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Year
Chaperone activity of alpha‐crystallins modulates intermediate filament assembly.
ID Nicholl, RA Quinlan
The EMBO journal 13 (4), 945-953, 1994
5101994
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, 282-306, 1985
5041985
Intermediate filament interactions can be altered by HSP27 and αB-crystallin
MD Perng, L Cairns, P Van Den IJssel, A Prescott, AM Hutcheson, ...
Journal of cell science 112 (13), 2099-2112, 1999
4531999
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
3322001
Lamin A/C binding protein LAP2α 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
3102002
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
2841985
[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
2811986
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
2742005
GFAP and its role in Alexander disease
RA Quinlan, M Brenner, JE Goldman, A Messing
Experimental cell research 313 (10), 2077-2087, 2007
2402007
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
2382001
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
2281984
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
2161982
Comparison of the small heat shock proteins αB-crystallin, MKBP, HSP25, HSP20, and cvHSP in heart and skeletal muscle
N Golenhofen, MD Perng, RA Quinlan, D Drenckhahn
Histochemistry and cell biology 122, 415-425, 2000
2122000
The growing world of small heat shock proteins: from structure to functions
S Carra, S Alberti, PA Arrigo, JL Benesch, IJ Benjamin, W Boelens, ...
Cell Stress and Chaperones 22 (4), 601-611, 2017
1992017
The cardiomyopathy and lens cataract mutation in αB-crystallin alters its protein structure, chaperone activity, and interaction with intermediate filaments in vitro
M Der Perng, PJ Muchowski, P van den IJssel, GJS Wu, AM Hutcheson, ...
Journal of Biological Chemistry 274 (47), 33235-33243, 1999
1971999
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
1922009
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
1891983
Ionizing radiation induced cataracts: Recent biological and mechanistic developments and perspectives for future research
EA Ainsbury, S Barnard, S Bright, C Dalke, M Jarrin, S Kunze, R Tanner, ...
Mutation Research/Reviews in Mutation Research 770, 238-261, 2016
1762016
Altered aggregation properties of mutant γ‐crystallins cause inherited cataract
A Sandilands, AM Hutcheson, HA Long, AR Prescott, G Vrensen, J Löster, ...
The EMBO journal, 2002
1702002
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
1512006
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