-
1
-
-
0021955150
-
Linear relationship of phlorizin-binding capacity and hexose uptake during differentiation in a clone of LLC-PK1 cells
-
Amsler K, Cook JS (1985) Linear relationship of phlorizin-binding capacity and hexose uptake during differentiation in a clone of LLC-PK1 cells. J Cell Physiol 122:254-258.
-
(1985)
J Cell Physiol
, vol.122
, pp. 254-258
-
-
Amsler, K.1
Cook, J.S.2
-
2
-
-
67649523527
-
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis
-
Anwar S, Riazuddin S, Ahmed ZM, Tasneem S, Ateeq-ul-Jaleel, Khan SY, Griffith AJ, Friedman TB, Riazuddin S (2009) SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis. J Hum Genet 54:266-270.
-
(2009)
J Hum Genet
, vol.54
, pp. 266-270
-
-
Anwar, S.1
Riazuddin, S.2
Ahmed, Z.M.3
Tasneem, S.4
Ateeq-ul-Jaleel5
Khan, S.Y.6
Griffith, A.J.7
Friedman, T.B.8
Riazuddin, S.9
-
3
-
-
0032487440
-
Small espin: A third actin-bundling protein and potential forked protein ortholog in brush border microvilli
-
Bartles JR, Zheng L, Li A, Wierda A, Chen B (1998) Small espin: a third actin-bundling protein and potential forked protein ortholog in brush border microvilli. J Cell Biol 143:107-119.
-
(1998)
J Cell Biol
, vol.143
, pp. 107-119
-
-
Bartles, J.R.1
Zheng, L.2
Li, A.3
Wierda, A.4
Chen, B.5
-
4
-
-
0034672784
-
Expression and localization of prestin and the sugar transporter GLUT-5 during development of electromotility in cochlear outer hair cells
-
Belyantseva IA, Adler HJ, Curi R, Frolenkov GI, Kachar B (2000) Expression and localization of prestin and the sugar transporter GLUT-5 during development of electromotility in cochlear outer hair cells. J Neurosci 20:RC116(1-5).
-
(2000)
J Neurosci
, vol.20
-
-
Belyantseva, I.A.1
Adler, H.J.2
Curi, R.3
Frolenkov, G.I.4
Kachar, B.5
-
5
-
-
0345133276
-
Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle
-
Belyantseva IA, Boger ET, Friedman TB (2003) Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle. Proc Natl Acad Sci U S A 100:13958-13963.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 13958-13963
-
-
Belyantseva, I.A.1
Boger, E.T.2
Friedman, T.B.3
-
6
-
-
13944260197
-
Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia
-
Belyantseva IA, Boger ET, Naz S, Frolenkov GI, Sellers JR, Ahmed ZM, Griffith AJ, Friedman TB (2005) Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia. Nat Cell Biol 7:148-156.
-
(2005)
Nat Cell Biol
, vol.7
, pp. 148-156
-
-
Belyantseva, I.A.1
Boger, E.T.2
Naz, S.3
Frolenkov, G.I.4
Sellers, J.R.5
Ahmed, Z.M.6
Griffith, A.J.7
Friedman, T.B.8
-
7
-
-
0033822063
-
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
-
Bitner-Glindzicz M, Lindley KJ, Rutland P, Blaydon D, Smith VV, Milla PJ, Hussain K, Furth-Lavi J, Cosgrove KE, Shepherd RM, Barnes PD, O'Brien RE, Farndon PA, Sowden J, Liu XZ, Scanlan MJ, Malcolm S, Dunne MJ, Aynsley-Green A, Glaser B (2000) A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene. Nat Genet 26:56-60.
-
(2000)
Nat Genet
, vol.26
, pp. 56-60
-
-
Bitner-Glindzicz, M.1
Lindley, K.J.2
Rutland, P.3
Blaydon, D.4
Smith, V.V.5
Milla, P.J.6
Hussain, K.7
Furth-Lavi, J.8
Cosgrove, K.E.9
Shepherd, R.M.10
Barnes, P.D.11
O'Brien, R.E.12
Farndon, P.A.13
Sowden, J.14
Liu, X.Z.15
Scanlan, M.J.16
Malcolm, S.17
Dunne, M.J.18
Aynsley-Green, A.19
Glaser, B.20
more..
-
8
-
-
12244277402
-
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle
-
Boëda B, El-Amraoui A, Bahloul A, Goodyear R, Daviet L, Blanchard S, Perfettini I, Fath KR, Shorte S, Reiners J, Houdusse A, Legrain P, Wolfrum U, Richardson G, Petit C (2002) Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle. EMBO J 21:6689-6699.
-
(2002)
EMBO J
, vol.21
, pp. 6689-6699
-
-
Boëda, B.1
El-Amraoui, A.2
Bahloul, A.3
Goodyear, R.4
Daviet, L.5
Blanchard, S.6
Perfettini, I.7
Fath, K.R.8
Shorte, S.9
Reiners, J.10
Houdusse, A.11
Legrain, P.12
Wolfrum, U.13
Richardson, G.14
Petit, C.15
-
9
-
-
0035168168
-
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
-
Bork JM, Peters LM, Riazuddin S, Bernstein SL, Ahmed ZM, Ness SL, Polomeno R, Ramesh A, Schloss M, Srisailpathy CR, Wayne S, Bellman S, Desmukh D, Ahmed Z, Khan SN, Kaloustian VM, Li XC, Lalwani A, Riazuddin S, Bitner- Glindzicz M, Nance WE, Liu XZ, Wistow G, Smith RJ, Griffith AJ, Wilcox ER, Friedman TB, Morell RJ (2001) Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet 68:26-37.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 26-37
-
-
Bork, J.M.1
Peters, L.M.2
Riazuddin, S.3
Bernstein, S.L.4
Ahmed, Z.M.5
Ness, S.L.6
Polomeno, R.7
Ramesh, A.8
Schloss, M.9
Srisailpathy, C.R.10
Wayne, S.11
Bellman, S.12
Desmukh, D.13
Ahmed, Z.14
Khan, S.N.15
Kaloustian, V.M.16
Li, X.C.17
Lalwani, A.18
Riazuddin, S.19
Bitner- Glindzicz, M.20
Nance, W.E.21
Liu, X.Z.22
Wistow, G.23
Smith, R.J.24
Griffith, A.J.25
Wilcox, E.R.26
Friedman, T.B.27
Morell, R.J.28
more..
