Papers associated with brain (and kcnq2)

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	A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.
	De novo pathogenic variants in neuronal differentiation factor 2 (NEUROD2) cause a form of early infantile epileptic encephalopathy., Sega AG., J Med Genet. February 1, 2019; 56 (2): 113-122.
	The KCNQ5 potassium channel mediates a component of the afterhyperpolarization current in mouse hippocampus., Tzingounis AV., Proc Natl Acad Sci U S A. June 1, 2010; 107 (22): 10232-7.
	Selective interaction of syntaxin 1A with KCNQ2: possible implications for specific modulation of presynaptic activity., Regev N., PLoS One. August 13, 2009; 4 (8): e6586.
	The role of S4 charges in voltage-dependent and voltage-independent KCNQ1 potassium channel complexes., Panaghie G., J Gen Physiol. February 1, 2007; 129 (2): 121-33.
	A spontaneous mutation involving Kcnq2 (Kv7.2) reduces M-current density and spike frequency adaptation in mouse CA1 neurons., Otto JF., J Neurosci. February 15, 2006; 26 (7): 2053-9.
	Conditional transgenic suppression of M channels in mouse brain reveals functions in neuronal excitability, resonance and behavior., Peters HC., Nat Neurosci. January 1, 2005; 8 (1): 51-60.
	Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2., Dedek K., Epilepsy Res. April 1, 2003; 54 (1): 21-7.
	Cloning and functional expression of rKCNQ2 K(+) channel from rat brain., Jow F., Brain Res Mol Brain Res. September 15, 2000; 80 (2): 269-78.
	Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+ channels involved in epilepsy., Schwake M., J Biol Chem. May 5, 2000; 275 (18): 13343-8.
	Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy., Schroeder BC., Nature. December 17, 1998; 396 (6712): 687-90.
	Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy., Yang WP., J Biol Chem. July 31, 1998; 273 (31): 19419-23.
	A potassium channel mutation in neonatal human epilepsy., Biervert C., Science. January 16, 1998; 279 (5349): 403-6.

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