Academic literature on the topic 'Proteine p126'

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Dissertations / Theses on the topic "Proteine p126"

1

Conseil, Valérie. "Etude des proteolyses en culture et in vitro de la proteine p126 de plasmodium falciparum." Lille 2, 1996. http://www.theses.fr/1996LIL2T007.

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2

Gilardeau, Truffinet Myriam. "Etude de l'influence de modifications chimiques non ambigues et de differents adjuvants sur l'immunogenicite du peptide nt47 de la proteine p126 de plasmodium falciparum." Lille 2, 1996. http://www.theses.fr/1996LIL2T006.

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3

Erhorn, Frauke. "Die Funktion von Juv-p120 im Verlauf der Infektion mit Litomosoides sigmodontis." Giessen : VVB Laufersweiler, 2008. http://d-nb.info/988285762/04.

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4

Tang, Kit Shing. "Stability, folding and evolution of the tumour suppressor protein p16." Thesis, University of Cambridge, 2001. https://www.repository.cam.ac.uk/handle/1810/251785.

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5

Bauer, Marcus [Verfasser]. "Expression des p16 Proteins in humanen Tumoren und Normalgeweben / Marcus Bauer." Hamburg : Staats- und Universitätsbibliothek Hamburg Carl von Ossietzky, 2020. http://d-nb.info/1236694937/34.

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6

Thullberg, Minna. "The cell cycle regulators p15, p16, p18 and p19 : functions and regulation during normal cell cycle and in multistep carcinogenesis /." Stockholm, 2000. http://diss.kib.ki.se/2000/91-628-4432-6/.

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7

Mutalik, Vimi Sunil. "Comparative Assessment of p16 Protein Expression in Normal and Dysplastic Oral Mucosal Epithelium." The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1530615395569555.

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8

Li, Junan. "Structural and functional studies on Tumor Suppressor INK4 Proteins P16(INK4A) and P18(INK4C) /." The Ohio State University, 2000. http://rave.ohiolink.edu/etdc/view?acc_num=osu1488194825665461.

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9

Junqueira, Mara de Souza. "Caracterização das vias de transformação maligna de uma nova linhagem estabelecida de melanoma murino." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/5/5155/tde-20092010-183837/.

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Ao longo dos processos de imortalização e transformação maligna, as células adquirem inúmeras alterações genéticas, que são causadas por fatores endógenos e exógenos como agentes biológicos e a geração de espécies reativas de oxigênio. Neste trabalho, uma linhagem celular espontaneamente transformada foi clonada a partir de explantes de embriões de camundongos C57bl/6. Esta linhagem mostrou-se produtora de pigmento escuro; a análise citoquímica e ultraestrutural permitiu caracterizar a linhagem como tendo origem melanocítica. A linhagem, denominada Mgal3, mostrou-se tumorigênica quando implant
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10

Wight, D. J. "Investigations into the function of the gammaretroviral protein p12 during the early stages of infection." Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1410320/.

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The retroviral structural proteins (encoded by gag) are not merely the architecture of the virus but carry out a diverse set of functions throughout the viral life cycle. Initially translated as a polyprotein, the Gag protein functions to encapsidate the genome and assemble retroviral particles at the budding sites. This polyprotein is then cleaved into the mature proteins: matrix (MA), capsid (CA) and nucleocapsid (NC) upon viral release. Most retroviruses also contain a small protein between MA and CA of unknown function. In Moloney murine leukaemia virus (Mo-MLV) this protein is p12. p12 co
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