Kobayashi Y - Search Results

1

Exonic point mutations in NADH-cytochrome B5 reductase genes of homozygotes for hereditary methemoglobinemia, types I and III: putative mechanisms of tissue-dependent enzyme deficiency.

Katsube T, Sakamoto N, Kobayashi Y, Seki R, Hirano M, Tanishima K, Tomoda A, Takazakura E, Yubisui T, Takeshita M, et al. Katsube T, et al. Among authors: kobayashi y. Am J Hum Genet. 1991 Apr;48(4):799-808. Am J Hum Genet. 1991. PMID: 1707593 Free PMC article.

2

Serine-proline replacement at residue 127 of NADH-cytochrome b5 reductase causes hereditary methemoglobinemia, generalized type.

Kobayashi Y, Fukumaki Y, Yubisui T, Inoue J, Sakaki Y. Kobayashi Y, et al. Blood. 1990 Apr 1;75(7):1408-13. Blood. 1990. PMID: 2107882 Free article.

3

The organization and the complete nucleotide sequence of the human NADH-cytochrome b5 reductase gene.

Tomatsu S, Kobayashi Y, Fukumaki Y, Yubisui T, Orii T, Sakaki Y. Tomatsu S, et al. Among authors: kobayashi y. Gene. 1989 Aug 15;80(2):353-61. doi: 10.1016/0378-1119(89)90299-0. Gene. 1989. PMID: 2479590

4

Structural role of serine 127 in the NADH-binding site of human NADH-cytochrome b5 reductase.

Yubisui T, Shirabe K, Takeshita M, Kobayashi Y, Fukumaki Y, Sakaki Y, Takano T. Yubisui T, et al. Among authors: kobayashi y. J Biol Chem. 1991 Jan 5;266(1):66-70. J Biol Chem. 1991. PMID: 1898726 Free article.

5

[Molecular analysis of the structure of the mutant NADH-cytochrome b5 reductase gene causing methemoglobinemia].

Kobayashi Y. Kobayashi Y. Fukuoka Igaku Zasshi. 1990 Jan;81(1):41-7. Fukuoka Igaku Zasshi. 1990. PMID: 2323714 Japanese.

6

Nonsense mutations at Arg-1947 in two cases of familial neurofibromatosis type 1 in Japanese.

Horiuchi T, Hatta N, Matsumoto M, Ohtsuka H, Collins FS, Kobayashi Y, Fujita S. Horiuchi T, et al. Among authors: kobayashi y. Hum Genet. 1994 Jan;93(1):81-3. doi: 10.1007/BF00218920. Hum Genet. 1994. PMID: 7903661 Free article.

7

The human interleukin-10 receptor gene maps to chromosome 11q23.3.

Taniyama T, Takai S, Miyazaki E, Fukumura R, Sato J, Kobayashi Y, Hirakawa T, Moore KW, Yamada K. Taniyama T, et al. Among authors: kobayashi y. Hum Genet. 1995 Jan;95(1):99-101. doi: 10.1007/BF00225083. Hum Genet. 1995. PMID: 7814035

8

A single nucleotide deletion in codon 123 of the beta-globin gene causes an inclusion body beta-thalassaemia trait: a novel elongated globin chain beta Makabe.

Fucharoen S, Kobayashi Y, Fucharoen G, Ohba Y, Miyazono K, Fukumaki Y, Takaku F. Fucharoen S, et al. Among authors: kobayashi y. Br J Haematol. 1990 Jul;75(3):393-9. doi: 10.1111/j.1365-2141.1990.tb04354.x. Br J Haematol. 1990. PMID: 2167124

9

A novel globin structural mutant, Showa-Yakushiji (beta 110 Leu-Pro) causing a beta-thalassemia phenotype.

Kobayashi Y, Fukumaki Y, Komatsu N, Ohba Y, Miyaji T, Miura Y. Kobayashi Y, et al. Blood. 1987 Nov;70(5):1688-91. Blood. 1987. PMID: 2822177 Free article.

10

NF1 gene mutations in Japanese with neurofibromatosis 1 (NF1).

Hatta N, Horiuchi T, Watanabe I, Kobayashi Y, Shirakata Y, Ohtsuka H, Minami T, Ueda K, Kokoroishi T, Fujita S. Hatta N, et al. Among authors: kobayashi y. Biochem Biophys Res Commun. 1995 Jul 17;212(2):697-704. doi: 10.1006/bbrc.1995.2025. Biochem Biophys Res Commun. 1995. PMID: 7542886

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

10,270 results

Search Page