-
1
-
-
0027772413
-
Connexin mutations in X-linked Charcot-Marie-Tooth disease
-
Bergoffen J, Scherer S S, Wang S et al. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science 1993: 262: 2039-2042.
-
(1993)
Science
, vol.262
, pp. 2039-2042
-
-
Bergoffen, J.1
Scherer, S.S.2
Wang, S.3
-
2
-
-
0028018967
-
Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease
-
Bruzzone R, White T W, Scherer S S, Fischbeck K H, Paul D L. Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease. Neuron 1994: 13: 1253-1260.
-
(1994)
Neuron
, vol.13
, pp. 1253-1260
-
-
Bruzzone, R.1
White, T.W.2
Scherer, S.S.3
Fischbeck, K.H.4
Paul, D.L.5
-
3
-
-
0028014579
-
Mutations in the connexin 32 gene in X-linked Charcot-Marie-Tooth disease
-
Fairweather N, Bell C, Cochrane S et al. Mutations in the connexin 32 gene in X-linked Charcot-Marie-Tooth disease. Hum Mol Genet 1994: 3: 29-34.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 29-34
-
-
Fairweather, N.1
Bell, C.2
Cochrane, S.3
-
4
-
-
0029060788
-
Mutations of the Connexin 43 gap-junction gene in patients with heart malformations and defects of laterality
-
Britz-Cunningham S H, Shah M M, Zuppan C W, Fletcher W H. Mutations of the Connexin 43 gap-junction gene in patients with heart malformations and defects of laterality [see comments]. N Engl J Med 1995: 332: 1323-1329.
-
(1995)
N Engl J Med
, vol.332
, pp. 1323-1329
-
-
Britz-Cunningham, S.H.1
Shah, M.M.2
Zuppan, C.W.3
Fletcher, W.H.4
-
5
-
-
0032780886
-
Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin
-
Berry V, Mackay D, Khaliq S et al. Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin. Hum Genet 1999: 105: 168-170.
-
(1999)
Hum Genet
, vol.105
, pp. 168-170
-
-
Berry, V.1
Mackay, D.2
Khaliq, S.3
-
6
-
-
0141498594
-
Connexin 46 mutations in autosomal dominant congenital cataract
-
Mackay D, Ionides A, Kibar Z et al. Connexin 46 mutations in autosomal dominant congenital cataract. Am J Hum Genet 1999: 64: 1357-1364.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1357-1364
-
-
Mackay, D.1
Ionides, A.2
Kibar, Z.3
-
7
-
-
0031959735
-
A missense mutation in the human connexin-50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q
-
Shiels A, Mackay D, Ionides A, Berry V, Moore A. A missense mutation in the human connexin-50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q. Am J Hum Genet 1998: 62: 526-532.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 526-532
-
-
Shiels, A.1
Mackay, D.2
Ionides, A.3
Berry, V.4
Moore, A.5
-
8
-
-
0031007349
-
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
-
Kelsell D P, Dunlop J, Stevens H P et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 1997: 387: 80-83.
-
(1997)
Nature
, vol.387
, pp. 80-83
-
-
Kelsell, D.P.1
Dunlop, J.2
Stevens, H.P.3
-
9
-
-
9844245885
-
Connexin 26 mutations associated with the most common form of nonsyndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
-
Zelante L, Gasparini P, Estivill X et al. Connexin 26 mutations associated with the most common form of nonsyndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Hum Mol Genet 1997: 6: 1605-1609.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1605-1609
-
-
Zelante, L.1
Gasparini, P.2
Estivill, X.3
-
10
-
-
9844252338
-
Prelingual deafness: High prevalence of a 30delG mutation in the connexin 26 gene
-
Denoyelle F, Weil D, Maw M A et al. Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. Hum Mol Genet 1997: 6: 2173-2177.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2173-2177
-
-
Denoyelle, F.1
Weil, D.2
Maw, M.A.3
-
11
-
-
0343726579
-
Autosomal recessive non-syndromic deafness (DFNA3/DFNB1): Connexin 26 mutation analysis in Middle Eastern and Caucasian populations
-
Lench N J, Mueller R F, Houseman M et al. Autosomal recessive non-syndromic deafness (DFNA3/DFNB1): connexin 26 mutation analysis in Middle Eastern and Caucasian populations. Am J Hum Genet 1997: 61: A22.
-
(1997)
Am J Hum Genet
, vol.61
-
-
Lench, N.J.1
Mueller, R.F.2
Houseman, M.3
-
12
-
-
0032492217
-
Connexin-26 mutations in sporadic and inherited sensorineural deafness
-
Estivill X, Fortina P, Surrey S et al. Connexin-26 mutations in sporadic and inherited sensorineural deafness. Lancet 1998: 351: 394-398.
-
(1998)
Lancet
, vol.351
, pp. 394-398
-
-
Estivill, X.1
Fortina, P.2
Surrey, S.3
-
13
-
-
0345055300
-
Connexin-26 mutations in sporadic non-syndromal sensorineural deafness
-
Lench N, Houseman M, Newton V, Van Camp G, Mueller R. Connexin-26 mutations in sporadic non-syndromal sensorineural deafness. Lancet 1998: 351: 415.
-
(1998)
Lancet
, vol.351
, pp. 415
-
-
Lench, N.1
Houseman, M.2
Newton, V.3
Van Camp, G.4
Mueller, R.5
-
14
-
-
0031949442
-
Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss
-
Kelley P M, Harris D J, Comer B C et al. Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss. Am J Hum Genet 1998: 62: 792-799.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 792-799
-
-
Kelley, P.M.1
Harris, D.J.2
Comer, B.C.3
-
15
-
-
0033575109
-
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness
-
Green G E, Scott D A, McDonald J M et al. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. Jama 1999: 281: 2211-2216.
-
(1999)
Jama
, vol.281
, pp. 2211-2216
-
-
Green, G.E.1
Scott, D.A.2
McDonald, J.M.3
-
16
-
-
0030696315
-
Two different connexin 26 mutations in an inbred kindred segregation non-syndromic recessive deafness: Implications for genetic studies in isolated populations
-
Carrasquillo M M, Zlotogora J, Barges S, Chakravarti A. Two different connexin 26 mutations in an inbred kindred segregation non-syndromic recessive deafness: implications for genetic studies in isolated populations. Hum Mol Genet 1997: 6: 2163-2172.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2163-2172
-
-
Carrasquillo, M.M.1
Zlotogora, J.2
Barges, S.3
Chakravarti, A.4
-
18
-
-
0031722150
-
Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma
-
Richard G, White T W, Smith L E et al. Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma. Hum Genet 1998: 103: 393-399.
