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Summary Expression Phenotypes Gene Literature (27) GO Terms (7) Nucleotides (60) Proteins (27) Interactants (189) Wiki
XB-GENEPAGE-5753498

Papers associated with dnah9



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GJA1 depletion causes ciliary defects by affecting Rab11 trafficking to the ciliary base., Jang DG, Kwon KY, Kweon YC, Kim BG, Myung K, Lee HS, Young Park C, Kwon T, Park TJ., Elife. August 25, 2022; 11                                       

DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes., Marquez J, Mann N, Arana K, Deniz E, Ji W, Konstantino M, Mis EK, Deshpande C, Jeffries L, McGlynn J, Hugo H, Widmeier E, Konrad M, Tasic V, Morotti R, Baptista J, Ellard S, Lakhani SA, Hildebrandt F, Khokha MK., J Med Genet. July 1, 2021; 58 (7): 453-464.                        

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.                        

Functional partitioning of a liquid-like organelle during assembly of axonemal dyneins., Lee C, Lee C, Cox RM, Papoulas O, Horani A, Drew K, Devitt CC, Brody SL, Marcotte EM, Wallingford JB., Elife. December 2, 2020; 9                             

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. March 15, 2020; 459 (2): 109-125.                                                                    

Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility., Robson A, Makova SZ, Barish S, Zaidi S, Mehta S, Drozd J, Jin SC, Gelb BD, Seidman CE, Chung WK, Lifton RP, Khokha MK, Brueckner M., Proc Natl Acad Sci U S A. July 9, 2019; 116 (28): 14049-14054.                                  

A dual function of FGF signaling in Xenopus left-right axis formation., Schneider I, Kreis J, Schweickert A, Blum M, Vick P., Development. May 10, 2019; 146 (9):                               

WDR5 regulates left-right patterning via chromatin-dependent and -independent functions., Kulkarni SS, Khokha MK., Development. November 28, 2018; 145 (23):                 

WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation., Kulkarni SS, Griffin JN, Date PP, Liem KF, Khokha MK., Dev Cell. September 10, 2018; 46 (5): 595-610.e3.                              

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.

An Early Function of Polycystin-2 for Left-Right Organizer Induction in Xenopus., Vick P, Kreis J, Schneider I, Tingler M, Getwan M, Thumberger T, Beyer T, Schweickert A, Blum M., iScience. April 27, 2018; 2 76-85.                                        

Leftward Flow Determines Laterality in Conjoined Twins., Tisler M, Thumberger T, Schneider I, Schweickert A, Blum M., Curr Biol. February 20, 2017; 27 (4): 543-548.                

CRISPR/Cas9: An inexpensive, efficient loss of function tool to screen human disease genes in Xenopus., Bhattacharya D, Marfo CA, Li D, Lane M, Khokha MK., Dev Biol. December 15, 2015; 408 (2): 196-204.            

ERK7 regulates ciliogenesis by phosphorylating the actin regulator CapZIP in cooperation with Dishevelled., Miyatake K, Kusakabe M, Takahashi C, Nishida E., Nat Commun. March 31, 2015; 6 6666.                

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.                      

The nodal inhibitor Coco is a critical target of leftward flow in Xenopus., Schweickert A, Vick P, Getwan M, Weber T, Schneider I, Eberhardt M, Beyer T, Pachur A, Blum M., Curr Biol. April 27, 2010; 20 (8): 738-43.      

Flow on the right side of the gastrocoel roof plate is dispensable for symmetry breakage in the frog Xenopus laevis., Vick P, Schweickert A, Weber T, Eberhardt M, Mencl S, Shcherbakov D, Beyer T, Blum M., Dev Biol. July 15, 2009; 331 (2): 281-91.                                        

FGF signalling during embryo development regulates cilia length in diverse epithelia., Neugebauer JM, Amack JD, Peterson AG, Bisgrove BW, Yost HJ., Nature. April 2, 2009; 458 (7238): 651-4.      

The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryos., Stubbs JL, Oishi I, Izpisúa Belmonte JC, Kintner C., Nat Genet. December 1, 2008; 40 (12): 1454-60.                

Cilia multifunctional organelles at the center of vertebrate left-right asymmetry., Basu B, Brueckner M., Curr Top Dev Biol. January 1, 2008; 85 151-74.

Xenopus Bicaudal-C is required for the differentiation of the amphibian pronephros., Tran U, Pickney LM, Ozpolat BD, Wessely O., Dev Biol. July 1, 2007; 307 (1): 152-64.                  

Cilia-driven leftward flow determines laterality in Xenopus., Schweickert A, Weber T, Beyer T, Vick P, Bogusch S, Feistel K, Blum M., Curr Biol. January 9, 2007; 17 (1): 60-6.        

Localization and loss-of-function implicates ciliary proteins in early, cytoplasmic roles in left-right asymmetry., Qiu D, Cheng SM, Wozniak L, McSweeney M, Perrone E, Levin M., Dev Dyn. September 1, 2005; 234 (1): 176-89.      

Left-right asymmetry: nodal points., Mercola M., J Cell Sci. August 15, 2003; 116 (Pt 16): 3251-7.      

Induction and patterning of the neural crest, a stem cell-like precursor population., LaBonne C, Bronner-Fraser M., J Neurobiol. August 1, 1998; 36 (2): 175-89.      

Vital dye labelling of Xenopus laevis trunk neural crest reveals multipotency and novel pathways of migration., Collazo A, Bronner-Fraser M, Fraser SE., Development. June 1, 1993; 118 (2): 363-76.

In situ analysis of neuronal dynamics and positional cues in the patterning of nerve connections., Fraser SE, O'Rourke NA., J Exp Biol. October 1, 1990; 153 61-70.

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