Connexins, Connexons, and Intercellular Communication, Annual Review of Biochemistry, vol.65, issue.1, pp.475-502, 1996. ,
DOI : 10.1146/annurev.bi.65.070196.002355
The gap junction cellular internet: connexin hemichannels enter the signalling limelight, Biochemical Journal, vol.397, issue.1, pp.1-14, 2006. ,
DOI : 10.1042/BJ20060175
Beyond the gap: functions of unpaired connexon channels, Nature Reviews Molecular Cell Biology, vol.4, issue.4, pp.285-94, 2003. ,
DOI : 10.1038/nrm1072
Heterotypic gap junction channel formation between heteromeric and homomeric Cx40 and Cx43 connexons, Am J Physiol Cell Physiol, vol.281, pp.1559-67, 2001. ,
Formation of Heterotypic Gap Junction Channels by Connexins 40 and 43, Circulation Research, vol.86, issue.2, pp.42-51, 2000. ,
DOI : 10.1161/01.RES.86.2.e42
Permeability of homotypic and heterotypic gap junction channels formed of cardiac connexins mCx30.2, Cx40, Cx43, and Cx45, AJP: Heart and Circulatory Physiology, vol.293, issue.3, pp.1729-1765, 2007. ,
DOI : 10.1152/ajpheart.00234.2007
Function of the voltage gate of gap junction channels: Selective exclusion of molecules, Proceedings of the National Academy of Sciences, vol.99, issue.2, pp.697-702, 2002. ,
DOI : 10.1073/pnas.022324499
Connexin channel permeability to cytoplasmic molecules, Progress in Biophysics and Molecular Biology, vol.94, issue.1-2, pp.120-163, 2007. ,
DOI : 10.1016/j.pbiomolbio.2007.03.011
Gap junctional channels are parts of multiprotein complexes, Biochimica et Biophysica Acta (BBA) - Biomembranes, vol.1818, issue.8, pp.1844-65, 2012. ,
DOI : 10.1016/j.bbamem.2011.12.009
Connexin43 interacts with ??arrestin: A pre-requisite for osteoblast survival induced by parathyroid hormone, Journal of Cellular Biochemistry, vol.144, issue.10, pp.2920-2950, 2011. ,
DOI : 10.1002/jcb.23208
Interaction of connexin43 and protein kinase C-delta during FGF2 signaling, BMC Biochemistry, vol.11, issue.1, p.14, 2010. ,
DOI : 10.1186/1471-2091-11-14
Mechanical stress-activated integrin ??5??1 induces opening of connexin 43 hemichannels, Proceedings of the National Academy of Sciences, vol.109, issue.9, pp.3359-64, 2012. ,
DOI : 10.1073/pnas.1115967109
Direct Regulation of Osteocytic Connexin 43 Hemichannels through AKT Kinase Activated by Mechanical Stimulation, Journal of Biological Chemistry, vol.289, issue.15, pp.10582-91, 2014. ,
DOI : 10.1074/jbc.M114.550608
Transduction of Cell Survival Signals by Connexin-43 Hemichannels, Journal of Biological Chemistry, vol.277, issue.10, pp.8648-57, 2002. ,
DOI : 10.1074/jbc.M108625200
An intact connexin43 is required to enhance signaling and gene expression in osteoblast-like cells, Journal of Cellular Biochemistry, vol.6, issue.11, pp.2542-50, 2013. ,
DOI : 10.1002/jcb.24603
Cardiac malformation in neonatal mice lacking connexin43, Science, vol.267, issue.5205, pp.1831-1835, 1995. ,
DOI : 10.1126/science.7892609
Connexin43 Deficiency Causes Delayed Ossification, Craniofacial Abnormalities, and Osteoblast Dysfunction, The Journal of Cell Biology, vol.114, issue.4, pp.931-975, 2000. ,
DOI : 10.1359/jbmr.1998.13.2.218
Delayed Osteoblastic Differentiation and Bone Development in Cx43 Knockout Mice, Toxicologic Pathology, vol.114, issue.7, pp.1046-55, 2011. ,
DOI : 10.1006/meth.2001.1262
