業績

ホーム＞業績＞２０１５年業績
２０１５年業績
  1. Tomoshige K, Matsumoto K, Tsuchiya T, Oikawa M, Miyazaki T, Yamasaki N, Mishima H, Kinoshita A, Kubo T, Fukushima K, Yoshiura KI, Nagayasu T. Germline mutations causing familial lung cancer. J Hum Genet. 2015 Oct;60(10):597-603. doi: 10.1038/jhg.2015.75. Epub 2015 Jul 16.
  2. Tamura S, Higuchi K, Tamaki M, Inoue C, Awazawa R, Mitsuki N, Nakazawa Y, Mishima H, Takahashi K, Kondo O, Imai K, Morio T, Ohara O, Ogi T, Furukawa F, Inoue M, Yoshiura KI, Kanazawa N. Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency. Clin Immunol. 2015 Oct;160(2):255-60. doi: 10.1016/j.clim.2015.07.004. Epub 2015 Jul 11.
  3. Oikawa M, Yano H, Matsumoto M, Otsubo R, Shibata K, Hayashi T, Abe K, Kinoshita N, Yoshiura KI, Nagayasu T. A novel diagnostic method targeting genomic instability in intracystic tumors of the breast. Breast Cancer. 2015 Sep;22(5):529-35. doi: 10.1007/s12282-013-0516-9. Epub 2014 Jan 9.
  4. Hasegawa Y, Miura K, Higashijima A, Abe S, Miura S, Yoshiura KI, Masuzaki H. Increased Levels of Cell-Free miR-517a and Decreased Levels of Cell-Free miR-518b in Maternal Plasma Samples From Placenta Previa Pregnancies at 32 Weeks of Gestation. Reprod Sci. 2015 Dec;22(12):1569-76. doi: 10.1177/1933719115589407. Epub 2015 Jun 2.
  5. Gohda Y, Oka S, Matsunaga T, Watanabe S, Yoshiura K, Kondoh T, Matsumoto T. Neonatal case of novel KMT2D mutation in Kabuki syndrome with severe hypoglycemia. Pediatr Int. 2015 Aug;57(4):726-8. doi: 10.1111/ped.12574. Epub 2015 May 5.
  6. Miura K, Higashijima A, Mishima H, Miura S, Kitajima M, Kaneuchi M, Yoshiura K, Masuzaki H. Pregnancy-associated microRNAs in plasma as potential molecular markers of ectopic pregnancy. Fertil Steril. 2015 May;103(5):1202-1208.e1. doi: 10.1016/j.fertnstert.2015.01.041. Epub 2015 Mar 13.
  7. Miura K, Higashijima A, Hasegawa Y, Abe S, Miura S, Kaneuchi M, Yoshiura KI, Masuzaki H. Circulating levels of maternal plasma cell-free miR-21 are associated with maternal body mass index and neonatal birth weight. Prenat Diagn. 2015 May;35(5):509-511. doi: 10.1002/pd.4509. Epub 2014 Nov 14. No abstract available.  
  8. Ohtsuka Y, Higashimoto K, Sasaki K, Jozaki K, Yoshinaga H, Okamoto N, Takama Y, Kubota A, Nakayama M, Yatsuki H, Nishioka K, Joh K, Mukai T, Yoshiura KI, Soejima H. Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome. Clin Genet. 2015 Sep;88(3):261-6. doi: 10.1111/cge.12496. Epub 2014 Nov 8
  9. Morisaki S, Miura K, Higashijima A, Abe S, Miura S, Hasegawa Y, Yoshida A, Kaneuchi M, Yoshiura KI, Masuzaki H. Effect of labor on plasma concentrations and postpartum clearance of cell-free, pregnancy-associated, placenta-specific microRNAs. Prenat Diagn. 2015 Jan; 35(1): 44-45. doi: 10.1002/pd.4479. [Epub ahead of print]