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A Cuevas

Showing results (81-90 of 268) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 1, 1995
The biochemical identification of carrier state in mothers of sporadic cases of X-linked recessive ichthyosisS A Cuevas-Covarrubias, S Kofman-Alfaro, E Orozco Orozco, et al.
Biomed Research International|May 7, 2015
β-Catenin-Dependent Signaling Pathway Contributes to Renal Fibrosis in Hypertensive RatsCatherina A Cuevas, Cheril Tapia-Rojas, Carlos Cespedes, et al.
Archivos Espanoles De Urologia|October 14, 2014
Ischaemic priapism as a presentation of chronic myeloid leukaemiaJ F Villegas Osorio, C Corchuelo Maíllo, A Cuevas Palomino, et al.
Molecular Syndromology|May 20, 2016
A Family with Craniofrontonasal Syndrome and a Mutation (p.G151S) in the EFNB1 Gene: Expanding the PhenotypeJaime Toral-López, Luz M González-Huerta, Olga Messina Baas, et al.
Biomed Research International|November 3, 2016
Corrigendum to "<i>β</i>-Catenin-Dependent Signaling Pathway Contributes to Renal Fibrosis in Hypertensive Rats"Catherina A Cuevas, Cheril Tapia-Rojas, Carlos Cespedes, et al.
American Journal of Physiology. Renal Physiology|May 25, 2012
Prostaglandin E2 EP3 receptor regulates cyclooxygenase-2 expression in the kidneyCarlos P Vio, Mariana Quiroz-Munoz, Catherina A Cuevas, et al.
The Journal of Investigative Dermatology|February 26, 2000
Mutation report: a novel partial deletion of exons 2-10 of the STS gene in recessive X-linked ichthyosisM Valdes-Flores, S H Kofman-Alfaro, A L Vaca, et al.
World Journal of Clinical Cases|December 3, 2020
Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case reportJaime Toral-Lopez, Luz María González Huerta, Olga Messina-Baas, et al.
Biochemistry and Molecular Biology International|July 1, 1993
Comparative analysis of human steroid sulfatase activity in prepubertal and postpubertal males and femalesS A Cuevas-Covarrubias, M A Juárez-Oropeza, R Miranda-Zamora, et al.
Annales De Genetique|January 1, 1979
Malformed genitalia in the 47,XYY genotypeH Rivera, A Hernandez, R Martinez y Martinez, et al.
Pageof 27

Showing results (81-90 of 268) with videos related to

Sort By:
Pageof 27
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
The biochemical identification of carrier state in mothers of sporadic cases of X-linked recessive ichthyosisS A Cuevas-Covarrubias, S Kofman-Alfaro, E Orozco Orozco, et al.
Biomed Research International|May 7, 2015
β-Catenin-Dependent Signaling Pathway Contributes to Renal Fibrosis in Hypertensive RatsCatherina A Cuevas, Cheril Tapia-Rojas, Carlos Cespedes, et al.
Archivos Espanoles De Urologia|October 14, 2014
Ischaemic priapism as a presentation of chronic myeloid leukaemiaJ F Villegas Osorio, C Corchuelo Maíllo, A Cuevas Palomino, et al.
Molecular Syndromology|May 20, 2016
A Family with Craniofrontonasal Syndrome and a Mutation (p.G151S) in the EFNB1 Gene: Expanding the PhenotypeJaime Toral-López, Luz M González-Huerta, Olga Messina Baas, et al.
Biomed Research International|November 3, 2016
Corrigendum to "<i>β</i>-Catenin-Dependent Signaling Pathway Contributes to Renal Fibrosis in Hypertensive Rats"Catherina A Cuevas, Cheril Tapia-Rojas, Carlos Cespedes, et al.
American Journal of Physiology. Renal Physiology|May 25, 2012
Prostaglandin E2 EP3 receptor regulates cyclooxygenase-2 expression in the kidneyCarlos P Vio, Mariana Quiroz-Munoz, Catherina A Cuevas, et al.
The Journal of Investigative Dermatology|February 26, 2000
Mutation report: a novel partial deletion of exons 2-10 of the STS gene in recessive X-linked ichthyosisM Valdes-Flores, S H Kofman-Alfaro, A L Vaca, et al.
World Journal of Clinical Cases|December 3, 2020
Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case reportJaime Toral-Lopez, Luz María González Huerta, Olga Messina-Baas, et al.
Biochemistry and Molecular Biology International|July 1, 1993
Comparative analysis of human steroid sulfatase activity in prepubertal and postpubertal males and femalesS A Cuevas-Covarrubias, M A Juárez-Oropeza, R Miranda-Zamora, et al.
Annales De Genetique|January 1, 1979
Malformed genitalia in the 47,XYY genotypeH Rivera, A Hernandez, R Martinez y Martinez, et al.
Pageof 27