Artigos de revistas sobre o tema "WDR41"
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Amick, Joseph, Arun Kumar Tharkeshwar, Catherine Amaya, e Shawn M. Ferguson. "WDR41 supports lysosomal response to changes in amino acid availability". Molecular Biology of the Cell 29, n.º 18 (setembro de 2018): 2213–27. http://dx.doi.org/10.1091/mbc.e17-12-0703.
Texto completo da fonteTalaia, Gabriel, Joseph Amick e 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 fevereiro de 2021): e2014941118. http://dx.doi.org/10.1073/pnas.2014941118.
Texto completo da fonteTang, 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 completo da fonteSHARMA, NISHA, REVANASIDDU D, SUSHIL KUMAR, BEENA SINHA, RAGINI KUMARI, I. D. GUPTA e ARCHANA VERMA. "Influence of WDR41 and ANKRD31 gene polymorphism on udder and teat type traits and mastitis in Karan Fries cows". Indian Journal of Animal Sciences 92, n.º 2 (10 de março de 2022): 215–21. http://dx.doi.org/10.56093/ijans.v92i2.122096.
Texto completo da fonteMcAlpine, 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 novembro de 2018): E11523—E11531. http://dx.doi.org/10.1073/pnas.1814753115.
Texto completo da fonteTang, Dan, Jingwen Sheng, Liangting Xu, Chuangye Yan e Shiqian Qi. "The C9orf72-SMCR8-WDR41 complex is a GAP for small GTPases". Autophagy 16, n.º 8 (17 de junho de 2020): 1542–43. http://dx.doi.org/10.1080/15548627.2020.1779473.
Texto completo da fonteFukatsu, Shoya, Hinami Sashi, Remina Shirai, Norio Takagi, Hiroaki Oizumi, Masahiro Yamamoto, Katsuya Ohbuchi, Yuki Miyamoto e Junji Yamauchi. "Rab11a Controls Cell Shape via C9orf72 Protein: Possible Relationships to Frontotemporal Dementia/Amyotrophic Lateral Sclerosis (FTDALS) Type 1". Pathophysiology 31, n.º 1 (9 de fevereiro de 2024): 100–116. http://dx.doi.org/10.3390/pathophysiology31010008.
Texto completo da fonteLiu, 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 janeiro de 2016): 181–98. http://dx.doi.org/10.1083/jcb.201506081.
Texto completo da fonteSnyder, Anthony J., Andrew T. Abad e Pranav Danthi. "A CRISPR-Cas9 screen reveals a role for WD repeat-containing protein 81 (WDR81) in the entry of late penetrating viruses". PLOS Pathogens 18, n.º 3 (23 de março de 2022): e1010398. http://dx.doi.org/10.1371/journal.ppat.1010398.
Texto completo da fonteLIU, Nan, e ChongLin YANG. "WDR91-WDR81 complex-dependent endolysosomal trafficking and neural development". SCIENTIA SINICA Vitae 49, n.º 7 (1 de julho de 2019): 798–805. http://dx.doi.org/10.1360/ssv-2019-0100.
Texto completo da fonteYang, Mei, Chen Liang, Kunchithapadam Swaminathan, Stephanie Herrlinger, Fan Lai, Ramin Shiekhattar e Jian-Fu Chen. "A C9ORF72/SMCR8-containing complex regulates ULK1 and plays a dual role in autophagy". Science Advances 2, n.º 9 (setembro de 2016): e1601167. http://dx.doi.org/10.1126/sciadv.1601167.
Texto completo da fonteNörpel, Julia, Simone Cavadini, Andreas D. Schenk, Alexandra Graff-Meyer, Daniel Hess, Jan Seebacher, Jeffrey A. Chao e Varun Bhaskar. "Structure of the human C9orf72-SMCR8 complex reveals a multivalent protein interaction architecture". PLOS Biology 19, n.º 7 (23 de julho de 2021): e3001344. http://dx.doi.org/10.1371/journal.pbio.3001344.
