Papers associated with skeletal element (and mmut)

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	Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome., Greenberg RS., Cell. September 5, 2019; 178 (6): 1421-1436.e24.
	SHH signaling directed by two oral epithelium-specific enhancers controls tooth and oral development., Sagai T., Sci Rep. October 11, 2017; 7 (1): 13004.
	A missense mutation accelerating the gating of the lysosomal Cl-/H+-exchanger ClC-7/Ostm1 causes osteopetrosis with gingival hamartomas in cattle., Sartelet A., Dis Model Mech. January 1, 2014; 7 (1): 119-28.
	Vertical signalling involves transmission of Hox information from gastrula mesoderm to neurectoderm., Bardine N., PLoS One. January 1, 2014; 9 (12): e115208.
	MCM2-7 form double hexamers at licensed origins in Xenopus egg extract., Gambus A., J Biol Chem. April 1, 2011; 286 (13): 11855-64.
	NARF, an nemo-like kinase (NLK)-associated ring finger protein regulates the ubiquitylation and degradation of T cell factor/lymphoid enhancer factor (TCF/LEF)., Yamada M., J Biol Chem. July 28, 2006; 281 (30): 20749-20760.
	Structural and functional role of the extracellular s5-p linker in the HERG potassium channel., Liu J., J Gen Physiol. November 1, 2002; 120 (5): 723-37.
	Autoregulation of Xvent-2B; direct interaction and functional cooperation of Xvent-2 and Smad1., Henningfeld KA., J Biol Chem. January 18, 2002; 277 (3): 2097-103.
	A mutation linked with Bartter's syndrome locks Kir 1.1a (ROMK1) channels in a closed state., Flagg TP., J Gen Physiol. November 1, 1999; 114 (5): 685-700.

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