✦ LIBER ✦

Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

✍ Scribed by Okazaki, Y.; Furuno, M.; Kasukawa, T.; Adachi, J.; Bono, H.; Kondo, S.; Nikaido, I.; Osato, N.; Saito, R.; Suzuki, H.

Book ID: 109890742
Publisher: Nature Publishing Group
Year: 2002
Tongue: English
Weight: 257 KB
Volume: 420
Category: Article
ISSN: 0028-0836
DOI: 10.1038/nature01266

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Large-scale sequencing based on full-len

Large-scale sequencing based on full-length-enriched cDNA libraries in pigs: contribution to annotation of the pig genome draft sequence

✍ Uenishi, Hirohide; Morozumi, Takeya; Toki, Daisuke; Eguchi-Ogawa, Tomoko; Rund, 📂 Article 📅 2012 🏛 BioMed Central 🌐 English ⚖ 415 KB

Large-scale sequencing of normalized ful

Large-scale sequencing of normalized full-length cDNA library of soybean seed at different developmental stages and analysis of the gene expression profiles based on ESTs

✍ Ai-Hua Sha; Chen Li; Xiao-Hong Yan; Zhi-Hui Shan; Xin-An Zhou; Mu-Lan Jiang; Han 📂 Article 📅 2011 🏛 Springer 🌐 English ⚖ 331 KB

Functional analysis of an ADAMTS10 signa

Functional analysis of an ADAMTS10 signal peptide mutation in Weill-Marchesani syndrome demonstrates a long-range effect on secretion of the full-length enzyme

✍ Wendy E. Kutz; Lauren W. Wang; Nathalie Dagoneau; Kazimir J. Odrcic; Valerie Cor 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 430 KB

We report the identification and functional analysis of the first missense ADAMTS10 mutation (c.73G4A; p.Ala25Thr) causing recessive Weill-Marchesani syndrome (WMS). The Ala25 residue affected by the missense mutation is at the À1 position relative to the ADAMTS10 signal peptidase cleavage site. p.A