-
(1998)
Hum Genet
, vol.103
, pp. 393-399
-
-
Richard, G.1
White, T.W.2
Smith, L.E.3
-
19
-
-
0032715472
-
Properties of connexin 26 gap junctional proteins derived from mutations associated with non-syndromal hereditary deafness
-
Martin P E, S L C, Casalotti S O, Forge A, Evans W H. Properties of connexin 26 gap junctional proteins derived from mutations associated with non-syndromal hereditary deafness [In Process Citation]. Hum Mol Genet 1999: 8: 2369-2376.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 2369-2376
-
-
Martin, P.E.1
C, S.L.2
Casalotti, S.O.3
Forge, A.4
Evans, W.H.5
-
20
-
-
0032575085
-
Connexin 26 gene linked to a dominant deafness
-
Denoyelle F, Lina-Granade G, Plauchu H et al. Connexin 26 gene linked to a dominant deafness [letter]. Nature 1998: 393: 319-320.
-
(1998)
Nature
, vol.393
, pp. 319-320
-
-
Denoyelle, F.1
Lina-Granade, G.2
Plauchu, H.3
-
21
-
-
0032846415
-
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
-
Grifa A, Wagner C A, D'Ambrosio L et al. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus [letter]. Nat Genet 1999: 23: 16-18.
-
(1999)
Nat Genet
, vol.23
, pp. 16-18
-
-
Grifa, A.1
Wagner, C.A.2
D'Ambrosio, L.3
-
22
-
-
17344373747
-
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
-
Xia J H, Liu C Y, Tang B S et al. Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment. Nat Genet 1998: 20: 370-373.
-
(1998)
Nat Genet
, vol.20
, pp. 370-373
-
-
Xia, J.H.1
Liu, C.Y.2
Tang, B.S.3
-
23
-
-
0031796918
-
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis
-
Richard G, Smith L E, Bailey R A et al. Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis. Nat Genet 1998: 20: 366-369.
-
(1998)
Nat Genet
, vol.20
, pp. 366-369
-
-
Richard, G.1
Smith, L.E.2
Bailey, R.A.3
-
24
-
-
0342421509
-
The spectrum of mutations in erythrokeratodermias-Novel and de novo mutations in GJB3
-
in press
-
Richard G, Brown K, Smith L et al. The spectrum of mutations in erythrokeratodermias-Novel and de novo mutations in GJB3. Hum Genet, in press 1999.
-
(1999)
Hum Genet
-
-
Richard, G.1
Brown, K.2
Smith, L.3
-
25
-
-
0033384991
-
Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis
-
Wilgoss A, Leigh I M, Barnes M R et al. Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis. J Invest Dermatol 1999: 113: 1119-1122.
-
(1999)
J Invest Dermatol
, vol.113
, pp. 1119-1122
-
-
Wilgoss, A.1
Leigh, I.M.2
Barnes, M.R.3
-
26
-
-
0032790899
-
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families
-
Maestrini E, Korge B P, Ocana-Sierra J et al. A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families. Hum Mol Genet 1999: 8: 1237-1243.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1237-1243
-
-
Maestrini, E.1
Korge, B.P.2
Ocana-Sierra, J.3
-
27
-
-
0029932193
-
Structure of gap junction intercellular channels
-
Yeager M, Nicholson B J. Structure of gap junction intercellular channels. Curr Opin Struct Biol 1996: 6: 183-192.
-
(1996)
Curr Opin Struct Biol
, vol.6
, pp. 183-192
-
-
Yeager, M.1
Nicholson, B.J.2
-
29
-
-
0032425020
-
Gap junctions in vascular smooth muscle
-
Brink P R. Gap junctions in vascular smooth muscle. Acta Physiol Scand 1998: 164: 349-356.
-
(1998)
Acta Physiol Scand
, vol.164
, pp. 349-356
-
-
Brink, P.R.1
-
30
-
-
0029776697
-
The life cycle of a connexin: Gap junction formation, removal, and degradation
-
Laird D W. The life cycle of a connexin: gap junction formation, removal, and degradation. J Bioenerg Biomembr 1996: 28: 311-318.
-
(1996)
J Bioenerg Biomembr
, vol.28
, pp. 311-318
-
-
Laird, D.W.1
-
31
-
-
0033012698
-
Trafficking, assembly, and function of a connexin43-green fluorescent protein chimera in live mammalian cells
-
Jordan K, Solan J L, Dominguez M et al. Trafficking, assembly, and function of a connexin43-green fluorescent protein chimera in live mammalian cells. Mol Biol Cell 1999: 10: 2033-2050.
-
(1999)
Mol Biol Cell
, vol.10
, pp. 2033-2050
-
-
Jordan, K.1
Solan, J.L.2
Dominguez, M.3
-
32
-
-
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
-
33
-
-
0000210839
-
Gating connexin 43 channels reconstituted in lipid vesicles by mitogen-activated protein kinase phosphorylation
-
Kim D Y, Kam Y, Koo S K, Joe C O. Gating connexin 43 channels reconstituted in lipid vesicles by mitogen-activated protein kinase phosphorylation. J Biol Chem 1999: 274: 5581-5587.
-
(1999)
J Biol Chem
, vol.274
, pp. 5581-5587
-
-
Kim, D.Y.1
Kam, Y.2
Koo, S.K.3
Joe, C.O.4
-
34
-
-
0031830342
-
Structure of cardiac gap junction intercellular channels
-
Yeager M. Structure of cardiac gap junction intercellular channels [In Process Citation]. J Struct Biol 1998: 121: 231-245.
-
(1998)
J Struct Biol
, vol.121
, pp. 231-245
-
-
Yeager, M.1
-
35
-
-
0033582686
-
Three-dimensional structure of a recombinant gap junction membrane channel
-
Unger V M, Kumar N M, Gilula N B, Yeager M. Three-dimensional structure of a recombinant gap junction membrane channel. Science 1999: 283: 1176-1180.
-
(1999)
Science
, vol.283
, pp. 1176-1180
-
-
Unger, V.M.1
Kumar, N.M.2
Gilula, N.B.3
Yeager, M.4
-
36
-
-
0029020099
-
Functional analysis of selective interactions among rodent connexins
-
White T W, Paul D L, Goodenough D A, Bruzzone R. Functional analysis of selective interactions among rodent connexins. Mol Biol Cell 1995: 6: 459-470.
-
(1995)
Mol Biol Cell
, vol.6
, pp. 459-470
-
-
White, T.W.1
Paul, D.L.2
Goodenough, D.A.3
Bruzzone, R.4
-
37
-
-
0026666944
-
Molecular analysis of voltage dependence of heterotypic gap junctions formed by connexins 26 and 32
-
discussion 193-195
-
Rubin J B, Verselis V K, Bennett M V, Bargiello T A. Molecular analysis of voltage dependence of heterotypic gap junctions formed by connexins 26 and 32. Biophys J 1992: 62: 183-193; discussion 193-195.
-
(1992)
Biophys J
, vol.62
, pp. 183-193
-
-
Rubin, J.B.1
Verselis, V.K.2
Bennett, M.V.3
Bargiello, T.A.4
-
38
-
-
0027442575
-
Identification of a proline residue as a transduction element involved in voltage gating of gap junctions
-
Suchyna T M, Xu L X, Gao F, Fourtner C R, Nicholson B J. Identification of a proline residue as a transduction element involved in voltage gating of gap junctions. Nature 1993: 365: 847-849.
