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フイブリノゲンγ鎖における遺伝子多型の検討
http://hdl.handle.net/10091/5186
http://hdl.handle.net/10091/518650083923-2df2-4f6d-9b8f-4dc9163eba64
| 名前 / ファイル | ライセンス | アクション |
|---|---|---|
Allied_Med20_05.pdf (346.2 kB)
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| Item type | 紀要論文 / Departmental Bulletin Paper(1) | |||||
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| 公開日 | 2010-03-01 | |||||
| タイトル | ||||||
| タイトル | フイブリノゲンγ鎖における遺伝子多型の検討 | |||||
| タイトル | ||||||
| タイトル | Studies on Genetic Polymorphism in Human Fibrinogen Gamma Chain | |||||
| 言語 | ||||||
| 言語 | jpn | |||||
| キーワード | ||||||
| 主題 | Fibrinogen, Gamma Chain, Genetic Polymorphism, DNA Sequence フィブリノゲン, γ鎖, 遺伝子多型, DNA塩基配列 |
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| 資源タイプ | ||||||
| 資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
| 資源タイプ | departmental bulletin paper | |||||
| 著者 |
寺澤, 文子
× 寺澤, 文子× 奥村, 伸生× 降旗, 謙一 |
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| 信州大学研究者総覧へのリンク | ||||||
| 表示名 | 奥村, 伸生 | |||||
| URL | http://soar-rd.shinshu-u.ac.jp/profile/ja.OVnmgCkh.html | |||||
| 出版者 | ||||||
| 出版者 | 信州大学医療技術短期大学部 | |||||
| 引用 | ||||||
| 内容記述タイプ | Other | |||||
| 内容記述 | 紀要 20: 31-36(1995) | |||||
| 書誌情報 |
紀要 巻 20, p. 31-36, 発行日 1995-02-28 |
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| 抄録 | ||||||
| 内容記述タイプ | Abstract | |||||
| 内容記述 | In the gene of human fibrinogen gamma chain, nucleotide poly(di)morphism has been reported at eight different positions. Among them, nucleotide 2543 is the middle base of the codon which encords residue 88 resulting in an amino acid substitution of Lysine to lsoleucine. However remaining seven mutations are silent. We examined frequency of genomic polymorphism for gamma chain nucleotide 2543 by DNA sequencing and effect of the amino acid substitution on fibrinogen function. DNA was isolated from peripheral nucleated cells of 11healthy volunteers and one patient with dysfibrinogenemia and the fourth exon of gamma chain containing the nucleotide 2543 was amplified by polymerase chain reaction(PCR). Nucleotide sequence was directry analyzed by Dye Deoxy Terminator method using an ABI 373A DNA sequencer. The nucleotide 2543 was A in all 12 samples. We investigated gamma chain sequence of a case of dysfibrinogenemia and found that the nucleotide 2543 was homozygous for A but heterozygous for G and C at nucleotide 9380, resulted in the substitution of Aspartic acid and Histidine. We conclude that Lysine at residue 88 of gamma chain is wild type and lsoleucine is a rare mutation. It was also suggested that this polymorphism was not responsible for the pathogenesis of the dysfibrinogenemia. | |||||
| 資源タイプ（コンテンツの種類） | ||||||
| 内容記述タイプ | Other | |||||
| 内容記述 | Article | |||||
| ISSN | ||||||
| 収録物識別子タイプ | ISSN | |||||
| 収録物識別子 | 0385-1982 | |||||
| 書誌レコードID | ||||||
| 収録物識別子タイプ | NCID | |||||
| 収録物識別子 | AN10402438 | |||||
