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The Journal of Experimental Medicine
|
June 22, 2016
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
Marije 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 Vesicles
Charles 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 osteoarthritis
Ingrid 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 malformations
Vanessa 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 Keratoderma
Annemieke 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 model
Ruizhi 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 characteristics
Henriët Springelkamp, Adriana I Iglesias, Aniket Mishra, et al.
Page
of 16
Search research articles
Search
Showing results (151-160 of 157) with videos related to
Sort By:
Page
of 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 syndrome
Marije 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 Vesicles
Charles 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 osteoarthritis
Ingrid 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 malformations
Vanessa 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 Keratoderma
Annemieke 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 model
Ruizhi 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 characteristics
Henriët Springelkamp, Adriana I Iglesias, Aniket Mishra, et al.
Page
of 16