-
(1993)
Nature
, vol.365
, pp. 847-849
-
-
Suchyna, T.M.1
Xu, L.X.2
Gao, F.3
Fourtner, C.R.4
Nicholson, B.J.5
-
39
-
-
0030052934
-
Heteromeric connexons in lens gap junction channels
-
Jiang J X, Goodenough D A. Heteromeric connexons in lens gap junction channels. Proc Natl Acad Sci U S A 1996: 93: 1287-1291.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 1287-1291
-
-
Jiang, J.X.1
Goodenough, D.A.2
-
40
-
-
0028964217
-
The gap junction proteins beta 1-connexin (connexin-32) and beta 2-connexin (connexin-26) can form heteromeric hemichannels
-
Stauffer K A. The gap junction proteins beta 1-connexin (connexin-32) and beta 2-connexin (connexin-26) can form heteromeric hemichannels. J Biol Chem 1995: 270: 6768-6772.
-
(1995)
J Biol Chem
, vol.270
, pp. 6768-6772
-
-
Stauffer, K.A.1
-
41
-
-
0026780731
-
Mutational analysis of gap junction formation
-
discussion 180-182
-
Dahl G, Werner R, Levine E, Rabadan-Diehl C. Mutational analysis of gap junction formation. Biophys J 1992: 62: 172-180; discussion 180-182.
-
(1992)
Biophys J
, vol.62
, pp. 172-180
-
-
Dahl, G.1
Werner, R.2
Levine, E.3
Rabadan-Diehl, C.4
-
42
-
-
0028915946
-
Specific permeability and selective formation of gap junction channels in connexin-transfected hela cells
-
Elfgang C, Eckert R, Lichtenberg-Frate H et al Specific permeability and selective formation of gap junction channels in connexin-transfected HeLa cells. J Cell Biol 1995: 129: 805-817.
-
(1995)
J Cell Biol
, vol.129
, pp. 805-817
-
-
Elfgang, C.1
Eckert, R.2
Lichtenberg-Frate, H.3
-
43
-
-
0030659574
-
Changing patterns of gap junctional intercellular communication and connexin distribution in mouse epidermis and hair follicles during embryonic development
-
Choudhry R, Pitts J D, Hodgins M B. Changing patterns of gap junctional intercellular communication and connexin distribution in mouse epidermis and hair follicles during embryonic development. Dev Dyn 1997: 210: 417 430.
-
(1997)
Dev Dyn
, vol.210
, pp. 417430
-
-
Choudhry, R.1
Pitts, J.D.2
Hodgins, M.B.3
-
44
-
-
0023029202
-
Patterns of junctional communication in skin
-
Kam E, Melville L, Pitts J D. Patterns of junctional communication in skin. J Invest Dermatol 1986: 87: 748-753.
-
(1986)
J Invest Dermatol
, vol.87
, pp. 748-753
-
-
Kam, E.1
Melville, L.2
Pitts, J.D.3
-
45
-
-
0029742875
-
The role of gap junction membrane channels in development
-
Lo C W The role of gap junction membrane channels in development. J Bioenerg Biomembr 1996: 28: 379-385.
-
(1996)
J Bioenerg Biomembr
, vol.28
, pp. 379-385
-
-
Lo, C.W.1
-
46
-
-
0030896499
-
Alterations in connexin expression and cell communication in healing corneal epithelium
-
Matic M, Petrov I N, Rosenfeld T, Wolosin J M. Alterations in connexin expression and cell communication in healing corneal epithelium. Invest Ophthalmol Vis Sci 1997: 38: 600-609.
-
(1997)
Invest Ophthalmol Vis Sci
, vol.38
, pp. 600-609
-
-
Matic, M.1
Petrov, I.N.2
Rosenfeld, T.3
Wolosin, J.M.4
-
47
-
-
0030025898
-
Expression of the gap junction proteins connexin31 and connexin43 correlates with communication compartments in extraembryonic tissues and in the gastrulating mouse embryo, respectively
-
Dahl E, Winterhager E, Reuss B et al. Expression of the gap junction proteins connexin31 and connexin43 correlates with communication compartments in extraembryonic tissues and in the gastrulating mouse embryo, respectively. J Cell Sci 1996: 109: 191-197.
-
(1996)
J Cell Sci
, vol.109
, pp. 191-197
-
-
Dahl, E.1
Winterhager, E.2
Reuss, B.3
-
48
-
-
0029738724
-
Size and selectivity of gap junction channels formed from different connexins
-
Veenstra R D. Size and selectivity of gap junction channels formed from different connexins. J Bioenerg Biomembr 1996: 28: 326-337.
-
(1996)
J Bioenerg Biomembr
, vol.28
, pp. 326-337
-
-
Veenstra, R.D.1
-
49
-
-
0028317052
-
Switch in gap junction protein expression is associated with selective changes in junctional permeability during keratinocyte differentiation
-
Brissette J L, Kumar N M, Gilula N B, Hall J E, Dotto G P. Switch in gap junction protein expression is associated with selective changes in junctional permeability during keratinocyte differentiation. Proc Natl Acad Sci U S A 1994: 91: 6453-6457.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 6453-6457
-
-
Brissette, J.L.1
Kumar, N.M.2
Gilula, N.B.3
Hall, J.E.4
Dotto, G.P.5
-
50
-
-
0029188095
-
Subcellular organization of calcium signalling in hepatocytes and the intact liver
-
Thomas A P, Renard-Rooney D C, Hajnoczky G et al. Subcellular organization of calcium signalling in hepatocytes and the intact liver. Ciba Found Symp 1995: 188: 18-35.
-
(1995)
Ciba Found Symp
, vol.188
, pp. 18-35
-
-
Thomas, A.P.1
Renard-Rooney, D.C.2
Hajnoczky, G.3
-
51
-
-
0033036692
-
Extent of intercellular calcium wave propagation is related to gap junction permeability and level of connexin-43 expression in astrocytes in primary cultures from four brain regions
-
Blomstrand F, Aberg N D, Eriksson P S, Hansson E, Ronnback L. Extent of intercellular calcium wave propagation is related to gap junction permeability and level of connexin-43 expression in astrocytes in primary cultures from four brain regions. Neuroscience 1999: 92: 255-265.
-
(1999)
Neuroscience
, vol.92
, pp. 255-265
-
-
Blomstrand, F.1
Aberg, N.D.2
Eriksson, P.S.3
Hansson, E.4
Ronnback, L.5
-
52
-
-
0032579554
-
Isoform composition of connexin channels determines selectivity among second messengers and uncharged molecules
-
Bevans C G, Kordel M, Rhee S K, Harris A L. Isoform composition of connexin channels determines selectivity among second messengers and uncharged molecules. J Biol Chem 1998: 273: 2808-2816.
-
(1998)
J Biol Chem
, vol.273
, pp. 2808-2816
-
-
Bevans, C.G.1
Kordel, M.2
Rhee, S.K.3
Harris, A.L.4
-
53
-
-
0033525038
-
Direct high affinity modulation of connexin channel activity by cyclic nucleotides
-
Bevans C G, Harris A E. Direct high affinity modulation of connexin channel activity by cyclic nucleotides [In Process Citation]. J Biol Chem 1999: 274: 3720-3725.
