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Year Number of Results
2003 1
2005 1
2006 2
2007 2
2008 2
2009 1
2010 3
2011 1
2012 4
2013 1
2015 1
2016 1
2017 4
2018 2
2019 1
2020 2
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2022 4
2023 3
2024 1

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Page 1
Generalized hypertrichosis syndromes in Mexico.
Aguayo-Orozco TA, Ríos-González BE, Castro-Martínez AG, Ruiz-Ramírez AV, Figuera LE. Aguayo-Orozco TA, et al. Among authors: figuera le. Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):1014-1022. doi: 10.1002/ajmg.c.31864. Epub 2020 Dec 7. Am J Med Genet C Semin Med Genet. 2020. PMID: 33283427
SOD2 Gene Variants (rs4880 and rs5746136) and Their Association with Breast Cancer Risk.
Gallegos-Arreola MP, Ramírez-Patiño R, Sánchez-López JY, Zúñiga-González GM, Figuera LE, Delgado-Saucedo JI, Gómez-Meda BC, Rosales-Reynoso MA, Puebla-Pérez AM, Lemus-Varela ML, Garibaldi-Ríos AF, Marín-Domínguez NA, Pacheco-Verduzco DP, Mohamed-Flores EA. Gallegos-Arreola MP, et al. Among authors: figuera le. Curr Issues Mol Biol. 2022 Oct 26;44(11):5221-5233. doi: 10.3390/cimb44110355. Curr Issues Mol Biol. 2022. PMID: 36354667 Free PMC article.
Severe Craniofacial Involvement due to Amniotic Band Sequence.
Becerra-Solano LE, Castañeda-Cisneros G, Corona-Rivera JR, Díaz-Rodríguez M, Figuera LE, López-Muñoz E, Nastasi-Catanese JA, Toscano-Flores JJ, Ramírez-Dueñas ML, García-Ortíz JE. Becerra-Solano LE, et al. Fetal Pediatr Pathol. 2018 Feb;37(1):27-37. doi: 10.1080/15513815.2017.1392663. Epub 2018 Jan 16. Fetal Pediatr Pathol. 2018. PMID: 29336649
Association of the rs8720 and rs12587 KRAS Gene Variants with Colorectal Cancer in a Mexican Population and Their Analysis In Silico.
Gallegos-Arreola MP, Garibaldi-Ríos AF, Cruz-Sánchez JI, Figuera LE, Ronquillo-Carreón CA, Rosales-Reynoso MA, Gómez-Meda BC, Carrillo-Dávila IA, Puebla-Pérez AM, Montoya-Fuentes H, Peralta-Leal V, Zúñiga-González GM. Gallegos-Arreola MP, et al. Cells. 2023 Jul 26;12(15):1941. doi: 10.3390/cells12151941. Cells. 2023. PMID: 37566020 Free PMC article.
Clinical and molecular features of 66 patients with musculocontractural Ehlers-Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14).
Minatogawa M, Unzaki A, Morisaki H, Syx D, Sonoda T, Janecke AR, Slavotinek A, Voermans NC, Lacassie Y, Mendoza-Londono R, Wierenga KJ, Jayakar P, Gahl WA, Tifft CJ, Figuera LE, Hilhorst-Hofstee Y, Maugeri A, Ishikawa K, Kobayashi T, Aoki Y, Ohura T, Kawame H, Kono M, Mochida K, Tokorodani C, Kikkawa K, Morisaki T, Kobayashi T, Nakane T, Kubo A, Ranells JD, Migita O, Sobey G, Kaur A, Ishikawa M, Yamaguchi T, Matsumoto N, Malfait F, Miyake N, Kosho T. Minatogawa M, et al. Among authors: figuera le. J Med Genet. 2022 Sep;59(9):865-877. doi: 10.1136/jmedgenet-2020-107623. Epub 2021 Nov 23. J Med Genet. 2022. PMID: 34815299 Free PMC article.
Potential Modifying Effect of the APOEε4 Allele on Age of Onset and Clinical Manifestations in Patients with Early-Onset Alzheimer's Disease with and without a Pathogenic Variant in PSEN1 in a Sample of the Mexican Population.
Valdez-Gaxiola CA, Maciel-Cruz EJ, Hernández-Peña R, Dumois-Petersen S, Rosales-Leycegui F, Gallegos-Arreola MP, Moreno-Ortiz JM, Figuera LE. Valdez-Gaxiola CA, et al. Among authors: figuera le. Int J Mol Sci. 2023 Oct 28;24(21):15687. doi: 10.3390/ijms242115687. Int J Mol Sci. 2023. PMID: 37958671 Free PMC article.
35 results