Masaaki Kagimoto - Concepedia

Concepedia

Author

Masaaki Kagimoto

The University of Texas Southwestern Medical Center

Also Known As

Kagimoto Masaaki, M Kagimoto, M. Kagimoto, Masaaki Kagimoto

24

Publications

1.2K

Citations

14

H-Index

39

Concepts

All Affiliations

The University of Texas Southwestern Medical Center Kyushu University University of Manitoba Southern Methodist University University of Alberta

MK

About

Masaaki Kagimoto is an author at The University of Texas Southwestern Medical Center specializing in biochemistry, medicine, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	10	10	548
2	Medicine	9	9	616
3	Natural Sciences	9	9	401
4	Engineering	1	1	12
5	Biomolecular Engineering	1	1	12

Masaaki Kagimoto

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17

Publications

1.2K

Citations

14

H-Index

	Year	Citations
Multiple mutations of the human cytochrome P450IID6 gene (CYP2D6) in poor metabolizers of debrisoquine. Study of the functional significance of individual mutations by expression of chimeric genes. Masaaki Kagimoto, Markus H. Heim, Keiko Kagimoto, Journal of Biological Chemistry Chimeric GenesGeneticsGenetic EpidemiologyHuman PolymorphismPathology	1990	267
Structural Characterization of Normal and Mutant Human Steroid 17α- Hydroxylase Genes: Molecular Basis of One Example of Combined 17α- Hydroxylase/17,20 Lyase Deficiency Masaaki Kagimoto, Jeremy S.D. Winter, Keiko Kagimoto, Molecular Endocrinology	1988	160
Rat P450<sub>17α</sub>from Testis: Characterization of a Full-Length cDNA Encoding a Unique Steroid Hydroxylase Capable of Catalyzing Both Δ<sup>4</sup>- and Δ<sup>5</sup>-Steroid-17,20-Lyase Reactions H. Richard Fevold, Matthew C. Lorence, John McCarthy, Molecular Endocrinology	1989	158
Transcriptional regulation of the bovine CYP17 (P-450(17)alpha) gene. Identification of two cAMP regulatory regions lacking the consensus cAMP-responsive element (CRE). Johan Lund, Dung-Ho Wu, Masaaki Kagimoto, Journal of Biological Chemistry Molecular RegulationGeneticsMolecular BiologyMolecular GeneticsGel Shift	1990	132
Deletion of a phenylalanine in the N-terminal region of human cytochrome P-45017α results in partial combined 17α-hydroxylase/17,20-lyase deficiency Toshihiko Yanase, Masaaki Kagimoto, Shingo Suzuki, Journal of Biological Chemistry	1989	96
Combined 17α-hydroxylase/17,20-lyase deficiency due to a stop codon in the N-terminal region of 17α-hydroxylase cytochrome P-450 Toshihiko Yanase, Masaaki Kagimoto, Nobuo Matsui, Molecular and Cellular Endocrinology Cellular EnzymologyBiochemistryNatural SciencesGenetics17α-Hydroxylase/17,20-lyase Deficiency	1988	54
Identification of a common molecular basis for combined 17?-hydroxylase/17,20-lyase deficiency in two Mennonite families Keiko Kagimoto, Michael R. Waterman, Masaaki Kagimoto, Human Genetics Aldehyde DehydrogenaseCellular EnzymologyBiochemistryCommon Molecular BasisGenetics	1989	50
Molecular basis of apparent isolated 17,20-lyase deficiency: compound heterozygous mutations in the C-terminal region (Arg(496) → Cys, Gln(461) → Stop) actually cause combined 17α-hydroxylase/17,20-lyase deficiency Toshihiko Yanase, Michael R. Waterman, M. Zachmann, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease C-terminal RegionBiochemistryNatural SciencesGeneticsBiochemical Genetics	1992	49
Structural characterization of the bovine CYP17 (17α-hydroxylase) gene C. Ramana Bhasker, Beverly S. Adler, Albert Dee, Archives of Biochemistry and Biophysics Bovine Cyp17BiochemistryNatural SciencesBiochemical GeneticsMolecular Biology	1989	44
The human c-Ha-<i>ras</i>2 is a processed pseudogene inactivated by numerous base substitutions Jun Miyoshi, Masaaki Kagimoto, Eiichi Soeda, Nucleic Acids Research	1984	32

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