-
(1999)
J Biol Chem
, vol.274
, pp. 3720-3725
-
-
Bevans, C.G.1
Harris, A.E.2
-
54
-
-
0032769955
-
Eocalization of regulatory protein binding sites in the proximal region of human myometrial connexin 43 gene
-
Echetebu C O, Ali M, Izban M G, MacKay E, Garfield R E. Eocalization of regulatory protein binding sites in the proximal region of human myometrial connexin 43 gene. Mol Hum Reprod 1999: 5: 757-766.
-
(1999)
Mol Hum Reprod
, vol.5
, pp. 757-766
-
-
Echetebu, C.O.1
Ali, M.2
Izban, M.G.3
MacKay, E.4
Garfield, R.E.5
-
55
-
-
0029035158
-
Use of alternate promoters for tissue-specific expression of the gene coding for connexin32
-
Neuhaus I M, Dahl G, Werner R. Use of alternate promoters for tissue-specific expression of the gene coding for connexin32. Gene 1995: 158: 257-262.
-
(1995)
Gene
, vol.158
, pp. 257-262
-
-
Neuhaus, I.M.1
Dahl, G.2
Werner, R.3
-
56
-
-
0029867989
-
A second alternative transcript of the gap junction gene connexin32 is expressed in murine Schwann cells and modulated in injured sciatic nerve
-
Sohl G, Gillen C, Bosse F et al. A second alternative transcript of the gap junction gene connexin32 is expressed in murine Schwann cells and modulated in injured sciatic nerve. Eur J Cell Biol 1996: 69: 267-275.
-
(1996)
Eur J Cell Biol
, vol.69
, pp. 267-275
-
-
Sohl, G.1
Gillen, C.2
Bosse, F.3
-
57
-
-
0033029594
-
Regulation of connexin32 and connexin43 gene expression by DNA methylation in rat liver cells
-
Piechocki M P, Burk R D, Ruch R J. Regulation of connexin32 and connexin43 gene expression by DNA methylation in rat liver cells. Carcinogenesis 1999: 20: 401-106.
-
(1999)
Carcinogenesis
, vol.20
, pp. 401-1106
-
-
Piechocki, M.P.1
Burk, R.D.2
Ruch, R.J.3
-
58
-
-
0028135352
-
Differential expression of the gap junction proteins connexin-45. -43, -40, -31, and -26 in mouse skin
-
Butterweck A, Elfgang K, Willeke K, Traub O. Differential expression of the gap junction proteins connexin-45. -43, -40, -31, and -26 in mouse skin. Eur J Cell Biol 1994: 65: 152-163.
-
(1994)
Eur J Cell Biol
, vol.65
, pp. 152-163
-
-
Butterweck, A.1
Elfgang, K.2
Willeke, K.3
Traub, O.4
-
59
-
-
0026541187
-
Four novel members of the connexin family of gap junction proteins. Molecular cloning, expression, and chromosome mapping
-
Haefliger J A, Bruzzone R, Jenkins N A et al. Four novel members of the connexin family of gap junction proteins. Molecular cloning, expression, and chromosome mapping. J Biol Chem 1992: 267: 2057-2064.
-
(1992)
J Biol Chem
, vol.267
, pp. 2057-2064
-
-
Haefliger, J.A.1
Bruzzone, R.2
Jenkins, N.A.3
-
60
-
-
0026801572
-
Two gap junction genes, connexin 31.1 and 30.3, are closely linked on mouse chromosome 4 and preferentially expressed in skin
-
Hennemann H, Dahl E, White J B et al. Two gap junction genes, connexin 31.1 and 30.3, are closely linked on mouse chromosome 4 and preferentially expressed in skin. J Biol Chem 1992: 267: 17225-17233.
-
(1992)
J Biol Chem
, vol.267
, pp. 17225-17233
-
-
Hennemann, H.1
Dahl, E.2
White, J.B.3
-
61
-
-
0026481014
-
Multiple gap junction are utilized during rat skin and hair development
-
Risek B, Klier F G, Gilula N B. Multiple gap junction are utilized during rat skin and hair development. Development 1992: 116: 639-651.
-
(1992)
Development
, vol.116
, pp. 639-651
-
-
Risek, B.1
Klier, F.G.2
Gilula, N.B.3
-
62
-
-
0031833255
-
Getting to the heart of gap junction pathology. Novartis Foundations Symposium: Gap junction-mediated intercellular signalling in health and disease
-
London, UK, 3-5 March 1998
-
Abdulla S. Getting to the heart of gap junction pathology. Novartis Foundations Symposium: Gap junction-mediated intercellular signalling in health and disease. London, UK, 3-5 March 1998. Mol Med Today 1998: 4: 192-193.
-
(1998)
Mol Med Today
, vol.4
, pp. 192-193
-
-
Abdulla, S.1
-
63
-
-
0026513477
-
Molecular cloning and expression of rat connexin40, a gap junction protein expressed in vascular smooth muscle
-
Beyer E C, Reed K E, Westphale E M, Kanter H E, Larson D M. Molecular cloning and expression of rat connexin40, a gap junction protein expressed in vascular smooth muscle. J Membr Biol 1992: 127: 69-76.
-
(1992)
J Membr Biol
, vol.127
, pp. 69-76
-
-
Beyer, E.C.1
Reed, K.E.2
Westphale, E.M.3
Kanter, H.E.4
Larson, D.M.5
-
64
-
-
0026674833
-
Gap-junctional protein connexin 43 is expressed in dermis and epidermis of human skin: Differential modulation by retinoids
-
Guo H, Acevedo P, Parsa F D, Bertram J S. Gap-junctional protein connexin 43 is expressed in dermis and epidermis of human skin: differential modulation by retinoids. J Invest Dermatol 1992: 99: 460-467.
-
(1992)
J Invest Dermatol
, vol.99
, pp. 460-467
-
-
Guo, H.1
Acevedo, P.2
Parsa, F.D.3
Bertram, J.S.4
-
65
-
-
0030901646
-
Differential regulation of connexin43 and connexin37 in endothelial cells by cell density, growth, and TGF-betal
-
Earson D M, Wrobleski M J, Sagar G D, Westphale E M, Beyer E C. Differential regulation of connexin43 and connexin37 in endothelial cells by cell density, growth, and TGF-betal. Am J Physiol 1997: 272: C405-415.
-
(1997)
Am J Physiol
, vol.272
-
-
Earson, D.M.1
Wrobleski, M.J.2
Sagar, G.D.3
Westphale, E.M.4
Beyer, E.C.5
-
66
-
-
0027409355
-
Molecular cloning and functional expression of human connexin37, an endothelial cell gap junction protein
-
Reed K E, Westphale E M, Larson D M et al. Molecular cloning and functional expression of human connexin37, an endothelial cell gap junction protein. J Clin Invest 1993: 91: 997-1004.
