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Showing 1 to 9 of 9 entries
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Comment on 'Childhood leukaemia close to high-voltage power lines--the Geocap study, 2002-2007'--odds ratio and confidence interval.

British journal of cancer

Magaña Torres MT, Gonzalez Garcia JR.
PMID: 23949155
Br J Cancer. 2013 Sep 03;109(5):1384-5. doi: 10.1038/bjc.2013.425. Epub 2013 Aug 15.

No abstract available.

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Magaña Torres MT, Gonzalez Garcia JR. Comment on 'Childhood leukaemia close to high-voltage power lines--the Geocap study, 2002-2007'--odds ratio and confidence interval. Br J Cancer. 2013;109(5):1384-5doi: 10.1038/bjc.2013.425.
Magaña Torres, M. T., & Gonzalez Garcia, J. R. (2013). Comment on 'Childhood leukaemia close to high-voltage power lines--the Geocap study, 2002-2007'--odds ratio and confidence interval. British journal of cancer, 109(5), 1384-5. https://doi.org/10.1038/bjc.2013.425
Magaña Torres, M T, and Gonzalez Garcia, J R. "Comment on 'Childhood leukaemia close to high-voltage power lines--the Geocap study, 2002-2007'--odds ratio and confidence interval." British journal of cancer vol. 109,5 (2013): 1384-5. doi: https://doi.org/10.1038/bjc.2013.425
Magaña Torres MT, Gonzalez Garcia JR. Comment on 'Childhood leukaemia close to high-voltage power lines--the Geocap study, 2002-2007'--odds ratio and confidence interval. Br J Cancer. 2013 Sep 03;109(5):1384-5. doi: 10.1038/bjc.2013.425. Epub 2013 Aug 15. PMID: 23949155; PMCID: PMC3778285.
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Association of polymorphisms of the .

Archives of medical science : AMS

González-Mercado A, Sánchez-López JY, Perea-Díaz FJ, Magaña-Torres MT, Salazar-Páramo M, González-López L, González-Mercado MG, Ibarra-Cortés B.
PMID: 31572484
Arch Med Sci. 2019 Sep;15(5):1352-1356. doi: 10.5114/aoms.2019.87410. Epub 2019 Aug 22.

No abstract available.

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González-Mercado A, Sánchez-López JY, Perea-Díaz FJ, et al. Association of polymorphisms of the . Arch Med Sci. 2019;15(5):1352-1356doi: 10.5114/aoms.2019.87410.
González-Mercado, A., Sánchez-López, J. Y., Perea-Díaz, F. J., Magaña-Torres, M. T., Salazar-Páramo, M., González-López, L., González-Mercado, M. G., & Ibarra-Cortés, B. (2019). Association of polymorphisms of the . Archives of medical science : AMS, 15(5), 1352-1356. https://doi.org/10.5114/aoms.2019.87410
González-Mercado, Anahi, et al. "Association of polymorphisms of the ." Archives of medical science : AMS vol. 15,5 (2019): 1352-1356. doi: https://doi.org/10.5114/aoms.2019.87410
González-Mercado A, Sánchez-López JY, Perea-Díaz FJ, Magaña-Torres MT, Salazar-Páramo M, González-López L, González-Mercado MG, Ibarra-Cortés B. Association of polymorphisms of the . Arch Med Sci. 2019 Sep;15(5):1352-1356. doi: 10.5114/aoms.2019.87410. Epub 2019 Aug 22. PMID: 31572484; PMCID: PMC6764302.
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Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population.

European review for medical and pharmacological sciences

Gallegos-Arreola MP, García Verdín PM, Magaña-Torres MT, Figuera LE, Zúñiga-González GM, Rosales-Reynoso MA, Gómez-Meda BC, Puebla-Pérez AM.
PMID: 34787849
Eur Rev Med Pharmacol Sci. 2021 Nov;25(21):6454-6464. doi: 10.26355/eurrev_202111_27088.

OBJECTIVE: Polymorphisms of the KRAS gene have been shown to be associated with cancer. However, their association with breast cancer (BC) has been inconsistent. The purpose of this study was to determine the frequency with which the rs61764370, rs9266,...

