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Kristjan Pomm

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Journal of Clinical Pathology|April 8, 2026
Morphological heterogeneity in testicular biopsies of infertile azoospermic men: the necessity of bilateral sampling and standardised reportingErik Tamp, Georgi Dzaparidze, Kristjan Pomm
International Journal of Molecular Sciences|December 24, 2021
<i>Mycoplasma genitalium</i> Provokes Seminal Inflammation among Infertile MalesStanislav Tjagur, Reet Mändar, Olev Poolamets, et al.
Asian Journal of Andrology|June 23, 2026
The long (GGN)n repeat tract in the androgen receptor gene exerts a negative effect on quantitative sperm parametersKristel Ehala-Aleksejev, Triin Kikas, Marina Grigorova, et al.
Human Reproduction (Oxford, England)|December 3, 2025
Microdeletion and microduplication syndromes, including recurrent rearrangements at 16p11.2 and 22q11.21, are enriched in unexplained male infertilityTriin Kikas, Avirup Dutta, Rain Inno, et al.
Human Reproduction Open|March 10, 2025
Significantly increased load of hereditary cancer-linked germline variants in infertile menAnu Valkna, Anna-Grete Juchnewitsch, Lisanna Põlluaas, et al.
Scientific Reports|January 11, 2023
Microdeletions and microduplications linked to severe congenital disorders in infertile menTriin Kikas, Anna Maria Punab, Laura Kasak, et al.
Elife|March 30, 2021
A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humansPille Hallast, Laura Kibena, Margus Punab, et al.
American Journal of Human Genetics|April 13, 2024
Toward clinical exomes in diagnostics and management of male infertilityKristiina Lillepea, Anna-Grete Juchnewitsch, Laura Kasak, et al.
Human Molecular Genetics|January 8, 2025
Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertilityTihana Marić, Helen Castillo-Madeen, Monika Logara Klarić, et al.
Frontiers in Endocrinology|April 24, 2024
Undiagnosed RASopathies in infertile menAnna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Journal of Clinical Pathology|April 8, 2026
Morphological heterogeneity in testicular biopsies of infertile azoospermic men: the necessity of bilateral sampling and standardised reportingErik Tamp, Georgi Dzaparidze, Kristjan Pomm
International Journal of Molecular Sciences|December 24, 2021
<i>Mycoplasma genitalium</i> Provokes Seminal Inflammation among Infertile MalesStanislav Tjagur, Reet Mändar, Olev Poolamets, et al.
Asian Journal of Andrology|June 23, 2026
The long (GGN)n repeat tract in the androgen receptor gene exerts a negative effect on quantitative sperm parametersKristel Ehala-Aleksejev, Triin Kikas, Marina Grigorova, et al.
Human Reproduction (Oxford, England)|December 3, 2025
Microdeletion and microduplication syndromes, including recurrent rearrangements at 16p11.2 and 22q11.21, are enriched in unexplained male infertilityTriin Kikas, Avirup Dutta, Rain Inno, et al.
Human Reproduction Open|March 10, 2025
Significantly increased load of hereditary cancer-linked germline variants in infertile menAnu Valkna, Anna-Grete Juchnewitsch, Lisanna Põlluaas, et al.
Scientific Reports|January 11, 2023
Microdeletions and microduplications linked to severe congenital disorders in infertile menTriin Kikas, Anna Maria Punab, Laura Kasak, et al.
Elife|March 30, 2021
A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humansPille Hallast, Laura Kibena, Margus Punab, et al.
American Journal of Human Genetics|April 13, 2024
Toward clinical exomes in diagnostics and management of male infertilityKristiina Lillepea, Anna-Grete Juchnewitsch, Laura Kasak, et al.
Human Molecular Genetics|January 8, 2025
Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertilityTihana Marić, Helen Castillo-Madeen, Monika Logara Klarić, et al.
Frontiers in Endocrinology|April 24, 2024
Undiagnosed RASopathies in infertile menAnna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Pageof 1