20470 IMGP4957

20470 IMGP4957



Wilms’ tumour

•    Wilms1 tumour (WT; nephroblastoma), a kidney ncoplasm, is one of the most frequentły occurring solid tumors of childhood.

*    I.oss of function of tumour suppressor gen es has been implicatcd iii the developmcnt of WT, and the Wilms' tumour suppressor gene WT1 (at chrom osom e 1 lpl3) was the second tumour suppressor gene to be doned. aftcr the retinoblastoma gene RB-1.

W Tl plays an essential role in kidney development, but is mutated in only approsimately 20% of WTs, which suggests that further lesions and genętic loci are involved in Wilms1 lumourigenesis.


Wyszukiwarka

Podobne podstrony:
83312 IMGP4959 Wilms’ tumour * The deveiopment of Wilms tumour u comples and is likely to invohc se
1US 6,359,145 BI IMIDAZOI.F. COMPOUNDS Iłiis applicalit.n is a 371 of WT Jm«M.W Jul. 22, 1999. lliC
Slajd50 (68) Gastrointestinal Stroma! Tumour (GIST) Rzadki rodzaj mięsaka -    0,2% n
UHAM071 54 ^ UNDERSTANDING HEADACHES AND M I G RAI N ES benign tumours are also a form of cancer. Th
Gazeta AMG nr 6/2012 Gdańsk International Paediatric Liver Tumours Consensus Meeting in Conjunc-tion
Wzrost guza nowotworowego log tumour celi burden    deoth    deot
IMGP4941 Suppressor gene RB1 (13ql4) p53 (17pl3) APC (5q21) WT-1 (11 p 13) NF-l (17qll> 
81896 Slajd19 (120) Efekt chemioterapii log celi survival bonę morrow -tumour — tumour becomes resis
RAK NERKI- patologia molekularna Tumourtype Clear celi Papillary (type I + II) Chromophobic Oncocyti
33 (475) 313,.ll Nephroblastoma (tumor Wilmsi) — nowotwór zarodkowy nerki (guz Wilms’a) r • A ® 9 ra
227 (21) 22 : Diagnostic approach to otitis extema Figurę 22 :17: Invasive mast celi tumour in the e
244 (20) necrolytic dermatitis (Figs 24 : 11) and uraemia-associated vasculitis (Fig. 24 : 12)), or

więcej podobnych podstron