dr. Boel De Paepe

Work address: Labo neuropathologie C. Heymanslaan 10
9000 Gent
Email: Boel.DePaepe@UGent.be

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The changed transcriptome of muscular dystrophy and inflammatory myopathy : contributions of non-coding RNAs to muscle damage and recovery

Boel De Paepe (UGent)

(2019) OBM GENETICS. 3(2).
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Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES

Willem De Ridder, Isabelle Nelson, Bob Asselbergh, Boel De Paepe (UGent) , Maud Beuvin, Rabah Ben Yaou, Cécile Masson, Anne Boland, Jean-François Deleuze, Thierry Maisonobe, et al.

(2019) NEUROLOGY-GENETICS. 5(2).
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- Conference Paper
- C3
- open access
Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma

Shanna Dewaele (UGent) , Katrien Vanderheyden, Boel De Paepe (UGent) , Louis Delhaye (UGent) , Fariba Nemati, Didier Decaudin, Sven Eyckerman (UGent) , Rudy Van Coster (UGent) , Jo Vandesompele (UGent) and Pieter Mestdagh (UGent)

(2019) Long noncoding RNAs : from molecular mechanism to functional genetics, Keystone symposium, Abstracts.
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Sporadic inclusion body myositis : an acquired mitochondrial disease with extras

Boel De Paepe (UGent)

(2019) BIOMOLECULES. 9(1).
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- Conference Paper
- C3
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Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma

Shanna Dewaele (UGent) , Katrien Vanderheyden, Boel De Paepe (UGent) , Fariba Nemati, Sergio Roman Roman, Rudy Van Coster (UGent) , Jo Vandesompele (UGent) and Pieter Mestdagh (UGent)

(2018) OncoPoint, 6th Research seminar, Abstracts.
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Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma

Shanna Dewaele (UGent) , Katrien Vanderheyden, Boel De Paepe (UGent) , Fariba Nemati, Sergio Roman Roman, Rudy Van Coster (UGent) , Jo Vandesompele (UGent) and Pieter Mestdagh (UGent)

(2018) Belgian Society for Human Genetics, 18th Annual meeting, Abstracts.
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- Journal Article
- A1
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Induction of osmolyte pathways in skeletal muscle inflammation : novel biomarkers for myositis

Boel De Paepe (UGent) , Jana Zschüntzsch, Tea Šokčević, Joachim Weis, Jens Schmidt and Jan De Bleecker (UGent)

(2018) FRONTIERS IN NEUROLOGY. 9.
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BVES loss-of-function mutations in limb-girdle muscular dystrophy 2X with cardiac conduction disorders

I Nelson, W De Ridder, B Asselbergh, Boel De Paepe (UGent) , M Beuvin, R Ben Yaou, A Boland, J Deleuze, T Maisonobe, B Eymard, et al.

(2018) NEUROMUSCULAR DISORDERS. 28(suppl. 2). p.S107-108
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- Conference Paper
- C3
Cyclic vomiting in a subject with homoplasmic m.14674T>C alteration

Elise Vantroys (UGent) , Boel De Paepe (UGent) , Joél Smet (UGent) , Femke Nachtergaele (UGent) , Sara Seneca, Arnaud Vanlander (UGent) and Rudy Van Coster (UGent)

(2018) In JOURNAL OF INHERITED METABOLIC DISEASE 41(suppl. 1). p.S160-S160
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The clinical heterogeneity of the NARS2 c.822G>C mutation clearly illustrated in two siblings : epilepsy and myopathy

Arnaud Vanlander (UGent) , Helene Verhelst (UGent) , Elise Vantroys (UGent) , Joél Smet (UGent) , Boel De Paepe (UGent) , Sarah Vergult (UGent) , Björn Menten (UGent) and Rudy Van Coster (UGent)

