✦ LIBER ✦

Proapoptotic effects of NARC 1 (= PCSK9), the gene encoding a novel serine proteinase

✍ Scribed by Brendan Bingham; Ru Shen; Smita Kotnis; C. Frederick Lo; Bradley A. Ozenberger; Nivedita Ghosh; Jeffrey D. Kennedy; J. Steven Jacobsen; Jill M. Grenier; Peter S. DiStefano; Lillian W. Chiang; Andrew Wood

Book ID: 102813852
Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 535 KB
Volume: 69A
Category: Article
ISSN: 0196-4763
DOI: 10.1002/cyto.a.20346

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

hBRAG, a novel B cell lineage cDNA encod

hBRAG, a novel B cell lineage cDNA encoding a type II transmembrane glycoprotein potentially involved in the regulation of recombination activating gene 1 (RAG1)

✍ Laurent K. Verkoczy; Philip A. Marsden; Neil L. Berinstein 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 295 KB 👁 1 views

A novel splice site mutation c.2278 (−1)

A novel splice site mutation c.2278 (−1) G>C in the TMPRSS6 gene causes deletion of the substrate binding site of the serine protease resulting in refractory iron deficiency anaemia

✍ Eunice S. Edison; Rekha Athiyarath; Thirugnanam Rajasekar; Mark Westerman; Alok 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 221 KB

Development of a novel non-human primate

Development of a novel non-human primate model for preclinical gene vector safety studies. Determining the effects of intracerebral HSV-1 inoculation in the common marmoset: a comparative study

✍ Deisboeck, T S; Wakimoto, H; Nestler, U; Louis, D N; Sehgal, P K; Simon, M; Chio 📂 Article 📅 2003 🏛 Nature Publishing Group 🌐 English ⚖ 292 KB

Two novel mutant alleles of the gene enc

Two novel mutant alleles of the gene encoding neurotrophic tyrosine kinase receptor type 1 (NTRK1) in a patient with congenital insensitivity to pain with anhidrosis: A splice junction mutation in intron 5 and cluster of four mutations in exon 15

✍ Marek Bodzioch; Katarzyna Lapicka; Charalampos Aslanidis; Marek Kacinski; Gerd S 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 34 KB 👁 3 views

Congenital insensitivity to pain with anhidrosis (CIPA), also called hereditary sensory and autonomic neuropathy type IV (HSAN IV), is caused by mutations of the NTRK1 gene coding for the neurotrophic tyrosine kinase receptor type 1. We report the results of the NTRK1 sequence analysis in a CIPA fam