Gotowa bibliografia na temat „Cellular immortalisation”
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Artykuły w czasopismach na temat "Cellular immortalisation"
Argyle, D., V. Ellsmore, E. A. Gault, A. F. Munro i L. Nasir. "Equine telomeres and telomerase in cellular immortalisation and ageing". Mechanisms of Ageing and Development 124, nr 6 (czerwiec 2003): 759–64. http://dx.doi.org/10.1016/s0047-6374(03)00104-0.
Pełny tekst źródłaThiers, B. H. "Cellular senescence in naevi and immortalisation in melanoma: a role for p16?" Yearbook of Dermatology and Dermatologic Surgery 2007 (styczeń 2007): 340–41. http://dx.doi.org/10.1016/s0093-3619(08)70622-1.
Pełny tekst źródłaGray-Schopfer, V. C., S. C. Cheong, H. Chong, J. Chow, T. Moss, Z. A. Abdel-Malek, R. Marais, D. Wynford-Thomas i D. C. Bennett. "Cellular senescence in naevi and immortalisation in melanoma: a role for p16?" British Journal of Cancer 95, nr 4 (sierpień 2006): 496–505. http://dx.doi.org/10.1038/sj.bjc.6603283.
Pełny tekst źródłaSonigra, Rakesh J., Shivanthi S. Kandiah i Caroline B. Wigley. "Spontaneous immortalisation of ensheathing cells from adult rat olfactory nerve". Glia 16, nr 3 (marzec 1996): 247–56. http://dx.doi.org/10.1002/(sici)1098-1136(199603)16:3<247::aid-glia7>3.0.co;2-z.
Pełny tekst źródłaKerr, Jonathan R. "Epstein-Barr virus (EBV) reactivation and therapeutic inhibitors". Journal of Clinical Pathology 72, nr 10 (17.07.2019): 651–58. http://dx.doi.org/10.1136/jclinpath-2019-205822.
Pełny tekst źródłaToussaint, Olivier, Patrick Dumont, Jose Remacle, Jean-Francois Dierick, Thierry Pascal, Christophe Frippiat, Joao Pedro Magalhaes, Stephanie Zdanov i Florence Chainiaux. "Stress-Induced Premature Senescence or Stress-Induced Senescence-Like Phenotype: OneIn VivoReality, Two Possible Definitions?" Scientific World JOURNAL 2 (2002): 230–47. http://dx.doi.org/10.1100/tsw.2002.100.
Pełny tekst źródłaNorton, J. D. "ID helix-loop-helix proteins in cell growth, differentiation and tumorigenesis". Journal of Cell Science 113, nr 22 (15.11.2000): 3897–905. http://dx.doi.org/10.1242/jcs.113.22.3897.
Pełny tekst źródłaArlett, Colin F., Michael H. L. Green, Anne Priestley, Susan A. Harcourt i Lynne V. Mayne. "Comparative Human Cellular Radiosensitivity: I. The Effect of SV40 Transformation and Immortalisation on the Gamma-irradiation Survival of Skin Derived Fibroblasts from Normal Individuals and from Ataxia-telangiectasia Patients and Heterozygotes". International Journal of Radiation Biology 54, nr 6 (styczeń 1988): 911–28. http://dx.doi.org/10.1080/09553008814552321.
Pełny tekst źródłaEvrard, C., M. Le Bert, I. Borde, P. Rouget, E. Galiana i R. Bemard. "Transfert de gènes dans les cellules nerveuses: immortalisation cellulaire et marquage génétique". médecine/sciences 7, nr 4 (1991): IX. http://dx.doi.org/10.4267/10608/4373.
Pełny tekst źródłaGiotopoulos, George, Wai-In Chan, David Ruau, Paolo Gallipoli, Alexis Fowler, Berthold Göttgens, Jan Van Deursen, Philip Cole i Brian Huntly. "The Epigenetic Regulators CBP and p300 Facilitate Leukemogenesis and Represent Therapeutic Targets In Acute Myeloid Leukemia (AML)". Blood 122, nr 21 (15.11.2013): 3732. http://dx.doi.org/10.1182/blood.v122.21.3732.3732.
Pełny tekst źródłaRozprawy doktorskie na temat "Cellular immortalisation"
Kan, Chin-Yi. "Human Papillomavirus in human breast cancer and cellular immortalisation". Sydney : University of New South Wales. Biotechnology and Biomolecular Sciences, 2007. http://www.library.unsw.edu.au/~thesis/adt-NUN/public/adt-NUN20071004.080541/.
Pełny tekst źródłaLinne, Hannah Louise. "Investigating telomerase regulation in human breast cancer cells : a search for telomerase repressor sequences localised to chromosome 3P". Thesis, Brunel University, 2015. http://bura.brunel.ac.uk/handle/2438/11620.
