Onderzoeker
Lien Van Eyck
- Disciplines:Systeembiologie, Moleculaire en celbiologie, Immunologie
Affiliaties
- Adaptieve Immunologie (Labo)
Lid
Vanaf1 okt 2012 → 2 okt 2016
Projecten
1 - 1 of 1
- Gain-of-function mutaties van NOD2 in Blau syndroom en early-onset sarcoïdose: onderzoek van immunologische en moleculaire mechanismen.Vanaf1 okt 2012 → 2 okt 2016Financiering: FWO mandaten
Publicaties
1 - 10 van 10
- A novel kindred with inherited STAT2 deficiency and severe viral illness(2017)
Auteurs: Leen Moens, Lien Van Eyck, Dirk Jochmans, Glynis Frans, Xavier Bossuyt, Patrick Matthys, Johan Neyts, Rik Gijsbers, Isabelle Meyts, Adrian Liston
Pagina's: 1995 - 1997 - Identification of disease-causing genetic variants in patients with severe early-onset immunological disorders: a whole-exome sequencing approach(2016)
Auteurs: Lien Van Eyck, Adrian Liston, Carine Wouters, Isabelle Meyts
- Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation(2016)
Auteurs: Vasiliki Lagou, Lien Van Eyck, James Dooley, Emanuela Pasciuto, Raf Sciot, Lien De Somer, Erika Van Nieuwenhove, An Goris, Carine Wouters, Adrian Liston
Pagina's: 332 - FAMILIAL AUTOINFLAMMATION WITH NEUTROPHILIC DERMATOSIS REVEALS A NOVEL REGULATORY MECHANISM OF PYRIN ACTIVATION(2016)
Auteurs: PJ Baker, Vasiliki Lagou, I Jeru, Lien Van Eyck, DA Parry, D Lawless, D De Nardo, JE Garcia-Perez, LF Dagley, C Holley, et al.
Pagina's: 54 - 55 - IFIH1 mutation causes systemic lupus erythematosus with selective IgA-deficiency(2015)
Auteurs: Lien Van Eyck, Lien De Somer, Simon Bornschein, Glynis Frans, Stephanie Humblet-Baron, Leen Moens, Francis de Zegher, Xavier Bossuyt, Carine Wouters, Adrian Liston
Pagina's: 1592 - 1597 - IFIH1 mutation causes systemic lupus erythematosus with selective IgA-deficiency(2015)
Auteurs: Lien Van Eyck, Lien De Somer, Diana Pombal, Simon Bornschein, Glynis Frans, Stephanie Humblet-Baron, Leen Moens, Francis de Zegher, Xavier Bossuyt, Carine Wouters, et al.
Pagina's: 1592 - 1597 - Hematopoietic stem cell transplantation rescues the immunologic phenotype and prevents vasculopathy in patients with adenosine deaminase 2 deficiency(2015)
Auteurs: Lien Van Eyck, Leen Moens, Glynis Frans, Heidi Schaballie, Gert De Hertogh, James Dooley, Xavier Bossuyt, Carine Wouters, Adrian Liston, Isabelle Meyts
Pagina's: 283 - 287 - Gain-of-function mutations in signal transducer and activator of transcription 1 (STAT1): Chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental shedding(2014)
Auteurs: Glynis Frans, Leen Moens, Heidi Schaballie, Lien Van Eyck, Edith Vermeulen, James Dooley, Dominique Declerck, Marleen Peumans, Christiane De Boeck, Ilse Hoffman, et al.
Pagina's: 1209 - 1213 - Mutant ADA2 in Vasculopathies(2014)
Auteurs: Lien Van Eyck, Adrian Liston, Carine Wouters
Pagina's: 480 - 480 - Olmsted syndrome: exploration of the immunological phenotype(2013)
Auteurs: Dina Danso-Abeam, James Dooley, Lien Van Eyck, Esther Hauben, Marc Van De Velde, Chris Van Geet, Heidi Schaballie, Diether Lambrechts, Dean Franckaert, Stephanie Humblet-Baron, et al.