Artículos de revistas sobre el tema "WDR11 complex"
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LIU, Nan y ChongLin YANG. "WDR91-WDR81 complex-dependent endolysosomal trafficking and neural development". SCIENTIA SINICA Vitae 49, n.º 7 (1 de julio de 2019): 798–805. http://dx.doi.org/10.1360/ssv-2019-0100.
Texto completoLiu, Kai, Youli Jian, Xiaojuan Sun, Chengkui Yang, Zhiyang Gao, Zhili Zhang, Xuezhao Liu et al. "Negative regulation of phosphatidylinositol 3-phosphate levels in early-to-late endosome conversion". Journal of Cell Biology 212, n.º 2 (18 de enero de 2016): 181–98. http://dx.doi.org/10.1083/jcb.201506081.
Texto completoBrauner, Raja, Joelle Bignon-Topalovic, Anu Bashamboo y Ken McElreavey. "Pituitary stalk interruption syndrome is characterized by genetic heterogeneity". PLOS ONE 15, n.º 12 (3 de diciembre de 2020): e0242358. http://dx.doi.org/10.1371/journal.pone.0242358.
Texto completoRapiteanu, Radu, Luther J. Davis, James C. Williamson, Richard T. Timms, J. Paul Luzio y Paul J. Lehner. "A Genetic Screen Identifies a Critical Role for the WDR81‐WDR91 Complex in the Trafficking and Degradation of Tetherin". Traffic 17, n.º 8 (25 de mayo de 2016): 940–58. http://dx.doi.org/10.1111/tra.12409.
Texto completoTang, Dan, Jingwen Sheng, Liangting Xu, Xiechao Zhan, Jiaming Liu, Hui Jiang, Xiaoling Shu et al. "Cryo-EM structure of C9ORF72–SMCR8–WDR41 reveals the role as a GAP for Rab8a and Rab11a". Proceedings of the National Academy of Sciences 117, n.º 18 (17 de abril de 2020): 9876–83. http://dx.doi.org/10.1073/pnas.2002110117.
Texto completoTalaia, Gabriel, Joseph Amick y Shawn M. Ferguson. "Receptor-like role for PQLC2 amino acid transporter in the lysosomal sensing of cationic amino acids". Proceedings of the National Academy of Sciences 118, n.º 8 (17 de febrero de 2021): e2014941118. http://dx.doi.org/10.1073/pnas.2014941118.
Texto completoHölzel, Michael, Michaela Rohrmoser, Martin Schlee, Thomas Grimm, Thomas Harasim, Anastassia Malamoussi, Anita Gruber-Eber et al. "Mammalian WDR12 is a novel member of the Pes1–Bop1 complex and is required for ribosome biogenesis and cell proliferation". Journal of Cell Biology 170, n.º 3 (25 de julio de 2005): 367–78. http://dx.doi.org/10.1083/jcb.200501141.
Texto completoAmick, Joseph, Arun Kumar Tharkeshwar, Catherine Amaya, y Shawn M. Ferguson. "WDR41 supports lysosomal response to changes in amino acid availability". Molecular Biology of the Cell 29, n.º 18 (septiembre de 2018): 2213–27. http://dx.doi.org/10.1091/mbc.e17-12-0703.
Texto completoRohrmoser, Michaela, Michael Hölzel, Thomas Grimm, Anastassia Malamoussi, Thomas Harasim, Mathias Orban, Iris Pfisterer, Anita Gruber-Eber, Elisabeth Kremmer y Dirk Eick. "Interdependence of Pes1, Bop1, and WDR12 Controls Nucleolar Localization and Assembly of the PeBoW Complex Required for Maturation of the 60S Ribosomal Subunit". Molecular and Cellular Biology 27, n.º 10 (12 de marzo de 2007): 3682–94. http://dx.doi.org/10.1128/mcb.00172-07.
Texto completoKile, Benjamin T., Athanasia D. Panopoulos, Roslynn A. Stirzaker, Douglas F. Hacking, Lubna H. Tahtamouni, Tracy A. Willson, Lisa A. Mielke et al. "Mutations in the cofilin partner Aip1/Wdr1 cause autoinflammatory disease and macrothrombocytopenia". Blood 110, n.º 7 (1 de octubre de 2007): 2371–80. http://dx.doi.org/10.1182/blood-2006-10-055087.
Texto completoTang, Dan, Jingwen Sheng, Liangting Xu, Chuangye Yan y Shiqian Qi. "The C9orf72-SMCR8-WDR41 complex is a GAP for small GTPases". Autophagy 16, n.º 8 (17 de junio de 2020): 1542–43. http://dx.doi.org/10.1080/15548627.2020.1779473.
