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Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype. , Ambrosini E., Hum Mol Genet. September 15, 2014; 23 (18): 4875-86.
Multiple interactions between cytoplasmic domains regulate slow deactivation of Kv11.1 channels. , Ng CA., J Biol Chem. September 12, 2014; 289 (37): 25822-32.
Custos controls β-catenin to regulate head development during vertebrate embryogenesis. , Komiya Y., Proc Natl Acad Sci U S A. September 9, 2014; 111 (36): 13099-104.
Cystic fibrosis transmembrane conductance regulator ( CFTR) potentiators protect G551D but not ΔF508 CFTR from thermal instability. , Liu X., Biochemistry. September 9, 2014; 53 (35): 5613-8.
Overexpression of p49/ STRAP alters cellular cytoskeletal structure and gross anatomy in mice. , Zhang X., BMC Cell Biol. September 2, 2014; 15 32.
Bile acids increase the activity of the epithelial Na+ channel. , Wiemuth D., Pflugers Arch. September 1, 2014; 466 (9): 1725-33.
Anion permeation in calcium-activated chloride channels formed by TMEM16A from Xenopus tropicalis. , Reyes JP., Pflugers Arch. September 1, 2014; 466 (9): 1769-77.
Transcription factor AP2 epsilon ( Tfap2e) regulates neural crest specification in Xenopus. , Hong CS ., Dev Neurobiol. September 1, 2014; 74 (9): 894-906.
Spatiotemporal lipid profiling during early embryo development of Xenopus laevis using dynamic ToF-SIMS imaging. , Tian H ., J Lipid Res. September 1, 2014; 55 (9): 1970-80.
A single codon insertion in PICALM is associated with development of familial subvalvular aortic stenosis in Newfoundland dogs. , Stern JA., Hum Genet. September 1, 2014; 133 (9): 1139-48.
Berberine attenuates spontaneous action potentials in sinoatrial node cells and the currents of human HCN4 channels expressed in Xenopus laevis oocytes. , Chen H ., Mol Med Rep. September 1, 2014; 10 (3): 1576-82.
Lariat intronic RNAs in the cytoplasm of Xenopus tropicalis oocytes. , Talhouarne GJ ., RNA. September 1, 2014; 20 (9): 1476-87.
Inhibition of the intestinal sodium-coupled glucose transporter 1 ( SGLT1) by extracts and polyphenols from apple reduces postprandial blood glucose levels in mice and humans. , Schulze C., Mol Nutr Food Res. September 1, 2014; 58 (9): 1795-808.
Symmetry breakage in the vertebrate embryo: when does it happen and how does it work? , Blum M ., Dev Biol. September 1, 2014; 393 (1): 109-23.
A Novel Long-Acting Glucagon-Like Peptide-1 Agonist with Improved Efficacy in Insulin Secretion and β-Cell Growth. , Kim HY ., Endocrinol Metab (Seoul). September 1, 2014; 29 (3): 320-7.
The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish. , Young T., Development. September 1, 2014; 141 (18): 3505-16.
myomiR-dependent switching of BAF60 variant incorporation into Brg1 chromatin remodeling complexes during embryo myogenesis. , Goljanek-Whysall K., Development. September 1, 2014; 141 (17): 3378-87.
Early expression of aromatase and the membrane estrogen receptor GPER in neuromasts reveals a role for estrogens in the development of the frog lateral line system. , Hamilton CK., Gen Comp Endocrinol. September 1, 2014; 205 242-50.
Cloning the sterol carrier protein 2 genes of Japanese toad (Bufo japonicus formosus) and Chinese toad (Bufo gargarizans) and its tissue expression analysis. , Ji YC., Dongwuxue Yanjiu. September 1, 2014; 35 (5): 398-403.
MHC class I limits hippocampal synapse density by inhibiting neuronal insulin receptor signaling. , Dixon-Salazar TJ., J Neurosci. August 27, 2014; 34 (35): 11844-56.
Fast phasic release properties of dopamine studied with a channel biosensor. , Kress GJ., J Neurosci. August 27, 2014; 34 (35): 11792-802.
APTE: identification of indirect read-out A-DNA promoter elements in genomes. , Whitley DC., BMC Bioinformatics. August 26, 2014; 15 288.
Hierarchical molecular events driven by oocyte-specific factors lead to rapid and extensive reprogramming. , Jullien J ., Mol Cell. August 21, 2014; 55 (4): 524-36.
BRCA1 is a histone- H2A-specific ubiquitin ligase. , Kalb R., Cell Rep. August 21, 2014; 8 (4): 999-1005.