-
(1993)
J Clin Invest
, vol.91
, pp. 997-1004
-
-
Reed, K.E.1
Westphale, E.M.2
Larson, D.M.3
-
67
-
-
0032415677
-
Characterization of the gap junction protein connexin37 in murine endothelium, respiratory epithelium, and after transfection in human HeLa cells
-
Traub O, Hertlein B, Kasper M et al. Characterization of the gap junction protein connexin37 in murine endothelium, respiratory epithelium, and after transfection in human HeLa cells. Eur J Cell Biol 1998: 77: 313-322.
-
(1998)
Eur J Cell Biol
, vol.77
, pp. 313-322
-
-
Traub, O.1
Hertlein, B.2
Kasper, M.3
-
68
-
-
0033591383
-
Molecular cloning and functional expression of the mouse gap junction gene connexin-57 in human HeLa cells
-
Manthey D, Bukauskas F, Lee C G, Kozak C A, Willecke K. Molecular cloning and functional expression of the mouse gap junction gene connexin-57 in human HeLa cells. J Biol Chem 1999: 274: 14716-14723.
-
(1999)
J Biol Chem
, vol.274
, pp. 14716-14723
-
-
Manthey, D.1
Bukauskas, F.2
Lee, C.G.3
Kozak, C.A.4
Willecke, K.5
-
69
-
-
0028361088
-
Expression of gap junction proteins cx26, cx31.1, cx37, and cx43 in developing and mature rat epidermis
-
Goliger J A, Paul D L. Expression of gap junction proteins cx26, cx31.1, cx37, and cx43 in developing and mature rat epidermis. Devel Dyn 1994: 200: 1-13.
-
(1994)
Devel Dyn
, vol.200
, pp. 1-13
-
-
Goliger, J.A.1
Paul, D.L.2
-
70
-
-
0027504845
-
Expression of gap junction proteins connexin 26 and 43 is modulated during differentiation of keratinocytes in newborn mouse epidermis
-
Kamibayashi Y, Oyamada M, Oyamada Y, Mori M. Expression of gap junction proteins connexin 26 and 43 is modulated during differentiation of keratinocytes in newborn mouse epidermis. J Invest Dermatol 1993: 101: 773-778.
-
(1993)
J Invest Dermatol
, vol.101
, pp. 773-778
-
-
Kamibayashi, Y.1
Oyamada, M.2
Oyamada, Y.3
Mori, M.4
-
71
-
-
0028998907
-
Aberrant expression of gap junction proteins (connexins) is associated with tumor progression during multistage mouse skin carcinogenesis in vivo
-
Kamibayashi Y, Oyamada Y, Mori M, Oyamada M. Aberrant expression of gap junction proteins (connexins) is associated with tumor progression during multistage mouse skin carcinogenesis in vivo. Carcinogenesis 1995: 16: 1287-1297.
-
(1995)
Carcinogenesis
, vol.16
, pp. 1287-1297
-
-
Kamibayashi, Y.1
Oyamada, Y.2
Mori, M.3
Oyamada, M.4
-
72
-
-
0023771349
-
Cell-to-cell communication within intact human skin
-
Salomon D. Saurat J H, Meda P. Cell-to-cell communication within intact human skin. J Clin Invest 1988: 82: 248-254.
-
(1988)
J Clin Invest
, vol.82
, pp. 248-254
-
-
Salomon, D.1
Saurat, J.H.2
Meda, P.3
-
73
-
-
0033024635
-
Upregulation of connexin 26 is a feature of keratinocyte differentiation in hyperproliferative epidermis, vaginal epithelium, and buccal epithelium
-
Lucke T, Choudhry R, Thorn R et al. Upregulation of connexin 26 is a feature of keratinocyte differentiation in hyperproliferative epidermis, vaginal epithelium, and buccal epithelium. J Invest Dermatol 1999: 112: 354-361.
-
(1999)
J Invest Dermatol
, vol.112
, pp. 354-361
-
-
Lucke, T.1
Choudhry, R.2
Thorn, R.3
-
74
-
-
0027993625
-
Topography of mammalian connexins in human skin
-
Salomon D, Masgrau E, Vischer S et al. Topography of mammalian connexins in human skin. J Invest Dermatol 1994: 103: 240-247.
-
(1994)
J Invest Dermatol
, vol.103
, pp. 240-247
-
-
Salomon, D.1
Masgrau, E.2
Vischer, S.3
-
75
-
-
0030666277
-
Ultrastructural localization of gap junction protein connexin 43 in normal human skin, basal cell carcinoma, and squamous cell carcinoma
-
Tada J, Hashimoto K. Ultrastructural localization of gap junction protein connexin 43 in normal human skin, basal cell carcinoma, and squamous cell carcinoma. J Cutan Pathol 1997: 24: 628-635.
-
(1997)
J Cutan Pathol
, vol.24
, pp. 628-635
-
-
Tada, J.1
Hashimoto, K.2
-
76
-
-
0012180336
-
Expression of epidermal connexins in erythrokeratodermia variabilis (EKV) and normal skin
-
Richard G, Andreoli J M, Compton J G. Expression of epidermal connexins in erythrokeratodermia variabilis (EKV) and normal skin. J Invest Dermatol 1997: 108: 587.
-
(1997)
J Invest Dermatol
, vol.108
, pp. 587
-
-
Richard, G.1
Andreoli, J.M.2
Compton, J.G.3
-
77
-
-
0028838703
-
Wounding alters epidermal connexin expression and gap junction-mediated intercellular communication
-
Goliger J A, Paul D L. Wounding alters epidermal connexin expression and gap junction-mediated intercellular communication. Mol Biol Cell 1995: 6: 1491-1501.
-
(1995)
Mol Biol Cell
, vol.6
, pp. 1491-1501
-
-
Goliger, J.A.1
Paul, D.L.2
-
78
-
-
0031860398
-
Upregulation of connexin 26 between keratinocytes of psoriatic lesions
-
Labarthe M R Bosco D, Saurat J H, Meda P, Salomon D. Upregulation of connexin 26 between keratinocytes of psoriatic lesions. J Invest Dermatol 1998: 111: 72-76.
-
(1998)
J Invest Dermatol
, vol.111
, pp. 72-76
-
-
Labarthe, M.R.1
Bosco, D.2
Saurat, J.H.3
Meda, P.4
Salomon, D.5
-
79
-
-
0031021159
-
Identification of aberrantly regulated genes in diseased skin using the cDNA differential display technique
-
Rivas M V, Jarvis E D, Morisaki S et al. Identification of aberrantly regulated genes in diseased skin using the cDNA differential display technique. J Invest Dermatol 1997: 108: 188-194.
-
(1997)
J Invest Dermatol
, vol.108
, pp. 188-194
-
-
Rivas, M.V.1
Jarvis, E.D.2
Morisaki, S.3
-
80
-
-
0029827447
-
Perturbation in connexin 43 and connexin 26 gap-junction expression in mouse skin hyperplasia and neoplasia
-
Sawey M J, Goldschmidt M H, Risek B, Gilula N B, Lo C W. Perturbation in connexin 43 and connexin 26 gap-junction expression in mouse skin hyperplasia and neoplasia. Mol Carcinog 1996: 17: 49-61.
