𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutations causing defective splicing in the human hprt gene

✍ Scribed by Björn Andersson; Sai-Mei Hou; Bo Lambert


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
698 KB
Volume
20
Category
Article
ISSN
0893-6692

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Splicing mutations at the HPRT locus in
✍ Anne-May Österholm; Sai-Mei Hou 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 183 KB 👁 3 views

We studied 58 splicing mutations originating in observed. The predicted change in three of the base vivo at the hypoxanthine guanine phosphoribosyl-substitutions would be a stop codon. The tandem transferase (HPRT) locus in T-cells of 30 nonsmoking mutation (CC r TT) occurred at position 550-551, ma

Molecular analysis of mutations affectin
✍ Anna M. Rossi; Ad D. Tates; Albert A. Van Zeeland; Harry Vrieling 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 570 KB

## Molecular analysis of hypoxanthine-guanine analyzed in more detail by sequencing the gephosphoribosyltransferase (hprt) cDNA from nomic regions flanking the mis-spliced exon. ## 6-thioguanine-resistant T-lymphocytes cloned Base pair substitutions or small deletions causfrom smoking and non-s

Reported in vivo splice-site mutations i
✍ Rhett P. Ketterling; Joni B. Drost; William A. Scaringe; Dong-zhou Liao; Jing-zh 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 497 KB 👁 2 views

Small consensus sequences have been defined for RNA splicing, but questions about splicing in humans remain unanswered. Analysis of germline mutations in the factor IX gene offers a highly advantageous system for studying the mutational process in humans. In a sample of 860 families with hemophilia