(2018) In JOURNAL OF INHERITED METABOLIC DISEASE 41(suppl. 1). p.S156-S156
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- Conference Paper
- C3
Complex III deficiency due to a homozygous mutation in the nuclear encoded subunit UQCRQ

Rudy Van Coster (UGent) , Joél Smet (UGent) , Boel De Paepe (UGent) , Elise Vantroys (UGent) , Femke Nachtergaele (UGent) , Sarah Vergult (UGent) , Björn Menten (UGent) , Arnaud Vanlander (UGent) and François-Guillaume Debray

(2018) In JOURNAL OF INHERITED METABOLIC DISEASE 41(suppl. 1). p.S153-S153
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NFAT5 and p38 MAPKs interact in muscle cells responding to osmotic and inflammatory stress and in polymyositis

Boel De Paepe (UGent) , Sandrine Herbelet (UGent) , Jens Schmidt and Jan De Bleecker (UGent)

(2018) JOURNAL OF NEUROMUSCULAR DISEASES. 5(suppl. 1). p.S139-S140
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Genetic background may contribute to the latitude-dependent prevalence of dermatomyositis and anti-TIF1-γ autoantibodies in adult patients with myositis

Joanna E Parkes, Simon Rothwell, Alexander Oldroyd, Hector Chinoy, Janine A Lamb, the Myositis Genetics Consortium (MYOGEN), Jan De Bleecker (UGent) and Boel De Paepe (UGent)

(2018) ARTHRITIS RESEARCH & THERAPY. 20.
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Localization and expression of nuclear factor of activated T-cells 5 in myoblasts exposed to pro-inflammatory cytokines or hyperosmolar stress and in biopsies from myositis patients

Sandrine Herbelet (UGent) , Elly De Vlieghere (UGent) , Amanda Gonçalves (UGent) , Boel De Paepe (UGent) , Karsten Schmidt, Eline Nys, Laurens Weynants, Joachim Weis, Gert Van Peer (UGent) , Jo Vandesompele (UGent) , et al.

(2018) FRONTIERS IN PHYSIOLOGY. 9.
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Nanoscopic X-ray fluorescence imaging and quantification of intracellular key-elements in cryofrozen Friedreich's ataxia fibroblasts

Björn De Samber (UGent) , Eline Meul (UGent) , Brecht Laforce (UGent) , Boel De Paepe (UGent) , Joél Smet (UGent) , Michiel De Bruyne (UGent) , Riet De Rycke (UGent) , Sylvain Bohic, Peter Cloetens, Rudy Van Coster (UGent) , et al.

(2018) PLOS ONE. 13(1).

Academic Bibliography

dr. Boel De Paepe

The changed transcriptome of muscular dystrophy and inflammatory myopathy : contributions of non-coding RNAs to muscle damage and recovery

Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES

Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma

Sporadic inclusion body myositis : an acquired mitochondrial disease with extras

Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma

Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma

Induction of osmolyte pathways in skeletal muscle inflammation : novel biomarkers for myositis

BVES loss-of-function mutations in limb-girdle muscular dystrophy 2X with cardiac conduction disorders

Cyclic vomiting in a subject with homoplasmic m.14674T>C alteration

The clinical heterogeneity of the NARS2 c.822G>C mutation clearly illustrated in two siblings : epilepsy and myopathy

Complex III deficiency due to a homozygous mutation in the nuclear encoded subunit UQCRQ

NFAT5 and p38 MAPKs interact in muscle cells responding to osmotic and inflammatory stress and in polymyositis

Genetic background may contribute to the latitude-dependent prevalence of dermatomyositis and anti-TIF1-γ autoantibodies in adult patients with myositis

Localization and expression of nuclear factor of activated T-cells 5 in myoblasts exposed to pro-inflammatory cytokines or hyperosmolar stress and in biopsies from myositis patients

Nanoscopic X-ray fluorescence imaging and quantification of intracellular key-elements in cryofrozen Friedreich's ataxia fibroblasts

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