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Momori Katsumi

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

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Cytogenetic and Genome Research|April 9, 2018
Somatically Acquired Isodicentric Y and Mosaic Loss of Chromosome Y in a Boy with HypospadiasMami Miyado, Koji Muroya, Momori Katsumi, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 21, 2015
SOX3 Overdosage Permits Normal Sex Development in Females with Random X InactivationMaki Igarashi, Hitoshi Mikami, Momori Katsumi, et al.
Scientific Reports|October 6, 2015
Parturition failure in mice lacking Mamld1Mami Miyado, Kenji Miyado, Momori Katsumi, et al.
Reproductive Medicine and Biology|April 11, 2020
Copy-number analysis of Y-linked loci in young men with non-obstructive azoospermia: Implications for the rarity of early onset mosaic loss of chromosome YErina Suzuki, Yoshitomo Kobori, Momori Katsumi, et al.
International Journal of Molecular Sciences|June 21, 2017
Knockout of Murine Mamld1 Impairs Testicular Growth and Daily Sperm Production but Permits Normal Postnatal Androgen Production and FertilityMami Miyado, Kaoru Yoshida, Kenji Miyado, et al.
Journal of Human Genetics|June 5, 2015
Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short statureMaki Fukami, Yasuhiro Naiki, Koji Muroya, et al.
Journal of Human Genetics|January 9, 2015
Copy-number variations in Y-chromosomal azoospermia factor regions identified by multiplex ligation-dependent probe amplificationKazuki Saito, Mami Miyado, Yoshitomo Kobori, et al.
Cytogenetic and Genome Research|March 14, 2015
Microhomology-mediated microduplication in the y chromosomal azoospermia factor a region in a male with mild asthenozoospermiaMomori Katsumi, Hiromichi Ishikawa, Yoko Tanaka, et al.
Journal of Cellular and Molecular Medicine|March 25, 2017
Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early pubertyMaki Fukami, Erina Suzuki, Yoko Izumi, et al.
Human Mutation|March 24, 2018
STX2 is a causative gene for nonobstructive azoospermiaShigeru Nakamura, Yoshitomo Kobori, Yoshihiko Ueda, et al.
Pageof 1

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

Sort By:
Pageof 1
Cytogenetic and Genome Research|April 9, 2018
Somatically Acquired Isodicentric Y and Mosaic Loss of Chromosome Y in a Boy with HypospadiasMami Miyado, Koji Muroya, Momori Katsumi, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 21, 2015
SOX3 Overdosage Permits Normal Sex Development in Females with Random X InactivationMaki Igarashi, Hitoshi Mikami, Momori Katsumi, et al.
Scientific Reports|October 6, 2015
Parturition failure in mice lacking Mamld1Mami Miyado, Kenji Miyado, Momori Katsumi, et al.
Reproductive Medicine and Biology|April 11, 2020
Copy-number analysis of Y-linked loci in young men with non-obstructive azoospermia: Implications for the rarity of early onset mosaic loss of chromosome YErina Suzuki, Yoshitomo Kobori, Momori Katsumi, et al.
International Journal of Molecular Sciences|June 21, 2017
Knockout of Murine Mamld1 Impairs Testicular Growth and Daily Sperm Production but Permits Normal Postnatal Androgen Production and FertilityMami Miyado, Kaoru Yoshida, Kenji Miyado, et al.
Journal of Human Genetics|June 5, 2015
Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short statureMaki Fukami, Yasuhiro Naiki, Koji Muroya, et al.
Journal of Human Genetics|January 9, 2015
Copy-number variations in Y-chromosomal azoospermia factor regions identified by multiplex ligation-dependent probe amplificationKazuki Saito, Mami Miyado, Yoshitomo Kobori, et al.
Cytogenetic and Genome Research|March 14, 2015
Microhomology-mediated microduplication in the y chromosomal azoospermia factor a region in a male with mild asthenozoospermiaMomori Katsumi, Hiromichi Ishikawa, Yoko Tanaka, et al.
Journal of Cellular and Molecular Medicine|March 25, 2017
Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early pubertyMaki Fukami, Erina Suzuki, Yoko Izumi, et al.
Human Mutation|March 24, 2018
STX2 is a causative gene for nonobstructive azoospermiaShigeru Nakamura, Yoshitomo Kobori, Yoshihiko Ueda, et al.
Pageof 1