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A Castilla

Showing results (191-200 of 201) with videos related to

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Plos One|August 2, 2022
Biodegradable microneedle patch for delivery of meloxicam for managing pain in cattleDavid A Castilla-Casadiego, Katherine A Miranda-Muñoz, Jesse L Roberts, et al.
Communications Biology|April 5, 2025
Trans-ethnic GWAS meta-analysis of idiopathic spermatogenic failure highlights the immune-mediated nature of Sertoli cell-only syndromeSara González-Muñoz, Yichen Long, Andrea Guzmán-Jiménez, et al.
Andrology|March 30, 2021
Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohortMiriam Cerván-Martín, Lara Bossini-Castillo, Rocío Rivera-Egea, et al.
Fertility and Sterility|July 22, 2020
Intronic variation of the SOHLH2 gene confers risk to male reproductive impairmentMiriam Cerván-Martín, M Irene Suazo-Sánchez, Rocío Rivera-Egea, et al.
Frontiers in Cell and Developmental Biology|January 2, 2023
Contribution of <i>TEX15</i> genetic variants to the risk of developing severe non-obstructive oligozoospermiaAndrea Guzmán-Jiménez, Sara González-Muñoz, Miriam Cerván-Martín, et al.
Journal of Personalized Medicine|January 1, 2021
Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic ImpairmentMiriam Cerván-Martín, Lara Bossini-Castillo, Rocío Rivera-Egea, et al.
Journal of Personalized Medicine|June 24, 2022
Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only SyndromeMiriam Cerván-Martín, Lara Bossini-Castillo, Andrea Guzmán-Jimenez, et al.
Human Reproduction (Oxford, England)|June 11, 2025
A genetic variant in the 3'-UTR of PIWIL4 confers risk for extreme phenotypes of male infertility by altering miR-215 and miR-136 binding affinitySara González-Muñoz, Miriam Cerván-Martín, Andrea Guzmán-Jiménez, et al.
Human Reproduction Open|December 16, 2024
A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failureAndrea Guzmán-Jiménez, Sara González-Muñoz, Miriam Cerván-Martín, et al.
Communications Biology|November 10, 2022
Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertilityMiriam Cerván-Martín, Frank Tüttelmann, Alexandra M Lopes, et al.
Pageof 21

Showing results (191-200 of 201) with videos related to

Sort By:
Pageof 21
Plos One|August 2, 2022
Biodegradable microneedle patch for delivery of meloxicam for managing pain in cattleDavid A Castilla-Casadiego, Katherine A Miranda-Muñoz, Jesse L Roberts, et al.
Communications Biology|April 5, 2025
Trans-ethnic GWAS meta-analysis of idiopathic spermatogenic failure highlights the immune-mediated nature of Sertoli cell-only syndromeSara González-Muñoz, Yichen Long, Andrea Guzmán-Jiménez, et al.
Andrology|March 30, 2021
Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohortMiriam Cerván-Martín, Lara Bossini-Castillo, Rocío Rivera-Egea, et al.
Fertility and Sterility|July 22, 2020
Intronic variation of the SOHLH2 gene confers risk to male reproductive impairmentMiriam Cerván-Martín, M Irene Suazo-Sánchez, Rocío Rivera-Egea, et al.
Frontiers in Cell and Developmental Biology|January 2, 2023
Contribution of <i>TEX15</i> genetic variants to the risk of developing severe non-obstructive oligozoospermiaAndrea Guzmán-Jiménez, Sara González-Muñoz, Miriam Cerván-Martín, et al.
Journal of Personalized Medicine|January 1, 2021
Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic ImpairmentMiriam Cerván-Martín, Lara Bossini-Castillo, Rocío Rivera-Egea, et al.
Journal of Personalized Medicine|June 24, 2022
Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only SyndromeMiriam Cerván-Martín, Lara Bossini-Castillo, Andrea Guzmán-Jimenez, et al.
Human Reproduction (Oxford, England)|June 11, 2025
A genetic variant in the 3'-UTR of PIWIL4 confers risk for extreme phenotypes of male infertility by altering miR-215 and miR-136 binding affinitySara González-Muñoz, Miriam Cerván-Martín, Andrea Guzmán-Jiménez, et al.
Human Reproduction Open|December 16, 2024
A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failureAndrea Guzmán-Jiménez, Sara González-Muñoz, Miriam Cerván-Martín, et al.
Communications Biology|November 10, 2022
Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertilityMiriam Cerván-Martín, Frank Tüttelmann, Alexandra M Lopes, et al.
Pageof 21