-
10
-
-
70450176317
-
Polarized traffic towards the cell surface: How to find the route
-
Carmosino M, Valenti G, Caplan M, Svelto M (2010) Polarized traffic towards the cell surface: how to find the route. Biol Cell 102:75-91.
-
(2010)
Biol Cell
, vol.102
, pp. 75-91
-
-
Carmosino, M.1
Valenti, G.2
Caplan, M.3
Svelto, M.4
-
11
-
-
0032741307
-
Espin contains an additional actin-binding site in its N terminus and is a major actin-bundling protein of the Sertoli cell-spermatid ectoplasmic specialization junctional plaque
-
Chen B, Li A, Wang D, Wang M, Zheng L, Bartles JR (1999) Espin contains an additional actin-binding site in its N terminus and is a major actin-bundling protein of the Sertoli cell-spermatid ectoplasmic specialization junctional plaque. Mol Biol Cell 10:4327-4339.
-
(1999)
Mol Biol Cell
, vol.10
, pp. 4327-4339
-
-
Chen, B.1
Li, A.2
Wang, D.3
Wang, M.4
Zheng, L.5
Bartles, J.R.6
-
12
-
-
15144351296
-
Conservation within the myosin motor domain: Implications for structure and function
-
Cope MJ, Whisstock J, Rayment I, Kendrick-Jones J (1996) Conservation within the myosin motor domain: implications for structure and function. Structure 4:969-987.
-
(1996)
Structure
, vol.4
, pp. 969-987
-
-
Cope, M.J.1
Whisstock, J.2
Rayment, I.3
Kendrick-Jones, J.4
-
13
-
-
42949132296
-
Prestin-based outer hair cell motility is necessary for mammalian cochlear amplification
-
Dallos P, Wu X, Cheatham MA, Gao J, Zheng J, Anderson CT, Jia S, Wang X, Cheng WH, Sengupta S, He DZ, Zuo J (2008) Prestin-based outer hair cell motility is necessary for mammalian cochlear amplification. Neuron 58:333-339.
-
(2008)
Neuron
, vol.58
, pp. 333-339
-
-
Dallos, P.1
Wu, X.2
Cheatham, M.A.3
Gao, J.4
Zheng, J.5
Anderson, C.T.6
Jia, S.7
Wang, X.8
Cheng, W.H.9
Sengupta, S.10
He, D.Z.11
Zuo, J.12
-
14
-
-
14944347399
-
Effects of cyclic nucleotides on the function of prestin
-
DOI 10.1113/jphysiol.2004.078857
-
Deák L, Zheng J, Orem A, Du GG, Aguiñaga S, Matsuda K, Dallos P (2005) Effects of cyclic nucleotides on the function of prestin. J Physiol 563:483-496. (Pubitemid 40360907)
-
(2005)
Journal of Physiology
, vol.563
, Issue.2
, pp. 483-496
-
-
Deak, L.1
Zheng, J.2
Orem, A.3
Du, G.-G.4
Aguinaga, S.5
Matsuda, K.6
Dallos, P.7
-
15
-
-
13544251711
-
Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at stereocilia tips and interact directly
-
Delprat B, Michel V, Goodyear R, Yamasaki Y, Michalski N, El-Amraoui A, Perfettini I, Legrain P, Richardson G, Hardelin JP, Petit C (2005) Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at stereocilia tips and interact directly. Hum Mol Genet 14:401-410.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 401-410
-
-
Delprat, B.1
Michel, V.2
Goodyear, R.3
Yamasaki, Y.4
Michalski, N.5
El-Amraoui, A.6
Perfettini, I.7
Legrain, P.8
Richardson, G.9
Hardelin, J.P.10
Petit, C.11
-
16
-
-
0035168151
-
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
-
DOI 10.1038/83660
-
Di Palma F, Holme RH, Bryda EC, Belyantseva IA, Pellegrino R, Kachar B, Steel KP, Noben-Trauth K (2001a) Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. Nat Genet 27:103-107. (Pubitemid 32044528)
-
(2001)
Nature Genetics
, vol.27
, Issue.1
, pp. 103-107
-
-
Palma, F.D.1
Holme, R.H.2
Bryda, E.C.3
Belyantseva, I.A.4
Pellegrino, R.5
Kachar, B.6
Steel, K.P.7
Noben-Trauth, K.8
-
17
-
-
0035960929
-
Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23)
-
DOI 10.1016/S0378-1119(01)00761-2, PII S0378111901007612
-
Di Palma F, Pellegrino R, Noben-Trauth K (2001b) Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23). Gene 281:31-41. (Pubitemid 34031902)
-
(2001)
Gene
, vol.281
, Issue.1-2
, pp. 31-41
-
-
Di Palma, F.1
Pellegrino, R.2
Noben-Trauth, K.3
-
18
-
-
32944469631
-
Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation
-
Donaudy F, Zheng L, Ficarella R, Ballana E, Carella M, Melchionda S, Estivill X, Bartles JR, Gasparini P (2006) Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation. J Med Genet 43:157-161.