Osteoblast connexin43 modulates skeletal architecture by regulating both arms of bone remodeling, Molecular Biology of the Cell, vol.22, issue.8, pp.1240-51, 2011. ,
DOI : 10.1091/mbc.E10-07-0571
Low peak bone mass and attenuated anabolic response to parathyroid hormone in mice with an osteoblast-specific deletion of connexin43, Journal of Cell Science, vol.119, issue.20, pp.4187-98, 2006. ,
DOI : 10.1242/jcs.03162
High Bone Mass in Mice Lacking Cx37 Because of Defective Osteoclast Differentiation, Journal of Biological Chemistry, vol.289, issue.12, pp.8508-8528, 2014. ,
DOI : 10.1074/jbc.M113.529735
Connexins and pannexins in the skeleton: gap junctions, hemichannels and more, Cellular and Molecular Life Sciences, vol.193, issue.Pt 2, pp.2853-67, 2015. ,
DOI : 10.1007/s00018-015-1963-6
Deletion of Connexin43 in Osteoblasts/Osteocytes Leads to Impaired Muscle Formation in Mice, Journal of Bone and Mineral Research, vol.89, issue.Pt 1, pp.596-605, 2014. ,
DOI : 10.1002/jbmr.2389
Connexin 43 Is Required for the Anti-Apoptotic Effect of Bisphosphonates on Osteocytes and Osteoblasts In Vivo, Journal of Bone and Mineral Research, vol.22, issue.11, pp.1712-1733, 2008. ,
DOI : 10.1093/hmg/ddm329
Enhanced Osteoclastic Resorption and Responsiveness to Mechanical Load in Gap Junction Deficient Bone, PLoS ONE, vol.102, issue.8, p.23516, 2011. ,
DOI : 10.1371/journal.pone.0023516.t001
Cell autonomous requirement of connexin 43 for osteocyte survival: Consequences for endocortical resorption and periosteal bone formation, Journal of Bone and Mineral Research, vol.133, issue.2, pp.374-89, 2012. ,
DOI : 10.1002/jbmr.548
Evidence for the role of connexin 43-mediated intercellular communication in the process of intracortical bone resorption via osteocytic osteolysis, BMC Musculoskeletal Disorders, vol.24, issue.5, p.122, 2014. ,
DOI : 10.1371/journal.pone.0033179
The amazing osteocyte, Journal of Bone and Mineral Research, vol.58, issue.(suppl1), pp.229-267, 2011. ,
DOI : 10.1002/jbmr.320
Connexin 43 Channels Are Essential for Normal Bone Structure and Osteocyte Viability, Journal of Bone and Mineral Research, vol.292, issue.2, pp.550-62, 2015. ,
DOI : 10.1002/jbmr.2374
Osteoblast and osteocyte-specific loss of Connexin43 results in delayed bone formation and healing during murine fracture healing, Journal of Orthopaedic Research, vol.10, issue.355 Suppl, pp.147-54, 2013. ,
DOI : 10.1002/jor.22178
Aged Male Rats Regenerate Cortical Bone with Reduced Osteocyte Density and Reduced Secretion of Nitric Oxide After Mechanical Stimulation, Calcified Tissue International, vol.30, issue.1, pp.484-94, 2014. ,
DOI : 10.1007/s00223-013-9832-5
Connexin 43 as a signaling platform for increasing the volume and spatial distribution of regenerated tissue, Proceedings of the National Academy of Sciences, vol.106, issue.32, pp.13219-13243, 2009. ,
DOI : 10.1073/pnas.0902622106
Cell communication and tissue engineering, Communicative & Integrative Biology, vol.3, issue.1, pp.53-59, 2010. ,
DOI : 10.4161/cib.3.1.9863
Cell-to-cell communication between osteogenic and endothelial lineages: implications for tissue engineering, Trends in Biotechnology, vol.27, issue.10, pp.562-71, 2009. ,
DOI : 10.1016/j.tibtech.2009.07.001
