Miyamoto T - Search Results

1

Male infertility and its causes in human.

Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Sengoku K. Miyamoto T, et al. Adv Urol. 2012;2012:384520. doi: 10.1155/2012/384520. Epub 2011 Oct 20. Adv Urol. 2012. PMID: 22046184 Free PMC article.

2

Current concepts of human azoospermia and its causes.

Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Sato H, Namiki M, Sengoku K. Miyamoto T, et al. Reprod Med Biol. 2010 Jun 16;9(3):121-127. doi: 10.1007/s12522-010-0054-5. eCollection 2010 Sep. Reprod Med Biol. 2010. PMID: 29699334 Free PMC article. Review.

3

A single nucleotide polymorphism in SPATA17 may be a genetic risk factor for Japanese patients with meiotic arrest.

Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Sakugawa N, Miyakawa H, Sato H, Namiki M, Okuyama A, Sengoku K. Miyamoto T, et al. Asian J Androl. 2009 Sep;11(5):623-8. doi: 10.1038/aja.2009.30. Epub 2009 Jun 1. Asian J Androl. 2009. PMID: 19483714 Free PMC article.

4

LMTK2 and PARP-2 gene polymorphism and azoospermia secondary to meiotic arrest.

Sakugawa N, Miyamoto T, Tsujimura A, Koh E, Miyagawa Y, Sato H, Namiki M, Okuyama A, Sengoku K. Sakugawa N, et al. Among authors: miyamoto t. J Assist Reprod Genet. 2009 Sep-Oct;26(9-10):545-52. doi: 10.1007/s10815-009-9347-1. Epub 2009 Oct 6. J Assist Reprod Genet. 2009. PMID: 19806447 Free PMC article.

5

Single nucleotide polymorphism in the UBR2 gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest.

Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Horikawa M, Saijo Y, Sengoku K. Miyamoto T, et al. J Assist Reprod Genet. 2011 Aug;28(8):743-6. doi: 10.1007/s10815-011-9576-y. Epub 2011 May 4. J Assist Reprod Genet. 2011. PMID: 21573678 Free PMC article.

6

Single-nucleotide polymorphisms in the SEPTIN12 gene may be a genetic risk factor for Japanese patients with Sertoli cell-only syndrome.

Miyakawa H, Miyamoto T, Koh E, Tsujimura A, Miyagawa Y, Saijo Y, Namiki M, Sengoku K. Miyakawa H, et al. Among authors: miyamoto t. J Androl. 2012 May-Jun;33(3):483-7. doi: 10.2164/jandrol.110.012146. Epub 2011 Jun 2. J Androl. 2012. PMID: 21636737

7

Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men.

Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Horikawa M, Saijo Y, Sengoku K. Miyamoto T, et al. J Assist Reprod Genet. 2012 Jan;29(1):47-51. doi: 10.1007/s10815-011-9679-5. Epub 2011 Nov 25. J Assist Reprod Genet. 2012. PMID: 22116646 Free PMC article.

8

Single-nucleotide polymorphisms in HORMAD1 may be a risk factor for azoospermia caused by meiotic arrest in Japanese patients.

Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Horikawa M, Saijo Y, Sengoku K. Miyamoto T, et al. Asian J Androl. 2012 Jul;14(4):580-3. doi: 10.1038/aja.2011.180. Epub 2012 Mar 12. Asian J Androl. 2012. PMID: 22407170 Free PMC article.

9

Male infertility and its genetic causes.

Miyamoto T, Minase G, Okabe K, Ueda H, Sengoku K. Miyamoto T, et al. J Obstet Gynaecol Res. 2015 Oct;41(10):1501-5. doi: 10.1111/jog.12765. Epub 2015 Jul 14. J Obstet Gynaecol Res. 2015. PMID: 26178295 Review.

10

Single-nucleotide polymorphisms in the human RAD21L gene may be a genetic risk factor for Japanese patients with azoospermia caused by meiotic arrest and Sertoli cell-only syndrome.

Minase G, Miyamoto T, Miyagawa Y, Iijima M, Ueda H, Saijo Y, Namiki M, Sengoku K. Minase G, et al. Among authors: miyamoto t. Hum Fertil (Camb). 2017 Sep;20(3):217-220. doi: 10.1080/14647273.2017.1292004. Epub 2017 Feb 21. Hum Fertil (Camb). 2017. PMID: 28635411

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