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Gallegos-Arreola MP, García Verdín PM, Magaña-Torres MT, et al. Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population. Eur Rev Med Pharmacol Sci. 2021;25(21):6454-6464doi: 10.26355/eurrev_202111_27088.
Gallegos-Arreola, M. P., García Verdín, P. M., Magaña-Torres, M. T., Figuera, L. E., Zúñiga-González, G. M., Rosales-Reynoso, M. A., Gómez-Meda, B. C., & Puebla-Pérez, A. M. (2021). Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population. European review for medical and pharmacological sciences, 25(21), 6454-6464. https://doi.org/10.26355/eurrev_202111_27088
Gallegos-Arreola, M P, et al. "Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population." European review for medical and pharmacological sciences vol. 25,21 (2021): 6454-6464. doi: https://doi.org/10.26355/eurrev_202111_27088
Gallegos-Arreola MP, García Verdín PM, Magaña-Torres MT, Figuera LE, Zúñiga-González GM, Rosales-Reynoso MA, Gómez-Meda BC, Puebla-Pérez AM. Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population. Eur Rev Med Pharmacol Sci. 2021 Nov;25(21):6454-6464. doi: 10.26355/eurrev_202111_27088. PMID: 34787849.
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Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population.

European review for medical and pharmacological sciences

Gallegos-Arreola MP, García Verdín PM, Magaña-Torres MT, Figuera LE, Zúñiga-González GM, Rosales-Reynoso MA, Gómez-Meda BC, Puebla-Pérez AM.
PMID: 34787849
Eur Rev Med Pharmacol Sci. 2021 Nov;25(21):6454-6464. doi: 10.26355/eurrev_202111_27088.

OBJECTIVE: Polymorphisms of the KRAS gene have been shown to be associated with cancer. However, their association with breast cancer (BC) has been inconsistent. The purpose of this study was to determine the frequency with which the rs61764370, rs9266,...

Cite
Gallegos-Arreola MP, García Verdín PM, Magaña-Torres MT, et al. Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population. Eur Rev Med Pharmacol Sci. 2021;25(21):6454-6464doi: 10.26355/eurrev_202111_27088.
Gallegos-Arreola, M. P., García Verdín, P. M., Magaña-Torres, M. T., Figuera, L. E., Zúñiga-González, G. M., Rosales-Reynoso, M. A., Gómez-Meda, B. C., & Puebla-Pérez, A. M. (2021). Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population. European review for medical and pharmacological sciences, 25(21), 6454-6464. https://doi.org/10.26355/eurrev_202111_27088
Gallegos-Arreola, M P, et al. "Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population." European review for medical and pharmacological sciences vol. 25,21 (2021): 6454-6464. doi: https://doi.org/10.26355/eurrev_202111_27088
Gallegos-Arreola MP, García Verdín PM, Magaña-Torres MT, Figuera LE, Zúñiga-González GM, Rosales-Reynoso MA, Gómez-Meda BC, Puebla-Pérez AM. Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population. Eur Rev Med Pharmacol Sci. 2021 Nov;25(21):6454-6464. doi: 10.26355/eurrev_202111_27088. PMID: 34787849.
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Predicting Pathogenicity of CDH1 Gene Variants in Patients with Early-onset Diffuse Gastric Cancer from Western Mexico.

Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion

García-Ruvalcaba A, Rizo de la Torre LDC, Magaña-Torres MT, Prado-Montes-de-Oca E, Ruiz-Ramírez AV, Rangel-Villalobos H, Aguilar-Velázquez JA, García-Muro AM, Sánchez-López JY.
PMID: 33465060
Rev Invest Clin. 2021 Jan 19; doi: 10.24875/RIC.20000470. Epub 2021 Jan 19.

BACKGROUND: Early-onset diffuse gastric cancer (EODGC) occurs at or before 50 years of age. Pathogenic mutations and germline deletions in the CDH1 gene (E-cadherin) are well-documented genetic factors associated with the causes of EODGC.OBJECTIVE: The objective of the study...

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García-Ruvalcaba A, Rizo de la Torre LDC, Magaña-Torres MT, et al. Predicting Pathogenicity of CDH1 Gene Variants in Patients with Early-onset Diffuse Gastric Cancer from Western Mexico. Rev Invest Clin. 2021;doi: 10.24875/RIC.20000470.
García-Ruvalcaba, A., Rizo de la Torre, L. D. C., Magaña-Torres, M. T., Prado-Montes-de-Oca, E., Ruiz-Ramírez, A. V., Rangel-Villalobos, H., Aguilar-Velázquez, J. A., García-Muro, A. M., & Sánchez-López, J. Y. (2021). Predicting Pathogenicity of CDH1 Gene Variants in Patients with Early-onset Diffuse Gastric Cancer from Western Mexico. Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion, . https://doi.org/10.24875/RIC.20000470
García-Ruvalcaba, Azaria, et al. "Predicting Pathogenicity of CDH1 Gene Variants in Patients with Early-onset Diffuse Gastric Cancer from Western Mexico." Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion vol. (2021). doi: https://doi.org/10.24875/RIC.20000470
García-Ruvalcaba A, Rizo de la Torre LDC, Magaña-Torres MT, Prado-Montes-de-Oca E, Ruiz-Ramírez AV, Rangel-Villalobos H, Aguilar-Velázquez JA, García-Muro AM, Sánchez-López JY. Predicting Pathogenicity of CDH1 Gene Variants in Patients with Early-onset Diffuse Gastric Cancer from Western Mexico. Rev Invest Clin. 2021 Jan 19; doi: 10.24875/RIC.20000470. Epub 2021 Jan 19. PMID: 33465060.
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Genomic instability in a chronic lymphocytic leukemia patient with mono-allelic deletion of the .

