Aoki Y - Search Results

1

Association between nonsyndromic cleft lip with or without cleft palate and the glutamic acid decarboxylase 67 gene in the Japanese population.

Kanno K, Suzuki Y, Yamada A, Aoki Y, Kure S, Matsubara Y. Kanno K, et al. Among authors: aoki y. Am J Med Genet A. 2004 May 15;127A(1):11-16. doi: 10.1002/ajmg.a.20649. Am J Med Genet A. 2004. PMID: 15103710

2

Isolation and characterization of mutations in the human holocarboxylase synthetase cDNA.

Suzuki Y, Aoki Y, Ishida Y, Chiba Y, Iwamatsu A, Kishino T, Niikawa N, Matsubara Y, Narisawa K. Suzuki Y, et al. Among authors: aoki y. Nat Genet. 1994 Oct;8(2):122-8. doi: 10.1038/ng1094-122. Nat Genet. 1994. PMID: 7842009

3

Purification and properties of bovine liver holocarboxylase synthetase.

Chiba Y, Suzuki Y, Aoki Y, Ishida Y, Narisawa K. Chiba Y, et al. Among authors: aoki y. Arch Biochem Biophys. 1994 Aug 15;313(1):8-14. doi: 10.1006/abbi.1994.1351. Arch Biochem Biophys. 1994. PMID: 8053691

4

Molecular analysis of holocarboxylase synthetase deficiency: a missense mutation and a single base deletion are predominant in Japanese patients.

Aoki Y, Suzuki Y, Sakamoto O, Li X, Takahashi K, Ohtake A, Sakuta R, Ohura T, Miyabayashi S, Narisawa K. Aoki Y, et al. Biochim Biophys Acta. 1995 Dec 12;1272(3):168-74. doi: 10.1016/0925-4439(95)00082-8. Biochim Biophys Acta. 1995. PMID: 8541348 Free article.

5

[Cloning of the holocarboxylase synthetase cDNA and identification of mutations prevalent in Japanese HCS-deficient patients].

Narisawa K, Suzuki Y, Aoki Y. Narisawa K, et al. Among authors: aoki y. Nihon Rinsho. 1996 Jan;54(1):259-67. Nihon Rinsho. 1996. PMID: 8587199 Review. Japanese.

6

Enzymatic diagnosis of holocarboxylase synthetase deficiency using apo-carboxyl carrier protein as a substrate.

Suzuki Y, Aoki Y, Sakamoto O, Li X, Miyabayashi S, Kazuta Y, Kondo H, Narisawa K. Suzuki Y, et al. Among authors: aoki y. Clin Chim Acta. 1996 Jul 15;251(1):41-52. doi: 10.1016/0009-8981(96)06291-2. Clin Chim Acta. 1996. PMID: 8814349

7

Characterization of mutant holocarboxylase synthetase (HCS): a Km for biotin was not elevated in a patient with HCS deficiency.

Aoki Y, Suzuki Y, Li X, Sakamoto O, Chikaoka H, Takita S, Narisawa K. Aoki Y, et al. Pediatr Res. 1997 Dec;42(6):849-54. doi: 10.1203/00006450-199712000-00021. Pediatr Res. 1997. PMID: 9396568

8

Two CPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: functional analysis and association with polymorphic haplotypes and two clinical phenotypes.

Wataya K, Akanuma J, Cavadini P, Aoki Y, Kure S, Invernizzi F, Yoshida I, Kira J, Taroni F, Matsubara Y, Narisawa K. Wataya K, et al. Among authors: aoki y. Hum Mutat. 1998;11(5):377-86. doi: 10.1002/(SICI)1098-1004(1998)11:5<377::AID-HUMU5>3.0.CO;2-E. Hum Mutat. 1998. PMID: 9600456

9

Identification of holocarboxylase synthetase (HCS) proteins in human placenta.

Hiratsuka M, Sakamoto O, Li X, Suzuki Y, Aoki Y, Narisawa K. Hiratsuka M, et al. Among authors: aoki y. Biochim Biophys Acta. 1998 Jun 11;1385(1):165-71. doi: 10.1016/s0167-4838(98)00032-6. Biochim Biophys Acta. 1998. PMID: 9630604

10

Molecular analysis of new Japanese patients with holocarboxylase synthetase deficiency.

Sakamoto O, Suzuki Y, Aoki Y, Li X, Hiratsuka M, Yanagihara K, Inui K, Okabe T, Yamaguchi S, Kudoh J, Shimizu N, Narisawa K. Sakamoto O, et al. Among authors: aoki y. J Inherit Metab Dis. 1998 Dec;21(8):873-4. doi: 10.1023/a:1005435121933. J Inherit Metab Dis. 1998. PMID: 9870216 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3,551 results

Search Page

Filters