메뉴 건너뛰기




Volumn 22, Issue 4, 1998, Pages 287-294

Allele loss in wilms tumors of chromosome arms 11q, 16q, and 22q correlates with clinicopathological parameters

Author keywords

[No Author keywords available]

Indexed keywords

ANAPLASTIC CARCINOMA; ARTICLE; CANCER RECURRENCE; CHROMOSOME 11Q; CHROMOSOME 16Q; CHROMOSOME 22Q; CHROMOSOME LOSS; CONTROLLED STUDY; DISEASE COURSE; HETEROZYGOSITY LOSS; HISTOPATHOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; MAJOR CLINICAL STUDY; NEPHROBLASTOMA; PRIORITY JOURNAL; PROGNOSIS;

EID: 0031747351     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199808)22:4<287::AID-GCC4>3.0.CO;2-R     Document Type: Article
Times cited : (79)

References (40)
  • 5
    • 0028892269 scopus 로고
    • Single nucleotide polymorphisms in the human E-cadherin gene
    • Becker KK, Reich U, Schott C, Hofler H (1995) Single nucleotide polymorphisms in the human E-cadherin gene. Hum Genet 96:739-740.
    • (1995) Hum Genet , vol.96 , pp. 739-740
    • Becker, K.K.1    Reich, U.2    Schott, C.3    Hofler, H.4
  • 8
    • 0030069636 scopus 로고    scopus 로고
    • The new SIOP (Stockholm) working classification of renal tumours of childhood. International Society of Paediatric Oncology (letter)
    • Delemarre JF, Sandstedt B, Harms D, Boccon-Gibod L, Vujanic GM (1996) The new SIOP (Stockholm) working classification of renal tumours of childhood. International Society of Paediatric Oncology (letter). Med Pediatr Oncol 26:145-146.
    • (1996) Med Pediatr Oncol , vol.26 , pp. 145-146
    • Delemarre, J.F.1    Sandstedt, B.2    Harms, D.3    Boccon-Gibod, L.4    Vujanic, G.M.5
  • 10
    • 0027459389 scopus 로고
    • The G401 cell line, utilized for studies of chromosomal changes in Wilms' tumor, is derived from a rhabdoid tumor of the kidney
    • Garvin AJ, Re GG, Tarnowski BI, Hazenmartin DJ, Sens DA (1993) The G401 cell line, utilized for studies of chromosomal changes in Wilms' tumor, is derived from a rhabdoid tumor of the kidney. Am J Pathol 142:375-380.
    • (1993) Am J Pathol , vol.142 , pp. 375-380
    • Garvin, A.J.1    Re, G.G.2    Tarnowski, B.I.3    Hazenmartin, D.J.4    Sens, D.A.5
  • 11
    • 0025098654 scopus 로고
    • Homozygous deletion in Wilms' tumours of a zinc-finger gene identified by chromosome jumping
    • Gessler M, Poustka A, Cavenee W, Neve RL, Orkin SH, Bruns GA (1990) Homozygous deletion in Wilms' tumours of a zinc-finger gene identified by chromosome jumping. Nature. 343:774-778.
    • (1990) Nature , vol.343 , pp. 774-778
    • Gessler, M.1    Poustka, A.2    Cavenee, W.3    Neve, R.L.4    Orkin, S.H.5    Bruns, G.A.6
  • 13
    • 0023683531 scopus 로고
    • Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11
    • Grundy P, Koufos A, Morgan K, Li KP, Meadows AT, Cavenee WK (1988) Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. Nature 366:374-376.
    • (1988) Nature , vol.366 , pp. 374-376
    • Grundy, P.1    Koufos, A.2    Morgan, K.3    Li, K.P.4    Meadows, A.T.5    Cavenee, W.K.6
  • 14
    • 0028351728 scopus 로고
    • Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome
    • Grundy PE, Telzerow PE, Breslow N, Moksness J, Huff V, Paterson MC (1994) Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome. Cancer Res 54:2331-2333.
    • (1994) Cancer Res , vol.54 , pp. 2331-2333
    • Grundy, P.E.1    Telzerow, P.E.2    Breslow, N.3    Moksness, J.4    Huff, V.5    Paterson, M.C.6
  • 15
    • 0029838115 scopus 로고    scopus 로고
    • Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: A preliminary analysis
    • Grundy P, Telzerow P, Moksness J, Breslow NE (1996) Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: A preliminary analysis. Med Pediatr Oncol 27:429-433.
    • (1996) Med Pediatr Oncol , vol.27 , pp. 429-433
    • Grundy, P.1    Telzerow, P.2    Moksness, J.3    Breslow, N.E.4
  • 16
    • 0028829767 scopus 로고
    • Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer
    • Hoggard N, Hey Y, Brintnell B, James L, Jones D, Mitchell E, Weissenbach J, Varley JM (1995) Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer. Genomics 30:233-243.
    • (1995) Genomics , vol.30 , pp. 233-243
    • Hoggard, N.1    Hey, Y.2    Brintnell, B.3    James, L.4    Jones, D.5    Mitchell, E.6    Weissenbach, J.7    Varley, J.M.8
  • 22
    • 0029864908 scopus 로고    scopus 로고
    • Immunohistochemical detection of p53 in Wilms' tumors correlates with unfavorable outcome
    • Lahoti C, Thorner P, Malkin ID, Yeger H (1996) Immunohistochemical detection of p53 in Wilms' tumors correlates with unfavorable outcome. Am J Pathol 148:1577-1589.
    • (1996) Am J Pathol , vol.148 , pp. 1577-1589
    • Lahoti, C.1    Thorner, P.2    Malkin, I.D.3    Yeger, H.4
  • 23
    • 0031214256 scopus 로고    scopus 로고
    • Allelic imbalance at chromosome 1q21 in Wilms' tumor
    • Law MH, Algar E, Little M (1997) Allelic imbalance at chromosome 1q21 in Wilms' tumor. Cancer Genet Cytogenet 97:54-59.
    • (1997) Cancer Genet Cytogenet , vol.97 , pp. 54-59
    • Law, M.H.1    Algar, E.2    Little, M.3
  • 25
    • 0030891372 scopus 로고    scopus 로고
    • A clinical overview of WT1 gene mutations
    • Little M, Wells C (1997) A clinical overview of WT1 gene mutations. Hum Mutat 9:209-225.
    • (1997) Hum Mutat , vol.9 , pp. 209-225
    • Little, M.1    Wells, C.2
  • 29
    • 0030610260 scopus 로고    scopus 로고
    • Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms' tumors
    • O'Keefe 13, Dao D, Zhao L, Sanderson R, Warburton D, Weiss L, Anyane-Yeboa K, Tycko B (1997) Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms' tumors. Am J Hum Genet 61:295-303.
    • (1997) Am J Hum Genet , vol.61 , pp. 295-303
    • O'Keefe, D.1    Dao, D.2    Zhao, L.3    Sanderson, R.4    Warburton, D.5    Weiss, L.6    Anyane-Yeboa, K.7    Tycko, B.8
  • 32
    • 0024505754 scopus 로고
    • Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells
    • Reeve AE, Sih SA, Raizis AM, Feinberg AP (1989) Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells. Mol Cell Biol 9:1799-1803.
    • (1989) Mol Cell Biol , vol.9 , pp. 1799-1803
    • Reeve, A.E.1    Sih, S.A.2    Raizis, A.M.3    Feinberg, A.P.4
  • 34
    • 0030032087 scopus 로고    scopus 로고
    • Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors
    • Schofield DE, Beckwith JB, Sklar J (1996) Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors. Genes Chromosomes Cancer 15:10-17.
    • (1996) Genes Chromosomes Cancer , vol.15 , pp. 10-17
    • Schofield, D.E.1    Beckwith, J.B.2    Sklar, J.3
  • 37
    • 0028935017 scopus 로고
    • Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms' tumor
    • Taniguchi T, Sullivan MJ, Ogawa O, Reeve AE (1995) Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms' tumor. Proc Natl Acad Sci USA 92:2159-2163.
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 2159-2163
    • Taniguchi, T.1    Sullivan, M.J.2    Ogawa, O.3    Reeve, A.E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.