岡野善行 (Yoshiyuki Okano) - マイポータル - researchmap

基本情報

所属: 大阪市立大学大学院医学研究科臨床医科学専攻（生殖発達医学大講座）医学研究科講師

学位: 医学博士

J-GLOBAL ID: 200901048709997395
researchmap会員ID: 1000056049

研究キーワード

1

Pediatrics

研究分野

2

学歴

4

受賞

3

MISC

37

A genetic factor for age-related cataract: Identification and characterization of a novel galactokinase variant, "Osaka," in Asians

Y Okano, M Asada, A Fujimoto, A Ohtake, K Murayama, KJ Hsiao, K Choeh, YL Yang, QX Cao, JKV Reichardt …

AMERICAN JOURNAL OF HUMAN GENETICS 68(4) 1036-1042 2001年4月
Two novel glucose-6-phosphate dehydrogenase variants found in newborn mass-screening for galactosaemia

Y Okano, A Fujimoto, T Miyagi, A Hirono, S Miwa, S Niihira, H Hirokawa, T Yamano

EUROPEAN JOURNAL OF PEDIATRICS 160(2) 105-108 2001年2月
Quantitative Beutler test for newborn mass screening of galactosemia using a fluorometric microplate reader

A Fujimoto, Y Okano, T Miyagi, G Isshiki, T Oura

CLINICAL CHEMISTRY 46(6) 806-810 2000年6月
Bone mineral density of the lumbar spine in very-low-birth-weight infants: a longitudinal study

H Ichiba, H Shintaku, M Fujimaru, C Hirai, Y Okano, M Funato

EUROPEAN JOURNAL OF PEDIATRICS 159(3) 215-218 2000年3月
Molecular basis for phenotypic heterogeneity in galactosemia: prediction of clinical phenotype from genotype in Japanese patients. 7: 757-764, 1999

Eur J Hum Genet 7 757-764 1999年
Molecular characterization of galactokinase deficiency in Japanese patients

Minoru Asada, Yoshiyuki Okano, Takuji Imamura, Itsujin Suyama, Yutaka Hase, Gen Isshiki

Journal of Human Genetics 44(6) 377-382 1999年
Cassical galactosemia and mutations at the galactose-1-phosphate uridyl transferase(GALT)gene(共著)

Hum Mutat 13 417-430 1999年
Molecular Characterization of 6-pyruvoyl-tetrahydropterin synthase deficiency in Japanese patients. (共著)

J Hum Genet. 44(3) 163-168 1999年
Neonatal mass screening of galactosemia for the recent 10 years in Osaka city.

J. Jpn Society for Mass-screening 8(3) 35-40 1998年
Usefulness of per-rectal portal scintigraphy with Tc-99m pertechnetate for galactosemia in infants

Susumu Shiomi, Nobumitsu Sasaki, Naoko Ikeoka, Tetsuo Kuroki, Yoshiyuki Okano, Joji Kawabe, Hironobu Ochi

Annals of Nuclear Medicine 12(6) 375-378 1998年
olecular characterization of phenylketonuria in Japanese patients(共著)

Hum Genet 103(5) 613-618 1998年
Human UDP-galactose 4'epimerase(GALE)gene and idetification of five missense mutation in patients with epimerase-deficiency galactosemia(共著)

Mol. Genet. Metab. 63(1) 26-30 1998年
Short tandem repeat polymorphisms in Japanese families with phenylketonuria(共著)

J. Inher. Metab. Dis. 19 375 1996年
Newborn mass screening and molecular genetics of phenylketonuria in East Asia

Southeast Asian Journal of Tropical Medicine and Public Health 26 123-129 1995年
MOLECULAR CHARACTERIZATION OF GALACTOSEMIA (TYPE-1) MUTATIONS IN JAPANESE

J ASHINO, Y OKANO, SUYAMA, I, T YAMAZAKI, M YOSHINO, J FURUYAMA, HC LIN, JKV REICHARDT, G ISSHIKI

HUMAN MUTATION 6(1) 36-43 1995年
Molecular Genetics of Phenylketonuria in East Asia

Okano Yoshiyuki

The bulletin of the Yamaguchi Medical School 41(3-4) 59-61 1994年
Molecular and Population genetics of phenyl ketonuria in Orientals : Correlation between phenotype and Genotype

Journal of Inherited Metabolic Disorders 17 156 1994年
Molecular characterization of phenylketonuric mutations in Japanese by analysis of phenylalanine hydroxylase mRNA from lymphoblast

Human Molecular Genetics 3(4) 659 1994年
Identification of three novel PKU mutations among Chinese: evidence for recombination or recurrent mutation at the OAH locus.(共著)

Genomics 13(1) 230-231 1992年
Multiple origins for phenylketo nuria in Europe (共著)

Am. J. Hum. Genet 51,1355-1365 1992年

もっとみる

所属学協会

7

共同研究・競争的資金等の研究課題

2