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asako horikoshi
(1 results)?
Subcritical Methanol Extraction of the Stone of Japanese Apricot Prunus mume Sieb. et Zucc.
Biomolecules. 2020 Jul 15;10(7):1047. doi: 10.3390/biom10071047.
Biomolecules. 2020.
PMID: 32679686
Free PMC article.
Phenolics profile of mume, Japanese apricot (Prunus mume Sieb. et Zucc.) fruit.
Mitani T, Horinishi A, Kishida K, Kawabata T, Yano F, Mimura H, Inaba N, Yamanishi H, Oe T, Negoro K, Mori H, Miyake Y, Hosoda A, Tanaka Y, Mori M, Ozaki Y.
Mitani T, et al. Among authors: horinishi a.
Biosci Biotechnol Biochem. 2013;77(8):1623-7. doi: 10.1271/bbb.130077. Epub 2013 Aug 7.
Biosci Biotechnol Biochem. 2013.
PMID: 23924723
Free article.
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Molecular characterization of Egyptian patients with glycogen storage disease type IIIa.
Endo Y, Fateen E, Aoyama Y, Horinishi A, Ebara T, Murase T, Shin YS, Okubo M.
Endo Y, et al. Among authors: horinishi a.
J Hum Genet. 2005;50(10):538-542. doi: 10.1007/s10038-005-0291-3. Epub 2005 Sep 28.
J Hum Genet. 2005.
PMID: 16189622
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Seven novel sequence variants in the human low density lipoprotein receptor related protein 5 (LRP5) gene.
Okubo M, Horinishi A, Kim DH, Yamamoto TT, Murase T.
Okubo M, et al. Among authors: horinishi a.
Hum Mutat. 2002 Feb;19(2):186. doi: 10.1002/humu.9012.
Hum Mutat. 2002.
PMID: 11793484
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Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and Turkey.
Endo Y, Horinishi A, Vorgerd M, Aoyama Y, Ebara T, Murase T, Odawara M, Podskarbi T, Shin YS, Okubo M.
Endo Y, et al. Among authors: horinishi a.
J Hum Genet. 2006;51(11):958-963. doi: 10.1007/s10038-006-0045-x. Epub 2006 Sep 19.
J Hum Genet. 2006.
PMID: 17047887
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A novel complex deletion-insertion mutation mediated by Alu repetitive elements leads to lipoprotein lipase deficiency.
Okubo M, Horinishi A, Saito M, Ebara T, Endo Y, Kaku K, Murase T, Eto M.
Okubo M, et al. Among authors: horinishi a.
Mol Genet Metab. 2007 Nov;92(3):229-33. doi: 10.1016/j.ymgme.2007.06.018. Epub 2007 Aug 13.
Mol Genet Metab. 2007.
PMID: 17706445
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Mutational and haplotype analysis of AGL in patients with glycogen storage disease type III.
Horinishi A, Okubo M, Tang NL, Hui J, To KF, Mabuchi T, Okada T, Mabuchi H, Murase T.
Horinishi A, et al.
J Hum Genet. 2002;47(2):55-9. doi: 10.1007/s100380200000.
J Hum Genet. 2002.
PMID: 11924557
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