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Summary Expression Phenotypes Gene Literature (156) GO Terms (16) Nucleotides (1832) Proteins (80) Interactants (665) Wiki
XB-GENEPAGE-484830

Papers associated with atp1a1



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Developmental regulation of cellular metabolism is required for intestinal elongation and rotation., Grzymkowski JK, Chiu YC, Jima DD, Wyatt BH, Jayachandran S, Stutts WL, Nascone-Yoder NM., Development. February 15, 2024; 151 (4):                                       

Phenotype-genotype relationships in Xenopus sox9 crispants provide insights into campomelic dysplasia and vertebrate jaw evolution., Hossain N, Igawa T, Suzuki M, Tazawa I, Nakao Y, Hayashi T, Suzuki N, Ogino H., Dev Growth Differ. October 1, 2023; 65 (8): 481-497.                  

The phenotypic spectrum of pathogenic ATP1A1 variants expands: the novel p.P600R substitution causes demyelinating Charcot-Marie-Tooth disease., Cinarli Yuksel F, Nicolaou P, Spontarelli K, Dohrn MF, Rebelo AP, Koutsou P, Georghiou A, Artigas P, Züchner SL, Kleopa KA, Christodoulou K., J Neurol. May 1, 2023; 270 (5): 2576-2590.            

RNA localization during early development of the axolotl., Šimková K, Naraine R, Vintr J, Soukup V, Šindelka R., Front Cell Dev Biol. January 1, 2023; 11 1260795.                        

Normal Table of Xenopus development: a new graphical resource., Zahn N, James-Zorn C, Ponferrada VG, Adams DS, Grzymkowski J, Buchholz DR, Nascone-Yoder NM, Horb M, Moody SA, Vize PD, Zorn AM., Development. July 15, 2022; 149 (14):                         

Embryonic and aglomerular kidney development in the bay pipefish, Syngnathus leptorhynchus., Maters BR, Stevenson E, Vize PD., PLoS One. May 12, 2022; 17 (5): e0267932.  

Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components., Hantel F, Liu H, Fechtner L, Neuhaus H, Ding J, Arlt D, Walentek P, Villavicencio-Lorini P, Gerhardt C, Hollemann T, Pfirrmann T., J Cell Sci. May 1, 2022; 135 (9):                                     

A revised mechanism of action of hyperaldosteronism-linked mutations in cytosolic domains of GIRK4 (KCNJ5)., Shalomov B, Handklo-Jamal R, Reddy HP, Theodor N, Bera AK, Dascal N., J Physiol. March 1, 2022; 600 (6): 1419-1437.

Deep learning is widely applicable to phenotyping embryonic development and disease., Naert T, Çiçek Ö, Ogar P, Bürgi M, Shaidani NI, Kaminski MM, Xu Y, Grand K, Vujanovic M, Prata D, Hildebrandt F, Brox T, Ronneberger O, Voigt FF, Helmchen F, Loffing J, Horb ME, Willsey HR, Lienkamp SS., Development. November 1, 2021; 148 (21):                                                                 

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

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations., Connaughton DM, Dai R, Owen DJ, Marquez J, Mann N, Graham-Paquin AL, Nakayama M, Coyaud E, Laurent EMN, St-Germain JR, Blok LS, Vino A, Klämbt V, Deutsch K, Wu CW, Kolvenbach CM, Kause F, Ottlewski I, Schneider R, Kitzler TM, Majmundar AJ, Buerger F, Onuchic-Whitford AC, Youying M, Kolb A, Salmanullah D, Chen E, van der Ven AT, Rao J, Ityel H, Seltzsam S, Rieke JM, Chen J, Vivante A, Hwang DY, Kohl S, Dworschak GC, Hermle T, Alders M, Bartolomaeus T, Bauer SB, Baum MA, Brilstra EH, Challman TD, Zyskind J, Costin CE, Dipple KM, Duijkers FA, Ferguson M, Fitzpatrick DR, Fick R, Glass IA, Hulick PJ, Kline AD, Krey I, Kumar S, Kumar S, Lu W, Marco EJ, Wentzensen IM, Mefford HC, Platzer K, Povolotskaya IS, Savatt JM, Shcherbakova NV, Senguttuvan P, Squire AE, Stein DR, Thiffault I, Voinova VY, Somers MJG, Ferguson MA, Traum AZ, Daouk GH, Daga A, Rodig NM, Terhal PA, van Binsbergen E, Eid LA, Tasic V, Rasouly HM, Lim TY, Ahram DF, Gharavi AG, Reutter HM, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Lifton RP, Xu H, Mane SM, Sanna-Cherchi S, Sharrocks AD, Raught B, Fisher SE, Bouchard M, Khokha MK, Shril S, Hildebrandt F., Am J Hum Genet. October 1, 2020; 107 (4): 727-742.

