Papers associated with brain (and hcn2)

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	HCN2 channel-induced rescue of brain, eye, heart and gut teratogenesis caused by nicotine, ethanol and aberrant notch signalling., Pai VP., Wound Repair Regen. November 1, 2022; 30 (6): 681-706.
	The HCN domain is required for HCN channel cell-surface expression and couples voltage- and cAMP-dependent gating mechanisms., Wang ZJ., J Biol Chem. June 12, 2020; 295 (24): 8164-8173.
	HCN2 Channel-Induced Rescue of Brain Teratogenesis via Local and Long-Range Bioelectric Repair., Pai VP., Front Cell Neurosci. January 1, 2020; 14 136.
	cAMP binds to closed, inactivated, and open sea urchin HCN channels in a state-dependent manner., Idikuda V., J Gen Physiol. February 4, 2019; 151 (2): 200-213.
	The VAMP-associated protein VAPB is required for cardiac and neuronal pacemaker channel function., Silbernagel N., FASEB J. November 1, 2018; 32 (11): 6159-6173.
	All four subunits of HCN2 channels contribute to the activation gating in an additive but intricate manner., Sunkara MR., J Gen Physiol. September 3, 2018; 150 (9): 1261-1271.
	Minimal molecular determinants of isoform-specific differences in efficacy in the HCN channel family., Alvarez-Baron CP., J Gen Physiol. August 6, 2018; 150 (8): 1203-1213.
	Ligand binding and activation properties of the purified bacterial cyclic nucleotide-gated channel SthK., Schmidpeter PAM., J Gen Physiol. June 4, 2018; 150 (6): 821-834.
	Activation gating in HCN2 channels., Hummert S., PLoS Comput Biol. March 22, 2018; 14 (3): e1006045.
	HCN2 Rescues brain defects by enforcing endogenous voltage pre-patterns., Pai VP., Nat Commun. March 8, 2018; 9 (1): 998.
	Booting up the organism during development: Pre-behavioral functions of the vertebrate brain in guiding body morphogenesis., Herrera-Rincon C., Commun Integr Biol. February 15, 2018; 11 (1): e1433440.
	HCN4 ion channel function is required for early events that regulate anatomical left-right patterning in a nodal and lefty asymmetric gene expression-independent manner., Pai VP., Biol Open. October 15, 2017; 6 (10): 1445-1457.
	The brain is required for normal muscle and nerve patterning during early Xenopus development., Herrera-Rincon C., Nat Commun. September 25, 2017; 8 (1): 587.
	Gabapentin Modulates HCN4 Channel Voltage-Dependence., Tae HS., Front Pharmacol. May 26, 2017; 8 554.
	Coordinating heart morphogenesis: A novel role for hyperpolarization-activated cyclic nucleotide-gated (HCN) channels during cardiogenesis in Xenopus laevis., Pitcairn E., Commun Integr Biol. May 10, 2017; 10 (3): e1309488.
	An N-terminal deletion variant of HCN1 in the epileptic WAG/Rij strain modulates HCN current densities., Wemhöner K., Front Mol Neurosci. November 3, 2015; 8 63.
	HCN2 channels: a permanent open state and conductance changes., Pittoors F., J Membr Biol. February 1, 2015; 248 (1): 67-81.
	Binding of the auxiliary subunit TRIP8b to HCN channels shifts the mode of action of cAMP., Hu L., J Gen Physiol. December 1, 2013; 142 (6): 599-612.
	Flavonoid regulation of HCN2 channels., Carlson AE., J Biol Chem. November 15, 2013; 288 (46): 33136-45.
	Flavonoid regulation of EAG1 channels., Carlson AE., J Gen Physiol. March 1, 2013; 141 (3): 347-58.
	Protein kinase C activation inhibits rat and human hyperpolarization activated cyclic nucleotide gated channel (HCN)1--mediated current in mammalian cells., Reetz O., Cell Physiol Biochem. January 1, 2013; 31 (4-5): 532-41.
	The hyperpolarization-activated cyclic nucleotide-gated HCN2 channel transports ammonium in the distal nephron., Carrisoza-Gaytán R., Kidney Int. October 1, 2011; 80 (8): 832-40.
	Local anesthetic inhibits hyperpolarization-activated cationic currents., Meng QT., Mol Pharmacol. May 1, 2011; 79 (5): 866-73.
	Association with the auxiliary subunit PEX5R/Trip8b controls responsiveness of HCN channels to cAMP and adrenergic stimulation., Zolles G., Neuron. June 25, 2009; 62 (6): 814-25.
	Associated changes in HCN2 and HCN4 transcripts and I(f) pacemaker current in myocytes., Zhang Q., Biochim Biophys Acta. May 1, 2009; 1788 (5): 1138-47.
	Mode shifts in the voltage gating of the mouse and human HCN2 and HCN4 channels., Elinder F., J Physiol. September 1, 2006; 575 (Pt 2): 417-31.
	Suppression of ih contributes to propofol-induced inhibition of mouse cortical pyramidal neurons., Chen X., J Neurophysiol. December 1, 2005; 94 (6): 3872-83.
	Impairment of hyperpolarization-activated, cyclic nucleotide-gated channel function by the intravenous general anesthetic propofol., Cacheaux LP., J Pharmacol Exp Ther. November 1, 2005; 315 (2): 517-25.
	Tyrosine kinase inhibition differentially regulates heterologously expressed HCN channels., Yu HG., Pflugers Arch. January 1, 2004; 447 (4): 392-400.
	KCNE2 modulates current amplitudes and activation kinetics of HCN4: influence of KCNE family members on HCN4 currents., Decher N., Pflugers Arch. September 1, 2003; 446 (6): 633-40.
	Regulation of hyperpolarization-activated HCN channel gating and cAMP modulation due to interactions of COOH terminus and core transmembrane regions., Wang J., J Gen Physiol. September 1, 2001; 118 (3): 237-50.
	Properties of hyperpolarization-activated pacemaker current defined by coassembly of HCN1 and HCN2 subunits and basal modulation by cyclic nucleotide., Chen S., J Gen Physiol. May 1, 2001; 117 (5): 491-504.
	Functional heteromerization of HCN1 and HCN2 pacemaker channels., Ulens C., J Biol Chem. March 2, 2001; 276 (9): 6069-72.

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