Texto completoMcAlpine, William, Lei Sun, Kuan-wen Wang, Aijie Liu, Ruchi Jain, Miguel San Miguel, Jianhui Wang et al. "Excessive endosomal TLR signaling causes inflammatory disease in mice with defective SMCR8-WDR41-C9ORF72 complex function". Proceedings of the National Academy of Sciences 115, n.º 49 (15 de noviembre de 2018): E11523—E11531. http://dx.doi.org/10.1073/pnas.1814753115.
Texto completoCastle, Christopher D., Erica K. Cassimere y Catherine Denicourt. "LAS1L interacts with the mammalian Rix1 complex to regulate ribosome biogenesis". Molecular Biology of the Cell 23, n.º 4 (15 de febrero de 2012): 716–28. http://dx.doi.org/10.1091/mbc.e11-06-0530.
Texto completoFanis, Pavlos, Nynke Gillemans, Ali Aghajanirefah, Farzin Pourfarzad, Jeroen Demmers, Fatemehsadat Esteghamat, Ratna K. Vadlamudi, Frank Grosveld, Sjaak Philipsen y Thamar B. van Dijk. "Five Friends of Methylated Chromatin Target of Protein-Arginine-Methyltransferase[Prmt]-1 (Chtop), a Complex Linking Arginine Methylation to Desumoylation". Molecular & Cellular Proteomics 11, n.º 11 (7 de agosto de 2012): 1263–73. http://dx.doi.org/10.1074/mcp.m112.017194.
Texto completoYang, Mei, Chen Liang, Kunchithapadam Swaminathan, Stephanie Herrlinger, Fan Lai, Ramin Shiekhattar y Jian-Fu Chen. "A C9ORF72/SMCR8-containing complex regulates ULK1 and plays a dual role in autophagy". Science Advances 2, n.º 9 (septiembre de 2016): e1601167. http://dx.doi.org/10.1126/sciadv.1601167.
Texto completoEveillard, Marion, Myriam Chevalier, Thomas Besnard, Benjamin Cogne, Alice Kuster, Stephane Bezieau, Marie C. Bene y Claire Beneteau. "Polymorphonuclears Display a New Type of Abnormal Cytologic Granules (Chediak Higashi-Like) in a Very Rare Syndrome Linked to a Biallelic Defect of WDR81". Blood 128, n.º 22 (2 de diciembre de 2016): 1331. http://dx.doi.org/10.1182/blood.v128.22.1331.1331.
Texto completoNörpel, Julia, Simone Cavadini, Andreas D. Schenk, Alexandra Graff-Meyer, Daniel Hess, Jan Seebacher, Jeffrey A. Chao y Varun Bhaskar. "Structure of the human C9orf72-SMCR8 complex reveals a multivalent protein interaction architecture". PLOS Biology 19, n.º 7 (23 de julio de 2021): e3001344. http://dx.doi.org/10.1371/journal.pbio.3001344.
Texto completoMoilanen, Anne-Mari, Jaana Rysä, Leena Kaikkonen, Teemu Karvonen, Erja Mustonen, Raisa Serpi, Zoltán Szabó et al. "WDR12, a Member of Nucleolar PeBoW-Complex, Is Up-Regulated in Failing Hearts and Causes Deterioration of Cardiac Function". PLOS ONE 10, n.º 4 (27 de abril de 2015): e0124907. http://dx.doi.org/10.1371/journal.pone.0124907.
Texto completoEfimenko, Evgeni, Oliver E. Blacque, Guangshuo Ou, Courtney J. Haycraft, Bradley K. Yoder, Jonathan M. Scholey, Michel R. Leroux y Peter Swoboda. "Caenorhabditis elegans DYF-2, an Orthologue of Human WDR19, Is a Component of the Intraflagellar Transport Machinery in Sensory Cilia". Molecular Biology of the Cell 17, n.º 11 (noviembre de 2006): 4801–11. http://dx.doi.org/10.1091/mbc.e06-04-0260.
Texto completoIshida, Yamato, Takuya Kobayashi, Shuhei Chiba, Yohei Katoh y Kazuhisa Nakayama. "Molecular basis of ciliary defects caused by compound heterozygous IFT144/WDR19 mutations found in cranioectodermal dysplasia". Human Molecular Genetics 30, n.º 3-4 (30 de enero de 2021): 213–25. http://dx.doi.org/10.1093/hmg/ddab034.
Texto completoDasgupta, Swapan, Anhquyen Le, Sandra Haudek, Mark Entman y Perumal Thiagarajan. "Cofilin-1 – Induced Actin Reorganization and Phosphatidylserine Exposure in Platelets". Blood 124, n.º 21 (6 de diciembre de 2014): 4153. http://dx.doi.org/10.1182/blood.v124.21.4153.4153.
