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Edgar A Otto

Showing results (1-10 of 118) with videos related to

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Nature Reviews. Nephrology|April 28, 2018
Is ciliary Hedgehog signalling dispensable in the kidneys?Edgar A Otto
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 9, 2006
Retinitis pigmentosa and renal failure in a patient with mutations in INVSJohn F O'Toole, Edgar A Otto, Yaacov Frishberg, et al.
Pediatric Nephrology (Berlin, Germany)|October 25, 2006
Mutational analysis in 119 families with nephronophthisisJohn F O'Toole, Edgar A Otto, Julia Hoefele, et al.
Pediatric Nephrology (Berlin, Germany)|July 8, 2010
Polycystic kidney and hepatic disease with mental retardation is nephronophthisis 11 caused by MKS3/TMEM67 mutationsTomás Seeman, Eva Seemanová, Gudrun Nuernberg, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
Renal-hepatic-pancreatic dysplasia: a sibship with skeletal and central nervous system anomalies and NPHP3 mutationLawrence Copelovitch, Maureen M O'Brien, Marta Guttenberg, et al.
Pediatric Nephrology (Berlin, Germany)|September 24, 2014
A boy with proteinuria and focal global glomerulosclerosis: Question and AnswersSidharth Kumar Sethi, Edgar A Otto, Sara Ma, et al.
Pediatric Nephrology (Berlin, Germany)|January 25, 2011
Pseudodominant inheritance of nephronophthisis caused by a homozygous NPHP1 deletionJulia Hoefele, Ahmet Nayir, Moumita Chaki, et al.
Journal of the American Society of Nephrology : JASN|January 18, 2008
NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisisEdgar A Otto, Melissa L Trapp, Ulla T Schultheiss, et al.
Journal of the American Society of Nephrology : JASN|January 22, 2005
Expression and phenotype analysis of the nephrocystin-1 and nephrocystin-4 homologs in Caenorhabditis elegansMatthias T F Wolf, Jeeyong Lee, Franziska Panther, et al.
Pediatric Nephrology (Berlin, Germany)|May 11, 2010
Homozygous NPHP1 deletions in Egyptian children with nephronophthisis including an infantile onset patientNeveen A Soliman, Friedhelm Hildebrandt, Susan J Allen, et al.
Pageof 12

Showing results (1-10 of 118) with videos related to

Sort By:
Pageof 12
Nature Reviews. Nephrology|April 28, 2018
Is ciliary Hedgehog signalling dispensable in the kidneys?Edgar A Otto
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 9, 2006
Retinitis pigmentosa and renal failure in a patient with mutations in INVSJohn F O'Toole, Edgar A Otto, Yaacov Frishberg, et al.
Pediatric Nephrology (Berlin, Germany)|October 25, 2006
Mutational analysis in 119 families with nephronophthisisJohn F O'Toole, Edgar A Otto, Julia Hoefele, et al.
Pediatric Nephrology (Berlin, Germany)|July 8, 2010
Polycystic kidney and hepatic disease with mental retardation is nephronophthisis 11 caused by MKS3/TMEM67 mutationsTomás Seeman, Eva Seemanová, Gudrun Nuernberg, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
Renal-hepatic-pancreatic dysplasia: a sibship with skeletal and central nervous system anomalies and NPHP3 mutationLawrence Copelovitch, Maureen M O'Brien, Marta Guttenberg, et al.
Pediatric Nephrology (Berlin, Germany)|September 24, 2014
A boy with proteinuria and focal global glomerulosclerosis: Question and AnswersSidharth Kumar Sethi, Edgar A Otto, Sara Ma, et al.
Pediatric Nephrology (Berlin, Germany)|January 25, 2011
Pseudodominant inheritance of nephronophthisis caused by a homozygous NPHP1 deletionJulia Hoefele, Ahmet Nayir, Moumita Chaki, et al.
Journal of the American Society of Nephrology : JASN|January 18, 2008
NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisisEdgar A Otto, Melissa L Trapp, Ulla T Schultheiss, et al.
Journal of the American Society of Nephrology : JASN|January 22, 2005
Expression and phenotype analysis of the nephrocystin-1 and nephrocystin-4 homologs in Caenorhabditis elegansMatthias T F Wolf, Jeeyong Lee, Franziska Panther, et al.
Pediatric Nephrology (Berlin, Germany)|May 11, 2010
Homozygous NPHP1 deletions in Egyptian children with nephronophthisis including an infantile onset patientNeveen A Soliman, Friedhelm Hildebrandt, Susan J Allen, et al.
Pageof 12