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Showing results (351-360 of 376) with videos related to

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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.
Journal of Vascular Surgery. Venous and Lymphatic Disorders|July 16, 2021
Surgical resection and graft replacement for primary inferior vena cava leiomyosarcoma: A multicenter experienceMichael Nooromid, Randall De Martino, Francesco Squizzato, et al.
Plos Genetics|April 5, 2013
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1Alexandra M Lopes, Kenneth I Aston, Emma Thompson, et al.
American Journal of Human Genetics|September 23, 2022
The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humansMargot J Wyrwoll, Channah M Gaasbeek, Ieva Golubickaite, et al.
Human Genetics|May 8, 2021
Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failureJimmaline J Hardy, Margot J Wyrwoll, William Mcfadden, et al.
Frontiers in Endocrinology|April 24, 2024
Undiagnosed RASopathies in infertile menAnna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Nature|October 13, 2017
Dynamic landscape and regulation of RNA editing in mammalsMeng How Tan, Qin Li, Raghuvaran Shanmugam, et al.
Nature Communications|August 9, 2024
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertilityBirgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, et al.
Human Molecular Genetics|July 23, 2015
Low-frequency germline variants across 6p22.2-6p21.33 are associated with non-obstructive azoospermia in Han Chinese menBixian Ni, Yuan Lin, Liangdan Sun, et al.
Nature|April 25, 2014
Guidelines for investigating causality of sequence variants in human diseaseD G MacArthur, T A Manolio, D P Dimmock, et al.
Pageof 38

Showing results (351-360 of 376) with videos related to

Sort By:
Pageof 38
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.
Journal of Vascular Surgery. Venous and Lymphatic Disorders|July 16, 2021
Surgical resection and graft replacement for primary inferior vena cava leiomyosarcoma: A multicenter experienceMichael Nooromid, Randall De Martino, Francesco Squizzato, et al.
Plos Genetics|April 5, 2013
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1Alexandra M Lopes, Kenneth I Aston, Emma Thompson, et al.
American Journal of Human Genetics|September 23, 2022
The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humansMargot J Wyrwoll, Channah M Gaasbeek, Ieva Golubickaite, et al.
Human Genetics|May 8, 2021
Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failureJimmaline J Hardy, Margot J Wyrwoll, William Mcfadden, et al.
Frontiers in Endocrinology|April 24, 2024
Undiagnosed RASopathies in infertile menAnna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Nature|October 13, 2017
Dynamic landscape and regulation of RNA editing in mammalsMeng How Tan, Qin Li, Raghuvaran Shanmugam, et al.
Nature Communications|August 9, 2024
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertilityBirgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, et al.
Human Molecular Genetics|July 23, 2015
Low-frequency germline variants across 6p22.2-6p21.33 are associated with non-obstructive azoospermia in Han Chinese menBixian Ni, Yuan Lin, Liangdan Sun, et al.
Nature|April 25, 2014
Guidelines for investigating causality of sequence variants in human diseaseD G MacArthur, T A Manolio, D P Dimmock, et al.
Pageof 38