Relevant bibliographies by topics / CEP104

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Academic literature on the topic 'CEP104'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "CEP104"

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Yamazoe, Takashi, Tomoaki Nagai, Shinya Umeda, Yuko Sugaya, and Kensaku Mizuno. "Roles of TOG and jelly-roll domains of centrosomal protein CEP104 in its functions in cilium elongation and Hedgehog signaling." Journal of Biological Chemistry 295, no. 43 (2020): 14723–36. http://dx.doi.org/10.1074/jbc.ra120.013334.

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Primary cilia are generated through the extension of the microtubule-based axoneme. Centrosomal protein 104 (CEP104) localizes to the tip of the elongating axoneme, and CEP104 mutations are linked to a ciliopathy, Joubert syndrome. Thus, CEP104 has been implicated in ciliogenesis. However, the mechanism by which CEP104 regulates ciliogenesis remains elusive. We report here that CEP104 is critical for cilium elongation but not for initiating ciliogenesis. We also demonstrated that the tumor-overexpressed gene (TOG) domain of CEP104 exhibits microtubule-polymerizing activity and that this activi
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Tolan, J. "Reading the Qur'an in Latin Christendom, 1140-1560." English Historical Review CXXIV, no. 508 (2009): 679–80. http://dx.doi.org/10.1093/ehr/cep104.

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Al-Jassar, Caezar, Antonina Andreeva, Deepak D. Barnabas, et al. "The Ciliopathy-Associated Cep104 Protein Interacts with Tubulin and Nek1 Kinase." Structure 25, no. 1 (2017): 146–56. http://dx.doi.org/10.1016/j.str.2016.11.014.

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Rezabkova, Lenka, Sebastian H. W. Kraatz, Anna Akhmanova, Michel O. Steinmetz, and Richard A. Kammerer. "Biophysical and Structural Characterization of the Centriolar Protein Cep104 Interaction Network." Journal of Biological Chemistry 291, no. 35 (2016): 18496–504. http://dx.doi.org/10.1074/jbc.m116.739771.

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Srour, Myriam, Fadi F. Hamdan, Dianalee McKnight, et al. "Joubert Syndrome in French Canadians and Identification of Mutations in CEP104." American Journal of Human Genetics 97, no. 5 (2015): 744–53. http://dx.doi.org/10.1016/j.ajhg.2015.09.009.

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Satish Tammana, T. V., D. Tammana, D. R. Diener, and J. Rosenbaum. "Centrosomal protein CEP104 (Chlamydomonas FAP256) moves to the ciliary tip during ciliary assembly." Journal of Cell Science 126, no. 21 (2013): 5018–29. http://dx.doi.org/10.1242/jcs.133439.

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Khoshbakht, Shahrouz, Maryam Beheshtian, Zohreh Fattahi, et al. "CEP104 and CEP290; Genes with Ciliary Functions Cause Intellectual Disability in Multiple Families." Archives of Iranian Medicine 24, no. 5 (2021): 364–73. http://dx.doi.org/10.34172/aim.2021.53.

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Frikstad, Kari-Anne M., Elisa Molinari, Marianne Thoresen, et al. "A CEP104-CSPP1 Complex Is Required for Formation of Primary Cilia Competent in Hedgehog Signaling." Cell Reports 28, no. 7 (2019): 1907–22. http://dx.doi.org/10.1016/j.celrep.2019.07.025.

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Graser, Susanne, York-Dieter Stierhof, Sébastien B. Lavoie, et al. "Cep164, a novel centriole appendage protein required for primary cilium formation." Journal of Cell Biology 179, no. 2 (2007): 321–30. http://dx.doi.org/10.1083/jcb.200707181.

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Primary cilia (PC) function as microtubule-based sensory antennae projecting from the surface of many eukaryotic cells. They play important roles in mechano- and chemosensory perception and their dysfunction is implicated in developmental disorders and severe diseases. The basal body that functions in PC assembly is derived from the mature centriole, a component of the centrosome. Through a small interfering RNA screen we found several centrosomal proteins (Ceps) to be involved in PC formation. One newly identified protein, Cep164, was indispensable for PC formation and hence characterized in
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Louka, Panagiota, Krishna Kumar Vasudevan, Mayukh Guha, et al. "Proteins that control the geometry of microtubules at the ends of cilia." Journal of Cell Biology 217, no. 12 (2018): 4298–313. http://dx.doi.org/10.1083/jcb.201804141.