Cell interactions between human progenitor-derived endothelial cells and human mesenchymal stem cells in a three-dimensional macroporous polysaccharide-based scaffold promote osteogenesis, Acta Biomaterialia, vol.9, issue.9, pp.8200-8213, 2013. ,
DOI : 10.1016/j.actbio.2013.05.025
Osteoinductivity of calcium phosphate mediated by connexin 43, Biomaterials, vol.34, issue.15, pp.3763-74, 2013. ,
DOI : 10.1016/j.biomaterials.2013.01.095
Connexin43 carboxyl-terminal peptides reduce scar progenitor and promote regenerative healing following skin wounding, Regenerative Medicine, vol.4, issue.2, pp.205-228, 2009. ,
DOI : 10.2217/17460751.4.2.205
A synthetic connexin 43 mimetic peptide augments corneal wound healing, Experimental Eye Research, vol.115, pp.178-88, 2013. ,
DOI : 10.1016/j.exer.2013.07.001
Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia, The American Journal of Human Genetics, vol.72, issue.2, pp.408-426, 2003. ,
DOI : 10.1086/346090
(Connexin 43) Mutation Causing Oculodentodigital Dysplasia Associated to Uncommon Features, Ophthalmic Genetics, vol.9, issue.1, pp.198-202, 2007. ,
DOI : 10.1001/archopht.123.10.1422
Variable expression of neurological phenotype in autosomal recessive oculodentodigital dysplasia of two sibs and review of the literature, European Journal of Pediatrics, vol.75, issue.7, pp.341-346, 2008. ,
DOI : 10.1007/s00431-007-0468-1
A homozygousGJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype, Human Mutation, vol.23, issue.3, p.286, 2004. ,
DOI : 10.1002/humu.9220
Neurological manifestations of the oculodentodigital dysplasia syndrome, Journal of Neurology, vol.249, issue.5, pp.584-95, 2002. ,
DOI : 10.1007/s004150200068
Lobar Distribution of Changes in Gray Matter and White Matter in Memory Clinic Patients: Detected Using Magnetization Transfer Imaging, American Journal of Neuroradiology, vol.28, issue.10, pp.1938-1980, 2007. ,
DOI : 10.3174/ajnr.A0687
Skin changes in oculo-dento-digital dysplasia are correlated with C-terminal truncations of connexin 43, American Journal of Medical Genetics Part A, vol.132, issue.4, pp.360-363, 2007. ,
DOI : 10.1002/ajmg.a.31558
Oculo-dento-digital dysplasia: Lack of genotype???phenotype correlation for GJA1 mutations and usefulness of neuro-imaging, European Journal of Medical Genetics, vol.53, issue.1, pp.19-22, 2010. ,
DOI : 10.1016/j.ejmg.2009.08.007
URL : https://hal.archives-ouvertes.fr/hal-00628409
causing oculodentodigital syndrome and primary lymphoedema in a three generation family, Clinical Genetics, vol.1131, issue.4, pp.378-81, 2013. ,
DOI : 10.1111/cge.12158
A case of oculodentodigital dysplasia syndrome with novel GJA1 gene mutation, Japanese Journal of Ophthalmology, vol.17, issue.5, pp.541-546, 2009. ,
DOI : 10.1007/s10384-009-0711-6
Oculodentodigital Dysplasia, Archives of Ophthalmology, vol.129, issue.6, pp.781-785, 2011. ,
DOI : 10.1001/archophthalmol.2011.113
A Novel GJA1 Mutation in Oculodentodigital Dysplasia with Progressive Spastic Paraplegia and Sensory Deficits, Internal Medicine, vol.51, issue.1, pp.93-101, 2012. ,
DOI : 10.2169/internalmedicine.51.5770
Cause Oculodentodigital syndrome, Journal of Dental Research, vol.87, issue.11, pp.1021-1027, 2008. ,
DOI : 10.1177/154405910808701108
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD), European Journal of Medical Genetics, vol.48, issue.4, pp.377-87, 2005. ,
