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Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes. , Neal SJ, Rajasekaran A, Jusić N, Taylor L , Read M, Alfandari D , Alfandari D , Pignoni F, Moody SA ., J Exp Zool B Mol Dev Evol. October 13, 2023;
Zmym4 is required for early cranial gene expression and craniofacial cartilage formation. , Jourdeuil K, Neilson KM , Cousin H , Tavares ALP, Majumdar HD, Alfandari D , Alfandari D , Moody SA ., Front Cell Dev Biol. January 1, 2023; 11 1274788.
Hnf1b renal expression directed by a distal enhancer responsive to Pax8. , Goea L, Buisson I , Bello V, Eschstruth A, Paces-Fessy M, Le Bouffant R , Chesneau A, Cereghini S, Riou JF , Umbhauer M ., Sci Rep. November 19, 2022; 12 (1): 19921.
Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease. , Coppenrath K , Tavares ALP, Shaidani NI , Wlizla M , Moody SA , Horb M ., Genesis. December 1, 2021; 59 (12): e23453.
Mcrs1 interacts with Six1 to influence early craniofacial and otic development. , Neilson KM , Keer S, Bousquet N, Macrorie O, Majumdar HD, Kenyon KL , Alfandari D , Alfandari D , Moody SA ., Dev Biol. November 1, 2020; 467 (1-2): 39-50.
Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development. , Shah AM, Krohn P, Baxi AB, Tavares ALP, Sullivan CH, Chillakuru YR, Majumdar HD, Neilson KM , Moody SA ., Dis Model Mech. March 3, 2020; 13 (3):
Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development. , Neilson KM , Abbruzzesse G , Kenyon K , Bartolo V, Krohn P, Alfandari D , Alfandari D , Moody SA ., Dev Biol. January 15, 2017; 421 (2): 171-182.
Over-expression of atf4 in Xenopus embryos interferes with neurogenesis and eye formation. , Liu JT , Yang Y , Guo XG, Chen M, Ding HZ, Chen YL , Chen YL , Wang MR., Dongwuxue Yanjiu. October 1, 2011; 32 (5): 485-91.