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	61.	Epidemiological Survey of Listeria monocytogenes in a gravlax salmon processing line. [electronic resource] by Cruz, C D Silvestre, F A Kinoshita, E M Landgraf, M Franco, B D G M Destro, M T Producer: 20130913 In: Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	[Complete resection of an advanced mediastinal nonseminomatous germ cell tumor with multiple distant metastases after down-staging by chemotherapy]. [electronic resource] by Usuda, K Sagawa, M Aikawa, H Ueno, M Tanaka, M Machida, Y Tsuchihara, K Masaki, Y Kinoshita, E Sakuma, T Producer: 20090903 In: Kyobu geka. The Japanese journal of thoracic surgery vol. 62 Availability: No items available. Save to lists Add to cart (remove)
	63.	Sequence of a variant thyroxine-binding globulin (TBG) in a family with partial TBG deficiency in Japanese (TBG-PDJ). [electronic resource] by Miura, Y Mori, Y Yamamori, I Tani, Y Murata, Y Yoshimoto, M Kinoshita, E Matsumoto, T Oiso, Y Seo, H Producer: 19941129 In: Endocrine journal vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	[Diurnal changes in lecithin: cholesterol acyltransferase (LCAT) activities and effects of oral fat load]. [electronic resource] by Shiina, Y Homma, Y Mikami, Y Shyu, K Yoshikawa, H Ishihara, J Sato, M Higashino, M Kinoshita, E Tagawa, R Producer: 19850528 In: Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Molecular analysis of a patient with Beckwith-Wiedemann syndrome, rhabdomyosarcoma and renal cell carcinoma. [electronic resource] by Matsumoto, T Kinoshita, E Maeda, H Niikawa, N Kurosaki, N Harada, N Yun, K Sawai, T Aoki, S Kondoh, T Producer: 19941014 In: The Japanese journal of human genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	[A case of Fabry's disease associated with lupus nephritis]. [electronic resource] by Majima, K Ishizaki, T Inoue, T Hori, Y Egami, J Oohara, A Nishida, H Miyake, Y Matsumoto, S Kinoshita, E Producer: 19930415 In: Nihon Jinzo Gakkai shi vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	67.	A point mutation at ATP-binding region of the ALD gene in a family with X-linked adrenoleukodystrophy. [electronic resource] by Matsumoto, T Kondoh, T Masuzaki, H Harada, N Matsusaka, T Kinoshita, E Takeo, G Tsujihata, M Suzuki, Y Tsuji, Y Producer: 19950303 In: The Japanese journal of human genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	DAX-1 gene mutations and deletions in Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism. [electronic resource] by Kinoshita, E Yoshimoto, M Motomura, K Kawaguchi, T Mori, R Baba, T Nishijo, K Hasegawa, T Momoi, T Yorihuji, T Producer: 19970724 In: Hormone research vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Analysis of a non-functional HNF-1alpha (TCF1) mutation in Japanese subjects with familial type 1 diabetes. [electronic resource] by Yoshiuchi, I Yamagata, K Yoshimoto, M Zhu, Q Yang, Q Nammo, T Uenaka, R Kinoshita, E Hanafusa, T Matsuzawa, Y Producer: 20020122 In: Human mutation vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	Classic steroid 11 beta-hydroxylase deficiency caused by a C-->G transversion in exon 7 of CYP11B1. [electronic resource] by Yang, L X Toda, K Miyahara, K Nomoto, S Kinoshita, E Baba, T Yoshimoto, M Araki, K Kurashige, T Hashimoto, K Producer: 19951221 In: Biochemical and biophysical research communications vol. 216 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia. [electronic resource] by Fofanova, O V Takamura, N Kinoshita, E Meerson, E M Iljina, V K Nechvolodova, O L Evgrafov, O V Peterkova, V A Yamashita, S Producer: 19990824 In: Endocrine journal vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	Rarity of PIT1 involvement in children from Russia with combined pituitary hormone deficiency. [electronic resource] by Fofanova, O V Takamura, N Kinoshita, E Yoshimoto, M Tsuji, Y Peterkova, V A Evgrafov, O V Dedov, I I Goncharov, N P Yamashita, S Producer: 19990205 In: American journal of medical genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Terreic acid, a quinone epoxide inhibitor of Bruton's tyrosine kinase. [electronic resource] by Kawakami, Y Hartman, S E Kinoshita, E Suzuki, H Kitaura, J Yao, L Inagaki, N Franco, A Hata, D Maeda-Yamamoto, M Fukamachi, H Nagai, H Kawakami, T Producer: 19990415 In: Proceedings of the National Academy of Sciences of the United States of America vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency. [electronic resource] by Fofanova, O Takamura, N Kinoshita, E Parks, J S Brown, M R Peterkova, V A Evgrafov, O V Goncharov, N P Bulatov, A A Dedov, I I Yamashita, S Producer: 19980729 In: The Journal of clinical endocrinology and metabolism vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	75.	A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency. [electronic resource] by Fofanova, O V Takamura, N Kinoshita, E Parks, J S Brown, M R Peterkova, V A Evgrafov, O V Goncharov, N P Bulatov, A A Dedov, I I Yamashita, S Producer: 20001219 In: Pituitary vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients. [electronic resource] by Kobayashi, S Uemura, H Kohda, T Nagai, T Chinen, Y Naritomi, K Kinoshita, E I Ohashi, H Imaizumi, K Tsukahara, M Sugio, Y Tonoki, H Kishino, T Tanaka, T Yamada, M Tsutsumi, O Niikawa, N Kaneko-Ishino, T Ishino, F Producer: 20020115 In: American journal of medical genetics vol. 104 Availability: No items available. Save to lists Add to cart (remove)