金澤正樹 (Masaki Kanazawa) - マイポータル - researchmap

基本情報

所属: 旧所属千葉大学医学部附属病院講師

学位: 医学博士(千葉大学)

J-GLOBAL ID: 200901090310430851
researchmap会員ID: 1000306503

外部リンク: http://www.ho.chiba-u.ac.jp/13/index.html

研究分野

1

ライフサイエンス / 胎児医学、小児成育学 /

学歴

2

- 1987年

山梨医科大学（YMU）, 医学部, 医学部医学科
- 1987年

山梨医科大学（YMU）

MISC

43

An mRNA amplification procedure with directional cDNA cloning and strand-specific cRNA synthesis for comprehensive gene expression analysis

S Ohtsuka, K Iwase, M Kato, N Seki, A Shimizu-Yabe, O Miyauchi, E Sakao, M Kanazawa, S Yamamoto, Y Kohno …

GENOMICS 84(4) 715-729 2004年10月
An mRNA amplification procedure with directional cDNA cloning and strand-specific cRNA synthesis for comprehensive gene expression analysis

S Ohtsuka, K Iwase, M Kato, N Seki, A Shimizu-Yabe, O Miyauchi, E Sakao, M Kanazawa, S Yamamoto, Y Kohno …

GENOMICS 84(4) 715-729 2004年10月
Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118R

K Kojima, S Kure, F Kamada, K Hao, A Ichinohe, K Sato, Y Aoki, S Yoichi, M Kubota, R Horikawa …

MOLECULAR GENETICS AND METABOLISM 81(4) 343-346 2004年4月
Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency.

J Hum Genet, 47,342-347. 2003年
Distinctly abnormal brain metabolism in late-onset ornithine transcarbamylase deficiency.

Neurology. 59(2),210-214. 2003年
Magnetic resonance imaging in late-onset ornithine transcarbamylase deficiency

A Kurihara, J Takanashi, M Tomita, K Kobayashi, A Ogawa, M Kanazawa, S Yamamoto, Y Kohno

BRAIN & DEVELOPMENT 25(1) 40-44 2003年1月
Complete recovery from fulminant hepatic failure with severe coma by living donor liver transplantation.

Hepatogastroenterology. 50, 515-518. 2003年
Distinctly abnormal brain metabolism in late-onset ornithine transcarbamylase deficiency.

Neurology. 59(2),210-214. 2003年
Magnetic resonance imaging in late-onset ornithine transcarbamylase deficiency

A Kurihara, J Takanashi, M Tomita, K Kobayashi, A Ogawa, M Kanazawa, S Yamamoto, Y Kohno

BRAIN & DEVELOPMENT 25(1) 40-44 2003年1月
Complete recovery from fulminant hepatic failure with severe coma by living donor liver transplantation.

Hepatogastroenterology. 50, 515-518. 2003年
Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency

Emi Ogawa, Masaki Kanazawa, Shigenori Yamamoto, Satoko Ohtsuka, Atsushi Ogawa, Akira Ohtake, Masaki Takayanagi, Yoichi Kohno

Journal of Human Genetics 47(7) 342-347 2002年
Monocyte chemoattractant protein 1 gene regulatory region polymorphism and serum levels of monocyte chemoattractant protein 1 in Japanese patients with Kawasaki disease.

Arthritis Rheum. 44,2211-2212. 2001年
Monocyte chemoattractant protein 1 gene regulatory region polymorphism and serum levels of monocyte chemoattractant protein 1 in Japanese patients with Kawasaki disease.

Arthritis Rheum. 44,2211-2212. 2001年
Identification of two novel mutations of the carnitine/ acylcarnitine translocase (CACT)gene in a patient with CACT deficiency(共著)

J. How Genet 82(3) 518 2000年
Quantitative analysis of cell allocation during live development, using the spf(ash)-heterozygous female mouse.(共著)

American Journal of Pathology 156(1) 65-75 2000年1月
Molecular analysis of hepatic carnitine palmitoyl transferase I deficiency(1) : cDNA and genomic DNA analysis of infants presenting with Reye-like illness.(共著)

Journal of Inherited Metabolic disease 23(Suppl 1) 115 2000年
Observation of dominant negative effects for ornithine transcarbamylase in cultured cells co-expressed with wild-type OTC and various mutant OTCs(共著)

Journal of Inherited Metabolic disease 23(Suppl 1) 55 2000年
Living related liver transplantation for Wilson disease presenting acute hepatic failure from heterozygous carrier(共著)

Journal of Interited Metabolic disease 23(Suppl 1) 265 2000年
Novel mutation of L718X in the ATP7A gene in a Japanese patient with classical Menkes disease, and four novel polymorphisms in the Japanese population(共著)

OGAWA A, YAMAMOTO S, KANAZAWA M, OGAWA E, TAKAYANAGI M, HASEGAWA S, KOHNO Y

Journal of Human Genetics 45(5) 315-317 2000年
Moleculer analysis of hepatic carnitine palmitoyl transferase (]G0001[) deficiency(2) : Expression of mutated CPTIA cDNAs in cos-7 cells

Journal of Inherited Metabolic disease 23(Suppl 1) 116 2000年

もっとみる

所属学協会

4

共同研究・競争的資金等の研究課題

4