Ogawa A - Search Results

1

Identification of three novel mutations in the MNK gene in three unrelated Japanese patients with classical Menkes disease.

Ogawa A, Yamamoto S, Takayanagi M, Kogo T, Kanazawa M, Kohno Y. Ogawa A, et al. J Hum Genet. 1999;44(3):206-9. doi: 10.1007/s100380050144. J Hum Genet. 1999. PMID: 10319589

2

Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency.

Ogawa E, Kanazawa M, Yamamoto S, Ohtsuka S, Ogawa A, Ohtake A, Takayanagi M, Kohno Y. Ogawa E, et al. Among authors: ogawa a. J Hum Genet. 2002;47(7):342-7. doi: 10.1007/s100380200047. J Hum Genet. 2002. PMID: 12111367

3

Two novel gene mutations (Glu174-->Lys, Phe383-->Tyr) causing the "hepatic" form of carnitine palmitoyltransferase II deficiency.

Yamamoto S, Abe H, Kohgo T, Ogawa A, Ohtake A, Hayashibe H, Sakuraba H, Suzuki Y, Aramaki S, Takayanagi M, Hasegawa S, Niimi H. Yamamoto S, et al. Among authors: ogawa a. Hum Genet. 1996 Jul;98(1):116-8. doi: 10.1007/s004390050170. Hum Genet. 1996. PMID: 8682496

4

An Ile/Val polymorphism at codon 1464 of the ATP7A gene.

Ogawa A, Yamamoto S, Takayanagi M, Kogo T, Kanazawa M, Kohno Y. Ogawa A, et al. J Hum Genet. 1999;44(6):423-4. doi: 10.1007/s100380050194. J Hum Genet. 1999. PMID: 10570920

5

Identification of two novel mutations of the carnitine/acylcarnitine translocase (CACT) gene in a patient with CACT deficiency.

Ogawa A, Yamamoto S, Kanazawa M, Takayanagi M, Hasegawa S, Kohno Y. Ogawa A, et al. J Hum Genet. 2000;45(1):52-5. doi: 10.1007/s100380050010. J Hum Genet. 2000. PMID: 10697964

6

Novel mutation of L718X in the ATP7A gene in a Japanese patient with classical Menkes disease, and four novel polymorphisms in the Japanese population.

Ogawa A, Yamamoto S, Kanazawa M, Ogawa E, Takayanagi M, Hasegawa S, Kohno Y. Ogawa A, et al. Among authors: ogawa e. J Hum Genet. 2000;45(5):315-7. doi: 10.1007/s100380070024. J Hum Genet. 2000. PMID: 11043517

7

Prenatal diagnosis of Menkes disease by genetic analysis and copper measurement.

Gu YH, Kodama H, Sato E, Mochizuki D, Yanagawa Y, Takayanagi M, Sato K, Ogawa A, Ushijima H, Lee CC. Gu YH, et al. Among authors: ogawa a. Brain Dev. 2002 Oct;24(7):715-8. doi: 10.1016/s0387-7604(02)00093-1. Brain Dev. 2002. PMID: 12427520

8

Monocyte chemoattractant protein 1 gene regulatory region polymorphism and serum levels of monocyte chemoattractant protein 1 in Japanese patients with Kawasaki disease.

Jibiki T, Terai M, Shima M, Ogawa A, Hamada H, Kanazawa M, Yamamoto S, Oana S, Kohno Y. Jibiki T, et al. Among authors: ogawa a. Arthritis Rheum. 2001 Sep;44(9):2211-2. doi: 10.1002/1529-0131(200109)44:9<2211::aid-art375>3.0.co;2-a. Arthritis Rheum. 2001. PMID: 11592387 Free article. No abstract available.

9

Copper metabolism after living donor liver transplantation for hepatic failure of Wilson's disease from a gene mutated donor.

Kobayashi S, Ochiai T, Hori S, Suzuki T, Shimizu T, Gunji Y, Shimada H, Yamamoto S, Ogawa A, Kohno Y, Sunaga M, Shimazu M, Tanaka K. Kobayashi S, et al. Among authors: ogawa a. Hepatogastroenterology. 2001 Sep-Oct;48(41):1259-61. Hepatogastroenterology. 2001. PMID: 11677941

10

Mutations of carnitine palmitoyltransferase II (CPT II) in Japanese patients with CPT II deficiency.

Yasuno T, Kaneoka H, Tokuyasu T, Aoki J, Yoshida S, Takayanagi M, Ohtake A, Kanazawa M, Ogawa A, Tojo K, Saito T. Yasuno T, et al. Among authors: ogawa a. Clin Genet. 2008 May;73(5):496-501. doi: 10.1111/j.1399-0004.2008.00986.x. Epub 2007 Mar 19. Clin Genet. 2008. PMID: 18363739

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