Cardiac arrhythmia induced by genetic silencing of 'funny' (f) channels is rescued by GIRK4 inactivation. , Mesirca P., Nat Commun. August 21, 2014; 5 4664.
cPKC regulates interphase nuclear size during Xenopus development. , Edens LJ., J Cell Biol. August 18, 2014; 206 (4): 473-83.
Clonal relationships impact neuronal tuning within a phylogenetically ancient vertebrate brain structure. , Muldal AM., Curr Biol. August 18, 2014; 24 (16): 1929-33.
Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus. , Roberts NA., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.
Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos. , Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
The XMAP215 family drives microtubule polymerization using a structurally diverse TOG array. , Fox JC., Mol Biol Cell. August 15, 2014; 25 (16): 2375-92.
Impaired liver function in Xenopus tropicalis exposed to benzo[a]pyrene: transcriptomic and metabolic evidence. , Regnault C., BMC Genomics. August 8, 2014; 15 666.
A tethered delivery mechanism explains the catalytic action of a microtubule polymerase. , Ayaz P., Elife. August 5, 2014; 3 e03069.
TPX2 levels modulate meiotic spindle size and architecture in Xenopus egg extracts. , Helmke KJ., J Cell Biol. August 4, 2014; 206 (3): 385-93.
A splice variant of the two-pore domain potassium channel TREK-1 with only one pore domain reduces the surface expression of full-length TREK-1 channels. , Rinné S., Pflugers Arch. August 1, 2014; 466 (8): 1559-70.
The role of voltage-gated calcium channels in neurotransmitter phenotype specification: Coexpression and functional analysis in Xenopus laevis. , Lewis BB ., J Comp Neurol. August 1, 2014; 522 (11): 2518-31.
Prolonged in vivo imaging of Xenopus laevis. , Hamilton PW., Dev Dyn. August 1, 2014; 243 (8): 1011-9.
CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance. , Schulz Y., Hum Genet. August 1, 2014; 133 (8): 997-1009.
Caging, but not air deprivation, slows tadpole growth and development in the amphibian Xenopus laevis. , Rose CS., J Exp Zool A Ecol Genet Physiol. August 1, 2014; 321 (7): 365-75.
Genomics, phylogeny and in silico analysis of mitochondrial glutathione S-transferase-kappa from the camel Camelus dromedarius. , Ataya FS., Res Vet Sci. August 1, 2014; 97 (1): 46-54.
Retinoic acid induced-1 ( Rai1) regulates craniofacial and brain development in Xenopus. , Tahir R ., Mech Dev. August 1, 2014; 133 91-104.
Upregulation of excitatory amino acid transporters by coexpression of Janus kinase 3. , Warsi J., J Membr Biol. August 1, 2014; 247 (8): 713-20.
Congenital heart disease protein 5 associates with CASZ1 to maintain myocardial tissue integrity. , Sojka S., Development. August 1, 2014; 141 (15): 3040-9.
Sirtuin inhibitor Ex-527 causes neural tube defects, ventral edema formations, and gastrointestinal malformations in Xenopus laevis embryos. , Ohata Y., Dev Growth Differ. August 1, 2014; 56 (6): 460-8.
Diverse functions of kindlin/fermitin proteins during embryonic development in Xenopus laevis. , Rozario T., Mech Dev. August 1, 2014; 133 203-17.
TPX2 knockdown suppressed hepatocellular carcinoma cell invasion via inactivating AKT signaling and inhibiting MMP2 and MMP9 expression. , Liu Q., Chin J Cancer Res. August 1, 2014; 26 (4): 410-7.
Controlling epithelial sodium channels with light using photoswitchable amilorides. , Schönberger M., Nat Chem. August 1, 2014; 6 (8): 712-9.
Simultaneous rather than ordered cleavage of two sites within the BMP4 prodomain leads to loss of ligand in mice. , Tilak A., Development. August 1, 2014; 141 (15): 3062-71.
Developmental hematopoiesis: ontogeny, genetic programming and conservation. , Ciau-Uitz A ., Exp Hematol. August 1, 2014; 42 (8): 669-83.
Gene regulatory networks governing lung specification. , Rankin SA , Rankin SA ., J Cell Biochem. August 1, 2014; 115 (8): 1343-50.
Disrupted coupling of gating charge displacement to Na+ current activation for DIIS4 mutations in hypokalemic periodic paralysis. , Mi W., J Gen Physiol. August 1, 2014; 144 (2): 137-45.