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Patrick H Maxwell

Showing results (141-150 of 168) with videos related to

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Plos Medicine|June 14, 2006
Mutation of von Hippel-Lindau tumour suppressor and human cardiopulmonary physiologyThomas G Smith, Jerome T Brooks, George M Balanos, et al.
Cancer Cell|October 22, 2011
Renal cyst formation in Fh1-deficient mice is independent of the Hif/Phd pathway: roles for fumarate in KEAP1 succination and Nrf2 signalingJulie Adam, Emine Hatipoglu, Linda O'Flaherty, et al.
The Journal of Clinical Investigation|January 12, 2008
Role of Gas6 in erythropoiesis and anemia in miceAnne Angelillo-Scherrer, Laurent Burnier, Diether Lambrechts, et al.
Cell Stem Cell|September 8, 2023
Generation of a humanized mesonephros in pigs from induced pluripotent stem cells via embryo complementationJiaowei Wang, Wenguang Xie, Nan Li, et al.
The Journal of Clinical Investigation|February 15, 2011
Prolyl hydroxylase 3 (PHD3) is essential for hypoxic regulation of neutrophilic inflammation in humans and miceSarah R Walmsley, Edwin R Chilvers, Alfred A Thompson, et al.
Nature Genetics|October 13, 2009
Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levelsJohn C Chambers, Weihua Zhang, Yun Li, et al.
The Journal of Biological Chemistry|January 6, 2017
Fumarylacetoacetate Hydrolase Knock-out Rabbit Model for Hereditary Tyrosinemia Type 1Li Li, Quanjun Zhang, Huaqiang Yang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 11, 2011
Cardiopulmonary function in two human disorders of the hypoxia-inducible factor (HIF) pathway: von Hippel-Lindau disease and HIF-2alpha gain-of-function mutationFederico Formenti, Philip A Beer, Quentin P P Croft, et al.
Plos One|March 24, 2017
A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general populationKonstantinos Voskarides, Charalambos Stefanou, Myrtani Pieri, et al.
Scientific Reports|August 25, 2017
Homozygous p.Ser267Phe in SLC10A1 is associated with a new type of hypercholanemia and implications for personalized medicineRuihong Liu, Chuming Chen, Xuefeng Xia, et al.
Pageof 17

Showing results (141-150 of 168) with videos related to

Sort By:
Pageof 17
Plos Medicine|June 14, 2006
Mutation of von Hippel-Lindau tumour suppressor and human cardiopulmonary physiologyThomas G Smith, Jerome T Brooks, George M Balanos, et al.
Cancer Cell|October 22, 2011
Renal cyst formation in Fh1-deficient mice is independent of the Hif/Phd pathway: roles for fumarate in KEAP1 succination and Nrf2 signalingJulie Adam, Emine Hatipoglu, Linda O'Flaherty, et al.
The Journal of Clinical Investigation|January 12, 2008
Role of Gas6 in erythropoiesis and anemia in miceAnne Angelillo-Scherrer, Laurent Burnier, Diether Lambrechts, et al.
Cell Stem Cell|September 8, 2023
Generation of a humanized mesonephros in pigs from induced pluripotent stem cells via embryo complementationJiaowei Wang, Wenguang Xie, Nan Li, et al.
The Journal of Clinical Investigation|February 15, 2011
Prolyl hydroxylase 3 (PHD3) is essential for hypoxic regulation of neutrophilic inflammation in humans and miceSarah R Walmsley, Edwin R Chilvers, Alfred A Thompson, et al.
Nature Genetics|October 13, 2009
Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levelsJohn C Chambers, Weihua Zhang, Yun Li, et al.
The Journal of Biological Chemistry|January 6, 2017
Fumarylacetoacetate Hydrolase Knock-out Rabbit Model for Hereditary Tyrosinemia Type 1Li Li, Quanjun Zhang, Huaqiang Yang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 11, 2011
Cardiopulmonary function in two human disorders of the hypoxia-inducible factor (HIF) pathway: von Hippel-Lindau disease and HIF-2alpha gain-of-function mutationFederico Formenti, Philip A Beer, Quentin P P Croft, et al.
Plos One|March 24, 2017
A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general populationKonstantinos Voskarides, Charalambos Stefanou, Myrtani Pieri, et al.
Scientific Reports|August 25, 2017
Homozygous p.Ser267Phe in SLC10A1 is associated with a new type of hypercholanemia and implications for personalized medicineRuihong Liu, Chuming Chen, Xuefeng Xia, et al.
Pageof 17