𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mosaic and polymorphic imprinting of the WT1 gene in humans

✍ Scribed by Jinno, Yoshihiro; Yun, Kankatsu; Nishiwaki, Kunihiko; Kubota, Takeo; Ogawa, Osamu; Reeve, Anthony E.; Niikawa, Norio


Book ID
109915394
Publisher
Nature Publishing Group
Year
1994
Tongue
English
Weight
567 KB
Volume
6
Category
Article
ISSN
1061-4036

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Genomic Organization of the Human WT1 Ge
✍ Tadokoro, Keiko ;Oki, Noriko ;Fujii, Hanako ;Ohshima, Akira ;Inoue, Tadashi ;Yam πŸ“‚ Article πŸ“… 1992 πŸ› Wiley (Blackwell Publishing) 🌐 English βš– 383 KB
A single base pair polymorphism in the W
✍ Natalie Groves; Paul N. Baird; Annette Hogg; John K. Cowell πŸ“‚ Article πŸ“… 1992 πŸ› Springer 🌐 English βš– 669 KB

The Wilms' tumor predisposition gene, WT1, was analysed exon-by-exon in a variety of tumours using the single-strand conformation polymorphism (SSCP) technique. A consistent variation in the usual band pattern for exon 7 was detected in this survey. On sequencing, a silent mutation was noted in codo

Mutations and polymorphisms in the human
✍ Katharina Engel; Wolfgang HΓΆhne; Johannes HΓ€berle πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 399 KB

Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1). Deficiency of ASS1 shows various clinical manifestations encompassing severely affected patients with fatal neonatal hyperammonemia as well as asymptom