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Cilia, essential motile and sensory organelles, have several compartments: the basal body, transition zone, and the middle and distal axoneme segments. The distal segment accommodates key functions, including cilium assembly and sensory activities. While the middle segment contains doublet microtubules (incomplete B-tubules fused to complete A-tubules), the distal segment contains only A-tubule extensions, and its existence requires coordination of microtubule length at the nanometer scale. We show that three conserved proteins, two of which are mutated in the ciliopathy Joubert syndrome, dete
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Dissertations / Theses on the topic "CEP104"

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Rocha, Jaqueline Maria Matias da. "The role of CEP164 in ciliogenesis in Drosophila melanogaster." Master's thesis, Universidade de Aveiro, 2013. http://hdl.handle.net/10773/12494.

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Mestrado em Biotecnologia - Biotecnologia Industrial e Ambiental<br>Cilia/flagella are microtubule (MT)-based oraganelle emanating from the surface of many eukaryotic cells. They are involved in a variety of processes including cell motility, fluid flow, and sensing processes. The skeleton of cilium, called axoneme, is templated from the basal body, a modified mature centriole required for centrosome formation. Mutations in human genes disrupting the function or structure of these organelles cause several human disorders, including infertility, ciliopathies, and cancer. In Drosophila melanoga
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Lamla, Stefan. "Functional characterisation of the centrosomal protein Cep170." Diss., lmu, 2009. http://nbn-resolving.de/urn:nbn:de:bvb:19-97838.

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Anderhub, Simon [Verfasser]. "Charakterisierung der Proteine CEP164 und ppdpf sowie deren Einordnung in den mitotischen Kontext / Simon Anderhub." Mainz : Universitätsbibliothek Mainz, 2013. http://d-nb.info/1033734136/34.

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Chamling, Xitiz. "Identification and characterization of CEP131 as a novel BBSome interacting protein." Diss., University of Iowa, 2014. https://ir.uiowa.edu/etd/4588.

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Bardet-Biedl syndrome (BBS) is a pleiotropic and genetically heterogeneous disorder, and a well-known ciliopathy. Nineteen different genes have been reported for BBS, mutations in which cause characteristic phenotypes including retinal degeneration, obesity, polydactyly, renal abnormalities, hypogenitalism and cognitive impairment. Protein products of eleven BBS genes are part of two major complexes: the BBSome complex and a CCT/CTRiC/BBS complex. The CCT/CTRiC/BBS complex assists in the formation of the BBSome complex, which in turn traffics numerous receptor proteins to the cilia. However, t
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Zanini, Marco. "Ciliogenesis Control Mechanisms in Cerebellar Neuron Progenitors." Thesis, Université Paris-Saclay (ComUE), 2019. http://www.theses.fr/2019SACLS475/document.

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Pendant le développement du cervelet, les progéniteurs des neurones granulaires (PNG) nécessitent la présence du cil primaire pour proliférer en réponse à Sonic Hedgehog (SHH). En effet, la prolifération dérégulée des PNGs peut conduire à la formation d'une tumeur pédiatrique maligne appelée SHH-médulloblastome (MB), de ce fait comprendre comment le cil primaire est régulé dans les PNGs est crucial.Nous montrons que le facteur de transcription Atoh1 contrôle la présence du cil primaire dans les PNGs in vitro et in vivo. En particulier, la suppression du cil primaire par l’inactivation génétiqu
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Sir, Joo-Hee. "Characterisation of the autosomal recessive primary microcephaly complex, CEP63-CEP152 in the vertebrate centrosome." Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608038.

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Schausten, Charlotte Verfasser], Rainer [Akademischer Betreuer] [Telle, and Georg [Akademischer Betreuer] Roth. "Untersuchungen zu Sinterverhalten und Gefügeentwicklung der Monazitkeramiken LaPO4, CePO4 und PrPO4 für die Endlagerung von Minoren Actinoiden / Charlotte Schausten ; Rainer Telle, Georg Roth." Aachen : Universitätsbibliothek der RWTH Aachen, 2020. http://d-nb.info/1227447086/34.

