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	1.	The human c-Ha-ras2 is a processed pseudogene inactivated by numerous base substitutions. [electronic resource] by Miyoshi, J Kagimoto, M Soeda, E Sakaki, Y Producer: 19840424 In: Nucleic acids research vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Multiple species of bovine adrenodoxin mRNA. Occurrence of two different mitochondrial precursor sequences associated with the same mature sequence. [electronic resource] by Okamura, T Kagimoto, M Simpson, E R Waterman, M R Producer: 19870904 In: The Journal of biological chemistry vol. 262 Availability: No items available. Save to lists Add to cart (remove)
	3.	Hemoglobin G Waimanalo: alpha 64 (E13) aspartic acid----asparagine observed in a Japanese family. [electronic resource] by Sugihara, J Yokota, E Kagimoto, M Naito, Y Imamura, T Producer: 19840625 In: Hemoglobin vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Deduced amino acid sequence of mature chicken testis ferredoxin. [electronic resource] by Kagimoto, K McCarthy, J L Waterman, M R Kagimoto, M Producer: 19881005 In: Biochemical and biophysical research communications vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Case report--relapse of hereditary spherocytosis following splenectomy. [electronic resource] by Satou, S Yokota, E Sugihara, J Kagimoto, M Imamura, T Producer: 19860228 In: Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	6.	Transcription of the bovine adrenodoxin gene produces two species of mRNA of which only one is translated into adrenodoxin. [electronic resource] by Kagimoto, M Kagimoto, K Simpson, E R Waterman, M R Producer: 19880727 In: The Journal of biological chemistry vol. 263 Availability: No items available. Save to lists Add to cart (remove)
	7.	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. [electronic resource] by Kagimoto, M Heim, M Kagimoto, K Zeugin, T Meyer, U A Producer: 19901116 In: The Journal of biological chemistry vol. 265 Availability: No items available. Save to lists Add to cart (remove)
	8.	Multiple facial hemangiomas and iron-deficiency anemia: blue rubber-bleb nevus syndrome. [electronic resource] by Ohishi, M Tanaka, Y Higuchi, Y Otsuka, T Kagimoto, M Niho, Y Producer: 19850408 In: Head & neck surgery vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Identification of two apolipoprotein variants, A-I Karatsu (Tyr 100-->His) and A-I Kurume (His 162-->Gln). [electronic resource] by Moriyama, K Sasaki, J Matsunaga, A Takada, Y Kagimoto, M Arakawa, K Producer: 19961017 In: Clinical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A common Chinese beta-thalassemia mutation found in a Japanese family. [electronic resource] by Naritomi, Y Nakashima, H Kagimoto, M Naito, Y Yokota, E Imamura, T Producer: 19900518 In: Human genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a stop codon in the N-terminal region of 17 alpha-hydroxylase cytochrome P-450. [electronic resource] by Yanase, T Kagimoto, M Matsui, N Simpson, E R Waterman, M R Producer: 19881208 In: Molecular and cellular endocrinology vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: molecular basis of one example of combined 17 alpha-hydroxylase/17,20 lyase deficiency. [electronic resource] by Kagimoto, M Winter, J S Kagimoto, K Simpson, E R Waterman, M R Producer: 19881018 In: Molecular endocrinology (Baltimore, Md.) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Deletion of a phenylalanine in the N-terminal region of human cytochrome P-450(17 alpha) results in partial combined 17 alpha-hydroxylase/17,20-lyase deficiency. [electronic resource] by Yanase, T Kagimoto, M Suzuki, S Hashiba, K Simpson, E R Waterman, M R Producer: 19891127 In: The Journal of biological chemistry vol. 264 Availability: No items available. Save to lists Add to cart (remove)
	14.	A new electrophoretic variant of hemoglobin (Munakata) in which a lysine residue is replaced by a methionine residue at position 90 of the alpha-chain. [electronic resource] by Sugihara, J Imamura, T Kagimoto, M Matsuo, T Yamada, H Imoto, T Yanase, T Producer: 19830527 In: Biochimica et biophysica acta vol. 744 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Identification of a common molecular basis for combined 17 alpha-hydroxylase/17,20-lyase deficiency in two Mennonite families. [electronic resource] by Kagimoto, K Waterman, M R Kagimoto, M Ferreira, P Simpson, E R Winter, J S Producer: 19890720 In: Human genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	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 17 alpha-hydroxylase/17,20-lyase deficiency. [electronic resource] by Yanase, T Waterman, M R Zachmann, M Winter, J S Simpson, E R Kagimoto, M Producer: 19921006 In: Biochimica et biophysica acta vol. 1139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Identification of abnormal hemoglobin (J Lome): beta 59 (E3) lysine----asparagine in a Japanese. [electronic resource] by Naritomi, Y Kawaguchi, T Naito, Y Kagimoto, M Yokota, E Hirakawa, M Imamura, T Producer: 19860609 In: Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	18.	Hemoglobin J Lome: beta 59 (E3) lysine replaced by asparagine observed in a Japanese family. [electronic resource] by Sugihara, J Nakashima, H Yokota, E Kagimoto, M Imamura, T Yamada, H Imoto, T Producer: 19840403 In: Hemoglobin vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Hemoglobin Hofu: beta 126 (H4) valine----glutamic acid observed in a Japanese family. [electronic resource] by Yokota, E Sugihara, J Kagimoto, M Naito, Y Matsuo, T Imamura, T Yamada, H Imoto, T Producer: 19850410 In: Hemoglobin vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Thalassemia in Japan. [electronic resource] by Imamura, T Yokota, E Naito, Y Kagimoto, M Naritomi, Y Kawaguchi, T Sugihara, J Ohta, Y Producer: 19860731 In: Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society vol. 48 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 26 results.