-
1
-
-
0029932193
-
Structure of gap junction intercellular channels
-
Yeager M, Nicholson BJ (1996) Structure of gap junction intercellular channels. Curr Opin Struct Biol 6: 183-192.
-
(1996)
Curr Opin Struct Biol
, vol.6
, pp. 183-192
-
-
Yeager, M.1
Nicholson, B.J.2
-
2
-
-
0035704411
-
Emerging issues of connexin channels: Biophysics fills the gap
-
Harris AL (2001) Emerging issues of connexin channels: biophysics fills the gap. Q Rev Biophys 34: 325-472.
-
(2001)
Q Rev Biophys
, vol.34
, pp. 325-472
-
-
Harris, A.L.1
-
3
-
-
0030028301
-
The gap junction communication channel
-
Kumar NM, Gilula. NB (1996) The gap junction communication channel. Cell, 81: 381-388.
-
(1996)
Cell
, vol.81
, pp. 381-388
-
-
Kumar, N.M.1
Gilula, N.B.2
-
4
-
-
0029096749
-
Physical characterization of gap junction membrane connexons (hemi-channels) isolated from rat liver
-
Cascio M, Kumar NM, Safarik R, Gilula NB (1995) Physical characterization of gap junction membrane connexons (hemi-channels) isolated from rat liver. J Biol Chem 270: 18643-18648.
-
(1995)
J Biol Chem
, vol.270
, pp. 18643-18648
-
-
Cascio, M.1
Kumar, N.M.2
Safarik, R.3
Gilula, N.B.4
-
5
-
-
0024095587
-
Topology of the 32-kd liver gap junction protein determined by site-directed antibody localizations
-
Milks LC, Kumar NM, Houghten R, Unwin N, Gilula NB (1988) Topology of the 32-kd liver gap junction protein determined by site-directed antibody localizations. EMBO J 7; 2967-2975,
-
(1988)
EMBO J
, vol.7
, pp. 2967-2975
-
-
Milks, L.C.1
Kumar, N.M.2
Houghten, R.3
Unwin, N.4
Gilula, N.B.5
-
6
-
-
0035754366
-
Connexin genes in the mouse and human genome
-
Eiberger J, Degen J, Romualdi A, Deutsch U, Willecke K, et al. (2001) Connexin genes in the mouse and human genome. Cell Common Adhes 8: 163-165.
-
(2001)
Cell Common Adhes
, vol.8
, pp. 163-165
-
-
Eiberger, J.1
Degen, J.2
Romualdi, A.3
Deutsch, U.4
Willecke, K.5
-
7
-
-
1642396591
-
Connexin disorders of the car, skin, and lens
-
Gerido DA, White TW (2004) Connexin disorders of the car, skin, and lens. Biochim Biophys Acta 1662: 159-170.
-
(2004)
Biochim Biophys Acta
, vol.1662
, pp. 159-170
-
-
Gerido, D.A.1
White, T.W.2
-
8
-
-
0027772413
-
Connexin mutations in X-linked Charcot-Marie-Tooth disease
-
Bergoffen J, Scherer SS, Wang S, Scott MO, Bone LJ, et al. (1993) Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science 262: 2039-2042.
-
(1993)
Science
, vol.262
, pp. 2039-2042
-
-
Bergoffen, J.1
Scherer, S.S.2
Wang, S.3
Scott, M.O.4
Bone, L.J.5
-
9
-
-
20444397355
-
Structural organization of gap junction channels
-
Sosinsky GE, Nicholson BJ (2005) Structural organization of gap junction channels. Biochim Biophys Acta 1711: 99-125.
-
(2005)
Biochim Biophys Acta
, vol.1711
, pp. 99-125
-
-
Sosinsky, G.E.1
Nicholson, B.J.2
-
10
-
-
0033582686
-
Three-dimensional structure of a recombinant gap junction membrane channel
-
Unger VM, Kumar NM, Gilula NB, Yeager M (1999) Three-dimensional structure of a recombinant gap junction membrane channel. Science 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
-
11
-
-
4644228547
-
A Calpha model for the transmembrane alpha helices of gap junction intercellular channels
-
Fleishman SJ, Unger VM, Yeager M, Ben Tal N (2004) A Calpha model for the transmembrane alpha helices of gap junction intercellular channels. Mol Cell 15: 879-888.
