Onderzoeker
Mohammad Jakir Hosen
- Disciplines:Pediatrie en neonatologie, Moleculaire en celbiologie, Systeembiologie, Verpleegkunde, Genetica
Affiliaties
- Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf15 okt 2010 → 14 okt 2015
Publicaties
1 - 10 van 16
- VEGFA variants as prognostic markers for the retinopathy in pseudoxanthoma elasticum(2020)
Auteurs: Eva De Vilder, Mohammad Jakir Hosen, Ludovic Martin, Julie De Zaeytijd, Jean-Marc Ebran, Olivier Vanakker
Pagina's: 74 - 79 - Association of variants in the VEGFA (Vascular Endothelial Growth Factor) gene with severe retinopathy in pseudoxanthoma elasticum: implications for molecular screening, counseling and management(2016)
Auteurs: Eva De Vilder, Mohammad Jakir Hosen, Ludovic Martin, Julie De Zaeytijd, Jean-Marc Ebran, Olivier Vanakker
Aantal pagina's: 1 - Efficiency of exome sequencing for the molecular diagnosis of Pseudoxanthoma Elasticum(2015)
Auteurs: Mohammad Jakir Hosen, Filip Van Nieuwerburgh, Wouter Steyaert, Dieter Deforce, Ludovic Martin, Georges Leftheriotis, Olivier Vanakker
Pagina's: 992 - 998 - Novel phenotypes and genes in pseudoxanthoma elasticum-related soft tissue mineralization: results of an integrative approach(2015)
Auteurs: Eva De Vilder, Mohammad Jakir Hosen, Ariana Kariminejad, Georges Lefthériotis, Filip Van Nieuwerburgh, Ludovic Martin, Olivier Vanakker
Aantal pagina's: 1 - Efficiency of exome sequencing for the molecular diagnosis and modifier gene identification in pseudoxanthoma elasticum(2015)
Auteurs: Eva De Vilder, Mohammad Jakir Hosen, Olivier Vanakker
Aantal pagina's: 1 - Novel insights in the pathogenesis of pseudoxanthoma elasticum(2015)
Auteurs: Mohammad Jakir Hosen
- Molecular docking simulations provide insights in the substrate binding sites and possible substrates of the ABCC6 transporter(2014)
Auteurs: Mohammad Jakir Hosen, Abdullah Zubaer, Simrika Thapa, Bijendra Khadka, Olivier Vanakker
- Perturbation of specific pro-mineralizing signalling pathways in human and murine pseudoxanthoma elasticum(2014)
Auteurs: Mohammad Jakir Hosen, Olivier Le Saux, Olivier Vanakker
- Retinitis pigmentosa, cutis laxa and pseudoxanthoma elasticum-like skin manifestations associated with GGCX mutations(2014)
Auteurs: Ariana Kariminejad, Bita Bozorgmehr, Abdolhamid Najafi, Atefeh Khoshaeen, Maryam Ghalandari, Hossein Najmabadi, Mohamad Hasan Kariminejad, Olivier Vanakker, Mohammad Jakir Hosen, Fransiska Malfait, et al.
Pagina's: 2331 - 2338 - Second family with the Boston-type craniosynostosis syndrome: novel mutation and expansion of the clinical spectrum(2013)
Auteurs: Alexander Janssen, Mohammad Jakir Hosen, Philippe Jeannin, Olivier Vanakker
Pagina's: 2352 - 2357