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Pilot genome-wide association study identifying novel risk loci for type 2 diabetes in a Maya population.
Gene. 2018 Nov 30;677:324-331. doi: 10.1016/j.gene.2018.08.041. Epub 2018 Aug 18.
Gene. 2018.
PMID: 30130595
Maya gene variants related to the risk of type 2 diabetes in a family-based association study.
Domínguez-Cruz MG, Muñoz ML, Totomoch-Serra A, García-Escalante MG, Burgueño J, Valadez-González N, Pinto-Escalante D, Díaz-Badillo A.
Domínguez-Cruz MG, et al. Among authors: garcia escalante mg.
Gene. 2020 Mar 10;730:144259. doi: 10.1016/j.gene.2019.144259. Epub 2019 Nov 21.
Gene. 2020.
PMID: 31759989
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Data on a genome-wide association study of type 2 diabetes in a Maya population.
Totomoch-Serra A, Domínguez-Cruz MG, Muñoz ML, García-Escalante MG, Burgueño J, Díaz-Badillo Á, Valadez-González N, Escalante DP.
Totomoch-Serra A, et al. Among authors: garcia escalante mg.
Data Brief. 2019 Nov 22;28:104866. doi: 10.1016/j.dib.2019.104866. eCollection 2020 Feb.
Data Brief. 2019.
PMID: 31872004
Free PMC article.
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[Effect of the Gly972Arg, SNP43 and Prol2Ala polymorphisms of the genes IRS1, CAPN10 and PPARG2 on secondary failure to sulphonylurea and metformin in patients with type 2 diabetes in Yucatán, México].
García-Escalante MG, Suárez-Solís VM, López-Avila MT, Pinto-Escalante Ddel C, Laviada-Molina H.
García-Escalante MG, et al.
Invest Clin. 2009 Mar;50(1):65-76.
Invest Clin. 2009.
PMID: 19418728
Spanish.
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Genetic variation of FTO: rs1421085 T>C, rs8057044 G>A, rs9939609 T>A, and copy number (CNV) in Mexican Mayan school-aged children with obesity/overweight and with normal weight.
González-Herrera L, Zavala-Castro J, Ayala-Cáceres C, Pérez-Mendoza G, López-González MJ, Pinto-Escalante D, Canto-Cetina T, García-Escalante MG, Rubi-Castellanos R, Contreras-Capetillo S, Herrera-Sanchez F, Méndez-Domínguez N, Alcocer-Gamboa A.
González-Herrera L, et al. Among authors: garcia escalante mg.
Am J Hum Biol. 2019 Jan;31(1):e23192. doi: 10.1002/ajhb.23192. Epub 2018 Dec 10.
Am J Hum Biol. 2019.
PMID: 30537186
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Analysis of Thiopurine S-Methyltransferase Deficient Alleles in Acute Lymphoblastic Leukemia Patients in Mexican Patients.
Jiménez-Morales S, Ramírez-Florencio M, Mejía-Aranguré JM, Núñez-Enríquez JC, Bekker-Mendez C, Torres-Escalante JL, Flores-Lujano J, Jiménez-Hernández E, Del Carmen Rodríguez-Zepeda M, Leal YA, González-Montalvo PM, Pantoja-Guillen F, Peñaloza-Gonzalez JG, Gutiérrez-Juárez EI, Núñez-Villegas NN, Pérez-Saldivar ML, Guerra-Castillo FX, Flores-Villegas LV, Ramos-Cervantes MT, Fragoso JM, García-Escalante MG, Del Carmen Pinto-Escalante D, Ramírez-Bello J, Hidalgo-Miranda A.
Jiménez-Morales S, et al. Among authors: garcia escalante mg.
Arch Med Res. 2016 Nov;47(8):615-622. doi: 10.1016/j.arcmed.2016.11.018.
Arch Med Res. 2016.
PMID: 28476189
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[Identifying deletions in the dystrophin gene and detecting carriers in families with Duchenne's/Becker's muscular dystrophy].
González-Herrera L, Gamas-Trujillo PA, García-Escalante MG, Castillo-Zapata I, Pinto-Escalante D.
González-Herrera L, et al. Among authors: garcia escalante mg.
Rev Neurol. 2009 Jan 16-31;48(2):66-70.
Rev Neurol. 2009.
PMID: 19173203
Free article.
Spanish.
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