-
(2004)
Mol Cell
, vol.15
, pp. 879-888
-
-
Fleishman, S.J.1
Unger, V.M.2
Yeager, M.3
Ben Tal, N.4
-
12
-
-
34547224262
-
Three-dimensional structure of a human connexin26 gap junction channel reveals a plug in the vestibule
-
Oshima A, Tani K, Hiroaki Y, Fujiyoshi Y, Sosinsky. GE (2007) Three-dimensional structure of a human connexin26 gap junction channel reveals a plug in the vestibule. Proc Natl Acad Sci U S A 104: 10034-10039.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 10034-10039
-
-
Oshima, A.1
Tani, K.2
Hiroaki, Y.3
Fujiyoshi, Y.4
Sosinsky, G.E.5
-
13
-
-
0037191101
-
Identification of amino acid residues lining the pore of a gap junction channel
-
Skerrett IM, Aronowitz J, Shin JH, Cymes G, Kasperek E, et al. (2002) Identification of amino acid residues lining the pore of a gap junction channel. J Cell Biol 159: 349-360.
-
(2002)
J Cell Biol
, vol.159
, pp. 349-360
-
-
Skerrett, I.M.1
Aronowitz, J.2
Shin, J.H.3
Cymes, G.4
Kasperek, E.5
-
14
-
-
0030897850
-
Identification of a pore lining segment in gap junction hemichannels
-
Zhou XW, Pfahnl A, Werner R, Hudder A, Llanes A, et al (1997) Identification of a pore lining segment in gap junction hemichannels. Biophys J 72: 1946-1953.
-
(1997)
Biophys J
, vol.72
, pp. 1946-1953
-
-
Zhou, X.W.1
Pfahnl, A.2
Werner, R.3
Hudder, A.4
Llanes, A.5
-
15
-
-
0346496117
-
Pore-lining residues identified by single channel SCAM sUdies in Cx46 hemichannels
-
Kronengold J, Trexler EB, Bukauskas FF, Bargiello TA, Verselis VK (2003) Pore-lining residues identified by single channel SCAM sUdies in Cx46 hemichannels. Cell Common Adhes 10: 193-199.
-
(2003)
Cell Common Adhes
, vol.10
, pp. 193-199
-
-
Kronengold, J.1
Trexler, E.B.2
Bukauskas, F.F.3
Bargiello, T.A.4
Verselis, V.K.5
-
16
-
-
0141919839
-
Single-channel SCAM identifies pore-lining residues in the first extracellular loop and first transmembrane domains of Cx46 hemichannels
-
Kronengold J, Trexler EB, Bukuskas FF, Bargiello TA, Verselis VK (2003) Single-channel SCAM identifies pore-lining residues in the first extracellular loop and first transmembrane domains of Cx46 hemichannels. J Gen Physiol 122: 389-405.
-
(2003)
J Gen Physiol
, vol.122
, pp. 389-405
-
-
Kronengold, J.1
Trexler, E.B.2
Bukuskas, F.F.3
Bargiello, T.A.4
Verselis, V.K.5
-
17
-
-
33747880802
-
Pathogenetic role of the deafness-related M34T mutation of Cx26
-
Bicego M, Beltramello M, Melchionda S, Carella M, Piazza V, et al. (2006) Pathogenetic role of the deafness-related M34T mutation of Cx26. Hum Mol Genet 15: 2569-2587.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2569-2587
-
-
Bicego, M.1
Beltramello, M.2
Melchionda, S.3
Carella, M.4
Piazza, V.5
-
18
-
-
34247886163
-
Unitary permeability of gap junction channels to second messengers measured by FRET microscopy
-
Hernandez VH, Bortolozzi M, Pertegato V, Beltramello M, Giarin MF, et al. (2007) Unitary permeability of gap junction channels to second messengers measured by FRET microscopy. Nat Methods 4: 353-358.
-
(2007)
Nat Methods
, vol.4
, pp. 353-358
-
-
Hernandez, V.H.1
Bortolozzi, M.2
Pertegato, V.3
Beltramello, M.4
Giarin, M.F.5
-
19
-
-
0033529269
-
Potassium and sodium binding to the outer mouth of the K+ channel
-
Guidoni L, Torre V, Carloni P (1999) Potassium and sodium binding to the outer mouth of the K+ channel. Biochemistry 38: 8599-8604.