Molecular cytogenetics

Nava-Rodríguez MP, Domínguez-Cruz MD, Aguilar-López LB, Borjas-Gutiérrez C, Magaña-Torres MT, González-García JR.
PMID: 30733830
Mol Cytogenet. 2019 Jan 31;12:2. doi: 10.1186/s13039-019-0417-5. eCollection 2019.

BACKGROUND: The most frequent cytogenetic abnormality detected in chronic lymphocytic leukemia (CLL) patients is the presence of a deletion within the chromosome band 13q14. Deletions can be heterogeneous in size, generally encompassing the CASE PRESENTATION: Cytogenetic and fluorescence in...

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Nava-Rodríguez MP, Domínguez-Cruz MD, Aguilar-López LB, et al. Genomic instability in a chronic lymphocytic leukemia patient with mono-allelic deletion of the . Mol Cytogenet. 2019;12:2doi: 10.1186/s13039-019-0417-5.
Nava-Rodríguez, M. P., Domínguez-Cruz, M. D., Aguilar-López, L. B., Borjas-Gutiérrez, C., Magaña-Torres, M. T., & González-García, J. R. (2019). Genomic instability in a chronic lymphocytic leukemia patient with mono-allelic deletion of the . Molecular cytogenetics, 122. https://doi.org/10.1186/s13039-019-0417-5
Nava-Rodríguez, María Paulina, et al. "Genomic instability in a chronic lymphocytic leukemia patient with mono-allelic deletion of the ." Molecular cytogenetics vol. 12 (2019): 2. doi: https://doi.org/10.1186/s13039-019-0417-5
Nava-Rodríguez MP, Domínguez-Cruz MD, Aguilar-López LB, Borjas-Gutiérrez C, Magaña-Torres MT, González-García JR. Genomic instability in a chronic lymphocytic leukemia patient with mono-allelic deletion of the . Mol Cytogenet. 2019 Jan 31;12:2. doi: 10.1186/s13039-019-0417-5. eCollection 2019. PMID: 30733830; PMCID: PMC6357463.
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Genetic variability in E6, E7 and L1 genes of Human Papillomavirus 62 and its prevalence in Mexico.

Infectious agents and cancer

Artaza-Irigaray C, Flores-Miramontes MG, Olszewski D, Magaña-Torres MT, López-Cardona MG, Leal-Herrera YA, Piña-Sánchez P, Jave-Suárez LF, Aguilar-Lemarroy A.
PMID: 28270859
Infect Agent Cancer. 2017 Mar 04;12:15. doi: 10.1186/s13027-017-0125-x. eCollection 2017.

BACKGROUND: Human papillomavirus (HPV) is the main etiological agent of cervical cancer, the third most common cancer among women globally and the second most frequent in Mexico. Persistent infection with high-risk HPV genotypes is associated with premalignant lesions and...

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Artaza-Irigaray C, Flores-Miramontes MG, Olszewski D, et al. Genetic variability in E6, E7 and L1 genes of Human Papillomavirus 62 and its prevalence in Mexico. Infect Agent Cancer. 2017;12:15doi: 10.1186/s13027-017-0125-x.
Artaza-Irigaray, C., Flores-Miramontes, M. G., Olszewski, D., Magaña-Torres, M. T., López-Cardona, M. G., Leal-Herrera, Y. A., Piña-Sánchez, P., Jave-Suárez, L. F., & Aguilar-Lemarroy, A. (2017). Genetic variability in E6, E7 and L1 genes of Human Papillomavirus 62 and its prevalence in Mexico. Infectious agents and cancer, 1215. https://doi.org/10.1186/s13027-017-0125-x
Artaza-Irigaray, Cristina, et al. "Genetic variability in E6, E7 and L1 genes of Human Papillomavirus 62 and its prevalence in Mexico." Infectious agents and cancer vol. 12 (2017): 15. doi: https://doi.org/10.1186/s13027-017-0125-x
Artaza-Irigaray C, Flores-Miramontes MG, Olszewski D, Magaña-Torres MT, López-Cardona MG, Leal-Herrera YA, Piña-Sánchez P, Jave-Suárez LF, Aguilar-Lemarroy A. Genetic variability in E6, E7 and L1 genes of Human Papillomavirus 62 and its prevalence in Mexico. Infect Agent Cancer. 2017 Mar 04;12:15. doi: 10.1186/s13027-017-0125-x. eCollection 2017. PMID: 28270859; PMCID: PMC5336664.
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Dup-24 bp in the CHIT1 Gene in Six Mexican Amerindian Populations.

