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XB--853454
Papers associated with celsr1 (and Disease Ontology)
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The contribution of de novo coding mutations to meningomyelocele., Ha YJ, Nisal A, Tang I, Lee C, Jhamb I, Wallace C, Howarth R, Schroeder S, Vong KI, Meave N, Jiwani F, Barrows C, Lee S, Jiang N, Patel A, Bagga K, Banka N, Friedman L, Blanco FA, Yu S, Rhee S, Jeong HS, Plutzer I, Major MB, Benoit B, Poüs C, Heffner C, Kibar Z, Bot GM, Northrup H, Au KS, Strain M, Ashley-Koch AE, Finnell RH, Le JT, Meltzer HS, Araujo C, Machado HR, Stevenson RE, Yurrita A, Mumtaz S, Ahmed A, Khara MH, Mutchinick OM, Medina-Bereciartu JR, Hildebrandt F, Melikishvili G, Marwan AI, Capra V, Noureldeen MM, Salem AMS, Issa MY, Zaki MS, Xu L, Lee JE, Shin D, Alkelai A, Shuldiner AR, Kingsmore SF, Murray SA, Gee HY, Miller WT, Tolias KF, Wallingford JB, Spina Bifida Sequencing Consortium, Kim S, Gleeson JG., Nature. May 26, 2025; 641 (8062): 419-426. |
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Disrupted endosomal trafficking of the Vangl-Celsr polarity complex underlies congenital anomalies in Xenopus trachea-esophageal morphogenesis., Edwards NA, Rankin SA, Kashyap A, Warren A, Agricola ZN, Kenny AP, Kofron M, Shen Y, Chung WK, Zorn AM., Dev Cell. May 21, 2025;  |
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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.  |
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Dishevelled Paralogs in Vertebrate Development: Redundant or Distinct?, Gentzel M, Schambony A., Front Cell Dev Biol. May 26, 2017; 5 59.  |
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The target of the NSD family of histone lysine methyltransferases depends on the nature of the substrate., Li Y, Trojer P, Xu CF, Cheung P, Kuo A, Drury WJ, Qiao Q, Neubert TA, Xu RM, Gozani O, Reinberg D., J Biol Chem. December 4, 2009; 284 (49): 34283-95.  |
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