-
(1999)
Biochemistry
, vol.38
, pp. 8599-8604
-
-
Guidoni, L.1
Torre, V.2
Carloni, P.3
-
20
-
-
10344261477
-
Conformational sampling and dynamics of membrane proteins from 10-nanosecond computer simulations
-
Faraldo-Gomez JD, Forrest LR, Baaden M, Bond PJ, Domene C, et al. (2004) Conformational sampling and dynamics of membrane proteins from 10-nanosecond computer simulations. Protein 57: 783-791.
-
(2004)
Protein
, vol.57
, pp. 783-791
-
-
Faraldo-Gomez, J.D.1
Forrest, L.R.2
Baaden, M.3
Bond, P.J.4
Domene, C.5
-
21
-
-
0035750729
-
Size seletivity between gap junction channels composed of different connexins
-
Gong XQ, Nicholson BJ (2001) Size seletivity between gap junction channels composed of different connexins. Cell Commun Adhes 8: 187-192.
-
(2001)
Cell Commun Adhes
, vol.8
, pp. 187-192
-
-
Gong, X.Q.1
Nicholson, B.J.2
-
22
-
-
33244478285
-
Selective defecfs in channel permeability associated with Cx32 mutations causing X-linked Charcot-Marie-Tooth disease
-
Bicego M, Morassutto S, Hernandez VH, Morgutti M, Mammano F, et al. (2006) Selective defecfs in channel permeability associated with Cx32 mutations causing X-linked Charcot-Marie-Tooth disease. Neurobiol Dis 21: 607-617.
-
(2006)
Neurobiol Dis
, vol.21
, pp. 607-617
-
-
Bicego, M.1
Morassutto, S.2
Hernandez, V.H.3
Morgutti, M.4
Mammano, F.5
-
23
-
-
0033063884
-
The role of a conserved proline residue in mediating conformational changes associated with voltage gating of Cx32 gap junctions
-
Ri Y, Ballesteros JA, Abrams CK, Oh S, Verselis VK, et al. (1999) The role of a conserved proline residue in mediating conformational changes associated with voltage gating of Cx32 gap junctions. Biophys J 76: 2887-2898.
-
(1999)
Biophys J
, vol.76
, pp. 2887-2898
-
-
Ri, Y.1
Ballesteros, J.A.2
Abrams, C.K.3
Oh, S.4
Verselis, V.K.5
-
24
-
-
0025663105
-
Strength and cooperativity of contributions of surface salt bridges to protein stability
-
Horovitz A, Serrano L, Avron B, Bycroft M, Fersht AR (1990) Strength and cooperativity of contributions of surface salt bridges to protein stability. J Mol Biol 216: 1031-1044.
-
(1990)
J Mol Biol
, vol.216
, pp. 1031-1044
-
-
Horovitz, A.1
Serrano, L.2
Avron, B.3
Bycroft, M.4
Fersht, A.R.5
-
25
-
-
0028204490
-
Do salt bridges stabilize proteins? A continuum electrostatic analysis
-
Hendsch ZS, Tidor B (1994) Do salt bridges stabilize proteins? A continuum electrostatic analysis. Protein Sci 3: 211-226.
-
(1994)
Protein Sci
, vol.3
, pp. 211-226
-
-
Hendsch, Z.S.1
Tidor, B.2
-
26
-
-
0037449718
-
Roles of Met-34, Cys-64, and Arg-75 in the assembly of human connexin 26. Implication for key amino acid residues for channel formation and function
-
Oshima A, Doi T, Mitsuoka K, Maeda S, Fujiyoshi Y (2003) Roles of Met-34, Cys-64, and Arg-75 in the assembly of human connexin 26. Implication for key amino acid residues for channel formation and function. J Biol Chem 278: 1807-1816.
-
(2003)
J Biol Chem
, vol.278
, pp. 1807-1816
-
-
Oshima, A.1
Doi, T.2
Mitsuoka, K.3
Maeda, S.4
Fujiyoshi, Y.5
-
27
-
-
24644458117
-
-
Chen Y, Deng Y, Ban X, Reuss L, Altenberg GA (2065) Mechanism of the defect in gap-junctional communication by expression of a connexin 26 mutant associated with dominant deafness. FASEB J 19: 1516-1518.
-
Chen Y, Deng Y, Ban X, Reuss L, Altenberg GA (2065) Mechanism of the defect in gap-junctional communication by expression of a connexin 26 mutant associated with dominant deafness. FASEB J 19: 1516-1518.
