Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lise Murphy"'
Autor:
Ingrid M. B. H. van de Laar, Eloisa Arbustini, Bart Loeys, Erik Björck, Lise Murphy, Maarten Groenink, Marlies Kempers, Janneke Timmermans, Jolien Roos-Hesselink, Kalman Benke, Guglielmina Pepe, Barbara Mulder, Zoltan Szabolcs, Gisela Teixidó-Turà, Leema Robert, Yaso Emmanuel, Arturo Evangelista, Alessandro Pini, Yskert von Kodolitsch, Guillaume Jondeau, Julie De Backer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Abstract The ACTA2 gene encodes for smooth muscle specific α-actin, a critical component of the contractile apparatus of the vascular smooth muscle cell. Pathogenic variants in the ACTA2 gene are the most frequently encountered genetic cause of non-
Externí odkaz:
https://doaj.org/article/28a3f413457f4d019b78d4411ab50cb3
Autor:
Alessandro Pini, Janneke Timmermans, Lise Murphy, Marlies Kempers, Guillaume Jondeau, Zoltán Szabolcs, Yaso Emmanuel, Arturo Evangelista, Yskert von Kodolitsch, Jolien W. Roos-Hesselink, Maarten Groenink, Bart Loeys, Kálmán Benke, Barbara J.M. Mulder, Julie De Backer, Ingrid M.B.H. van de Laar, Gisela Teixido-Tura, Erik Björck, Guglielmina Pepe, Leema Robert, Eloisa Arbustini
Publikováno v:
Orphanet journal of rare diseases, 14(1). BioMed Central
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 14, 264
Scientia
Orphanet Journal of Rare Diseases, 14, 1, pp. 264
Orphanet Journal of Rare Diseases, 14(1):264. BioMed Central Ltd.
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
ORPHANET JOURNAL OF RARE DISEASES
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 14, 264
Scientia
Orphanet Journal of Rare Diseases, 14, 1, pp. 264
Orphanet Journal of Rare Diseases, 14(1):264. BioMed Central Ltd.
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
ORPHANET JOURNAL OF RARE DISEASES
Malaltia aòrtica; Dissecció; Aneurisma aòrtic toràcic Enfermedad aórtica; Disección; Aneurisma de aorta torácica Aortic disease; Dissection; Thoracic aortic aneurysm The ACTA2 gene encodes for smooth muscle specific α-actin, a critical compon
Autor:
Susan M. Twine, Arthur G. Szabo, Patrik Callis, Michael T. Cash, Lise Murphy, Robert S. Phillips
Publikováno v:
The Journal of Physical Chemistry B. 107:637-645
The biosynthetic incorporation of tryptophan analogues into proteins using plasmid expression systems has been shown to offer advantages in fluorescence spectroscopic studies of the molecular details of the interacting segments of protein−protein c