𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Novel mutant phenotypes of a dark-germinating mutantdkg1in the fernCeratopteris richardii

✍ Scribed by Hiroyuki Kamachi; Eishi Matsunaga; Munenori Noguchi; Hiroshi Inoue

Book ID
106302380
Publisher
Springer
Year
2004
Tongue
English
Weight
527 KB
Volume
117
Category
Article
ISSN
0918-9440

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

A novel phenotype of an excision-repair
A novel phenotype of an excision-repair mutant in Neurospora crassa: Mutagen sensitivity of the mus-18 mutant is specific to UV
✍ Ishii, Chizu ;Nakamura, Kiyoshi ;Inoue, Hirokazu πŸ“‚ Article πŸ“… 1991 πŸ› Springer 🌐 English βš– 871 KB

A UV-sensitive mutant has been isolated from UV-mutagenized conidia of Neurospora crassa. The mutation responsible for the lesion was mapped in linkage group VL, proximal to the nucleolus organizer region. We designated the mutant mus-18. The sensitivity of the mus-18 mutant to UV-irradiation was no

Crigler-Najjar syndrome in The Netherlan
Crigler-Najjar syndrome in The Netherlands: Identification of four novel UGT1A1 alleles, genotype–phenotype correlation, and functional analysis of 10 missense mutants
✍ Nina Sneitz; Conny T. Bakker; Robert J. de Knegt; Dicky J.J. Halley; Moshe Finel πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 192 KB

Crigler-Najjar syndrome (CN), caused by deficiency of UGT isoform 1A1 (UGT1A1), is characterized by severe unconjugated hyperbilirubinemia. In this study we have analyzed 19 CN patients diagnosed in The Netherlands (18) and in Belgium (1), and have identified 14 different UGT1A1 mutations, four of w

Molecular genetics of the long QT syndro
Molecular genetics of the long QT syndrome: Two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindred
✍ Kirsi Saarinen; Heikki Swan; Katariina Kainulainen; Lauri Toivonen; Matti Viitas πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 213 KB πŸ‘ 3 views

At least three different gene loci were recently shown to account for the long QT syndrome (LQTS), a monogenic disorder with altered myocardial repolarization and occurrence of life-threatening cardiac arrhythmias. We screened 44 unrelated probands for mutations of the gene encoding the cardiac pota