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BMJ Open
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September 15, 2020
Currently prescribed drugs in the UK that could upregulate or downregulate ACE2 in COVID-19 disease: a systematic review
Hajira Dambha-Miller, Ali Albasri, Sam Hodgson, et al.
Human Mutation
|
April 30, 2014
A novel ZRS mutation leads to preaxial polydactyly type 2 in a heterozygous form and Werner mesomelic syndrome in a homozygous form
Julia E VanderMeer, Reymundo Lozano, Miao Sun, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium
|
February 25, 2011
Analysis of user behavior in accessing electronic medical record systems in emergency departments
Jan Horsky, Matthew B Allen, Allison R Wilcox, et al.
Molecular Neuropsychiatry
|
September 8, 2017
Low-Density Neuronal Cultures from Human Induced Pluripotent Stem Cells
Peter Dimitrion, Yun Zhi, Dennis Clayton, et al.
Vector Borne and Zoonotic Diseases (Larchmont, N.Y.)
|
April 6, 2006
West Nile virus antibodies in avian species of Georgia, USA: 2000-2004
Samantha E J Gibbs, Andrew B Allison, Michael J Yabsley, et al.
American Journal of Medical Genetics
|
May 5, 2001
"Baby rattle" pelvis dysplasia
V Cormier-Daire, R Savarirayan, R S Lachman, et al.
Bone
|
April 6, 2010
FGFR3 signaling induces a reversible senescence phenotype in chondrocytes similar to oncogene-induced premature senescence
Pavel Krejci, Jirina Prochazkova, Jiri Smutny, et al.
Molecular and Cellular Biology
|
October 27, 2010
Mitogen-activated protein kinases promote WNT/beta-catenin signaling via phosphorylation of LRP6
Igor Červenka, Joshua Wolf, Jan Mašek, et al.
The New Phytologist
|
October 14, 2020
Plant traits related to precipitation sensitivity of species and communities in semiarid shortgrass prairie
Kevin R Wilcox, Dana M Blumenthal, Julie A Kray, et al.
Nature Genetics
|
March 21, 1998
A mutation in PDS causes non-syndromic recessive deafness
X C Li, L A Everett, A K Lalwani, et al.
Page
of 80
Search research articles
Search
Showing results (541-550 of 791) with videos related to
Sort By:
Page
of 80
BMJ Open
|
September 15, 2020
Currently prescribed drugs in the UK that could upregulate or downregulate ACE2 in COVID-19 disease: a systematic review
Hajira Dambha-Miller, Ali Albasri, Sam Hodgson, et al.
Human Mutation
|
April 30, 2014
A novel ZRS mutation leads to preaxial polydactyly type 2 in a heterozygous form and Werner mesomelic syndrome in a homozygous form
Julia E VanderMeer, Reymundo Lozano, Miao Sun, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium
|
February 25, 2011
Analysis of user behavior in accessing electronic medical record systems in emergency departments
Jan Horsky, Matthew B Allen, Allison R Wilcox, et al.
Molecular Neuropsychiatry
|
September 8, 2017
Low-Density Neuronal Cultures from Human Induced Pluripotent Stem Cells
Peter Dimitrion, Yun Zhi, Dennis Clayton, et al.
Vector Borne and Zoonotic Diseases (Larchmont, N.Y.)
|
April 6, 2006
West Nile virus antibodies in avian species of Georgia, USA: 2000-2004
Samantha E J Gibbs, Andrew B Allison, Michael J Yabsley, et al.
American Journal of Medical Genetics
|
May 5, 2001
"Baby rattle" pelvis dysplasia
V Cormier-Daire, R Savarirayan, R S Lachman, et al.
Bone
|
April 6, 2010
FGFR3 signaling induces a reversible senescence phenotype in chondrocytes similar to oncogene-induced premature senescence
Pavel Krejci, Jirina Prochazkova, Jiri Smutny, et al.
Molecular and Cellular Biology
|
October 27, 2010
Mitogen-activated protein kinases promote WNT/beta-catenin signaling via phosphorylation of LRP6
Igor Červenka, Joshua Wolf, Jan Mašek, et al.
The New Phytologist
|
October 14, 2020
Plant traits related to precipitation sensitivity of species and communities in semiarid shortgrass prairie
Kevin R Wilcox, Dana M Blumenthal, Julie A Kray, et al.
Nature Genetics
|
March 21, 1998
A mutation in PDS causes non-syndromic recessive deafness
X C Li, L A Everett, A K Lalwani, et al.
Page
of 80