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au.\*:("SHIMADZU M")

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Results 1 to 13 of 13

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THE J BAND OF THE MALACHITE GREEN-POLY(ALPHA -L-GLUTAMIC ACID) COMPLEXE: THE CONDITIONS FOR ITS APPEARANCE IN AQUEOUS SOLUTIONSYAMAOKA K; SHIMADZU M.1982; CHEM. LETT.; ISSN 0366-7022; JPN; DA. 1982; NO 4; PP. 583-586; BIBL. 9 REF.Article

STUDIES ON FURAN DERIVATIVES. XII: NUCLEOPHILIC SUBSTITUTION OF METHYL 5-NITRO-2-FURANCARBOXYLATE. PREPARATION OF METHYL 5-PHENOXY-2-FURANCARBOXYLATESTANAKA A; USUI T; SHIMADZU M et al.1981; J. HETEROCYCL. CHEM.; ISSN 0022-152X; USA; DA. 1981; VOL. 18; NO 6; PP. 1241-1244; BIBL. 6 REF.Article

CHARACTERIZATION OF A RADIATION-RESISTANT ACINETOBACTERNISHIMURA Y; KAIRIYAMA E; SHIMADZU M et al.1981; Z. ALLG. MIKROBIOL.; ISSN 0044-2208; DDR; DA. 1981; VOL. 21; NO 2; PP. 125-130; BIBL. 11 REF.Article

Comparison of gyrA and parC mutations and resistance levels among fluoroquinolone-resistant isolates and laboratory-derived mutants of oral streptococciKANEKO, A; SASAKI, J; SHIMADZU, M et al.Journal of antimicrobial chemotherapy (Print). 2000, Vol 45, Num 6, pp 771-775, issn 0305-7453Article

Dopa-responsive dystonia simulating spastic paraplegia due to tyrosine hydroxylase (TH) gene mutationsFURUKAWA, Y; GRAF, W. D; WONG, H et al.Neurology. 2001, Vol 56, Num 2, pp 260-263, issn 0028-3878Article

Assignment of SFA-1 (PETA-3), a member of the transmembrane 4 superfamily, to human chromosome 11p15.5 by fluorescence in situ hybridizationHASEGAWA, H; KISHIMOTO, K; YANAGISAWA, K et al.Genomics (San Diego, Calif.). 1997, Vol 40, Num 1, pp 193-196, issn 0888-7543Article

A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCRKUBOTA, T; NONOYAMA, S; TONOKI, H et al.Human genetics. 1999, Vol 104, Num 1, pp 49-55, issn 0340-6717Article

Familial lethal inheritance of a mutated paternal gene in females causing X-linked ornithine transcarbamylase (OTC) deficiencyKOMAKI, S; MATSUURA, T; OYANAGI, K et al.American journal of medical genetics. 1997, Vol 69, Num 2, pp 177-181, issn 0148-7299Article

Recombinant adeno-associated virus-mediated gene transfer into human leukemia cell linesITOU, T; MIYAMURA, K; ABE, A et al.International journal of hematology. 1998, Vol 67, Num 1, pp 27-35, issn 0925-5710Article

Molecular and biochemical aspects of hereditary progressive and dopa-responsive dystoniaFURUKAWA, Y; SHIMADZU, M; HORNYKIEWICZ, O et al.Advances in neurology. 1998, Vol 78, pp 267-282, issn 0091-3952Conference Paper

Mutations of the CD40 ligand gene in 13 Japanese patients with X-linked hyper-IgM syndromeNONOYAMA, S; SHIMADZU, M; TORU, H et al.Human genetics. 1997, Vol 99, Num 5, pp 624-627, issn 0340-6717Article

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 adultMATSUDA, I; MATSUURA, T; SHIMADZU, M et al.Journal of medical genetics. 1996, Vol 33, Num 8, pp 645-648, issn 0022-2593Article

GTP-cyclohydrolase I gene mutations in hereditary progressive and dopa-responsive dystoniaFURUKAWA, Y; SHIMADZU, M; KISH, S. J et al.Annals of neurology. 1996, Vol 39, Num 5, pp 609-617, issn 0364-5134Article

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