Research Topics
Genomes and Genes | Patricia CantoSummaryCountry: Mexico Publications
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Publications
Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequencesPatricia Canto
Research Unit in Developmental Biology, , , Instituto Mexicano del Seguro Social, Cuauhtemoc Av 330, Col Doctores CP 06725, , DF,
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...- Screening for mutations in the SRY gene in patients with mixed gonadal dysgenesis or with Turner syndrome and Y mosaicismPatricia 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... 
TNFRSF11B gene haplotype and its association with bone mineral density variations in postmenopausal Mexican-Mestizo womenDavid 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...- A novel mutation of the insulin-like 3 gene in patients with cryptorchidismPatricia 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... 
Analysis of polymorphisms in interleukin-10, interleukin-6, and interleukin-1 receptor antagonist in Mexican-Mestizo women with pre-eclampsiaElith 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...- 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 patientsFelipe 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... - DNA binding activity studies and computational approach of mutant SRY in patients with 46, XY complete pure gonadal dysgenesisIrene 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... - Screening for mutations in the WNT-4 gene in patients with 46,XX true hermaphroditismPatricia 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... - Delta-sarcoglycan gene polymorphism frequency in Amerindian and Mestizo populations of MexicoRosa 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... - Mutational analysis of the luteinizing hormone receptor gene in two individuals with Leydig cell tumorsPatricia 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... - Analysis of polymorphisms in genes (AGT, MTHFR, GPIIIa, and GSTP1) associated with hypertension, thrombophilia and oxidative stress in Mestizo and Amerindian populations of MéxicoRocio 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... - Caveolae and non-caveolae lipid raft microdomains of human umbilical vein endothelial cells contain utrophin-associated protein complexesIsrael 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... - Risk factors and impact on bone mineral density in postmenopausal Mexican mestizo womenDavid 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... - Methylenetetrahydrofolate reductase C677T and glutathione S-transferase P1 A313G are associated with a reduced risk of preeclampsia in Maya-Mestizo womenPatricia 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...