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Cardiovascular Research
|
October 14, 2003
Vascular endothelial growth factor-D expression in human atherosclerotic lesions
Juha Rutanen, Pia Leppänen, Tiina T Tuomisto, et al.
The American Journal of Pathology
|
April 12, 2002
Expression of vascular endothelial growth factor and vascular endothelial growth factor receptor-2 (KDR/Flk-1) in ischemic skeletal muscle and its regeneration
Tuomas T Rissanen, Ismo Vajanto, Mikko O Hiltunen, et al.
Annals of Medicine
|
April 3, 2012
Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population
Pertti Jääskeläinen, Tiina Heliö, Katriina Aalto-Setälä, et al.
Science (New York, N.Y.)
|
November 10, 2018
Quantifying the contribution of recessive coding variation to developmental disorders
Hilary C Martin, Wendy D Jones, Rebecca McIntyre, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 24, 2021
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
Tomoko Nakanishi, Sara Pigazzini, Frauke Degenhardt, et al.
Biorxiv : the Preprint Server for Biology
|
March 3, 2021
A single-cell and spatial atlas of autopsy tissues reveals pathology and cellular targets of SARS-CoV-2
Toni M Delorey, Carly G K Ziegler, Graham Heimberg, et al.
Nature
|
April 29, 2021
COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets
Toni M Delorey, Carly G K Ziegler, Graham Heimberg, et al.
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Search research articles
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Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
Cardiovascular Research
|
October 14, 2003
Vascular endothelial growth factor-D expression in human atherosclerotic lesions
Juha Rutanen, Pia Leppänen, Tiina T Tuomisto, et al.
The American Journal of Pathology
|
April 12, 2002
Expression of vascular endothelial growth factor and vascular endothelial growth factor receptor-2 (KDR/Flk-1) in ischemic skeletal muscle and its regeneration
Tuomas T Rissanen, Ismo Vajanto, Mikko O Hiltunen, et al.
Annals of Medicine
|
April 3, 2012
Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population
Pertti Jääskeläinen, Tiina Heliö, Katriina Aalto-Setälä, et al.
Science (New York, N.Y.)
|
November 10, 2018
Quantifying the contribution of recessive coding variation to developmental disorders
Hilary C Martin, Wendy D Jones, Rebecca McIntyre, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 24, 2021
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
Tomoko Nakanishi, Sara Pigazzini, Frauke Degenhardt, et al.
Biorxiv : the Preprint Server for Biology
|
March 3, 2021
A single-cell and spatial atlas of autopsy tissues reveals pathology and cellular targets of SARS-CoV-2
Toni M Delorey, Carly G K Ziegler, Graham Heimberg, et al.
Nature
|
April 29, 2021
COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets
Toni M Delorey, Carly G K Ziegler, Graham Heimberg, et al.
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