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van den Born

Showing results (611-620 of 717) with videos related to

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Plos One|October 8, 2015
Toll-Like Receptor Family Polymorphisms Are Associated with Primary Renal Diseases but Not with Renal Outcomes Following Kidney TransplantationMark C Dessing, Jesper Kers, Jeffrey Damman, et al.
The Lancet Regional Health. Europe|December 20, 2021
Differences in SARS-CoV-2 infections during the first and second wave of SARS-CoV-2 between six ethnic groups in Amsterdam, the Netherlands: A population-based longitudinal serological studyLiza Coyer, Anders Boyd, Janke Schinkel, et al.
Physiological Genomics|January 24, 2013
SLC22A2 is associated with tubular creatinine secretion and bias of estimated GFR in renal transplantationAnna Reznichenko, Steef J Sinkeler, Harold Snieder, et al.
Investigative Ophthalmology & Visual Science|May 31, 2014
IMPG2-associated retinitis pigmentosa displays relatively early macular involvementRamon A C van Huet, Rob W J Collin, Anna M Siemiatkowska, et al.
Cell Stem Cell|January 21, 2010
Lgr5(+ve) stem cells drive self-renewal in the stomach and build long-lived gastric units in vitroNick Barker, Meritxell Huch, Pekka Kujala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2025
Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosaTamar Hayman, Shai Ovadia, Jaya Krishnan, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 12, 2018
Profiling proliferative cells and their progeny in damaged murine heartsKai Kretzschmar, Yorick Post, Marie Bannier-Hélaouët, et al.
BMC Medical Genetics|September 6, 2012
UMOD as a susceptibility gene for end-stage renal diseaseAnna Reznichenko, Carsten A Böger, Harold Snieder, et al.
Human Genetics|June 27, 2003
Novel types of mutation in the choroideremia ( CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exonJosé A J M van den Hurk, Dorien J R van de Pol, Bernd Wissinger, et al.
Investigative Ophthalmology & Visual Science|December 17, 2008
A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorderKarin W Littink, Maria M van Genderen, Rob W J Collin, et al.
Pageof 72

Showing results (611-620 of 717) with videos related to

Sort By:
Pageof 72
Plos One|October 8, 2015
Toll-Like Receptor Family Polymorphisms Are Associated with Primary Renal Diseases but Not with Renal Outcomes Following Kidney TransplantationMark C Dessing, Jesper Kers, Jeffrey Damman, et al.
The Lancet Regional Health. Europe|December 20, 2021
Differences in SARS-CoV-2 infections during the first and second wave of SARS-CoV-2 between six ethnic groups in Amsterdam, the Netherlands: A population-based longitudinal serological studyLiza Coyer, Anders Boyd, Janke Schinkel, et al.
Physiological Genomics|January 24, 2013
SLC22A2 is associated with tubular creatinine secretion and bias of estimated GFR in renal transplantationAnna Reznichenko, Steef J Sinkeler, Harold Snieder, et al.
Investigative Ophthalmology & Visual Science|May 31, 2014
IMPG2-associated retinitis pigmentosa displays relatively early macular involvementRamon A C van Huet, Rob W J Collin, Anna M Siemiatkowska, et al.
Cell Stem Cell|January 21, 2010
Lgr5(+ve) stem cells drive self-renewal in the stomach and build long-lived gastric units in vitroNick Barker, Meritxell Huch, Pekka Kujala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2025
Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosaTamar Hayman, Shai Ovadia, Jaya Krishnan, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 12, 2018
Profiling proliferative cells and their progeny in damaged murine heartsKai Kretzschmar, Yorick Post, Marie Bannier-Hélaouët, et al.
BMC Medical Genetics|September 6, 2012
UMOD as a susceptibility gene for end-stage renal diseaseAnna Reznichenko, Carsten A Böger, Harold Snieder, et al.
Human Genetics|June 27, 2003
Novel types of mutation in the choroideremia ( CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exonJosé A J M van den Hurk, Dorien J R van de Pol, Bernd Wissinger, et al.
Investigative Ophthalmology & Visual Science|December 17, 2008
A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorderKarin W Littink, Maria M van Genderen, Rob W J Collin, et al.
Pageof 72