Yuasa I - Search Results

1

Anti-steatosis compounds from leaves of Mallotus furetianus.

Huang X, Xu M, Shirahata T, Li W, Koike K, Kojima-Yuasa A, Yuasa I, Kobayashi Y. Huang X, et al. Among authors: yuasa i. Nat Prod Res. 2018 Jun;32(12):1459-1462. doi: 10.1080/14786419.2017.1350664. Epub 2017 Jul 10. Nat Prod Res. 2018. PMID: 28693358

2

Characterization of an acidic polysaccharide isolated from the leaves of Corchorus olitorius (Moroheiya).

Ohtani K, Okai K, Yamashita U, Yuasa I, Misaki A. Ohtani K, et al. Among authors: yuasa i. Biosci Biotechnol Biochem. 1995 Mar;59(3):378-81. doi: 10.1271/bbb.59.378. Biosci Biotechnol Biochem. 1995. PMID: 7766172 Free article.

3

Novel TSC2 mutation in a patient with pulmonary tuberous sclerosis: lack of loss of heterozygosity in a lung cyst.

Zhang H, Yamamoto T, Nanba E, Kitamura Y, Terada T, Akaboshi S, Yuasa I, Ohtani K, Nakamoto S, Takeshita K, Ohno K. Zhang H, et al. Among authors: yuasa i. Am J Med Genet. 1999 Feb 19;82(5):368-70. doi: 10.1002/(sici)1096-8628(19990219)82:5<368::aid-ajmg2>3.0.co;2-i. Am J Med Genet. 1999. PMID: 10069705

4

Human orosomucoid polymorphism: molecular basis of the three common ORM1 alleles, ORM1*F1, ORM1*F2, and ORM1*S.

Yuasa I, Umetsu K, Vogt U, Nakamura H, Nanba E, Tamaki N, Irizawa Y. Yuasa I, et al. Hum Genet. 1997 Mar;99(3):393-8. doi: 10.1007/s004390050378. Hum Genet. 1997. PMID: 9050929

5

Mutation in the exon 10 (R173W) of the hydroxymethylbilane synthase gene in two unrelated Japanese families with acute intermittent porphyria.

Tomie Y, Horie Y, Tajima F, Kitaoka S, Nanba E, Yuasa I, Kawasaki H. Tomie Y, et al. Among authors: yuasa i. Res Commun Mol Pathol Pharmacol. 1998 Jan;99(1):5-15. Res Commun Mol Pathol Pharmacol. 1998. PMID: 9523350

6

Increased expression of beta-hexosaminidase alpha chain in cultured skin fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome type I.

Ichisaka S, Ohno K, Yuasa I, Nanba E, Sakuraba H, Suzuki Y. Ichisaka S, et al. Among authors: yuasa i. Brain Dev. 1998 Aug;20(5):302-6. doi: 10.1016/s0387-7604(98)00035-7. Brain Dev. 1998. PMID: 9760999

7

[CDG syndrome(congenital disorders of glycosylation)].

Yuasa I, Ohno K. Yuasa I, et al. Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):493-5. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11032006 Review. Japanese. No abstract available.

8

The carbohydrate deficient glycoprotein syndrome in three Japanese children.

Ohno K, Yuasa I, Akaboshi S, Itoh M, Yoshida K, Ehara H, Ochiai Y, Takeshita K. Ohno K, et al. Among authors: yuasa i. Brain Dev. 1992 Jan;14(1):30-5. doi: 10.1016/s0387-7604(12)80276-2. Brain Dev. 1992. PMID: 1590525

9

Prenatal diagnosis of congenital myotonic dystrophy in two Japanese families: direct mutation analysis by a non-radioisotope PCR method and haplotype analysis with flanking DNA markers.

Nanba E, Ito T, Kadowaki K, Makio A, Nakagawa M, Yamamoto T, Yuasa I, Takeshita K. Nanba E, et al. Among authors: yuasa i. Brain Dev. 1996 Mar-Apr;18(2):122-6. doi: 10.1016/0387-7604(95)00111-5. Brain Dev. 1996. PMID: 8733903

10

Carbohydrate-deficient glycoprotein syndrome: electrophoretic study of multiple serum glycoproteins.

Yuasa I, Ohno K, Hashimoto K, Iijima K, Yamashita K, Takeshita K. Yuasa I, et al. Brain Dev. 1995 Jan-Feb;17(1):13-9. doi: 10.1016/0387-7604(94)00099-j. Brain Dev. 1995. PMID: 7762756

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