-
1
-
-
0024148392
-
Junctional communication and cellular differentiation
-
Pitts J.D., Finbow M.E., Kam E. Junctional communication and cellular differentiation. Br. J. Cancer 1988, (Suppl. 9):52-57.
-
(1988)
Br. J. Cancer
, Issue.SUPPL. 9
, pp. 52-57
-
-
Pitts, J.D.1
Finbow, M.E.2
Kam, E.3
-
2
-
-
0035985057
-
Structural and functional diversity of connexin genes in the mouse and human genome
-
Willecke K., Eiberger J., Degen J., Eckardt D., Romualdi A., et al. Structural and functional diversity of connexin genes in the mouse and human genome. Biol. Chem. 2002, 383:725-737.
-
(2002)
Biol. Chem.
, vol.383
, pp. 725-737
-
-
Willecke, K.1
Eiberger, J.2
Degen, J.3
Eckardt, D.4
Romualdi, A.5
-
3
-
-
0029974655
-
Connections with connexins: the molecular basis of direct intercellular signaling
-
Bruzzone R., White T.W., Paul D.L. Connections with connexins: the molecular basis of direct intercellular signaling. Eur. J. Biochem. 1996, 238:1-27.
-
(1996)
Eur. J. Biochem.
, vol.238
, pp. 1-27
-
-
Bruzzone, R.1
White, T.W.2
Paul, D.L.3
-
4
-
-
84864471439
-
RhoA GTPase switch controls Cx43-hemichannel activity through the contractile system
-
Ponsaerts R., D'hondt C., Hertens F., Parys J.B., Leybaert L., et al. RhoA GTPase switch controls Cx43-hemichannel activity through the contractile system. PLoS One 2012, 7:e42074.
-
(2012)
PLoS One
, vol.7
-
-
Ponsaerts, R.1
D'hondt, C.2
Hertens, F.3
Parys, J.B.4
Leybaert, L.5
-
5
-
-
84872102097
-
Involvement of connexin43 hemichannel in ATP release after γ-irradiation
-
Ohshima Y., Tsukimoto M., Harada H., Kojima S. Involvement of connexin43 hemichannel in ATP release after γ-irradiation. J. Radiat. Res. 2012, 53:551-557.
-
(2012)
J. Radiat. Res.
, vol.53
, pp. 551-557
-
-
Ohshima, Y.1
Tsukimoto, M.2
Harada, H.3
Kojima, S.4
-
6
-
-
13644252915
-
Cochlear gap junctions coassembled from Cx26 and 30 show faster intercellular Ca2+ signaling than homomeric counterparts
-
Sun J., Ahmad S., Chen S., Tang W., Zhang Y., et al. Cochlear gap junctions coassembled from Cx26 and 30 show faster intercellular Ca2+ signaling than homomeric counterparts. Am. J. Physiol. Cell. Physiol. 2005, 288:C613-C623.
-
(2005)
Am. J. Physiol. Cell. Physiol.
, vol.288
-
-
Sun, J.1
Ahmad, S.2
Chen, S.3
Tang, W.4
Zhang, Y.5
-
7
-
-
2442637577
-
Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear
-
Cohen-Salmon M., Maxeiner S., Krüger O., Theis M., Willecke K., et al. Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear. Cell Tissue Res. 2004, 316:15-22.
-
(2004)
Cell Tissue Res.
, vol.316
, pp. 15-22
-
-
Cohen-Salmon, M.1
Maxeiner, S.2
Krüger, O.3
Theis, M.4
Willecke, K.5
-
8
-
-
28944449812
-
The role of gap junctions in health and disease
-
Anand R.J., Hackam D.J. The role of gap junctions in health and disease. Crit. Care Med. 2005, 33:S535-S538.
-
(2005)
Crit. Care Med.
, vol.33
-
-
Anand, R.J.1
Hackam, D.J.2
-
9
-
-
1842665165
-
An expression atlas of connexin genes in the mouse
-
Buniello A., Montanaro D., Volinia S., Gasparini P., Marigo V. An expression atlas of connexin genes in the mouse. Genomics 2004, 83:812-820.
