Search research articles
Contact Us
Filters
Showing results (451-460 of 464) with videos related to
Page
of 47
Sort By:
Kidney International
|
January 22, 2020
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis
Tilman 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 nephrolithiasis
Amar 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 models
Chunyan 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 hole
Grant 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 Syndrome
Jillian 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 conference
Frank 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 Recipients
Nina 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 nephrocalcinosis
Ankana 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 CAKUT
Steve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Page
of 47
Search research articles
Search
Showing results (451-460 of 464) with videos related to
Sort By:
Page
of 47
Kidney International
|
January 22, 2020
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis
Tilman 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 nephrolithiasis
Amar 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 models
Chunyan 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 hole
Grant 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 Syndrome
Jillian 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 conference
Frank 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 Recipients
Nina 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 nephrocalcinosis
Ankana 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 CAKUT
Steve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Page
of 47