Thomas Geuens

Thomas Geuens

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Thomas Geuens

Thomas Geuens

Publications by authors named "Thomas Geuens"

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Vascular bioengineering of scaffolds derived from human discarded transplant kidneys using human pluripotent stem cell-derived endothelium.

Authors:
Daniëlle G Leuning Franca M R Witjas Mehdi Maanaoui Annemarie M A de Graaf Ellen Lievers Thomas Geuens Christina M Avramut Loes E Wiersma Cathelijne W van den Berg Wendy M P J Sol Hetty de Boer Gangqi Wang Vanessa L S LaPointe Johan van der Vlag Cees van Kooten Bernard M van den Berg Melissa H Little Marten A Engelse Ton J Rabelink

Am J Transplant 2019 May 10;19(5):1328-1343. Epub 2019 Jan 10.

Department of Nephrology, Leiden University Medical Center, Leiden, The Netherlands.

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http://doi.wiley.com/10.1111/ajt.15200
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http://dx.doi.org/10.1111/ajt.15200DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590331PMC
May 2019

Novel insights in the disease biology of mutant small heat shock proteins in neuromuscular diseases.

Authors:
Elias Adriaenssens Thomas Geuens Jonathan Baets Andoni Echaniz-Laguna Vincent Timmerman

Brain 2017 Oct;140(10):2541-2549

Peripheral Neuropathy Research Group, Institute Born Bunge, University of Antwerp, Antwerpen, Belgium.

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http://academic.oup.com/brain/article/140/10/2541/4082543
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http://dx.doi.org/10.1093/brain/awx187DOI Listing
October 2017

Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations.

Authors:
Andoni Echaniz-Laguna Thomas Geuens Philippe Petiot Yann Péréon Elias Adriaenssens Mansour Haidar Simona Capponi Thierry Maisonobe Emmanuel Fournier Odile Dubourg Bertrand Degos François Salachas Timothée Lenglet Bruno Eymard Emilien Delmont Jean Pouget Raul Juntas Morales Cyril Goizet Philippe Latour Vincent Timmerman Tanya Stojkovic

Hum Mutat 2017 05 25;38(5):556-568. Epub 2017 Feb 25.

Neuromuscular Disease Centre, Hôpital de la Pitié-Salpétrière, APHP, Paris, France.

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http://dx.doi.org/10.1002/humu.23189DOI Listing
May 2017

Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease.

Authors:
Thomas Geuens Vicky De Winter Nicholas Rajan Tilmann Achsel Ligia Mateiu Leonardo Almeida-Souza Bob Asselbergh Delphine Bouhy Michaela Auer-Grumbach Claudia Bagni Vincent Timmerman

Acta Neuropathol Commun 2017 01 11;5(1). Epub 2017 Jan 11.

Peripheral Neuropathy Group, Department of Molecular Genetics, VIB, Institute Born Bunge and University of Antwerp, Antwerpen, Belgium.

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http://dx.doi.org/10.1186/s40478-016-0407-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225548PMC
January 2017

Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1.

Authors:
Simona Capponi Thomas Geuens Alessandro Geroldi Paola Origone Simonetta Verdiani Elena Cichero Elias Adriaenssens Vicky De Winter Monica Bandettini di Poggio Marco Barberis Adriano Chiò Paola Fossa Paola Mandich Emilia Bellone Vincent Timmerman

Hum Mutat 2016 11 30;37(11):1202-1208. Epub 2016 Aug 30.

VIB Department of Molecular Genetics, Peripheral Neuropathy Group, Born Bunge Foundation, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1002/humu.23062DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108433PMC
November 2016

The hnRNP family: insights into their role in health and disease.

Authors:
Thomas Geuens Delphine Bouhy Vincent Timmerman

Hum Genet 2016 08 23;135(8):851-67. Epub 2016 May 23.

Peripheral Neuropathy Group, VIB Molecular Genetics Department, University of Antwerp-CDE, Parking P4, Building V, Room 1.30, Universiteitsplein 1, 2610, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s00439-016-1683-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947485PMC
August 2016

Characterization of New Transgenic Mouse Models for Two Charcot-Marie-Tooth-Causing HspB1 Mutations using the Rosa26 Locus.

Authors:
Delphine Bouhy Thomas Geuens Vicky De Winter Leonardo Almeida-Souza Istvan Katona Joachim Weis Tino Hochepied Steven Goossens Jody J Haigh Sophie Janssens Vincent Timmerman

J Neuromuscul Dis 2016 05;3(2):183-200

Peripheral Neuropathy Group, VIB Department of Molecular Genetics and Institute Born Bunge, University of Antwerp, Antwerpen, Belgium.

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http://dx.doi.org/10.3233/JND-150144DOI Listing
May 2016

Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.

Authors:
Katia Hardies Carolien G F de Kovel Sarah Weckhuysen Bob Asselbergh Thomas Geuens Tine Deconinck Abdelkrim Azmi Patrick May Eva Brilstra Felicitas Becker Nina Barisic Dana Craiu Kees P J Braun Dennis Lal Holger Thiele Julian Schubert Yvonne Weber Ruben van 't Slot Peter Nürnberg Rudi Balling Vincent Timmerman Holger Lerche Stuart Maudsley Ingo Helbig Arvid Suls Bobby P C Koeleman Peter De Jonghe

Brain 2015 Nov 17;138(Pt 11):3238-50. Epub 2015 Sep 17.

3 Departments of Medical Genetics and Child Neurology, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://brain.oxfordjournals.org/content/brain/138/11/3238.fu
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http://www.brain.oxfordjournals.org/lookup/doi/10.1093/brain
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http://dx.doi.org/10.1093/brain/awv263DOI Listing
November 2015

Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritance.

Authors:
Kristien Peeters Ivan Litvinenko Bob Asselbergh Leonardo Almeida-Souza Teodora Chamova Thomas Geuens Elke Ydens Magdalena Zimoń Joy Irobi Els De Vriendt Vicky De Winter Tinne Ooms Vincent Timmerman Ivailo Tournev Albena Jordanova

Am J Hum Genet 2013 Jun 9;92(6):955-64. Epub 2013 May 9.

Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, Antwerp 2610, Belgium; Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp 2610, Belgium.

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http://dx.doi.org/10.1016/j.ajhg.2013.04.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675262PMC
June 2013