-
(2006)
J Med Genet
, vol.43
, pp. 157-161
-
-
Donaudy, F.1
Zheng, L.2
Ficarella, R.3
Ballana, E.4
Carella, M.5
Melchionda, S.6
Estivill, X.7
Bartles, J.R.8
Gasparini, P.9
-
19
-
-
0030604722
-
Crystal structures of a complexed and peptide-free membrane protein- Binding domain: Molecular basis of peptide recognition by PDZ
-
DOI 10.1016/S0092-8674(00)81307-0
-
Doyle DA, Lee A, Lewis J, Kim E, Sheng M, MacKinnon R (1996) Crystal structures of a complexed and peptide-free membrane protein-binding domain: molecular basis of peptide recognition by PDZ. Cell 85:1067-1076. (Pubitemid 26231173)
-
(1996)
Cell
, vol.85
, Issue.7
, pp. 1067-1076
-
-
Doyle, D.A.1
Lee, A.2
Lewis, J.3
Kim, E.4
Sheng, M.5
MacKinnon, R.6
-
20
-
-
27844517356
-
Usher I syndrome: Unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells
-
DOI 10.1242/jcs.02636
-
El-Amraoui A, Petit C (2005) Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells. J Cell Sci 118:4593-4603. (Pubitemid 41646370)
-
(2005)
Journal of Cell Science
, vol.118
, Issue.20
, pp. 4593-4603
-
-
El-Amraoui, A.1
Petit, C.2
-
21
-
-
16944366606
-
Pendred syndrome is caused by mutations in the putative sulphate transporter gene (PDS)
-
Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, Adawi F, Hazani E, Nassir E, Baxevanis AD, Sheffield VC, Green ED (1997) Pendred syndrome is caused by mutations in the putative sulphate transporter gene (PDS). Nat Genet 17:411-422.
-
(1997)
Nat Genet
, vol.17
, pp. 411-422
-
-
Everett, L.A.1
Glaser, B.2
Beck, J.C.3
Idol, J.R.4
Buchs, A.5
Heyman, M.6
Adawi, F.7
Hazani, E.8
Nassir, E.9
Baxevanis, A.D.10
Sheffield, V.C.11
Green, E.D.12
-
22
-
-
16844374089
-
The building blocks for basolateral vesicles in polarized epithelial cells
-
Fölsch H (2005) The building blocks for basolateral vesicles in polarized epithelial cells. Trends Cell Biol 15:222-228.
-
(2005)
Trends Cell Biol
, vol.15
, pp. 222-228
-
-
Fölsch, H.1
-
23
-
-
0032692619
-
A novel clathrin adaptor complex mediates basolateral targeting in polarized epithelial cells
-
Fölsch H, Ohno H, Bonifacino JS, Mellman I (1999) A novel clathrin adaptor complex mediates basolateral targeting in polarized epithelial cells. Cell 99:189-198.
-
(1999)
Cell
, vol.99
, pp. 189-198
-
-
Fölsch, H.1
Ohno, H.2
Bonifacino, J.S.3
Mellman, I.4
-
24
-
-
46749092031
-
The dimensions and composition of stereociliary rootlets in mammalian cochlear hair cells: Comparison between high- And low-frequency cells and evidence for a connection to the lateral membrane
-
Furness DN, Mahendrasingam S, Ohashi M, Fettiplace R, Hackney CM (2008) The dimensions and composition of stereociliary rootlets in mammalian cochlear hair cells: comparison between high- and low-frequency cells and evidence for a connection to the lateral membrane. J Neurosci 28:6342-6353.
-
(2008)
J Neurosci
, vol.28
, pp. 6342-6353
-
-
Furness, D.N.1
Mahendrasingam, S.2
Ohashi, M.3
Fettiplace, R.4
Hackney, C.M.5
-
25
-
-
0032883413
-
Structural mechanism of muscle contraction
-
Geeves MA, Holmes KC (1999) Structural mechanism of muscle contraction. Annu Rev Biochem 68:687-728.
-
(1999)
Annu Rev Biochem
, vol.68
, pp. 687-728
-
-
Geeves, M.A.1
Holmes, K.C.2
-
26
-
-
33746786784
-
Molecular determinants for differential membrane trafficking of PMCA1 and PMCA2 in mammalian hair cells
-
DOI 10.1242/jcs.03030
-
Grati M, Aggarwal N, Strehler EE, Wenthold RJ (2006) Molecular determinants for differential membrane trafficking of PMCA1 and PMCA2 in mammalian hair cells. J Cell Sci 119:2995-3007. (Pubitemid 44177878)
-
(2006)
Journal of Cell Science
, vol.119
, Issue.14
, pp. 2995-3007
-
-
Grati, M.1
Aggarwal, N.2
Strehler, E.E.3
Wenthold, R.J.4
-
27
-
-
65549085188
-
Harmonin mutations cause mechanotransduction defects in cochlear hair cells
-
Grillet N, Xiong W, Reynolds A, Kazmierczak P, Sato T, Lillo C, Dumont RA, Hintermann E, Sczaniecka A, Schwander M, Williams D, Kachar B, Gillespie PG, Müller U (2009) Harmonin mutations cause mechanotransduction defects in cochlear hair cells. Neuron 62:375-387.
-
(2009)
Neuron
, vol.62
, pp. 375-387
-
-
Grillet, N.1
Xiong, W.2
Reynolds, A.3
Kazmierczak, P.4
Sato, T.5
Lillo, C.6
Dumont, R.A.7
Hintermann, E.8
Sczaniecka, A.9
Schwander, M.10
Williams, D.11
Kachar, B.12
Gillespie, P.G.13
Müller, U.14
-
28
-
-
0034740693
-
Mechanism and role of PDZ domains in signaling complex assembly
-
Harris BZ, Lim WA (2001) Mechanism and role of PDZ domains in signaling complex assembly. J Cell Sci 114:3219-3231.
