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J Bissler

Showing results (51-60 of 96) with videos related to

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Plos One|February 10, 2011
Cell cycle control and DNA damage response of conditionally immortalized urothelial cellsBradley P Dixon, Jeff Henry, Brian J Siroky, et al.
Neuro-Ophthalmology (Aeolus Press)|April 7, 2025
Neuro-Ophthalmic Characteristics of Patients with Tuberous Sclerosis Complex at a Tertiary Care Referral CentreBarbara D Smith, Lyba A Naseer, Aaron E Rice, et al.
Biology|May 28, 2022
Single Gene Mutations in <i>Pkd1</i> or <i>Tsc2</i> Alter Extracellular Vesicle Production and TraffickingPrashant Kumar, Fahad Zadjali, Ying Yao, et al.
International Journal of Molecular Sciences|March 7, 2020
Tuberous Sclerosis Complex Axis Controls Renal Extracellular Vesicle Production and Protein ContentFahad Zadjali, Prashant Kumar, Ying Yao, et al.
Plos One|October 13, 2017
Pooled analysis of menstrual irregularities from three major clinical studies evaluating everolimus for the treatment of tuberous sclerosis complexSteven Sparagana, David N Franz, Darcy A Krueger, et al.
Journal of the American Society of Nephrology : JASN|February 11, 2014
Characterization of renal toxicity in mice administered the marine biotoxin domoic AcidJason A Funk, Michael G Janech, Joshua C Dillon, et al.
Genes & Diseases|January 10, 2022
<i>Tsc2</i> mutation induces renal tubular cell nonautonomous diseasePrashant Kumar, Fahad Zadjali, Ying Yao, et al.
American Journal of Physiology. Cell Physiology|October 27, 2006
Spermidine/spermine N1-acetyltransferase overexpression in kidney epithelial cells disrupts polyamine homeostasis, leads to DNA damage, and causes G2 arrestKamyar Zahedi, John J Bissler, Zhaohui Wang, et al.
Proceedings of the Association of American Physicians|March 1, 1997
Molecular defects in hereditary angioneurotic edemaJ J Bissler, K S Aulak, V H Donaldson, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 27, 1994
A cluster of mutations within a short triplet repeat in the C1 inhibitor geneJ J Bissler, M Cicardi, V H Donaldson, et al.
Pageof 10

Showing results (51-60 of 96) with videos related to

Sort By:
Pageof 10
Plos One|February 10, 2011
Cell cycle control and DNA damage response of conditionally immortalized urothelial cellsBradley P Dixon, Jeff Henry, Brian J Siroky, et al.
Neuro-Ophthalmology (Aeolus Press)|April 7, 2025
Neuro-Ophthalmic Characteristics of Patients with Tuberous Sclerosis Complex at a Tertiary Care Referral CentreBarbara D Smith, Lyba A Naseer, Aaron E Rice, et al.
Biology|May 28, 2022
Single Gene Mutations in <i>Pkd1</i> or <i>Tsc2</i> Alter Extracellular Vesicle Production and TraffickingPrashant Kumar, Fahad Zadjali, Ying Yao, et al.
International Journal of Molecular Sciences|March 7, 2020
Tuberous Sclerosis Complex Axis Controls Renal Extracellular Vesicle Production and Protein ContentFahad Zadjali, Prashant Kumar, Ying Yao, et al.
Plos One|October 13, 2017
Pooled analysis of menstrual irregularities from three major clinical studies evaluating everolimus for the treatment of tuberous sclerosis complexSteven Sparagana, David N Franz, Darcy A Krueger, et al.
Journal of the American Society of Nephrology : JASN|February 11, 2014
Characterization of renal toxicity in mice administered the marine biotoxin domoic AcidJason A Funk, Michael G Janech, Joshua C Dillon, et al.
Genes & Diseases|January 10, 2022
<i>Tsc2</i> mutation induces renal tubular cell nonautonomous diseasePrashant Kumar, Fahad Zadjali, Ying Yao, et al.
American Journal of Physiology. Cell Physiology|October 27, 2006
Spermidine/spermine N1-acetyltransferase overexpression in kidney epithelial cells disrupts polyamine homeostasis, leads to DNA damage, and causes G2 arrestKamyar Zahedi, John J Bissler, Zhaohui Wang, et al.
Proceedings of the Association of American Physicians|March 1, 1997
Molecular defects in hereditary angioneurotic edemaJ J Bissler, K S Aulak, V H Donaldson, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 27, 1994
A cluster of mutations within a short triplet repeat in the C1 inhibitor geneJ J Bissler, M Cicardi, V H Donaldson, et al.
Pageof 10