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Showing results (371-380 of 453) with videos related to

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Clinical Journal of the American Society of Nephrology : CJASN|May 14, 2011
Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigreesYiannis Athanasiou, Konstantinos Voskarides, Daniel P Gale, et al.
Frontiers in Oncology|October 11, 2021
Corrigendum: VHL-Mediated Regulation of CHCHD4 and Mitochondrial FunctionThomas Briston, Jenna M Stephen, Luke W Thomas, et al.
Plos One|March 22, 2013
Epistatic role of the MYH9/APOL1 region on familial hematuria genesKonstantinos Voskarides, Panayiota Demosthenous, Louiza Papazachariou, et al.
Human Mutation|January 12, 2005
Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese familiesSuqin Chen, Chun Song, Hui Guo, et al.
Frontiers in Oncology|October 20, 2018
VHL-Mediated Regulation of CHCHD4 and Mitochondrial FunctionThomas Briston, Jenna M Stephen, Luke W Thomas, et al.
Blood|February 15, 2007
Lack of endothelial cell survivin causes embryonic defects in angiogenesis, cardiogenesis, and neural tube closureFemke Zwerts, Florea Lupu, Astrid De Vriese, et al.
International Journal of Cancer|July 21, 2007
Erythropoietin gene expression in renal carcinoma is considerably more frequent than paraneoplastic polycythemiaMichael S Wiesener, Philine Münchenhagen, Markus Gläser, et al.
Cancer Research|May 23, 2002
Expression of hypoxia-inducible factors in human renal cancer: relationship to angiogenesis and to the von Hippel-Lindau gene mutationKevin J Turner, John W Moore, Adam Jones, et al.
Cancer Cell|July 19, 2002
HIF activation identifies early lesions in VHL kidneys: evidence for site-specific tumor suppressor function in the nephronStefano J Mandriota, Kevin J Turner, David R Davies, et al.
The Journal of Pathology|September 19, 2006
Evolution of VHL tumourigenesis in nerve root tissueA O Vortmeyer, M G B Tran, W Zeng, et al.
Pageof 46

Showing results (371-380 of 453) with videos related to

Sort By:
Pageof 46
Clinical Journal of the American Society of Nephrology : CJASN|May 14, 2011
Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigreesYiannis Athanasiou, Konstantinos Voskarides, Daniel P Gale, et al.
Frontiers in Oncology|October 11, 2021
Corrigendum: VHL-Mediated Regulation of CHCHD4 and Mitochondrial FunctionThomas Briston, Jenna M Stephen, Luke W Thomas, et al.
Plos One|March 22, 2013
Epistatic role of the MYH9/APOL1 region on familial hematuria genesKonstantinos Voskarides, Panayiota Demosthenous, Louiza Papazachariou, et al.
Human Mutation|January 12, 2005
Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese familiesSuqin Chen, Chun Song, Hui Guo, et al.
Frontiers in Oncology|October 20, 2018
VHL-Mediated Regulation of CHCHD4 and Mitochondrial FunctionThomas Briston, Jenna M Stephen, Luke W Thomas, et al.
Blood|February 15, 2007
Lack of endothelial cell survivin causes embryonic defects in angiogenesis, cardiogenesis, and neural tube closureFemke Zwerts, Florea Lupu, Astrid De Vriese, et al.
International Journal of Cancer|July 21, 2007
Erythropoietin gene expression in renal carcinoma is considerably more frequent than paraneoplastic polycythemiaMichael S Wiesener, Philine Münchenhagen, Markus Gläser, et al.
Cancer Research|May 23, 2002
Expression of hypoxia-inducible factors in human renal cancer: relationship to angiogenesis and to the von Hippel-Lindau gene mutationKevin J Turner, John W Moore, Adam Jones, et al.
Cancer Cell|July 19, 2002
HIF activation identifies early lesions in VHL kidneys: evidence for site-specific tumor suppressor function in the nephronStefano J Mandriota, Kevin J Turner, David R Davies, et al.
The Journal of Pathology|September 19, 2006
Evolution of VHL tumourigenesis in nerve root tissueA O Vortmeyer, M G B Tran, W Zeng, et al.
Pageof 46