✦ LIBER ✦

Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma

✍ Scribed by Harbour, J William; Roberson, Elisha D O; Anbunathan, Hima; Onken, Michael D; Worley, Lori A; Bowcock, Anne M

Book ID: 121344414
Publisher: Nature Publishing Group
Year: 2013
Tongue: English
Weight: 235 KB
Volume: 45
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng.2523

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Exome sequencing identifies recurrent so

Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

✍ Martin, Marcel; Maßhöfer, Lars; Temming, Petra; Rahmann, Sven; Metz, Claudia; Bo 📂 Article 📅 2013 🏛 Nature Publishing Group 🌐 English ⚖ 402 KB

Exome sequencing identifies recurrent mu

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

✍ Quesada, Víctor; Conde, Laura; Villamor, Neus; Ordóñez, Gonzalo R; Jares, Pedro; 📂 Article 📅 2011 🏛 Nature Publishing Group 🌐 English ⚖ 936 KB

Mutations of the SF3B1 splicing factor i

Mutations of the SF3B1 splicing factor in chronic lymphocytic leukemia: association with progression and fludarabine-refractoriness

✍ Rossi, D.; Bruscaggin, A.; Spina, V.; Rasi, S.; Khiabanian, H.; Messina, M.; Fan 📂 Article 📅 2011 🏛 American Society of Hematology 🌐 English ⚖ 766 KB

Mutations at codon 61 of the Ha-ras prot

Mutations at codon 61 of the Ha-ras proto-oncogene in precancerous liver lesions of the B6C3F1 mouse

✍ Albrecht Buchmann; Johanna Mahr; Richard Bauer-Hofmann; Michael Schwarz 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 464 KB

ederal Republic of Germany Liver tumors of the B6C3F1 mouse frequently contain mutations at specific sites of codon 61 of the Ha-ras proto-oncogene. To address whether these mutations occur early or late during carcinogenesis, w e analyzed mutations in the Ha-ras gene in small precancerous liver les

Recurrent missense mutations at the firs

Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries

✍ Yuanhong Ma; Ming-Sun Liu; David Chitayat; Taco Bruin; Ulrike Beisiegel; Pascale 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 742 KB

Communicated by Ronald G. Worton Mutations in the lipoprotein lipase (LPL) gene are the most common cause of familial chylomicron. emia. Here we define the molecular basis of LPL deficiency in four patients of German, French, Dutch, and Chinese descent. We show that two of the probands of Dutch and

Spontaneous mutation at codon 61 of the

Spontaneous mutation at codon 61 of the Ha-ras gene in the nascent liver of B6C3F1, C3H/He and C57BL/6 mice

✍ Beth A. Moulds; Jay I. Goodman 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 645 KB