Literatura académica sobre el tema "Crispr-case9"
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Artículos de revistas sobre el tema "Crispr-case9"
Ma, Yiqiong, Duilio Michele Potenza, Guillaume Ajalbert, Andrea Brenna, Cui Zhu, Xiu-Fen Ming y Zhihong Yang. "Paracrine Effects of Renal Proximal Tubular Epithelial Cells on Podocyte Injury under Hypoxic Conditions Are Mediated by Arginase-II and TGF-β1". International Journal of Molecular Sciences 24, n.º 4 (10 de febrero de 2023): 3587. http://dx.doi.org/10.3390/ijms24043587.
Texto completoAbid, Pakeeza, Muhammad Babar Malook, Sidra Adil Khan, Muhammad Riaz, Hassan Rehman Ali y Kashif Kareem. "Use of CRISPER/CASE9 System in Engineering Plant Resistant to Gemini Virus, an Emerging Threat". International Journal of Pathogen Research 12, n.º 5 (25 de agosto de 2023): 37–43. http://dx.doi.org/10.9734/ijpr/2023/v12i5241.
Texto completoShi, Qizhen, Jeremy G. Mattson, Scot A. Fahs y Robert R. Montgomery. "The Severe Spontaneous Bleeding Phenotype in a Novel Hemophilia a Rat Model with an Inversion Mutation Is Rescued By Platelet-Targeted FVIII Expression". Blood 132, Supplement 1 (29 de noviembre de 2018): 219. http://dx.doi.org/10.1182/blood-2018-99-112165.
Texto completoLu, Junru y Guan Jiang. "The journey of CAR-T therapy in hematological malignancies". Molecular Cancer 21, n.º 1 (8 de octubre de 2022). http://dx.doi.org/10.1186/s12943-022-01663-0.
Texto completoWang, Li, Bo Li, Ran-Ran Su, Shi-Peng Wang, Zi-Yuan Xia, Cai-Yun Xie y Yue-Qin Tang. "Screening novel genes by a comprehensive strategy to construct multiple stress-tolerant industrial Saccharomyces cerevisiae with prominent bioethanol production". Biotechnology for Biofuels and Bioproducts 15, n.º 1 (21 de enero de 2022). http://dx.doi.org/10.1186/s13068-022-02109-x.
Texto completoTesis sobre el tema "Crispr-case9"
Hamouri, Fatima. "Contrôle optique de l'activité de protéines et de l'expression de gènes, par photo-activation du cyclofène cagé, pour l’étude de l’initiation du cancer". Electronic Thesis or Diss., Sorbonne université, 2020. http://www.theses.fr/2020SORUS235.
Texto completoThe zebrafish has become an increasingly popular and valuable cancer model over the past decades. While most of these models are generated by expressing mammalian oncogenes under tissue-specific promoters, here we describe a method that allows for the precise optical control of oncogene expression or inactivation in live zebrafish. Thus, this technique allows for the induction of tumor phenotypes by activating the constitutive expression of a typical human oncogene, KRASG12V, in selected tissues and single cells without tissue-specific promoters in live zebrafish. We also demonstrate the optical control of oncogene expression as KRASG12V, CMYC and BRAFV600E as well as the control of the expression and the activity of the CRISPR-Cas9 system. In addition, it should be noted that accurate manipulation of gene expression is essential to understand most biological processes. Therefore, our work presents a novel approach to initiate and study cancer in zebrafish. Finally, it is also worth noting that the high spatio-temporal resolution of this method makes it a valuable tool for studying cancer initiation from single cells