Texto completo da fonteLeray, Xavier, Rossella Conti, Yan Li, Cécile Debacker, Florence Castelli, François Fenaille, Anselm A. Zdebik, Michael Pusch e 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 completo da fonteWada, Kouko, Manae Sato, Nanase Araki, Masahiro Kumeta, Yuya Hirai, Kunio Takeyasu, Kazuhiro Furukawa e Tsuneyoshi Horigome. "Dynamics of WD-repeat containing proteins in SSU processome components". Biochemistry and Cell Biology 92, n.º 3 (junho de 2014): 191–99. http://dx.doi.org/10.1139/bcb-2014-0007.
Texto completo da fonteRapiteanu, Radu, Luther J. Davis, James C. Williamson, Richard T. Timms, J. Paul Luzio e 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 maio de 2016): 940–58. http://dx.doi.org/10.1111/tra.12409.
Texto completo da fonteLiu, Kai, Ruxiao Xing, Youli Jian, Zhiyang Gao, Xinli Ma, Xiaojuan Sun, Yang Li et al. "WDR91 is a Rab7 effector required for neuronal development". Journal of Cell Biology 216, n.º 10 (31 de agosto de 2017): 3307–21. http://dx.doi.org/10.1083/jcb.201705151.
Texto completo da fonteSeibler, Philip, Lena F. Burbulla, Marija Dulovic, Simone Zittel, Johanne Heine, Thomas Schmidt, Franziska Rudolph et al. "Iron overload is accompanied by mitochondrial and lysosomal dysfunction in WDR45 mutant cells". Brain 141, n.º 10 (30 de agosto de 2018): 3052–64. http://dx.doi.org/10.1093/brain/awy230.
Texto completo da fonteAring, Luisa, Eun-kyeong Choi e Young-Ah Seo. "WDR45 Contributes to Iron Accumulation Through Dysregulation of Neuronal Iron Homeostasis". Current Developments in Nutrition 4, Supplement_2 (29 de maio de 2020): 1188. http://dx.doi.org/10.1093/cdn/nzaa057_004.
Texto completo da fonteLiu, Xuezhao, Yang Li, Xin Wang, Ruxiao Xing, Kai Liu, Qiwen Gan, Changyong Tang et al. "The BEACH-containing protein WDR81 coordinates p62 and LC3C to promote aggrephagy". Journal of Cell Biology 216, n.º 5 (12 de abril de 2017): 1301–20. http://dx.doi.org/10.1083/jcb.201608039.
Texto completo da fonteLiu, Xuezhao, Limin Yin, Tianyou Li, Lingxi Lin, Jie Zhang e Yang Li. "Reduction of WDR81 impairs autophagic clearance of aggregated proteins and cell viability in neurodegenerative phenotypes". PLOS Genetics 17, n.º 3 (17 de março de 2021): e1009415. http://dx.doi.org/10.1371/journal.pgen.1009415.
Texto completo da fonteKannan, Meghna, Efil Bayam, Christel Wagner, Bruno Rinaldi, Perrine F. Kretz, Peggy Tilly, Marna Roos et al. "WD40-repeat 47, a microtubule-associated protein, is essential for brain development and autophagy". Proceedings of the National Academy of Sciences 114, n.º 44 (12 de outubro de 2017): E9308—E9317. http://dx.doi.org/10.1073/pnas.1713625114.
Texto completo da fonteWang, Jie, Xiao-Lin Kou, Cheng Chen, Mei Wang, Cui Qi, Jing Wang, Wei-Yan You, Gang Hu, Jiong Chen e Jun Gao. "Hippocampal Wdr1 Deficit Impairs Learning and Memory by Perturbing F-actin Depolymerization in Mice". Cerebral Cortex 29, n.º 10 (22 de dezembro de 2018): 4194–207. http://dx.doi.org/10.1093/cercor/bhy301.
Texto completo da fonteDiaw, Sokhna Haissatou, Christos Ganos, Simone Zittel, Kirstin Plötze-Martin, Leonora Kulikovskaja, Melissa Vos, Ana Westenberger, Aleksandar Rakovic, Katja Lohmann e Marija Dulovic-Mahlow. "Mutant WDR45 Leads to Altered Ferritinophagy and Ferroptosis in β-Propeller Protein-Associated Neurodegeneration". International Journal of Molecular Sciences 23, n.º 17 (23 de agosto de 2022): 9524. http://dx.doi.org/10.3390/ijms23179524.
