Journal articles on the topic 'WDR11 complex'
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LIU, Nan, and ChongLin YANG. "WDR91-WDR81 complex-dependent endolysosomal trafficking and neural development." SCIENTIA SINICA Vitae 49, no. 7 (July 1, 2019): 798–805. http://dx.doi.org/10.1360/ssv-2019-0100.
Full textLiu, 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, no. 2 (January 18, 2016): 181–98. http://dx.doi.org/10.1083/jcb.201506081.
Full textBrauner, Raja, Joelle Bignon-Topalovic, Anu Bashamboo, and Ken McElreavey. "Pituitary stalk interruption syndrome is characterized by genetic heterogeneity." PLOS ONE 15, no. 12 (December 3, 2020): e0242358. http://dx.doi.org/10.1371/journal.pone.0242358.
Full textRapiteanu, Radu, Luther J. Davis, James C. Williamson, Richard T. Timms, J. Paul Luzio, and Paul J. Lehner. "A Genetic Screen Identifies a Critical Role for the WDR81‐WDR91 Complex in the Trafficking and Degradation of Tetherin." Traffic 17, no. 8 (May 25, 2016): 940–58. http://dx.doi.org/10.1111/tra.12409.
Full textTang, 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, no. 18 (April 17, 2020): 9876–83. http://dx.doi.org/10.1073/pnas.2002110117.
Full textTalaia, Gabriel, Joseph Amick, and 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, no. 8 (February 17, 2021): e2014941118. http://dx.doi.org/10.1073/pnas.2014941118.
Full textHölzel, 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, no. 3 (July 25, 2005): 367–78. http://dx.doi.org/10.1083/jcb.200501141.
Full textAmick, Joseph, Arun Kumar Tharkeshwar, Catherine Amaya,, and Shawn M. Ferguson. "WDR41 supports lysosomal response to changes in amino acid availability." Molecular Biology of the Cell 29, no. 18 (September 2018): 2213–27. http://dx.doi.org/10.1091/mbc.e17-12-0703.
Full textRohrmoser, Michaela, Michael Hölzel, Thomas Grimm, Anastassia Malamoussi, Thomas Harasim, Mathias Orban, Iris Pfisterer, Anita Gruber-Eber, Elisabeth Kremmer, and 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, no. 10 (March 12, 2007): 3682–94. http://dx.doi.org/10.1128/mcb.00172-07.
Full textKile, 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, no. 7 (October 1, 2007): 2371–80. http://dx.doi.org/10.1182/blood-2006-10-055087.
Full textTang, Dan, Jingwen Sheng, Liangting Xu, Chuangye Yan, and Shiqian Qi. "The C9orf72-SMCR8-WDR41 complex is a GAP for small GTPases." Autophagy 16, no. 8 (June 17, 2020): 1542–43. http://dx.doi.org/10.1080/15548627.2020.1779473.
Full textMcAlpine, 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, no. 49 (November 15, 2018): E11523—E11531. http://dx.doi.org/10.1073/pnas.1814753115.
Full textCastle, Christopher D., Erica K. Cassimere, and Catherine Denicourt. "LAS1L interacts with the mammalian Rix1 complex to regulate ribosome biogenesis." Molecular Biology of the Cell 23, no. 4 (February 15, 2012): 716–28. http://dx.doi.org/10.1091/mbc.e11-06-0530.
Full textFanis, Pavlos, Nynke Gillemans, Ali Aghajanirefah, Farzin Pourfarzad, Jeroen Demmers, Fatemehsadat Esteghamat, Ratna K. Vadlamudi, Frank Grosveld, Sjaak Philipsen, and 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, no. 11 (August 7, 2012): 1263–73. http://dx.doi.org/10.1074/mcp.m112.017194.
Full textYang, Mei, Chen Liang, Kunchithapadam Swaminathan, Stephanie Herrlinger, Fan Lai, Ramin Shiekhattar, and Jian-Fu Chen. "A C9ORF72/SMCR8-containing complex regulates ULK1 and plays a dual role in autophagy." Science Advances 2, no. 9 (September 2016): e1601167. http://dx.doi.org/10.1126/sciadv.1601167.
Full textEveillard, Marion, Myriam Chevalier, Thomas Besnard, Benjamin Cogne, Alice Kuster, Stephane Bezieau, Marie C. Bene, and 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, no. 22 (December 2, 2016): 1331. http://dx.doi.org/10.1182/blood.v128.22.1331.1331.
