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Journal of the American Society of Nephrology : JASN
|
April 14, 2006
Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults
David S Geller, Junhui Zhang, Maria-Christina Zennaro, et al.
Journal of the American College of Cardiology
|
March 29, 2008
Hypoxia, hypoxia-inducible transcription factor, and macrophages in human atherosclerotic plaques are correlated with intraplaque angiogenesis
Judith C Sluimer, Jean-Marie Gasc, Job L van Wanroij, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
October 27, 2006
Angiogenic activity of human chorionic gonadotropin through LH receptor activation on endothelial and epithelial cells of the endometrium
Sarah Berndt, Sophie Perrier d'Hauterive, Silvia Blacher, et al.
Hypertension (Dallas, Tex. : 1979)
|
April 12, 2017
Transcriptome Analysis of Human Reninomas as an Approach to Understanding Juxtaglomerular Cell Biology
Alexandre G Martini, Lucie K Xa, Marie-Josée Lacombe, et al.
Developmental Cell
|
January 18, 2011
Robo4 maintains vessel integrity and inhibits angiogenesis by interacting with UNC5B
Alexander W Koch, Thomas Mathivet, Bruno Larrivée, et al.
The Journal of Clinical Investigation
|
November 18, 2003
Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency
Robert S Jackson, John W M Creemers, I Sadaf Farooqi, et al.
Journal of the American Society of Nephrology : JASN
|
June 23, 2006
Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the Renin-Angiotensin system
Mireille Lacoste, Yi Cai, Liliane Guicharnaud, et al.
The Journal of Clinical Investigation
|
April 16, 2019
ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration
Takuo Hirose, Alfredo Cabrera-Socorro, David Chitayat, et al.
Human Mutation
|
November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis
Olivier Gribouval, Vincent Morinière, Audrey Pawtowski, et al.
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of 8
Search research articles
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Showing results (71-80 of 79) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 79 results.
Journal of the American Society of Nephrology : JASN
|
April 14, 2006
Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults
David S Geller, Junhui Zhang, Maria-Christina Zennaro, et al.
Journal of the American College of Cardiology
|
March 29, 2008
Hypoxia, hypoxia-inducible transcription factor, and macrophages in human atherosclerotic plaques are correlated with intraplaque angiogenesis
Judith C Sluimer, Jean-Marie Gasc, Job L van Wanroij, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
October 27, 2006
Angiogenic activity of human chorionic gonadotropin through LH receptor activation on endothelial and epithelial cells of the endometrium
Sarah Berndt, Sophie Perrier d'Hauterive, Silvia Blacher, et al.
Hypertension (Dallas, Tex. : 1979)
|
April 12, 2017
Transcriptome Analysis of Human Reninomas as an Approach to Understanding Juxtaglomerular Cell Biology
Alexandre G Martini, Lucie K Xa, Marie-Josée Lacombe, et al.
Developmental Cell
|
January 18, 2011
Robo4 maintains vessel integrity and inhibits angiogenesis by interacting with UNC5B
Alexander W Koch, Thomas Mathivet, Bruno Larrivée, et al.
The Journal of Clinical Investigation
|
November 18, 2003
Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency
Robert S Jackson, John W M Creemers, I Sadaf Farooqi, et al.
Journal of the American Society of Nephrology : JASN
|
June 23, 2006
Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the Renin-Angiotensin system
Mireille Lacoste, Yi Cai, Liliane Guicharnaud, et al.
The Journal of Clinical Investigation
|
April 16, 2019
ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration
Takuo Hirose, Alfredo Cabrera-Socorro, David Chitayat, et al.
Human Mutation
|
November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis
Olivier Gribouval, Vincent Morinière, Audrey Pawtowski, et al.
Page
of 8