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Rob Willemsen

Showing results (151-160 of 157) with videos related to

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The Journal of Experimental Medicine|June 22, 2016
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndromeMarije E C Meuwissen, Rachel Schot, Sofija Buta, et al.
Journal of the American Society of Nephrology : JASN|March 30, 2021
Comparing Approaches to Normalize, Quantify, and Characterize Urinary Extracellular VesiclesCharles J Blijdorp, Omar A Z Tutakhel, Thomas A Hartjes, et al.
Nature Genetics|January 11, 2011
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritisIngrid M B H van de Laar, Rogier A Oldenburg, Gerard Pals, et al.
Circulation Research|May 3, 2012
NPHP4 variants are associated with pleiotropic heart malformationsVanessa M French, Ingrid M B H van de Laar, Marja W Wessels, et al.
The Journal of Investigative Dermatology|September 16, 2023
Disruption of TUFT1, a Desmosome-Associated Protein, Causes Skin Fragility, Woolly Hair, and Palmoplantar KeratodermaAnnemieke J M H Verkerk, Daniela Andrei, Mathilde C S C Vermeer, et al.
Acta Neuropathologica|April 29, 2023
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical modelRuizhi Deng, Eva Medico-Salsench, Anita Nikoncuk, et al.
Human Molecular Genetics|January 12, 2017
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristicsHenriët Springelkamp, Adriana I Iglesias, Aniket Mishra, et al.
Pageof 16

Showing results (151-160 of 157) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 157 results.
The Journal of Experimental Medicine|June 22, 2016
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndromeMarije E C Meuwissen, Rachel Schot, Sofija Buta, et al.
Journal of the American Society of Nephrology : JASN|March 30, 2021
Comparing Approaches to Normalize, Quantify, and Characterize Urinary Extracellular VesiclesCharles J Blijdorp, Omar A Z Tutakhel, Thomas A Hartjes, et al.
Nature Genetics|January 11, 2011
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritisIngrid M B H van de Laar, Rogier A Oldenburg, Gerard Pals, et al.
Circulation Research|May 3, 2012
NPHP4 variants are associated with pleiotropic heart malformationsVanessa M French, Ingrid M B H van de Laar, Marja W Wessels, et al.
The Journal of Investigative Dermatology|September 16, 2023
Disruption of TUFT1, a Desmosome-Associated Protein, Causes Skin Fragility, Woolly Hair, and Palmoplantar KeratodermaAnnemieke J M H Verkerk, Daniela Andrei, Mathilde C S C Vermeer, et al.
Acta Neuropathologica|April 29, 2023
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical modelRuizhi Deng, Eva Medico-Salsench, Anita Nikoncuk, et al.
Human Molecular Genetics|January 12, 2017
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristicsHenriët Springelkamp, Adriana I Iglesias, Aniket Mishra, et al.
Pageof 16