-
-
-
-
28
-
-
8944253782
-
X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): New mutations in the connexin32 gene
-
Ressot C, Latour P, Blanquet-Grossard F, Sturtz F, Duthel S, et al. (1996) X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 gene. Hum Genet 98: 172-175.
-
(1996)
Hum Genet
, vol.98
, pp. 172-175
-
-
Ressot, C.1
Latour, P.2
Blanquet-Grossard, F.3
Sturtz, F.4
Duthel, S.5
-
29
-
-
33749376891
-
The structural context of disease-causing mutations in gap junctions
-
Fleishman SJ, Sabag AD, Ophir E, Avraham KB, Ben Tal N (2006) The structural context of disease-causing mutations in gap junctions. J Biol Chem 281: 28958-28963.
-
(2006)
J Biol Chem
, vol.281
, pp. 28958-28963
-
-
Fleishman, S.J.1
Sabag, A.D.2
Ophir, E.3
Avraham, K.B.4
Ben Tal, N.5
-
30
-
-
0038810233
-
Correlated motion and die effect of distal mutations in dihydrofolate reductase
-
Rod TH, Radkiewicz JL, Brooks CL III (2003) Correlated motion and die effect of distal mutations in dihydrofolate reductase. Proc Natl Acad Sci U S A 100: 6980-6985.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 6980-6985
-
-
Rod, T.H.1
Radkiewicz, J.L.2
Brooks III, C.L.3
-
31
-
-
0032948117
-
Mutations in the peripheral myclin genes and associated genes in inherited peripheral neuropathies
-
Nelis E, Haites N, Van Broeckhoven C (1999) Mutations in the peripheral myclin genes and associated genes in inherited peripheral neuropathies. Hum Mutat 13: 11-28.
-
(1999)
Hum Mutat
, vol.13
, pp. 11-28
-
-
Nelis, E.1
Haites, N.2
Van Broeckhoven, C.3
-
32
-
-
0031949442
-
Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNBI) hearing loss
-
Kelley PM, Harris DJ, Comer BC, Askew JW, Fowler T, et al. (1998) Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNBI) hearing loss. Am J Hum Genet 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
Askew, J.W.4
Fowler, T.5
-
33
-
-
12344304163
-
Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness
-
Beltramello M, Piazza V, Bukauskas FF, Pozzan T. Mammano F (2005) Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness. Nat Cell Biol 7: 63-69.
-
(2005)
Nat Cell Biol
, vol.7
, pp. 63-69
-
-
Beltramello, M.1
Piazza, V.2
Bukauskas, F.F.3
Pozzan, T.4
Mammano, F.5
-
34
-
-
27844535720
-
Molecular simulations and lipid-protein interactions: Potassium channels and other membrane proteins
-
Sansom MS, Bond PJ, Deol SS, Grottesi A, Haider S, et al. (2005) Molecular simulations and lipid-protein interactions: potassium channels and other membrane proteins. Biochem Soc Trans 33: 916-920.
-
(2005)
Biochem Soc Trans
, vol.33
, pp. 916-920
-
-
Sansom, M.S.1
Bond, P.J.2
Deol, S.S.3
Grottesi, A.4
Haider, S.5
-
35
-
-
0035253804
-
Transmembrane alpha-helices in the gap junction membrane channel: Systematic search of packing models based on the pair potential function
-
Nunn RS, Macke TJ, Olson AJ, Yeager M (2001) Transmembrane alpha-helices in the gap junction membrane channel: systematic search of packing models based on the pair potential function. Microsc Res Tech 52: 344-351.
-
(2001)
Microsc Res Tech
, vol.52
, pp. 344-351
-
-
Nunn, R.S.1
Macke, T.J.2
Olson, A.J.3
Yeager, M.4
-
36
-
-
34249059596
-
Molecular modeling and mutagenesis of gap junction channels
-
Kovacs JA, Baker KA, Altenberg GA, Abagyan R, Yeager M (2007) Molecular modeling and mutagenesis of gap junction channels. Prog Biophys Mol Biol 94: 15-28.