-
(1996)
Mol Carcinog
, vol.17
, pp. 49-61
-
-
Sawey, M.J.1
Goldschmidt, M.H.2
Risek, B.3
Gilula, N.B.4
Lo, C.W.5
-
81
-
-
0030752665
-
In vivo modulation of connexins 43 and 26 of human epidermis by topical retinoic acid treatment
-
Masgrau-Peya E, Salomon D, Saurat J H, Meda P. In vivo modulation of connexins 43 and 26 of human epidermis by topical retinoic acid treatment. J Histochem Cytochem 1997: 45: 1207-1215.
-
(1997)
J Histochem Cytochem
, vol.45
, pp. 1207-1215
-
-
Masgrau-Peya, E.1
Salomon, D.2
Saurat, J.H.3
Meda, P.4
-
82
-
-
0031800637
-
Modulation of gap junction expression during transient hyperplasia of rat epidermis
-
Risek B, Pozzi A, Gilula N B. Modulation of gap junction expression during transient hyperplasia of rat epidermis. J Cell Sci 1998: 111: 1395-1404.
-
(1998)
J Cell Sci
, vol.111
, pp. 1395-1404
-
-
Risek, B.1
Pozzi, A.2
Gilula, N.B.3
-
83
-
-
0028808365
-
The expression of gap junctional proteins during different stages of mouse skin carcinogenesis
-
Budunova I V, Carbajal S, Slaga T J. The expression of gap junctional proteins during different stages of mouse skin carcinogenesis. Carcinogenesis 1995: 16: 2717-2724.
-
(1995)
Carcinogenesis
, vol.16
, pp. 2717-2724
-
-
Budunova, I.V.1
Carbajal, S.2
Slaga, T.J.3
-
84
-
-
0032904443
-
Disruption of gap junctional intercellular communication in human renal cancer cell lines
-
Noguchi M, Nomata K, Watanabe J I et al. Disruption of gap junctional intercellular communication in human renal cancer cell lines. Urology 1999: 53: 218-222.
-
(1999)
Urology
, vol.53
, pp. 218-222
-
-
Noguchi, M.1
Nomata, K.2
Watanabe, J.I.3
-
85
-
-
0029979440
-
Connexin expression in epidermal cell lines from SENCAR mouse skin tumors
-
Budunova I V, Carbajal S, Viaje A, Slaga T J. Connexin expression in epidermal cell lines from SENCAR mouse skin tumors. Mol Carcinog 1996: 15: 190-201.
-
(1996)
Mol Carcinog
, vol.15
, pp. 190-201
-
-
Budunova, I.V.1
Carbajal, S.2
Viaje, A.3
Slaga, T.J.4
-
86
-
-
0033034577
-
Genetic and epigenetic changes of intercellular communication genes during multistage carcinogenesis
-
Yamasaki H, Omori Y, Zaidan-Dagli M L et al. Genetic and epigenetic changes of intercellular communication genes during multistage carcinogenesis. Cancer Detect Prev 1999: 23: 273-279.
-
(1999)
Cancer Detect Prev
, vol.23
, pp. 273-279
-
-
Yamasaki, H.1
Omori, Y.2
Zaidan-Dagli, M.L.3
-
87
-
-
0028939358
-
Negative growth control of HeLa cells by connexin genes: Connexin species specificity
-
Mesnil M, Krutovskikh V, Piccoli C et al. Negative growth control of HeLa cells by connexin genes: connexin species specificity. Cancer Res 1995: 55: 629-639.
-
(1995)
Cancer Res
, vol.55
, pp. 629-639
-
-
Mesnil, M.1
Krutovskikh, V.2
Piccoli, C.3
-
88
-
-
0026646956
-
Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines
-
Lee S W, Tomasetto C, Paul D, Keyomarsi K, Sager R. Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines. J Cell Biol 1992: 118: 1213-1221.
-
(1992)
J Cell Biol
, vol.118
, pp. 1213-1221
-
-
Lee, S.W.1
Tomasetto, C.2
Paul, D.3
Keyomarsi, K.4
Sager, R.5
-
89
-
-
18744437083
-
Role of connexin (gap junction) genes in cell growth control: Approach with site-directed mutagenesis and dominant-negative effects
-
Omori Y, Duflot-Dancer A, Mesnil M, Yamasaki H. Role of connexin (gap junction) genes in cell growth control: approach with site-directed mutagenesis and dominant-negative effects. Toxicol Lett 1998: 96-97: 105-110.
-
(1998)
Toxicol Lett
, vol.96-97
, pp. 105-110
-
-
Omori, Y.1
Duflot-Dancer, A.2
Mesnil, M.3
Yamasaki, H.4
-
90
-
-
0031785706
-
Mutated connexin43 proteins inhibit rat glioma cell growth suppression mediated by wildtype connexin43 in a dominant-negative manner
-
Omori Y, Yamasaki H. Mutated connexin43 proteins inhibit rat glioma cell growth suppression mediated by wildtype connexin43 in a dominant-negative manner. Int J Cancer 1998: 78: 446-453.
-
(1998)
Int J Cancer
, vol.78
, pp. 446-453
-
-
Omori, Y.1
Yamasaki, H.2
-
91
-
-
0030809793
-
Dominant-negative abrogation of connexin-mediated cell growth control by mutant connexin genes
-
Duflot-Dancer A, Mesnil M, Yamasaki H. Dominant-negative abrogation of connexin-mediated cell growth control by mutant connexin genes. Oncogene 1997: 15: 2151-2158.
-
(1997)
Oncogene
, vol.15
, pp. 2151-2158
-
-
Duflot-Dancer, A.1
Mesnil, M.2
Yamasaki, H.3
-
92
-
-
0029996360
-
Bystander killing of cancer cells by herpes simplex virus thymidine kinase gene is mediated by connexins
-
Mesnil M, Piccoli C, Tiraby G, Willecke K, Yamasaki H. Bystander killing of cancer cells by herpes simplex virus thymidine kinase gene is mediated by connexins. Proc Natl Acad Sci U S A 1996: 93: 1831-1835.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 1831-1835
-
-
Mesnil, M.1
Piccoli, C.2
Tiraby, G.3
Willecke, K.4
Yamasaki, H.5
-
93
-
-
0029161615
-
The "by-stander effect": Association of U-87 cell death with ganciclovir-mediated apoptosis of nearby cells and lack of effect in athymic mice
-
Colombo B M, Benedetti S, Ottolenghi S et al. The "by-stander effect": association of U-87 cell death with ganciclovir-mediated apoptosis of nearby cells and lack of effect in athymic mice. Hum Gene Ther 1995: 6: 763-772.
-
(1995)
Hum Gene Ther
, vol.6
, pp. 763-772
-
-
Colombo, B.M.1
Benedetti, S.2
Ottolenghi, S.3
-
94
-
-
0030750649
-
A tumor suppressor gene, Cx26, also mediates the bystander effect in HeLa cells
-
Mesnil M, Piccoli C, Yamasaki H. A tumor suppressor gene, Cx26, also mediates the bystander effect in HeLa cells. Cancer Res 1997: 57: 2929-2932.