-
(2001)
J Cell Sci
, vol.114
, pp. 3219-3231
-
-
Harris, B.Z.1
Lim, W.A.2
-
29
-
-
34547623918
-
Quality control of eukaryotic mRNA: Safeguarding cells from abnormal mRNA function
-
DOI 10.1101/gad.1566807
-
Isken O, Maquat LE (2007) Quality control of eukaryotic mRNA: safeguarding cells from abnormal mRNA function. Genes Dev 21:1833-1856. (Pubitemid 47204924)
-
(2007)
Genes and Development
, vol.21
, Issue.15
, pp. 1833-1856
-
-
Isken, O.1
Maquat, L.E.2
-
30
-
-
35449005942
-
Lateral wall protein content mediates alterations in cochlear outer hair cell mechanics before and after hearing onset
-
DOI 10.1002/cm.20217
-
Jensen-Smith H, Hallworth R (2007) Lateral wall protein content mediates alterations in cochlear outer hair cell mechanics before and after hearing onset. Cell Motil Cytoskeleton 64:705-717. (Pubitemid 350194533)
-
(2007)
Cell Motility and the Cytoskeleton
, vol.64
, Issue.9
, pp. 705-717
-
-
Jensen-Smith, H.1
Hallworth, R.2
-
31
-
-
0028075559
-
Postnatal development of the hamster cochlea. II. Growth and differentiation of stereocilia bundles
-
DOI 10.1002/cne.903500204
-
Kaltenbach JA, Falzarano PR, Simpson TH (1994) Postnatal development of the hamster cochlea. II. Growth and differentiation of stereocilia bundles. J Comp Neurol 350:187-198. (Pubitemid 24346678)
-
(1994)
Journal of Comparative Neurology
, vol.350
, Issue.2
, pp. 187-198
-
-
Kaltenbach, J.A.1
Falzarano, P.R.2
Simpson, T.H.3
-
32
-
-
34548509448
-
Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells
-
DOI 10.1038/nature06091, PII NATURE06091
-
Kazmierczak P, Sakaguchi H, Tokita J, Wilson-Kubalek EM, Milligan RA, Müller U, Kachar B (2007) Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells. Nature 449:87-91. (Pubitemid 47373771)
-
(2007)
Nature
, vol.449
, Issue.7158
, pp. 87-91
-
-
Kazmierczak, P.1
Sakaguchi, H.2
Tokita, J.3
Wilson-Kubalek, E.M.4
Milligan, R.A.5
Muller, U.6
Kachar, B.7
-
33
-
-
0036783931
-
Immunocytochemical localization of pendrin in intercalated cell subtypes in rat and mouse kidney
-
Kim YH, Kwon TH, Frische S, Kim J, Tisher CC, Madsen KM, Nielsen S (2002) Immunocytochemical localization of pendrin in intercalated cell subtypes in rat and mouse kidney. Am J Physiol Renal Physiol 283:F744-F754.
-
(2002)
Am J Physiol Renal Physiol
, vol.283
-
-
Kim, Y.H.1
Kwon, T.H.2
Frische, S.3
Kim, J.4
Tisher, C.C.5
Madsen, K.M.6
Nielsen, S.7
-
35
-
-
34447276474
-
The Structural Coupling between ATPase Activation and Recovery Stroke in the Myosin II Motor
-
DOI 10.1016/j.str.2007.06.008, PII S0969212607002146
-
Koppole S, Smith JC, Fischer S (2007) The structural coupling between ATPase activation and recovery stroke in the myosin II motor. Structure 15:825-837. (Pubitemid 47042437)
-
(2007)
Structure
, vol.15
, Issue.7
, pp. 825-837
-
-
Koppole, S.1
Smith, J.C.2
Fischer, S.3
-
36
-
-
18844448958
-
Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development
-
Lagziel A, Ahmed ZM, Schultz JM, Morell RJ, Belyantseva IA, Friedman TB (2005) Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development. Dev Biol 280:295-306.
-
(2005)
Dev Biol
, vol.280
, pp. 295-306
-
-
Lagziel, A.1
Ahmed, Z.M.2
Schultz, J.M.3
Morell, R.J.4
Belyantseva, I.A.5
Friedman, T.B.6
-
37
-
-
70349215361
-
Expression of cadherin 23 isoforms is not conserved: Implications for a mouse model of Usher syndrome type 1D
-
Lagziel A, Overlack N, Bernstein SL, Morell RJ, Wolfrum U, Friedman TB (2009) Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D. Mol Vis 15:1843-1857.
-
(2009)
Mol Vis
, vol.15
, pp. 1843-1857
-
-
Lagziel, A.1
Overlack, N.2
Bernstein, S.L.3
Morell, R.J.4
Wolfrum, U.5
Friedman, T.B.6
-
38
-
-
44449102085
-
A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth
-
Lefèvre G, Michel V, Weil D, Lepelletier L, Bizard E, Wolfrum U, Hardelin JP, Petit C (2008) A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. Development 135:1427-1437.
-
(2008)
Development
, vol.135
, pp. 1427-1437
-
-
Lefèvre, G.1
Michel, V.2
Weil, D.3
Lepelletier, L.4
Bizard, E.5
Wolfrum, U.6
Hardelin, J.P.7
Petit, C.8
-
39
-
-
39149139311
-
Architecture of the mouse utricle: Macular organization and hair bundle heights
-
Li A, Xue J, Peterson EH (2008) Architecture of the mouse utricle: macular organization and hair bundle heights. J Neurophysiol 99:718-733.
