117 related articles for article (PubMed ID: 10920996)
1. [The structure, function and mutation of Rb gene promoter in normal individuals and retinoblastoma patients].
Huang Q; Wang J; Tao Y
Zhonghua Zhong Liu Za Zhi; 1998 May; 20(3):165-7. PubMed ID: 10920996
[TBL] [Abstract][Full Text] [Related]
2. The retinoblastoma binding factor 1 (RBF-1) site in RB gene promoter binds preferentially E4TF1, a member of the Ets transcription factors family.
Savoysky E; Mizuno T; Sowa Y; Watanabe H; Sawada J; Nomura H; Ohsugi Y; Handa H; Sakai T
Oncogene; 1994 Jul; 9(7):1839-46. PubMed ID: 8208529
[TBL] [Abstract][Full Text] [Related]
3. [The status of p53 gene in the primary retinoblastoma].
Huang Q
Zhonghua Yan Ke Za Zhi; 1999 Jul; 35(4):248-51. PubMed ID: 11835813
[TBL] [Abstract][Full Text] [Related]
4. [Gene diagnosis and genetic counselling of Rb gene mutations in retinoblastoma patients and their family members].
Huang Q; Dryja TP; Yandell DW
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Apr; 15(2):65-8. PubMed ID: 9531640
[TBL] [Abstract][Full Text] [Related]
5. Retinoblastoma binding factor 1 site in the core promoter region of the human RB gene is activated by hGABP/E4TF1.
Sowa Y; Shiio Y; Fujita T; Matsumoto T; Okuyama Y; Kato D; Inoue J; Sawada J; Goto M; Watanabe H; Handa H; Sakai T
Cancer Res; 1997 Aug; 57(15):3145-8. PubMed ID: 9242441
[TBL] [Abstract][Full Text] [Related]
6. Overview of RB gene mutations in patients with retinoblastoma. Implications for clinical genetic screening.
Harbour JW
Ophthalmology; 1998 Aug; 105(8):1442-7. PubMed ID: 9709755
[TBL] [Abstract][Full Text] [Related]
7. A silencer element in the retinoblastoma tumor-suppressor gene.
Ohtani-Fujita N; Fujita T; Takahashi R; Robbins PD; Dryja TP; Sakai T
Oncogene; 1994 Jun; 9(6):1703-11. PubMed ID: 8183566
[TBL] [Abstract][Full Text] [Related]
8. [Distinct Rb gene point mutations in families showing low penetrance of hereditary retinoblastoma].
Huang Q; Dryja TP; Yandell DW
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Jun; 15(3):139-42. PubMed ID: 9621119
[TBL] [Abstract][Full Text] [Related]
9. [Mutations of several tumor suppressor genes in primary retinoblastoma].
Huang Q; Tao Y; Yandell DW
Zhonghua Zhong Liu Za Zhi; 1999 Jan; 21(1):10-2. PubMed ID: 11776785
[TBL] [Abstract][Full Text] [Related]
10. A novel mutation in the promotor region in a family with a mild form of retinoblastoma indicates the location of a new regulatory domain for the RB1 gene.
Cowell JK; Bia B; Akoulitchev A
Oncogene; 1996 Jan; 12(2):431-6. PubMed ID: 8570221
[TBL] [Abstract][Full Text] [Related]
11. Loss of heterozygosity and mutations are the major mechanisms of RB1 gene inactivation in Chinese with sporadic retinoblastoma.
Choy KW; Pang CP; Yu CB; Wong HL; Ng JS; Fan DS; Lo KW; Chai JT; Wang J; Fu W; Lam DS
Hum Mutat; 2002 Nov; 20(5):408. PubMed ID: 12402348
[TBL] [Abstract][Full Text] [Related]
12. Genomic organization of the human retinoblastoma gene.
T'Ang A; Wu KJ; Hashimoto T; Liu WY; Takahashi R; Shi XH; Mihara K; Zhang FH; Chen YY; Du C
Oncogene; 1989 Apr; 4(4):401-7. PubMed ID: 2717184
[TBL] [Abstract][Full Text] [Related]
13. Retinoic acid upregulates cone arrestin expression in retinoblastoma cells through a Cis element in the distal promoter region.
Li A; Zhu X; Craft CM
Invest Ophthalmol Vis Sci; 2002 May; 43(5):1375-83. PubMed ID: 11980849
[TBL] [Abstract][Full Text] [Related]
14. [Low-penetrance retinoblastoma due to exons 24 and 25 deletions in the Rb1 gene].
Du C; Jiang Y; Gallie BL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Oct; 19(5):370-4. PubMed ID: 12362308
[TBL] [Abstract][Full Text] [Related]
15. [Diagnosis of a predisposition of retinoblastoma at the DNA level].
Murakami Y
Gan To Kagaku Ryoho; 1991 Jan; 18(1):44-50. PubMed ID: 1670986
[TBL] [Abstract][Full Text] [Related]
16. [Spectrum and frequencies of RB1 gene structural defects in retinoblastoma].
Babenko OV; Saakian SV; Brovkina AF; Kozlova VM; Strel'nikov VV; Zaletaev DV; Nemtsova MV
Mol Biol (Mosk); 2002; 36(4):623-9. PubMed ID: 12173465
[TBL] [Abstract][Full Text] [Related]
17. Abnormal gene expression profiles in unaffected parents of patients with hereditary-type retinoblastoma.
Chuang EY; Chen X; Tsai MH; Yan H; Li CY; Mitchell JB; Nagasawa H; Wilson PF; Peng Y; Fitzek MM; Bedford JS; Little JB
Cancer Res; 2006 Apr; 66(7):3428-33. PubMed ID: 16585164
[TBL] [Abstract][Full Text] [Related]
18. Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.
Nichols KE; Houseknecht MD; Godmilow L; Bunin G; Shields C; Meadows A; Ganguly A
Hum Mutat; 2005 Jun; 25(6):566-74. PubMed ID: 15884040
[TBL] [Abstract][Full Text] [Related]
19. p53 gene gets altered by various mechanisms: studies in childhood sarcomas and retinoblastoma.
Ghule P; Kadam PA; Jambhekar N; Bamne M; Pai S; Nair C; Banavali S; Puri A; Agarwal M
Med Sci Monit; 2006 Dec; 12(12):BR385-396. PubMed ID: 17136003
[TBL] [Abstract][Full Text] [Related]
20. A point mutation affecting an SP1 binding site in the promoter of the ferrochelatase gene impairs gene transcription and causes erythropoietic protoporphyria.
Di Pierro E; Cappellini MD; Mazzucchelli R; Moriondo V; Mologni D; Zanone Poma B; Riva A
Exp Hematol; 2005 May; 33(5):584-91. PubMed ID: 15850836
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]