Kiwaki K - Search Results

1

In vivo correction with recombinant adenovirus of 4-hydroxyphenylpyruvic acid dioxygenase deficiencies in strain III mice.

Kubo S, Kiwaki K, Awata H, Katoh H, Kanegae Y, Saito I, Yamamoto T, Miyazaki J, Matsuda I, Endo F. Kubo S, et al. Among authors: kiwaki k. Hum Gene Ther. 1997 Jan 1;8(1):65-71. doi: 10.1089/hum.1997.8.1-65. Hum Gene Ther. 1997. PMID: 8989996 Free article.

2

Gene therapy for ornithine transcarbamylase deficiency.

Kiwaki K, Matsuda I. Kiwaki K, et al. Acta Paediatr Jpn. 1996 Apr;38(2):189-92. doi: 10.1111/j.1442-200x.1996.tb03467.x. Acta Paediatr Jpn. 1996. PMID: 8677801 Review.

3

Correction of ornithine transcarbamylase deficiency in adult spf(ash) mice and in OTC-deficient human hepatocytes with recombinant adenoviruses bearing the CAG promoter.

Kiwaki K, Kanegae Y, Saito I, Komaki S, Nakamura K, Miyazaki JI, Endo F, Matsuda I. Kiwaki K, et al. Hum Gene Ther. 1996 May 1;7(7):821-30. doi: 10.1089/hum.1996.7.7-821. Hum Gene Ther. 1996. PMID: 8860834

4

Complete rescue of lethal albino c14CoS mice by null mutation of 4-hydroxyphenylpyruvate dioxygenase and induction of apoptosis of hepatocytes in these mice by in vivo retrieval of the tyrosine catabolic pathway.

Endo F, Kubo S, Awata H, Kiwaki K, Katoh H, Kanegae Y, Saito I, Miyazaki J, Yamamoto T, Jakobs C, Hattori S, Matsuda I. Endo F, et al. Among authors: kiwaki k. J Biol Chem. 1997 Sep 26;272(39):24426-32. doi: 10.1074/jbc.272.39.24426. J Biol Chem. 1997. PMID: 9305902 Free article.

5

Identification of two new aberrant splicings in the ornithine carbamoyltransferase (OCT) gene in two patients with early and late onset OCT deficiency.

Matsuura T, Hoshide R, Komaki S, Kiwaki K, Endo F, Nakamura S, Jitosho T, Matsuda I. Matsuura T, et al. Among authors: kiwaki k. J Inherit Metab Dis. 1995;18(3):273-82. doi: 10.1007/BF00710415. J Inherit Metab Dis. 1995. PMID: 7474892

6

Expression of four mutant human ornithine transcarbamylase genes in cultured Cos 1 cells relates to clinical phenotypes.

Matsuura T, Hoshide R, Setoyama C, Komaki S, Kiwaki K, Endo F, Nishikawa S, Matsuda I. Matsuura T, et al. Among authors: kiwaki k. Hum Genet. 1994 Feb;93(2):129-34. doi: 10.1007/BF00210596. Hum Genet. 1994. PMID: 8112735

7

[Gene therapy for ornithine transcarbamylase deficiency].

Matsuda I, Kiwaki K, Komaki S, Hoshide R, Matsuura T, Endo F. Matsuda I, et al. Among authors: kiwaki k. Tanpakushitsu Kakusan Koso. 1995 Dec;40(17):2759-64. Tanpakushitsu Kakusan Koso. 1995. PMID: 8584733 Review. Japanese. No abstract available.

8

X-inactivation pattern in the liver of a manifesting female with ornithine transcarbamylase (OTC) deficiency.

Yorifuji T, Muroi J, Uematsu A, Tanaka K, Kiwaki K, Endo F, Matsuda I, Nagasaka H, Furusho K. Yorifuji T, et al. Among authors: kiwaki k. Clin Genet. 1998 Oct;54(4):349-53. doi: 10.1034/j.1399-0004.1998.5440415.x. Clin Genet. 1998. PMID: 9831349

9

Phenotypic variability in male patients carrying the mutant ornithine transcarbamylase (OTC) allele, Arg40His, ranging from a child with an unfavourable prognosis to an asymptomatic older adult.

Matsuda I, Matsuura T, Nishiyori A, Komaki S, Hoshide R, Matsumoto T, Funakoshi M, Kiwaki K, Endo F, Hata A, Shimadzu M, Yoshino M. Matsuda I, et al. Among authors: kiwaki k. J Med Genet. 1996 Aug;33(8):645-8. doi: 10.1136/jmg.33.8.645. J Med Genet. 1996. PMID: 8863155 Free PMC article.

10

Familial lethal inheritance of a mutated paternal gene in females causing X-linked ornithine transcarbamylase (OTC) deficiency.

Komaki S, Matsuura T, Oyanagi K, Hoshide R, Kiwaki K, Endo F, Shimadzu M, Matsuda I. Komaki S, et al. Among authors: kiwaki k. Am J Med Genet. 1997 Mar 17;69(2):177-81. doi: 10.1002/(sici)1096-8628(19970317)69:2<177::aid-ajmg12>3.0.co;2-i. Am J Med Genet. 1997. PMID: 9056557

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