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J H Smith

Showing results (451-460 of 588) with videos related to

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American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 20, 2016
Screening of Living Kidney Donors for Genetic Diseases Using a Comprehensive Genetic Testing StrategyC P Thomas, M A Mansilla, R Sompallae, et al.
Human Mutation|January 29, 2008
Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BORDana J Orten, Stephanie M Fischer, Jessica L Sorensen, et al.
Nature Communications|November 5, 2022
On-microscope staging of live cells reveals changes in the dynamics of transcriptional bursting during differentiationD M Jeziorska, E A J Tunnacliffe, J M Brown, et al.
Neurobiology of Disease|July 19, 2005
Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cellsLut Van Laer, Markus Pfister, Sofie Thys, et al.
Clinical Pharmacology and Therapeutics|May 25, 2021
Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 GenotypeJohn Henry McDermott, Joshua Wolf, Keito Hoshitsuki, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2013
CFTR-deficient pigs display peripheral nervous system defects at birthLeah R Reznikov, Qian Dong, Jeng-Haur Chen, et al.
Frontiers in Immunology|February 10, 2025
Novel immunochromatographic test for rapid detection of anti-factor H autoantibodies with an assessment of its clinical relevanceSantiago Rodríguez de Córdoba, Andrea Reparaz, Daniel Sanchez, et al.
Frontiers in Immunology|September 7, 2021
Selective Binding of Heparin/Heparan Sulfate Oligosaccharides to Factor H and Factor H-Related Proteins: Therapeutic Potential for C3 GlomerulopathiesMarkus A Loeven, Marissa L Maciej-Hulme, Cansu Yanginlar, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Molecular characterization of a novel X-linked syndrome involving developmental delay and deafnessMichael S Hildebrand, Michelle G de Silva, Tiong Yang Tan, et al.
Journal of Medical Genetics|November 22, 2005
Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)M A Abrera-Abeleda, C Nishimura, J L H Smith, et al.
Pageof 59

Showing results (451-460 of 588) with videos related to

Sort By:
Pageof 59
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 20, 2016
Screening of Living Kidney Donors for Genetic Diseases Using a Comprehensive Genetic Testing StrategyC P Thomas, M A Mansilla, R Sompallae, et al.
Human Mutation|January 29, 2008
Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BORDana J Orten, Stephanie M Fischer, Jessica L Sorensen, et al.
Nature Communications|November 5, 2022
On-microscope staging of live cells reveals changes in the dynamics of transcriptional bursting during differentiationD M Jeziorska, E A J Tunnacliffe, J M Brown, et al.
Neurobiology of Disease|July 19, 2005
Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cellsLut Van Laer, Markus Pfister, Sofie Thys, et al.
Clinical Pharmacology and Therapeutics|May 25, 2021
Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 GenotypeJohn Henry McDermott, Joshua Wolf, Keito Hoshitsuki, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2013
CFTR-deficient pigs display peripheral nervous system defects at birthLeah R Reznikov, Qian Dong, Jeng-Haur Chen, et al.
Frontiers in Immunology|February 10, 2025
Novel immunochromatographic test for rapid detection of anti-factor H autoantibodies with an assessment of its clinical relevanceSantiago Rodríguez de Córdoba, Andrea Reparaz, Daniel Sanchez, et al.
Frontiers in Immunology|September 7, 2021
Selective Binding of Heparin/Heparan Sulfate Oligosaccharides to Factor H and Factor H-Related Proteins: Therapeutic Potential for C3 GlomerulopathiesMarkus A Loeven, Marissa L Maciej-Hulme, Cansu Yanginlar, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Molecular characterization of a novel X-linked syndrome involving developmental delay and deafnessMichael S Hildebrand, Michelle G de Silva, Tiong Yang Tan, et al.
Journal of Medical Genetics|November 22, 2005
Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)M A Abrera-Abeleda, C Nishimura, J L H Smith, et al.
Pageof 59