✦ LIBER ✦

A new detection method for ATRX gene mutations using a mismatch-specific endonuclease

✍ Scribed by Takahito Wada; Yoshimitsu Fukushima; Shinji Saitoh

Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 176 KB
Volume: 140A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.31310

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Site-Specific DNA Cleavage on a Solid Su

Site-Specific DNA Cleavage on a Solid Support: A Method for Mismatch Detection

✍ Sandra Thoeni; Christoph J. Kressierer; Bernd Giese 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 151 KB

A new method for detecting clotting in s

A new method for detecting clotting in shunts used for haemodialysis

✍ J. R. Salaman; J. Chu; D. L. Crosby 📂 Article 📅 1973 🏛 John Wiley and Sons 🌐 English ⚖ 361 KB 👁 1 views

Immunohistochemical detection of mismatc

Immunohistochemical detection of mismatch repair gene proteins as a useful tool for the identification of colorectal carcinoma with the mutator phenotype

✍ P. Chaves; C. Cruz; P. Lage; I. Claro; M. Cravo; C. N. Leitão; J. Soares 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 128 KB 👁 2 views

Comparison of heteroduplex analysis, dir

Comparison of heteroduplex analysis, direct sequencing, and enzyme mismatch cleavage for detecting mutations in a large gene, FBN1

✍ Bo Yuan; Jeanne P. Thomas; Yskert von Kodolitsch; Reed E. Pyeritz 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 250 KB 👁 1 views

Analysis of large genes for mutations of clinical relevance is complicated by intragenic heterogeneity, sensitivity, and cost of the methods available, and in the case of many conditions, specificity of the genetic alterations detected. We examined the FBN1 gene for mutations in people who had Marfa

A rapid method for detecting the predomi

A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene

✍ Joel E. Straughen; Juliana Johnson; Donna McLaren; Maria Proytcheva; Nathan Elli 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 157 KB

Bloom's syndrome (BS) is a rare, autosomal recessive disease characterized by sun sensitivity, short stature, and predisposition to cancer. Although rare in the general population, BS is more common in the Ashkenazi Jewish population (German, 1993). The isolation of the gene for BS, known as BLM, ha

A highly sensitive method for K-ras muta

A highly sensitive method for K-ras mutation detection is useful in diagnosis of gastrointestinal cancer

✍ Pere Puig; Eulàlia Urgell; Gabriel Capellá; Francesc Josep Sancho; Joan Pujol; J 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 French ⚖ 63 KB 👁 2 views

## Detection of molecular features such as K-ras mutations has been used to evaluate potential tumour markers in a wide variety of clinical samples. Here we have applied a recently developed highly sensitive method for detection of K-ras codon 12 mutations to colorectal and pancreatic cancer diagno