DOI : 10.1016/j.ejmg.2005.05.003
Novel Connexin 43 (GJA1) mutation causes oculo-dento-digital dysplasia with curly hair, American Journal of Medical Genetics, vol.193, issue.2, pp.152-159, 2004. ,
DOI : 10.1002/ajmg.a.20614
Oculodentodigital dysplasia. A case report, Minerva Stomatol, vol.54, pp.453-462, 2005. ,
Congenital heart defects in oculodentodigital dysplasia: Report of two cases, American Journal of Medical Genetics Part A, vol.53, issue.12, pp.3150-3154, 2013. ,
DOI : 10.1002/ajmg.a.36159
Three novel GJA1 missense substitutions resulting in oculo-dento-digital dysplasia (ODDD) ??? Further extension of the mutational spectrum, Gene, vol.539, issue.1, pp.157-61, 2014. ,
DOI : 10.1016/j.gene.2014.01.066
A novelGJA1 missense mutation in a Polish child with oculodentodigital dysplasia, Journal of Applied Genetics, vol.24, issue.3, pp.297-306, 2009. ,
DOI : 10.1007/BF03195687
Bigenic connexin mutations in a patient with hidrotic ectodermal dysplasia, Eur J Dermatol, vol.15, pp.75-84, 2005. ,
A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis, Eur J Dermatol, vol.16, pp.241-246, 2006. ,
Syndromic and non-syndromic disease-linked Cx43 mutations, FEBS Letters, vol.386, issue.8, pp.1339-1387, 2014. ,
DOI : 10.1016/j.febslet.2013.12.022
mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype, Human Mutation, vol.16, issue.Pt 3, pp.724-757, 2009. ,
DOI : 10.1002/humu.20958
Letter to the editor: Novel GJA1 mutation in oculodentodigital dysplasia, Am J Med Genet A, vol.139, pp.48-57, 2005. ,
Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly, Journal of Medical Genetics, vol.41, issue.1, pp.60-67, 2004. ,
DOI : 10.1136/jmg.2003.012005
A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma, Am J Med Genet A, vol.132, pp.171-175, 2005. ,
A Novel Mutation in the GJA1 Gene in a Family With Oculodentodigital Dysplasia, Archives of Ophthalmology, vol.123, issue.10, pp.1422-1428, 2005. ,
DOI : 10.1001/archopht.123.10.1422
Clinical and genetic variability of oculodentodigital dysplasia, Clinical Genetics, vol.119, issue.3, pp.71-73, 2006. ,
DOI : 10.1111/j.1399-0004.2006.00631.x
A Novel Autosomal Recessive GJA1 Missense Mutation Linked to Craniometaphyseal Dysplasia, PLoS ONE, vol.18, issue.8, p.73576, 2013. ,
DOI : 10.1371/journal.pone.0073576.s001
Connexin43 Mutation Causes Heterogeneous Gap Junction Loss and Sudden Infant Death, Circulation, vol.125, issue.3, pp.474-81, 2012. ,
DOI : 10.1161/CIRCULATIONAHA.111.057224
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome, Journal of Medical Genetics, vol.43, issue.7, p.37, 2006. ,
DOI : 10.1136/jmg.2005.037655
Myogenic bladder defects in mouse models of human oculodentodigital dysplasia, Biochemical Journal, vol.6, issue.3, pp.441-450, 2014. ,
DOI : 10.1152/ajpcell.00122.2007
Gap junction remodeling and cardiac arrhythmogenesis in a murine model of oculodentodigital dysplasia, Proceedings of the National Academy of Sciences, vol.104, issue.51, pp.20512-20518, 2007. ,
DOI : 10.1073/pnas.0705472105
The severity of mammary gland developmental defects is linked to the overall functional status of Cx43 as revealed by genetically modified mice, Biochemical Journal, vol.6, issue.2, pp.401-414, 2013. ,
DOI : 10.1126/science.7892609
