608. doi: 10.1016/j.jtbi.2023.111608. Epub 2023 Aug 16. J Theor Biol. 2023. PMID: 37595867 Free article.
Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia.
Rodríguez A, Yang C, Furutani E, García de Teresa B, Velázquez M, Filiatrault J, Sambel LA, Phan T, Flores-Guzmán P, Sánchez S, Monsiváis Orozco A, Mayani H, Bolukbasi OV, Färkkilä A, Epperly M, Greenberger J, Shimamura A, Frías S, Grompe M, Parmar K, D'Andrea AD. Rodríguez A, et al. Among authors: garcia de teresa b. Exp Hematol. 2021 Jan;93:70-84.e4. doi: 10.1016/j.exphem.2020.11.002. Epub 2020 Nov 7. Exp Hematol. 2021. PMID: 33166613 Free PMC article.
MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia.
Rodríguez A, Zhang K, Färkkilä A, Filiatrault J, Yang C, Velázquez M, Furutani E, Goldman DC, García de Teresa B, Garza-Mayén G, McQueen K, Sambel LA, Molina B, Torres L, González M, Vadillo E, Pelayo R, Fleming WH, Grompe M, Shimamura A, Hautaniemi S, Greenberger J, Frías S, Parmar K, D'Andrea AD. Rodríguez A, et al. Among authors: garcia de teresa b. Cell Stem Cell. 2021 Jan 7;28(1):33-47.e8. doi: 10.1016/j.stem.2020.09.004. Epub 2020 Sep 29. Cell Stem Cell. 2021. PMID: 32997960 Free PMC article.
WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways.
Rodríguez A, Naveja JJ, Torres L, García de Teresa B, Juárez-Figueroa U, Ayala-Zambrano C, Azpeitia E, Mendoza L, Frías S. Rodríguez A, et al. Among authors: garcia de teresa b. Front Genet. 2019 May 3;10:411. doi: 10.3389/fgene.2019.00411. eCollection 2019. Front Genet. 2019. PMID: 31130988 Free PMC article.
FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México.
García-de Teresa B, Frias S, Molina B, Villarreal MT, Rodriguez A, Carnevale A, López-Hernández G, Vollbrechtshausen L, Olaya-Vargas A, Torres L. García-de Teresa B, et al. Mol Genet Genomic Med. 2019 Jun;7(6):e710. doi: 10.1002/mgg3.710. Epub 2019 May 1. Mol Genet Genomic Med. 2019. PMID: 31044565 Free PMC article.
Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.
Barrientos-Rios R, Frias S, Velázquez-Aragón JA, Villaroel CE, Sánchez S, Molina B, Martínez A, Carnevale A, García-de-Teresa B, Bonilla E, Alvarado-Araiza CD, Valderrama-Hernández A, Ríos-Gallardo PT, Calzada-León R, Altamirano-Bustamante N, Torres L. Barrientos-Rios R, et al. Among authors: garcia de teresa b. Gynecol Endocrinol. 2019 Sep;35(9):772-776. doi: 10.1080/09513590.2019.1582626. Epub 2019 Mar 19. Gynecol Endocrinol. 2019. PMID: 30887870
16 results