Related Experiment Video

Updated: Jul 12, 2025

Detection of Rare Mutations in CtDNA Using Next Generation Sequencing
11:11

Detection of Rare Mutations in CtDNA Using Next Generation Sequencing

Published on: August 24, 2017

16.9K

The eQTL analysis to discover unique eGFR-related SNPs for the Taiwanese population

Ping-Hsun Wu1,2, Johnathan Lin3,4, Mei-Chuan Kuo1,2

  • 1Division of Nephrology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.

Journal of Nephrology
|October 19, 2023
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
07:00

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene

Published on: April 1, 2019

10.1K
Visualizing Genetic Variants, Short Targets, and Point Mutations in the Morphological Tissue Context with an RNA In Situ Hybridization Assay
10:57

Visualizing Genetic Variants, Short Targets, and Point Mutations in the Morphological Tissue Context with an RNA In Situ Hybridization Assay

Published on: August 14, 2018

10.7K

Related Experiment Videos

Last Updated: Jul 12, 2025

Detection of Rare Mutations in CtDNA Using Next Generation Sequencing
11:11

Detection of Rare Mutations in CtDNA Using Next Generation Sequencing

Published on: August 24, 2017

16.9K
A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
07:00

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene

Published on: April 1, 2019

10.1K
Visualizing Genetic Variants, Short Targets, and Point Mutations in the Morphological Tissue Context with an RNA In Situ Hybridization Assay
10:57

Visualizing Genetic Variants, Short Targets, and Point Mutations in the Morphological Tissue Context with an RNA In Situ Hybridization Assay

Published on: August 14, 2018

10.7K

Related Concept Videos

Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

15.2K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.2K

Articles linked to this work by shared authors, journal, and citation graph.

Fecal Metabolomic Profiles by LDL-C Target Achievement Status in Statin-treated Patients: A Cross-sectional Study.

Journal of lipid research·2026

IEU-Net: Sequence learning of internal texture and external morphology for sonographic kidney segmentation.

Computer methods and programs in biomedicine·2026

Independent and joint effect of genetic susceptibility and long-term PM2.5 exposure on coronary artery disease risk: A large-scale cohort study.

Ecotoxicology and environmental safety·2026

Diabetic Retinopathy Severity and Heart Failure Outcomes in Type 2 Diabetes Mellitus.

Journal of diabetes·2026

Kidney measures and cerebral white matter hyperintensity severity in chronic kidney disease stratified by type 2 diabetes mellitus status.

Diabetes research and clinical practice·2026

Distinct longitudinal trajectories of alkaline phosphatase and parathyroid hormone at dialysis initiation predict mortality in incident hemodialysis patients.

BMC nephrology·2026

Graft Renal Vein Pulsatility as a Marker of Systemic Venous Congestion in Kidney Transplant Recipients: Concordance with the VExUS Score and Implications for Hemodynamic Management.

Journal of nephrology·2026

Impact of recombinant human growth hormone treatment in children with growth disorders secondary to nephrotic syndrome.

Journal of nephrology·2026

Atypical hemolytic uremic syndrome in kidney transplantation.

Journal of nephrology·2026

Glow-food illuminating nutritional value and enhancing taste in chronic kidney disease: a Mediterranean perspective.

Journal of nephrology·2026

Serum N-terminal pro-B-type natriuretic peptide and physical performance in middle-aged and older patients with chronic kidney disease.

Journal of nephrology·2026

Unexpected finding of AA amyloidosis with novel genetic variants in the MEFV gene in patients undergoing kidney biopsy for proteinuria. A case series.

Journal of nephrology·2026

Heat, home-based assault and domestic and family violence injuries: Evidence from hospital emergency department presentations.

Social science & medicine (1982)·2026

Violent death and Post-traumatic pulmonary embolism during hospital admission.

Forensic science, medicine, and pathology·2026

Psychiatric emergency events and risk factors among patients with severe mental disorders: an 8-year retrospective analysis in an urban district of Beijing.

Frontiers in psychiatry·2026

Three-Year Single-Center Retrospective Comparison of Total Extraperitoneal Versus Transabdominal Preperitoneal Approach Laparoscopic Groin Hernia Repair: Postoperative Complications and Operative Performance.

Annali italiani di chirurgia·2026

Electroconvulsive Therapy in Denmark From 2017 to 2025: A Nationwide Register-Based Study.

The journal of ECT·2026

Potassium Citrate vs Thiazides for Empiric Stone Prevention: A Propensity-Matched Analysis.

Urology·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies
Jove
Visualize
Contact Us