Functional Characterization of Connexin43 Mutations Found in Patients With Oculodentodigital Dysplasia, Circulation Research, vol.96, issue.10, pp.83-91, 2005. ,
DOI : 10.1161/01.RES.0000168369.79972.d2
The potency of the fs260 connexin43 mutant to impair keratinocyte differentiation is distinct from other disease-linked connexin43 mutants, Biochemical Journal, vol.45, issue.3, pp.473-83, 2010. ,
DOI : 10.1111/1523-1747.ep12616154
Functional Characterization of a GJA1 Frameshift Mutation Causing Oculodentodigital Dysplasia and Palmoplantar Keratoderma, Journal of Biological Chemistry, vol.281, issue.42, pp.31801-31812, 2006. ,
DOI : 10.1074/jbc.M605961200
Some Oculodentodigital Dysplasia-Associated Cx43 Mutations Cause Increased Hemichannel Activity in Addition to Deficient Gap Junction Channels, Journal of Membrane Biology, vol.148, issue.1-3, pp.9-17, 2007. ,
DOI : 10.1007/s00232-007-9055-7
Differential Potency of Dominant Negative Connexin43 Mutants in Oculodentodigital Dysplasia, Journal of Biological Chemistry, vol.282, issue.26, pp.19190-202, 2007. ,
DOI : 10.1074/jbc.M609653200
Autosomal recessive GJA1 (Cx43) gene mutations cause oculodentodigital dysplasia by distinct mechanisms, Journal of Cell Science, vol.126, issue.13, pp.2857-66, 2013. ,
DOI : 10.1242/jcs.123315
Functional Characterization of Oculodentodigital Dysplasia-Associated Cx43 Mutants, Cell Communication & Adhesion, vol.13, issue.5-6, pp.279-92, 2005. ,
DOI : 10.1080/cac.10.4-6.445.450
Oculodentodigital Dysplasia-causing Connexin43 Mutants Are Non-functional and Exhibit Dominant Effects on Wild-type Connexin43, Journal of Biological Chemistry, vol.280, issue.12, pp.11458-66, 2005. ,
DOI : 10.1074/jbc.M409564200
Connexin43 Modulation of Osteoblast/Osteocyte Apoptosis: A Potential Therapeutic Target?, Journal of Bone and Mineral Research, vol.23, issue.11, pp.1709-1720, 2008. ,
DOI : 10.1210/en.2004-1414
Connexin43 mediates direct intercellular communication in human osteoblastic cell networks., Journal of Clinical Investigation, vol.91, issue.5, pp.1888-96, 1993. ,
DOI : 10.1172/JCI116406
The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans, Human Molecular Genetics, vol.17, issue.4, pp.539-54, 2008. ,
DOI : 10.1093/hmg/ddm329
-Golgi Compartment of Osteoblastic Cells, The Journal of Cell Biology, vol.103, issue.4, pp.847-57, 1997. ,
DOI : 10.1091/mbc.6.4.459
URL : https://hal.archives-ouvertes.fr/hal-00697582
Cell???cell communication in the osteoblast/osteocyte lineage, Archives of Biochemistry and Biophysics, vol.473, issue.2, pp.188-92, 2008. ,
DOI : 10.1016/j.abb.2008.04.005
Molecular Mechanisms of Osteoblast/Osteocyte Regulation by Connexin43, Calcified Tissue International, vol.47, issue.pt 8, pp.55-67, 2014. ,
DOI : 10.1007/s00223-013-9742-6
Determining how defects in connexin43 cause skeletal disease, genesis, vol.6, issue.2, pp.75-82, 2013. ,
DOI : 10.1002/dvg.22349
Beyond gap junctions: Connexin43 and bone cell signaling, Bone, vol.52, issue.1, pp.157-66, 2013. ,
DOI : 10.1016/j.bone.2012.09.030
Gap junction and hemichannel functions in osteocytes, Bone, vol.54, issue.2, pp.205-217, 2013. ,
DOI : 10.1016/j.bone.2012.08.132
Development of Mice with Osteoblast-Specific Connexin43 Gene Deletion, Cell Communication & Adhesion, vol.4, issue.4-6, pp.445-50, 2003. ,
DOI : 10.1016/8756-3282(96)00047-6
