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Ablation of connexin43 in smooth muscle cells of the mouse intestine: functional insights into physiology and morphology.
- Published in:
- Cell & Tissue Research, 2007, v. 327, n. 2, p. 333, doi. 10.1007/s00441-006-0281-6
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- Article
Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression.
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- Human Genetics, 2002, v. 111, n. 2, p. 190, doi. 10.1007/s00439-002-0750-2
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- Publication type:
- Article
Involvement of the Cytoplasmic C-Terminal Domain of Connexin43 in Neuronal Migration.
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- Journal of Neuroscience, 2009, v. 29, n. 7, p. 2009, doi. 10.1523/JNEUROSCI.5025-08.2009
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- Article
A Central Role of Connexin 43 in Hypoxic Preconditioning.
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- Journal of Neuroscience, 2008, v. 28, n. 3, p. 681, doi. 10.1523/JNEUROSCI.3827-07.2008
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- Article
The Impact of Astrocytic Gap Junctional Coupling on Potassium Buffering in the Hippocampus.
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- Journal of Neuroscience, 2006, v. 26, n. 20, p. 5438, doi. 10.1523/JNEUROSCI.0037-06.2006
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- Publication type:
- Article
Transgenic Expression of Human Connexin32 in Myelinating Schwann Cells Prevents Demyelination in Connexin32-Null Mice.
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- Journal of Neuroscience, 2005, v. 25, n. 6, p. 1550, doi. 10.1523/JNEUROSCI.3082-04.2005
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- Publication type:
- Article
Deletion of Connexin45 in Mouse Retinal Neurons Disrupts the Rod/Cone Signaling Pathway between AII Amacrine and ON Cone Bipolar Cells and Leads to Impaired Visual Transmission.
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- Journal of Neuroscience, 2005, v. 25, n. 3, p. 566, doi. 10.1523/JNEUROSCI.3232-04.2005
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- Article
Expression of Connexin36 in Cone Pedicles and OFF-Cone Bipolar Cells of the Mouse Retina.
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- Journal of Neuroscience, 2004, v. 24, n. 13, p. 3325, doi. 10.1523/JNEUROSCI.5598-03.2004
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- Publication type:
- Article
Ceramide synthase 4 deficiency in mice causes lipid alterations in sebum and results in alopecia.
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- Biochemical Journal, 2014, v. 461, n. 1, p. 147, doi. 10.1042/BJ20131242
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- Article
Physiologic regulation of heart rate and blood pressure involves connexin 36-containing gap junctions.
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- FASEB Journal, 2017, v. 31, n. 9, p. 3966, doi. 10.1096/fj.201600919RR
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- Article
Dual reporter approaches for identification of Cre efficacy and astrocyte heterogeneity.
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- FASEB Journal, 2012, v. 26, n. 11, p. 4576, doi. 10.1096/fj.12-207183
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- Publication type:
- Article
Connexin-43 upregulation in micrometastases and tumor vasculature and its role in tumor cell attachment to pulmonary endothelium.
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- BMC Medicine, 2008, v. 6, p. 1, doi. 10.1186/1741-7015-6-20
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- Publication type:
- Article
Quantified CSF antibody reactivity against myelin in multiple sclerosis.
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- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 12, p. 1116, doi. 10.1002/acn3.264
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- Publication type:
- Article
Correction to: Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice.
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- 2018
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- Correction Notice
Defective ceramide synthases in mice cause reduced amplitudes in electroretinograms and altered sphingolipid composition in retina and cornea.
- Published in:
- European Journal of Neuroscience, 2016, v. 44, n. 1, p. 1700, doi. 10.1111/ejn.13260
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- Publication type:
- Article
A novel type of interplexiform amacrine cell in the mouse retina.
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- European Journal of Neuroscience, 2009, v. 30, n. 2, p. 217, doi. 10.1111/j.1460-9568.2009.06808.x
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- Publication type:
- Article
Connexin32-null mice develop demyelinating peripheral neuropathy.
