近藤郁子 (Ikuko Kondo) - マイポータル - researchmap

基本情報

所属: 旧所属愛媛大学医学部医学科教授

学位: 医学博士(筑波大学)

J-GLOBAL ID: 200901098098235904
researchmap会員ID: 1000039769

研究キーワード

6

研究分野

5

経歴

6

1989年 - 1992年

琉球大学教授
1989年 - 1992年

University of Ryukyu, Professor
1992年

- 愛媛工学教授
1992年

- Ehime University Professor
1975年 - 1988年

筑波大学(基礎医学系人類遺伝学) 講師
1975年 - 1988年

筑波大学

学歴

2

- 1967年

徳島大学, 医学部, 医学科
- 1967年

徳島大学

MISC

41

A novel giant gene CSMD3 encoding a protein with CUB and sushi multiple domains: a candidate gene for benign adult familial myoclonic epilepsy on human chromosome 8q23.3-q24.1

A Shimizu, S Asakawa, T Sasaki, S Yamazaki, H Yamagata, J Kudoh, S Minoshima, Kondo, I, N Shimizu

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 309(1) 143-154 2003年9月
Patients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?

Journal of Medical Genetics 40(5):e52. 2003年
Polymorphism of the monocyte chemoattractant protein(MCP-1)gene is associated with the plasma level of MCP-1 but not with carotid intima-media thickness.

TABARA Yasuharu, KOHARA Katsuhiko, YAMAMOTO Yoshikuni, IGASE Michiya, NAKURA Jun, KONDO Ikuko, MIKI Tetsuro

Hypertension Research 26(9):677-83(9) 677-683 2003年
Patients with the R133C mutation: is their phenotype differend from patients with rett syndrome eith other mutations?

Journal of Medical Genetics 40: e52 2003年
Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

K Kitamura, M Yanazawa, N Sugiyama, H Miura, A Iizuka-Kogo, M Kusaka, K Omichi, R Suzuki, Y Kato-Fukui, K Kamiirisa …

NATURE GENETICS 32(3) 359-369 2002年11月
Screening of SLC25A13 mutations in early and late onset Patients with Citrin Deficiency and in the Japanese Population : Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations

Human Mutation 19, 122-130 2002年
The-4, 752 C/T polymorphism in the Presenilin / gene increased the risk of Alzheimer's desease in apolipoprotein E4 cancers

Internal Medicine 41, 823-828 2002年
Human biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase gene (MCCA): cDNA sequence, genomic organization, localization to chromosomal band 3q27, and expression

K Obata, T Fukuda, R Morishita, S Abe, S Asakawa, S Yamaguchi, M Yoshino, K Ihara, K Murayama, K Shigemoto …

GENOMICS 72(2) 145-152 2001年3月
Mutation analysis of the methyl-CpG-binding protein 2 (MECP2) in Peti patents with preserved speech

Brain & Development 23, S157-S160 2001年
A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome

MEGURO M

Nat Genet 28(1) 19-20 2001年
Genetic association between Alzheimer disease and the alpha-synuclein gene

Miho Matsubara, Hidehisa Yamagata, Kouzin Kamino, Takuo Nomura, Katsuhiko Kohara, Ikuko Kondo, Tetsuro Miki

Dementia and Geriatric Cognitive Disorders 12(2) 106-109 2001年
Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome

K Obata, T Matsuishi, Y Yamashita, T Fukuda, K Kuwajima, Horiuchi, I, S Nagamitsu, R Iwanaga, A Kimura, Omori, I …

JOURNAL OF MEDICAL GENETICS 37(8) 608-610 2000年8月
Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24

NM Plaster, E Uyama, M Uchino, T Ikeda, KM Flanigan, Kondo, I, LJ Ptacek

NEUROLOGY 53(6) 1180-1183 1999年10月
Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I

Kiyomi Mizugishi, Keiko Yamanaka, Katsuko Kuwajima, Isao Yuasa, Kazuhiro Shigemoto, Ikuko Kondo

Brain and Development 21(4) 223-228 1999年6月1日
Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)(1-2) polymorphism and contribution to founder effect

K Mizushima, M Watanabe, Kondo, I, K Okamoto, M Shizuka, K Abe, M Aoki, M Shoji

JOURNAL OF MEDICAL GENETICS 36(2) 112-114 1999年2月
The gene mutated in adult-onset type (]G0002[) citrullinaemia encodes a putative mitochondrial carrier protein

Nature Genetics 22(2) 159-165 1999年
An Acil polymorphism in the 3' untranslated region of the human phosphomannomutase 2(PMM2)gene

Journal of Human Gentics 44(4) 266-267 1999年
Missense mutations in phosphomannomutase 2 gene in two Japanese families with carbohydrate-deficient glycoprotein syndrome type 1

Kondo, I, K Mizugishi, Y Yoneda, T Hashimoto, K Kuwajima, Yuasa, I, K Shigemoto, Y Kuroda

CLINICAL GENETICS 55(1) 50-54 1999年1月
Genetic association between susceptibility to Parkinson's disease and α1-antichymotrypsin polymorphism

Mitsutoshi Yamamoto, Ikuko Kondo, Norio Ogawa, Masato Asanuma, Yoshiaki Yamashita, Yoshikuni Mizuno

Brain Research 759(1) 153-155 1997年6月6日
Early-childhood progressive myoclonus epilepsy presenting as partial seizures in dentatorubral-pallidoluysian atrophy

H Hattori, Y Higuchi, T Okuno, R Asato, M Fukumoto, Kondo, I

EPILEPSIA 38(3) 271-274 1997年3月

もっとみる

所属学協会

6

共同研究・競争的資金等の研究課題

10