SCOPUS 정보 검색 플랫폼

Volumn 60, Issue 22, 2000, Pages 6339-6345

The RB1 gene is the target of chromosome 13 deletions in malignant fibrous histiocytoma

(7) Chibon, Frédéric a Mairal, Aline a Fréneaux, Paul a Terrier, Philippe b Coindre, Jean Michel c Sastre, Xavier a Aurias, Alain a

a INSTITUT CURIE (France)

b INSTITUT GUSTAVE ROUSSY (France)

c INSTITUT BERGONIÉ (France)

Author keywords

[No Author keywords available]

Indexed keywords

RETINOBLASTOMA PROTEIN;

ADULT; ARTICLE; CARCINOGENESIS; CHROMOSOME DELETION 13; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONSENSUS SEQUENCE; CONTROLLED STUDY; DELETION MUTANT; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE INACTIVATION; GENE LOCATION; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MALE; MALIGNANT FIBROUS HISTIOCYTOMA; NUCLEOTIDE REPEAT; PRIORITY JOURNAL; PROTEIN EXPRESSION; RETINOBLASTOMA; TUMOR SUPPRESSOR GENE;

ALLELIC IMBALANCE; BLOTTING, SOUTHERN; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 13; CONSENSUS SEQUENCE; FEMALE; GENES, RETINOBLASTOMA; HISTIOCYTOMA, BENIGN FIBROUS; HUMANS; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MICROSATELLITE REPEATS; MUTATION; NUCLEIC ACID HYBRIDIZATION;

EID: 0033709408 PISSN: 00085472 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (55)

References (16)

1
- 0032901704
- Loss of chromosome 13 is the most frequent genomic imbalance in malignant fibrous histiocytomas. A comparative genomic hybridization analysis of a series of 30 cases
- (1999) Cancer Genet. Cytogenet. , vol.11 , pp. 134-138
- Mairal, A.¹ Terrier, P.² Chibon, F.³ Sastre, X.⁴ Lecesne, A.⁵ Aurias, A.⁶

2
- 0026495364
- Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
- (1992) Science (Washington DC) , vol.258 , pp. 818-821
- Kallionemi, A.¹ Kallionemi, O.P.² Sudar, D.³ Rutovitz, D.⁴ Gray, J.W.⁵ Waldman, F.⁶ Pinkel, D.⁷

3
- 0031912459
- High-resolution YAC-cosmid-STS map of human chromosome 13
- (1998) Genomics , vol.47 , pp. 26-43
- Cayanis, E.¹ Russo, J.J.² Kalachikov, S.³ Ye, X.⁴ Park, S.H.⁵ Sunjevaric, I.⁶ Bonaldo, M.F.⁷ Lawton, L.⁸ Venkatraj, V.S.⁹ Schon, E.¹⁰ Soares, M.B.¹¹ Rothstein, R.¹² Warburton, D.¹³ Edelman, I.S.¹⁴ Zhang, P.¹⁵ Efstratiadis, A.¹⁶ Fischer, S.G.¹⁷

4
- 0028327448
- Isolation and characterization of a panel of cosmids which allows unequivocal identification of chromosome deletions involving the RB1 gene using fluorescence in situ hybridization
- (1994) J. Med. Genet. , vol.31 , pp. 334-337
- Cowell, J.K.¹ Jaju, R.² Kempski, H.³

5
- 0031916210
- Cytogenetic and molecular analysis of a t(1;22)(p36;q11.2) in a rhabdoid tumor with a putative homozygous deletion of chromosome 22
- (1998) Genes Chromosomes Cancer , vol.21 , pp. 82-89
- Rosty, C.¹ Peter, M.² Zucman, J.³ Validire, P.⁴ Delattre, O.⁵ Aurias, A.⁶

6
- 13344259999
- A comprehensive genetic map of the human genome based on 5,264 microsatellites
- (1996) Nature (Lond.) , vol.380 , pp. 152-154
- Dib, C.¹ Faure, S.² Fizames, C.³ Samson, D.⁴ Drouot, N.⁵ Vignal, A.⁶ Millasseau, P.⁷ Marc, S.⁸ Hazan, J.⁹ Seboun, E.¹⁰ Lathrop, M.¹¹ Gyapay, G.¹² Morissette, J.¹³ Weissenbach, J.¹⁴

