| ○種別 (必須): | □ | 学術論文 (審査論文)
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| ○言語 (必須): | □ | 英語
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| ○カテゴリ (推奨): |
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| ○学究種別 (推奨): |
| ○組織 (推奨): |
| ○著者 (必須): | 1. | (英) Akagi Reiko (日) (読)
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| 2. | (英) Inoue Rikako (日) (読)
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| 3. | (英) Muranaka Shikibu (日) (読)
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| 4. | 田原 強 ([徳島大学.先端研究推進センター.バイオイメージング研究部門])
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| 5. | (英) Taketani Shigeru (日) (読)
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| 6. | (英) Anderson Karl E (日) (読)
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| 7. | (英) Phillips John D (日) (読)
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| 8. | (英) Sassa Shigeru (日) (読)
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| ○題名 (必須): | □ | (英) Dual gene defects involving delta-aminolaevulinate dehydratase and coproporphyrinogen oxidase in a porphyria patient. (日)
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| ○副題 (任意): |
| ○要約 (任意): | □ | (英) Summary A Caucasian male had symptoms of acute porphyria, with increases in urinary delta-aminolaevulinic acid (ALA), porphobilinogen (PBG) and coproporphyrin that were consistent with hereditary coproporphyria (HCP). However, a greater than expected increase in ALA, compared with PBG, and a substantial increase in erythrocyte zinc protoporphyrin, suggested additional ALA dehydratase (ALAD) deficiency. Nucleotide sequence analysis of coproporphyrinogen oxidase (CPO) cDNA of the patient, but not of the parents, revealed a novel nucleotide transition G835-->C, resulting in an amino acid change, G279R. The mutant CPO protein expressed in Escherichia coli was unstable, and produced about 5% of activity compared with the wild-type CPO. Erythrocyte ALAD activity was 32% of normal in the proband. Nucleotide sequence analysis of cloned ALAD cDNAs from the patient revealed a C36-->G base transition (F12L amino acid change). The F12L ALAD mutation, which was found in the mother and a brother, was previously described, and is known to lack any enzyme activity. This patient thus represents the first case of porphyria where both CPO and ALAD deficiencies were demonstrated at the molecular level. (日)
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| ○キーワード (推奨): | 1. | (英) Adult (日) (読)
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| 2. | (英) Coproporphyria, Hereditary (日) (読)
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| 3. | (英) Coproporphyrinogen Oxidase (日) (読)
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| 4. | (英) DNA Mutational Analysis (日) (読)
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| 5. | (英) DNA, Complementary (日) (読)
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| 6. | (英) Erythrocytes (日) (読)
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| 7. | (英) Female (日) (読)
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| 8. | (英) Humans (日) (読)
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| 9. | (英) Male (日) (読)
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| 10. | (英) Models, Molecular (日) (読)
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| 11. | (英) Pedigree (日) (読)
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| 12. | (英) Porphobilinogen Synthase (日) (読)
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| ○発行所 (推奨): |
| ○誌名 (必須): | □ | British Journal of Haematology (British Society for Haematology)
(pISSN: 0007-1048, eISSN: 1365-2141)
| ○ISSN (任意): | □ | 0007-1048
ISSN: 0007-1048
(pISSN: 0007-1048, eISSN: 1365-2141) Title: British journal of haematologyTitle(ISO): Br J HaematolSupplier: British Society for HaematologyPublisher: Blackwell (NLM Catalog)
(Wiley)
(Scopus)
(CrossRef)
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| ○巻 (必須): | □ | 132
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| ○号 (必須): | □ | 2
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| ○頁 (必須): | □ | 237 243
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| ○都市 (任意): |
| ○年月日 (必須): | □ | 西暦 2006年 1月 初日 (平成 18年 1月 初日)
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| ○URL (任意): |
| ○DOI (任意): | □ | 10.1111/j.1365-2141.2005.05852.x (→Scopusで検索)
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| ○PMID (任意): | □ | 16398658 (→Scopusで検索)
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| ○備考 (任意): | 1. | (英) PublicationType: Case Reports (日)
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| 2. | (英) PublicationType: Journal Article (日)
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| 3. | (英) PublicationType: Research Support, N.I.H., Extramural (日)
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| 4. | (英) PublicationType: Research Support, Non-U.S. Gov't (日)
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