Ogawa E - Search Results

1

Compound heterozygous mutations in the cholesterol side-chain cleavage enzyme gene (CYP11A) cause congenital adrenal insufficiency in humans.

Katsumata N, Ohtake M, Hojo T, Ogawa E, Hara T, Sato N, Tanaka T. Katsumata N, et al. Among authors: ogawa e. J Clin Endocrinol Metab. 2002 Aug;87(8):3808-13. doi: 10.1210/jcem.87.8.8763. J Clin Endocrinol Metab. 2002. PMID: 12161514

2

Novel CYP17A1 mutation in a Japanese patient with combined 17alpha-hydroxylase/17,20-lyase deficiency.

Katsumata N, Ogawa E, Fujiwara I, Fujikura K. Katsumata N, et al. Among authors: ogawa e. Metabolism. 2010 Feb;59(2):275-8. doi: 10.1016/j.metabol.2009.07.024. Epub 2009 Sep 29. Metabolism. 2010. PMID: 19793597

3

Kallmann syndrome phenotype in a female patient with CHARGE syndrome and CHD7 mutation.

Ogata T, Fujiwara I, Ogawa E, Sato N, Udaka T, Kosaki K. Ogata T, et al. Among authors: ogawa e. Endocr J. 2006 Dec;53(6):741-3. doi: 10.1507/endocrj.k06-099. Epub 2006 Sep 7. Endocr J. 2006. PMID: 16960397 Free article.

4

Hypospadias in a male patient with 21-hydroxylase deficiency.

Kojima-Ishii K, Fujiwara I, Katsumata N, Kanno J, Ogawa E, Tsuchiya S. Kojima-Ishii K, et al. Among authors: ogawa e. Endocr J. 2008 Dec;55(6):1051-4. doi: 10.1507/endocrj.k07e-175. Epub 2008 Aug 22. Endocr J. 2008. PMID: 18719294 Free article.

5

Infant formula with galacto-oligosaccharides (OM55N) stimulates the growth of indigenous bifidobacteria in healthy term infants.

Matsuki T, Tajima S, Hara T, Yahagi K, Ogawa E, Kodama H. Matsuki T, et al. Among authors: ogawa e. Benef Microbes. 2016 Sep;7(4):453-61. doi: 10.3920/BM2015.0168. Epub 2016 Apr 27. Benef Microbes. 2016. PMID: 27120106 Clinical Trial.

6

Effects of individual mutations in the P-450(C21) pseudogene on the P-450(C21) activity and their distribution in the patient genomes of congenital steroid 21-hydroxylase deficiency.

Higashi Y, Hiromasa T, Tanae A, Miki T, Nakura J, Kondo T, Ohura T, Ogawa E, Nakayama K, Fujii-Kuriyama Y. Higashi Y, et al. Among authors: ogawa e. J Biochem. 1991 Apr;109(4):638-44. doi: 10.1093/oxfordjournals.jbchem.a123433. J Biochem. 1991. PMID: 1869518 Free article.

7

Molecular analysis of Japanese patients with steroid 21-hydroxylase deficiency.

Asanuma A, Ohura T, Ogawa E, Sato S, Igarashi Y, Matsubara Y, Iinuma K. Asanuma A, et al. Among authors: ogawa e. J Hum Genet. 1999;44(5):312-7. doi: 10.1007/s100380050167. J Hum Genet. 1999. PMID: 10496074

8

Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus.

Kuwahara M, Iwai K, Ooeda T, Igarashi T, Ogawa E, Katsushima Y, Shinbo I, Uchida S, Terada Y, Arthus MF, Lonergan M, Fujiwara TM, Bichet DG, Marumo F, Sasaki S. Kuwahara M, et al. Among authors: ogawa e. Am J Hum Genet. 2001 Oct;69(4):738-48. doi: 10.1086/323643. Epub 2001 Aug 30. Am J Hum Genet. 2001. PMID: 11536078 Free PMC article.

9

Gonadal suppression by a GnRH analogue does not alter somatic growth in rats with complete GH deficiency.

Ogawa E, Breier BH, Fujiwara I, Iinuma K. Ogawa E, et al. J Endocrinol. 2000 Aug;166(2):355-61. doi: 10.1677/joe.0.1660355. J Endocrinol. 2000. PMID: 10927624

10

A novel intronic mutation of the TAZ ( G4.5) gene in a patient with Barth syndrome: creation of a 5' splice donor site with variant GC consensus and elongation of the upstream exon.

Sakamoto O, Ohura T, Katsushima Y, Fujiwara I, Ogawa E, Miyabayashi S, Iinuma K. Sakamoto O, et al. Among authors: ogawa e. Hum Genet. 2001 Nov;109(5):559-63. doi: 10.1007/s00439-001-0612-3. Epub 2001 Oct 13. Hum Genet. 2001. PMID: 11735032

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