JIMD reports

Da Silva-José TD, Juárez-Rendón KJ, Juárez-Osuna JA, Porras-Dorantes A, Valladares-Salgado A, Cruz M, Gonzalez-Ibarra M, Soto AG, Magaña-Torres MT, Sandoval-Ramírez L, García-Ortiz JE.
PMID: 25967229
JIMD Rep. 2015;23:123-7. doi: 10.1007/8904_2015_442. Epub 2015 May 13.

Chitotriosidase (CHIT, EC 3.2.1.14) is an enzyme secreted by activated macrophages with the ability to hydrolyze the chitin of pathogens. The high activity of this enzyme has been used as a secondary biomarker of response to treatment in patients...

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Da Silva-José TD, Juárez-Rendón KJ, Juárez-Osuna JA, et al. Dup-24 bp in the CHIT1 Gene in Six Mexican Amerindian Populations. JIMD Rep. 2015;23:123-7doi: 10.1007/8904_2015_442.
Da Silva-José, T. D., Juárez-Rendón, K. J., Juárez-Osuna, J. A., Porras-Dorantes, A., Valladares-Salgado, A., Cruz, M., Gonzalez-Ibarra, M., Soto, A. G., Magaña-Torres, M. T., Sandoval-Ramírez, L., & García-Ortiz, J. E. (2015). Dup-24 bp in the CHIT1 Gene in Six Mexican Amerindian Populations. JIMD reports, 23123-7. https://doi.org/10.1007/8904_2015_442
Da Silva-José, T D, et al. "Dup-24 bp in the CHIT1 Gene in Six Mexican Amerindian Populations." JIMD reports vol. 23 (2015): 123-7. doi: https://doi.org/10.1007/8904_2015_442
Da Silva-José TD, Juárez-Rendón KJ, Juárez-Osuna JA, Porras-Dorantes A, Valladares-Salgado A, Cruz M, Gonzalez-Ibarra M, Soto AG, Magaña-Torres MT, Sandoval-Ramírez L, García-Ortiz JE. Dup-24 bp in the CHIT1 Gene in Six Mexican Amerindian Populations. JIMD Rep. 2015;23:123-7. doi: 10.1007/8904_2015_442. Epub 2015 May 13. PMID: 25967229; PMCID: PMC4484898.
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Clinical and molecular characterization of Costello syndrome in unrelated Mexican patients.

Clinical dysmorphology

Ríos-González BE, Rodríguez-Ortiz JF, Castro-Martínez AG, Magaña-Torres MT, Barros-Núñez P.
PMID: 34845155
Clin Dysmorphol. 2021 Nov 29; doi: 10.1097/MCD.0000000000000405. Epub 2021 Nov 29.

This study intends to describe for the first time a cohort of Mexican patients with Costello syndrome. The five exons of the HRAS gene were amplified in DNA samples from 13 patients with a clinical suspicion of Costello syndrome....

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Ríos-González BE, Rodríguez-Ortiz JF, Castro-Martínez AG, et al. Clinical and molecular characterization of Costello syndrome in unrelated Mexican patients. Clin Dysmorphol. 2021;doi: 10.1097/MCD.0000000000000405.
Ríos-González, B. E., Rodríguez-Ortiz, J. F., Castro-Martínez, A. G., Magaña-Torres, M. T., & Barros-Núñez, P. (2021). Clinical and molecular characterization of Costello syndrome in unrelated Mexican patients. Clinical dysmorphology, . https://doi.org/10.1097/MCD.0000000000000405
Ríos-González, Blanca E, et al. "Clinical and molecular characterization of Costello syndrome in unrelated Mexican patients." Clinical dysmorphology vol. (2021). doi: https://doi.org/10.1097/MCD.0000000000000405
Ríos-González BE, Rodríguez-Ortiz JF, Castro-Martínez AG, Magaña-Torres MT, Barros-Núñez P. Clinical and molecular characterization of Costello syndrome in unrelated Mexican patients. Clin Dysmorphol. 2021 Nov 29; doi: 10.1097/MCD.0000000000000405. Epub 2021 Nov 29. PMID: 34845155.
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Showing 1 to 9 of 9 entries