Full textNörpel, Julia, Simone Cavadini, Andreas D. Schenk, Alexandra Graff-Meyer, Daniel Hess, Jan Seebacher, Jeffrey A. Chao, and Varun Bhaskar. "Structure of the human C9orf72-SMCR8 complex reveals a multivalent protein interaction architecture." PLOS Biology 19, no. 7 (July 23, 2021): e3001344. http://dx.doi.org/10.1371/journal.pbio.3001344.
Full textMoilanen, 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, no. 4 (April 27, 2015): e0124907. http://dx.doi.org/10.1371/journal.pone.0124907.
Full textEfimenko, Evgeni, Oliver E. Blacque, Guangshuo Ou, Courtney J. Haycraft, Bradley K. Yoder, Jonathan M. Scholey, Michel R. Leroux, and 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, no. 11 (November 2006): 4801–11. http://dx.doi.org/10.1091/mbc.e06-04-0260.
Full textIshida, Yamato, Takuya Kobayashi, Shuhei Chiba, Yohei Katoh, and Kazuhisa Nakayama. "Molecular basis of ciliary defects caused by compound heterozygous IFT144/WDR19 mutations found in cranioectodermal dysplasia." Human Molecular Genetics 30, no. 3-4 (January 30, 2021): 213–25. http://dx.doi.org/10.1093/hmg/ddab034.
Full textDasgupta, Swapan, Anhquyen Le, Sandra Haudek, Mark Entman, and Perumal Thiagarajan. "Cofilin-1 – Induced Actin Reorganization and Phosphatidylserine Exposure in Platelets." Blood 124, no. 21 (December 6, 2014): 4153. http://dx.doi.org/10.1182/blood.v124.21.4153.4153.
Full textLeray, Xavier, Rossella Conti, Yan Li, Cécile Debacker, Florence Castelli, François Fenaille, Anselm A. Zdebik, Michael Pusch, and Bruno Gasnier. "Arginine-selective modulation of the lysosomal transporter PQLC2 through a gate-tuning mechanism." Proceedings of the National Academy of Sciences 118, no. 32 (August 3, 2021): e2025315118. http://dx.doi.org/10.1073/pnas.2025315118.
Full textCapra, Anna Paola, Maria Angela La Rosa, Sara Briguori, Rosa Civa, Chiara Passarelli, Emanuele Agolini, Antonio Novelli, and Silvana Briuglia. "Coexistence of Genetic Diseases Is a New Clinical Challenge: Three Unrelated Cases of Dual Diagnosis." Genes 14, no. 2 (February 14, 2023): 484. http://dx.doi.org/10.3390/genes14020484.
Full textPeng, X., and 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, no. 11 (November 1995): 6273–82. http://dx.doi.org/10.1128/mcb.15.11.6273.
Full textNworah, Chinenye, and Bashir Sule. "INVESTIGATING THE RELATIONSHIPS BETWEEN EXPRESSED CANCER RELATED GENES AND SURVIVAL OF PATIENTS WITH BREAST CANCER." FUDMA JOURNAL OF SCIENCES 5, no. 2 (July 7, 2021): 327–33. http://dx.doi.org/10.33003/fjs-2021-0502-553.
Full textKim, 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, no. 6 (May 25, 2015): 927–38. http://dx.doi.org/10.1084/jem.20142384.
Full textBerning, Daniel, Hannah Adams, Heidi Luc, and Joshua B. Gross. "In-Frame Indel Mutations in the Genome of the Blind Mexican Cavefish, Astyanax mexicanus." Genome Biology and Evolution 11, no. 9 (August 19, 2019): 2563–73. http://dx.doi.org/10.1093/gbe/evz180.
Full textCortellino, 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, no. 1 (January 2009): 225–37. http://dx.doi.org/10.1016/j.ydbio.2008.10.020.
Full textSAHA, Nirmalya, James Ropa, Lili Chen, Hsiang-Yu Hu, Maria Mysliwski, Ann Friedman, Ivan Maillard, and 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 (November 29, 2018): 1280. http://dx.doi.org/10.1182/blood-2018-99-118703.
Full textCastro, 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 (June 3, 2022). http://dx.doi.org/10.3389/fped.2022.887658.