-
(2008)
J Neurophysiol
, vol.99
, pp. 718-733
-
-
Li, A.1
Xue, J.2
Peterson, E.H.3
-
40
-
-
0346849715
-
Espin cross-links cause the elongation of microvillus-type parallel actin bundles in vivo
-
Loomis PA, Zheng L, Sekerková G, Changyaleket B, Mugnaini E, Bartles JR (2003) Espin cross-links cause the elongation of microvillus-type parallel actin bundles in vivo. J Cell Biol 163:1045-1055.
-
(2003)
J Cell Biol
, vol.163
, pp. 1045-1055
-
-
Loomis, P.A.1
Zheng, L.2
Sekerková, G.3
Changyaleket, B.4
Mugnaini, E.5
Bartles, J.R.6
-
41
-
-
33646683606
-
Targeted wild-type and jerker espins reveal a novel WH2 domain-dependent way to make actin bundles in cells
-
Loomis PA, Kelly AE, Zheng L, Changyaleket B, Sekerková G, Mugnaini E, Ferreira A, Mullins RD, Bartles JR (2006) Targeted wild-type and jerker espins reveal a novel, WH2 domain-dependent way to make actin bundles in cells. J Cell Sci 119:1655-1665.
-
(2006)
J Cell Sci
, vol.119
, pp. 1655-1665
-
-
Loomis, P.A.1
Kelly, A.E.2
Zheng, L.3
Changyaleket, B.4
Sekerková, G.5
Mugnaini, E.6
Ferreira, A.7
Mullins, R.D.8
Bartles, J.R.9
-
42
-
-
0043168114
-
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
-
Mburu P, Mustapha M, Varela A, Weil D, El-Amraoui A, Holme RH, Rump A, Hardisty RE, Blanchard S, Coimbra RS, Perfettini I, Parkinson N, Mallon AM, Glenister P, Rogers MJ, Paige AJ, Moir L, Clay J, Rosenthal A, Liu XZ, Blanco G, Steel KP, Petit C, Brown SD (2003) Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31. Nat Genet 34:421-428.
-
(2003)
Nat Genet
, vol.34
, pp. 421-428
-
-
Mburu, P.1
Mustapha, M.2
Varela, A.3
Weil, D.4
El-Amraoui, A.5
Holme, R.H.6
Rump, A.7
Hardisty, R.E.8
Blanchard, S.9
Coimbra, R.S.10
Perfettini, I.11
Parkinson, N.12
Mallon, A.M.13
Glenister, P.14
Rogers, M.J.15
Paige, A.J.16
Moir, L.17
Clay, J.18
Rosenthal, A.19
Liu, X.Z.20
Blanco, G.21
Steel, Kp.22
Petit, C.23
Brown, S.D.24
more..
-
43
-
-
34548809124
-
Rab-GTPase-dependent endocytic recycling of Kv1.5 in atrial myocytes
-
McEwen DP, Schumacher SM, Li Q, Benson MD, Iñiguez-Lluhí JA, Van Genderen KM, Martens JR (2007) Rab-GTPase-dependent endocytic recycling of Kv1.5 in atrial myocytes. J Biol Chem 282:29612-29620.
-
(2007)
J Biol Chem
, vol.282
, pp. 29612-29620
-
-
McEwen, D.P.1
Schumacher, S.M.2
Li, Q.3
Benson, M.D.4
Iñiguez-Lluhí, J.A.5
Van Genderen, K.M.6
Martens, J.R.7
-
44
-
-
73949146587
-
Harmonin b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells
-
Michalski N, Michel V, Caberlotto E, Lefèvre GM, van Aken AF, Tinevez JY, Bizard E, Houbron C, Weil D, Hardelin JP, Richardson GP, Kros CJ, Martin P, Petit C (2009) Harmonin b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells. Pflugers Arch 459:115-130.
-
(2009)
Pflugers Arch
, vol.459
, pp. 115-130
-
-
Michalski, N.1
Michel, V.2
Caberlotto, E.3
Lefèvre, G.M.4
Van Aken, A.F.5
Tinevez, J.Y.6
Bizard, E.7
Houbron, C.8
Weil, D.9
Hardelin, J.P.10
Richardson, G.P.11
Kros, C.J.12
Martin, P.13
Petit, C.14
-
45
-
-
18844363457
-
Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells
-
Michel V, Goodyear RJ, Weil D, Marcotti W, Perfettini I, Wolfrum U, Kros CJ, Richardson GP, Petit C (2005) Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells. Dev Biol 280:281-294.
-
(2005)
Dev Biol
, vol.280
, pp. 281-294
-
-
Michel, V.1
Goodyear, R.J.2
Weil, D.3
Marcotti, W.4
Perfettini, I.5
Wolfrum, U.6
Kros, C.J.7
Richardson, G.P.8
Petit, C.9
-
46
-
-
1242317663
-
The SLC26 gene family of multifunctional anion exchangers
-
Mount DB, Romero MF (2004) The SLC26 gene family of multifunctional anion exchangers. Pflugers Arch 447:710-721.
-
(2004)
Pflugers Arch
, vol.447
, pp. 710-721
-
-
Mount, D.B.1
Romero, M.F.2
-
47
-
-
50849144332
-
Cadherins and mechanotransduction by hair cells
-
Müller U (2008) Cadherins and mechanotransduction by hair cells. Curr Opin Cell Biol 20:557-566.