Pełny tekst źródłaParouchev, Alexandre. "Immortalisation et transplantation de cellules hépatiques simiennes : modèles de thérapie cellulaire hépatique". Paris 7, 2010. http://www.theses.fr/2010PA077099.
Pełny tekst źródłaOrthotopic liver transplantation is the only available cure for certain metabolic deficiencies. But, lack of donors and complications related to immunosuppression urge the development of alternatives therapies such as hepatocyte transplantation. However, trials with adult hepatocytes have been so far disappointing. We have explored two directions. As a model for an alternative source of hépatocytes, we have characterized a line of simian fetal hepatic cells (IPFLS), immortalized by SV40-T antigen. In vitro these cells conserve their proliferative capacity and their hepatic bipotent progenitor phenotype. The immortalization is reversible after Cre-mediated excision of the oncogene. In vivo, they are non tumorigenic and differentiate into hepatocytes, with no in situ proliferation. However, the important karyotype instability underlines the need for new immortali2ation strategies. Moreover, ex vivo gene therapy is considered as an alternative to hepatocyte allotransplantation. We have set up conditions for efficient transduction of freshly-isolated and cryopreserved, adult, simian hepatocytes in suspension by HIV-1-derived recombinant lentiviruses, expressing GFP under transcriptional control of the hepatospecific promoter of the human apolipoprotein A-II gene. The in vivo persistence and fonction of cryopreserved cells is demonstrated by the presence of transduced hepatocytes three months after transplantation into the liver of immunodeficient mice. Thus the nonhuman primate appears as a good preclinical model for the development of liver-directed ex vivo gene therapy strategies
Bernard, Rozenn. "Transfert de gènes dans des précurseurs gliaux : immortalisation cellulaire, prolifération et différenciation des lignées établies". Paris 11, 1994. http://www.theses.fr/1994PA11T009.
Pełny tekst źródłaAllain, Jean-Etienne. "Immortalisation et transplantation de cellules foetales hépatiques simiennes et humaines : modèles de thérapie cellulaire hépatique". Paris 7, 2002. http://www.theses.fr/2002PA077004.
Pełny tekst źródłaBayad, Jamal. "Immortalisation de lignées cellulaires hépatocytaires : expression et régulation des enzymes du métabolisme des xenobiotiques". Nancy 1, 1991. http://www.theses.fr/1991NAN10450.
Pełny tekst źródłaDelgado, Charris Jean-Paul. "Caractérisation phénotypique et moléculaire des cellules progénitrices foetales hépatiques simiennes et humaines". Paris 11, 2006. http://www.theses.fr/2006PA114825.
Pełny tekst źródłaThe liver is a target organ for cell-based therapies. The use of human adult hepatocytes for such approaches is limited by the lack of donors, the absence of proliferation and low cell engraftment. We characterized a simian bipotent hepatoblast line (IPFLS) immortalized in our lab by using the Sv40 virus T oncogene flanked by LoxP sites, at different population doublings (PD). We showed that immortalization process was reversible after Cre recombinase mediated retroviral gene transfer. We also showed a telomerase activity reduction correlated with telomere shortening and chromosomal rearrangements at 120 PD. After transplantation in the liver of immunocompromised mice, IPFLS cells were differentiated into hepatocytes but did not proliferate. We contributed to the isolation and characterization of early fetal human heptoblasts/hepatocytes (10-12 weeks). After transplantation, these cells repopulated more efficiently the liver of transplanted mice than IPFLS cells. Human hepatoblasts, contrary tu adult hepatocytes, have an in vitro migration and invasion potential which is enhanced by the Hepatocyte Growth Factor (HGF). This process is correlated with an up regulation in the secretion and activation of matrix metalloproteinases 2 and 9 and the activation of the ERK pathway. Transplantation of hepatoblasts stimulated with HGF into new born mice improves cell spreading in the liver parenchyma. These results suggest that human hepatoblasts have specific properties which allow the improvement of cell engraftement
Aure, Karine. "Physiopathologie moléculaire et cellulaire des maladies mitochondriales à présentation neurologique". Paris 6, 2007. http://www.theses.fr/2007PA066281.
Pełny tekst źródłaDJELLOUL, SIHAM. "Immortalisation des cellules epitheliales digestives par l'oncogene grand t de sv40 : consequences sur la transformation, la differenciation et l'effet antiproliferatif du tgf1". Paris 6, 1997. http://www.theses.fr/1997PA066066.
Pełny tekst źródłaBORDE, ISABELLE. "Transfert de genes et immortalisation de precurseurs de cellules nerveuses murines. Etude de la proliferation et de la differenciation des lignees immortalisees". Paris 7, 1994. http://www.theses.fr/1994PA077012.
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