A. Horinishi

发表

Proanthocyanidin in the fruit of Japanese apricot (Prunus mume Sieb. et Zucc.) and their structural estimation by HPLC-ESI-MS/MS

T. Shoji, E. Nomura, Y. Ozaki, 2021 .

Seven novel sequence variants in the human low density lipoprotein receptor related protein 5 (LRP5) gene

Tokuo T. Yamamoto, M. Okubo, T. Murase, 2002, Human mutation.

Heterogeneous mutations in the glycogen-debranching enzyme gene are responsible for glycogen storage disease type IIIa in Japan

K. Hayasaka, M. Okubo, T. Murase, 1999, Human Genetics.

Subcritical Methanol Extraction of the Stone of Japanese Apricot Prunus mume Sieb. et Zucc.

T. Mitani, A. Hosoda, Yoshie Tanaka, 2020, Biomolecules.

Chemical Features of Phenolic Extracts Prepared on an Industrial Scale from a Processing Byproduct of the Japanese Apricot, Mume Fruit (Prunus mume Sieb.et Zucc.)

T. Mitani, Y. Ozaki, Nobuya Inaba, 2017 .

Characterization of Phenolics in the Flesh Tissue of 'Tsuyuakane', a Red Flesh Type of Japanese Apricot (Prunus mume Sieb. et Zucc.) and its Effect on Postprandial Blood Glucose Levels in Rats

K. Kishida, Y. Ozaki, A. Horinishi, 2017, Food Preservation Science.

Phenolics Profile of Mume, Japanese Apricot (Prunus mume Sieb. et Zucc.) Fruit

K. Kishida, H. Mori, F. Yano, 2013, Bioscience, biotechnology, and biochemistry.

Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and Turkey

M. Vorgerd, M. Odawara, M. Okubo, 2006, Journal of Human Genetics.

Molecular characterization of Egyptian patients with glycogen storage disease type IIIa

M. Okubo, T. Ebara, Y. Aoyama, 2005, Journal of Human Genetics.

No evidence of accelerated atherosclerosis in a 66-yr-old chylomicronemia patient homozygous for the nonsense mutation (Tyr61-->stop) in the lipoprotein lipase gene.

M. Adachi, T. Hirano, M. Okubo, 2001, Atherosclerosis.

Phenolic Extract from Japanese Apricot Fruit (Prunus Mume Sieb et Zucc.) Inhibits Disaccharidase Activity in the Small Intestine and Suppresses the Postprandial Elevation of Glucose Levels in Rats

K. Kishida, Y. Ozaki, A. Horinishi, 2014, Food Preservation Science.

Detection of a new compound heterozygote (del G916/G1401A) for lipoprotein lipase deficiency and a comparative haplotype analysis of the mutant lipoprotein lipase gene from Japanese patients.

M. Okubo, T. Murase, N. Yamada, 1999, Atherosclerosis.

Letter to the Editor Detection of a new compound heterozygote (del G 916 :G1401A) for lipoprotein lipase deficiency and a comparative haplotype analysis of the mutant lipoprotein lipase gene from Japanese patients

M. Okubo, T. Murase, N. Yamada, 1999 .

Mutational and haplotype analysis of AGL in patients with glycogen storage disease type III

H. Mabuchi, K. To, N. Tang, 2002, Journal of Human Genetics.

Compound heterozygous patient with glycogen storage disease type III: identification of two novel AGL mutations, a donor splice site mutation of Chinese origin and a 1-bp deletion of Japanese origin.

K. Hayasaka, M. Okubo, T. Murase, 2000, American journal of medical genetics.

Glycogen storage disease type IIIa: first report of a causative missense mutation (G1448R) of the glycogen debranching enzyme gene found in a homozygous patient

K. Chihara, M. Okubo, T. Murase, 1999, Human mutation.

A novel complex deletion-insertion mutation mediated by Alu repetitive elements leads to lipoprotein lipase deficiency.

K. Kaku, M. Okubo, T. Ebara, 2007, Molecular genetics and metabolism.

1176C Polymorphism in Japanese patients with glycogen storage disease type 1a

M. Okubo, T. Murase, A. Horinishi, 1999, Human Genetics.