Na/K Pump Mutations Associated with Primary Hyperaldosteronism Cause Loss of Function., Meyer DJ, Gatto C, Artigas P., Biochemistry. April 2, 2019; 58 (13): 1774-1785.

Dynamin Binding Protein Is Required for Xenopus laevis Kidney Development., DeLay BD, Baldwin TA, Miller RK., Front Physiol. January 1, 2019; 10 143.                                

Asymmetric distribution of biomolecules of maternal origin in the Xenopus laevis egg and their impact on the developmental plan., Sindelka R, Abaffy P, Qu Y, Tomankova S, Sidova M, Naraine R, Kolar M, Peuchen E, Sun L, Dovichi N, Kubista M., Sci Rep. May 29, 2018; 8 (1): 8315.                

Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2., Lassuthova P, Rebelo AP, Ravenscroft G, Lamont PJ, Davis MR, Manganelli F, Feely SM, Bacon C, Brožková DŠ, Haberlova J, Mazanec R, Tao F, Saghira C, Abreu L, Courel S, Powell E, Buglo E, Bis DM, Baxter MF, Ong RW, Marns L, Lee YC, Bai Y, Isom DG, Barro-Soria R, Chung KW, Scherer SS, Larsson HP, Laing NG, Choi BO, Seeman P, Shy ME, Santoro L, Zuchner S., Am J Hum Genet. March 1, 2018; 102 (3): 505-514.

Tissue-Specific Gene Inactivation in Xenopus laevis: Knockout of lhx1 in the Kidney with CRISPR/Cas9., DeLay BD, Corkins ME, Hanania HL, Salanga M, Deng JM, Sudou N, Taira M, Horb ME, Miller RK., Genetics. February 1, 2018; 208 (2): 673-686.                        

On the effect of hyperaldosteronism-inducing mutations in Na/K pumps., Meyer DJ, Gatto C, Artigas P., J Gen Physiol. November 6, 2017; 149 (11): 1009-1028.                      

Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM, Tosic J, Kresbach C, Engel H, Klockenbusch J, Müller AL, Pichler R, Grahammer F, Kretz O, Huber TB, Walz G, Arnold SJ, Lienkamp SS., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.                  

Evolution of the α-Subunit of Na/K-ATPase from Paramecium to Homo sapiens: Invariance of Transmembrane Helix Topology., Morrill GA, Kostellow AB, Liu L, Gupta RK, Askari A., J Mol Evol. May 1, 2016; 82 (4-5): 183-98.              

Tuning of the Na,K-ATPase by the beta subunit., Hilbers F, Kopec W, Isaksen TJ, Holm TH, Lykke-Hartmann K, Nissen P, Khandelia H, Poulsen H., Sci Rep. February 5, 2016; 6 20442.          

Cardiac glycosides induced toxicity in human cells expressing α1-, α2-, or α3-isoforms of Na-K-ATPase., Cherniavsky Lev M, Karlish SJ, Garty H., Am J Physiol Cell Physiol. July 15, 2015; 309 (2): C126-35.

Congenital chloride-losing diarrhea in a Mexican child with the novel homozygous SLC26A3 mutation G393W., Reimold FR, Balasubramanian S, Doroquez DB, Shmukler BE, Zsengeller ZK, Saslowsky D, Thiagarajah JR, Stillman IE, Lencer WI, Wu BL, Villalpando-Carrion S, Alper SL., Front Physiol. June 9, 2015; 6 179.                  

