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Showing results (631-640 of 664) with videos related to

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American Journal of Nephrology|June 7, 2021
Plasma Mucin-1 (CA15-3) Levels in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 MutationsPetr Vylet'al, Kendrah Kidd, Hannah C Ainsworth, et al.
The Journal of Vascular Access|January 23, 2021
PATENCY-2 trial of vonapanitase to promote radiocephalic fistula use for hemodialysis and secondary patencyEric K Peden, John F Lucas, Barry J Browne, et al.
Drug Delivery|May 2, 2026
Local application of otoprotective compounds other than sodium thiosulfate to prevent cisplatin-induced hearing loss: a systematic reviewAmirhossein Masroor, Nienke Streefkerk, Martine Van Grotel, et al.
Human Molecular Genetics|July 29, 2016
Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6Hana Hartmannová, Lenka Piherová, Kateřina Tauchmannová, et al.
Journal of Nephrology|January 31, 2022
The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene ProjectElhussein A E Elhassan, Susan L Murray, Dervla M Connaughton, et al.
Kidney International|March 26, 2026
A Missense Mutation in the SAA1 Protein Causing Hereditary Amyloid A AmyloidosisNelson Leung, Aleš Hnízda, Ellen D McPhail, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 4, 2008
Phase III prevention trial of fenretinide in patients with resected non-muscle-invasive bladder cancerAnita L Sabichi, Seth P Lerner, E Neely Atkinson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 10, 2022
An intermediate-effect size variant in <i>UMOD</i> confers risk for chronic kidney diseaseEric Olinger, Céline Schaeffer, Kendrah Kidd, et al.
Kidney International|August 5, 2020
An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypesMartina Živná, Kendrah Kidd, Mohamad Zaidan, et al.
BMC Nephrology|December 19, 2024
Eight-fold increased COVID-19 mortality in autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations: an observational studyKendrah O Kidd, Adrienne H Williams, Abbigail Taylor, et al.
Pageof 67

Showing results (631-640 of 664) with videos related to

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Pageof 67
American Journal of Nephrology|June 7, 2021
Plasma Mucin-1 (CA15-3) Levels in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 MutationsPetr Vylet'al, Kendrah Kidd, Hannah C Ainsworth, et al.
The Journal of Vascular Access|January 23, 2021
PATENCY-2 trial of vonapanitase to promote radiocephalic fistula use for hemodialysis and secondary patencyEric K Peden, John F Lucas, Barry J Browne, et al.
Drug Delivery|May 2, 2026
Local application of otoprotective compounds other than sodium thiosulfate to prevent cisplatin-induced hearing loss: a systematic reviewAmirhossein Masroor, Nienke Streefkerk, Martine Van Grotel, et al.
Human Molecular Genetics|July 29, 2016
Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6Hana Hartmannová, Lenka Piherová, Kateřina Tauchmannová, et al.
Journal of Nephrology|January 31, 2022
The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene ProjectElhussein A E Elhassan, Susan L Murray, Dervla M Connaughton, et al.
Kidney International|March 26, 2026
A Missense Mutation in the SAA1 Protein Causing Hereditary Amyloid A AmyloidosisNelson Leung, Aleš Hnízda, Ellen D McPhail, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 4, 2008
Phase III prevention trial of fenretinide in patients with resected non-muscle-invasive bladder cancerAnita L Sabichi, Seth P Lerner, E Neely Atkinson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 10, 2022
An intermediate-effect size variant in <i>UMOD</i> confers risk for chronic kidney diseaseEric Olinger, Céline Schaeffer, Kendrah Kidd, et al.
Kidney International|August 5, 2020
An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypesMartina Živná, Kendrah Kidd, Mohamad Zaidan, et al.
BMC Nephrology|December 19, 2024
Eight-fold increased COVID-19 mortality in autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations: an observational studyKendrah O Kidd, Adrienne H Williams, Abbigail Taylor, et al.
Pageof 67