Literatura académica sobre el tema "Cdc42 isoformes"
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Artículos de revistas sobre el tema "Cdc42 isoformes"
Ravindran, Priyadarshini y Andreas W. Püschel. "An isoform-specific function of Cdc42 in regulating mammalian Exo70 during axon formation". Life Science Alliance 6, n.º 3 (21 de diciembre de 2022): e202201722. http://dx.doi.org/10.26508/lsa.202201722.
Texto completoJansson, Thomas, Marisol Castillo-Castrejon, Madhulika B. Gupta, Theresa L. Powell y Fredrick J. Rosario. "Down-regulation of placental Cdc42 and Rac1 links mTORC2 inhibition to decreased trophoblast amino acid transport in human intrauterine growth restriction". Clinical Science 134, n.º 1 (enero de 2020): 53–70. http://dx.doi.org/10.1042/cs20190794.
Texto completoKolyada, Alexey Y., Kathleen N. Riley y Ira M. Herman. "Rho GTPase signaling modulates cell shape and contractile phenotype in an isoactin-specific manner". American Journal of Physiology-Cell Physiology 285, n.º 5 (noviembre de 2003): C1116—C1121. http://dx.doi.org/10.1152/ajpcell.00177.2003.
Texto completoFediuk, Jena, Anurag S. Sikarwar, Nora Nolette y Shyamala Dakshinamurti. "Thromboxane-induced actin polymerization in hypoxic neonatal pulmonary arterial myocytes involves Cdc42 signaling". American Journal of Physiology-Lung Cellular and Molecular Physiology 307, n.º 11 (1 de diciembre de 2014): L877—L887. http://dx.doi.org/10.1152/ajplung.00036.2014.
Texto completoWirth, Alexander, Chen Chen-Wacker, Yao-Wen Wu, Nataliya Gorinski, Mikhail A. Filippov, Ghanshyam Pandey y Evgeni Ponimaskin. "Dual lipidation of the brain-specific Cdc42 isoform regulates its functional properties". Biochemical Journal 456, n.º 3 (22 de noviembre de 2013): 311–22. http://dx.doi.org/10.1042/bj20130788.
Texto completoZhou, Rihong, Zhen Guo, Charles Watson, Emily Chen, Rong Kong, Wenxian Wang y Xuebiao Yao. "Polarized Distribution of IQGAP Proteins in Gastric Parietal Cells and Their Roles in Regulated Epithelial Cell Secretion". Molecular Biology of the Cell 14, n.º 3 (marzo de 2003): 1097–108. http://dx.doi.org/10.1091/mbc.e02-07-0425.
Texto completoFotiadou, Poppy P., Chiaki Takahashi, Hasan N. Rajabi y Mark E. Ewen. "Wild-Type NRas and KRas Perform Distinct Functions during Transformation". Molecular and Cellular Biology 27, n.º 19 (16 de julio de 2007): 6742–55. http://dx.doi.org/10.1128/mcb.00234-07.
Texto completoCARGINALE, Vincenzo, Rosaria SCUDIERO, Clemente CAPASSO, Antonio CAPASSO, Peter KILLE, Guido di PRISCO y Elio PARISI. "Cadmium-induced differential accumulation of metallothionein isoforms in the Antarctic icefish, which exhibits no basal metallothionein protein but high endogenous mRNA levels". Biochemical Journal 332, n.º 2 (1 de junio de 1998): 475–81. http://dx.doi.org/10.1042/bj3320475.
Texto completoChen, Hung-Hsi, Yu-Chiuan Wang y Ming-Ji Fann. "Identification and Characterization of the CDK12/Cyclin L1 Complex Involved in Alternative Splicing Regulation". Molecular and Cellular Biology 26, n.º 7 (1 de abril de 2006): 2736–45. http://dx.doi.org/10.1128/mcb.26.7.2736-2745.2006.
Texto completoScalia, Pierluigi, Carmen Merali, Carlos Barrero, Antonio Suma, Vincenzo Carnevale, Salim Merali y Stephen J. Williams. "Novel Isoform DTX3c Associates with UBE2N-UBA1 and Cdc48/p97 as Part of the EphB4 Degradation Complex Regulated by the Autocrine IGF-II/IRA Signal in Malignant Mesothelioma". International Journal of Molecular Sciences 24, n.º 8 (17 de abril de 2023): 7380. http://dx.doi.org/10.3390/ijms24087380.
Texto completoTesis sobre el tema "Cdc42 isoformes"
Ravichandran, Yamini. "Cdc42 isoforms : localization, functions and regulation". Electronic Thesis or Diss., Sorbonne université, 2020. http://www.theses.fr/2020SORUS405.
Texto completoMutations in proteins cause diverse developmental disorders, particularly for individuals with rare diseases or for whom a unifying clinical diagnosis is unknown. Cdc42 is one such protein; vital for establishing cell polarity, a crucial step in many biological processes such as cell migration, division and immune responses. Not surprisingly, mutations in Cdc42 cause a range of diseases such as growth dysregulation, facial dysmorphism and neurodevelopmental, immunological, and hematological abnormalities. In vertebrates there are two isoforms of Cdc42. The first being the ubiquitous isoform, has almost exclusively been studied and the role of the second isoform, being the brain isoform, is largely unknown. We have shown that the two isoforms are localized differently in cells. The ubiquitous isoform is mostly found in the cell cytoplasm and at the plasma membrane, while the Brain isoform localizes at the Golgi apparatus and on intracellular vesicles. We have also shown that the two isoforms carry out different functions during cell migration, suggesting that the differences between these two isoforms which only differs by the last 10 amino acids are responsible for their distinct localisation and function. Interestingly, a mutation in the C-ter sequence of Cdc42 ubiquitous isoform alters Cdc42 localisation and causes a generalized pustular psoriasis disease. Two main objectives have been studied in this project 1) the impact of the last amino acids of the protein in Cdc42 localization; and 2) new regulatory mechanisms of Cdc42 responsible for its intracellular localization. These findings will bring a better understanding of pathologies related to Cdc42 mutations
Fediuk, Jena. "Thromboxane receptor signaling and Rho GTPase activation on actin polymerization and contraction in hypoxic neonatal pulmonary arterial myocytes". Am J Physiol Lung Cell Mol Physiol, 2012. http://hdl.handle.net/1993/23862.
Texto completoKiso, Marina. "Long isoform of VEGF stimulates cell migration of breast cancer by filopodia formation via NRP1/ARHGAP17/Cdc42 regulatory network". Kyoto University, 2018. http://hdl.handle.net/2433/235980.
Texto completoActas de conferencias sobre el tema "Cdc42 isoformes"
Kiso, Marina, Sunao Tanaka, Masakazu Toi y Fumiaki Sato. "Abstract 2862: Long isoform of VEGF stimulates cell migration of breast cancer by filopodia formation via NRP1/ARHGAP17/Cdc42 regulatory network". En Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-2862.
Texto completoKiso, Marina, Sunao Tanaka, Masakazu Toi y Fumiaki Sato. "Abstract 2862: Long isoform of VEGF stimulates cell migration of breast cancer by filopodia formation via NRP1/ARHGAP17/Cdc42 regulatory network". En Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-2862.
Texto completo