Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 31


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.

J Neurosci. 2008 Jun 18;28(25):6342-53. doi: 10.1523/JNEUROSCI.1154-08.2008.


Cytoplasmic gamma-actin is not required for skeletal muscle development but its absence leads to a progressive myopathy.

Sonnemann KJ, Fitzsimons DP, Patel JR, Liu Y, Schneider MF, Moss RL, Ervasti JM.

Dev Cell. 2006 Sep;11(3):387-97.


Tracking down the different forms of nuclear actin.

Jockusch BM, Schoenenberger CA, Stetefeld J, Aebi U.

Trends Cell Biol. 2006 Aug;16(8):391-6. Epub 2006 Jul 7.


Arginylation of beta-actin regulates actin cytoskeleton and cell motility.

Karakozova M, Kozak M, Wong CC, Bailey AO, Yates JR 3rd, Mogilner A, Zebroski H, Kashina A.

Science. 2006 Jul 14;313(5784):192-6. Epub 2006 Jun 22.


The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles.

McGee J, Goodyear RJ, McMillan DR, Stauffer EA, Holt JR, Locke KG, Birch DG, Legan PK, White PC, Walsh EJ, Richardson GP.

J Neurosci. 2006 Jun 14;26(24):6543-53.


A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.

Rendtorff ND, Zhu M, Fagerheim T, Antal TL, Jones M, Teslovich TM, Gillanders EM, Barmada M, Teig E, Trent JM, Friderici KH, Stephan DA, Tranebjaerg L.

Eur J Hum Genet. 2006 Oct;14(10):1097-105. Epub 2006 Jun 14.


A mutation of beta -actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia.

Procaccio V, Salazar G, Ono S, Styers ML, Gearing M, Davila A, Jimenez R, Juncos J, Gutekunst CA, Meroni G, Fontanella B, Sontag E, Sontag JM, Faundez V, Wainer BH.

Am J Hum Genet. 2006 Jun;78(6):947-60. Epub 2006 Apr 21.


Differential distribution of beta- and gamma-actin in guinea-pig cochlear sensory and supporting cells.

Furness DN, Katori Y, Mahendrasingam S, Hackney CM.

Hear Res. 2005 Sep;207(1-2):22-34.


An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal.

Rzadzinska AK, Schneider ME, Davies C, Riordan GP, Kachar B.

J Cell Biol. 2004 Mar 15;164(6):887-97.


A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26).

van Wijk E, Krieger E, Kemperman MH, De Leenheer EM, Huygen PL, Cremers CW, Cremers FP, Kremer H.

J Med Genet. 2003 Dec;40(12):879-84.


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.

J Cell Biol. 2003 Dec 8;163(5):1045-55. Epub 2003 Dec 1.


Actin filament turnover regulated by cross-linking accounts for the size, shape, location, and number of actin bundles in Drosophila bristles.

Tilney LG, Connelly PS, Ruggiero L, Vranich KA, Guild GM.

Mol Biol Cell. 2003 Oct;14(10):3953-66. Epub 2003 Jul 25.


Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).

Zhu M, Yang T, Wei S, DeWan AT, Morell RJ, Elfenbein JL, Fisher RA, Leal SM, Smith RJ, Friderici KH.

Am J Hum Genet. 2003 Nov;73(5):1082-91. Epub 2003 Sep 16.


Long continuous actin bundles in Drosophila bristles are constructed by overlapping short filaments.

Guild GM, Connelly PS, Ruggiero L, Vranich KA, Tilney LG.

J Cell Biol. 2003 Sep 15;162(6):1069-77.


Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier.

Liberman MC, Gao J, He DZ, Wu X, Jia S, Zuo J.

Nature. 2002 Sep 19;419(6904):300-4. Epub 2002 Aug 28.


Rapid renewal of auditory hair bundles.

Schneider ME, Belyantseva IA, Azevedo RB, Kachar B.

Nature. 2002 Aug 22;418(6900):837-8.


Functional anatomy of auditory brainstem nuclei: application to the anatomical basis of brainstem auditory evoked potentials.

Biacabe B, Chevallier JM, Avan P, Bonfils P.

Auris Nasus Larynx. 2001 Jan;28(1):85-94. Review.


A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25.

Morell RJ, Friderici KH, Wei S, Elfenbein JL, Friedman TB, Fisher RA.

Genomics. 2000 Jan 1;63(1):1-6.


Sorting of actin isoforms in chicken auditory hair cells.

Höfer D, Ness W, Drenckhahn D.

J Cell Sci. 1997 Mar;110 ( Pt 6):765-70.

Items per page

Supplemental Content

Write to the Help Desk