Inge Everaert
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Explore the profile of Inge Everaert including associated specialties, affiliations and a list of published articles.
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36
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Recent Articles
11.
Everaert I, Baron G, Barbaresi S, Gilardoni E, Coppa C, Carini M, et al.
Amino Acids
. 2018 Oct;
51(1):103-114.
PMID: 30302566
Carnosine (beta-alanyl-L-histidine) and its methylated analogue anserine are present in relevant concentrations in the omnivore human diet. Several studies reported promising therapeutic potential for carnosine in various rodent models of...
12.
Stautemas J, Everaert I, Lefevere F, Derave W
Front Nutr
. 2018 Sep;
5:70.
PMID: 30175101
The ergogenic response following long-term ingestion of β-alanine shows a high inter-individual variation. It is hypothesized that this variation is partially caused by a variable pharmacokinetic response induced by inferior...
13.
Blancquaert L, Baguet A, Bex T, Volkaert A, Everaert I, Delanghe J, et al.
Br J Nutr
. 2018 Mar;
119(7):759-770.
PMID: 29569535
Balanced vegetarian diets are popular, although they are nearly absent in creatine and carnosine and contain considerably less carnitine than non-vegetarian diets. Few longitudinal intervention studies investigating the effect of...
14.
AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse model
Verhelle A, Nair N, Everaert I, Van Overbeke W, Supply L, Zwaenepoel O, et al.
Hum Mol Genet
. 2017 Jun;
26(15):3030.
PMID: 28605435
No abstract available.
15.
AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse model
Verhelle A, Nair N, Everaert I, Van Overbeke W, Supply L, Zwaenepoel O, et al.
Hum Mol Genet
. 2017 Mar;
26(7):1353-1364.
PMID: 28334940
Gelsolin amyloidosis is a dominantly inherited, incurable type of amyloidosis. A single point mutation in the gelsolin gene (G654A is most common) results in the loss of a Ca2+ binding...
16.
Blancquaert L, Everaert I, Missinne M, Baguet A, Stegen S, Volkaert A, et al.
Med Sci Sports Exerc
. 2017 Jan;
49(3):602-609.
PMID: 28106620
Purpose: Carnosine is a dipeptide composed of β-alanine and L-histidine and is present in skeletal muscle. Chronic oral β-alanine supplementation can induce muscle carnosine loading and is therefore seen as...
17.
Kaczmarek D, Lochynski D, Everaert I, Pawlak M, Derave W, Celichowski J
J Appl Physiol (1985)
. 2016 May;
121(1):164-72.
PMID: 27197862
The physiological role of the muscle histidyl dipeptides carnosine and anserine in contractile function of various types of muscle fibers in vivo is poorly understood. Ten adult male Wistar rats...
18.
Blancquaert L, Baba S, Kwiatkowski S, Stautemas J, Stegen S, Barbaresi S, et al.
J Physiol
. 2016 Apr;
594(17):4849-63.
PMID: 27062388
Key Points: Using recombinant DNA technology, the present study provides the first strong and direct evidence indicating that β-alanine is an efficient substrate for the mammalian transaminating enzymes 4-aminobutyrate-2-oxoglutarate transaminase...
19.
de Courten B, Kurdiova T, de Courten M, Belan V, Everaert I, Vician M, et al.
PLoS One
. 2015 Oct;
10(10):e0138707.
PMID: 26439389
Background: Carnosine is a naturally present dipeptide abundant in skeletal muscle and an over-the counter food additive. Animal data suggest a role of carnosine supplementation in the prevention and treatment...
20.
Stegen S, Everaert I, Deldicque L, Vallova S, de Courten B, Ukropcova B, et al.
PLoS One
. 2015 Mar;
10(3):e0121062.
PMID: 25803044
Objective: Muscle carnosine and its methylated form anserine are histidine-containing dipeptides. Both dipeptides have the ability to quench reactive carbonyl species and previous studies have shown that endogenous tissue levels...