7
- 0028067338
- Two distinct deleted regions on the short arm of chromosome 1 in neuroblastoma
- (1994) Genes Chromosomes Cancer , vol.10 , pp. 275-281
- Schleiermacher, G.¹ Peter, M.² Michon, J.³ Hugot, J.P.⁴ Vielh, P.⁵ Zucke, J.M.⁶ Magdelenat, H.⁷ Thomas, G.⁸ Delattre, O.⁹

8
- 0023473012
- Deletions of a DNA sequence in retinoblastoma and mesenchymal tumors: Organization of the sequence and its encoded protein
- (1987) Proc. Natl. Acad. Sci. USA , vol.84 , pp. 9059-9063
- Friend, S.H.¹ Horowitz, J.M.² Gerber, M.R.³ Wang, X.F.⁴ Bogenmann, E.⁵ Li, F.P.⁶ Weinberg, R.A.⁷

9
- 0026417618
- Analysis of alterations in the retinoblastoma gene and tumor grade in bone and soft-tissue sarcomas
- (1991) J. Natl. Cancer Inst. , vol.83 , pp. 194-200
- Wunder, J.S.¹ Czitrom, A.A.² Kandel, R.³ Andrulis, I.L.⁴

10
- 0028871328
- Altered patterns of retinoblastoma gene product expression in adult soft-tissue sarcomas
- (1995) Br. J. Cancer , vol.72 , pp. 986-991
- Karpeh, M.S.¹ Brennan, M.F.² Cance, W.G.³ Woodruff, J.M.⁴ Pollack, D.⁵ Casper, E.S.⁶ Dudas, M.E.⁷ Latres, E.⁸ Drobnjak, M.⁹ Cordon-Cardo, C.¹⁰

11
- 0030824829
- Loss of RB and MTS1/CDKN2 (p16) expression in human sarcomas
- (1997) Hum. Pathol. , vol.28 , pp. 893-898
- Cohen, J.A.¹ Geradts, J.²

12
- 0028907719
- Spectrum of germline mutations in the RB1 gene: A study of 232 patients with hereditary and non-hereditary retinoblastoma
- (1995) Hum. Mol. Genet. , vol.4 , pp. 383-388
- Blanquet, V.¹ Turleau, C.² Gross-Morand, M.S.³ Senamaud-Beaufort, C.⁴ Doz, F.⁵ Besmond, C.⁶

13
- 0027962591
- Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma
- (1994) Hum. Genet. , vol.94 , pp. 491-496
- Greger, V.¹ Debus, N.² Lohmann, D.³ Hopping, W.⁴ Passarge, E.⁵ Horsthemke, B.⁶

14
- 0030848575
- Hypermethylation in the retinoblastoma gene is associated with unilateral, sporadic retinoblastoma
- (1997) Cancer Genet. Cytogenet. , vol.98 , pp. 43-49
- Ohtani-Fujita, N.¹ Dryja, T.P.² Rapaport, J.M.³ Fujita, T.⁴ Matsumura, S.⁵ Ozasa, K.⁶ Watanabe, Y.⁷ Hayashi, K.⁸ Maeda, K.⁹ Kinoshita, S.¹⁰ Matsumura, T.¹¹ Ohnishi, Y.¹² Hotta, Y.¹³ Takahashi, R.¹⁴ Kato, M.V.¹⁵ Ishizaki, K.¹⁶ Sasaki, M.S.¹⁷ Horsthemke, B.¹⁸ Minoda, K.¹⁹ Sakai, T.²⁰ more..

15
- 0027325420
- Malignant fibrous histiocytoma in childhood
- (1993) Cancer (Phila.) , vol.71 , pp. 4077-4083
- Cole, C.H.¹ Magee, J.F.² Gianoulis, M.³ Rogers, P.C.⁴

16
- 0031402818
- Second primary tumours in hereditary and nonhereditary retinoblastoma patients treated with megavoltage external beam irradiation
- (1997) Doc. Ophthalmol. , vol.93 , pp. 337-344
- Imhof, S.M.¹ Moll, A.C.² Hofman, P.³ Mourits, M.P.⁴ Schipper, J.⁵ Tan, K.E.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.