-
(2008)
Curr Opin Cell Biol
, vol.20
, pp. 557-566
-
-
Müller, U.1
-
48
-
-
38349104748
-
The varitint-waddler (Va) deafness mutation in TRPML3 generates constitutive, inward rectifying currents and causes cell degeneration
-
Nagata K, Zheng L, Madathany T, Castiglioni AJ, Bartles JR, García-Añoveros J (2008) The varitint-waddler (Va) deafness mutation in TRPML3 generates constitutive, inward rectifying currents and causes cell degeneration. Proc Natl Acad Sci U S A 105:353-358.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 353-358
-
-
Nagata, K.1
Zheng, L.2
Madathany, T.3
Castiglioni, A.J.4
Bartles, J.R.5
García-Añoveros, J.6
-
49
-
-
34948880109
-
Mutational spectrum of MYO15A: The large N-terminal extension of myosin XVa is required for hearing
-
Nal N, Ahmed ZM, Erkal E, Alper OM, Lüleci G, Dinç O, Waryah AM, Ain Q, Tasneem S, Husnain T, Chattaraj P, Riazuddin S, Boger E, Ghosh M, Kabra M, Riazuddin S, Morell RJ, Friedman TB (2007) Mutational spectrum of MYO15A: The large N-terminal extension of myosin XVa is required for hearing. Hum Mutat 28:1014-1019.
-
(2007)
Hum Mutat
, vol.28
, pp. 1014-1019
-
-
Nal, N.1
Ahmed, Z.M.2
Erkal, E.3
Alper, O.M.4
Lüleci, G.5
Dinç, O.6
Waryah, A.M.7
Ain, Q.8
Tasneem, S.9
Husnain, T.10
Chattaraj, P.11
Riazuddin, S.12
Boger, E.13
Ghosh, M.14
Kabra, M.15
Riazuddin, S.16
Morell, R.J.17
Friedman, T.B.18
-
50
-
-
27744513304
-
N-terminal-mediated homomultimerization of prestin, the outer hair cell motor protein
-
Navaratnam D, Bai JP, Samaranayake H, Santos-Sacchi J (2005) N-terminal-mediated homomultimerization of prestin, the outer hair cell motor protein. Biophys J 89:3345-3352.
-
(2005)
Biophys J
, vol.89
, pp. 3345-3352
-
-
Navaratnam, D.1
Bai, J.P.2
Samaranayake, H.3
Santos-Sacchi, J.4
-
51
-
-
2942593267
-
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction
-
Naz S, Griffith AJ, Riazuddin S, Hampton LL, Battey JF Jr, Khan SN, Riazuddin S, Wilcox ER, Friedman TB (2004) Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction. J Med Genet 41:591-595.
-
(2004)
J Med Genet
, vol.41
, pp. 591-595
-
-
Naz, S.1
Griffith, A.J.2
Riazuddin, S.3
Hampton, L.L.4
Battey Jr., J.F.5
Khan, S.N.6
Riazuddin, S.7
Wilcox, E.R.8
Friedman, T.B.9
-
52
-
-
65249180705
-
Assembling stable hair cell tip link complex via multidentate interactions between harmonin and cadherin 23
-
Pan L, Yan J, Wu L, Zhang M (2009) Assembling stable hair cell tip link complex via multidentate interactions between harmonin and cadherin 23. Proc Natl Acad Sci U S A 106:5575-5580.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 5575-5580
-
-
Pan, L.1
Yan, J.2
Wu, L.3
Zhang, M.4
-
53
-
-
72849115649
-
Twinfilin 2 regulates actin filament lengths in cochlear stereocilia
-
Peng AW, Belyantseva IA, Hsu PD, Friedman TB, Heller S (2009) Twinfilin 2 regulates actin filament lengths in cochlear stereocilia. J Neurosci 29:15083-15088.
-
(2009)
J Neurosci
, vol.29
, pp. 15083-15088
-
-
Peng, A.W.1
Belyantseva, I.A.2
Hsu, P.D.3
Friedman, T.B.4
Heller, S.5
-
54
-
-
33846794288
-
Structural polymorphism of the actin-espin system: A prototypical system of filaments and linkers in stereocilia
-
Purdy KR, Bartles JR, Wong GC (2007) Structural polymorphism of the actin-espin system: a prototypical system of filaments and linkers in stereocilia. Phys Rev Lett 98:058105.
-
(2007)
Phys Rev Lett
, vol.98
, pp. 058105
-
-
Purdy, K.R.1
Bartles, J.R.2
Wong, G.C.3
-
55
-
-
0029024879
-
Structural interpretation of the mutations in the β-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy
-
Rayment I, Holden HM, Sellers JR, Fananapazir L, Epstein ND (1995) Structural interpretation of the mutations in the β-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy. Proc Natl Acad Sci U S A 92:3864-3868.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 3864-3868
-
-
Rayment, I.1
Holden, H.M.2
Sellers, J.R.3
Fananapazir, L.4
Epstein, N.D.5
-
56
-
-
33646856845
-
Molecular basis of human Usher syndrome: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease
-
Reiners J, Nagel-Wolfrum K, Jürgens K, Märker T, Wolfrum U (2006) Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease. Exp Eye Res 83:97-119.
-
(2006)
Exp Eye Res
, vol.83
, pp. 97-119
-
-
Reiners, J.1
Nagel-Wolfrum, K.2
Jürgens, K.3
Märker, T.4
Wolfrum, U.5
-
57
-
-
0034463973
-
Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells
-
Royaux IE, Suzuki K, Mori A, Katoh R, Everett LA, Kohn LD, Green ED (2000) Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells. Endocrinology 141:839-845.
-
(2000)
Endocrinology
, vol.141
, pp. 839-845
-
-
Royaux, I.E.1
Suzuki, K.2
Mori, A.3
Katoh, R.4
Everett, L.A.5
Kohn, L.D.6
Green, E.D.7
-
58
-
-
0141729459
-
Localization and functional studies of pendrin the mouse inner ear provide insight about the etiology of deafness in pendred syndrome
-
Royaux IE, Belyantseva IA, Wu T, Kachar B, Everett LA, Marcus DC, Green ED (2003) Localization and functional studies of pendrin the mouse inner ear provide insight about the etiology of deafness in pendred syndrome. J Assoc Res Otolaryngol 4:394-404.
