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Showing results (1221-1230 of 1,228) with videos related to

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Pediatric Pulmonology|January 17, 2025
Angiotensin-Converting Enzyme 2 (G8790A) Gene Polymorphism as a Risk Factor for COVID-19 in Egyptian Children and AdolescentsAhmed A A Ibraheem, Sarah A Saleh, Ahmed A Emam, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 12, 2017
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic SyndromeJillian K Warejko, Weizhen Tan, Ankana Daga, et al.
Nature Communications|May 19, 2018
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatmentShazia Ashraf, Hiroki Kudo, Jia Rao, et al.
Journal of the American Society of Nephrology : JASN|August 26, 2018
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary TractAmelie T van der Ven, Dervla M Connaughton, Hadas Ityel, et al.
Pediatric Research|January 4, 2024
Association of ACE1 I/D polymorphism and susceptibility to COVID-19 in Egyptian children and adolescentsNaglaa F Boraey, Marwa A Bebars, Ali A Wahba, et al.
Physical Review Letters|December 15, 2018
Constraints on Primordial Gravitational Waves Using Planck, WMAP, and New BICEP2/Keck Observations through the 2015 SeasonP A R Ade, Z Ahmed, R W Aikin, et al.
Physical Review Letters|October 22, 2021
Improved Constraints on Primordial Gravitational Waves using Planck, WMAP, and BICEP/Keck Observations through the 2018 Observing SeasonP A R Ade, Z Ahmed, M Amiri, et al.
Nature Genetics|August 15, 2017
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephalyDaniela A Braun, Jia Rao, Geraldine Mollet, et al.
Pageof 123

Showing results (1221-1230 of 1,228) with videos related to

Sort By:
Pageof 123
You have reached the last page of results.This site can display upto 1,228 results.
Pediatric Pulmonology|January 17, 2025
Angiotensin-Converting Enzyme 2 (G8790A) Gene Polymorphism as a Risk Factor for COVID-19 in Egyptian Children and AdolescentsAhmed A A Ibraheem, Sarah A Saleh, Ahmed A Emam, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 12, 2017
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic SyndromeJillian K Warejko, Weizhen Tan, Ankana Daga, et al.
Nature Communications|May 19, 2018
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatmentShazia Ashraf, Hiroki Kudo, Jia Rao, et al.
Journal of the American Society of Nephrology : JASN|August 26, 2018
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary TractAmelie T van der Ven, Dervla M Connaughton, Hadas Ityel, et al.
Pediatric Research|January 4, 2024
Association of ACE1 I/D polymorphism and susceptibility to COVID-19 in Egyptian children and adolescentsNaglaa F Boraey, Marwa A Bebars, Ali A Wahba, et al.
Physical Review Letters|December 15, 2018
Constraints on Primordial Gravitational Waves Using Planck, WMAP, and New BICEP2/Keck Observations through the 2015 SeasonP A R Ade, Z Ahmed, R W Aikin, et al.
Physical Review Letters|October 22, 2021
Improved Constraints on Primordial Gravitational Waves using Planck, WMAP, and BICEP/Keck Observations through the 2018 Observing SeasonP A R Ade, Z Ahmed, M Amiri, et al.
Nature Genetics|August 15, 2017
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephalyDaniela A Braun, Jia Rao, Geraldine Mollet, et al.
Pageof 123