✦ LIBER ✦

MiR-1246: A new link of the p53 family with cancer and Down syndrome

✍ Scribed by Liao, Jun-ming; Zhou, Xiang; Zhang, Yu; Lu, Hua

Book ID: 120319353
Publisher: Landes Bioscience
Year: 2012
Tongue: English
Weight: 518 KB
Volume: 11
Category: Article
ISSN: 1538-4101
DOI: 10.4161/cc.20809

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Absence of germline mutations in exons 5

Absence of germline mutations in exons 5–9 of the p53 gene in patients with Li-Fraumeni-like (SBLA) and familial adenomatous polyposis heritable cancer syndromes

✍ Stephen K. Moore; Nicola Zambrano; Henry T. Lynch; Martin Lipkin; Levy Kopelovic 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 561 KB

Down syndrome and coeliac disease: five

Down syndrome and coeliac disease: five new cases with a review of the literature

✍ M. I. Hilhorst; M. Brink; E. A. K. Wauters; R. H. J. Houwen 📂 Article 📅 1993 🏛 Springer 🌐 English ⚖ 359 KB

A population-based assessment of the hea

A population-based assessment of the health, functional status, and consequent family impact among children with Down syndrome

✍ Laura A. Schieve; Sheree L. Boulet; Michael D. Kogan; Kim Van Naarden-Braun; Col 📂 Article 📅 2011 🏛 Elsevier 🌐 English ⚖ 179 KB

Family cancer syndrome: A study of the k

Family cancer syndrome: A study of the kindred of a man with osteogenic sarcoma of the mandible

✍ Glendon M. Gardner; Joseph R. Steiniger 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 526 KB

Study of the origin of nondisjunction in

Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms

✍ Stinissen, Piet ;Van Roy, Bernadette ;Van Camp, Guy ;Backhovens, Hubert ;Partoen 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 400 KB 👁 2 views

We analyzed the possibility of inherited predisposition to nondisjunction in a family with two cases of Down syndrome using restriction fragment length polymorphisms and cytogenetic heteromorphisms. In both patients the extra chromosome 21 was the result of a nondisjunction event at first meiotic di

Renal cysts and diabetes syndrome linked

Renal cysts and diabetes syndrome linked to mutations of the hepatocyte nuclear factor-1β gene: Description of a new family with associated liver involvement

✍ Alberto Montoli; Giacomo Colussi; Ornella Massa; Roberta Caccia; Gianfranco Rizz 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 49 KB