𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Carotenoid and vitamin intake,von Hippel-Lindaugene mutations and sporadic renal cell carcinoma

✍ Scribed by Boukje A. C. van Dijk; Leo J. Schouten; Egbert Oosterwijk; Christina A. Hulsbergen-van de Kaa; Lambertus A. L. M. Kiemeney; R. Alexandra Goldbohm; Jack A. Schalken; Piet A. van den Brandt


Publisher
Springer Netherlands
Year
2007
Tongue
English
Weight
201 KB
Volume
19
Category
Article
ISSN
0957-5243

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Vitamin and carotenoid intake and risk o
✍ Teresa T. Fung; Donna Spiegelman; Kathleen M. Egan; Edward Giovannucci; David J. πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 French βš– 80 KB πŸ‘ 2 views

## Abstract Our objective was to examine prospectively the intake of vitamins A (including retinol and total vitamin A), C and E; folate; total carotene; and several individual carotenoids (α‐carotene, β‐carotene, β‐cryptoxanthin and lutein/zeaxanthin) in relation to incidence of SCC of the skin in

Cytogenetic characterization of renal ce
✍ M. David Goodman; Barbara K. Goodman; Matthew B. Lubin; Rhona R. Schreck; Glenn πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 534 KB

We report the case of a 26-year-old man with von Hippel-Lindau syndrome (VHL) and two renal cell carcinomas (RCC), one of which was studied cytogenetically. Chromosomal analysis of the RCC showed a translocation that involved chromosomes 3 and 8 with subsequent loss of the derivative chromosome 8. T

Copy number profiling in von hippel-lind
✍ Salwati Shuib; Wenbin Wei; Hariom Sur; Mark R. Morris; Dominic McMullan; Eleanor πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 802 KB

## Abstract Germline mutations in the __VHL__ tumor suppressor gene cause von Hippel‐Lindau (VHL) disease and somatic __VHL__ mutations occur in the majority of clear cell renal cell carcinoma (cRCC). To compare copy number abnormalities (CNAs) between cRCC from VHL patients and sporadic cRCC cases

Lack of mutation of the folliculin gene
✍ Anett Nagy; Dmitri Zoubakov; Zorica Stupar; Gyula Kovacs πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 French βš– 193 KB

## Abstract Germline mutation of the folliculin gene (BHD) at chromosome 17p11.2 is associated with the development of multiplex hamartomas of the hair follicles, chromophobe renal cell carcinomas (RCC) and renal oncocytomas (RO). We have analyzed the folliculin gene with sequencing for mutations a