✦ LIBER ✦

APC gene: database of germline and somatic mutations in human tumors and cell lines

✍ Scribed by Beroud, C

Book ID: 124095880
Publisher: Oxford University Press
Year: 1996
Tongue: English
Weight: 70 KB
Volume: 24
Category: Article
ISSN: 0305-1048
DOI: 10.1093/nar/24.1.121

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Germ-line and somatic mutations of the A

Germ-line and somatic mutations of the APC gene in patients with turcot syndrome and analysis of APC mutations in brain tumors

✍ Takahiro Mori; Hiroki Nagase; Akira Horii; Yasuo Miyoshi; Shuichi Nakatsuru; Tak 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 453 KB 👁 1 views

## Abstract The Turcot syndrome (TS) is a rare, probably autosomal recessive, disorder characterized by development of primary neuroepithelial tumors of the central nervous system (CNS) and numerous adenomatous colorectal polyps. To examine the possible involvement of mutations of the __APC__ gene,

Germline versus somatic mutations of the

Germline versus somatic mutations of the APC gene: Evidence for mechanistic differences

✍ Brendan Marshall; Gloria Isidro; Raquel Carvalhas; Maria Guida Boavida 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 101 KB 👁 2 views

Comparative analysis of germline and som

Comparative analysis of germline and somatic microlesion mutational spectra in 17 human tumor suppressor genes

✍ Dobril Ivanov; Stephen E. Hamby; Peter D. Stenson; Andrew D. Phillips; Hildegard 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 260 KB

Mutations associated with tumorigenesis may either arise somatically or can be inherited through the germline. We performed a comparison of somatic, germline, shared (found in both soma and germline) and somatic recurrent mutational spectra for 17 human tumor suppressor genes, which focused upon mis

Absence of KLF6 gene mutations in human

Absence of KLF6 gene mutations in human astrocytic tumors and cell lines

✍ Pasi A. Koivisto; Xiaohui Zhang; Satu-Leena Sallinen; Pauli Sallinen; Heikki J. 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 French ⚖ 49 KB 👁 1 views

Loss of heterozygosity (LOH) on chromosome 10 is the most common genetic changes in glioblastomas of World Health Organization (WHO) Grade IV. [1][2][3][4][5][6][7] In most cases, the allelic losses involve loci along the entire chromosome, a finding in line with monosomy 10. LOH on chromosome 10 ma

IARC p53 mutation database: A relational

IARC p53 mutation database: A relational database to compile and analyze p53 mutations in human tumors and cell lines

✍ Tina Hernandez-Boussard; Patricia Rodriguez-Tome; Ruggero Montesano; Pierre Hain 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 252 KB 👁 2 views

Communicated by

The Human Prohibitin (PHB) Gene Family a

The Human Prohibitin (PHB) Gene Family and Its Somatic Mutations in Human Tumors

✍ Takaaki Sato; Takashi Sakamoto; Ken-ichi Takita; Hiroko Saito; Keiko Okui; Yusuk 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 186 KB