Krizia Tuand
Overview
Explore the profile of Krizia Tuand including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
151
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0
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Recent Articles
11.
Declercq J, Brouwers B, Pruniau V, Stijnen P, de Faudeur G, Tuand K, et al.
PLoS One
. 2015 Aug;
10(8):e0135502.
PMID: 26275221
The Nestin-Cre driver mouse line has mild hypopituitarism, reduced body weight, a metabolic phenotype and reduced anxiety. Although several causes have been suggested, a comprehensive explanation is still lacking. In...
12.
Declercq J, Brouwers B, Pruniau V, Stijnen P, Tuand K, Meulemans S, et al.
Biomed Res Int
. 2015 Jul;
2015:148651.
PMID: 26167473
Proprotein convertases are subtilisin-like serine endoproteases that cleave and hence activate a variety of proproteins, including growth factors, receptors, metalloproteases, and extracellular matrix proteins. Therefore, it has been suggested that...
13.
Stijnen P, Tuand K, Varga T, Franks P, Aertgeerts B, Creemers J
Am J Epidemiol
. 2015 Apr;
181(9):733-4.
PMID: 25861817
No abstract available.
14.
Stijnen P, Tuand K, Varga T, Franks P, Aertgeerts B, Creemers J
Am J Epidemiol
. 2014 Oct;
180(11):1051-65.
PMID: 25355447
Congenital deficiency of the proprotein convertase subtilisine/kexin type 1 gene (PCSK1), which encodes proprotein convertase 1/3, causes a severe multihormonal disorder marked by early-onset obesity. The single nucleotide polymorphisms (SNPs)...
15.
Nuytens K, Tuand K, Fu Q, Stijnen P, Pruniau V, Meulemans S, et al.
PLoS One
. 2014 Oct;
9(10):e109598.
PMID: 25333629
Two knockout mouse models for the autism candidate gene Neurobeachin (Nbea) have been generated independently. Although both models have similar phenotypes, one striking difference is the dwarf phenotype observed in...
16.
Nuytens K, Tuand K, Di Michele M, Boonen K, Waelkens E, Freson K, et al.
Mol Autism
. 2013 Nov;
4(1):43.
PMID: 24188528
Background: Neurobeachin (NBEA) has been identified as a candidate gene for autism spectrum disorders (ASD) in several unrelated patients with alterations in the NBEA gene. The exact function of NBEA,...