Developmental expression analysis of Na, K-ATPase α subunits in Xenopus., Rahman MM, Tae HJ, Cho HS, Shin GW, Park BY., Dev Genes Evol. April 1, 2015; 225 (2): 105-11.

The alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform., Dichmann DS, Walentek P, Harland RM., Cell Rep. February 3, 2015; 10 (4): 527-36.                    

Signals governing the trafficking and mistrafficking of a ciliary GPCR, rhodopsin., Lodowski KH, Lee R, Ropelewski P, Nemet I, Tian G, Imanishi Y., J Neurosci. August 21, 2013; 33 (34): 13621-38.                      

ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3., Hoff S, Halbritter J, Epting D, Frank V, Nguyen TM, van Reeuwijk J, Boehlke C, Schell C, Yasunaga T, Helmstädter M, Mergen M, Filhol E, Boldt K, Horn N, Ueffing M, Otto EA, Eisenberger T, Elting MW, van Wijk JA, Bockenhauer D, Sebire NJ, Rittig S, Vyberg M, Ring T, Pohl M, Pape L, Neuhaus TJ, Elshakhs NA, Koon SJ, Harris PC, Grahammer F, Huber TB, Kuehn EW, Kramer-Zucker A, Bolz HJ, Roepman R, Saunier S, Walz G, Hildebrandt F, Bergmann C, Lienkamp SS., Nat Genet. August 1, 2013; 45 (8): 951-6.                                

Postnatal regulation of X,K-ATPases in rat skin and conserved lateroapical polarization of Na,K-ATPase in vertebrate epidermis., Pestov NB, Korneenko TV, Shakhparonov MI, Modyanov NN., Exp Dermatol. June 1, 2013; 22 (6): 423-5.

Urotensin II receptor (UTR) exists in hyaline chondrocytes: a study of peripheral distribution of UTR in the African clawed frog, Xenopus laevis., Konno N, Fujii Y, Imae H, Kaiya H, Mukuda T, Miyazato M, Matsuda K, Uchiyama M., Gen Comp Endocrinol. May 1, 2013; 185 44-56.                          

Regulation of G-protein signaling via Gnas is required to regulate proximal tubular growth in the Xenopus pronephros., Zhang B, Romaker D, Ferrell N, Wessely O., Dev Biol. April 1, 2013; 376 (1): 31-42.                        

The C-terminal cavity of the Na,K-ATPase analyzed by docking and electrophysiology., Paulsen PA, Jurkowski W, Apostolov R, Lindahl E, Nissen P, Poulsen H., Mol Membr Biol. March 1, 2013; 30 (2): 195-205.

Regeneration of functional pronephric proximal tubules after partial nephrectomy in Xenopus laevis., Caine ST, Mclaughlin KA., Dev Dyn. March 1, 2013; 242 (3): 219-29.          

Measuring cation transport by Na,K- and H,K-ATPase in Xenopus oocytes by atomic absorption spectrophotometry: an alternative to radioisotope assays., Dürr KL, Tavraz NN, Spiller S, Friedrich T., J Vis Exp. February 19, 2013; (72): e50201.

Plasma membrane events associated with the meiotic divisions in the amphibian oocyte: insights into the evolution of insulin transduction systems and cell signaling., Morrill GA, Kostellow AB, Moore RD, Gupta RK., BMC Dev Biol. January 23, 2013; 13 3.              

Exon capture and bulk segregant analysis: rapid discovery of causative mutations using high-throughput sequencing., del Viso F, Bhattacharya D, Kong Y, Gilchrist MJ, Khokha MK., BMC Genomics. November 21, 2012; 13 649.                  

Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development., Chang JT, Lowery LA, Sive H., Dev Biol. August 15, 2012; 368 (2): 312-22.

Control of gastric H,K-ATPase activity by cations, voltage and intracellular pH analyzed by voltage clamp fluorometry in Xenopus oocytes., Dürr KL, Tavraz NN, Friedrich T., PLoS One. January 1, 2012; 7 (3): e33645.            

