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Summary Anatomy Item Literature (1250) Expression Attributions Wiki
XB-ANAT-720

Papers associated with proximal

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Meiosis initiation: a story of two sexes in all creatures great and small., Sou IF., Biochem J. October 29, 2021; 478 (20): 3791-3805.      


The enpp4 ectonucleotidase regulates kidney patterning signalling networks in Xenopus embryos., Massé K., Commun Biol. October 7, 2021; 4 (1): 1158.                                


Huntingtin CAG expansion impairs germ layer patterning in synthetic human 2D gastruloids through polarity defects., Galgoczi S., Development. October 1, 2021; 148 (19):               


Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease., Getwan M., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):                                                   


Bicc1 and Dicer regulate left-right patterning through post-transcriptional control of the Nodal inhibitor Dand5., Maerker M., Nat Commun. September 16, 2021; 12 (1): 5482.                              


Auto-inhibitory intramolecular S5/S6 interaction in the TRPV6 channel regulates breast cancer cell migration and invasion., Cai R., Commun Biol. August 19, 2021; 4 (1): 990.              


The dorsal blastopore lip is a source of signals inducing planar cell polarity in the Xenopus neural plate., Mancini P., Biol Open. July 15, 2021; 10 (7):                 


DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes., Marquez J., J Med Genet. July 1, 2021; 58 (7): 453-464.                        


Tau, XMAP215/Msps and Eb1 co-operate interdependently to regulate microtubule polymerisation and bundle formation in axons., Hahn I., PLoS Genet. July 1, 2021; 17 (7): e1009647.              


Structural insight into BRCA1-BARD1 complex recruitment to damaged chromatin., Dai L., Mol Cell. July 1, 2021; 81 (13): 2765-2777.e6.  


Smad2 and Smad3 differentially modulate chordin transcription via direct binding on the distal elements in gastrula Xenopus embryos., Kumar V., Biochem Biophys Res Commun. June 25, 2021; 559 168-175.          


Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness., Schlingmann KP., J Am Soc Nephrol. June 1, 2021; 32 (6): 1498-1512.


Secreted inhibitors drive the loss of regeneration competence in Xenopus limbs., Aztekin C., Development. June 1, 2021; 148 (11):                                             


Fibroblast dedifferentiation as a determinant of successful regeneration., Lin TY., Dev Cell. May 17, 2021; 56 (10): 1541-1551.e6.                    


Chemical Catalysis Intervening to Histone Epigenetics., Nozaki T., Acc Chem Res. May 4, 2021; 54 (9): 2313-2322.


Diversity of functional alterations of the ClC-5 exchanger in the region of the proton glutamate in patients with Dent disease 1., Sakhi I., Hum Mutat. May 1, 2021; 42 (5): 537-550.


Functional-genomic analysis reveals intraspecies diversification of antiviral receptor transporter proteins in Xenopus laevis., Boys IN., PLoS Genet. May 1, 2021; 17 (5): e1009578.              


FAX-RIC enables robust profiling of dynamic RNP complex formation in multicellular organisms in vivo., Na Y., Nucleic Acids Res. March 18, 2021; 49 (5): e28.            


Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome., Mann N., J Am Soc Nephrol. March 1, 2021; 32 (3): 580-596.    


Xenopus epidermal and endodermal epithelia as models for mucociliary epithelial evolution, disease, and metaplasia., Walentek P., Genesis. February 1, 2021; 59 (1-2): e23406.          


Manipulating water for amphibian conservation., Mathwin R., Conserv Biol. February 1, 2021; 35 (1): 24-34.


Nucleoporin NUP205 plays a critical role in cilia and congenital disease., Marquez J., Dev Biol. January 1, 2021; 469 46-53.                        


Iron uptake mediated by the plant-derived chelator nicotianamine in the small intestine., Murata Y., J Biol Chem. January 1, 2021; 296 100195.            


Genetic and Physiological Effects of Insulin on Human Urate Homeostasis., Mandal AK., Front Physiol. January 1, 2021; 12 713710.              


Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1., Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.                                                    


The Secreted Protein Disulfide Isomerase Ag1 Lost by Ancestors of Poorly Regenerating Vertebrates Is Required for Xenopus laevis Tail Regeneration., Ivanova AS., Front Cell Dev Biol. January 1, 2021; 9 738940.                  


