Luc J Peelman
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Explore the profile of Luc J Peelman including associated specialties, affiliations and a list of published articles.
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Articles
38
Citations
527
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Recent Articles
1.
Pavani K, XueFeng G, Chunduru J, Meese T, Peelman L, Van Nieuwerburgh F, et al.
Reproduction
. 2023 Dec;
PMID: 38063339
MicroRNAs (miRNAs), which can be carried inside extracellular vesicles (EVs), play a crucial role in regulating embryo development up to the blastocyst stage. Yet, the molecular mechanisms underlying blastocyst development...
2.
Van Poucke M, Van Renterghem E, Peterson M, van den Berg M, Stock E, Peelman L, et al.
J Vet Intern Med
. 2022 Sep;
36(5):1597-1606.
PMID: 36054182
Background: Primary congenital hypothyroidism (CH) is a rare endocrine disorder in cats with a largely unknown genetic cause. Objectives: Describe the clinical presentation of CH in 11 affected cats and...
3.
Schipper T, Storms G, Janssens G, Schoofs S, Capiau E, Verdonck D, et al.
Animals (Basel)
. 2022 Aug;
12(15).
PMID: 35953997
Corneal sequestra are ophthalmic lesions that are remarkably common in Persian, Himalayan and exotic cats. In this study, the genetic aspects of this disease were investigated in a population of...
4.
Schipper T, Ohlsson A, Longeri M, Hayward J, Mouttham L, Ferrari P, et al.
Anim Genet
. 2022 May;
53(4):526-529.
PMID: 35634705
Hypertrophic cardiomyopathy (HCM) is a common and potentially fatal heart disease in many cat breeds. An intronic variant in TNNT2, c.95-108G>A, was recently reported as the cause of HCM in...
5.
Schipper T, Van Poucke M, Sonck L, Smets P, Ducatelle R, Broeckx B, et al.
Eur J Hum Genet
. 2019 Jun;
27(11):1724-1730.
PMID: 31164718
Hypertrophic cardiomyopathy (HCM) is the most common inherited human heart disease. The same disease has a high prevalence in cats, where it is also suspected to be inherited. More than...
6.
Van Poucke M, Stee K, Sonck L, Stock E, Bosseler L, Van Dorpe J, et al.
Eur J Hum Genet
. 2019 Jun;
27(10):1561-1568.
PMID: 31160700
Clinical, pathological, and genetic findings of a primary hereditary ataxia found in a Malinois dog family are described and compared with its human counterpart. Based on the family history and...
7.
Van Poucke M, Stee K, Bhatti S, Vanhaesebrouck A, Bosseler L, Peelman L, et al.
Eur J Hum Genet
. 2016 Dec;
25(2):222-226.
PMID: 27966545
SeSAME/EAST syndrome is a multisystemic disorder in humans, characterised by seizures, sensorineural deafness, ataxia, developmental delay and electrolyte imbalance. It is exclusively caused by homozygous or compound heterozygous variations in...
8.
Wang W, Degroote J, Van Ginneken C, Van Poucke M, Vergauwen H, Dam T, et al.
FASEB J
. 2015 Oct;
30(2):863-73.
PMID: 26514167
Neonates with intrauterine growth restriction (IUGR) show lower efficiency of nutrient utilization compared to normal birth weight (NBW) newborns. This study was conducted using neonatal piglets as a model to...
9.
Van Poucke M, Martle V, Van Brantegem L, Ducatelle R, Van Ham L, Bhatti S, et al.
Eur J Hum Genet
. 2015 Oct;
24(6):852-6.
PMID: 26486469
Alexander disease (AxD) is a fatal neurodegenerative disorder of astrocyte dysfunction in man, for which already a number of causal variants are described, mostly de novo dominant missense variants in...
10.
Svobodova K, Horak P, Stratil A, Bartenschlager H, Van Poucke M, Chalupova P, et al.
Mol Biol Rep
. 2015 Mar;
42(8):1257-64.
PMID: 25749814
Eukaryotic translation elongation factor 1 alpha (EEF1A) plays a key role in protein synthesis. In higher vertebrates EEF1A occurs in two isoforms, EEF1A1 and EEF1A2, encoded by distinct genes. The...