Hasegawa Y - Search Results

1

Molecular basis of non-syndromic hypospadias: systematic mutation screening and genome-wide copy-number analysis of 62 patients.

Kon M, Suzuki E, Dung VC, Hasegawa Y, Mitsui T, Muroya K, Ueoka K, Igarashi N, Nagasaki K, Oto Y, Hamajima T, Yoshino K, Igarashi M, Kato-Fukui Y, Nakabayashi K, Hayashi K, Hata K, Matsubara Y, Moriya K, Ogata T, Nonomura K, Fukami M. Kon M, et al. Among authors: hasegawa y. Hum Reprod. 2015 Mar;30(3):499-506. doi: 10.1093/humrep/deu364. Epub 2015 Jan 20. Hum Reprod. 2015. PMID: 25605705

2

Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation: analysis of the X-inactivation patterns.

Matsuo M, Muroya K, Nanao K, Hasegawa Y, Terasaki H, Kosaki K, Ogata T. Matsuo M, et al. Among authors: hasegawa y. Am J Med Genet. 2000 Apr 10;91(4):267-72. Am J Med Genet. 2000. PMID: 10766981 Review.

3

Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: a clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata.

Hasegawa T, Ogata T, Hasegawa Y, Honda M, Nagai T, Fukushima Y, Nakahori Y, Matsuo N. Hasegawa T, et al. Among authors: hasegawa y. Hum Genet. 1996 May;97(5):564-7. doi: 10.1007/BF02281861. Hum Genet. 1996. PMID: 8655131

4

Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients.

Ogata T, Muroya K, Matsuo N, Shinohara O, Yorifuji T, Nishi Y, Hasegawa Y, Horikawa R, Tachibana K. Ogata T, et al. Among authors: hasegawa y. J Clin Endocrinol Metab. 2001 Nov;86(11):5498-508. doi: 10.1210/jcem.86.11.8058. J Clin Endocrinol Metab. 2001. PMID: 11701728 Clinical Trial.

5

GATA3 abnormalities and the phenotypic spectrum of HDR syndrome.

Muroya K, Hasegawa T, Ito Y, Nagai T, Isotani H, Iwata Y, Yamamoto K, Fujimoto S, Seishu S, Fukushima Y, Hasegawa Y, Ogata T. Muroya K, et al. Among authors: hasegawa t, hasegawa y. J Med Genet. 2001 Jun;38(6):374-80. doi: 10.1136/jmg.38.6.374. J Med Genet. 2001. PMID: 11389161 Free PMC article.

6

Changes in serum concentrations of immunoreactive inhibin during the oestrous cycle of the rat.

Hasegawa Y, Miyamoto K, Igarashi M. Hasegawa Y, et al. J Endocrinol. 1989 Apr;121(1):91-100. doi: 10.1677/joe.0.1210091. J Endocrinol. 1989. PMID: 2715763

7

Rapid identification of mutations in the glucocerebrosidase gene of Gaucher disease patients by analysis of single-strand conformation polymorphisms.

Kawame H, Hasegawa Y, Eto Y, Maekawa K. Kawame H, et al. Among authors: hasegawa y. Hum Genet. 1992 Nov;90(3):294-6. doi: 10.1007/BF00220082. Hum Genet. 1992. PMID: 1487244

8

Glycogen storage disease type Ib: structural and mutational analysis of the microsomal glucose-6-phosphate transporter gene.

Hou DC, Kure S, Suzuki Y, Hasegawa Y, Hara Y, Inoue T, Kida Y, Matsubara Y, Narisawa K. Hou DC, et al. Among authors: hasegawa y. Am J Med Genet. 1999 Sep 17;86(3):253-7. doi: 10.1002/(sici)1096-8628(19990917)86:3<253::aid-ajmg11>3.0.co;2-7. Am J Med Genet. 1999. PMID: 10482875

9

[Mechanism of inhibition of hypothalamic pituitary-ovarian function in streptozotocin-diabetic mature female rats].

Taniguchi Y, Hasegawa Y, Igarashi M. Taniguchi Y, et al. Among authors: hasegawa y. Nihon Sanka Fujinka Gakkai Zasshi. 1984 Apr;36(4):557-63. Nihon Sanka Fujinka Gakkai Zasshi. 1984. PMID: 6232328 Japanese.

10

Heterogeneous mutations in the glycogen-debranching enzyme gene are responsible for glycogen storage disease type IIIa in Japan.

Okubo M, Horinishi A, Takeuchi M, Suzuki Y, Sakura N, Hasegawa Y, Igarashi T, Goto K, Tahara H, Uchimoto S, Omichi K, Kanno H, Hayasaka K, Murase T. Okubo M, et al. Among authors: hasegawa y. Hum Genet. 2000 Jan;106(1):108-15. doi: 10.1007/s004390051017. Hum Genet. 2000. PMID: 10982190

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