Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

1,822 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Efficacy of short-term treatment of pertussis with clarithromycin and azithromycin.
Aoyama T, Sunakawa K, Iwata S, Takeuchi Y, Fujii R. Aoyama T, et al. J Pediatr. 1996 Nov;129(5):761-4. doi: 10.1016/s0022-3476(96)70163-4. J Pediatr. 1996. PMID: 8917247 Clinical Trial.
Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency.
Cox GF, Souri M, Aoyama T, Rockenmacher S, Varvogli L, Rohr F, Hashimoto T, Korson MS. Cox GF, et al. Among authors: aoyama t. J Pediatr. 1998 Aug;133(2):247-53. doi: 10.1016/s0022-3476(98)70228-8. J Pediatr. 1998. PMID: 9709714
Secondary carnitine deficiency in the newborn period in twins of a mother with partial ornithine transcarbamylase deficiency.
Nagao M, Tsuchiyama A, Aoyama T, Mori T, Oyanagi K. Nagao M, et al. Among authors: aoyama t. J Pediatr. 1989 Oct;115(4):611-4. doi: 10.1016/s0022-3476(89)80296-3. J Pediatr. 1989. PMID: 2795359 No abstract available.
Caspase-dependent and serine protease-dependent DNA fragmentation of myocytes in the ischemia-reperfused rabbit heart: these inhibitors do not reduce infarct size.
Minatoguchi S, Kariya T, Uno Y, Arai M, Nishida Y, Hashimoto K, Wang N, Aoyama T, Takemura G, Fujiwara T, Fujiwara H. Minatoguchi S, et al. Among authors: aoyama t. Jpn Circ J. 2001 Oct;65(10):907-11. doi: 10.1253/jcj.65.907. Jpn Circ J. 2001. PMID: 11665797
[Peroxisome proliferator-activated receptor beta(delta) (PPAR beta(delta))].
Sugiyama E, Tanaka N, Aoyama T. Sugiyama E, et al. Among authors: aoyama t. Nihon Rinsho. 2001 Feb;59 Suppl 2:301-4. Nihon Rinsho. 2001. PMID: 11351593 Review. Japanese. No abstract available.
Assignment of the gene for very-long-chain acyl-CoA dehydrogenase (Acadvl) to mouse chromosome band 11B2-B5 by in situ hybridization.
Orii KO, Saito-Ohara F, Ikeuchi T, Orii T, Kondo N, Aoyama T, Hashimoto T. Orii KO, et al. Among authors: aoyama t. Cytogenet Cell Genet. 1997;78(1):25-6. doi: 10.1159/000134619. Cytogenet Cell Genet. 1997. PMID: 9345900 No abstract available.
Age-dependent PPARα activation induces hepatic sulfatide accumulation in transgenic mice carrying the hepatitis C virus core gene.
Tian Y, Yang Y, Zhang X, Nakajima T, Tanaka N, Sugiyama E, Kamijo Y, Lu Y, Moriya K, Koike K, Gonzalez FJ, Aoyama T. Tian Y, et al. Among authors: aoyama t. Glycoconj J. 2016 Dec;33(6):927-936. doi: 10.1007/s10719-016-9703-1. Epub 2016 Jun 18. Glycoconj J. 2016. PMID: 27318478 Free PMC article.
Genomic and mutational analysis of the mitochondrial trifunctional protein beta-subunit (HADHB) gene in patients with trifunctional protein deficiency.
Orii KE, Aoyama T, Wakui K, Fukushima Y, Miyajima H, Yamaguchi S, Orii T, Kondo N, Hashimoto T. Orii KE, et al. Among authors: aoyama t. Hum Mol Genet. 1997 Aug;6(8):1215-24. doi: 10.1093/hmg/6.8.1215. Hum Mol Genet. 1997. PMID: 9259266
We detected two mutations in the HADHB gene from two Japanese patients, an exonic single T insertion which created a new cryptic 5' splice site and a G1331A transition (R411 K). ...
We detected two mutations in the HADHB gene from two Japanese patients, an exonic single T insertion which created a new cryptic 5' s …
Molecular basis of very long chain acyl-CoA dehydrogenase deficiency in three Israeli patients: identification of a complex mutant allele with P65L and K247Q mutations, the former being an exonic mutation causing exon 3 skipping.
Watanabe H, Orii KE, Fukao T, Song XQ, Aoyama T, IJlst L, Ruiter J, Wanders RJ, Kondo N. Watanabe H, et al. Among authors: aoyama t. Hum Mutat. 2000;15(5):430-8. doi: 10.1002/(SICI)1098-1004(200005)15:5<430::AID-HUMU4>3.0.CO;2-1. Hum Mutat. 2000. PMID: 10790204
Patient 1 was homozygous for a complex mutant allele containing two alterations, including a 194C>T transition (P65L) and 739A>C transversion (K247Q); in the case of P65L, the amino acid change does not reduce enzyme activity. ...
Patient 1 was homozygous for a complex mutant allele containing two alterations, including a 194C>T transition (P65L) and 739A> …
Formation of the enzyme complex in mitochondria is required for function of trifunctional beta-oxidation protein.
Orii KE, Aoyama T, Souri M, Jiang LL, Orii KO, Hayashi S, Yamaguchi S, Kondo N, Orii T, Hashimoto T. Orii KE, et al. Among authors: aoyama t. Biochem Biophys Res Commun. 1996 Feb 27;219(3):773-7. doi: 10.1006/bbrc.1996.0309. Biochem Biophys Res Commun. 1996. PMID: 8645256
1,822 results
Jump to page
Feedback