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J Bissler

Showing results (11-20 of 96) with videos related to

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Clinical Pediatrics|March 1, 1988
Alimentary tract duplications in children: case and literature reviewJ J Bissler, R L Klein
Therapeutic Advances in Urology|December 9, 2016
Optimal treatment of tuberous sclerosis complex associated renal angiomyolipomata: a systematic reviewJohn J Bissler, John C Kingswood
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 12, 2018
Renal manifestation of tuberous sclerosis complexJohn J Bissler, J Christopher Kingswood
Biology|September 28, 2023
Physiologically Based Pharmacokinetic Modeling of Extracellular VesiclesPrashant Kumar, Darshan Mehta, John J Bissler
Behring Institute Mitteilungen|December 1, 1993
Mutations in the C1 inhibitor gene that result in hereditary angioneurotic edemaA E Davis, J J Bissler, M Cicardi
Molecular Medicine (Cambridge, Mass.)|February 17, 1999
C1 inhibitor gene sequence facilitates frameshift mutationsJ J Bissler, Q S Meng, T Emery
Pediatric Nephrology (Berlin, Germany)|December 15, 2010
Clinical and molecular insights into tuberous sclerosis complex renal diseaseBrian J Siroky, Hong Yin, John J Bissler
Cell Cycle (Georgetown, Tex.)|August 19, 2007
Cell cycle-and proteasome-dependent formation of etoposide-induced replication protein A (RPA) or Mre11/Rad50/Nbs1 (MRN) complex repair fociJacob G Robison, Kathleen Dixon, John J Bissler
Critical Reviews in Oncogenesis|February 3, 2023
Progress in Tuberous Sclerosis Complex Renal DiseaseJohn J Bissler, Dinah Batchelor, J Christopher Kingswood
Pediatric Nephrology (Berlin, Germany)|January 22, 2010
Glomerulocystic kidney diseaseJohn J Bissler, Brian J Siroky, Hong Yin
Pageof 10

Showing results (11-20 of 96) with videos related to

Sort By:
Pageof 10
Clinical Pediatrics|March 1, 1988
Alimentary tract duplications in children: case and literature reviewJ J Bissler, R L Klein
Therapeutic Advances in Urology|December 9, 2016
Optimal treatment of tuberous sclerosis complex associated renal angiomyolipomata: a systematic reviewJohn J Bissler, John C Kingswood
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 12, 2018
Renal manifestation of tuberous sclerosis complexJohn J Bissler, J Christopher Kingswood
Biology|September 28, 2023
Physiologically Based Pharmacokinetic Modeling of Extracellular VesiclesPrashant Kumar, Darshan Mehta, John J Bissler
Behring Institute Mitteilungen|December 1, 1993
Mutations in the C1 inhibitor gene that result in hereditary angioneurotic edemaA E Davis, J J Bissler, M Cicardi
Molecular Medicine (Cambridge, Mass.)|February 17, 1999
C1 inhibitor gene sequence facilitates frameshift mutationsJ J Bissler, Q S Meng, T Emery
Pediatric Nephrology (Berlin, Germany)|December 15, 2010
Clinical and molecular insights into tuberous sclerosis complex renal diseaseBrian J Siroky, Hong Yin, John J Bissler
Cell Cycle (Georgetown, Tex.)|August 19, 2007
Cell cycle-and proteasome-dependent formation of etoposide-induced replication protein A (RPA) or Mre11/Rad50/Nbs1 (MRN) complex repair fociJacob G Robison, Kathleen Dixon, John J Bissler
Critical Reviews in Oncogenesis|February 3, 2023
Progress in Tuberous Sclerosis Complex Renal DiseaseJohn J Bissler, Dinah Batchelor, J Christopher Kingswood
Pediatric Nephrology (Berlin, Germany)|January 22, 2010
Glomerulocystic kidney diseaseJohn J Bissler, Brian J Siroky, Hong Yin
Pageof 10