-
(2007)
Prog Biophys Mol Biol
, vol.94
, pp. 15-28
-
-
Kovacs, J.A.1
Baker, K.A.2
Altenberg, G.A.3
Abagyan, R.4
Yeager, M.5
-
37
-
-
0030930298
-
Screening for connexin 32 mutations in Charrot-Marie-Tooth disease families with possible X-linked inheritance
-
Silander K, Meretoja P, Pihko H, Juvonen V, Issakainen J, et al. (1997) Screening for connexin 32 mutations in Charrot-Marie-Tooth disease families with possible X-linked inheritance. Hum Genet 100: 391-397.
-
(1997)
Hum Genet
, vol.100
, pp. 391-397
-
-
Silander, K.1
Meretoja, P.2
Pihko, H.3
Juvonen, V.4
Issakainen, J.5
-
38
-
-
0029942648
-
Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth disease
-
Tan CC, Ainsworth PJ, Hahn AF, MacLeod PM (1996) Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth disease. Hum Mutat, 7: 167-171.
-
(1996)
Hum Mutat
, vol.7
, pp. 167-171
-
-
Tan, C.C.1
Ainsworth, P.J.2
Hahn, A.F.3
MacLeod, P.M.4
-
39
-
-
0031796918
-
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis
-
Richard G, Smith LE, Bailey RA, Itin P, Hohl D, et al. (1998) Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis. Nat Genet 20: 366-369.
-
(1998)
Nat Genet
, vol.20
, pp. 366-369
-
-
Richard, G.1
Smith, L.E.2
Bailey, R.A.3
Itin, P.4
Hohl, D.5
-
40
-
-
0030013202
-
Connexins, connexons, and intercellular communication
-
Goodenough DA, Goliger JA, Paul DL (1996) Connexins, connexons, and intercellular communication. Annu Rev Biochem 65: 475-502.
-
(1996)
Annu Rev Biochem
, vol.65
, pp. 475-502
-
-
Goodenough, D.A.1
Goliger, J.A.2
Paul, D.L.3
-
41
-
-
0030696315
-
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: Implications for genetic studies in isolated populations
-
Carrasquillo MM. Zlotogora J. S. Chakravarti A (1997) Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations. Hum Mol Genet 6: 2163-2172.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2163-2172
-
-
Carrasquillo, M.M.1
Zlotogora, J.S.2
Chakravarti, A.3
-
42
-
-
0037413825
-
Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness
-
Bruzzone R, Veronesi V, Gomes D, Bicego M, Duval N, et al. (2003) Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness. FEBS Lett 533: 79-88.
-
(2003)
FEBS Lett
, vol.533
, pp. 79-88
-
-
Bruzzone, R.1
Veronesi, V.2
Gomes, D.3
Bicego, M.4
Duval, N.5
-
43
-
-
25444475775
-
Lipid rafts prepared by different methods contain different connexin channels, but gap junctions are not lipid rafts
-
Locke D, Liu J, Harris AL (2005) Lipid rafts prepared by different methods contain different connexin channels, but gap junctions are not lipid rafts. Biochemistry 44: 13027-13042.
-
(2005)
Biochemistry
, vol.44
, pp. 13027-13042
-
-
Locke, D.1
Liu, J.2
Harris, A.L.3
-
44
-
-
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, Gouider R; Tardieu S, et al. (1997) Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families. Hum Mutat 10: 443-452.
-
(1997)
Hum Mutat
, vol.10
, pp. 443-452
-
-
Rouger, H.1
LeGuern, E.2
Birouk, N.3
Gouider, R.4
Tardieu, S.5
-
45
-
-
0033812813
-
Connexin26 mutations associated with nonsyndromic hearing loss
-
Park HJ, Hahn SH, Chun YM, Park K, Kim HN (2000) Connexin26 mutations associated with nonsyndromic hearing loss. Laryngoscope 110: 1535-1538.
-
(2000)
Laryngoscope
, vol.110
, pp. 1535-1538
-
-
Park, H.J.1
Hahn, S.H.2
Chun, Y.M.3
Park, K.4
Kim, H.N.5
-
46
-
-
0030896412
-
Connexin32 gene mutations in X-linked dominant Charcol-Marie-Tooth disease (CMTX1)
-
Janssen EA. Kemp S, Hensels GW, Sie OG, Die-Smulders CE, et al. (1997) Connexin32 gene mutations in X-linked dominant Charcol-Marie-Tooth disease (CMTX1).. Hum Genet 99: 501-505.
