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Showing results (311-320 of 318) with videos related to

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Nature Communications|February 25, 2016
FAT1 mutations cause a glomerulotubular nephropathyHeon Yung Gee, Carolin E Sadowski, Pardeep K Aggarwal, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 2, 2020
Identifying Outcomes Important to Patients with Glomerular Disease and Their CaregiversSimon A Carter, Talia Gutman, Charlotte Logeman, et al.
Nature Communications|May 19, 2019
Functional rare and low frequency variants in BLK and BANK1 contribute to human lupusSimon H Jiang, Vicki Athanasopoulos, Julia I Ellyard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.
Kidney International Reports|January 10, 2022
A Focus Group Study of Self-Management in Patients With Glomerular DiseaseSimon A Carter, Claris Teng, Talia Gutman, et al.
Biorxiv : the Preprint Server for Biology|April 28, 2025
Polymorphic tandem repeats influence cell type-specific gene expression across the human immune landscapeHope A Tanudisastro, Anna S E Cuomo, Ben Weisburd, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 30, 2023
Gaining Wings to FLY: Using Drosophila Oogenesis as an Entry Point for Citizen Scientists in Laboratory ResearchDara M Ruiz-Whalen, Christopher P Aichele, Ebony R Dyson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variantsAdam M Bournazos, Lisa G Riley, Shobhana Bommireddipalli, et al.
Pageof 32

Showing results (311-320 of 318) with videos related to

Sort By:
Pageof 32
You have reached the last page of results.This site can display upto 318 results.
Nature Communications|February 25, 2016
FAT1 mutations cause a glomerulotubular nephropathyHeon Yung Gee, Carolin E Sadowski, Pardeep K Aggarwal, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 2, 2020
Identifying Outcomes Important to Patients with Glomerular Disease and Their CaregiversSimon A Carter, Talia Gutman, Charlotte Logeman, et al.
Nature Communications|May 19, 2019
Functional rare and low frequency variants in BLK and BANK1 contribute to human lupusSimon H Jiang, Vicki Athanasopoulos, Julia I Ellyard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.
Kidney International Reports|January 10, 2022
A Focus Group Study of Self-Management in Patients With Glomerular DiseaseSimon A Carter, Claris Teng, Talia Gutman, et al.
Biorxiv : the Preprint Server for Biology|April 28, 2025
Polymorphic tandem repeats influence cell type-specific gene expression across the human immune landscapeHope A Tanudisastro, Anna S E Cuomo, Ben Weisburd, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 30, 2023
Gaining Wings to FLY: Using Drosophila Oogenesis as an Entry Point for Citizen Scientists in Laboratory ResearchDara M Ruiz-Whalen, Christopher P Aichele, Ebony R Dyson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variantsAdam M Bournazos, Lisa G Riley, Shobhana Bommireddipalli, et al.
Pageof 32