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Dyrk1a is required for craniofacial development in Xenopus laevis. , Johnson HK, Wahl SE , Sesay F, Litovchick L, Dickinson AJ ., Dev Biol. July 1, 2024; 511 63-75.
Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes. , Lansdon LA, Dickinson A , Arlis S, Liu H , Hlas A, Hahn A, Bonde G, Long A, Standley J, Tyryshkina A, Wehby G, Lee NR, Daack-Hirsch S, Mohlke K, Girirajan S, Darbro BW, Cornell RA, Houston DW , Murray JC, Manak JR., Am J Hum Genet. January 5, 2023; 110 (1): 71-91.
Recognition of H2AK119ub plays an important role in RSF1-regulated early Xenopus development. , Parast SM, Yu D, Chen C , Dickinson AJ , Chang C , Wang H., Front Cell Dev Biol. January 1, 2023; 11 1168643.
Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disorders. , Wyatt BH, Raymond TO, Lansdon LA, Darbro BW, Murray JC, Manak JR, Dickinson AJG ., Genesis. February 1, 2021; 59 (1-2): e23394.
Desmoplakin is required for epidermal integrity and morphogenesis in the Xenopus laevis embryo. , Bharathan NK, Dickinson AJG ., Dev Biol. June 15, 2019; 450 (2): 115-131.
Transcriptome analysis of Xenopus orofacial tissues deficient in retinoic acid receptor function. , Wahl SE , Wyatt BH, Turner SD, Dickinson AJG ., BMC Genomics. November 3, 2018; 19 (1): 795.
E-cigarette aerosol exposure can cause craniofacial defects in Xenopus laevis embryos and mammalian neural crest cells. , Kennedy AE , Kandalam S, Olivares-Navarrete R, Dickinson AJG ., PLoS One. September 8, 2017; 12 (9): e0185729.
Role of JNK during buccopharyngeal membrane perforation, the last step of embryonic mouth formation. , Houssin NS, Bharathan NK, Turner SD, Dickinson AJ ., Dev Dyn. February 1, 2017; 246 (2): 100-115.
Using frogs faces to dissect the mechanisms underlying human orofacial defects. , Dickinson AJ ., Semin Cell Dev Biol. March 1, 2016; 51 54-63.
Budgett's frog (Lepidobatrachus laevis): A new amphibian embryo for developmental biology. , Amin NM , Womble M , Ledon-Rettig C, Hull M, Dickinson A , Nascone-Yoder N ., Dev Biol. September 15, 2015; 405 (2): 291-303.
The role of folate metabolism in orofacial development and clefting. , Wahl SE , Kennedy AE , Wyatt BH, Moore AD, Pridgen DE, Cherry AM, Mavila CB, Dickinson AJ ., Dev Biol. September 1, 2015; 405 (1): 108-22.
Quantification of orofacial phenotypes in Xenopus. , Kennedy AE , Dickinson AJ ., J Vis Exp. November 6, 2014; (93): e52062.
Retinoic acid induced-1 ( Rai1) regulates craniofacial and brain development in Xenopus. , Tahir R , Kennedy A , Elsea SH, Dickinson AJ ., Mech Dev. August 1, 2014; 133 91-104.
The extreme anterior domain is an essential craniofacial organizer acting through Kinin- Kallikrein signaling. , Jacox L, Sindelka R , Chen J , Rothman A, Dickinson A , Sive H ., Cell Rep. July 24, 2014; 8 (2): 596-609.
Quantitative analysis of orofacial development and median clefts in Xenopus laevis. , Kennedy AE , Dickinson AJ ., Anat Rec (Hoboken). May 1, 2014; 297 (5): 834-55.
Facial transplants in Xenopus laevis embryos. , Jacox LA, Dickinson AJ , Sive H ., J Vis Exp. March 26, 2014; (85):
Median facial clefts in Xenopus laevis: roles of retinoic acid signaling and homeobox genes. , Kennedy AE , Dickinson AJ ., Dev Biol. May 1, 2012; 365 (1): 229-40.
The Wnt antagonists Frzb-1 and Crescent locally regulate basement membrane dissolution in the developing primary mouth. , Dickinson AJ , Sive HL ., Development. April 1, 2009; 136 (7): 1071-81.
Positioning the extreme anterior in Xenopus: cement gland, primary mouth and anterior pituitary. , Dickinson A , Sive H ., Semin Cell Dev Biol. August 1, 2007; 18 (4): 525-33.
Development of the primary mouth in Xenopus laevis. , Dickinson AJ , Sive H ., Dev Biol. July 15, 2006; 295 (2): 700-13.
Identification of a BMP inhibitor-responsive promoter module required for expression of the early neural gene zic1. , Tropepe V , Li S, Dickinson A , Gamse JT, Sive HL ., Dev Biol. January 15, 2006; 289 (2): 517-29.