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Andrology
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March 30, 2021
Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort
Miriam 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 impairment
Miriam 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 oligozoospermia
Andrea 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 Impairment
Miriam 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 Syndrome
Miriam Cerván-Martín, Lara Bossini-Castillo, Andrea Guzmán-Jimenez, 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 failure
Andrea 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 infertility
Miriam Cerván-Martín, Frank Tüttelmann, Alexandra M Lopes, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 67) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 67 results.
Andrology
|
March 30, 2021
Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort
Miriam 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 impairment
Miriam 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 oligozoospermia
Andrea 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 Impairment
Miriam 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 Syndrome
Miriam Cerván-Martín, Lara Bossini-Castillo, Andrea Guzmán-Jimenez, 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 failure
Andrea 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 infertility
Miriam Cerván-Martín, Frank Tüttelmann, Alexandra M Lopes, et al.
Page
of 7