Patricia Canto

Summary

Country: Mexico

Publications

  1. ncbi request reprint Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences
    Patricia Canto
    Research Unit in Developmental Biology, Hospital de Pediatria, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Cuauhtemoc Av 330, Col Doctores CP 06725, Mexico, DF, Mexico
    Cancer Genet Cytogenet 150:70-2. 2004
  2. ncbi request reprint Screening for mutations in the SRY gene in patients with mixed gonadal dysgenesis or with Turner syndrome and Y mosaicism
    Patricia Canto
    Research Unit in Developmental Biology, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Hospital de Pediatria, Mexico, D F, Mexico
    Eur J Obstet Gynecol Reprod Biol 115:55-8. 2004
  3. pmc Analysis of polymorphisms in interleukin-10, interleukin-6, and interleukin-1 receptor antagonist in Mexican-Mestizo women with pre-eclampsia
    Elith Yazmin Valencia Villalvazo
    División de Investigación Biomédica, Subdirección de Enseñanza e Investigación, Centro Medico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Mexico, D F, Mexico
    Genet Test Mol Biomarkers 16:1263-9. 2012
  4. doi request reprint Analysis of polymorphisms and haplotypes in genes associated with vascular tone, hypertension and oxidative stress in Mexican-Mestizo women with severe preeclampsia
    Ramón Mauricio Coral-Vázquez
    Seccion de Posgrado, Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico, D F, Mexico Subdirección de Enseñanza e Investigación, Centro Medico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Mexico, D F, Mexico
    Clin Biochem 46:627-32. 2013
  5. doi request reprint Impact of genetic variants of IL-6, IL6R, LRP5, ESR1 and SP7 genes on bone mineral density in postmenopausal Mexican-Mestizo women with obesity
    Juan Pablo Mendez
    Unidad de Investigación en Obesidad, Facultad de Medicina, Universidad Nacional Autonoma de Mexico, Mexico, D F, Mexico Clínica de Obesidad, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico, D F, Mexico
    Gene 528:216-20. 2013
  6. pmc JAG1 and COL1A1 polymorphisms and haplotypes in relation to bone mineral density variations in postmenopausal Mexican-Mestizo Women
    David Rojano-Mejía
    División de Investigación Biomédica, Subdirección de Enseñanza e Investigación, Centro Medico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, San Lorenzo No 502, 2nd piso Col del Valle, Delegacion Benito Juarez, C P 03100, Mexico, D F, Mexico
    Age (Dordr) 35:471-8. 2013
  7. doi request reprint TNFRSF11B gene haplotype and its association with bone mineral density variations in postmenopausal Mexican-Mestizo women
    David Rojano-Mejía
    División de Investigación Biomédica, Subdirección de Enseñanza e Investigación, Centro Medico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Mexico, D F, Mexico
    Maturitas 71:49-54. 2012
  8. ncbi request reprint A novel mutation of the insulin-like 3 gene in patients with cryptorchidism
    Patricia Canto
    Research Unit in Developmental Biology, Hospital de Pediatria, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, D F, Mexico
    J Hum Genet 48:86-90. 2003
  9. ncbi request reprint Screening for mutations in the WNT-4 gene in patients with 46,XX true hermaphroditism
    Patricia Canto
    Research Unit in Developmental Biology, Hospital de Pediatria, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico, DF, Mexico
    Mol Genet Metab 83:341-3. 2004
  10. doi request reprint Molecular analysis of the SRD5A2 in 46,XY subjects with incomplete virilization: the P212R substitution of the steroid 5alpha-reductase 2 may constitute an ancestral founder mutation in Mexican patients
    Felipe Vilchis
    Departamento de Biologia de la Reproduccion, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico, D F, Mexico
    J Androl 31:358-64. 2010

Collaborators

  • Felipe Vilchis
  • Sebastian Carranza-Lira
  • Juan Carlos Zenteno
  • Susana Kofman-Alfaro
  • Guadalupe Aguilar-Madrid
  • Ramón Mauricio Coral-Vázquez
  • David Rojano-Mejía
  • Agustín Coronel
  • Juan Pablo Mendez
  • Samuel Canizales-Quinteros
  • Thelma Canto-Cetina
  • Elith Yazmin Valencia Villalvazo
  • Guillermo López-Medina
  • Rosa María Ordoñez-Razo
  • Josué Joram Castro
  • Juan Fernando Romero Arauz
  • Jaime Hernández Rivera
  • Leticia Cortes Espinosa
  • Roberto Ibarra
  • Ramon M Coral-Vazquez
  • Israel Ramirez-Sanchez
  • Haydee Rosas-Vargas
  • Rocio Juárez-Velázquez
  • Irene Sánchez-Moreno
  • Ruth Soriano
  • Eduardo García-García
  • Marvin Antonio Soriano-Ursúa
  • Pablo Damian-Matsumura
  • Belem Ramírez Regalado
  • María José Casas
  • María C Aguirre-García
  • Javier Pedraza
  • David Rojano Mejía
  • Jesús Benitez-Granados
  • Juan Carlos Falcón
  • Patricia Mendoza-Lorenzo
  • Enrique Méndez-Bolaina
  • María Del Carmen Aguirre García
  • Guillermo Ceballos-Reyes
  • Lucila Polanco Reyes
  • Eleazar Lara-Padilla
  • Carlos Palma-Flores
  • Sandra Romero-Hidalgo
  • Alejandro Zentella-Dehesa
  • Maria C Hernández-Chiu
  • Leticia Cortes-Espinosa
  • Alma Vergara-López
  • Guadalupe Vilchis-Dorantes
  • Fernando Minauro-Sanmiguel
  • Ramon Coral-Vazquez
  • Maricela Rodriguez-Cruz
  • Fabio Salamanca-Gomez
  • Ana Claudia Velázquez Wong
  • Rosenda Peñaloza
  • Maricela Rodríguez
  • Hector Rangel-Villalobos
  • Edgardo Reyes
  • Bulmaro Cisneros
  • Patricia Munguía
  • Mario Bermúdez de León

