Yoshiura K - Search Results

1

Predominantly placenta-expressed mRNAs in maternal plasma as predictive markers for twin-twin transfusion syndrome.

Miura K, Higashijima A, Miura S, Mishima H, Yamasaki K, Abe S, Hasegawa Y, Kaneuchi M, Yoshida A, Kinoshita A, Yoshiura K, Masuzaki H. Miura K, et al. Among authors: yoshiura k. Prenat Diagn. 2014 Apr;34(4):345-9. doi: 10.1002/pd.4307. Epub 2014 Jan 17. Prenat Diagn. 2014. PMID: 24375464

2

The gene TSGA14, adjacent to the imprinted gene MEST, escapes genomic imprinting.

Yamada T, Kayashima T, Yamasaki K, Ohta T, Yoshiura Ki, Matsumoto N, Fujimoto S, Niikawa N, Kishino T. Yamada T, et al. Among authors: yoshiura ki. Gene. 2002 Apr 17;288(1-2):57-63. doi: 10.1016/s0378-1119(02)00428-6. Gene. 2002. PMID: 12034494

3

The novel imprinted carboxypeptidase A4 gene ( CPA4) in the 7q32 imprinting domain.

Kayashima T, Yamasaki K, Yamada T, Sakai H, Miwa N, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Kanetake H, Ishino F, Niikawa N, Kishino T. Kayashima T, et al. Among authors: yoshiura k. Hum Genet. 2003 Mar;112(3):220-6. doi: 10.1007/s00439-002-0891-3. Epub 2003 Jan 28. Hum Genet. 2003. PMID: 12552318

4

Atp10a, the mouse ortholog of the human imprinted ATP10A gene, escapes genomic imprinting.

Kayashima T, Yamasaki K, Joh K, Yamada T, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Mukai T, Niikawa N, Kishino T. Kayashima T, et al. Among authors: yoshiura k. Genomics. 2003 Jun;81(6):644-7. doi: 10.1016/s0888-7543(03)00077-6. Genomics. 2003. PMID: 12782135

5

TGFB1 mutations in four new families with Camurati-Engelmann disease: confirmation of independently arising LAP-domain-specific mutations.

Kinoshita A, Fukumaki Y, Shirahama S, Miyahara A, Nishimura G, Haga N, Namba A, Ueda H, Hayashi H, Ikegawa S, Seidel J, Niikawa N, Yoshiura KI. Kinoshita A, et al. Am J Med Genet A. 2004 May 15;127A(1):104-107. doi: 10.1002/ajmg.a.20671. Am J Med Genet A. 2004. PMID: 15103729 No abstract available.

6

Isolated congenital anosmia with morphologically normal olfactory bulb in two Iranian families: a new clinical entity?

Ghadami M, Majidzadeh-A K, Morovvati S, Damavandi E, Nishimura G, Komatsu K, Kinoshita A, Najafi MT, Niikawa N, Yoshiura K. Ghadami M, et al. Among authors: yoshiura k. Am J Med Genet A. 2004 Jun 15;127A(3):307-9. doi: 10.1002/ajmg.a.30025. Am J Med Genet A. 2004. PMID: 15150785

7

The IHPK1 gene is disrupted at the 3p21.31 breakpoint of t(3;9) in a family with type 2 diabetes mellitus.

Kamimura J, Wakui K, Kadowaki H, Watanabe Y, Miyake K, Harada N, Sakamoto M, Kinoshita A, Yoshiura KI, Ohta T, Kishino T, Ishikawa M, Kasuga M, Fukushima Y, Niikawa N, Matsumoto N. Kamimura J, et al. Among authors: yoshiura ki. J Hum Genet. 2004;49(7):360-365. doi: 10.1007/s10038-004-0158-z. Epub 2004 Jun 18. J Hum Genet. 2004. PMID: 15221640

8

Heterozygous TGFBR2 mutations in Marfan syndrome.

Mizuguchi T, Collod-Beroud G, Akiyama T, Abifadel M, Harada N, Morisaki T, Allard D, Varret M, Claustres M, Morisaki H, Ihara M, Kinoshita A, Yoshiura K, Junien C, Kajii T, Jondeau G, Ohta T, Kishino T, Furukawa Y, Nakamura Y, Niikawa N, Boileau C, Matsumoto N. Mizuguchi T, et al. Among authors: yoshiura k. Nat Genet. 2004 Aug;36(8):855-60. doi: 10.1038/ng1392. Epub 2004 Jul 4. Nat Genet. 2004. PMID: 15235604 Free PMC article.

9

Labor increases maternal DNA contamination in cord blood.

Masuzaki H, Miura K, Miura S, Yoshiura K, Mapendano CK, Nakayama D, Yoshimura S, Niikawa N, Ishimaru T. Masuzaki H, et al. Among authors: yoshiura k. Clin Chem. 2004 Sep;50(9):1709-11. doi: 10.1373/clinchem.2004.036517. Clin Chem. 2004. PMID: 15331519 No abstract available.

10

Placental mRNA in maternal plasma and its clinical application to the evaluation of placental status in a pregnant woman with placenta previa-percreta.

Masuzaki H, Miura K, Yoshiura K, Yamasaki K, Miura S, Yoshimura S, Nakayama D, Mapendano CK, Niikawa N, Ishimaru T. Masuzaki H, et al. Among authors: yoshiura k. Clin Chem. 2005 May;51(5):923-5. doi: 10.1373/clinchem.2005.047803. Clin Chem. 2005. PMID: 15855676 No abstract available.

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