Miyamoto T - Search Results

1

A family of oculofaciocardiodental syndrome (OFCD) with a novel BCOR mutation and genomic rearrangements involving NHS.

Kondo Y, Saitsu H, Miyamoto T, Nishiyama K, Tsurusaki Y, Doi H, Miyake N, Ryoo NK, Kim JH, Yu YS, Matsumoto N. Kondo Y, et al. Among authors: miyamoto t. J Hum Genet. 2012 Mar;57(3):197-201. doi: 10.1038/jhg.2012.4. Epub 2012 Feb 2. J Hum Genet. 2012. PMID: 22301464

2

Pathogenic mutations in two families with congenital cataract identified with whole-exome sequencing.

Kondo Y, Saitsu H, Miyamoto T, Lee BJ, Nishiyama K, Nakashima M, Tsurusaki Y, Doi H, Miyake N, Kim JH, Yu YS, Matsumoto N. Kondo Y, et al. Among authors: miyamoto t. Mol Vis. 2013;19:384-9. Epub 2013 Feb 18. Mol Vis. 2013. PMID: 23441109 Free PMC article.

3

An atypical case of SPG56/CYP2U1-related spastic paraplegia presenting with delayed myelination.

Minase G, Miyatake S, Nabatame S, Arai H, Koshimizu E, Mizuguchi T, Nakashima M, Miyake N, Saitsu H, Miyamoto T, Sengoku K, Matsumoto N. Minase G, et al. Among authors: miyamoto t. J Hum Genet. 2017 Nov;62(11):997-1000. doi: 10.1038/jhg.2017.77. Epub 2017 Jul 20. J Hum Genet. 2017. PMID: 28725025

4

Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest.

Sato H, Miyamoto T, Yogev L, Namiki M, Koh E, Hayashi H, Sasaki Y, Ishikawa M, Lamb DJ, Matsumoto N, Birk OS, Niikawa N, Sengoku K. Sato H, et al. Among authors: miyamoto t. J Hum Genet. 2006;51(6):533-540. doi: 10.1007/s10038-006-0394-5. Epub 2006 May 9. J Hum Genet. 2006. PMID: 16683055

5

Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract.

Miyamoto T, Yu YS, Sato H, Hayashi H, Sakugawa N, Ishikawa M, Sengoku K. Miyamoto T, et al. Turk J Pediatr. 2007 Jul-Sep;49(3):334-6. Turk J Pediatr. 2007. PMID: 17990594

6

The human ASCL2 gene escaping genomic imprinting and its expression pattern.

Miyamoto T, Hasuike S, Jinno Y, Soejima H, Yun K, Miura K, Ishikawa M, Niikawa N. Miyamoto T, et al. J Assist Reprod Genet. 2002 May;19(5):240-4. doi: 10.1023/a:1015362903486. J Assist Reprod Genet. 2002. PMID: 12099555 Free PMC article.

7

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 Free article.

8

Azoospermia in patients heterozygous for a mutation in SYCP3.

Miyamoto T, Hasuike S, Yogev L, Maduro MR, Ishikawa M, Westphal H, Lamb DJ. Miyamoto T, et al. Lancet. 2003 Nov 22;362(9397):1714-9. doi: 10.1016/S0140-6736(03)14845-3. Lancet. 2003. PMID: 14643120

9

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.

10

Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest.

Miyamoto T, Koh E, Sakugawa N, Sato H, Hayashi H, Namiki M, Sengoku K. Miyamoto T, et al. J Assist Reprod Genet. 2008 Nov-Dec;25(11-12):553-7. doi: 10.1007/s10815-008-9270-x. Epub 2008 Oct 22. J Assist Reprod Genet. 2008. PMID: 18941885 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

4,202 results

Search Page

Filters