Detail Information

Publications18

  1. ncbi request reprint Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences
    Patricia Canto
    Research Unit in Developmental Biology, Hospital de Pediatria, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Cuauhtemoc Av 330, Col Doctores CP 06725, Mexico, DF, Mexico
    Cancer Genet Cytogenet 150:70-2. 2004
    ..Because of the high proportion (33%) of gonadal tumors in patients with Y-chromosome sequences found among our patients of mestizo origin, adequate counseling regarding a gonadectomy should be given...
  2. ncbi request reprint Screening for mutations in the SRY gene in patients with mixed gonadal dysgenesis or with Turner syndrome and Y mosaicism
    Patricia Canto
    Research Unit in Developmental Biology, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Hospital de Pediatria, Mexico, D F, Mexico
    Eur J Obstet Gynecol Reprod Biol 115:55-8. 2004
    ..To investigate the presence of mutations in the open reading frame (ORF), as well as on the 5' and 3', flanking regions of the SRY gene in patients with mixed gonadal dysgenesis (MGD) or with Turner syndrome (TS) and Y mosaicism...
  3. pmc Analysis of polymorphisms in interleukin-10, interleukin-6, and interleukin-1 receptor antagonist in Mexican-Mestizo women with pre-eclampsia
    Elith Yazmin Valencia Villalvazo
    División de Investigación Biomédica, Subdirección de Enseñanza e Investigación, Centro Medico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Mexico, D F, Mexico
    Genet Test Mol Biomarkers 16:1263-9. 2012
    ..To our knowledge, this is the first time that these three polymorphisms were analyzed together with gene-gene interaction in women with PE...
  4. doi request reprint Analysis of polymorphisms and haplotypes in genes associated with vascular tone, hypertension and oxidative stress in Mexican-Mestizo women with severe preeclampsia
    Ramón Mauricio Coral-Vázquez
    Seccion de Posgrado, Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico, D F, Mexico Subdirección de Enseñanza e Investigación, Centro Medico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Mexico, D F, Mexico
    Clin Biochem 46:627-32. 2013
    ..We investigated the possible association among three polymorphisms in eNOS (as well their haplotypes): one of MTHFR, one of GSTP1 and one of AGT, with severe preeclampsia in Mexican-Mestizo women...
  5. doi request reprint Impact of genetic variants of IL-6, IL6R, LRP5, ESR1 and SP7 genes on bone mineral density in postmenopausal Mexican-Mestizo women with obesity
    Juan Pablo Mendez
    Unidad de Investigación en Obesidad, Facultad de Medicina, Universidad Nacional Autonoma de Mexico, Mexico, D F, Mexico Clínica de Obesidad, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico, D F, Mexico
    Gene 528:216-20. 2013
    ....
  6. pmc JAG1 and COL1A1 polymorphisms and haplotypes in relation to bone mineral density variations in postmenopausal Mexican-Mestizo Women
    David Rojano-Mejía
    División de Investigación Biomédica, Subdirección de Enseñanza e Investigación, Centro Medico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, San Lorenzo No 502, 2nd piso Col del Valle, Delegacion Benito Juarez, C P 03100, Mexico, D F, Mexico
    Age (Dordr) 35:471-8. 2013
    ..Our results suggest that the rs1800012 polymorphism of the COL1A1, in addition to one haplotype, were significantly associated with BMD variation in Mexican-Mestizo postmenopausal women...
  7. doi request reprint TNFRSF11B gene haplotype and its association with bone mineral density variations in postmenopausal Mexican-Mestizo women
    David Rojano-Mejía
    División de Investigación Biomédica, Subdirección de Enseñanza e Investigación, Centro Medico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Mexico, D F, Mexico
    Maturitas 71:49-54. 2012
    ..The aim of this study was to investigate the possible association among three SNPs of TNFRSF11B and their haplotypes with the presence of BMD variations in postmenopausal Mexican Mestizo women...
  8. ncbi request reprint A novel mutation of the insulin-like 3 gene in patients with cryptorchidism
    Patricia Canto
    Research Unit in Developmental Biology, Hospital de Pediatria, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, D F, Mexico
    J Hum Genet 48:86-90. 2003
    ..This finding provides new evidence that INSL3 is involved in testicular descent in humans; however, mutations of this gene are not a frequent cause of cryptorchidism...
  9. ncbi request reprint Screening for mutations in the WNT-4 gene in patients with 46,XX true hermaphroditism
    Patricia Canto
    Research Unit in Developmental Biology, Hospital de Pediatria, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico, DF, Mexico
    Mol Genet Metab 83:341-3. 2004
    ..Direct sequencing of all five exons demonstrated no mutant alleles in any of the patients. The possibility of the existence of causative mutations in the untranslated regions of WNT-4, or within introns cannot be ruled out...
