Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Josef T Prchal

Showing results (211-220 of 241) with videos related to

Pageof 25
Sort By:
Blood Cells, Molecules & Diseases|September 3, 2013
Iron deficiency modifies gene expression variation induced by augmented hypoxia sensingXu Zhang, Wei Zhang, Shwu-Fan Ma, et al.
Haematologica|January 29, 2008
Elevated homocysteine, glutathione and cysteinylglycine concentrations in patients homozygous for the Chuvash polycythemia VHL mutationAdelina I Sergueeva, Galina Y Miasnikova, Daniel J Okhotin, et al.
Haematologica|October 2, 2010
Elevated tricuspid regurgitation velocity and decline in exercise capacity over 22 months of follow up in children and adolescents with sickle cell anemiaVictor R Gordeuk, Caterina P Minniti, Mehdi Nouraie, et al.
Plos One|December 4, 2009
Angiogenic and inflammatory markers of cardiopulmonary changes in children and adolescents with sickle cell diseaseXiaomei Niu, Mehdi Nouraie, Andrew Campbell, et al.
Oncotarget|December 31, 2016
Evolutionary selected Tibetan variants of HIF pathway and risk of lung cancerLucie Lanikova, N Scott Reading, Hao Hu, et al.
Nature Genetics|November 5, 2002
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemiaSonny O Ang, Hua Chen, Kiichi Hirota, et al.
American Journal of Human Genetics|November 4, 2017
Natural Selection on Genes Related to Cardiovascular Health in High-Altitude Adapted AndeansJacob E Crawford, Ricardo Amaru, Jihyun Song, et al.
Blood|November 8, 2003
The worldwide distribution of the VHL 598C>T mutation indicates a single founding eventEnli Liu, Melanie J Percy, Christopher I Amos, et al.
Human Molecular Genetics|February 8, 2017
A genetic variation associated with plasma erythropoietin and a non-coding transcript of PRKAR1A in sickle cell diseaseXu Zhang, Binal N Shah, Wei Zhang, et al.
Iscience|April 2, 2021
<i>HIF2A</i> gain-of-function mutation modulates the stiffness of smooth muscle cells and compromises vascular mechanicsXin Yi Chan, Eugenia Volkova, Joon Eoh, et al.
Pageof 25

Showing results (211-220 of 241) with videos related to

Sort By:
Pageof 25
Blood Cells, Molecules & Diseases|September 3, 2013
Iron deficiency modifies gene expression variation induced by augmented hypoxia sensingXu Zhang, Wei Zhang, Shwu-Fan Ma, et al.
Haematologica|January 29, 2008
Elevated homocysteine, glutathione and cysteinylglycine concentrations in patients homozygous for the Chuvash polycythemia VHL mutationAdelina I Sergueeva, Galina Y Miasnikova, Daniel J Okhotin, et al.
Haematologica|October 2, 2010
Elevated tricuspid regurgitation velocity and decline in exercise capacity over 22 months of follow up in children and adolescents with sickle cell anemiaVictor R Gordeuk, Caterina P Minniti, Mehdi Nouraie, et al.
Plos One|December 4, 2009
Angiogenic and inflammatory markers of cardiopulmonary changes in children and adolescents with sickle cell diseaseXiaomei Niu, Mehdi Nouraie, Andrew Campbell, et al.
Oncotarget|December 31, 2016
Evolutionary selected Tibetan variants of HIF pathway and risk of lung cancerLucie Lanikova, N Scott Reading, Hao Hu, et al.
Nature Genetics|November 5, 2002
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemiaSonny O Ang, Hua Chen, Kiichi Hirota, et al.
American Journal of Human Genetics|November 4, 2017
Natural Selection on Genes Related to Cardiovascular Health in High-Altitude Adapted AndeansJacob E Crawford, Ricardo Amaru, Jihyun Song, et al.
Blood|November 8, 2003
The worldwide distribution of the VHL 598C>T mutation indicates a single founding eventEnli Liu, Melanie J Percy, Christopher I Amos, et al.
Human Molecular Genetics|February 8, 2017
A genetic variation associated with plasma erythropoietin and a non-coding transcript of PRKAR1A in sickle cell diseaseXu Zhang, Binal N Shah, Wei Zhang, et al.
Iscience|April 2, 2021
<i>HIF2A</i> gain-of-function mutation modulates the stiffness of smooth muscle cells and compromises vascular mechanicsXin Yi Chan, Eugenia Volkova, Joon Eoh, et al.
Pageof 25