井田博幸 (Hiroyuki Ida) - マイポータル - researchmap

基本情報

所属: 東京慈恵会医科大学ＤＮＡ医学研究所小児科学講座，DNA研究所遺伝子治療部門助教授

学位: 医学博士(東京慈恵会医科大学)

J-GLOBAL ID: 200901099074077000
researchmap会員ID: 5000002889

研究キーワード

4

研究分野

1

ライフサイエンス / 胎児医学、小児成育学 /

経歴

8

学歴

2

- 1981年

東京慈恵会医科大学, 医学部
東京慈恵会医科大学

委員歴

3

受賞

5

MISC

43

Enzyme enhancement activity of N-octyl-β-valienamine on β-glucosidase mutants associated with Gaucher disease.

K Lei, H Ninomiya, M Suzuki, T Inoue, M Sawa, M Iida, H Ida, Y Eto, S Ogawa, K Ohno …

Biochimica et biophysica acta 1772(5) 587-596 2007年5月
Pseudo-gaucher cell proliferation associated with myelodysplastic syndrome

Takeshi Saito, Noriko Usui, Osamu Asai, Nobuaki Dobashi, Hiroyuki Ida, Makio Kawakami, Shingo Yano, Hiroshi Osawa, Yutaka Takei, Shinobu Takahara …

INTERNATIONAL JOURNAL OF HEMATOLOGY 85(4) 350-353 2007年5月
Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease: Identification of four novel mutations

H. Ida, O. M. Rennert, H. Kawame, K. Maekawa, Y. Eto

Journal of Inherited Metabolic Disease 20(1) 67-73 1997年
Ida H and Eto Y. Biochemical and morphological studies ofdorsal root ganglion and its cultured cells from twitchermouse (murine globoid cell leukodystrophy).

Brain and Development 12 : 412-416 1990年
Dopaminergic neuronal dysfunction associated with parkinsonism in both a Gaucher disease patient and cerrier.

S Kono, K Shirakawa, Y Ouchi, M Sakamoto, H Ida, T Sugiura, H Tomiyama, H Suzuki, Y Takahashi, H Miyajima …

J Neurol Sci (525) 181-4
Ida H,Umezawa F,Kasai E,Eto Y and Maekawa K.An accumulation of galactocerebroside in kidney from mousegloboid cell leukodystrophy(twitcher).

Biochem Biophys Res Commun 1982 ; 109 : 634-638
Ida H,Maekawa K,Ochiai Y,Yamazaki Y and Tsuzura S.Neurological features of children with cerebral palsy whoreceived very early treatment.

Jikeikai Med J 1987 ; 34 : 211-218
Ida H, Rennert OM, Watabe K, Eto Y and Maekawa K.Pathological and biochemical studies of fetal Krabbedisease.

Brain and Development 1994 ; 16 : 480-488
Ida H, Rennert OM, Maekawa K and Eto Y. Identification ofthree novel mutations in the acid sphingomyelinase gene ofJapanese patients with Niemann-Pick disease thpe A and B.

Hum Mutat 1996 ; 7 : 65-68
Ida H, Rennert OM, Kobayashi M and Eto Y. Effects ofenzyme replacement tharapy in thirteen Japanese Paediatricpatients with Gaucher disease.

Eur J Pediatr 2001 ; 160 : 21-5
Ida H, Rennert OM, Kawame H, Ito T, Maekawa K and Eto Y.Mutation screening of 17 Japanese patients with neuropathicGaucher disease.

Hum Genet 1996 ; 98 : 167-171
Ida H, Rennert OM, Kato S, Ueda T, Oishi K, Maekawa K andEto Y. Severe skeletal complications in Japanese patientswith type 1 Gaucher disease.

J Inher Metab Dis 1999 ; 22 : 63-73
Ida H, Rennert OM, Iwasawa K, Kobayashi M and Eto Y.Clinical and genetic studies of Japanese homozygotes for theGaucher disease L444P mutation.

Hum Genet 1999 ; 105 : 120-126
Ida H, Rennert OM, Ito T, Maekawa K and Eto Y. Type 1Gaucher disease : phenotypic expression and natural history.

Blood Cells, Molecules, and Diseases 1998 ; 24 : 73-81
Ida H, Rennert OM, Ito T, Maekawa K and Eto Y. Clinical andgenetic studies of five fatal cases of Japanese Gaucherdisease type 1.

Acta Paediatr Jpn 1996 ; 38 : 233-236
Ida H, Rennert OM, Eto Y and Chan WY. Cloning of a humanacid sphingomyelinase cDNA with a new mutation thatrenders the enzyme inactive.

J Biochem 1993 ; 114 : 15-20
Ida H, Kusano K, SUzuki H, Tokoro T and Eto Y.Galactosylceramide and galactosylsphingosine loadingstudies in cultured skin fibroblasts in human and murinegloboid cell leukodystrophy.

Biochem Biophys Res Commun 1990 ; 166 : 1053-1060
Ida H, Kawame F, Kim SU and Eto Y. Abnormality in culturedoligodendrocytes and Schwann cells isolated from twitchermouse.

Molecular and Chemical Neuropathology 1991 ; 13 : 195-204
Ida H, Iwasawa K, Kawame H, Rennert OM, Maekawa K and EtoY. Characteristics of gene mutations among 32 unrelatedJapanese Gaucher disease patients : absence of the commonJewish 84GG and 1226G mutations.

Hum Genet 1995 ; 95 : 717-720
Ida H, Eto Y and Maekawa K. Neurotoxicity of psychosine inneural cell cultures : The pathogenesis of Krabbe's disease.

Jikeikai Med J 1993 ; 40 : 171-176

もっとみる

所属学協会

8

共同研究・競争的資金等の研究課題

2

先天代謝異常症

厚生労働科学研究費補助金 1989年
Inborn Errors of Metabolism

Health and Labour Sciences Research Grants 1989年