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Schausten, Charlotte [Verfasser], Rainer [Akademischer Betreuer] Telle, and Georg [Akademischer Betreuer] Roth. "Untersuchungen zu Sinterverhalten und Gefügeentwicklung der Monazitkeramiken LaPO4, CePO4 und PrPO4 für die Endlagerung von Minoren Actinoiden / Charlotte Schausten ; Rainer Telle, Georg Roth." Aachen : Universitätsbibliothek der RWTH Aachen, 2020. http://d-nb.info/1227447086/34.

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Huang, Han-Chiang, and 黃漢強. "Overexpressed Cep170 localizes to acentrosomal puncta and promotes neurite outgrowth." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/92897006679658144092.

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碩士<br>國立交通大學<br>生物科技學系<br>104<br>Microtubule is the major cytoskeleton in neuron, and regulates various crucial neuron developmental processes. To understand how microtubule cytoskeleton influences neuronal development, we have previously utilized quantitative proteomics to examine microtubule-associated proteomes in mouse embryonal carcinoma cells (P19 cells) before and after neuronal differentiation. One of the proteins on microtubules exhibiting substantial and significant increase upon neuronal differentiation is centrosomal protein 170 (Cep170). This suggests that it plays a role in regul
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Srour, Myriam. "Genetic Landscape of Joubert syndrome in French Canadians." Thèse, 2015. http://hdl.handle.net/1866/13027.

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Le syndrome de Joubert est une maladie récessive caractérisée par une malformation congénitale distincte du tronc cérébral et du cervelet, associée à une anomalie des mouvements oculaires (apraxie oculomotrice), une respiration irrégulière, un retard de développement, et une ataxie à la démarche. Au cours de la dernière décennie, plus de 20 gènes responsables ont été identifiés, tous ayant un rôle important dans la structure et la fonction des cils primaires. Ainsi, le syndrome de Joubert est considéré une ciliopathie. Bien que le Syndrome de Joubert ait été décrit pour la première fois dans
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Books on the topic "CEP104"

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Loizou, Christopher. Slavers of Karg (Cursed Empire) (CEP004). Spartans Unleashed, 2005.

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Loizou, Chris. Thargos Atlas (Cursed Empire) (CEP013). Spartans Unleashed, 2004.

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Loizou, Chris. Darkun Sourcebook (Cursed Empire) (CEP002). Spartans Unleashed, 2004.

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Loizou, Christopher. Blood of Heroes (Cursed Empire) (CEP015). Spartans Unleashed, 2005.

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Loizou, Christopher. Dark Clouds of War (Cursed Empire) (CEP007). Spartans Unleashed, 2005.

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Loizoo, Chris. Cursed Empire Second Edition (Crimson Empire) (CEP008). Spartans Unleashed, 2004.

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Book chapters on the topic "CEP104"

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Suski, W., and T. Palewski. "CePS4." In Pnictides and Chalcogenides II. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/10713485_327.

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Kouass, Salah, Amor Fadhalaoui, Hassouna Dhaouadi, and Fathi Touati. "Designing and Synthesis of (Cd2+, Li+), Cr3+, Bi3+ Doped CePO4 Materials Optical, Electrochemical, Ionic Conductivity Analysis." In Electrochemical Impedance Spectroscopy. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.91330.

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Most of the work has been done on the optical properties of the rare earth doped CePO4, so there are few studies on the effect of metal ion doping on CePO4. The doping improves the properties of the compounds and can lead to new properties. It is the first time, that multi- ionic doping process is used in the CePO4matrix, in order to improve the ionic conductivity and the electrochemical stability. The low percentage of (Cd2+, Li+), Cr3+, Bi3+ dopant affect the structure showing a weak decrease in the lattice parameters compared to the CePO4. Impedance spectroscopy analysis was used to analyze the electrical behavior of samples as a function of frequency at different temperatures. The total electrical conductivity plots obtained from impedance spectra shows an increase of the total conductivity as Li, Cr-content increases. The determined energy gap values decrease with increasingly Li+, Cr3+ and Bi3+ doping content. Electrochemical tests showed an improved capacity when increasing the Li+, Cr3+ and Bi3+ content and a stable cycling performance.
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Conference papers on the topic "CEP104"

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Bhonsule, S. U., S. P. Wankhede, and S. V. Moharil. "Synthesis and photoluminescence in Yb doped cerium phosphate CePO4." In 2ND INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5032814.

