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A Baum

Showing results (451-460 of 464) with videos related to

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Kidney International|January 22, 2020
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosisTilman Jobst-Schwan, Verena Klämbt, Maureen Tarsio, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 26, 2022
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasisAmar J Majmundar, Eugen Widmeier, John F Heneghan, et al.
American Journal of Medical Genetics. Part A|January 18, 2022
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse modelsChunyan Wang, Steve Seltzsam, Bixia Zheng, et al.
Applied and Environmental Microbiology|June 9, 2019
Bacillus thuringiensis Cry1Da_7 and Cry1B.868 Protein Interactions with Novel Receptors Allow Control of Resistant Fall Armyworms, Spodoptera frugiperda (J.E. Smith)Yanfei Wang, Jinling Wang, Xiaoran Fu, et al.
Nature|June 10, 2016
Cold, clumpy accretion onto an active supermassive black holeGrant R Tremblay, J B Raymond Oonk, Françoise Combes, et al.
Hypertension (Dallas, Tex. : 1979)|February 28, 2018
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic SyndromeJillian K Warejko, Markus Schueler, Asaf Vivante, et al.
Journal of Vascular Surgery|May 22, 2002
Nature and significance of endoleaks and endotension: summary of opinions expressed at an international conferenceFrank J Veith, Richard A Baum, Takao Ohki, et al.
Journal of the American Society of Nephrology : JASN|January 19, 2019
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant RecipientsNina Mann, Daniela A Braun, Kassaundra Amann, et al.
Kidney International|September 13, 2017
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosisAnkana Daga, Amar J Majmundar, Daniela A Braun, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUTSteve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Pageof 47

Showing results (451-460 of 464) with videos related to

Sort By:
Pageof 47
Kidney International|January 22, 2020
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosisTilman Jobst-Schwan, Verena Klämbt, Maureen Tarsio, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 26, 2022
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasisAmar J Majmundar, Eugen Widmeier, John F Heneghan, et al.
American Journal of Medical Genetics. Part A|January 18, 2022
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse modelsChunyan Wang, Steve Seltzsam, Bixia Zheng, et al.
Applied and Environmental Microbiology|June 9, 2019
Bacillus thuringiensis Cry1Da_7 and Cry1B.868 Protein Interactions with Novel Receptors Allow Control of Resistant Fall Armyworms, Spodoptera frugiperda (J.E. Smith)Yanfei Wang, Jinling Wang, Xiaoran Fu, et al.
Nature|June 10, 2016
Cold, clumpy accretion onto an active supermassive black holeGrant R Tremblay, J B Raymond Oonk, Françoise Combes, et al.
Hypertension (Dallas, Tex. : 1979)|February 28, 2018
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic SyndromeJillian K Warejko, Markus Schueler, Asaf Vivante, et al.
Journal of Vascular Surgery|May 22, 2002
Nature and significance of endoleaks and endotension: summary of opinions expressed at an international conferenceFrank J Veith, Richard A Baum, Takao Ohki, et al.
Journal of the American Society of Nephrology : JASN|January 19, 2019
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant RecipientsNina Mann, Daniela A Braun, Kassaundra Amann, et al.
Kidney International|September 13, 2017
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosisAnkana Daga, Amar J Majmundar, Daniela A Braun, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUTSteve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Pageof 47