Texto completoLeray, Xavier, Rossella Conti, Yan Li, Cécile Debacker, Florence Castelli, François Fenaille, Anselm A. Zdebik, Michael Pusch y Bruno Gasnier. "Arginine-selective modulation of the lysosomal transporter PQLC2 through a gate-tuning mechanism". Proceedings of the National Academy of Sciences 118, n.º 32 (3 de agosto de 2021): e2025315118. http://dx.doi.org/10.1073/pnas.2025315118.
Texto completoCapra, Anna Paola, Maria Angela La Rosa, Sara Briguori, Rosa Civa, Chiara Passarelli, Emanuele Agolini, Antonio Novelli y Silvana Briuglia. "Coexistence of Genetic Diseases Is a New Clinical Challenge: Three Unrelated Cases of Dual Diagnosis". Genes 14, n.º 2 (14 de febrero de 2023): 484. http://dx.doi.org/10.3390/genes14020484.
Texto completoPeng, X. y S. M. Mount. "Genetic enhancement of RNA-processing defects by a dominant mutation in B52, the Drosophila gene for an SR protein splicing factor." Molecular and Cellular Biology 15, n.º 11 (noviembre de 1995): 6273–82. http://dx.doi.org/10.1128/mcb.15.11.6273.
Texto completoNworah, Chinenye y Bashir Sule. "INVESTIGATING THE RELATIONSHIPS BETWEEN EXPRESSED CANCER RELATED GENES AND SURVIVAL OF PATIENTS WITH BREAST CANCER". FUDMA JOURNAL OF SCIENCES 5, n.º 2 (7 de julio de 2021): 327–33. http://dx.doi.org/10.33003/fjs-2021-0502-553.
Texto completoKim, Man Lyang, Jae Jin Chae, Yong Hwan Park, Dominic De Nardo, Roslynn A. Stirzaker, Hyun-Ja Ko, Hazel Tye et al. "Aberrant actin depolymerization triggers the pyrin inflammasome and autoinflammatory disease that is dependent on IL-18, not IL-1β". Journal of Experimental Medicine 212, n.º 6 (25 de mayo de 2015): 927–38. http://dx.doi.org/10.1084/jem.20142384.
Texto completoBerning, Daniel, Hannah Adams, Heidi Luc y Joshua B. Gross. "In-Frame Indel Mutations in the Genome of the Blind Mexican Cavefish, Astyanax mexicanus". Genome Biology and Evolution 11, n.º 9 (19 de agosto de 2019): 2563–73. http://dx.doi.org/10.1093/gbe/evz180.
Texto completoCortellino, Salvatore, Chengbing Wang, Baolin Wang, Maria Rosaria Bassi, Elena Caretti, Delphine Champeval, Amelie Calmont et al. "Defective ciliogenesis, embryonic lethality and severe impairment of the Sonic Hedgehog pathway caused by inactivation of the mouse complex A intraflagellar transport gene Ift122/Wdr10, partially overlapping with the DNA repair gene Med1/Mbd4". Developmental Biology 325, n.º 1 (enero de 2009): 225–37. http://dx.doi.org/10.1016/j.ydbio.2008.10.020.
Texto completoSAHA, Nirmalya, James Ropa, Lili Chen, Hsiang-Yu Hu, Maria Mysliwski, Ann Friedman, Ivan Maillard y Andrew G. Muntean. "The PAF1c Subunit Cdc73 Is Essential for Hematopoiesis and Displays Differential Gene Regulation in MLL-AF9 Driven Leukemia". Blood 132, Supplement 1 (29 de noviembre de 2018): 1280. http://dx.doi.org/10.1182/blood-2018-99-118703.
Texto completoCastro, Sebastián, Franco G. Brunello, Gabriela Sansó, Paula Scaglia, María Esnaola Azcoiti, Agustín Izquierdo, Florencia Villegas et al. "Delayed Puberty Due to a WDR11 Truncation at Its N-Terminal Domain Leading to a Mild Form of Ciliopathy Presenting With Dissociated Central Hypogonadism: Case Report". Frontiers in Pediatrics 10 (3 de junio de 2022). http://dx.doi.org/10.3389/fped.2022.887658.
Texto completoNavarro Negredo, Paloma, James R. Edgar, Paul T. Manna, Robin Antrobus y Margaret S. Robinson. "The WDR11 complex facilitates the tethering of AP-1-derived vesicles". Nature Communications 9, n.º 1 (9 de febrero de 2018). http://dx.doi.org/10.1038/s41467-018-02919-4.
Texto completoFabbri-Scallet, Helena, Ralf Werner, Mara S. Guaragna, Juliana G. R. de Andrade, Andrea T. Maciel-Guerra, Nadine C. Hornig, Olaf Hiort, Gil Guerra-Júnior y Maricilda P. de Mello. "Can Non-Coding <b><i>NR5A1</i></b> Gene Variants Explain Phenotypes of Disorders of Sex Development?" Sexual Development, 28 de junio de 2022, 1–9. http://dx.doi.org/10.1159/000524956.
