Masaki Kanazawa - My portal - researchmap

Profile Information

Affiliation: Former Institution / Organization Chiba University Hospital

Degree: (BLANK)(Chiba University)

J-GLOBAL ID: 200901090310430851
researchmap Member ID: 1000306503

External link: http://www.ho.chiba-u.ac.jp/13/index.html

Research Areas

1

Life sciences / Fetal medicine/Pediatrics /

Education

2

- 1987

Yamanashi Medical University
- 1987

Faculty of Medicine, Yamanashi Medical University

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, Oct, 2004
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, Oct, 2004
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, Apr, 2004
Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency.

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

Neurology., 59(2),210-214., 2003
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, Jan, 2003
Complete recovery from fulminant hepatic failure with severe coma by living donor liver transplantation.

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

Neurology., 59(2),210-214., 2003
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, Jan, 2003
Complete recovery from fulminant hepatic failure with severe coma by living donor liver transplantation.

Hepatogastroenterology., 50, 515-518., 2003
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
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
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
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
Quantitative analysis of cell allocation during liver development, using the spf(ash)-heterozygous female mouse

N Shiojiri, M Sano, S Inujima, M Nitou, M Kanazawa, M Mori

AMERICAN JOURNAL OF PATHOLOGY, 156(1) 65-75, Jan, 2000
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
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
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
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
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

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Professional Memberships

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Research Projects

4