User:JonSDSUGrad/Sandbox/TEST11 Retinoblastoma protein
From Wikipedia, the free encyclopedia
Retinoblastoma 1 (including osteosarcoma), also known as RB1, is a human gene.
Retinoblastoma (RB) is an embryonic malignant neoplasm of retinal origin. It almost always presents in early childhood and is often bilateral. Spontaneous regression ('cure') occurs in some cases.[supplied by OMIM][1]
[edit] References
[edit] Further reading
- Momand J, Wu HH, Dasgupta G (2000). "MDM2--master regulator of the p53 tumor suppressor protein.". Gene 242 (1-2): 15-29. PMID 10721693.
- Zheng L, Lee WH (2003). "Retinoblastoma tumor suppressor and genome stability.". Adv. Cancer Res. 85: 13-50. PMID 12374284.
- Classon M, Harlow E (2003). "The retinoblastoma tumour suppressor in development and cancer.". Nat. Rev. Cancer 2 (12): 910-7. doi: . PMID 12459729.
- Lai H, Ma F, Lai S (2003). "Identification of the novel role of pRB in eye cancer.". J. Cell. Biochem. 88 (1): 121-7. doi: . PMID 12461781.
- Simin K, Wu H, Lu L, et al. (2006). "pRb inactivation in mammary cells reveals common mechanisms for tumor initiation and progression in divergent epithelia.". PLoS Biol. 2 (2): E22. doi: . PMID 14966529.
- Lohmann DR, Gallie BL (2004). "Retinoblastoma: revisiting the model prototype of inherited cancer.". American journal of medical genetics. Part C, Seminars in medical genetics 129 (1): 23-8. doi: . PMID 15264269.
- Clemo NK, Arhel NJ, Barnes JD, et al. (2005). "The role of the retinoblastoma protein (Rb) in the nuclear localization of BAG-1: implications for colorectal tumour cell survival.". Biochem. Soc. Trans. 33 (Pt 4): 676-8. doi: . PMID 16042572.
- RodrÃguez-Cruz M, del Prado M, Salcedo M (2006). "[Genomic retinoblastoma perspectives: implications of tumor supressor gene RB1]". Rev. Invest. Clin. 57 (4): 572-81. PMID 16315642.
- Knudsen ES, Knudsen KE (2006). "Retinoblastoma tumor suppressor: where cancer meets the cell cycle.". Exp. Biol. Med. (Maywood) 231 (7): 1271-81. PMID 16816134.