Papers associated with uqcc6 (and OMIM)

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	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.
	De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome., Ufartes R, Berger H, Till K, Salinas G, Sturm M, Altmüller J, Nürnberg P, Thiele H, Funke R, Apeshiotis N, Langen H, Wollnik B, Borchers A, Pauli S., Hum Genet. November 1, 2020; 139 (11): 1363-1379.
	Interplay of TRIM2 E3 Ubiquitin Ligase and ALIX/ESCRT Complex: Control of Developmental Plasticity During Early Neurogenesis., Lokapally A, Neuhaus H, Herfurth J, Hollemann T., Cells. July 20, 2020; 9 (7):
	Musculocontractural Ehlers-Danlos syndrome and neurocristopathies: dermatan sulfate is required for Xenopus neural crest cells to migrate and adhere to fibronectin., Gouignard N, Maccarana M, Strate I, von Stedingk K, Malmström A, Pera EM., Dis Model Mech. June 1, 2016; 9 (6): 607-20.
	Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis., Barnett C, Yazgan O, Kuo HC, Malakar S, Thomas T, Fitzgerald A, Harbour W, Henry JJ, Krebs JE., Mech Dev. January 1, 2012; 129 (9-12): 324-38.
	Expression of the gene encoding the beta-amyloid precursor protein APP in Xenopus laevis., van den Hurk WH, Bloemen M, Martens GJ., Brain Res Mol Brain Res. December 16, 2001; 97 (1): 13-20.
	Chloride dependence of hyperpolarization-activated chloride channel gates., Pusch M, Jordt SE, Stein V, Jentsch TJ., J Physiol. March 1, 1999; 515 ( Pt 2) 341-53.

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