✦ LIBER ✦

Mutation screening of theMERIT40gene encoding a novel BRCA1 and RAP80 interacting protein in breast cancer families

✍ Scribed by Szilvia Solyom; Jeffery Patterson-Fortin; Katri Pylkäs; Roger A. Greenberg; Robert Winqvist

Book ID: 106378318
Publisher: Springer US
Year: 2009
Tongue: English
Weight: 180 KB
Volume: 120
Category: Article
ISSN: 0167-6806
DOI: 10.1007/s10549-009-0453-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Identification of a novel splice-site mu

Identification of a novel splice-site mutation of the BRCA1 gene in two breast cancer families: Screening reveals low frequency in Icelandic breast cancer patients

✍ Jon Thor Bergthorsson; Adalbjorg Jonasdottir; Gudrun Johannesdottir; Adalgeir Ar 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 479 KB 👁 1 views

Analysis of the genes coding for the BRC

Analysis of the genes coding for the BRCA1-interacting proteins, RAP80 and Abraxas (CCDC98), in high-risk, non-BRCA1/2, multiethnic breast cancer cases

✍ David J. Novak; Nelly Sabbaghian; Philippe Maillet; Pierre O. Chappuis; William 📂 Article 📅 2008 🏛 Springer US 🌐 English ⚖ 184 KB

Mutational analysis of the LMO4 gene, en

Mutational analysis of the LMO4 gene, encoding a BRCA1-interacting protein, in breast carcinomas

✍ Kate D. Sutherland; Jane E. Visvader; David Y.H. Choong; Eleanor Y.M. Sum; Geoff 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 French ⚖ 131 KB

## Abstract The LIM domain‐only genes __LMO1__ and __LMO2__ are translocated in acute T cell leukemia (T‐ALL) and have been shown to be oncogenes in T lymphoid cells. LMO4, the fourth member of this family, is overexpressed in more than 50% of sporadic breast cancers, suggesting a role in breast on

Identification of a recurrent BRCA1 muta

Identification of a recurrent BRCA1 mutation in German breast-cancer and/or ovarian-cancer families

✍ Wera Hofmann; Burkhard Jandrig; Elvira Classen; Carolin Nestle-Kraemling; Jenny 📂 Article 📅 2001 🏛 Springer-Verlag 🌐 English ⚖ 69 KB

BRCA1 mutations in South African breast

BRCA1 mutations in South African breast and/or ovarian cancer families: Evidence of a novel founder mutation in Afrikaner families

✍ Michelle D. Reeves; Tali M. Yawitch; Nerina C. van der Merwe; Hester J. van den 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 French ⚖ 89 KB 👁 1 views

## Abstract Germ‐line mutations within __BRCA1__ are responsible for different proportions of inherited susceptibility to breast/ovarian cancer, and the spectrum of mutations within this gene is often unique to certain populations. At this time, there have been no reports regarding the role of __BR

Detection of BRCA1 and BRCA2 mutations i

Detection of BRCA1 and BRCA2 mutations in breast cancer families by a comprehensive two-stage screening procedure

✍ Eva Spitzer; Mohammad R. Abbaszadegan; Frank Schmidt; Andrea Hauser; Ute Buwitt; 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 French ⚖ 101 KB 👁 2 views

We have developed a 2-stage protocol for BRCA1 and BRCA2 mutation screening from blood spot paper. Stage 1 screening was aimed to analyze patients at highest risk for the most common disease-associated sequence variants listed in the BIC database. Accordingly, stage1 testing implied detection of 18