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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., Am J Hum Genet. January 5, 2023; 110 (1): 71-91.
E-liquids and vanillin flavoring disrupts retinoic acid signaling and causes craniofacial defects in Xenopus embryos. , Dickinson AJG., Dev Biol. January 1, 2022; 481 14-29.
Bioelectric signaling: Reprogrammable circuits underlying embryogenesis, regeneration, and cancer. , Levin M ., Cell. April 15, 2021;
Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disorders. , Wyatt BH., Genesis. February 1, 2021; 59 (1-2): e23394.
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. , Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration. , Schwenty-Lara J., Hum Mol Genet. January 15, 2020; 29 (2): 305-319.
CALHM3 Is Essential for Rapid Ion Channel-Mediated Purinergic Neurotransmission of GPCR-Mediated Tastes. , Ma Z., Neuron. May 2, 2018; 98 (3): 547-561.e10.
Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans. , Lansdon LA., Genetics. January 1, 2018; 208 (1): 283-296.
Mouth development. , Chen J ., Wiley Interdiscip Rev Dev Biol. September 1, 2017; 6 (5):
In vitro models of cranial neural crest development toward toxicity tests: frog, mouse, and human. , Suga M., Oral Dis. July 1, 2017; 23 (5): 559-565.
Role of JNK during buccopharyngeal membrane perforation, the last step of embryonic mouth formation. , Houssin NS., Dev Dyn. February 1, 2017; 246 (2): 100-115.
Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome. , Devotta A., Dev Biol. July 15, 2016; 415 (2): 371-382.
The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery. , Toriyama M., Nat Genet. June 1, 2016; 48 (6): 648-56.
Using frogs faces to dissect the mechanisms underlying human orofacial defects. , Dickinson AJ ., Semin Cell Dev Biol. March 1, 2016; 51 54-63.
Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy. , Zaharieva IT., Brain. March 1, 2016; 139 (Pt 3): 674-91.
Genetics, Morphology, Advertisement Calls, and Historical Records Distinguish Six New Polyploid Species of African Clawed Frog (Xenopus, Pipidae) from West and Central Africa. , Evans BJ ., PLoS One. December 16, 2015; 10 (12): e0142823.
The role of folate metabolism in orofacial development and clefting. , Wahl SE ., Dev Biol. September 1, 2015; 405 (1): 108-22.
Spindle orientation processes in epithelial growth and organisation. , Panousopoulou E., Semin Cell Dev Biol. October 1, 2014; 34 124-32.
Quantitative analysis of orofacial development and median clefts in Xenopus laevis. , Kennedy AE ., Anat Rec (Hoboken). May 1, 2014; 297 (5): 834-55.
Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome. , Karpinski BA., Dis Model Mech. February 1, 2014; 7 (2): 245-57.
Median facial clefts in Xenopus laevis: roles of retinoic acid signaling and homeobox genes. , Kennedy AE ., Dev Biol. May 1, 2012; 365 (1): 229-40.
Hedgehog signalling in development of the secondary palate. , Cobourne MT., Front Oral Biol. January 1, 2012; 16 52-9.
Combinatorial roles for BMPs and Endothelin 1 in patterning the dorsal- ventral axis of the craniofacial skeleton. , Alexander C., Development. December 1, 2011; 138 (23): 5135-46.
Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice. , Rainger J., PLoS Genet. July 1, 2011; 7 (7): e1002114.
Sox9 function in craniofacial development and disease. , Lee YH , Lee YH ., Genesis. April 1, 2011; 49 (4): 200-8.
SPLUNC1 expression reduces surface levels of the epithelial sodium channel (ENaC) in Xenopus laevis oocytes. , Rollins BM., Channels (Austin). January 1, 2010; 4 (4): 255-9.
SPLUNC1 regulates airway surface liquid volume by protecting ENaC from proteolytic cleavage. , Garcia-Caballero A., Proc Natl Acad Sci U S A. July 7, 2009; 106 (27): 11412-7.
Maternal Interferon Regulatory Factor 6 is required for the differentiation of primary superficial epithelia in Danio and Xenopus embryos. , Sabel JL., Dev Biol. January 1, 2009; 325 (1): 249-62.
Tissue engineering in cleft palate and other congenital malformations. , Panetta NJ., Pediatr Res. May 1, 2008; 63 (5): 545-51.
Chemical rescue of cleft palate and midline defects in conditional GSK-3beta mice. , Liu KJ , Liu KJ ., Nature. March 1, 2007; 446 (7131): 79-82.
Cholesterol homeostasis in development: the role of Xenopus 7-dehydrocholesterol reductase ( Xdhcr7) in neural development. , Tadjuidje E ., Dev Dyn. August 1, 2006; 235 (8): 2095-110.
Identification and developmental expression analysis of a novel homeobox gene closely linked to the mouse Twirler mutation. , Liu H ., Gene Expr Patterns. August 1, 2006; 6 (6): 632-6.
Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test. , Juriloff DM., Birth Defects Res A Clin Mol Teratol. August 1, 2006; 76 (8): 574-9.
Loss of the Sall3 gene leads to palate deficiency, abnormalities in cranial nerves, and perinatal lethality. , Parrish M., Mol Cell Biol. August 1, 2004; 24 (16): 7102-12.
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features. , Roessler E., Proc Natl Acad Sci U S A. November 11, 2003; 100 (23): 13424-9.
Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. , Jezewski PA., J Med Genet. June 1, 2003; 40 (6): 399-407.
A new member of the spalt like zinc finger protein family, Msal-3, is expressed in the CNS and sites of epithelial/mesenchymal interaction. , Ott T., Mech Dev. March 1, 2001; 101 (1-2): 203-7.
Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development. , Mo R., Development. January 1, 1997; 124 (1): 113-23.
Multiple defects and perinatal death in mice deficient in follistatin. , Matzuk MM., Nature. March 23, 1995; 374 (6520): 360-3.
Functional analysis of activins during mammalian development. , Matzuk MM., Nature. March 23, 1995; 374 (6520): 354-6.
Endogenous distribution of retinoids during normal development and teratogenesis in the mouse embryo. , Horton C., Dev Dyn. March 1, 1995; 202 (3): 312-23.
Calcium-binding proteins in chemoreceptors of Xenopus laevis. , Kerschbaum HH., Tissue Cell. January 1, 1992; 24 (5): 719-24.
Hyaluronan as a propellant for epithelial movement: the development of semicircular canals in the inner ear of Xenopus. , Haddon CM., Development. June 1, 1991; 112 (2): 541-50.
Development and ciliation of the palate in two frogs, Bombina and Xenopus; a comparative study. , LeCluyse EL., Tissue Cell. January 1, 1985; 17 (6): 853-64.