-
(2004)
Genomics
, vol.83
, pp. 812-820
-
-
Buniello, A.1
Montanaro, D.2
Volinia, S.3
Gasparini, P.4
Marigo, V.5
-
10
-
-
0037165262
-
A deletion involving the connexin 30 gene in nonsyndromic hearing impairment
-
Del Castillo I., Villamar M., Moreno-Pelayo M.A., del Castillo F.J., Alvarez A., et al. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment. N. Engl. J. Med. 2002, 346:243-249.
-
(2002)
N. Engl. J. Med.
, vol.346
, pp. 243-249
-
-
Del Castillo, I.1
Villamar, M.2
Moreno-Pelayo, M.A.3
del Castillo, F.J.4
Alvarez, A.5
-
11
-
-
9144251659
-
Prevalence and evolutionary origins of the del (GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study
-
Del Castillo I., Moreno-Pelayo M.A., Del Castillo F.J., Brownstein Z., Marlin S., et al. Prevalence and evolutionary origins of the del (GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study. Am. J. Hum. Genet. 2003, 73:1452-1458.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 1452-1458
-
-
Del Castillo, I.1
Moreno-Pelayo, M.A.2
Del Castillo, F.J.3
Brownstein, Z.4
Marlin, S.5
-
12
-
-
14044263546
-
GJB2 mutations in keratitis-ichthyosis-deafness syndrome including its fatal form
-
Janecke A.R., Hennies H.C., Günther B., Gansl G., Smolle J., et al. GJB2 mutations in keratitis-ichthyosis-deafness syndrome including its fatal form. Am. J. Med. Genet. A 2005, 133:128-131.
-
(2005)
Am. J. Med. Genet. A
, vol.133
, pp. 128-131
-
-
Janecke, A.R.1
Hennies, H.C.2
Günther, B.3
Gansl, G.4
Smolle, J.5
-
13
-
-
33845505914
-
A novel mechanism for connexin 26 mutation linked deafness: cell death caused by leaky gap junction hemichannels
-
Stong B.C., Chang Q., Ahmad S., Lin X. A novel mechanism for connexin 26 mutation linked deafness: cell death caused by leaky gap junction hemichannels. Laryngoscope 2006, 116:2205-2210.
-
(2006)
Laryngoscope
, vol.116
, pp. 2205-2210
-
-
Stong, B.C.1
Chang, Q.2
Ahmad, S.3
Lin, X.4
-
14
-
-
84055176143
-
The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome
-
Mese G., Sellitto C., Li L., Wang H.Z., Valiunas V., et al. The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome. Mol. Biol. Cell 2011, 22:4776-4786.
-
(2011)
Mol. Biol. Cell
, vol.22
, pp. 4776-4786
-
-
Mese, G.1
Sellitto, C.2
Li, L.3
Wang, H.Z.4
Valiunas, V.5
-
15
-
-
0347364631
-
Molecular basis of calcium regulation in connexin-32 hemichannels
-
Gómez-Hernández J.M., de Miguel M., Larrosa B., González D., Barrio L.C. Molecular basis of calcium regulation in connexin-32 hemichannels. Proc. Natl. Acad. Sci. U.S.A. 2003, 100:16030-16035.
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 16030-16035
-
-
Gómez-Hernández, J.M.1
de Miguel, M.2
Larrosa, B.3
González, D.4
Barrio, L.C.5
-
16
-
-
0035046041
-
Single-cell electroporation for gene transfer in vivo
-
Haas K., Sin W.C., Javaherian A., Li Z., Cline H.T. Single-cell electroporation for gene transfer in vivo. Neuron 2001, 29:583-591.
-
(2001)
Neuron
, vol.29
, pp. 583-591
-
-
Haas, K.1
Sin, W.C.2
Javaherian, A.3
Li, Z.4
Cline, H.T.5
-
17
-
-
0027295398
-
Properties of a nonjunctional current expressed from a rat connexin46 cDNA in xenopus oocytes
-
Ebihara L., Steiner E. Properties of a nonjunctional current expressed from a rat connexin46 cDNA in xenopus oocytes. J. Gen. Physiol. 1993, 102:59-74.
