Heidi Rommelaere
Overview
Explore the profile of Heidi Rommelaere including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
12
Citations
188
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Desmyter A, Spinelli S, Boutton C, Saunders M, Blachetot C, de Haard H, et al.
Front Immunol
. 2017 Sep;
8:884.
PMID: 28871249
The heterodimeric cytokine interleukin (IL) 23 comprises the IL12-shared p40 subunit and an IL23-specific subunit, p19. Together with IL12 and IL27, IL23 sits at the apex of the regulatory mechanisms...
2.
Terryn S, Francart A, Rommelaere H, Stortelers C, Van Gucht S
PLoS Negl Trop Dis
. 2016 Aug;
10(8):e0004902.
PMID: 27483431
Post-exposure prophylaxis (PEP) against rabies infection consists of a combination of passive immunisation with plasma-derived human or equine immune globulins and active immunisation with vaccine delivered shortly after exposure. Since...
3.
Terryn S, Francart A, Lamoral S, Hultberg A, Rommelaere H, Wittelsberger A, et al.
PLoS One
. 2014 Oct;
9(10):e109367.
PMID: 25347556
Rabies virus causes lethal brain infection in about 61000 people per year. Each year, tens of thousands of people receive anti-rabies prophylaxis with plasma-derived immunoglobulins and vaccine soon after exposure....
4.
Vandamme D, Lambert E, Waterschoot D, Cognard C, Vandekerckhove J, Ampe C, et al.
Biochim Biophys Acta
. 2009 Apr;
1793(7):1259-71.
PMID: 19393268
Nemaline myopathy is a neuromuscular disorder, characterized by muscle weakness and hypotonia and is, in 20% of the cases, caused by mutations in the gene encoding alpha-skeletal muscle actin, ACTA1....
5.
Vandamme D, Lambert E, Waterschoot D, Tondeleir D, Vandekerckhove J, Machesky L, et al.
BMC Res Notes
. 2009 Mar;
2:40.
PMID: 19284548
Background: Nemaline myopathy is a neuromuscular disorder characterized by the presence of nemaline bodies in patient muscles. 20% of the cases are associated with alpha-skeletal muscle actin mutations. We previously...
6.
Vandamme D, Rommelaere H, Lambert E, Waterschoot D, Vandekerckhove J, Constantin B, et al.
Cell Motil Cytoskeleton
. 2009 Feb;
66(4):179-92.
PMID: 19206168
Central core disease (CCD), congenital fibre type disproportion (CFTD), and nemaline myopathy (NM) are earlyonset clinically heterogeneous congenital myopathies, characterized by generalized muscle weakness and hypotonia. All three diseases are...
7.
Bathe F, Rommelaere H, Machesky L
BMC Cell Biol
. 2007 Jan;
8:2.
PMID: 17227580
Background: About 20 % of nemaline myopathies are thus far related to skeletal muscle alpha-actin. Seven actin mutants located in different parts of the actin molecule and linked to different...
8.
Neirynck K, Waterschoot D, Vandekerckhove J, Ampe C, Rommelaere H
J Mol Biol
. 2005 Nov;
355(1):124-38.
PMID: 16300788
The chaperones prefoldin and the cytosolic chaperonin CCT-containing TCP-1 (CCT) guide the cytoskeletal protein actin to its native conformation. Performing an alanine scan of actin, we identified discrete recognition determinants...
9.
Rommelaere H, Waterschoot D, Neirynck K, Vandekerckhove J, Ampe C
Biol Proced Online
. 2004 Oct;
6:235-249.
PMID: 15514698
Recombinant production and biochemical analysis of actin mutants has been hampered by the fact that actin has an absolute requirement for the eukaryotic chaperone CCT to reach its native state....
10.
Costa C, Rommelaere H, Waterschoot D, Sethi K, Nowak K, Laing N, et al.
J Cell Sci
. 2004 Jul;
117(Pt 15):3367-77.
PMID: 15226407
Mutations in the gene encoding alpha-skeletal-muscle actin, ACTA1, cause congenital myopathies of various phenotypes that have been studied since their discovery in 1999. Although much is now known about the...