-
(2003)
J Assoc Res Otolaryngol
, vol.4
, pp. 394-404
-
-
Royaux, I.E.1
Belyantseva, I.A.2
Wu, T.3
Kachar, B.4
Everett, L.A.5
Marcus, D.C.6
Green, E.D.7
-
59
-
-
2942585053
-
Espins are multifunctional actin cytoskeletal regulatory proteins in the microvilli of chemosensory and mechanosensory cells
-
Sekerková G, Zheng L, Loomis PA, Changyaleket B, Whitlon DS, Mugnaini E, Bartles JR (2004) Espins are multifunctional actin cytoskeletal regulatory proteins in the microvilli of chemosensory and mechanosensory cells. J Neurosci 24:5445-5456.
-
(2004)
J Neurosci
, vol.24
, pp. 5445-5456
-
-
Sekerková, G.1
Zheng, L.2
Loomis, P.A.3
Changyaleket, B.4
Whitlon, D.S.5
Mugnaini, E.6
Bartles, J.R.7
-
60
-
-
33644756413
-
Differential expression of espin isoforms during epithelial morphogenesis, stereociliogenesis and postnatal maturation in the developing inner ear
-
Sekerková G, Zheng L, Mugnaini E, Bartles JR (2006) Differential expression of espin isoforms during epithelial morphogenesis, stereociliogenesis and postnatal maturation in the developing inner ear. Dev Biol 291:83-95.
-
(2006)
Dev Biol
, vol.291
, pp. 83-95
-
-
Sekerková, G.1
Zheng, L.2
Mugnaini, E.3
Bartles, J.R.4
-
61
-
-
50049122837
-
3- secretion and in regulation of CFTR in the parotid duct
-
3- secretion and in regulation of CFTR in the parotid duct. J Physiol 586:3813-3824.
-
(2008)
J Physiol
, vol.586
, pp. 3813-3824
-
-
Shcheynikov, N.1
Yang, D.2
Wang, Y.3
Zeng, W.4
Karniski, L.P.5
So, I.6
Wall, S.M.7
Muallem, S.8
-
62
-
-
70849098334
-
Cooperativity and frustration in protein-mediated parallel actin bundles
-
Shin H, Purdy Drew KR, Bartles JR, Wong GC, Grason GM (2009) Cooperativity and frustration in protein-mediated parallel actin bundles. Phys Rev Lett 103:238102.
-
(2009)
Phys Rev Lett
, vol.103
, pp. 238102
-
-
Shin, H.1
Purdy Drew, K.R.2
Bartles, J.R.3
Wong, G.C.4
Grason, G.M.5
-
63
-
-
0037069346
-
The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions
-
Siemens J, Kazmierczak P, Reynolds A, Sticker M, Littlewood-Evans A, Müller U (2002) The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions. Proc Natl Acad Sci U S A 99:14946-14951.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 14946-14951
-
-
Siemens, J.1
Kazmierczak, P.2
Reynolds, A.3
Sticker, M.4
Littlewood-Evans, A.5
Müller, U.6
-
64
-
-
2342421512
-
Cadherin 23 is a component of the tip link in hair-cell stereocilia
-
Siemens J, Lillo C, Dumont RA, Reynolds A, Williams DS, Gillespie PG, Müller U (2004) Cadherin 23 is a component of the tip link in hair-cell stereocilia. Nature 428:950-955.
-
(2004)
Nature
, vol.428
, pp. 950-955
-
-
Siemens, J.1
Lillo, C.2
Dumont, R.A.3
Reynolds, A.4
Williams, D.S.5
Gillespie, P.G.6
Müller, U.7
-
65
-
-
24344508126
-
The unconventional myosin-VIIa associates with lysosomes
-
Soni LE, Warren CM, Bucci C, Orten DJ, Hasson T (2005) The unconventional myosin-VIIa associates with lysosomes. Cell Motil Cytoskeleton 62:13-26.
-
(2005)
Cell Motil Cytoskeleton
, vol.62
, pp. 13-26
-
-
Soni, L.E.1
Warren, C.M.2
Bucci, C.3
Orten, D.J.4
Hasson, T.5
-
67
-
-
0022909002
-
Actin filaments, stereocilia, and hair cells of the bird cochlea. III. the development and differentiation of hair cells and stereocilia
-
Tilney LG, Tilney MS, Saunders JS, DeRosier DJ (1986) Actin filaments, stereocilia, and hair cells of the bird cochlea. III. The development and differentiation of hair cells and stereocilia. Dev Biol 116:100-118.
-
(1986)
Dev Biol
, vol.116
, pp. 100-118
-
-
Tilney, L.G.1
Tilney, M.S.2
Saunders, J.S.3
DeRosier, D.J.4
-
68
-
-
0036218579
-
MYO1A (brush border myosin I) dynamics in the brush border of LLC-PK1-CL4 cells
-
Tyska MJ, Mooseker MS (2002) MYO1A (brush border myosin I) dynamics in the brush border of LLC-PK1-CL4 cells. Biophys J 82:1869-1883.
-
(2002)
Biophys J
, vol.82
, pp. 1869-1883
-
-
Tyska, M.J.1
Mooseker, M.S.2
-
69
-
-
0033816925
-
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
-
Verpy E, Leibovici M, Zwaenepoel I, Liu XZ, Gal A, Salem N, Mansour A, Blanchard S, Kobayashi I, Keats BJ, Slim R, Petit C (2000) A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nat Genet 26:51-55.