-
(1993)
J. Gen. Physiol.
, vol.102
, pp. 59-74
-
-
Ebihara, L.1
Steiner, E.2
-
18
-
-
0032913131
-
Gating of cx46 gap junction hemichannels by calcium and voltage
-
Pfahnl A., Dahl G. Gating of cx46 gap junction hemichannels by calcium and voltage. Pflugers. Arch. 1999, 437:345-353.
-
(1999)
Pflugers. Arch.
, vol.437
, pp. 345-353
-
-
Pfahnl, A.1
Dahl, G.2
-
19
-
-
0037099393
-
Conformational changes in surface structures of isolated connexin 26 gap junctions
-
Müller D.J., Hand G.M., Engel A., Sosinsky G.E. Conformational changes in surface structures of isolated connexin 26 gap junctions. EMBO J. 2002, 21:3598-3607.
-
(2002)
EMBO J.
, vol.21
, pp. 3598-3607
-
-
Müller, D.J.1
Hand, G.M.2
Engel, A.3
Sosinsky, G.E.4
-
20
-
-
38749094820
-
A familial case of Keratitis-ichthyosis-deafness (KID) syndrome with the GJB2 mutation G45E
-
Jonard L., Feldmann D., Parsy C., Freitag S., Sinico M., et al. A familial case of Keratitis-ichthyosis-deafness (KID) syndrome with the GJB2 mutation G45E. Eur. J. Med. Genet. 2008, 51:35-43.
-
(2008)
Eur. J. Med. Genet.
, vol.51
, pp. 35-43
-
-
Jonard, L.1
Feldmann, D.2
Parsy, C.3
Freitag, S.4
Sinico, M.5
-
21
-
-
33746817088
-
Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome
-
Griffith A.J., Yang Y., Pryor S.P., Park H.J., Jabs E.W., et al. Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome. Laryngoscope 2006, 116:1404-1408.
-
(2006)
Laryngoscope
, vol.116
, pp. 1404-1408
-
-
Griffith, A.J.1
Yang, Y.2
Pryor, S.P.3
Park, H.J.4
Jabs, E.W.5
-
22
-
-
80052411907
-
Connexin32 can restore hearing in connexin26 deficient mice
-
Degen J., Schütz M., Dicke N., Strenzke N., Jokwitz M., et al. Connexin32 can restore hearing in connexin26 deficient mice. Eur. J. Cell Biol. 2011, 90:817-824.
-
(2011)
Eur. J. Cell Biol.
, vol.90
, pp. 817-824
-
-
Degen, J.1
Schütz, M.2
Dicke, N.3
Strenzke, N.4
Jokwitz, M.5
-
23
-
-
70349266854
-
Molecular cloning and evolutionary analysis of the GJA1 (connexin43) gene from bats (Chiroptera)
-
Wang L., Li G., Wang J., Ye S., Jones G., et al. Molecular cloning and evolutionary analysis of the GJA1 (connexin43) gene from bats (Chiroptera). Genet. Res. (Camb) 2009, 91:101-109.
-
(2009)
Genet. Res. (Camb)
, vol.91
, pp. 101-109
-
-
Wang, L.1
Li, G.2
Wang, J.3
Ye, S.4
Jones, G.5
-
24
-
-
84865455412
-
Contractility in type III cochlear fibrocytes is dependent on non-muscle myosin II and intercellular gap junctional coupling
-
Kelly J.J., Forge A., Jagger D.J. Contractility in type III cochlear fibrocytes is dependent on non-muscle myosin II and intercellular gap junctional coupling. J. Assoc. Res. Otolaryngol. 2012, 13:473-484.
-
(2012)
J. Assoc. Res. Otolaryngol.
, vol.13
, pp. 473-484
-
-
Kelly, J.J.1
Forge, A.2
Jagger, D.J.3
|