| Search Results |
The H2A.Z and NuRD associated protein HMG20A controls early head and heart developmental transcription programs., Herchenröther A, Gossen S, Friedrich T, Reim A, Daus N, Diegmüller F, Leers J, Sani HM, Gerstner S, Schwarz L, Stellmacher I, Szymkowiak LV, Nist A, Stiewe T, Borggrefe T, Mann M, Mackay JP, Bartkuhn M, Borchers A, Lan J, Hake SB., Nat Commun. January 28, 2023; 14 (1): 472. 
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Development and metamorphosis in frogs deficient in the thyroid hormone transporter MCT8., Sterner ZR, Jabrah A, Shaidani NI, Horb ME, Dockery R, Paul B, Buchholz DR., Gen Comp Endocrinol. January 15, 2023; 331 114179.
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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, 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.
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Tissue-specific expression of carbohydrate sulfotransferases drives keratan sulfate biosynthesis in the notochord and otic vesicles of Xenopus embryos., Yasuoka Y., Front Cell Dev Biol. January 1, 2023; 11 957805.
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A CRISPR/Cas-Based Method for Precise DNA Integration in Xenopus laevis Oocytes Followed by Intracytoplasmic Sperm Injection (ICSI) Fertilization., Martin SA., Methods Mol Biol. January 1, 2023; 2633 131-143.
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CRISPR/Cas9 Gene Disruption Studies in F0 Xenopus Tadpoles: Understanding Development and Disease in the Frog., Abu-Daya A, Godwin A., Methods Mol Biol. January 1, 2023; 2633 111-130.
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CRISPR-Cas9-Based Functional Analysis in Amphibians: Xenopus laevis, Xenopus tropicalis, and Pleurodeles waltl., Suzuki M, Iida M, Hayashi T, Suzuki KT., Methods Mol Biol. January 1, 2023; 2637 341-357.
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An Efficient CRISPR-Cas9 Method to Knock Out MiRNA Expression in Xenopus Tropicalis., Godden AM, Antonaci M, Wheeler GN., Methods Mol Biol. January 1, 2023; 2630 231-241.
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Identification of novel genes including NAV2 associated with isolated tall stature., Weiss B, Ott T, Vick P, Lui JC, Roeth R, Vogel S, Waldmüller S, Hoffmann S, Baron J, Wit JM, Rappold GA., Front Endocrinol (Lausanne). January 1, 2023; 14 1258313.
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The G213D variant in Nav1.5 alters sodium current and causes an arrhythmogenic phenotype resulting in a multifocal ectopic Purkinje-related premature contraction phenotype in human-induced pluripotent stem cell-derived cardiomyocytes., Calloe K, Geryk M, Freude K, Treat JA, Vold VA, Frederiksen HRS, Broendberg AK, Frederiksen TC, Jensen HK, Cordeiro JM., Europace. December 9, 2022; 24 (12): 2015-2027.
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