-
(1997)
Cancer Res
, vol.57
, pp. 2929-2932
-
-
Mesnil, M.1
Piccoli, C.2
Yamasaki, H.3
-
96
-
-
9844222499
-
Linkage studies in erythrokeratodermias: Fine mapping, genetic heterogeneity and analysis of candidate genes
-
Richard G, Lin J P, Smith L et al. Linkage studies in erythrokeratodermias: fine mapping, genetic heterogeneity and analysis of candidate genes. J Invest Dermatol 1997: 109: 666-671.
-
(1997)
J Invest Dermatol
, vol.109
, pp. 666-671
-
-
Richard, G.1
Lin, J.P.2
Smith, L.3
-
97
-
-
4243781359
-
Erythrokeratodermia figurata variabilis: Immunocytochemistry and ultrastructure
-
Itin P H, Pittelkow M R. Erythrokeratodermia figurata variabilis: immunocytochemistry and ultrastructure. Dermatologica 1990: 181: 175A.
-
(1990)
Dermatologica
, vol.181
-
-
Itin, P.H.1
Pittelkow, M.R.2
-
98
-
-
0013880963
-
Erythrokeratodermia variabilis. Report of three cases and review of the literature
-
Brown J, Kierland R R. Erythrokeratodermia variabilis. Report of three cases and review of the literature. Arch Dermatol 1966: 93: 194-201.
-
(1966)
Arch Dermatol
, vol.93
, pp. 194-201
-
-
Brown, J.1
Kierland, R.R.2
-
99
-
-
0015049773
-
Erythrokeratodermia variabilis. An enzyme histochemical and ultrastructural study
-
Vandersteen P R, Muller S A. Erythrokeratodermia variabilis. An enzyme histochemical and ultrastructural study. Arch Dermatol 1971: 103: 362-370.
-
(1971)
Arch Dermatol
, vol.103
, pp. 362-370
-
-
Vandersteen, P.R.1
Muller, S.A.2
-
100
-
-
0022578594
-
Erythrokeratodermia variabilis treated with isotretinoin. A clinical, histologic, and ultrastructural study
-
Rappaport I P, Goldes J A, Goltz R W. Erythrokeratodermia variabilis treated with isotretinoin. A clinical, histologic, and ultrastructural study. Arch Dermatol 1986: 122: 441-445.
-
(1986)
Arch Dermatol
, vol.122
, pp. 441-445
-
-
Rappaport, I.P.1
Goldes, J.A.2
Goltz, R.W.3
-
101
-
-
0020381063
-
Epidermal langerhans cells in erythrokeratodermia variabilis. Histochemical and ultrastructural investigations before and after treatment with etretinate (RO 10-9359)
-
van der Schroeff J G, Ruiter D J, Bots G T. Epidermal Langerhans cells in erythrokeratodermia variabilis. Histochemical and ultrastructural investigations before and after treatment with etretinate (RO 10-9359). Arch Dermatol Res 1982: 274: 339-348.
-
(1982)
Arch Dermatol Res
, vol.274
, pp. 339-348
-
-
Van Der Schroeff, J.G.1
Ruiter, D.J.2
Bots, G.T.3
-
102
-
-
0025809412
-
Is erythrokeratoderma one disorder? A clinical and ultrastructural study of two siblings
-
MacFarlane A W, Chapman S J, Verbov J L. Is erythrokeratoderma one disorder? A clinical and ultrastructural study of two siblings. Br J Dermatol 1991: 124: 487-491.
-
(1991)
Br J Dermatol
, vol.124
, pp. 487-491
-
-
MacFarlane, A.W.1
Chapman, S.J.2
Verbov, J.L.3
-
103
-
-
0030763564
-
The molecular pathology of progressive symmetric erythrokeratoderma: A frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope
-
Ishida-Yamamoto A, McGrath J A, Lam H et al. The molecular pathology of progressive symmetric erythrokeratoderma: a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope. Am J Hum Genet 1997: 61: 581-585.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 581-585
-
-
Ishida-Yamamoto, A.1
McGrath, J.A.2
Lam, H.3
-
104
-
-
0030846028
-
Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis
-
Korge B P, Ishida-Yamamoto A, Punter C et al Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis. J Invest Dermatol 1997: 109: 604-609.
-
(1997)
J Invest Dermatol
, vol.109
, pp. 604-609
-
-
Korge, B.P.1
Ishida-Yamamoto, A.2
Punter, C.3
-
105
-
-
15844391073
-
A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome
-
Maestrini E, Monaco A P, McGrath J A et al. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Nat Genet 1996: 13: 70-77.
-
(1996)
Nat Genet
, vol.13
, pp. 70-77
-
-
Maestrini, E.1
Monaco, A.P.2
McGrath, J.A.3
-
106
-
-
0021743075
-
Genetic linkage between erythrokeratodermia variabilis and Rh locus
-
van der Schroeff J G, Nijenhuis L E, Meera Khan P et al. Genetic linkage between erythrokeratodermia variabilis and Rh locus. Hum Genet 1984: 68: 165-168.
-
(1984)
Hum Genet
, vol.68
, pp. 165-168
-
-
Van Der Schroeff, J.G.1
Nijenhuis, L.E.2
Meera Khan, P.3
-
108
-
-
0032813517
-
A genetic polymorphism in connexin 37 as a prognostic marker for atherosclerotic plaque development
-
Boerma M, Forsberg L, Van Zeijl L et al. A genetic polymorphism in connexin 37 as a prognostic marker for atherosclerotic plaque development. J Intern Med 1999: 246:211-218.
-
(1999)
J Intern Med
, vol.246
, pp. 211-218
-
-
Boerma, M.1
Forsberg, L.2
Van Zeijl, L.3
-
109
-
-
0026474825
-
Chromosomal assignments of mouse connexin genes, coding for gap junctional proteins, by somatic cell hybridization
-
Schwarz H J, Chang Y S, Hennemann H et al. Chromosomal assignments of mouse connexin genes, coding for gap junctional proteins, by somatic cell hybridization. Somat Cell Mol Genet 1992: 18: 351-359.
-
(1992)
Somat Cell Mol Genet
, vol.18
, pp. 351-359
-
-
Schwarz, H.J.1
Chang, Y.S.2
Hennemann, H.3
-
110
-
-
0032581383
-
Human gap junction protein connexin31: Molecular cloning and expression analysis
-
Wenzel K, Manthey D, Willecke K, Grzeschik K H, Traub O. Human gap junction protein connexin31: molecular cloning and expression analysis. Biochem Biophys Res Commun 1998: 248: 910-915.
-
(1998)
Biochem Biophys Res Commun
, vol.248
, pp. 910-915
-
-
Wenzel, K.1
Manthey, D.2
Willecke, K.3
Grzeschik, K.H.4
Traub, O.5
-
111
-
-
0028340086
-
Rat connexins 30.3 and 31 are expressed in the kidney
-
Tucker M A, Barajas L. Rat connexins 30.3 and 31 are expressed in the kidney. Exp Cell Res 1994: 213: 224-230.