Full textNavarro Negredo, Paloma, James R. Edgar, Paul T. Manna, Robin Antrobus, and Margaret S. Robinson. "The WDR11 complex facilitates the tethering of AP-1-derived vesicles." Nature Communications 9, no. 1 (February 9, 2018). http://dx.doi.org/10.1038/s41467-018-02919-4.
Full textFabbri-Scallet, Helena, Ralf Werner, Mara S. Guaragna, Juliana G. R. de Andrade, Andrea T. Maciel-Guerra, Nadine C. Hornig, Olaf Hiort, Gil Guerra-Júnior, and Maricilda P. de Mello. "Can Non-Coding <b><i>NR5A1</i></b> Gene Variants Explain Phenotypes of Disorders of Sex Development?" Sexual Development, June 28, 2022, 1–9. http://dx.doi.org/10.1159/000524956.
Full textMi, 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 (November 12, 2021). http://dx.doi.org/10.3389/fonc.2021.751792.
Full textTao, 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 (September 28, 2021). http://dx.doi.org/10.3389/fonc.2021.741142.
Full textGordon, Jacob, Fleur L. Chapus, Elizabeth G. Viverette, Jason G. Williams, Leesa J. Deterding, Juno M. Krahn, Mario J. Borgnia, Joseph Rodriguez, Alan J. Warren, and Robin E. Stanley. "Cryo-EM reveals the architecture of the PELP1-WDR18 molecular scaffold." Nature Communications 13, no. 1 (November 9, 2022). http://dx.doi.org/10.1038/s41467-022-34610-0.
Full textAmick, Joseph, Arun Kumar Tharkeshwar, Gabriel Talaia, and Shawn M. Ferguson. "PQLC2 recruits the C9orf72 complex to lysosomes in response to cationic amino acid starvation." Journal of Cell Biology 219, no. 1 (December 18, 2019). http://dx.doi.org/10.1083/jcb.201906076.
Full textSu, Ming-Yuan, Simon A. Fromm, Jonathan Remis, Daniel B. Toso, and James H. Hurley. "Structural basis for the ARF GAP activity and specificity of the C9orf72 complex." Nature Communications 12, no. 1 (June 18, 2021). http://dx.doi.org/10.1038/s41467-021-24081-0.
Full textKalmár, Tibor, Katalin Szakszon, Zoltán Maróti, Alíz Zimmermann, Adrienn Máté, Melinda Zombor, Csaba Bereczki, and László Sztriha. "A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia." Journal of Pediatric Genetics, May 28, 2020. http://dx.doi.org/10.1055/s-0040-1712916.
Full textMcCool, Mason A., Amber F. Buhagiar, Carson J. Bryant, Lisa M. Ogawa, Laura Abriola, Yulia V. Surovtseva, and Susan J. Baserga. "Human pre-60S assembly factors link rRNA transcription to pre-rRNA processing." RNA, November 2, 2022, rna.079149.122. http://dx.doi.org/10.1261/rna.079149.122.
Full textBolger-Munro, Madison, Kate Choi, Faith Cheung, Yi Tian Liu, May Dang-Lawson, Nikola Deretic, Connor Keane, and 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 (April 13, 2021). http://dx.doi.org/10.3389/fcell.2021.649433.
Full textTur-Gracia, Sara, and Narcisa Martinez-Quiles. "Emerging functions of cytoskeletal proteins in immune diseases." Journal of Cell Science 134, no. 3 (February 1, 2021). http://dx.doi.org/10.1242/jcs.253534.
Full textXia, Pengcheng, Jing Chen, Xiaohui Bai, Ming Li, Le Wang, and 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, no. 1 (May 30, 2022). http://dx.doi.org/10.1186/s12883-022-02724-z.
Full textXiao, Shangxi, Paul M. McKeever, Agnes Lau, and Janice Robertson. "Synaptic localization of C9orf72 regulates post-synaptic glutamate receptor 1 levels." Acta Neuropathologica Communications 7, no. 1 (October 24, 2019). http://dx.doi.org/10.1186/s40478-019-0812-5.
Full textCao, Jing, and Lei Yuan. "Identification of key genes for hypertrophic cardiomyopathy using integrated network analysis of differential lncRNA and gene expression." Frontiers in Cardiovascular Medicine 9 (August 4, 2022). http://dx.doi.org/10.3389/fcvm.2022.946229.
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