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Proteomes|March 2, 2017
Immature Seed Endosperm and Embryo Proteomics of the Lotus (Nelumbo Nucifera Gaertn.) by One-Dimensional Gel-Based Tandem Mass Spectrometry and a Comparison with the Mature Endosperm ProteomeCarlo F Moro, Yoichiro Fukao, Junko Shibato, et al.European Journal of Pediatrics|December 29, 2000
Milder childhood form of very long-chain acyl-CoA dehydrogenase deficiency in a 6-year-old Japanese boyT Doi, W Abo, M Tateno, et al.Journal of Chromatography. B, Biomedical Sciences and Applications|August 3, 2001
Urinary organic acids in peroxisomal disorders: a simple screening methodS Yamaguchi, M Iga, M Kimura, et al.Journal of Inherited Metabolic Disease|July 24, 2010
A neonatal-onset succinyl-CoA:3-ketoacid CoA transferase (SCOT)-deficient patient with T435N and c.658-666dupAACGTGATT p.N220_I222dup mutations in the OXCT1 geneToshiyuki Fukao, Tomohiro Ishii, Naoko Amano, et al.Cancer Research|July 1, 1995
Mutations of p16Ink4/CDKN2 and p15Ink4B/MTS2 genes in biliary tract cancersS Yoshida, T Todoroki, Y Ichikawa, et al.Thrombosis and Haemostasis|December 1, 1994
Recombinant variants of tissue-type plasminogen activator containing amino acid substitutions in the fibronectin finger-like domain and the kringle 1 domainH Yahara, K Matsumoto, H Maruyama, et al.International Journal of Pediatric Otorhinolaryngology|August 22, 2009
Congenital inner ear malformations without sensorineural hearing loss in childrenMichio Ozeki, Zenichiro Kato, Hideo Sasai, et al.Molecular Genetics and Metabolism|December 16, 2006
Single-base substitution at the last nucleotide of exon 6 (c.671G>A), resulting in the skipping of exon 6, and exons 6 and 7 in human succinyl-CoA:3-ketoacid CoA transferase (SCOT) geneKeitaro Yamada, Toshiyuki Fukao, Gaixiu Zhang, et al.European Journal of Cancer (Oxford, England : 1990)|December 8, 2006
Alcohol consumption is associated with an increased risk of distal colon and rectal cancer in Japanese men: the Miyagi Cohort StudyMunira Akhter, Shinichi Kuriyama, Naoki Nakaya, et al.The Tohoku Journal of Experimental Medicine|June 15, 2010
Carnitine palmitoyltransferase 2 deficiency: the time-course of blood and urinary acylcarnitine levels during initial L-carnitine supplementationTomohiro Hori, Toshiyuki Fukao, Hironori Kobayashi, et al.Pageof 123