Texto completo da fonteHuang, Huang, Jidong Yan, Xi Lan, Yuanxu Guo, Mengyao Sun, Yitong Zhao, Fujun Zhang, Jian Sun e Shemin Lu. "LncRNA WDR11-AS1 Promotes Extracellular Matrix Synthesis in Osteoarthritis by Directly Interacting with RNA-Binding Protein PABPC1 to Stabilize SOX9 Expression". International Journal of Molecular Sciences 24, n.º 1 (3 de janeiro de 2023): 817. http://dx.doi.org/10.3390/ijms24010817.
Texto completo da fonteSuárez-Carrillo, Alejandra, Mónica Álvarez-Córdoba, Ana Romero-González, Marta Talaverón-Rey, Suleva Povea-Cabello, Paula Cilleros-Holgado, Rocío Piñero-Pérez et al. "Antioxidants Prevent Iron Accumulation and Lipid Peroxidation, but Do Not Correct Autophagy Dysfunction or Mitochondrial Bioenergetics in Cellular Models of BPAN". International Journal of Molecular Sciences 24, n.º 19 (26 de setembro de 2023): 14576. http://dx.doi.org/10.3390/ijms241914576.
Texto completo da fonteTaylor, Kathryne E., e Karen L. Mossman. "Cellular Protein WDR11 Interacts with Specific Herpes Simplex Virus Proteins at thetrans-Golgi Network To Promote Virus Replication". Journal of Virology 89, n.º 19 (15 de julho de 2015): 9841–52. http://dx.doi.org/10.1128/jvi.01705-15.
Texto completo da fonteLin, Chi, Juan Wang, Long Ouyang, Huaxin Duan e Shasha Fan. "WDR4 as a potential indicator of clinical prognosis and immunotherapy in hepatocellular carcinoma." Journal of Clinical Oncology 42, n.º 16_suppl (1 de junho de 2024): e16275-e16275. http://dx.doi.org/10.1200/jco.2024.42.16_suppl.e16275.
Texto completo da fonteDasgupta, Swapan Kumar, Qi Da, Anhquyen Le, Miguel A. Cruz e Perumal Thiagarajan. "Wdr1-Mediated Actin Reorganization Is Essential for Integrin αIIbβ3 Activation in Platelets". Blood 126, n.º 23 (3 de dezembro de 2015): 2231. http://dx.doi.org/10.1182/blood.v126.23.2231.2231.
Texto completo da fonteJussara Maria Gonçalves, João Luiz Dornelles Bastos, Elena Riet Correa Rivero e Mabel Mariela Rodríguez Cordeiro. "Immunoexpression of tumor suppressor protein p53 and deubiquitinating enzymes in oral squamous cell carcinoma". RSBO 19, n.º 1 (6 de junho de 2022): 10–07. http://dx.doi.org/10.21726/rsbo.v19i1.1753.
Texto completo da fonteWang, Yu-Jia, Eko Mugiyanto, Yun-Ting Peng, Wan-Chen Huang, Wan-Hsuan Chou, Chi-Chiu Lee, Yu-Shiuan Wang et al. "Genetic Association of the Functional WDR4 Gene in Male Fertility". Journal of Personalized Medicine 11, n.º 8 (30 de julho de 2021): 760. http://dx.doi.org/10.3390/jpm11080760.
Texto completo da fonteBowes, Charnese, Michael Redd, Malika Yousfi, Muriel Tauzin, Emi Murayama e Philippe Herbomel. "Coronin 1A depletion restores the nuclear stability and viability of Aip1/Wdr1-deficient neutrophils". Journal of Cell Biology 218, n.º 10 (30 de agosto de 2019): 3258–71. http://dx.doi.org/10.1083/jcb.201901024.
