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XB--5753498
Papers associated with dnah9 (and Disease Ontology)
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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.  |
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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.  |
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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.  |
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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. |
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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.  |
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WDR5 regulates left-right patterning via chromatin-dependent and -independent functions., Kulkarni SS, Khokha MK., Development. November 28, 2018; 145 (23):  |
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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. March 15, 2020; 459 (2): 109-125.  |
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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  |
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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.  |
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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.  |
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