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J H Smith

Showing results (421-430 of 588) with videos related to

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Journal of the American Society of Nephrology : JASN|August 3, 2013
Soluble CR1 therapy improves complement regulation in C3 glomerulopathyYuzhou Zhang, Carla M Nester, Danniele G Holanda, et al.
Human Genetics|February 19, 2022
DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing lossFengxiao Bu, Mingjun Zhong, Qinyi Chen, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locusNicole C Meyer, Fatemeh Alasti, Carla J Nishimura, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 15, 2007
Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunitRick F Nelson, Kevin A Glenn, Yuzhou Zhang, et al.
Molecular Immunology|August 5, 2016
Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion geneXue Xiao, Cybele Ghossein, Agustín Tortajada, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 9, 2009
No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch populationIsabelle Schrauwen, Melissa Thys, Kathleen Vanderstraeten, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2010
Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing childrenWilliam J Kimberling, Michael S Hildebrand, A Eliot Shearer, et al.
Hearing Research|February 19, 2017
Genetic variants in the peripheral auditory system significantly affect adult cochlear implant performanceA Eliot Shearer, Robert W Eppsteiner, Kathy Frees, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 19, 2012
The genetics of the alternative pathway of complement in the pathogenesis of HELLP syndromeFrancesca Crovetto, Nicolò Borsa, Barbara Acaia, et al.
Kidney International Reports|February 12, 2024
Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 GlomerulopathyJill J Hauer, Yuzhou Zhang, Renee Goodfellow, et al.
Pageof 59

Showing results (421-430 of 588) with videos related to

Sort By:
Pageof 59
Journal of the American Society of Nephrology : JASN|August 3, 2013
Soluble CR1 therapy improves complement regulation in C3 glomerulopathyYuzhou Zhang, Carla M Nester, Danniele G Holanda, et al.
Human Genetics|February 19, 2022
DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing lossFengxiao Bu, Mingjun Zhong, Qinyi Chen, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locusNicole C Meyer, Fatemeh Alasti, Carla J Nishimura, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 15, 2007
Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunitRick F Nelson, Kevin A Glenn, Yuzhou Zhang, et al.
Molecular Immunology|August 5, 2016
Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion geneXue Xiao, Cybele Ghossein, Agustín Tortajada, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 9, 2009
No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch populationIsabelle Schrauwen, Melissa Thys, Kathleen Vanderstraeten, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2010
Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing childrenWilliam J Kimberling, Michael S Hildebrand, A Eliot Shearer, et al.
Hearing Research|February 19, 2017
Genetic variants in the peripheral auditory system significantly affect adult cochlear implant performanceA Eliot Shearer, Robert W Eppsteiner, Kathy Frees, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 19, 2012
The genetics of the alternative pathway of complement in the pathogenesis of HELLP syndromeFrancesca Crovetto, Nicolò Borsa, Barbara Acaia, et al.
Kidney International Reports|February 12, 2024
Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 GlomerulopathyJill J Hauer, Yuzhou Zhang, Renee Goodfellow, et al.
Pageof 59