✦ LIBER ✦

Deletion of chromosome 3p in three tumor types associated with Von Hippel-Lindau Disease (VHL)

✍ Scribed by Kalman Tory; Hiltrud Brauch; Marston Linehan; David Barba; Edward Oldfield; Michele Filling-Katz; Yusuke Nakamura; Ray White; Bernd Seizinger; Michael I. Lerman; Berton Zbar

Book ID: 119104297
Publisher: Elsevier Science
Year: 1989
Tongue: English
Weight: 61 KB
Volume: 41
Category: Article
ISSN: 0165-4608
DOI: 10.1016/0165-4608(89)90289-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Association of Type O Blood with Pancrea

Association of Type O Blood with Pancreatic Neuroendocrine Tumors in Von Hippel–Lindau Syndrome

✍ Weisbrod, Allison B.; Liewehr, David J.; Steinberg, Seth M.; Patterson, Erin E.; 📂 Article 📅 2012 🏛 Springer 🌐 English ⚖ 257 KB

Von HippelLindau disease maps to the re

Von HippelLindau disease maps to the region of chromosome 3 associated with renal cell carcinoma

✍ Seizinger, B. R.; Rouleau, G. A.; Ozelius, L. J.; Lane, A. H.; Farmer, G. E.; La 📂 Article 📅 1988 🏛 Nature Publishing Group 🌐 English ⚖ 228 KB

Proximal 3p deletion in renal cell carci

Proximal 3p deletion in renal cell carcinoma cells from a patient with von Hippel-Lindau disease

✍ Charles R. King; R.Neil Schimke; Terry Arthur; Barbara Davoren; Debra Collins 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 220 KB

Clinical presentation of Von Hippel Lind

Clinical presentation of Von Hippel Lindau syndrome type 2B associated with VHL p.A149S mutation in a large Turkish family

✍ T. Mete, D. Berker, E. Yilmaz, G. Ozgen, Y. Yalcin, M. Tuna, D. Ciliz, M. Onen… 📂 Article 📅 2013 🏛 Springer 🌐 English ⚖ 345 KB

Loss of heterozygosity on the short arm

Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von hippel-lindau disease-associated, and familial pheochromocytoma

✍ Martha A. Zeiger; Berton Zbar; Harry Keiser; W. Marston Linehan; James R. Gnarra 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 490 KB 👁 1 views

## Pheochromocytomas occur sporadically and are associated with several dominantly inherited cancer syndromes, including von Hippel-Lindau (VHL) disease. We examined 14 pheochromocytomas (four from VHL patients, nine from sporadic patients, and one from a patient with familial pheochromocytoma) fo

Inactivation of the von Hippel–Lindau (V

Inactivation of the von Hippel–Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: Evidence for a VHL-independent pathway in clear cell renal tumourigenesis

✍ Steven C. Clifford; Amanda H. Prowse; Nabeel A. Affara; Charles H. C. M. Buys; E 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 149 KB 👁 2 views

Inactivation of tumour suppressor gene(s) (TSGs) on 3p appears to be a critical event in the pathogenesis of clear cell renal cell carcinoma (CC-RCC). Analysis of loss of heterozygosity (LOH) in sporadic RCC samples has implicated roles for TSGs in three specific regions of 3p in RCC development: (1