Narisawa K - Search Results

1

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: narisawa k. Nat Genet. 1994 Oct;8(2):122-8. doi: 10.1038/ng1094-122. Nat Genet. 1994. PMID: 7842009

2

Purification and properties of bovine liver holocarboxylase synthetase.

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

3

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. Among authors: narisawa k. 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.

4

[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. Nihon Rinsho. 1996 Jan;54(1):259-67. Nihon Rinsho. 1996. PMID: 8587199 Review. Japanese.

5

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: narisawa k. Clin Chim Acta. 1996 Jul 15;251(1):41-52. doi: 10.1016/0009-8981(96)06291-2. Clin Chim Acta. 1996. PMID: 8814349

6

Purification and properties of bovine and human holocarboxylase synthetases.

Suzuki Y, Narisawa K. Suzuki Y, et al. Among authors: narisawa k. Methods Enzymol. 1997;279:386-93. doi: 10.1016/s0076-6879(97)79043-8. Methods Enzymol. 1997. PMID: 9211291 Review. No abstract available.

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. Among authors: narisawa k. Pediatr Res. 1997 Dec;42(6):849-54. doi: 10.1203/00006450-199712000-00021. Pediatr Res. 1997. PMID: 9396568

8

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: narisawa k. Biochim Biophys Acta. 1998 Jun 11;1385(1):165-71. doi: 10.1016/s0167-4838(98)00032-6. Biochim Biophys Acta. 1998. PMID: 9630604

9

Identification and characterization of mutations in patients with holocarboxylase synthetase deficiency.

Aoki Y, Li X, Sakamoto O, Hiratsuka M, Akaishi H, Xu L, Briones P, Suormala T, Baumgartner ER, Suzuki Y, Narisawa K. Aoki Y, et al. Among authors: narisawa k. Hum Genet. 1999 Feb;104(2):143-8. doi: 10.1007/s004390050927. Hum Genet. 1999. PMID: 10190325

10

Relationship between kinetic properties of mutant enzyme and biochemical and clinical responsiveness to biotin in holocarboxylase synthetase deficiency.

Sakamoto O, Suzuki Y, Li X, Aoki Y, Hiratsuka M, Suormala T, Baumgartner ER, Gibson KM, Narisawa K. Sakamoto O, et al. Among authors: narisawa k. Pediatr Res. 1999 Dec;46(6):671-6. doi: 10.1203/00006450-199912000-00004. Pediatr Res. 1999. PMID: 10590022

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

242 results

Search Page

Filters