Progesterone-induced changes in the phosphoryl potential during the meiotic divisions in amphibian oocytes: role of Na/K-ATPase., Morrill GA, Dowd TL, Kostellow AB, Gupta RK., BMC Dev Biol. January 26, 2011; 11 67.                

The two C-terminal tyrosines stabilize occluded Na/K pump conformations containing Na or K ions., Vedovato N, Gadsby DC., J Gen Physiol. July 1, 2010; 136 (1): 63-82.                      

Activity-dependent regulation of mitochondrial motility by calcium and Na/K-ATPase at nodes of Ranvier of myelinated nerves., Zhang CL, Ho PL, Kintner DB, Sun D, Chiu SY., J Neurosci. March 10, 2010; 30 (10): 3555-66.

E2P state stabilization by the N-terminal tail of the H,K-ATPase beta-subunit is critical for efficient proton pumping under in vivo conditions., Dürr KL, Abe K, Tavraz NN, Friedrich T., J Biol Chem. July 24, 2009; 284 (30): 20147-54.

Functional significance of E2 state stabilization by specific alpha/beta-subunit interactions of Na,K- and H,K-ATPase., Dürr KL, Tavraz NN, Dempski RE, Bamberg E, Friedrich T., J Biol Chem. February 6, 2009; 284 (6): 3842-54.

Requirement of Wnt/beta-catenin signaling in pronephric kidney development., Lyons JP, Miller RK, Zhou X, Weidinger G, Deroo T, Denayer T, Park JI, Ji H, Hong JY, Li A, Moon RT, Jones EA, Vleminckx K, Vleminckx K, Vize PD, McCrea PD., Mech Dev. January 1, 2009; 126 (3-4): 142-59.        

Ankyrin-B is required for coordinated expression of beta-2-spectrin, the Na/K-ATPase and the Na/Ca exchanger in the inner segment of rod photoreceptors., Kizhatil K, Sandhu NK, Peachey NS, Bennett V., Exp Eye Res. January 1, 2009; 88 (1): 57-64.  

Deletion of the chloride transporter Slc26a9 causes loss of tubulovesicles in parietal cells and impairs acid secretion in the stomach., Xu J, Song P, Miller ML, Borgese F, Barone S, Riederer B, Wang Z, Alper SL, Forte JG, Shull GE, Ehrenfeld J, Seidler U, Soleimani M., Proc Natl Acad Sci U S A. November 18, 2008; 105 (46): 17955-60.

The fourth extracellular loop of the alpha subunit of Na,K-ATPase. Functional evidence for close proximity with the second extracellular loop., Capendeguy O, Iwaszkiewicz J, Michielin O, Horisberger JD., J Biol Chem. October 10, 2008; 283 (41): 27850-27858.

Human FXYD2 G41R mutation responsible for renal hypomagnesemia behaves as an inward-rectifying cation channel., Sha Q, Pearson W, Burcea LC, Wigfall DA, Schlesinger PH, Nichols CG, Mercer RW., Am J Physiol Renal Physiol. July 1, 2008; 295 (1): F91-9.

Characterization of Na,K-ATPase and H,K-ATPase enzymes with glycosylation-deficient beta-subunit variants by voltage-clamp fluorometry in Xenopus oocytes., Dürr KL, Tavraz NN, Zimmermann D, Bamberg E, Friedrich T., Biochemistry. April 8, 2008; 47 (14): 4288-97.

Collectrin/tmem27 is expressed at high levels in all segments of the developing Xenopus pronephric nephron and in the Wolffian duct., McCoy KE, Zhou X, Zhou X, Vize PD., Gene Expr Patterns. April 1, 2008; 8 (4): 271-4.        

Phosphorylation of phospholemman (FXYD1) by protein kinases A and C modulates distinct Na,K-ATPase isozymes., Bibert S, Roy S, Schaer D, Horisberger JD, Geering K., J Biol Chem. January 4, 2008; 283 (1): 476-486.

H,K-ATPase protein localization and Kir4.1 function reveal concordance of three axes during early determination of left-right asymmetry., Aw S, Adams DS, Qiu D, Levin M., Mech Dev. January 1, 2008; 125 (3-4): 353-72.    

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