✦ LIBER ✦

Insertional DNA and spontaneous mutation at the white locus in Drosophila simulans

✍ Scribed by Inoue, Yoshihiro H. ;Yamamoto, Masa-Toshi

Publisher: Springer
Year: 1987
Tongue: English
Weight: 806 KB
Volume: 209
Category: Article
ISSN: 0026-8925
DOI: 10.1007/bf00329842

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Crouzon-like craniofacial dysmorphology

Crouzon-like craniofacial dysmorphology in the mouse is caused by an insertional mutation at the Fgf3/Fgf4 locus

✍ Mark B.L. Carlton; William H. Colledge; Martin J. Evans 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 529 KB

Retroviral insertional mutagenesis by means of ES cells has resulted in a new autosomal dominant mutation causing craniofacial dysmorphology in the mouse (Bulgy-eye, Bey). Heterozygous Bey mice are viable and fertile but show facial shortening with increased interorbital distance and precocious clos

DNA sequence of the Doe retroposon in th

DNA sequence of the Doe retroposon in the white-one mutant of Drosophila melanogaster and of secondary insertions in the phenotypically altered derivatives white honey and white-eosin

✍ O'Hare, K. ;Alley, M. R. K. ;Cullingford, T. E. ;Driver, A. ;Sanderson, M. J. 📂 Article 📅 1991 🏛 Springer 🌐 English ⚖ 858 KB

We analysed the structure of the white locus of Drosophila melanogaster in a family of related white mutants. The white-one mutant has bleach white eyes, and a Doc transposable element is inserted into the promotor region of the white locus. The DNA sequence of this Doc insertion was determined, and

Spontaneous mutation spectrum at the lam

Spontaneous mutation spectrum at the lambda cII locus in liver, lung, and spleen tissue of Big Blue® transgenic mice

✍ P.R. Harbach; D.M. Zimmer; A.L. Filipunas; W.B. Mattes; C.S. Aaron 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 241 KB 👁 2 views

Big Blue ® mice harbor a recoverable transgene in a lambda/LIZ shuttle vector. In the standard assay, in vivo mutations are measured in the bacterial lacI gene using a labor-intensive color plaque assay. Applying a simpler assay : Proc Natl Acad Sci USA 93:9073-9078], we measured mutations in the la

Spectrum of phenylketonuria mutations in

Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus

✍ Monique Berthelon; Catherine Caillaud; Françoise Rey; Philippe Labrune; Dominiqu 📂 Article 📅 1991 🏛 Springer 🌐 English ⚖ 396 KB

A total of 252 chromosomes from 126 patients with phenylalanine hydroxylase (PAH) deficiencies were analyzed for both mutant genotypes and restriction fragment length polymorphism (RFLP) haplotypes at the PAH locus. The mutant genes studied originated either from Western Europe (116 alleles) or from