Attenuated Response to In Vivo Mechanical Loading in Mice With Conditional Osteoblast Ablation of the Connexin43 Gene (Gja1), Journal of Bone and Mineral Research, vol.281, issue.6, pp.879-86, 2008. ,
DOI : 10.1359/jbmr.080222
Connexin43 deficiency reduces the sensitivity of cortical bone to the effects of muscle paralysis, Journal of Bone and Mineral Research, vol.87, issue.(Suppl 1), pp.2151-60, 2011. ,
DOI : 10.1002/jbmr.425
Biochemical evidence for gap junctions and Cx43 expression in immortalized human chondrocyte cell line: a potential model in the study of cell communication in human chondrocytes, Osteoarthritis and Cartilage, vol.22, issue.4, pp.586-90, 2014. ,
DOI : 10.1016/j.joca.2014.02.002
Articular chondrocyte network mediated by gap junctions: role in metabolic cartilage homeostasis, Annals of the Rheumatic Diseases, vol.62, issue.(Pt 1), pp.275-84, 2015. ,
DOI : 10.1136/annrheumdis-2013-204244
Isolation of Pluripotent Neural Crest-Derived Stem Cells from Adult Human Tissues by Connexin-43 Enrichment, Stem Cells and Development, vol.22, issue.21, pp.2906-2920, 2013. ,
DOI : 10.1089/scd.2013.0090
Bone morphogenetic protein-2 modulation of chondrogenic differentiation in vitro involves gap junction-mediated intercellular communication, Journal of Cellular Physiology, vol.11, issue.2, pp.233-276, 2002. ,
DOI : 10.1002/jcp.10168
Connexin43 hemichannels mediate small molecule exchange between chondrocytes and matrix in biomechanicallystimulated temporomandibular joint cartilage. Osteoarthritis Cartilage, pp.822-852, 2014. ,
Human Articular Chondrocytes Express Multiple Gap Junction Proteins, The American Journal of Pathology, vol.182, issue.4, pp.1337-1383, 2013. ,
DOI : 10.1016/j.ajpath.2012.12.018
Connexin 43 deficiency desensitizes bone to the effects of mechanical unloading through modulation of both arms of bone remodeling, Bone, vol.57, issue.1, pp.76-83, 2013. ,
DOI : 10.1016/j.bone.2013.07.022
Age-related changes in gap junctional intercellular communication in osteoblastic cells, Journal of Orthopaedic Research, vol.282, issue.12, pp.1979-84, 2012. ,
DOI : 10.1002/jor.22172
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia, Development, vol.132, issue.19, pp.4375-86, 2005. ,
DOI : 10.1242/dev.02011
The G60S connexin 43 mutation activates the osteoblast lineage and results in a resorption-stimulating bone matrix and abrogation of old-age-related bone loss, Journal of Bone and Mineral Research, vol.89, issue.22, pp.2400-2413, 2013. ,
DOI : 10.1002/jbmr.1965
Roles of gap junctions and hemichannels in bone cell functions and in signal transmission of mechanical stress, Frontiers in Bioscience, vol.12, issue.1, pp.1450-62, 2007. ,
DOI : 10.2741/2159
Bisphosphonates improve trabecular bone mass and normalize cortical thickness in ovariectomized, osteoblast connexin43 deficient mice, Bone, vol.51, issue.4, pp.787-94, 2012. ,
DOI : 10.1016/j.bone.2012.06.018
Enhanced Periosteal and Endocortical Responses to Axial Tibial Compression Loading in Conditional Connexin43 Deficient Mice, PLoS ONE, vol.7, issue.9, p.44222, 2012. ,
DOI : 10.1371/journal.pone.0044222.s005
Connexin 43 deficiency attenuates loss of trabecular bone and prevents suppression of cortical bone formation during unloading, Journal of Bone and Mineral Research, vol.88, issue.4, pp.2359-72, 2012. ,