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- Glia, 1998, v. 24, n. 1, p. 8, doi. 10.1002/(SICI)1098-1136(199809)24:1<8::AID-GLIA2>3.0.CO;2-3
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- Publication type:
- Article
Cardiac Conduction Abnormalities in Mice Lacking the Gap Junction Protein Connexin40.
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- Journal of Cardiovascular Electrophysiology, 1999, v. 10, n. 10, p. 1380, doi. 10.1111/j.1540-8167.1999.tb00194.x
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- Publication type:
- Article
Exacerbation of experimental autoimmune encephalomyelitis in ceramide synthase 6 knockout mice is associated with enhanced activation/migration of neutrophils.
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- Immunology & Cell Biology, 2015, v. 93, n. 9, p. 825, doi. 10.1038/icb.2015.47
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- Publication type:
- Article
Ceramide synthase 2 facilitates S1P-dependent egress of thymocytes into the circulation in mice.
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- European Journal of Immunology, 2017, v. 47, n. 4, p. 677, doi. 10.1002/eji.201646623
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- Article
Extracellular Ca<sup>2+</sup> Acts as a Mediator of Communication from Neurons to Glia.
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- Science Signaling, 2012, v. 5, n. 208, p. 1, doi. 10.1126/scisignal.2002160
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- Article
Fast skeletal myofibers of mdx mouse, model of Duchenne muscular dystrophy, express connexin hemichannels that lead to apoptosis.
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- Cellular & Molecular Life Sciences, 2016, v. 73, n. 13, p. 2583, doi. 10.1007/s00018-016-2132-2
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- Article
Expression and modulation of connexin30.2, a novel gap junction protein in the mouse retina.
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- Visual Neuroscience, 2010, v. 27, n. 3/4, p. 91, doi. 10.1017/S0952523810000131
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- Article
Subcellular distribution of connexin45 in OFF bipolar cells of the mouse retina.
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- Journal of Comparative Neurology, 2011, v. 519, n. 3, p. 433, doi. 10.1002/cne.22526
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- Article
Expression patterns of connexin genes in mouse retina.
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- Journal of Comparative Neurology, 2000, v. 425, n. 2, p. 193, doi. 10.1002/1096-9861(20000918)425:2<193::AID-CNE3>3.0.CO;2-N
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- Article
Altered epidermal lipid processing and calcium distribution in the KID syndrome mouse model Cx26S17F.
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- FEBS Letters, 2015, v. 589, n. 15, p. 1904, doi. 10.1016/j.febslet.2015.05.047
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- Article
The Clouston syndrome mutation connexin30 A88V leads to hyperproliferation of sebaceous glands and hearing impairments in mice.
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- FEBS Letters, 2014, v. 588, n. 9, p. 1795, doi. 10.1016/j.febslet.2014.03.040
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- Publication type:
- Article
Altered Dye Diffusion and Upregulation of Connexin37 in Mouse Aortic Endothelium Deficient in Connexin40.
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- Journal of Vascular Research, 2002, v. 39, n. 2, p. 160, doi. 10.1159/000057764
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- Publication type:
- Article
Developmental regulation of connexin 40 gene expression in mouse heart correlates with the differentiation of the conduction system.
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- Developmental Dynamics, 1995, v. 204, n. 4, p. 358, doi. 10.1002/aja.1002040403
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- Article
The electrical behaviour of rat connexin46 gap junction channels expressed in transfected HeLa cells.
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- Pflügers Archiv: European Journal of Physiology, 2003, v. 446, n. 6, p. 714, doi. 10.1007/s00424-003-1129-5
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- Article
Dilated bile canaliculi and attenuated decrease of nerve-dependent bile secretion in connexin32-deficient mouse liver.
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- Pflügers Archiv: European Journal of Physiology, 2001, v. 442, n. 6, p. 961, doi. 10.1007/s004240100623
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- Publication type:
- Article
Connexin hemichannel-mediated CO<sub>2</sub>-dependent release of ATP in the medulla oblongata contributes to central respiratory chemosensitivity.