-
(1997)
Hum Genet
, vol.99
, pp. 501-505
-
-
Janssen, E.A.1
Kemp, S.2
Hensels, G.W.3
Sie, O.G.4
Die-Smulders, C.E.5
-
47
-
-
0035805077
-
Functional alterations in gap junction channels formed by mutant Forms of connexin 32: Evidence for loss of function as a pathogenic mechanism in the X-linked form of Charcot-Marie-Tooth disease
-
Abrams CK, Freidin MM, Versclis VK, Bennett MV, Bargiello TA (2001) Functional alterations in gap junction channels formed by mutant Forms of connexin 32: evidence for loss of function as a pathogenic mechanism in the X-linked form of Charcot-Marie-Tooth disease. Brain Res 900: 9-25.
-
(2001)
Brain Res
, vol.900
, pp. 9-25
-
-
Abrams, C.K.1
Freidin, M.M.2
Versclis, V.K.3
Bennett, M.V.4
Bargiello, T.A.5
-
48
-
-
0026646956
-
Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines
-
Lee SW, Tomasetto C, Paul D, Keyomarsi K, Sager R (1992) Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines. J Cell Biol 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
-
49
-
-
0030777706
-
Changes in permeability-caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease
-
Oh S, Ri Y, Bennett MV. Trexler EB, Verselis VK, et al. (1997) Changes in permeability-caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease. Neuron 19: 927-938.
-
(1997)
Neuron
, vol.19
, pp. 927-938
-
-
Oh, S.1
Ri, Y.2
Bennett, M.V.3
Trexler, E.B.4
Verselis, V.K.5
-
50
-
-
0032100768
-
Connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease show two distinct behaviors: Loss of function and altered gating properties
-
Ressot C, Gomes D, Dautigny A, Pham-Dinh D, Bruzzone R (1998) Connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease show two distinct behaviors: loss of function and altered gating properties. J Neurosci 18: 4063-4075.
-
(1998)
J Neurosci
, vol.18
, pp. 4063-4075
-
-
Ressot, C.1
Gomes, D.2
Dautigny, A.3
Pham-Dinh, D.4
Bruzzone, R.5
-
51
-
-
0023521842
-
Analysis of the relationship between side-chain conformation and secondary structure in globular proteins
-
McGregor MJ, Islam SA, Sternberg MJ (1987) Analysis of the relationship between side-chain conformation and secondary structure in globular proteins. J Mol Biol 198: 295-310.
-
(1987)
J Mol Biol
, vol.198
, pp. 295-310
-
-
McGregor, M.J.1
Islam, S.A.2
Sternberg, M.J.3
-
52
-
-
18544388829
-
Connexin 26 mutations in cases of sensorineural deafness in eastern Austria
-
Frei K, Szuhai K, Lucas T, Weipoltshammer K, Schofer C, et al. (2002) Connexin 26 mutations in cases of sensorineural deafness in eastern Austria. Eur J Hum Genet 10: 427-432.
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 427-432
-
-
Frei, K.1
Szuhai, K.2
Lucas, T.3
Weipoltshammer, K.4
Schofer, C.5
-
53
-
-
27244452111
-
Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions
-
Zhang Y, Tang W, Ahmad S, Sipp JA, Chen P, et al. (2005) Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions. Proc Natl Acad Sci U S A 102: 15201-15206.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 15201-15206
-
-
Zhang, Y.1
Tang, W.2
Ahmad, S.3
Sipp, J.A.4
Chen, P.5
-
54
-
-
0036432888
-
-
Common JE, Becker D, Di WL, Leigh IM; O'Toole EA, et al. (2002) Functional studies of human skin disease- and deafness-associated connexin 30 mutations. Biochem Biophys Res Common 298: 651-656.
-
Common JE, Becker D, Di WL, Leigh IM; O'Toole EA, et al. (2002) Functional studies of human skin disease- and deafness-associated connexin 30 mutations. Biochem Biophys Res Common 298: 651-656.
-
-
-
-
55
-
-
0031021107
-
Mutation analysis of the connexin 32 (Cx32) gcne in Charcot-Marie-Tooth neuropathy type 1: Identification of five new mutation
-
Nelis E. Simokovic S. Timmerman V, Lofgren A, Rackhovens H. et al. (1997) Mutation analysis of the connexin 32 (Cx32) gcne in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutation. Hum Mutat 9: 47-52.
