Velazquez-Soto, Henry, Fernanda Real, and Maria C. Jiménez-Martínez. «Historical evolution, overview, and therapeutic manipulation of co-stimulatory molecules.» World Journal of Immunology 1 (2022): 1-8. 10.5411/wji.v12.i1.1
Cubillo-Martínez AA, Pereyra MA, Garfias Y, Guluarte C, Zenteno E, Sánchez-Salgado JL. Extracellular traps involved in invertebrate immune mechanisms. Fish Shellfish Immunol. 2022 Feb;121:380-386. doi: 10.1016/j.fsi.2022.01.024. Epub 2022 Jan 16. PMID: 35045319.
The Mexican Consortium of Epidemiological Studies for the Prevention, Diagnosis, and Control of Chronic Kidney Disease: a review of collaborating studies. Córtes-Valencia A, Ortíz-Rodríguez S, Balderas N, Catzin-Kuhlmann A, Correa-Rotter R, González-Villalpando C, Jiménez-Corona A, López-Ridaura R, Mejía M, Salmerón J, Tamayo J, Lajous M, Denova-Gutiérrez E. Salud Pública de México 2022 (en press)
Feasibility of a Bi-national Consulate-based Teleophthalmology Screening and Referral Protocol for Diabetic retinopathy among Mexican Migrants in the United States. Foreman J, Lahiff M, Hernández EG, Jiménez-Corona A, Matsui R, Cuadros J, Pizano S, Peters H, Castañeda X, Maus M. J Health Care Poor Underserved. 2022;33(1):221-233. doi: 10.1353/hpu.2022.0017.PMID: 35153216
Novel CHRDL1 mutation causing X-linked megalocornea in a family with mild anterior segment manifestations in carrier females. Arce-Gonzalez R, Chacon-Camacho OF, Navas-Perez A, Gonzalez-Gonzalez MC, Martinez-Aguilar A, Zenteno JC. Ophthalmic Genet. 2022 Apr;43(2):224-229. doi: 10.1080/13816810.2021.2002917. Epub 2021 Nov 29. PMID: 34844512
Contribution of APOA5, APOC3, CETP, ABCA1 and SIK3 genetic variants to hypertriglyceridemia development in Mexican HIV-patients receiving antiretroviral therapy. Bautista-Martínez JS, Mata-Marín JA, Sandoval-Ramírez JL, Chaparro-Sánchez A, Manjarrez-Téllez B, Uribe-Noguez LA, Gaytán-Martínez J, Núñez-Armendáriz M, Cruz-Sánchez A, Núñez-Rodríguez N, Iván MA, Morales-González GS, Álvarez-Mendoza JP, Pérez-Barragán E, Ríos-De Los Ríos J, Contreras-Chávez GG, Tapia-Magallanes DM, Ribas-Aparicio RM, Díaz-López M, Olivares-Labastida A, Gómez-Delgado A, Torres J, Miranda-Duarte A, Zenteno JC, Pompa-Mera EN.Pharmacogenet Genomics. 2022 Apr 1;32(3):101-110. doi: 10.1097/FPC.0000000000000458. PMID: 34693928
Detailed phenotypic description of stromal corneal dystrophy in a large pedigree carrying the uncommon TGFBI p.Ala546Asp pathogenic variant. Irusteta L, Ramírez-Miranda A, Navas-Pérez A, Montes-Almanza L, Arteaga J, García-Martínez F, Graue-Hernández E, Zenteno JC. Ophthalmic Genet. 2022 Apr 26:1-5. doi: 10.1080/13816810.2022.2068047. Online ahead of print. PMID: 35470743
AUTOSOMAL DOMINANT MÜLLER CELL SHEEN DYSTROPHY: Clinical, Histopathologic, and Genetic Assessment in an Extended Family With Long Follow-Up. Dalma-Weiszhausz J, Chacón-Camacho O, Chevez-Barrios P, Zenteno JC, Franco-Cárdenas V, García-Montaño LA, Pérez-Bravo J, García-Montalvo IA, Jiménez-Sierra JM, Dalma A. Retina. 2022 May 1;42(5):981-991. doi: 10.1097/IAE.0000000000003413. PMID: 35125479
A new missense variant in RAB3GAP2 in a family with muscular dystrophy-short stature and defective autophagy: An expansion of the micro/Martsolf spectrum or a new phenotype?. Mora-Roldan GA, Galaviz-Hernandez C, Hiebert-Froese J, Hernandez A, Montes L, Duran-Pasten ML, Gazarian K, Zenteno JC. Am J Med Genet A. 2022 Jul;188(7):1972-1978. doi: 10.1002/ajmg.a.62723. Epub 2022 Mar 11. PMID: 35274444
