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Summary Expression Phenotypes Gene Literature (27) GO Terms (1) Nucleotides (278) Proteins (47) Interactants (270) Wiki
XB--973604

Papers associated with cfd



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Transmembrane serine protease 2 (TMPRSS2) proteolytically activates the epithelial sodium channel (ENaC) by cleaving the channel's γ-subunit., Sure F, Bertog M, Afonso S, Diakov A, Rinke R, Madej MG, Wittmann S, Gramberg T, Korbmacher C, Ilyaskin AV., J Biol Chem. June 1, 2022; 298 (6): 102004.                                        

Foxm1 regulates neural progenitor fate during spinal cord regeneration., Pelzer D, Phipps LS, Thuret R, Gallardo-Dodd CJ, Baker SM, Dorey K., EMBO Rep. September 6, 2021; 22 (9): e50932.                        

The secreted BMP antagonist ERFE is required for the development of a functional circulatory system in Xenopus., Melchert J, Henningfeld KA, Richts S, Lingner T, Jonigk D, Pieler T., Dev Biol. March 15, 2020; 459 (2): 138-148.                                

A multichannel computer-driven system to raise aquatic embryos under selectable hypoxic conditions., Metikala S, Neuhaus H, Hollemann T., Hypoxia (Auckl). January 12, 2018; 6 1-9.      

The cardiac-restricted protein ADP-ribosylhydrolase-like 1 is essential for heart chamber outgrowth and acts on muscle actin filament assembly., Smith SJ, Towers N, Saldanha JW, Shang CA, Mahmood SR, Taylor WR, Mohun TJ., Dev Biol. August 15, 2016; 416 (2): 373-88.                                                      

Suppression of vascular network formation by chronic hypoxia and prolyl-hydroxylase 2 (phd2) deficiency during vertebrate development., Metikala S, Neuhaus H, Hollemann T., Angiogenesis. April 1, 2016; 19 (2): 119-31.  

The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning., Schlosser G, Patthey C, Shimeld SM., Dev Biol. May 1, 2014; 389 (1): 98-119.            

Xenopus cadherin 5 is specifically expressed in endothelial cells of the developing vascular system., Neuhaus H, Metikala S, Hollemann T., Int J Dev Biol. January 1, 2014; 58 (1): 51-6.            

Activin ligands are required for the re-activation of Smad2 signalling after neurulation and vascular development in Xenopus tropicalis., Nagamori Y, Roberts S, Maciej M, Dorey K., Int J Dev Biol. January 1, 2014; 58 (10-12): 783-91.            

VEGFA-dependent and -independent pathways synergise to drive Scl expression and initiate programming of the blood stem cell lineage in Xenopus., Ciau-Uitz A, Pinheiro P, Kirmizitas A, Zuo J, Patient R., Development. June 1, 2013; 140 (12): 2632-42.                                                                                                                            

Uncoupling VEGFA functions in arteriogenesis and hematopoietic stem cell specification., Leung A, Ciau-Uitz A, Pinheiro P, Monteiro R, Zuo J, Vyas P, Patient R, Porcher C., Dev Cell. January 28, 2013; 24 (2): 144-58.                                

Hippo signaling components, Mst1 and Mst2, act as a switch between self-renewal and differentiation in Xenopus hematopoietic and endothelial progenitors., Nejigane S, Takahashi S, Haramoto Y, Michiue T, Asashima M., Int J Dev Biol. January 1, 2013; 57 (5): 407-14.                      

Proteolytic activation of the epithelial sodium channel (ENaC) by the cysteine protease cathepsin-S., Haerteis S, Krappitz M, Bertog M, Krappitz A, Baraznenok V, Henderson I, Lindström E, Murphy JE, Bunnett NW, Korbmacher C., Pflugers Arch. October 1, 2012; 464 (4): 353-65.                  

Plasmin and chymotrypsin have distinct preferences for channel activating cleavage sites in the γ subunit of the human epithelial sodium channel., Haerteis S, Krappitz M, Diakov A, Krappitz A, Rauh R, Korbmacher C., J Gen Physiol. October 1, 2012; 140 (4): 375-89.                      

Mapping gene expression in two Xenopus species: evolutionary constraints and developmental flexibility., Yanai I, Peshkin L, Jorgensen P, Kirschner MW., Dev Cell. April 19, 2011; 20 (4): 483-96.            

Detection of dynamic spatiotemporal response to periodic chemical stimulation in a Xenopus embryonic tissue., Kim Y, Joshi SD, Messner WC, LeDuc PR, Davidson LA., PLoS One. January 7, 2011; 6 (1): e14624.        

Xenopus er71 is involved in vascular development., Neuhaus H, Müller F, Hollemann T., Dev Dyn. December 1, 2010; 239 (12): 3436-45.            

A mutation of the epithelial sodium channel associated with atypical cystic fibrosis increases channel open probability and reduces Na+ self inhibition., Rauh R, Diakov A, Tzschoppe A, Korbmacher J, Azad AK, Cuppens H, Cassiman JJ, Dötsch J, Sticht H, Korbmacher C., J Physiol. April 15, 2010; 588 (Pt 8): 1211-25.

XRASGRP2 is essential for blood vessel formation during Xenopus development., Suzuki K, Takahashi S, Haramoto Y, Onuma Y, Nagamine K, Okabayashi K, Hashizume K, Iwanaka T, Asashima M., Int J Dev Biol. January 1, 2010; 54 (4): 609-15.            

The delta-subunit of the epithelial sodium channel (ENaC) enhances channel activity and alters proteolytic ENaC activation., Haerteis S, Krueger B, Korbmacher C, Rauh R., J Biol Chem. October 16, 2009; 284 (42): 29024-40.

In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M, Ito Y, Chan T, Michiue T, Nakanishi M, Suzuki K, Hitachi K, Okabayashi K, Kondow A, Ariizumi T., Dev Dyn. June 1, 2009; 238 (6): 1309-20.                      

SHP-2 is required for the maintenance of cardiac progenitors., Langdon YG, Goetz SC, Berg AE, Swanik JT, Conlon FL., Development. November 1, 2007; 134 (22): 4119-30.    

(NDRG2) stimulates amiloride-sensitive Na+ currents in Xenopus laevis oocytes and fisher rat thyroid cells., Wielpütz MO, Lee IH, Dinudom A, Boulkroun S, Farman N, Cook DI, Korbmacher C, Rauh R., J Biol Chem. September 21, 2007; 282 (38): 28264-73.

Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis., Inui M, Fukui A, Ito Y, Asashima M., Dev Biol. October 1, 2006; 298 (1): 188-200.                

A novel gene, Ami is expressed in vascular tissue in Xenopus laevis., Inui M, Asashima M., Gene Expr Patterns. August 1, 2006; 6 (6): 613-9.        

The gamma-subunit of ENaC is more important for channel surface expression than the beta-subunit., Konstas AA, Korbmacher C., Am J Physiol Cell Physiol. February 1, 2003; 284 (2): C447-56.

Influence of voltage and extracellular Na(+) on amiloride block and transport kinetics of rat epithelial Na(+) channel expressed in Xenopus oocytes., Segal A, Awayda MS, Eggermont J, Van Driessche W, Weber WM., Pflugers Arch. March 1, 2002; 443 (5-6): 882-91.

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