DOI : 10.1002/jbmr.1687
A ubiquitous family of putative gap junction molecules, Current Biology, vol.10, issue.13, pp.473-477, 2000. ,
DOI : 10.1016/S0960-9822(00)00576-5
Pannexin 1 and pannexin 3 are glycoproteins that exhibit many distinct characteristics from the connexin family of gap junction proteins, Journal of Cell Science, vol.120, issue.21, pp.3772-83, 2007. ,
DOI : 10.1242/jcs.009514
Pannexin 1 channels mediate ???find-me??? signal release and membrane permeability during apoptosis, Nature, vol.168, issue.7317, pp.863-870, 2010. ,
DOI : 10.1038/nature09413
Pannexin1 Channels Contain a Glycosylation Site That Targets the Hexamer to the Plasma Membrane, Journal of Biological Chemistry, vol.282, issue.43, pp.31733-31776, 2007. ,
DOI : 10.1074/jbc.M702422200
The biochemistry and function of pannexin channels, Biochimica et Biophysica Acta (BBA) - Biomembranes, vol.1828, issue.1, pp.15-22, 2013. ,
DOI : 10.1016/j.bbamem.2012.01.017
Pannexin membrane channels are mechanosensitive conduits for ATP, FEBS Letters, vol.102, issue.1-3, pp.65-73, 2004. ,
DOI : 10.1016/j.febslet.2004.07.009
channel, hemichannel, and gap junction to promote osteoblast differentiation, The Journal of Cell Biology, vol.1719, issue.7, pp.1257-74, 2011. ,
DOI : 10.1083/jcb.201101050.dv
ATP Released by Electrical Stimuli Elicits Calcium Transients and Gene Expression in Skeletal Muscle, Journal of Biological Chemistry, vol.284, issue.50, pp.34490-505, 2009. ,
DOI : 10.1074/jbc.M109.057315
Activation of neuronal P2X7 receptor???pannexin-1 mediates death of enteric neurons during colitis, Nature Medicine, vol.279, issue.4, pp.600-604, 2012. ,
DOI : 10.1152/ajpgi.00067.2006
Activation of pannexin 1 channels by ATP through P2Y receptors and by cytoplasmic calcium, FEBS Letters, vol.293, issue.1, pp.239-283, 2006. ,
DOI : 10.1016/j.febslet.2005.12.004
Calcium-dependent block of P2X7 receptor channel function is allosteric, The Journal of General Physiology, vol.198, issue.4, pp.437-52, 2011. ,
DOI : 10.1523/JNEUROSCI.2390-10.2010
Non-junction functions of pannexin-1 channels, Trends in Neurosciences, vol.33, issue.2, pp.93-102, 2010. ,
DOI : 10.1016/j.tins.2009.11.007
Activation of Pannexin-1 Hemichannels Augments Aberrant Bursting in the Hippocampus, Science, vol.322, issue.5907, pp.1555-1564, 2008. ,
DOI : 10.1126/science.1165209
Ischemia Opens Neuronal Gap Junction Hemichannels, Science, vol.312, issue.5775, pp.924-931, 2006. ,
DOI : 10.1126/science.1126241
Loss of Pannexin 1 Attenuates Melanoma Progression by Reversion to a Melanocytic Phenotype, Journal of Biological Chemistry, vol.287, issue.34, pp.29184-93, 2012. ,
DOI : 10.1074/jbc.M112.377176
Extracellular ATP acts on P2Y2 purinergic receptors to facilitate HIV-1 infection, The Journal of Experimental Medicine, vol.50, issue.9, pp.1823-1857, 2011. ,
DOI : 10.1128/CVI.00166-07
Implications of pannexin 1 and pannexin 3 for keratinocyte differentiation, Journal of Cell Science, vol.123, issue.8, pp.1363-72, 2010. ,
DOI : 10.1242/jcs.056093
Pannexin 3 is a novel target for Runx2, expressed by osteoblasts and mature growth plate chondrocytes, Journal of Bone and Mineral Research, vol.39, issue.2, pp.2911-2933, 2011. ,
DOI : 10.1002/jbmr.509
