✦ LIBER ✦

Absence of IDH2 codon 172 mutation in common human cancers

✍ Scribed by Sang Wook Park; Nak Gyun Chung; Ji Youn Han; Hyeon Seok Eom; Ji Youl Lee; Nam Jin Yoo; Sug Hyung Lee

Publisher: John Wiley and Sons
Year: 2009
Tongue: French
Weight: 44 KB
Volume: 125
Category: Article
ISSN: 0020-7136
DOI: 10.1002/ijc.24647

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutational analysis of IDH1 codon 132 in

Mutational analysis of IDH1 codon 132 in glioblastomas and other common cancers

✍ Mi Ran Kang; Min Sung Kim; Ji Eun Oh; Yoo Ri Kim; Sang Yong Song; Seong Il Seo; 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 French ⚖ 128 KB

## Abstract Missense somatic mutations in __IDH1__ gene affecting codon 132 have recently been reported in glioblastoma multiforme (GBM) and other gliomas. The recurrent nature of the __IDH1__ mutations in the same amino acid strongly suggests that the mutations may play important roles in the path

Absence of EGFR mutation in the kinase d

Absence of EGFR mutation in the kinase domain in common human cancers besides non-small cell lung cancer

✍ Jong Woo Lee; Young Hwa Soung; Su Young Kim; Won Sang Park; Suk Woo Nam; Jung Yo 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 French ⚖ 61 KB 👁 1 views

Absence of GNAI2 codon 179 oncogene muta

Absence of GNAI2 codon 179 oncogene mutations in inflammatory bowel disease

✍ Dr. Wen Jie Zhang; Dr. Walter A. Koltun; Anna F. Tilberg; Michael J. Page; Micha 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 392 KB

The human GNAI2 gene coding for G protein, Gai2, is located on chromosome 3p21 in proximity to the region where an inflammatory bowel disease (IBD) locus has been suggested. Gai2-deficient mice develop a lethal diffuse colitis that resembles human ulcerative colitis (UC) and frequently progresses to

Frameshift mutation at codon 642 of the

Frameshift mutation at codon 642 of the hMLH1 gene in human endometrial cancer

✍ Shinichi Fukushige; Shigeru Wakatsuki; Satoru Nagase; Akira Horii 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 212 KB

## MUTATION NOTES single-strand conformational polymorphism (SSCP) analysis, 22 exons and 196 bp of the 5' region of the PDEB gene were screened. Primers were derived from Riess et al. (1992). The samples corresponding to the two affected RP patients had an altered migration band in exon 13 compar

Loh and mutation analysis of CDKN2 in pr

Loh and mutation analysis of CDKN2 in primary human ovarian cancers

✍ Ian G. Campbell; Gareth Beynon; Michael Davis; Pat Englefield 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 French ⚖ 735 KB

The CDKNZ gene encodes a cell cycle regulatory protein and is located on chromosome 9 ~2 1 , a region deleted in a wide variety of primary tumours. While mutations in the CDKNZ gene itself are frequently observed in tumour cell lines, they are less common in primary turnouts. We have investigated th

Absence of common activating mutations o

Absence of common activating mutations of the epidermal growth factor receptor gene in thyroid cancers from American and Japanese patients

✍ Julio C. Ricarte-Filho; Michiko Matsuse; Christopher Lau; Mabel Ryder; Eijun Nis 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 French ⚖ 735 KB