Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Valerie L R M Verstraeten"'
Publikováno v:
JAAD Case Reports, 16, 74-76. Elsevier Inc.
JAAD Case Reports, Vol 16, Iss, Pp 74-76 (2021)
JAAD Case Reports
JAAD Case Reports, Vol 16, Iss, Pp 74-76 (2021)
JAAD Case Reports
Dermatomyositis is an inflammatory myopathy that affects children and adults. It can present without muscle involvement in the case of amyopathic dermatomyositis. Whereas the juvenile variant is often associated with calcinosis cutis, the adult varia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e67734bce83c17785d5d4162578d51eb
https://cris.maastrichtuniversity.nl/en/publications/66a90131-677a-4e66-8af6-ba294c200f7f
https://cris.maastrichtuniversity.nl/en/publications/66a90131-677a-4e66-8af6-ba294c200f7f
Publikováno v:
Dermatitis, 32(6), E100-E101. Decker Publishing
Publikováno v:
Contact Dermatitis
Contact Dermatitis, 80(3), 166-167. Wiley
Contact Dermatitis, 80(3), 166-167. Wiley
Autor:
Frederik Houben, Ingrid P.C. Krapels, M. Coorens, Valerie L. R. M. Verstraeten, Frans C. S. Ramaekers, Carlo Marcelis, G. J. J. Kierkels, W. De Vos, Jos L. V. Broers, Miriam A.F. Kamps, A. van den Wijngaard
Publikováno v:
Histochemistry and Cell Biology, 139(1), 119-134. Springer Verlag
Histochemistry and Cell Biology, 139, 119-34
Histochemistry and Cell Biology, 139, 1, pp. 119-34
Histochemistry and Cell Biology, 139, 119-34
Histochemistry and Cell Biology, 139, 1, pp. 119-34
Item does not contain fulltext There is growing evidence that laminopathies, diseases associated with mutations in the LMNA gene, are caused by a combination of mechanical and gene regulatory distortions. Strikingly, there is a large variability in d
Autor:
Frank P. T. Baaijens, Carlijn V. Bouten, C Chiara Tamiello, Arthur van den Wijngaard, Jos L. V. Broers, Miriam A.F. Kamps, Valerie L. R. M. Verstraeten
Publikováno v:
Nucleus, 4(1), 61-73. Landes Bioscience
Nucleus
Nucleus
Laminopathies, mainly caused by mutations in the LMNA gene, are a group of inherited diseases with a highly variable penetrance; i.e., the disease spectrum in persons with identical LMNA mutations range from symptom-free conditions to severe cardiomy
Autor:
Lana A. Peckham, Jan Lammerding, Brian C. Capell, Elizabeth G. Nabel, Michelle Olive, Stephen G. Young, Loren G. Fong, Francis S. Collins, Valerie L. R. M. Verstraeten
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 108(12), 4997-5002. National Academy of Sciences
Despite the success of protein farnesyltransferase inhibitors (FTIs) in the treatment of certain malignancies, their mode of action is incompletely understood. Dissecting the molecular pathways affected by FTIs is important, particularly because this
Autor:
Maurice A.M. van Steensel, Jos L. V. Broers, Miriam A.F. Kamps, Valerie L. R. M. Verstraeten, Johan Renes, P.M. Steijlen, Fons Verheyen, Frans C. S. Ramaekers, Martin Wabitsch, Helma J.H. Kuijpers
Publikováno v:
Histochemistry and Cell Biology
Histochemistry and Cell Biology, 135(3), 251-61. Springer Verlag
Histochemistry and Cell Biology, 135(3), 251-61. Springer Verlag
A thorough understanding of fat cell biology is necessary to counter the epidemic of obesity. Although molecular pathways governing adipogenesis are well delineated, the structure of the nuclear lamina and nuclear-cytoskeleton junction in this proces
Publikováno v:
Circulation Research. 106:234-237
See related articles, pages 346–353 More than one-third of cases of dilated cardiomyopathy (DCM) are caused by inherited mutations, with 5% to 10% of these mutations being linked to the LMNA gene encoding the nuclear envelope proteins lamin A and C
Autor:
Eric R. Schreiter, Jan Lammerding, William A. Chutkow, Parth Patwari, Valerie L. R. M. Verstraeten, Richard T. Lee, Kiersten Cummings
Publikováno v:
Journal of Biological Chemistry. 284:24996-25003
Thioredoxin-interacting protein (Txnip), originally characterized as an inhibitor of thioredoxin, is now known to be a critical regulator of glucose metabolism in vivo. Txnip is a member of the alpha-arrestin protein family; the alpha-arrestins are r
Autor:
Michel van Geel, Salla Keskitalo, Jorge Frank, J. C. J. M. Veraart, Valerie L. R. M. Verstraeten, Peter M. Steijlen, Maurice A.M. van Steensel, Caroline A. Heckman, Wolfgang Holnthoner, Reno S. Bladergroen, Kari Alitalo
Publikováno v:
Journal of Investigative Dermatology. 129(2):509-512