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Summary Expression Gene Literature (508) GO Terms (23) Nucleotides (1111) Proteins (38) Interactants (968) Wiki
XB--966886

Papers associated with rho (and Disease Ontology)

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Results 1 - 21 of 21 results

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Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R, Ververi A, Beleza-Meireles A, Ji W, Mis E, Patterson QT, Griffin JN, Bhujel N, Chang CA, Dixit A, Konstantino M, Healy C, Hannan S, Neo N, Cash A, Li D, Bhoj E, Zackai EH, Cleaver R, Baralle D, McEntagart M, Newbury-Ecob R, Scott R, Hurst JA, Au PYB, Hosey MT, Khokha M, Marciano DK, Lakhani SA, Liu KJ, Liu KJ., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.                  


Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders., Barbosa S, Greville-Heygate S, Bonnet M, Godwin A, Fagotto-Kaufmann C, Kajava AV, Laouteouet D, Mawby R, Wai HA, Dingemans AJM, Hehir-Kwa J, Willems M, Capri Y, Mehta SG, Cox H, Goudie D, Vansenne F, Turnpenny P, Vincent M, Cogné B, Lesca G, Hertecant J, Rodriguez D, Keren B, Burglen L, Gérard M, Putoux A, null null, Cantagrel V, Siquier-Pernet K, Rio M, Banka S, Sarkar A, Steeves M, Parker M, Clement E, Moutton S, Tran Mau-Them F, Piton A, de Vries BBA, Guille M, Debant A, Schmidt S, Baralle D., Am J Hum Genet. January 1, 2020; 106 (3): 338-355.                            


Electrophysiological Changes During Early Steps of Retinitis Pigmentosa., Bocchero U, Tam BM, Chiu CN, Torre V, Moritz OL., Invest Ophthalmol Vis Sci. January 1, 2019; 60 (4): 933-943.              


ECT2 associated to PRICKLE1 are poor-prognosis markers in triple-negative breast cancer., Daulat AM, Finetti P, Revinski D, Silveira Wagner M, Camoin L, Audebert S, Birnbaum D, Kodjabachian L, Borg JP, Bertucci F., Br J Cancer. January 1, 2019; 120 (9): 931-940.        


Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary Clearance., Bustamante-Marin XM, Yin WN, Sears PR, Werner ME, Brotslaw EJ, Mitchell BJ, Jania CM, Zeman KL, Rogers TD, Herring LE, Refabért L, Thomas L, Amselem S, Escudier E, Legendre M, Grubb BR, Knowles MR, Zariwala MA, Ostrowski LE., Am J Hum Genet. January 1, 2019; 104 (2): 229-245.                                  


Targeting TMEM176B Enhances Antitumor Immunity and Augments the Efficacy of Immune Checkpoint Blockers by Unleashing Inflammasome Activation., Segovia M, Russo S, Jeldres M, Mahmoud YD, Perez V, Duhalde M, Charnet P, Rousset M, Victoria S, Veigas F, Louvet C, Vanhove B, Floto RA, Anegon I, Cuturi MC, Girotti MR, Rabinovich GA, Hill M., Cancer Cell. January 1, 2019; 35 (5): 767-781.e6.                              


CRISPR/Cas9 disease models in zebrafish and Xenopus: The genetic renaissance of fish and frogs., Naert T, Vleminckx K, Vleminckx K., Drug Discov Today Technol. August 1, 2018; 28 41-52.


Nosip functions during vertebrate eye and cranial cartilage development., Flach H, Krieg J, Hoffmeister M, Dietmann P, Reusch A, Wischmann L, Kernl B, Riegger R, Oess S, Kühl SJ., Dev Dyn. January 1, 2018; 247 (9): 1070-1082.                


Retinal tissue preparation for high-resolution live imaging of photoreceptors expressing multiple transgenes., Haeri M, Zhuo X, Haeri M, Knox BE., MethodsX. January 1, 2018; 5 1140-1147.    


Fgfr signaling is required as the early eye field forms to promote later patterning and morphogenesis of the eye., Atkinson-Leadbeater K, Hehr CL, McFarlane S., Dev Dyn. September 23, 2017; .              


An Epha4/Sipa1l3/Wnt pathway regulates eye development and lens maturation., Rothe M, Kanwal N, Dietmann P, Seigfried FA, Hempel A, Schütz D, Reim D, Engels R, Linnemann A, Schmeisser MJ, Bockmann J, Kühl M, Boeckers TM, Kühl SJ., Development. January 1, 2017; 144 (2): 321-333.                              


Opposing Effects of Valproic Acid Treatment Mediated by Histone Deacetylase Inhibitor Activity in Four Transgenic X. laevis Models of Retinitis Pigmentosa., Vent-Schmidt RYJ, Wen RH, Zong Z, Chiu CN, Tam BM, May CG, Moritz OL., J Neurosci. January 1, 2017; 37 (4): 1039-1054.                  


Usher syndrome type 1-associated cadherins shape the photoreceptor outer segment., Schietroma C, Parain K, Estivalet A, Aghaie A, Boutet de Monvel J, Picaud S, Sahel JA, Perron M, El-Amraoui A, Petit C., J Cell Biol. January 1, 2017; 216 (6): 1849-1864.                  


Modeling Dominant and Recessive Forms of Retinitis Pigmentosa by Editing Three Rhodopsin-Encoding Genes in Xenopus Laevis Using Crispr/Cas9., Feehan JM, Chiu CN, Stanar P, Tam BM, Ahmed SN, Moritz OL., Sci Rep. January 1, 2017; 7 (1): 6920.              


Photoactivation-induced instability of rhodopsin mutants T4K and T17M in rod outer segments underlies retinal degeneration in X. laevis transgenic models of retinitis pigmentosa., Tam BM, Noorwez SM, Kaushal S, Kono M, Moritz OL., J Neurosci. October 1, 2014; 34 (40): 13336-48.              


The severe autosomal dominant retinitis pigmentosa rhodopsin mutant Ter349Glu mislocalizes and induces rapid rod cell death., Hollingsworth TJ, Gross AK., J Biol Chem. October 4, 2013; 288 (40): 29047-55.  


SHP-2 acts via ROCK to regulate the cardiac actin cytoskeleton., Langdon Y, Tandon P, Paden E, Duddy J, Taylor JM, Conlon FL., Development. March 1, 2012; 139 (5): 948-57.                


Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning., Fakhro KA, Choi M, Ware SM, Belmont JW, Towbin JA, Lifton RP, Khokha MK, Brueckner M., Proc Natl Acad Sci U S A. February 15, 2011; 108 (7): 2915-20.                      


Xenopus laevis P23H rhodopsin transgene causes rod photoreceptor degeneration that is more severe in the ventral retina and is modulated by light., Zhang R, Oglesby E, Marsh-Armstrong N., Exp Eye Res. April 1, 2008; 86 (4): 612-21.          


Dark rearing rescues P23H rhodopsin-induced retinal degeneration in a transgenic Xenopus laevis model of retinitis pigmentosa: a chromophore-dependent mechanism characterized by production of N-terminally truncated mutant rhodopsin., Tam BM, Moritz OL., J Neurosci. August 22, 2007; 27 (34): 9043-53.              


Opsin activation as a cause of congenital night blindness., Jin S, Cornwall MC, Oprian DD., Nat Neurosci. July 1, 2003; 6 (7): 731-5.

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