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Summary Expression Phenotypes Gene Literature (11) GO Terms (24) Nucleotides (288) Proteins (53) Interactants (1118) Wiki
XB-GENEPAGE-974981

Papers associated with cul3



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Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ, Moers V, Yan J, Souopgui J, Quan XJ, De Geest N, Kricha S, Hassan BA, Bellefroid EJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.              


Cullin mediates degradation of RhoA through evolutionarily conserved BTB adaptors to control actin cytoskeleton structure and cell movement., Chen Y, Yang Z, Meng M, Zhao Y, Dong N, Yan H, Liu L, Ding M, Peng HB, Shao F., Mol Cell. September 24, 2009; 35 (6): 841-55.                                                  


The CUL3-KLHL18 ligase regulates mitotic entry and ubiquitylates Aurora-A., Moghe S, Jiang F, Miura Y, Cerny RL, Tsai MY, Furukawa M., Biol Open. February 15, 2012; 1 (2): 82-91.                


Hyperkalemic hypertension-associated cullin 3 promotes WNK signaling by degrading KLHL3., McCormick JA, Yang CL, Zhang C, Davidge B, Blankenstein KI, Terker AS, Yarbrough B, Meermeier NP, Park HJ, McCully B, West M, Borschewski A, Himmerkus N, Bleich M, Bachmann S, Mutig K, Argaiz ER, Gamba G, Singer JD, Ellison DH., J Clin Invest. November 1, 2014; 124 (11): 4723-36.


Cell-fate determination by ubiquitin-dependent regulation of translation., Werner A, Iwasaki S, McGourty CA, Medina-Ruiz S, Teerikorpi N, Fedrigo I, Ingolia NT, Rape M., Nature. September 24, 2015; 525 (7570): 523-7.                            


ROMK expression remains unaltered in a mouse model of familial hyperkalemic hypertension caused by the CUL3Δ403-459 mutation., Murthy M, Kurz T, O'Shaughnessy KM., Physiol Rep. July 1, 2016; 4 (13):             


A proteomic analysis of LRRK2 binding partners reveals interactions with multiple signaling components of the WNT/PCP pathway., Salašová A, Yokota C, Potěšil D, Zdráhal Z, Bryja V, Arenas E., Mol Neurodegener. July 11, 2017; 12 (1): 54.  


Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis., Louis-Dit-Picard H, Kouranti I, Rafael C, Loisel-Ferreira I, Chavez-Canales M, Abdel-Khalek W, Argaiz ER, Baron S, Vacle S, Migeon T, Coleman R, Do Cruzeiro M, Hureaux M, Thurairajasingam N, Decramer S, Girerd X, O'Shaugnessy K, Mulatero P, Roussey G, Tack I, Unwin R, Vargas-Poussou R, Staub O, Grimm R, Welling PA, Gamba G, Clauser E, Hadchouel J, Jeunemaitre X., J Clin Invest. December 1, 2020; 130 (12): 6379-6394.


Role of KLHL3 and dietary K+ in regulating KS-WNK1 expression., Ostrosky-Frid M, Chávez-Canales M, Zhang J, Andrukhova O, Argaiz ER, Lerdo-de-Tejada F, Murillo-de-Ozores A, Sanchez-Navarro A, Rojas-Vega L, Bobadilla NA, Vazquez N, Castañeda-Bueno M, Alessi DR, Gamba G., Am J Physiol Renal Physiol. May 1, 2021; 320 (5): F734-F747.                    


Pleiotropy of autism-associated chromatin regulators., Lasser M, Sun N, Xu Y, Xu Y, Wang S, Drake S, Law K, Gonzalez S, Wang B, Drury V, Castillo O, Zaltsman Y, Dea J, Bader E, McCluskey KE, State MW, Willsey AJ, Willsey HR., Development. July 15, 2023; 150 (14):                   


Profiling ubiquitin signalling with UBIMAX reveals DNA damage- and SCFβ-Trcp1-dependent ubiquitylation of the actin-organizing protein Dbn1., Colding-Christensen CS, Kakulidis ES, Arroyo-Gomez J, Hendriks IA, Arkinson C, Fábián Z, Gambus A, Mailand N, Duxin JP, Nielsen ML., Nat Commun. December 14, 2023; 14 (1): 8293.        

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