Katsumi M - Search Results

1

Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations.

Nakamura S, Miyado M, Saito K, Katsumi M, Nakamura A, Kobori Y, Tanaka Y, Ishikawa H, Yoshida A, Okada H, Hata K, Nakabayashi K, Okamura K, Ogata H, Matsubara Y, Ogata T, Nakai H, Fukami M. Nakamura S, et al. Among authors: katsumi m. Andrology. 2017 Jul;5(4):824-831. doi: 10.1111/andr.12378. Andrology. 2017. PMID: 28718531 Free article.

2

Copy-number variations in Y-chromosomal azoospermia factor regions identified by multiplex ligation-dependent probe amplification.

Saito K, Miyado M, Kobori Y, Tanaka Y, Ishikawa H, Yoshida A, Katsumi M, Saito H, Kubota T, Okada H, Ogata T, Fukami M. Saito K, et al. Among authors: katsumi m. J Hum Genet. 2015 Mar;60(3):127-31. doi: 10.1038/jhg.2014.115. Epub 2015 Jan 8. J Hum Genet. 2015. PMID: 25566757

3

Microhomology-mediated microduplication in the y chromosomal azoospermia factor a region in a male with mild asthenozoospermia.

Katsumi M, Ishikawa H, Tanaka Y, Saito K, Kobori Y, Okada H, Saito H, Nakabayashi K, Matsubara Y, Ogata T, Fukami M, Miyado M. Katsumi M, et al. Cytogenet Genome Res. 2014;144(4):285-9. doi: 10.1159/000377649. Epub 2015 Mar 6. Cytogenet Genome Res. 2014. PMID: 25765000

4

SOX3 Overdosage Permits Normal Sex Development in Females with Random X Inactivation.

Igarashi M, Mikami H, Katsumi M, Miyado M, Izumi Y, Ogata T, Fukami M. Igarashi M, et al. Among authors: katsumi m. Sex Dev. 2015;9(3):125-9. doi: 10.1159/000377653. Epub 2015 Mar 17. Sex Dev. 2015. PMID: 25791725

5

Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early puberty.

Fukami M, Suzuki E, Izumi Y, Torii T, Narumi S, Igarashi M, Miyado M, Katsumi M, Fujisawa Y, Nakabayashi K, Hata K, Umezawa A, Matsubara Y, Yamauchi J, Ogata T. Fukami M, et al. Among authors: katsumi m. J Cell Mol Med. 2017 Oct;21(10):2623-2626. doi: 10.1111/jcmm.13146. Epub 2017 Mar 24. J Cell Mol Med. 2017. PMID: 28338294 Free PMC article.

6

STX2 is a causative gene for nonobstructive azoospermia.

Nakamura S, Kobori Y, Ueda Y, Tanaka Y, Ishikawa H, Yoshida A, Katsumi M, Saito K, Nakamura A, Ogata T, Okada H, Nakai H, Miyado M, Fukami M. Nakamura S, et al. Among authors: katsumi m. Hum Mutat. 2018 Jun;39(6):830-833. doi: 10.1002/humu.23423. Epub 2018 Apr 10. Hum Mutat. 2018. PMID: 29570232

7

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 Y.

Suzuki E, Kobori Y, Katsumi M, Ushijima K, Uchiyama T, Okada H, Miyado M, Fukami M. Suzuki E, et al. Among authors: katsumi m. Reprod Med Biol. 2020 Mar 2;19(2):178-181. doi: 10.1002/rmb2.12321. eCollection 2020 Apr. Reprod Med Biol. 2020. PMID: 32273824 Free PMC article.

8

Knockout of Murine Mamld1 Impairs Testicular Growth and Daily Sperm Production but Permits Normal Postnatal Androgen Production and Fertility.

Miyado M, Yoshida K, Miyado K, Katsumi M, Saito K, Nakamura S, Ogata T, Fukami M. Miyado M, et al. Among authors: katsumi m. Int J Mol Sci. 2017 Jun 19;18(6):1300. doi: 10.3390/ijms18061300. Int J Mol Sci. 2017. PMID: 28629181 Free PMC article.

9

Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short stature.

Fukami M, Naiki Y, Muroya K, Hamajima T, Soneda S, Horikawa R, Jinno T, Katsumi M, Nakamura A, Asakura Y, Adachi M, Ogata T, Kanzaki S; Japanese SHOX study group. Fukami M, et al. Among authors: katsumi m. J Hum Genet. 2015 Sep;60(9):553-6. doi: 10.1038/jhg.2015.53. Epub 2015 Jun 4. J Hum Genet. 2015. PMID: 26040210

10

Parturition failure in mice lacking Mamld1.

Miyado M, Miyado K, Katsumi M, Saito K, Nakamura A, Shihara D, Ogata T, Fukami M. Miyado M, et al. Among authors: katsumi m. Sci Rep. 2015 Oct 5;5:14705. doi: 10.1038/srep14705. Sci Rep. 2015. PMID: 26435405 Free PMC article.

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