r.a.quinlan
Title
Cited by
Cited by
Year
Patterns of expression and organization of cytokeratin intermediate filaments
RA Quinlan, DL Schiller, M Hatzfeld, T Achtstätter, R Moll, JL Jorcano, ...
Annals of the New York Academy of Sciences 455 (1), 282-306, 1985
4891985
Chaperone activity of alpha‐crystallins modulates intermediate filament assembly.
ID Nicholl, RA Quinlan
The EMBO journal 13 (4), 945-953, 1994
4821994
Intermediate filament interactions can be altered by HSP27 and alphaB-crystallin
MD Perng, L Cairns, P Van Den IJssel, A Prescott, AM Hutcheson, ...
Journal of cell science 112 (13), 2099-2112, 1999
4151999
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans
V Berry, P Francis, MA Reddy, D Collyer, E Vithana, I MacKay, G Dawson, ...
The American Journal of Human Genetics 69 (5), 1141-1145, 2001
2962001
Lamin A/C binding protein LAP2 is required for nuclear anchorage of retinoblastoma protein
E Markiewicz, T Dechat, R Foisner, RA Quinlan, CJ Hutchison
Molecular biology of the cell 13 (12), 4401-4413, 2002
2872002
[34] Separation of cytokeratin polypeptides by gel electrophoretic and chromatographic techniques and their identification by immunoblotting
T Achtstaetter, M Hatzfeld, RA Quinlan, DC Parmelee, WW Franke
Methods in enzymology 134, 355-371, 1986
2781986
Identification of a distinct soluble subunit of an intermediate filament protein: tetrameric vimentin from living cells
P Soellner, RA Quinlan, WW Franke
Proceedings of the National Academy of Sciences 82 (23), 7929-7933, 1985
2541985
Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease
R Li, AB Johnson, G Salomons, JE Goldman, S Naidu, R Quinlan, B Cree, ...
Annals of neurology 57 (3), 310-326, 2005
2392005
Heterotypic tetramer (A2D2) complexes of non-epidermal keratins isolated from cytoskeletons of rat hepatocytes and hepatoma cells
RA Quinlan, JA Cohlberg, DL Schiller, M Hatzfeld, WW Franke
Journal of molecular biology 178 (2), 365-388, 1984
2221984
Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6
DA Kleinjan, A Seawright, A Schedl, RA Quinlan, S Danes, ...
Human molecular genetics 10 (19), 2049-2059, 2001
2162001
GFAP and its role in Alexander disease
RA Quinlan, M Brenner, JE Goldman, A Messing
Experimental cell research 313 (10), 2077-2087, 2007
2092007
Heteropolymer filaments of vimentin and desmin in vascular smooth muscle tissue and cultured baby hamster kidney cells demonstrated by chemical crosslinking
RA Quinlan, WW Franke
Proceedings of the National Academy of Sciences 79 (11), 3452-3456, 1982
1981982
Comparison of the small heat shock proteins B-crystallin, MKBP, HSP25, HSP20, and cvHSP in heart and skeletal muscle
N Golenhofen, M Der Perng, RA Quinlan, D Drenckhahn
Histochemistry and cell biology 122 (5), 415-425, 2000
1872000
The cardiomyopathy and lens cataract mutation in alphaB-crystallin alters its protein structure, chaperone activity, and interaction with intermediate filaments in vitro.
MD Perng, PJ Muchowski, P van Den IJssel, GJ Wu, AM Hutcheson, ...
The Journal of biological chemistry 274 (47), 33235-33243, 1999
1781999
Molecular Interactions in Intermediate‐Sized Filaments Revealed by Chemical Cross‐Linking: Heteropholymers of Vimentin and Glial Filament Protein in Cultured Human Glima Cells
RA QUINLAN, WW FRANKE
European journal of biochemistry 132 (3), 477-484, 1983
1771983
Altered aggregation properties of mutant ‐crystallins cause inherited cataract
A Sandilands, AM Hutcheson, HA Long, AR Prescott, G Vrensen, J Löster, ...
The EMBO journal 21 (22), 6005-6014, 2002
1482002
Functions of the intermediate filament cytoskeleton in the eye lens
S Song, A Landsbury, R Dahm, Y Liu, Q Zhang, RA Quinlan
The Journal of clinical investigation 119 (7), 1837-1848, 2009
1382009
Proteolytic modification of acidic and basic keratins during terminal differentiation of mouse and human epidermis
PE BOWDEN, RA Quinlan, D Breitkreutz, NE Fusenig
European journal of biochemistry 142 (1), 29-36, 1984
1361984
The Alexander disease–causing glial fibrillary acidic protein mutant, R416W, accumulates into rosenthal fibers by a pathway that involves filament aggregation and the…
M Der Perng, M Su, SF Wen, R Li, T Gibbon, AR Prescott, M Brenner, ...
The American Journal of Human Genetics 79 (2), 197-213, 2006
1352006
Vimentin and CP49/filensin form distinct networks in the lens which are independently modulated during lens fibre cell differentiation
A Sandilands, AR Prescott, JM Carter, AM Hutcheson, RA Quinlan, ...
Journal of cell science 108 (4), 1397-1406, 1995
1341995
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