  10. doi request reprint Molecular analysis of the SRD5A2 in 46,XY subjects with incomplete virilization: the P212R substitution of the steroid 5alpha-reductase 2 may constitute an ancestral founder mutation in Mexican patients
    Felipe Vilchis
    Departamento de Biologia de la Reproduccion, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico, D F, Mexico
    J Androl 31:358-64. 2010
    ..Regarding the frequency of the p.P212R mutation in our population and its presence throughout all of our country, it allows us to hypothesize that the presence of this mutation may constitute a founder gene effect...
  11. doi request reprint DNA binding activity studies and computational approach of mutant SRY in patients with 46, XY complete pure gonadal dysgenesis
    Irene Sánchez-Moreno
    Instituto Mexicano del Seguro Social, Unidad de Investigación Médica en Biología del Desarrollo, Centro Medico Nacional Siglo XXI, Coordinacion de Investigacion en Salud, Mexico, D F, Mexico
    Mol Cell Endocrinol 299:212-8. 2009
    ..In conclusion, we identified two SRY mutations and a polymorphism in two patients with 46,XY complete PGD, demonstrating the importance of the carboxy-terminal region of SRY in DNA binding activity...
  12. doi request reprint Delta-sarcoglycan gene polymorphism frequency in Amerindian and Mestizo populations of Mexico
    Rosa María Ordoñez-Razo
    Unidad de Investigacion Medica en Genetica Humana, Hospital de Pediatria, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico
    Genet Test Mol Biomarkers 14:237-40. 2010
    ..05). These data show that the distribution of the C allele is higher in Mexican populations studied and consequently it is necessary to define if this may be associated with genetic susceptibility for HCM in the Mexican patients...
  13. pmc In Vitro and Molecular Modeling Analysis of Two Mutant Desert Hedgehog Proteins Associated with 46,XY Gonadal Dysgenesis
    Josué Joram Castro
    1 División de Investigación Biomédica, Subdirección de Enseñanza e Investigación, Centro Medico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Mexico, D F, Mexico
    DNA Cell Biol 32:524-30. 2013
    ..Our results suggest that both mutations have a deleterious effect on the expression of the DHH mutant proteins. ..
  14. ncbi request reprint Mutational analysis of the luteinizing hormone receptor gene in two individuals with Leydig cell tumors
    Patricia Canto
    Research Unit in Developmental Biology, Hospital de Pediatria, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico, D F, Mexico
    Am J Med Genet 108:148-52. 2002
    ..Our results confirm the fact that somatic activating mutations of gonadotropin receptors are involved in gonadal tumorigenesis...
  15. doi request reprint Analysis of polymorphisms in genes (AGT, MTHFR, GPIIIa, and GSTP1) associated with hypertension, thrombophilia and oxidative stress in Mestizo and Amerindian populations of México
    Rocio Juárez-Velázquez
    Hospital de Pediatria, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico, D F, Mexico
    Dis Markers 28:323-31. 2010
    ..Our results show the genetic diversity among different Mexican populations and with other racial groups...
  16. doi request reprint Caveolae and non-caveolae lipid raft microdomains of human umbilical vein endothelial cells contain utrophin-associated protein complexes
    Israel Ramirez-Sanchez
    Seccion de Posgrado, Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico, D F, Mexico
    Biochimie 94:1884-90. 2012
    ..Together these results suggest that UAPC located in caveolae and non-caveolae lipid raft domains of HUVECs may have a mechanosensory function that could participate in the control of eNOS activity...
  17. doi request reprint Risk factors and impact on bone mineral density in postmenopausal Mexican mestizo women
    David Rojano-Mejía
    División de Investigación Biomédica, Subdirección de Enseñanza e Investigación, Centro Medico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Mexico, D F, Mexico
    Menopause 18:302-6. 2011
    ..The aim of this study was to analyze several risk factors related to the development of osteoporosis in postmenopausal Mexican mestizo women...
  18. doi request reprint Methylenetetrahydrofolate reductase C677T and glutathione S-transferase P1 A313G are associated with a reduced risk of preeclampsia in Maya-Mestizo women
    Patricia Canto
    Medical Research Unit in Developmental Biology, National Medical Center XXI Century, Instituto Mexicano del Seguro Social, Mexico, DF, Mexico
    Hypertens Res 31:1015-9. 2008
    ..008 and p = 0.013, respectively). Our results suggest, for the first time, that the MTHFR 677T and GSTP1 313G polymorphisms confer a significantly decreased risk of developing preeclampsia in the Mexican Maya-Mestizo population...