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Livasy, Chad A., Kimberly Limentani, Benjamin C. Calhoun, and Steven Limentani. "Abstract P4-15-07: HER2 positive (HER2/CEP17 ratio≥2.0) invasive mammary carcinomas with average <4.0 HER2 and <2.0 CEP17 signals/cell: Clinicopathologic features, correlation with HER2 immunohistochemistry and response to neoadjuvant chemotherapy." In Thirty-Seventh Annual CTRC-AACR San Antonio Breast Cancer Symposium; December 9-13, 2014; San Antonio, TX. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.sabcs14-p4-15-07.

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Tengblad, O., M. Mårtensson, E. Nacher, et al. "CEPA4: A LaBr/LaCl Phoswich Prototype Array for Simultaneous Detection of High-Energy Gamma and Proton Radiation." In Proceedings of the Conference on Advances in Radioactive Isotope Science (ARIS2014). Journal of the Physical Society of Japan, 2015. http://dx.doi.org/10.7566/jpscp.6.030132.

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Tse, CH, AM Gown, LC Goldstein, et al. "Amplification involving the CEP17 region may lead to false negative results of HER2 gene amplification by FISH." In CTRC-AACR San Antonio Breast Cancer Symposium: 2008 Abstracts. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/0008-5472.sabcs-1079.

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Sharma, Cristian, Padmini Narayanan, Michael Sharma, et al. "Abstract 1723: Novel drug candidates CEP1430 and CEP1507 against cancer stem cells and circulating tumor cells in advanced stage pancreatic cancer." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-1723.

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Lambein, K., Bockstal M. Van, M. Praet, et al. "P4-18-06: Relationship between Pathological Features, Her2 Protein Expression, and HER2 and CEP17 Copy Numbers in DCIS." In Abstracts: Thirty-Fourth Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 6‐10, 2011; San Antonio, TX. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/0008-5472.sabcs11-p4-18-06.

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Sharma, Michael, Maulik Jain, Cristian Sharma, et al. "Abstract 3889: Novel drug candidates cep1430 and cep1507 for targeting pancreatic patient-derived xenograft cancer stem cell and circulating tumor cell models." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-3889.

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Singer, CF, YY Tan, F. Fitzal, et al. "Abstract P1-09-10: Pathological complete response to neoadjuvant trastuzumab is dependent on HER2/CEP17 ratio in HER2-amplified early breast cancer." In Abstracts: 2016 San Antonio Breast Cancer Symposium; December 6-10, 2016; San Antonio, Texas. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.sabcs16-p1-09-10.

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Tse, CH, HC Hwang, LC Goldstein, et al. "P4-09-04: Do Decreased CEP17 Signals Indicate the Presence of “Monosomy” in Breast Cancer? A Study of HER2 Gene Status and HER2 Immunohistochemistry." In Abstracts: Thirty-Fourth Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 6‐10, 2011; San Antonio, TX. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/0008-5472.sabcs11-p4-09-04.

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Park, Hwan-Seo, In-Tae Kim, Hwan-Young Kim, Byeung Gil Ahn, and Han-Soo Lee. "Characteristics on the SAP-Based Wasteform Containing Radioactive Molten Salt Waste." In ASME 2009 12th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2009. http://dx.doi.org/10.1115/icem2009-16137.

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This study investigated a unique wasteform containing molten salt wastes which are generated from the pyro-process for the spent fuel treatment. Using a conventional sol-gel process, SiO2-Al2O3-P2O5 (SAP) inorganic material reactive to metal chlorides were prepared. By using this inorganic composite, a monolithic wasteform were sucessfully fabricated via a simple process, reaction at 650°C and sintering at 1100°C. This unique wasteform should be qualified if it meets the requirements for final disposal. For this reasons, this paper characterized its chemical durability, physical properties, mo
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