-
(1997)
Hum Mutat
, vol.9
, pp. 47-52
-
-
Nelis, E.1
Simokovic, S.2
Timmerman, V.3
Lofgren, A.4
Rackhovens, H.5
-
56
-
-
9844245885
-
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
-
Zelante L, Gasparini P, Estivill X, Melchionda S, D'Agruma L, et al. (1997) Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Hum Mol Genet 6: 1605-1609.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1605-1609
-
-
Zelante, L.1
Gasparini, P.2
Estivill, X.3
Melchionda, S.4
D'Agruma, L.5
-
57
-
-
0032727332
-
-
Murgia A, Orzan E, Polli R, Martella M, Minanzi et. al. (1999) Cx26 deafness: mutation analysis and clinical variability. J Med Genet 36: 829-832.
-
Murgia A, Orzan E, Polli R, Martella M, Minanzi et. al. (1999) Cx26 deafness: mutation analysis and clinical variability. J Med Genet 36: 829-832.
-
-
-
-
58
-
-
28144444402
-
GJB2 mutations and degree of hearing loss: A multicenter study
-
Snoeckx RL, Huygen PL, Feldmann D, Marlin S, Dentayelle F, et al. (2005) GJB2 mutations and degree of hearing loss: a multicenter study. Am J Hum Genet 77: 945-957.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 945-957
-
-
Snoeckx, R.L.1
Huygen, P.L.2
Feldmann, D.3
Marlin, S.4
Dentayelle, F.5
-
59
-
-
0036705666
-
Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression
-
Thonnissen E, Rabionet R, Arbones ML, Estivill X, Willecke K, et al. (2002) Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression. Hum Genet 111: 190-197.
-
(2002)
Hum Genet
, vol.111
, pp. 190-197
-
-
Thonnissen, E.1
Rabionet, R.2
Arbones, M.L.3
Estivill, X.4
Willecke, K.5
-
60
-
-
33645047652
-
Ioss of function mutations of the GJB2 gene detected in patients with DENBI-associated hearing impairment
-
Palmada M, Schmalisch K, Bohmer C, Schug N, Pfister M, et al. (2006) Ioss of function mutations of the GJB2 gene detected in patients with DENBI-associated hearing impairment. Neurobiol Dis 22: 112-118.
-
(2006)
Neurobiol Dis
, vol.22
, pp. 112-118
-
-
Palmada, M.1
Schmalisch, K.2
Bohmer, C.3
Schug, N.4
Pfister, M.5
-
61
-
-
49749128979
-
-
Case DA, Darden TA, Cheatham III TE, Simmerling CL, Wang J, et al. (2004) Amber 8 0, University of California, San Francisco.
-
Case DA, Darden TA, Cheatham III TE, Simmerling CL, Wang J, et al. (2004) Amber 8 0, University of California, San Francisco.
-
-
-
-
62
-
-
14244273182
-
Theory and applications of the generalized Born solvation model in macromolecular simulations
-
Tsui V, Case DA (2000) Theory and applications of the generalized Born solvation model in macromolecular simulations. Biopolymers 56: 275-291.
-
(2000)
Biopolymers
, vol.56
, pp. 275-291
-
-
Tsui, V.1
Case, D.A.2
-
63
-
-
0029011701
-
A second generation force field for the simulation of proteins, nucleic acids, and organic molecules
-
Cornell WD, Cieplak P, Bayly CI, Gould IR, Merz KM, et al. (1995) A second generation force field for the simulation of proteins, nucleic acids, and organic molecules. J Am Chem Soc 117: 5179-5197.
-
(1995)
J Am Chem Soc
, vol.117
, pp. 5179-5197
-
-
Cornell, W.D.1
Cieplak, P.2
Bayly, C.I.3
Gould, I.R.4
Merz, K.M.5
-
64
-
-
33646940952
-
Numerical integration of the Cartesian equations of motion of a system with constraints: Molecular dynamics of n-Alkanes
-
Ryckaert JP, Ciccotti G, Berendsen HJ (1977) Numerical integration of the Cartesian equations of motion of a system with constraints: molecular dynamics of n-Alkanes. J Comput Phys 23: 327-341.
-
(1977)
J Comput Phys
, vol.23
, pp. 327-341
-
-
Ryckaert, J.P.1
Ciccotti, G.2
Berendsen, H.J.3
-
65
-
-
0032478818
-
The structure of the potassium channel: Molecular basis of K+ conduction and selectivity
-
Doyle DA, Morais CJ, Pfuetzner RA, Kuo A, Gulbis JM, et al. (1998) The structure of the potassium channel: molecular basis of K+ conduction and selectivity. Science 280: 69-77.