Texto completo da fonteMontenont, Emilie, Christina Echagarruga, Nicole Allen, Elisa Araldi, Yajaira Suarez e Jeffrey S. Berger. "Platelet WDR1 suppresses platelet activity and is associated with cardiovascular disease". Blood 128, n.º 16 (20 de outubro de 2016): 2033–42. http://dx.doi.org/10.1182/blood-2016-03-703157.
Texto completo da fonteZhu, Jinhong, Xiaoping Liu, Wei Chen, Yuxiang Liao, Jiabin Liu, Li Yuan, Jichen Ruan e Jing He. "Association of RNA m7G Modification Gene Polymorphisms with Pediatric Glioma Risk". BioMed Research International 2023 (24 de janeiro de 2023): 1–10. http://dx.doi.org/10.1155/2023/3678327.
Texto completo da fonteKile, 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 outubro de 2007): 2371–80. http://dx.doi.org/10.1182/blood-2006-10-055087.
Texto completo da fonteChoi, Jin-Tae, Yeseul Choi, Yujin Lee, Seung-Heon Lee, Seun Kang, Kyung-Tae Lee e Yong-Sun Bahn. "The hybrid RAVE complex plays V-ATPase-dependent and -independent pathobiological roles in Cryptococcus neoformans". PLOS Pathogens 19, n.º 10 (9 de outubro de 2023): e1011721. http://dx.doi.org/10.1371/journal.ppat.1011721.
Texto completo da fonteDogrusöz, Mehmet, Andrea Ruschel Trasel, Jinfeng Cao, Selҫuk Ҫolak, Sake I. van Pelt, Wilma G. M. Kroes, Amina F. A. S. Teunisse et al. "Differential Expression of DNA Repair Genes in Prognostically-Favorable versus Unfavorable Uveal Melanoma". Cancers 11, n.º 8 (2 de agosto de 2019): 1104. http://dx.doi.org/10.3390/cancers11081104.
Texto completo da fonteSuh, Myung Whan, Dong Hoon Shin, Ho Sun Lee, Ji Yeong Park, Chong Sun Kim e Seung Ha Oh. "WDR1 expression in the normal and noise-damaged chick vestibule". Journal of Vestibular Research 17, n.º 4 (1 de abril de 2008): 163–70. http://dx.doi.org/10.3233/ves-2007-17402.
Texto completo da fonteNagappa, Madhu, Parayil S. Bindu, Sanjib Sinha, Rose D. Bharath, Mangalore Sandhya, Jitender Saini, Pavagada S. Mathuranath e Arun B. Taly. "Palatal Tremor Revisited: Disorder with Nosological Diversity and Etiological Heterogeneity". Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 45, n.º 2 (18 de dezembro de 2017): 243–47. http://dx.doi.org/10.1017/cjn.2017.273.
Texto completo da fonteStanding, Ariane S. I., Dessislava Malinova, Ying Hong, Julien Record, Dale Moulding, Michael P. Blundell, Karolin Nowak et al. "Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1". Journal of Experimental Medicine 214, n.º 1 (19 de dezembro de 2016): 59–71. http://dx.doi.org/10.1084/jem.20161228.
Texto completo da fonteLee, Hye Eun, Min Kyo Jung, Seul Gi Noh, Hye Bin Choi, Se hyun Chae, Jae Hyeok Lee e Ji Young Mun. "Iron Accumulation and Changes in Cellular Organelles in WDR45 Mutant Fibroblasts". International Journal of Molecular Sciences 22, n.º 21 (28 de outubro de 2021): 11650. http://dx.doi.org/10.3390/ijms222111650.
Texto completo da fonteDubner, R., D. R. Kenshalo, W. Maixner, M. C. Bushnell e J. L. Oliveras. "The correlation of monkey medullary dorsal horn neuronal activity and the perceived intensity of noxious heat stimuli". Journal of Neurophysiology 62, n.º 2 (1 de agosto de 1989): 450–57. http://dx.doi.org/10.1152/jn.1989.62.2.450.