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- Journal of Physiology, 2010, v. 588, n. 20, p. 3901, doi. 10.1113/jphysiol.2010.192088
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- Article
Gating, permselectivity and pH-dependent modulation of channels formed by connexin57, a major connexin of horizontal cells in the mouse retina.
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- Journal of Physiology, 2009, v. 587, n. 13, p. 3251, doi. 10.1113/jphysiol.2009.171496
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- Article
Loss of ceramide synthase 3 causes lethal skin barrier disruption.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 586, doi. 10.1093/hmg/ddr494
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- Article
The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis–ichthyosis–deafness syndrome.
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- Human Molecular Genetics, 2011, v. 20, n. 1, p. 28, doi. 10.1093/hmg/ddq429
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- Publication type:
- Article
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.
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- Human Molecular Genetics, 2010, v. 19, n. 24, p. 4759, doi. 10.1093/hmg/ddq402
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- Publication type:
- Article
Loss of connexin43-mediated gap junctional coupling in the mesenchyme of limb buds leads to altered expression of morphogens in mice.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2899, doi. 10.1093/hmg/ddp227
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- Article
The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.
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- Human Molecular Genetics, 2008, v. 17, n. 4, p. 539, doi. 10.1093/hmg/ddm329
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- Publication type:
- Article
The Connexin31 F137L mutant mouse as a model for the human skin disease Erythrokeratodermia variabilis (EKV).
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- Human Molecular Genetics, 2007, v. 16, n. 10, p. 1216, doi. 10.1093/hmg/ddm068
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- Publication type:
- Article
Expression of Cx26, Cx32 AND Cx43 gap junction proteins in normal and neoplastic human tissues.
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- International Journal of Cancer, 1992, v. 51, n. 4, p. 522, doi. 10.1002/ijc.2910510404
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- Publication type:
- Article
Cell-Specific Cre Recombinase Expression Allows Selective Ablation of Glutamate Receptors from Mouse Horizontal Cells.
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- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0083076
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- Article
Connexin45 Is Expressed in Vascular Smooth Muscle but Its Function Remains Elusive.
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- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0042287
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- Article
Ganglion Cell Adaptability: Does the Coupling of Horizontal Cells Play a Role?
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- PLoS ONE, 2008, v. 3, n. 3, p. 1, doi. 10.1371/journal.pone.0001714
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- Article
Connexin47 Protein Phosphorylation and Stability in Oligodendrocytes Depend on Expression of Connexin43 Protein in Astrocytes to Olfaction.
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- Journal of Neuroscience, 2013, v. 33, n. 18, p. 7985, doi. 10.1523/JNEUROSCI.5874-12.2013
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- Article
Ablation of Retinal Horizontal Cells from Adult Mice Leads to Rod Degeneration and Remodeling in the Outer Retina.
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- Journal of Neuroscience, 2012, v. 32, n. 31, p. 10713, doi. 10.1523/JNEUROSCI.0442-12.2012
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- Article
Panglial Gap Junctional Communication is Essential for Maintenance of Myelin in the CNS.
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- Journal of Neuroscience, 2012, v. 32, n. 22, p. 7499, doi. 10.1523/JNEUROSCI.0392-12.2012
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- Article
The Role of Neuronal Connexins 36 and 45 in Shaping Spontaneous Firing Patterns in the Developing Retina.
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- Journal of Neuroscience, 2011, v. 31, n. 27, p. 9998, doi. 10.1523/JNEUROSCI.5640-10.2011
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- Article
Expression of connexin genes in the human retina.
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- 2010
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- Publication type:
- journal article
Expression of connexin genes in the human retina.
- Published in:
- BMC Ophthalmology, 2010, v. 10, p. 27, doi. 10.1186/1471-2415-10-27
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- Article
Pathologic and Phenotypic Alterations in a Mouse Expressing a Connexin47 Missense Mutation That Causes Pelizaeus-Merzbacher--Like Disease in Humans.
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- PLoS Genetics, 2011, v. 7, n. 7, p. 1, doi. 10.1371/journal.pgen.1002146
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- Article