Differential effect of simvastatin on activation of Rac(1) vs.activation of the heat shock protein 27-mediated pathway upon oxidativestress, in human smooth muscle cells
(2002)
Journal Article
Negre-Aminou, P., van Leeuwen, R., van Thiel, G., van den IJssel, P., de Jong, W., Quinlan, R., & Cohen, L. (2002). Differential effect of simvastatin on activation of Rac(1) vs.activation of the heat shock protein 27-mediated pathway upon oxidativestress, in human smooth muscle cells. Biochemical Pharmacology, 64(10), 1483-1491
Outputs (136)
Altered aggregation properties of mutant gamma-crystallins cause inherited cataract (2002)
Journal Article
Sandilands, A., Hutcheson, A., Long, H., Prescott, A., Vrensen, G., Löster, J., …Quinlan, R. (2002). Altered aggregation properties of mutant gamma-crystallins cause inherited cataract. The EMBO Journal, 21(22), 6005-6014. https://doi.org/10.1093/emboj/cdf609Protein inclusions are associated with a diverse group of human diseases ranging from localized neurological disorders through to systemic non-neuropathic diseases. Here, we present evidence that the formation of intranuclear inclusions is a key even... Read More about Altered aggregation properties of mutant gamma-crystallins cause inherited cataract.
Association of the nuclear matrix component NuMA with the Cajal bodyand nuclear speckle compartments during transitions in transcriptionalactivity in lens cell differentiation (2002)
Journal Article
Gribbon, C., Dahm, R., Prescott, A., & Quinlan, R. (2002). Association of the nuclear matrix component NuMA with the Cajal bodyand nuclear speckle compartments during transitions in transcriptionalactivity in lens cell differentiation. European Journal of Cell Biology, 81(10), 557-566. https://doi.org/10.1078/0171-9335-00275The transcriptional status of cells can be deduced from the staining pattern of various nuclear markers such as the Cajal body, nucleolus and nuclear speckles. In this study we have used these markers to correlate transcriptional status with cell dif... Read More about Association of the nuclear matrix component NuMA with the Cajal bodyand nuclear speckle compartments during transitions in transcriptionalactivity in lens cell differentiation.
Localization of two conserved cis-acting enhancer regions for thefilensin gene promoter that direct lens-specific expression (2002)
Journal Article
Masaki, S., Yonezawa, S., & Quinlan, R. (2002). Localization of two conserved cis-acting enhancer regions for thefilensin gene promoter that direct lens-specific expression. Experimental Eye Research, 75(3), 295-305
Theoretical considerations regarding the study "Alpha-B crystallin gene(CRYAB) mutation causes dominant congenital posterior polar cataract inhumans" - Reply (2002)
Journal Article
Berry, V., Francis, P., Reddy, M., Collyer, D., Vithana, E., MacKay, I., …Quinlan, R. (2002). Theoretical considerations regarding the study "Alpha-B crystallin gene(CRYAB) mutation causes dominant congenital posterior polar cataract inhumans" - Reply. American Journal of Human Genetics, 71(3), 685-686
Translocation of small heat shock proteins to the actin cytoskeletonupon proteasomal inhibition (2002)
Journal Article
Verschuure, P., Croes, Y., van den IJssel, P., Quinlan, R., de Jong, W., & Boelens, W. (2002). Translocation of small heat shock proteins to the actin cytoskeletonupon proteasomal inhibition. Journal of Molecular and Cellular Cardiology, 34(2), 117-128
Alpha-b crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans (2001)
Journal Article
Berry, V., Francis, P., Reddy, M., Collyer, D., Vithana, E., MacKay, I., …Quinlan, R. (2001). Alpha-b crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans. American Journal of Human Genetics, 69(5), 1141-1145. https://doi.org/10.1086/324158Congenital cataracts are an important cause of bilateral visual impairment in infants. In a four-generation family of English descent, we mapped dominant congenital posterior polar cataract to chromosome 11q22-q22.3. The maximum LOD score, 3.92 at re... Read More about Alpha-b crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans.
Antiischemic effects of SB203580 are mediated through the inhibition ofp38 alpha mitogen-activated protein kinase - Evidence from ectopicexpression of an inhibition-resistant kinase (2001)
Journal Article
Martin, J., Avkiran, M., Quinlan, R., Cohen, P., & Marber, M. (2001). Antiischemic effects of SB203580 are mediated through the inhibition ofp38 alpha mitogen-activated protein kinase - Evidence from ectopicexpression of an inhibition-resistant kinase. Circulation Research, 89(9), 750-752
Aniridia-associated translocations, DNase hypersensitivity, sequencecomparison and transgenic analysis redefine the functional domain ofPAX6 (2001)
Journal Article
Kleinjan, D., Seawright, A., Schedl, A., Quinlan, R., Danes, S., & van Heyningen, V. (2001). Aniridia-associated translocations, DNase hypersensitivity, sequencecomparison and transgenic analysis redefine the functional domain ofPAX6. Human Molecular Genetics, 10(19), 2049-2059
Expression of individual lamins in basal cell carcinomas of the skin (2001)
Journal Article
Venables, R., McLean, S., Luny, D., Moteleb, E., Morley, S., Quinlan, R., …Hutchison, C. (2001). Expression of individual lamins in basal cell carcinomas of the skin. British Journal of Cancer, 84(4), 512-519. https://doi.org/10.1054/bjoc.2000.1632