Incidence of zinc and copper deficiency in Japan.

Por Matsuda, I, Higashi, A
Publicado em 1988

Comparative analysis of Pseudomonas syringae pv. actinidiae and pv. phaseolicola based on phaseolotoxin-resistant ornithine carbamoyltransferase gene (argK) and 16S-23S rRNA interg...

Por Sawada, H, Takeuchi, T, Matsuda, I
Publicado em 1997

PCR detection of Ti and Ri plasmids from phytopathogenic Agrobacterium strains.

Por Sawada, H, Ieki, H, Matsuda, I
Publicado em 1995

Hyperlipidaemia during persistent peritoneal dialysis.

Por Matsuda, I, Maeda, T, Takase, A, Arashima, S
Publicado em 1972

Screening for late neonatal vitamin K deficiency by acarboxyprothrombin in dried blood spots.

Por Motohara, K, Endo, F, Matsuda, I
Publicado em 1987

Dosage schedule of gentamicin for chronic renal insufficiency in children.

Por Yoshioka, H, Takimoto, M, Matsuda, I, Hattori, S
Publicado em 1978

A murine model for type III tyrosinemia: lack of immunologically detectable 4-hydroxyphenylpyruvic acid dioxygenase enzyme protein in a novel mouse strain with hypertyrosinemia.

Por Endo, F, Katoh, H, Yamamoto, S, Matsuda, I
Publicado em 1991

A single nucleotide change in the prolidase gene in fibroblasts from two patients with polypeptide positive prolidase deficiency. Expression of the mutant enzyme in NIH 3T3 cells.

Por Tanoue, A, Endo, F, Kitano, A, Matsuda, I
Publicado em 1990

Mucinous Cystadenocarcinoma of the Colon during Pregnancy

Por Shoji, T., Sakurai, N., Misumi, K., Matsuda, I., Terada, T.
Publicado em 2009

Structure of the rat argininosuccinate lyase gene: close similarity to chicken delta-crystallin genes.

Por Matsubasa, T, Takiguchi, M, Amaya, Y, Matsuda, I, Mori, M
Publicado em 1989

Inactive form of erythrocyte carbonic anhydrase B in patients with primary renal tubular acidosis.

Por Kondo, T, Taniguchi, N, Taniguchi, K, Matsuda, I, Murao, M
Publicado em 1978

Altered kinetic properties of the branched-chain alpha-keto acid dehydrogenase complex due to mutation of the beta-subunit of the branched-chain alpha-keto acid decarboxylase (E1)...

Por Indo, Y, Kitano, A, Endo, F, Akaboshi, I, Matsuda, I
Publicado em 1987

Carbamyl phosphate synthetase I deficiency. One base substitution in an exon of the CPS I gene causes a 9-basepair deletion due to aberrant splicing.

Por Hoshide, R, Matsuura, T, Haraguchi, Y, Endo, F, Yoshinaga, M, Matsuda, I
Publicado em 1993

Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene...

Por Tanoue, A, Endo, F, Akaboshi, I, Oono, T, Arata, J, Matsuda, I
Publicado em 1991

Molecular cloning and nucleotide sequence of cDNA for human liver arginase.

Por Haraguchi, Y, Takiguchi, M, Amaya, Y, Kawamoto, S, Matsuda, I, Mori, M
Publicado em 1987

Correspondence

Por Endo, F., Matsukura, M., Maeda, T., Ueno, T., Matsuda, I., Sakazaki, E., Morioka, T.
Publicado em 1978

An 11-base-pair DNA sequence motif apparently unique to the human interleukin 4 gene confers responsiveness to T-cell activation signals.

Por Abe, E, De Waal Malefyt, R, Matsuda, I, Arai, K, Arai, N
Publicado em 1992

Maple syrup urine disease caused by a partial deletion in the inner E2 core domain of the branched chain alpha-keto acid dehydrogenase complex due to aberrant splicing. A single ba...

Por Mitsubuchi, H, Nobukuni, Y, Akaboshi, I, Indo, Y, Endo, F, Matsuda, I
Publicado em 1991

Maple syrup urine disease. Complete primary structure of the E1 beta subunit of human branched chain alpha-ketoacid dehydrogenase complex deduced from the nucleotide sequence and a...

Por Nobukuni, Y, Mitsubuchi, H, Endo, F, Akaboshi, I, Asaka, J, Matsuda, I
Publicado em 1990

Constitutive production of multiple colony-stimulating factors in patients with lung cancer associated with neutrophilia.

Por Adachi, N., Yamaguchi, K., Morikawa, T., Suzuki, M., Matsuda, I., Abe, M. K.
Publicado em 1994