-
(1994)
Exp Cell Res
, vol.213
, pp. 224-230
-
-
Tucker, M.A.1
Barajas, L.2
-
112
-
-
0025831254
-
Molecular cloning and characterization of a new member of the gap junction gene family, connexin-31
-
Hoh J H, John S A, Revel J P. Molecular cloning and characterization of a new member of the gap junction gene family, connexin-31. J Biol Chem 1991: 266: 6524-6531.
-
(1991)
J Biol Chem
, vol.266
, pp. 6524-6531
-
-
Hoh, J.H.1
John, S.A.2
Revel, J.P.3
-
113
-
-
0030723591
-
Altered trafficking of mutant connexin32
-
Deschenes S M, Walcott J L, Wexler T L, Scherer S S, Fischbeck K H. Altered trafficking of mutant connexin32. J Neurosci 1997: 17: 9077-9084.
-
(1997)
J Neurosci
, vol.17
, pp. 9077-9084
-
-
Deschenes, S.M.1
Walcott, J.L.2
Wexler, T.L.3
Scherer, S.S.4
Fischbeck, K.H.5
-
114
-
-
0028299152
-
Opposite voltage gating polarities of two closely related connexins
-
Verselis V K, Ginter C S, Bargiello T A. Opposite voltage gating polarities of two closely related connexins. Nature 1994: 368: 348-351.
-
(1994)
Nature
, vol.368
, pp. 348-351
-
-
Verselis, V.K.1
Ginter, C.S.2
Bargiello, T.A.3
-
115
-
-
0030013202
-
Connexins, connexons, and intercellular communication
-
Goodenough D A, Goliger J A, Paul D L. Connexins, Connexons, and intercellular communication. Annu Rev Biochem 1996: 65: 475-502.
-
(1996)
Annu Rev Biochem
, vol.65
, pp. 475-502
-
-
Goodenough, D.A.1
Goliger, J.A.2
Paul, D.L.3
-
116
-
-
16944366517
-
Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 Cx32 mutations in 35 families
-
Rouger H, LeGuern E, Birouk N et al. Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families. Hum Mutat 1997: 10: 443-452.
-
(1997)
Hum Mutat
, vol.10
, pp. 443-452
-
-
Rouger, H.1
LeGuern, E.2
Birouk, N.3
-
117
-
-
0017031961
-
Knuckle pads, leuconychia, deafness, and keratosis palmoplantaris
-
Crosby E F, Vidurrizaga R H. Knuckle pads, leuconychia, deafness, and keratosis palmoplantaris. Johns Hopkins Med J 1976: 139: S90-S92.
-
(1976)
Johns Hopkins Med J
, vol.139
-
-
Crosby, E.F.1
Vidurrizaga, R.H.2
-
118
-
-
0029914419
-
Hereditary palmoplantar keratoderma with deafness
-
Fitzgerald D A, Verbov J L. Hereditary palmoplantar keratoderma with deafness. J Dermatol 1996: 134: 939-942.
-
(1996)
J Dermatol
, vol.134
, pp. 939-942
-
-
Fitzgerald, D.A.1
Verbov, J.L.2
-
119
-
-
0024349474
-
Familäre zirkumskripte palmoplantarkeratose mil schallempfindungsschwerhörigkeit und sporadischem
-
Gloor M, Gross M, Happle R, Gehring W. Familäre zirkumskripte Palmoplantarkeratose mil Schallempfindungsschwerhörigkeit und sporadischem CHILD Syndrom Hautarzt 1989: 40: 304-307.
-
(1989)
CHILD Syndrom Hautarzt
, vol.40
, pp. 304-307
-
-
Gloor, M.1
Gross, M.2
Happle, R.3
Gehring, W.4
-
120
-
-
84943208996
-
Diffuse palmoplantar keratoderma with deafness
-
Hatamochi A, Nakagawa S H U. Diffuse palmoplantar keratoderma with deafness. Arch Dermatol 1982: 118: 605-607.
-
(1982)
Arch Dermatol
, vol.118
, pp. 605-607
-
-
Hatamochi, A.1
Nakagawa, S.H.U.2
-
121
-
-
0026584664
-
Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generations
-
Sharland M, Bleach N R, Goberdhan P D, Patton M A. Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generations. J Med Genet 1992: 29: 50-52.
-
(1992)
J Med Genet
, vol.29
, pp. 50-52
-
-
Sharland, M.1
Bleach, N.R.2
Goberdhan, P.D.3
Patton, M.A.4
-
122
-
-
0023359292
-
Palmoplantar keratoderma, deafness and atopy
-
Verbov J L. Palmoplantar keratoderma, deafness and atopy. Br J Dermatol 1987: 116: 881-882.
-
(1987)
Br J Dermatol
, vol.116
, pp. 881-882
-
-
Verbov, J.L.1
-
123
-
-
0001245331
-
Keratoma hereditarium mutilans
-
Vohwinkel K H. Keratoma hereditarium mutilans. Arch Derm Syph 1929: 158: 354-364.
-
(1929)
Arch Derm Syph
, vol.158
, pp. 354-364
-
-
Vohwinkel, K.H.1
-
124
-
-
0031933645
-
Connexin mutations and hearing loss
-
Scott D A, Kraft M L, Stone E M, Sheffield V C, Smith R J. Connexin mutations and hearing loss [letter]. Nature 1998: 391: 32.
-
(1998)
Nature
, vol.391
, pp. 32
-
-
Scott, D.A.1
Kraft, M.L.2
Stone, E.M.3
Sheffield, V.C.4
Smith, R.J.5
-
125
-
-
0343291144
-
Connexin mutations in skin disease and deafness: Genotype versus phenotype
-
Kelsell D, Wilgoss A, Leigh I. Connexin mutations in skin disease and deafness: Genotype versus phenotype. J Invest Dermatol 1999: 113: 433.
-
(1999)
J Invest Dermatol
, vol.113
, pp. 433
-
-
Kelsell, D.1
Wilgoss, A.2
Leigh, I.3
-
126
-
-
4243786319
-
Transdominant negative effect of a novel connexin-26 mutation on connexin-43 channels as possible mechanism for cutaneous phenotype
-
Rouan F, White T, Paul D, Uitto J, Richard G. Transdominant negative effect of a novel connexin-26 mutation on connexin-43 channels as possible mechanism for cutaneous phenotype. Mol Biol Cell 1999: 10: 402a.
-
(1999)
Mol Biol Cell
, vol.10
-
-
Rouan, F.1
White, T.2
Paul, D.3
Uitto, J.4
Richard, G.5
-
127
-
-
0042040636
-
The skin phenotypes of dominant Connexin 26 mutations
-
Hodgins M, Munro C, Shore L et al. The skin phenotypes of dominant Connexin 26 mutations. J Invest Dermatol 1999: 113: 444.
-
(1999)
J Invest Dermatol
, vol.113
, pp. 444
-
-
Hodgins, M.1
Munro, C.2
Shore, L.3
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