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van den Born

Showing results (621-630 of 717) with videos related to

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American Journal of Human Genetics|July 15, 2014
Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophySusanne Roosing, Ideke J C Lamers, Erik de Vrieze, et al.
Cell|November 1, 2002
The beta-catenin/TCF-4 complex imposes a crypt progenitor phenotype on colorectal cancer cellsMarc van de Wetering, Elena Sancho, Cornelis Verweij, et al.
Cardiovascular Research|May 14, 2016
The role of ADAMTS13 in acute myocardial infarction: cause or consequence?Elise S Eerenberg, Paul F A Teunissen, Bert-Jan van den Born, et al.
Molecular Vision|June 19, 2014
Novel compound heterozygous NMNAT1 variants associated with Leber congenital amaurosisAnna M Siemiatkowska, L Ingeborgh van den Born, Maria M van Genderen, et al.
BMJ Open|October 30, 2023
Associations between spirometric impairments and microvascular complications in type 2 diabetes: a cross-sectional studyCharles F Hayfron-Benjamin, Charles Agyemang, Bert-Jan H van den Born, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|April 9, 2009
Climate change and food safety: an emerging issue with special focus on EuropeM Miraglia, H J P Marvin, G A Kleter, et al.
Human Mutation|August 19, 2021
PRPH2 mutation update: In silico assessment of 245 reported and 7 novel variants in patients with retinal diseaseManon H C A Peeters, Mubeen Khan, Anoek A M B Rooijakkers, et al.
HLA|May 19, 2025
Repeated HLA-DRB1 and HLA-DQB1 Mismatches Without Preformed DSA Affect Graft Survival, Rejection and DSA Development: A Multicenter AnalysisD A J van den Broek, S Meziyerh, D van der Helm, et al.
Investigative Ophthalmology & Visual Science|October 17, 2019
Late-Onset Stargardt Disease Due to Mild, Deep-Intronic ABCA4 AllelesEsmee H Runhart, Dyon Valkenburg, Stéphanie S Cornelis, et al.
Genes|January 11, 2018
Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate GenesGaluh D N Astuti, L Ingeborgh van den Born, M Imran Khan, et al.
Pageof 72

Showing results (621-630 of 717) with videos related to

Sort By:
Pageof 72
American Journal of Human Genetics|July 15, 2014
Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophySusanne Roosing, Ideke J C Lamers, Erik de Vrieze, et al.
Cell|November 1, 2002
The beta-catenin/TCF-4 complex imposes a crypt progenitor phenotype on colorectal cancer cellsMarc van de Wetering, Elena Sancho, Cornelis Verweij, et al.
Cardiovascular Research|May 14, 2016
The role of ADAMTS13 in acute myocardial infarction: cause or consequence?Elise S Eerenberg, Paul F A Teunissen, Bert-Jan van den Born, et al.
Molecular Vision|June 19, 2014
Novel compound heterozygous NMNAT1 variants associated with Leber congenital amaurosisAnna M Siemiatkowska, L Ingeborgh van den Born, Maria M van Genderen, et al.
BMJ Open|October 30, 2023
Associations between spirometric impairments and microvascular complications in type 2 diabetes: a cross-sectional studyCharles F Hayfron-Benjamin, Charles Agyemang, Bert-Jan H van den Born, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|April 9, 2009
Climate change and food safety: an emerging issue with special focus on EuropeM Miraglia, H J P Marvin, G A Kleter, et al.
Human Mutation|August 19, 2021
PRPH2 mutation update: In silico assessment of 245 reported and 7 novel variants in patients with retinal diseaseManon H C A Peeters, Mubeen Khan, Anoek A M B Rooijakkers, et al.
HLA|May 19, 2025
Repeated HLA-DRB1 and HLA-DQB1 Mismatches Without Preformed DSA Affect Graft Survival, Rejection and DSA Development: A Multicenter AnalysisD A J van den Broek, S Meziyerh, D van der Helm, et al.
Investigative Ophthalmology & Visual Science|October 17, 2019
Late-Onset Stargardt Disease Due to Mild, Deep-Intronic ABCA4 AllelesEsmee H Runhart, Dyon Valkenburg, Stéphanie S Cornelis, et al.
Genes|January 11, 2018
Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate GenesGaluh D N Astuti, L Ingeborgh van den Born, M Imran Khan, et al.
Pageof 72