Pannexin 3 regulates intracellular ATP/cAMP levels and promotes chondrocyte differentiation, Journal of Biological Chemistry, vol.285, issue.24, pp.18948-58, 2010. ,
DOI : 10.1074/jbc.M110.127027
Diverse Subcellular Distribution Profiles of Pannexin1 and Pannexin3, Cell Communication & Adhesion, vol.12, issue.1-2, pp.133-175, 2008. ,
DOI : 10.1016/j.neuroscience.2007.01.061
Cell-Cell Communication Beyond Connexins: The Pannexin Channels, Physiology, vol.21, issue.2, pp.103-117, 2006. ,
DOI : 10.1152/physiol.00048.2005
Analysis of the extracellular matrix vesicle proteome in mineralizing osteoblasts, Journal of Cellular Physiology, vol.24, issue.2, pp.325-360, 2007. ,
DOI : 10.1002/jcp.20826
Microarray Analyses of Gene Expression during Chondrocyte Differentiation Identifies Novel Regulators of Hypertrophy, Molecular Biology of the Cell, vol.16, issue.11, pp.5316-5349, 2005. ,
DOI : 10.1091/mbc.E05-01-0084
Connexin- and Pannexin-Based Channels in Normal Skeletal Muscles and Their Possible Role in Muscle Atrophy, The Journal of Membrane Biology, vol.142, issue.Suppl 1, pp.10-1007, 2012. ,
DOI : 10.1007/s00232-012-9485-8
Pannexins in ischemia-induced neurodegeneration, Proceedings of the National Academy of Sciences, vol.108, issue.51, pp.20772-20779, 2011. ,
DOI : 10.1073/pnas.1018262108
Global and cartilage-specific deletion of Panx3 prevents the development of surgically induced osteoarthritis, J. Molec. Medicine, 2015. ,
Arthritis in Canada: what do we know and what should we know?, J Rheumatol, vol.72, pp.39-41, 2005. ,
Osteoarthritis, Journal of Cellular Physiology, vol.26, issue.3, pp.626-660, 2007. ,
DOI : 10.1002/jcp.21258
Pathobiology of Osteoarthritis: Pathomechanisms and Potential Therapeutic Targets, Current Drug Targets, vol.8, issue.2, pp.271-82, 2007. ,
DOI : 10.2174/138945007779940160
Hypertrophic differentiation of chondrocytes in osteoarthritis: the developmental aspect of degenerative joint disorders, Arthritis Research & Therapy, vol.12, issue.5, p.216, 2010. ,
DOI : 10.1186/ar3117
Cartilage biology in osteoarthritis???lessons from developmental biology, Nature Reviews Rheumatology, vol.237, issue.11, pp.654-63, 2011. ,
DOI : 10.1038/nrrheum.2011.129
Increased Intercellular Communication through Gap Junctions May Contribute to Progression of Osteoarthritis, Clinical Orthopaedics and Related Research, vol.422, pp.224-256, 2004. ,
DOI : 10.1097/01.blo.0000129346.29945.3b
Identification of shoulder osteoarthritis biomarkers: comparison between shoulders with and without osteoarthritis, Journal of Shoulder and Elbow Surgery, vol.24, issue.3, pp.382-90, 2015. ,
DOI : 10.1016/j.jse.2014.11.039
Silencing the expression of connexin 43 decreases inflammation and joint destruction in experimental arthritis, Journal of Orthopaedic Research, vol.7, issue.4, pp.525-555, 2013. ,
DOI : 10.1002/jor.22263
Proteomic Analysis of Connexin 43 Reveals Novel Interactors Related to Osteoarthritis, Molecular & Cellular Proteomics, vol.14, issue.7, pp.1831-1876, 2015. ,
DOI : 10.1074/mcp.M115.050211
Global analyses of gene expression in early experimental osteoarthritis, Arthritis & Rheumatism, vol.44, issue.427, pp.1854-68, 2007. ,
DOI : 10.1002/art.22711
Differentiating connexin hemichannels and pannexin channels in cellular ATP release, FEBS Letters, vol.133, issue.8, pp.1379-88, 2014. ,
DOI : 10.1016/j.febslet.2014.02.004