Editorial: Kidney cancer - A unique opportunity for the development of disease specific therapy

被引:8
作者
Linehan, WM [1 ]
机构
[1] NCI, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S0022-5347(05)64156-0
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:2411 / 2412
页数:2
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共 18 条
[1]   Regression of metastatic renal-cell carcinoma after nonmyeloablative allogeneic peripheral-blood stem-cell transplantation [J].
Childs, R ;
Chernoff, A ;
Contentin, N ;
Bahceci, E ;
Schrump, D ;
Leitman, S ;
Read, EJ ;
Tisdale, J ;
Dunbar, C ;
Linehan, WM ;
Young, NS ;
Barrett, AJ ;
Clave, E ;
Epperson, D ;
Mayo, V .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (11) :750-758
[2]   Rising incidence of renal cell cancer in the United States [J].
Chow, WH ;
Devesa, SS ;
Warren, JL ;
Fraumeni, JF .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (17) :1628-1631
[3]   MUTATIONS OF THE VHL TUMOR-SUPPRESSOR GENE IN RENAL-CARCINOMA [J].
GNARRA, JR ;
TORY, K ;
WENG, Y ;
SCHMIDT, L ;
WEI, MH ;
LI, H ;
LATIF, F ;
LIU, S ;
CHEN, F ;
DUH, FM ;
LUBENSKY, I ;
DUAN, DR ;
FLORENCE, C ;
POZZATTI, R ;
WALTHER, MM ;
BANDER, NH ;
GROSSMAN, HB ;
BRAUCH, H ;
POMER, S ;
BROOKS, JD ;
ISAACS, WB ;
LERMAN, MI ;
ZBAR, B ;
LINEHAN, WM .
NATURE GENETICS, 1994, 7 (01) :85-90
[4]   Parenchymal sparing surgery in patients with hereditary renal cell carcinoma: 10-year experience [J].
Herring, JC ;
Enquist, EG ;
Chernoff, A ;
Linehan, WM ;
Choyke, PL ;
Walther, MM .
JOURNAL OF UROLOGY, 2001, 165 (03) :777-781
[5]   IDENTIFICATION OF THE VONHIPPEL-LINDAU DISEASE TUMOR-SUPPRESSOR GENE [J].
LATIF, F ;
TORY, K ;
GNARRA, J ;
YAO, M ;
DUH, FM ;
ORCUTT, ML ;
STACKHOUSE, T ;
KUZMIN, I ;
MODI, W ;
GEIL, L ;
SCHMIDT, L ;
ZHOU, FW ;
LI, H ;
WEI, MH ;
CHEN, F ;
GLENN, G ;
CHOYKE, P ;
WALTHER, MM ;
WENG, YK ;
DUAN, DSR ;
DEAN, M ;
GLAVAC, D ;
RICHARDS, FM ;
CROSSEY, PA ;
FERGUSONSMITH, MA ;
LEPASLIER, D ;
CHUMAKOV, I ;
COHEN, D ;
CHINAULT, AC ;
MAHER, ER ;
LINEHAN, WM ;
ZBAR, B ;
LERMAN, MI .
SCIENCE, 1993, 260 (5112) :1317-1320
[6]   Inherited susceptibility to uterine leiomyomas and renal cell cancer [J].
Launonen, V ;
Vierimaa, O ;
Kiuru, M ;
Isola, J ;
Roth, S ;
Pukkala, E ;
Sistonen, P ;
Herva, R ;
Aaltonen, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (06) :3387-3392
[7]  
Linehan W.M., 2002, GENETIC BASIS HUMAN
[8]   Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dube syndrome [J].
Nickerson, ML ;
Warren, MB ;
Toro, JR ;
Matrosova, V ;
Glenn, G ;
Turner, ML ;
Duray, P ;
Merino, M ;
Choyke, P ;
Pavlovich, CP ;
Sharma, N ;
Walther, M ;
Munroe, D ;
Hill, R ;
Maher, E ;
Greenberg, C ;
Lerman, MI ;
Linehan, WM ;
Zbar, B ;
Schmidt, LS .
CANCER CELL, 2002, 2 (02) :157-164
[9]   Ubiquitination of hypoxia-inducible factor requires direct binding to the β-domain of the von Hippel-Lindau protein [J].
Ohh, M ;
Park, CW ;
Ivan, N ;
Hoffman, MA ;
Kim, TY ;
Huang, LE ;
Pavletich, N ;
Chau, V ;
Kaelin, WG .
NATURE CELL BIOLOGY, 2000, 2 (07) :423-427
[10]   Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas [J].
Schmidt, L ;
Duh, FM ;
Chen, F ;
Kishida, T ;
Glenn, G ;
Choyke, P ;
Scherer, SW ;
Zhuang, ZP ;
Lubensky, I ;
Dean, M ;
Allikmets, R ;
Chidambaram, A ;
Bergerheim, UR ;
Feltis, JT ;
Casadevall, C ;
Zamarron, A ;
Bernues, M ;
Richard, S ;
Lips, CJM ;
Walther, MM ;
Tsui, LC ;
Geil, L ;
Orcutt, ML ;
Stackhouse, T ;
Lipan, J ;
Slife, L ;
Brauch, H ;
Decker, J ;
Niehans, G ;
Hughson, MD ;
Moch, H ;
Storkel, S ;
Lerman, MI ;
Linehan, WM ;
Zbar, B .
NATURE GENETICS, 1997, 16 (01) :68-73