-
(1998)
Science
, vol.280
, pp. 69-77
-
-
Doyle, D.A.1
Morais, C.J.2
Pfuetzner, R.A.3
Kuo, A.4
Gulbis, J.M.5
-
66
-
-
0032512619
-
Rapid refinement of protein interfaces incorporating solvation: Application to the docking problem
-
Jackson RM, Gabb HA, Stemberg MJ (1998) Rapid refinement of protein interfaces incorporating solvation: application to the docking problem. J Mol Biol 276: 265-285.
-
(1998)
J Mol Biol
, vol.276
, pp. 265-285
-
-
Jackson, R.M.1
Gabb, H.A.2
Stemberg, M.J.3
-
67
-
-
0034664682
-
Structure of the amino terminus of a gap junction protein
-
Purnick PE, Benjamin DC, Verselis VK, Bargiello TA, Dowd TL (2000) Structure of the amino terminus of a gap junction protein. Arch Biochem Biophys 381: 181-190.
-
(2000)
Arch Biochem Biophys
, vol.381
, pp. 181-190
-
-
Purnick, P.E.1
Benjamin, D.C.2
Verselis, V.K.3
Bargiello, T.A.4
Dowd, T.L.5
-
68
-
-
0032498942
-
The pattern of disulfide linkages in the extracellular loop regions of connexin 32 suggests a model for the docking interface of gap junctions
-
Foote CI, Zhou L, Zhu X, Nicholson BJ (1998) The pattern of disulfide linkages in the extracellular loop regions of connexin 32 suggests a model for the docking interface of gap junctions. J Cell Biol 140: 1187-1197.
-
(1998)
J Cell Biol
, vol.140
, pp. 1187-1197
-
-
Foote, C.I.1
Zhou, L.2
Zhu, X.3
Nicholson, B.J.4
-
69
-
-
0027136282
-
Comparative protein modelling by satisfaction of spatial restraints
-
Sali A, Blundell TL (1993) Comparative protein modelling by satisfaction of spatial restraints. J Mol Biol 234: 779-815.
-
(1993)
J Mol Biol
, vol.234
, pp. 779-815
-
-
Sali, A.1
Blundell, T.L.2
-
70
-
-
0028991962
-
Modeling mutations and homologous proteins
-
Sali A (1995) Modeling mutations and homologous proteins. Curr Opin Biotechnol 6: 437-451.
-
(1995)
Curr Opin Biotechnol
, vol.6
, pp. 437-451
-
-
Sali, A.1
-
71
-
-
33847025691
-
The role of phosphorylation on the structure and dynamics of phospholamban: A model from molecular simulation
-
Pantano S, Carafoli E (2007) The role of phosphorylation on the structure and dynamics of phospholamban: a model from molecular simulation. Proteins 66: 930-940.
-
(2007)
Proteins
, vol.66
, pp. 930-940
-
-
Pantano, S.1
Carafoli, E.2
-
72
-
-
0037099393
-
Conformational changes in surface structures of isolated connexin 26 gap junctions
-
Muller DJ, Hand GM, Engel A, Sosinsky GE (2002) Conformational changes in surface structures of isolated connexin 26 gap junctions. EMBO J 21: 3598-3607.
-
(2002)
EMBO J
, vol.21
, pp. 3598-3607
-
-
Muller, D.J.1
Hand, G.M.2
Engel, A.3
Sosinsky, G.E.4
-
74
-
-
33846823909
-
Particle Mesh Ewald: An N log(N) method for Ewald sums in large systems
-
Darden TA, York D (1993) Particle Mesh Ewald: an N log(N) method for Ewald sums in large systems. J Chem Phys 98: 10089-10094.
-
(1993)
J Chem Phys
, vol.98
, pp. 10089-10094
-
-
Darden, T.A.1
York, D.2
-
77
-
-
0032780181
-
Situs: A package for docking crystal structures into low-resolution maps from electron microscopy
-
Wriggers W, Milligan RA, McCammon JA (1999) Situs: A package for docking crystal structures into low-resolution maps from electron microscopy. J Struct Biol 125: 185-195.
-
(1999)
J Struct Biol
, vol.125
, pp. 185-195
-
-
Wriggers, W.1
Milligan, R.A.2
McCammon, J.A.3
|