-
(2000)
Nat Genet
, vol.26
, pp. 51-55
-
-
Verpy, E.1
Leibovici, M.2
Zwaenepoel, I.3
Liu, X.Z.4
Gal, A.5
Salem, N.6
Mansour, A.7
Blanchard, S.8
Kobayashi, I.9
Keats, B.J.10
Slim, R.11
Petit, C.12
-
70
-
-
34547700102
-
The micromachinery of mechanotransduction in hair cells
-
Vollrath MA, Kwan KY, Corey DP (2007) The micromachinery of mechanotransduction in hair cells. Annu Rev Neurosci 30:339-365.
-
(2007)
Annu Rev Neurosci
, vol.30
, pp. 339-365
-
-
Vollrath, M.A.1
Kwan, K.Y.2
Corey, D.P.3
-
71
-
-
32844471085
-
Survival and morphology of auditory neurons in dissociated cultures of newborn mouse spiral ganglion
-
Whitlon DS, Ketels KV, Coulson MT, Williams T, Grover M, Edpao W, Richter CP (2006) Survival and morphology of auditory neurons in dissociated cultures of newborn mouse spiral ganglion. Neuroscience 138:653-662.
-
(2006)
Neuroscience
, vol.138
, pp. 653-662
-
-
Whitlon, D.S.1
Ketels, K.V.2
Coulson, M.T.3
Williams, T.4
Grover, M.5
Edpao, W.6
Richter, C.P.7
-
72
-
-
56149115057
-
MAGI-1, a candidate stereociliary scaffolding protein associates with the tip-link component cadherin 23
-
Xu Z, Peng AW, Oshima K, Heller S (2008) MAGI-1, a candidate stereociliary scaffolding protein, associates with the tip-link component cadherin 23. J Neurosci 28:11269-11276.
-
(2008)
J Neurosci
, vol.28
, pp. 11269-11276
-
-
Xu, Z.1
Peng, A.W.2
Oshima, K.3
Heller, S.4
-
73
-
-
38349054763
-
Human deafness mutation E385D disrupts the mechanochemical coupling and subcellular targeting of myosin-1a
-
Yengo CM, Ananthanarayanan SK, Brosey CA, Mao S, Tyska MJ (2008) Human deafness mutation E385D disrupts the mechanochemical coupling and subcellular targeting of myosin-1a. Biophys J 94:L5-L7.
-
(2008)
Biophys J
, vol.94
-
-
Yengo, C.M.1
Ananthanarayanan, S.K.2
Brosey, C.A.3
Mao, S.4
Tyska, M.J.5
-
74
-
-
33847270136
-
Mechanochemical coupling in the myosin motor domain. II. Analysis of critical residues
-
Yu H, Ma L, Yang Y, Cui Q (2007) Mechanochemical coupling in the myosin motor domain. II. Analysis of critical residues. PLoS Comput Biol 3:e23.
-
(2007)
PLoS Comput Biol
, vol.3
-
-
Yu, H.1
Ma, L.2
Yang, Y.3
Cui, Q.4
-
75
-
-
33744981140
-
Prestin is expressed on the whole outer hair cell basolateral surface
-
Yu N, Zhu ML, Zhao HB (2006) Prestin is expressed on the whole outer hair cell basolateral surface. Brain Res 1095:51-58.
-
(2006)
Brain Res
, vol.1095
, pp. 51-58
-
-
Yu, N.1
Zhu, M.L.2
Zhao, H.B.3
-
76
-
-
0034636553
-
Prestin is the motor protein of cochlear outer hair cells
-
Zheng J, Shen W, He DZ, Long KB, Madison LD, Dallos P (2000) Prestin is the motor protein of cochlear outer hair cells. Nature 405:149-155.
-
(2000)
Nature
, vol.405
, pp. 149-155
-
-
Zheng, J.1
Shen, W.2
He, D.Z.3
Long, K.B.4
Madison, L.D.5
Dallos, P.6
-
77
-
-
0037326334
-
Genomic characterization and expression of mouse prestin, the motor protein of outer hair cells
-
Zheng J, Long KB, Matsuda KB, Madison LD, Ryan AD, Dallos PD (2003) Genomic characterization and expression of mouse prestin, the motor protein of outer hair cells. Mamm Genome 14:87-96.
-
(2003)
Mamm Genome
, vol.14
, pp. 87-96
-
-
Zheng, J.1
Long, K.B.2
Matsuda, K.B.3
Madison, L.D.4
Ryan, A.D.5
Dallos, P.D.6
-
78
-
-
23744456610
-
The C-terminus of prestin influences nonlinear capacitance and plasma membrane targeting
-
Zheng J, Du GG, Matsuda K, Orem A, Aguiñaga S, Deák L, Navarrete E, Madison LD, Dallos P (2005) The C-terminus of prestin influences nonlinear capacitance and plasma membrane targeting. J Cell Sci 118:2987-2996.
-
(2005)
J Cell Sci
, vol.118
, pp. 2987-2996
-
-
Zheng, J.1
Du, G.G.2
Matsuda, K.3
Orem, A.4
Aguiñaga, S.5
Deák, L.6
Navarrete, E.7
Madison, L.D.8
Dallos, P.9
-
79
-
-
0034604349
-
The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins
-
Zheng L, Sekerková G, Vranich K, Tilney LG, Mugnaini E, Bartles JR (2000) The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins. Cell 102: 377-385.
-
(2000)
Cell
, vol.102
, pp. 377-385
-
-
Zheng, L.1
Sekerková, G.2
Vranich, K.3
Tilney, L.G.4
Mugnaini, E.5
Bartles, J.R.6
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