Tsutsumi M - Search Results

1

Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome.

Tsuge I, Morishita M, Kato T, Tsutsumi M, Inagaki H, Mori Y, Yamawaki K, Inuo C, Ieda K, Ohye T, Hayakawa A, Kurahashi H. Tsuge I, et al. Among authors: tsutsumi m. Hum Genome Var. 2015 Feb 12;2:15003. doi: 10.1038/hgv.2015.3. eCollection 2015. Hum Genome Var. 2015. PMID: 27081519 Free PMC article.

2

An identification of the HLA-F null allele in Japanese.

Uchigiri C, Mizuno S, Wada K, Tsutsumi M, Kato T, Kamiya T, Ozawa K. Uchigiri C, et al. Among authors: tsutsumi m. Immunogenetics. 1997;45(6):466-7. doi: 10.1007/s002510050236. Immunogenetics. 1997. PMID: 9089112 No abstract available.

3

Mutations of the SYCP3 gene in women with recurrent pregnancy loss.

Bolor H, Mori T, Nishiyama S, Ito Y, Hosoba E, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Kato T, Tong M, Nishizawa H, Pryor-Koishi K, Kitaoka E, Sawada T, Nishiyama Y, Udagawa Y, Kurahashi H. Bolor H, et al. Among authors: tsutsumi m. Am J Hum Genet. 2009 Jan;84(1):14-20. doi: 10.1016/j.ajhg.2008.12.002. Epub 2008 Dec 24. Am J Hum Genet. 2009. PMID: 19110213 Free PMC article.

4

Recent advance in our understanding of the molecular nature of chromosomal abnormalities.

Kurahashi H, Bolor H, Kato T, Kogo H, Tsutsumi M, Inagaki H, Ohye T. Kurahashi H, et al. Among authors: tsutsumi m. J Hum Genet. 2009 May;54(5):253-60. doi: 10.1038/jhg.2009.35. Epub 2009 Apr 17. J Hum Genet. 2009. PMID: 19373258 Review.

5

Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.

Kurahashi H, Inagaki H, Kato T, Hosoba E, Kogo H, Ohye T, Tsutsumi M, Bolor H, Tong M, Emanuel BS. Kurahashi H, et al. Among authors: tsutsumi m. Hum Mol Genet. 2009 Sep 15;18(18):3397-406. doi: 10.1093/hmg/ddp279. Epub 2009 Jun 11. Hum Mol Genet. 2009. PMID: 19520744 Free PMC article.

6

Paternal origin of the de novo constitutional t(11;22)(q23;q11).

Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville MV, Medne L, Zackai EH, Emanuel BS, Kurahashi H. Ohye T, et al. Among authors: tsutsumi m. Eur J Hum Genet. 2010 Jul;18(7):783-7. doi: 10.1038/ejhg.2010.20. Epub 2010 Feb 24. Eur J Hum Genet. 2010. PMID: 20179746 Free PMC article.

7

Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia.

Nishizawa H, Kato T, Ota S, Nishiyama S, Pryor-Koishi K, Suzuki M, Tsutsumi M, Inagaki H, Kurahashi H, Udagawa Y. Nishizawa H, et al. Among authors: tsutsumi m. Am J Reprod Immunol. 2010 Jul 1;64(1):68-76. doi: 10.1111/j.1600-0897.2010.00820.x. Epub 2010 Feb 28. Am J Reprod Immunol. 2010. PMID: 20192952

8

Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humans.

Kogo H, Kowa-Sugiyama H, Yamada K, Bolor H, Tsutsumi M, Ohye T, Inagaki H, Taniguchi M, Toda T, Kurahashi H. Kogo H, et al. Among authors: tsutsumi m. J Hum Genet. 2010 May;55(5):293-9. doi: 10.1038/jhg.2010.26. Epub 2010 Mar 26. J Hum Genet. 2010. PMID: 20339383

9

Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.

Tong M, Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Wang J, Emanuel BS, Kurahashi H. Tong M, et al. Among authors: tsutsumi m. Hum Mol Genet. 2010 Jul 1;19(13):2630-7. doi: 10.1093/hmg/ddq150. Epub 2010 Apr 13. Hum Mol Genet. 2010. PMID: 20392709 Free PMC article.

10

The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.

Kurahashi H, Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS. Kurahashi H, et al. Among authors: tsutsumi m. Clin Genet. 2010 Oct;78(4):299-309. doi: 10.1111/j.1399-0004.2010.01445.x. Clin Genet. 2010. PMID: 20507342 Free PMC article. Review.

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