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American Journal of Human Genetics
|
July 17, 2020
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility
Margot J Wyrwoll, Şehime G Temel, Liina Nagirnaja, 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 (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 affinity
Sara 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 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.
Nature Communications
|
December 26, 2022
Diverse monogenic subforms of human spermatogenic failure
Liina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, et al.
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of 5
Search research articles
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Showing results (41-50 of 47) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 47 results.
American Journal of Human Genetics
|
July 17, 2020
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility
Margot J Wyrwoll, Şehime G Temel, Liina Nagirnaja, 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 (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 affinity
Sara 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 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.
Nature Communications
|
December 26, 2022
Diverse monogenic subforms of human spermatogenic failure
Liina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, et al.
Page
of 5