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Summary Expression Gene Literature (14) GO Terms (2) Nucleotides (219) Proteins (31) Interactants (321) Wiki
XB-GENEPAGE-995462

Papers associated with stom

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CFAP43 modulates ciliary beating in mouse and Xenopus., Rachev E, Schuster-Gossler K, Fuhl F, Ott T, Tveriakhina L, Beckers A, Hegermann J, Boldt K, Mai M, Kremmer E, Ueffing M, Blum M, Gossler A., Dev Biol. January 1, 2020; 459 (2): 109-125.                                                                    


Timing is everything: Reiterative Wnt, BMP and RA signaling regulate developmental competence during endoderm organogenesis., Rankin SA, Rankin SA, McCracken KW, Luedeke DM, Han L, Wells JM, Shannon JM, Zorn AM., Dev Biol. January 1, 2018; 434 (1): 121-132.          


The Lhx1-Ldb1 complex interacts with Furry to regulate microRNA expression during pronephric kidney development., Espiritu EB, Crunk AE, Bais A, Hochbaum D, Cervino AS, Phua YL, Butterworth MB, Goto T, Ho J, Hukriede NA, Cirio MC., Sci Rep. January 1, 2018; 8 (1): 16029.                                      


Subunit composition of a DEG/ENaC mechanosensory channel of Caenorhabditis elegans., Chen Y, Bharill S, Isacoff EY, Chalfie M., Proc Natl Acad Sci U S A. September 15, 2015; 112 (37): 11690-5.


Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome., Flatt JF, Guizouarn H, Burton NM, Borgese F, Tomlinson RJ, Forsyth RJ, Baldwin SA, Levinson BE, Quittet P, Aguilar-Martinez P, Delaunay J, Stewart GW, Bruce LJ., Blood. November 10, 2011; 118 (19): 5267-77.


A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis., Iolascon A, De Falco L, Borgese F, Esposito MR, Avvisati RA, Izzo P, Piscopo C, Guizouarn H, Biondani A, Pantaleo A, De Franceschi L., Haematologica. August 1, 2009; 94 (8): 1049-59.


A single conserved proline residue determines the membrane topology of stomatin., Kadurin I, Huber S, Gründer S., Biochem J. March 15, 2009; 418 (3): 587-94.


Taurine uptake across the human intestinal brush-border membrane is via two transporters: H+-coupled PAT1 (SLC36A1) and Na+- and Cl(-)-dependent TauT (SLC6A6)., Anderson CM, Howard A, Walters JR, Ganapathy V, Thwaites DT., J Physiol. February 15, 2009; 587 (Pt 4): 731-44.                


MEC-2 and MEC-6 in the Caenorhabditis elegans sensory mechanotransduction complex: auxiliary subunits that enable channel activity., Brown AL, Liao Z, Goodman MB., J Gen Physiol. June 1, 2008; 131 (6): 605-16.            


Exploring nervous system transcriptomes during embryogenesis and metamorphosis in Xenopus tropicalis using EST analysis., Fierro AC, Thuret R, Coen L, Perron M, Demeneix BA, Wegnez M, Gyapay G, Weissenbach J, Wincker P, Mazabraud A, Pollet N., BMC Genomics. July 10, 2007; 8 118.        


MEC-2 is recruited to the putative mechanosensory complex in C. elegans touch receptor neurons through its stomatin-like domain., Zhang S, Arnadottir J, Keller C, Caldwell GA, Yao CA, Chalfie M., Curr Biol. November 9, 2004; 14 (21): 1888-96.


Left-right asymmetric morphogenesis in the Xenopus digestive system., Muller JK, Prather DR, Nascone-Yoder NM., Dev Dyn. December 1, 2003; 228 (4): 672-82.          


The mechanosensory protein MEC-6 is a subunit of the C. elegans touch-cell degenerin channel., Chelur DS, Ernstrom GG, Goodman MB, Yao CA, Chen L, O' Hagan R, Chalfie M., Nature. December 12, 2002; 420 (6916): 669-73.


MEC-2 regulates C. elegans DEG/ENaC channels needed for mechanosensation., Goodman MB, Ernstrom GG, Chelur DS, O'Hagan R, Yao CA, Chalfie M., Nature. February 28, 2002; 415 (6875): 1039-42.

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