Texto completoMi, Lanjuan, Qinghui Qi, Haowen Ran, Lishu Chen, Da Li, Dake Xiao, Jiaqi Wu et al. "Suppression of Ribosome Biogenesis by Targeting WD Repeat Domain 12 (WDR12) Inhibits Glioma Stem-Like Cell Growth". Frontiers in Oncology 11 (12 de noviembre de 2021). http://dx.doi.org/10.3389/fonc.2021.751792.
Texto completoTao, Zhonghua, Jianxia Liu, Ting Li, Hong Xu, Kai Chen, Jian Zhang, Hao Zhou et al. "Profiling Receptor Tyrosine Kinase Fusions in Chinese Breast Cancers". Frontiers in Oncology 11 (28 de septiembre de 2021). http://dx.doi.org/10.3389/fonc.2021.741142.
Texto completoGordon, Jacob, Fleur L. Chapus, Elizabeth G. Viverette, Jason G. Williams, Leesa J. Deterding, Juno M. Krahn, Mario J. Borgnia, Joseph Rodriguez, Alan J. Warren y Robin E. Stanley. "Cryo-EM reveals the architecture of the PELP1-WDR18 molecular scaffold". Nature Communications 13, n.º 1 (9 de noviembre de 2022). http://dx.doi.org/10.1038/s41467-022-34610-0.
Texto completoAmick, Joseph, Arun Kumar Tharkeshwar, Gabriel Talaia y Shawn M. Ferguson. "PQLC2 recruits the C9orf72 complex to lysosomes in response to cationic amino acid starvation". Journal of Cell Biology 219, n.º 1 (18 de diciembre de 2019). http://dx.doi.org/10.1083/jcb.201906076.
Texto completoSu, Ming-Yuan, Simon A. Fromm, Jonathan Remis, Daniel B. Toso y James H. Hurley. "Structural basis for the ARF GAP activity and specificity of the C9orf72 complex". Nature Communications 12, n.º 1 (18 de junio de 2021). http://dx.doi.org/10.1038/s41467-021-24081-0.
Texto completoKalmár, Tibor, Katalin Szakszon, Zoltán Maróti, Alíz Zimmermann, Adrienn Máté, Melinda Zombor, Csaba Bereczki y László Sztriha. "A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia". Journal of Pediatric Genetics, 28 de mayo de 2020. http://dx.doi.org/10.1055/s-0040-1712916.
Texto completoMcCool, Mason A., Amber F. Buhagiar, Carson J. Bryant, Lisa M. Ogawa, Laura Abriola, Yulia V. Surovtseva y Susan J. Baserga. "Human pre-60S assembly factors link rRNA transcription to pre-rRNA processing". RNA, 2 de noviembre de 2022, rna.079149.122. http://dx.doi.org/10.1261/rna.079149.122.
Texto completoBolger-Munro, Madison, Kate Choi, Faith Cheung, Yi Tian Liu, May Dang-Lawson, Nikola Deretic, Connor Keane y Michael R. Gold. "The Wdr1-LIMK-Cofilin Axis Controls B Cell Antigen Receptor-Induced Actin Remodeling and Signaling at the Immune Synapse". Frontiers in Cell and Developmental Biology 9 (13 de abril de 2021). http://dx.doi.org/10.3389/fcell.2021.649433.
Texto completoTur-Gracia, Sara y Narcisa Martinez-Quiles. "Emerging functions of cytoskeletal proteins in immune diseases". Journal of Cell Science 134, n.º 3 (1 de febrero de 2021). http://dx.doi.org/10.1242/jcs.253534.
Texto completoXia, Pengcheng, Jing Chen, Xiaohui Bai, Ming Li, Le Wang y Zhiming Lu. "Key gene network related to primary ciliary dyskinesia in hippocampus of patients with Alzheimer’s disease revealed by weighted gene co-expression network analysis". BMC Neurology 22, n.º 1 (30 de mayo de 2022). http://dx.doi.org/10.1186/s12883-022-02724-z.
Texto completoXiao, Shangxi, Paul M. McKeever, Agnes Lau y Janice Robertson. "Synaptic localization of C9orf72 regulates post-synaptic glutamate receptor 1 levels". Acta Neuropathologica Communications 7, n.º 1 (24 de octubre de 2019). http://dx.doi.org/10.1186/s40478-019-0812-5.
Texto completoCao, Jing y Lei Yuan. "Identification of key genes for hypertrophic cardiomyopathy using integrated network analysis of differential lncRNA and gene expression". Frontiers in Cardiovascular Medicine 9 (4 de agosto de 2022). http://dx.doi.org/10.3389/fcvm.2022.946229.
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