Texto completo da fonteChudler, E. H., F. Anton, R. Dubner e D. R. Kenshalo. "Responses of nociceptive SI neurons in monkeys and pain sensation in humans elicited by noxious thermal stimulation: effect of interstimulus interval". Journal of Neurophysiology 63, n.º 3 (1 de março de 1990): 559–69. http://dx.doi.org/10.1152/jn.1990.63.3.559.
Texto completo da fonteKuhns, Douglas B., Danielle L. Fink, Uimook Choi, Colin Sweeney, Karen Lau, Debra Long Priel, Dara Riva et al. "Cytoskeletal abnormalities and neutrophil dysfunction in WDR1 deficiency". Blood 128, n.º 17 (27 de outubro de 2016): 2135–43. http://dx.doi.org/10.1182/blood-2016-03-706028.
Texto completo da fonteAdang, Laura A., Amy Pizzino, Alka Malhotra, Holly Dubbs, Catherine Williams, Omar Sherbini, Anna-Kaisa Anttonen et al. "Phenotypic and Imaging Spectrum Associated With WDR45". Pediatric Neurology 109 (agosto de 2020): 56–62. http://dx.doi.org/10.1016/j.pediatrneurol.2020.03.005.
Texto completo da fonteMaixner, W., R. Dubner, D. R. Kenshalo, M. C. Bushnell e J. L. Oliveras. "Responses of monkey medullary dorsal horn neurons during the detection of noxious heat stimuli". Journal of Neurophysiology 62, n.º 2 (1 de agosto de 1989): 437–49. http://dx.doi.org/10.1152/jn.1989.62.2.437.
Texto completo da fonteFujibuchi, Taketsugu, Yasuhito Abe, Takashi Takeuchi, Yoshinori Imai, Yoshiaki Kamei, Ryuichi Murase, Norifumi Ueda, Kazuhiro Shigemoto, Haruyasu Yamamoto e Katsumi Kito. "AIP1/WDR1 supports mitotic cell rounding". Biochemical and Biophysical Research Communications 327, n.º 1 (fevereiro de 2005): 268–75. http://dx.doi.org/10.1016/j.bbrc.2004.11.156.
Texto completo da fonteCurtis, Claire, Jane F. Apperley, Raymond Dang, Michael Jeng, Jason Gotlib, Nicholas C. P. Cross e Francis H. Grand. "The Platelet-Derived Growth Factor Receptor beta Fuses to Two Distinct Loci at 3p21 in Imatinib Responsive Chronic Eosinophilic Leukemia." Blood 106, n.º 11 (16 de novembro de 2005): 3253. http://dx.doi.org/10.1182/blood.v106.11.3253.3253.
Texto completo da fonteFujimura, Akiko, Yuki Hayashi, Kazashi Kato, Yuichiro Kogure, Mutsuro Kameyama, Haruka Shimamoto, Hiroaki Daitoku, Akiyoshi Fukamizu, Toru Hirota e Keiji Kimura. "Identification of a novel nucleolar protein complex required for mitotic chromosome segregation through centromeric accumulation of Aurora B". Nucleic Acids Research 48, n.º 12 (1 de junho de 2020): 6583–96. http://dx.doi.org/10.1093/nar/gkaa449.
Texto completo da fonteCevik, Sebiha, Xiaoyu Peng, Tina Beyer, Mustafa S. Pir, Ferhan Yenisert, Franziska Woerz, Felix Hoffmann et al. "WDR31 displays functional redundancy with GTPase-activating proteins (GAPs) ELMOD and RP2 in regulating IFT complex and recruiting the BBSome to cilium". Life Science Alliance 6, n.º 8 (19 de maio de 2023): e202201844. http://dx.doi.org/10.26508/lsa.202201844.
Texto completo da fonteLucaciu, Laura A., Radu Seicean, Alina Uifălean, Maria Iacobescu, Cristina A. Iuga e Andrada Seicean. "Unveiling Distinct Proteomic Signatures in Complicated Crohn’s Disease That Could Predict the Disease Course". International Journal of Molecular Sciences 24, n.º 23 (30 de novembro de 2023): 16966. http://dx.doi.org/10.3390/ijms242316966.
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