抄録
Using a PCR strategy based on an initial set of 15 couples of primers designed from the known cDNA sequence, we identified 18 introns in the human RET proto-oncogene and sequenced the corresponding 5' and 3' exon-intron junctions. This approach was successful in locating all the introns contained in fragments short enough to be amplified by PCR. Thus 19 exons were identified which, together with the previously reported exon subjected to alternative splicing, brings the total number of RET exons to 20. This information is relevant for the screening of recently reported missense mutations of RET which cause Multiple Endocrine Neoplasia 2A (MEN2A) and for the search of additional point mutations of the same gene which might cause two other neural crest disorders, MEN2B and Hirschsprung disease, mapping in the same region as MEN2A.
| 本文言語 | 英語 |
|---|---|
| ページ(範囲) | 1288-1295 |
| ページ数 | 8 |
| ジャーナル | Biochemical and Biophysical Research Communications |
| 巻 | 196 |
| 号 | 3 |
| DOI | |
| 出版ステータス | 出版済み - 15-11-1993 |
| 外部発表 | はい |
UN SDG
この成果は、次の持続可能な開発目標に貢献しています
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SDG 3 すべての人に健康と福祉を
All Science Journal Classification (ASJC) codes
- 生物理学
- 生化学
- 分子生物学
- 細胞生物学
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「Exon structure and flanking intronic sequences of the human RET proto-oncogene」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。引用スタイル
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