Wnt-inducible Lrp6-APEX2 interacting proteins identify ESCRT machinery and Trk-fused gene as components of the Wnt signaling pathway., Colozza G., Sci Rep. December 9, 2020; 10 (1): 21555.            


Rare heterozygous GDF6 variants in patients with renal anomalies., Martens H., Eur J Hum Genet. December 1, 2020; 28 (12): 1681-1693.                      


Preliminary indications that recombinant human IL-16 attracts and stimulates lymphocytes of the amphibian, Xenopus laevis implying an ancestral role for CD4 as a cytokine receptor., Gillis J., Cytokine. December 1, 2020; 136 155254.


Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts., Sulerud T., Mol Biol Cell. December 1, 2020; 31 (25): 2791-2802.          


Anatomical and histological analyses reveal that tail repair is coupled with regrowth in wild-caught, juvenile American alligators (Alligator mississippiensis)., Xu C., Sci Rep. November 18, 2020; 10 (1): 20122.                


Monocarboxylate transporter 12 as a guanidinoacetate efflux transporter in renal proximal tubular epithelial cells., Jomura R., Biochim Biophys Acta Biomembr. November 1, 2020; 1862 (11): 183434.


von Willebrand factor D and EGF domains is an evolutionarily conserved and required feature of blastemas capable of multitissue appendage regeneration., Leigh ND., Evol Dev. July 1, 2020; 22 (4): 297-311.        


DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain., Kyono Y., Dev Biol. June 15, 2020; 462 (2): 180-196.                                                    


A comparative analysis of fibroblast growth factor receptor signalling during Xenopus development., Brunsdon H., Biol Cell. May 1, 2020; 112 (5): 127-139.                


14-3-3 targets keratin intermediate filaments to mechanically sensitive cell-cell contacts., Mariani RA., Mol Biol Cell. April 15, 2020; 31 (9): 930-943.              


CFAP43 modulates ciliary beating in mouse and Xenopus., Rachev E., Dev Biol. March 15, 2020; 459 (2): 109-125.                                                                    


Family-wide Structural and Biophysical Analysis of Binding Interactions among Non-clustered δ-Protocadherins., Harrison OJ., Cell Rep. February 25, 2020; 30 (8): 2655-2671.e7.              


Disrupted ER membrane protein complex-mediated topogenesis drives congenital neural crest defects., Marquez J., J Clin Invest. February 3, 2020; 130 (2): 813-826.                                


Identification and characterization of the Atlantic salmon peptide transporter 1a., Gomes AS., Am J Physiol Cell Physiol. January 1, 2020; 318 (1): C191-C204.


The roles and controls of GATA factors in blood and cardiac development., Dobrzycki T., IUBMB Life. January 1, 2020; 72 (1): 39-44.


Structural complementarity facilitates E7820-mediated degradation of RBM39 by DCAF15., Faust TB., Nat Chem Biol. January 1, 2020; 16 (1): 7-14.          


SLC20A1 Is Involved in Urinary Tract and Urorectal Development., Rieke JM., Front Cell Dev Biol. January 1, 2020; 8 567.                                


Renal Reabsorptive Transport of Uric Acid Precursor Xanthine by URAT1 and GLUT9., Arakawa H., Biol Pharm Bull. January 1, 2020; 43 (11): 1792-1798.


Lissamphibian limbs and the origins of tetrapod hox domains., Woltering JM., Dev Biol. December 15, 2019; 456 (2): 138-144.        


Evaluating pathogenicity of SLC34A3-Ser192Leu, a frequent European missense variant in disorders of renal phosphate wasting., Schönauer R., Urolithiasis. December 1, 2019; 47 (6): 511-519.        


DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract., Blackburn ATM., Genet Med. December 1, 2019; 21 (12): 2755-2764.            


POPDC3 Gene Variants Associate with a New Form of Limb Girdle Muscular Dystrophy., Vissing J., Ann Neurol. December 1, 2019; 86 (6): 832-843.


The mechanosensitive ion channel TRAAK is localized to the mammalian node of Ranvier., Brohawn SG., Elife. November 1, 2019; 8                     


Update on the Role of the Non-Canonical Wnt/Planar Cell Polarity Pathway in Neural Tube Defects., Wang M., Cells. October 4, 2019; 8 (10):     

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