Related Experiment Video

Updated: Jul 7, 2025

Identifying DNA Mutations in Purified Hematopoietic Stem/Progenitor Cells
11:06

Identifying DNA Mutations in Purified Hematopoietic Stem/Progenitor Cells

Published on: February 24, 2014

13.1K

Cell perturbation and lasers illuminate the genetics of latent blood cell traits

Andrew D Johnson1,2

  • 1Population Sciences Branch, Division of Intramural Research, National Heart, Lung and Blood Institute, Framingham, MA, USA. Johnsonad2@nhlbi.nih.gov.

Nature Genetics
|December 22, 2023
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Characterizing Mutational Load and Clonal Composition of Human Blood
07:58

Characterizing Mutational Load and Clonal Composition of Human Blood

Published on: July 11, 2019

7.4K
Laser Microdissection for Species-Agnostic Single-Tissue Applications
08:57

Laser Microdissection for Species-Agnostic Single-Tissue Applications

Published on: March 31, 2022

2.2K

Related Experiment Videos

Last Updated: Jul 7, 2025

Identifying DNA Mutations in Purified Hematopoietic Stem/Progenitor Cells
11:06

Identifying DNA Mutations in Purified Hematopoietic Stem/Progenitor Cells

Published on: February 24, 2014

13.1K
Characterizing Mutational Load and Clonal Composition of Human Blood
07:58

Characterizing Mutational Load and Clonal Composition of Human Blood

Published on: July 11, 2019

7.4K
Laser Microdissection for Species-Agnostic Single-Tissue Applications
08:57

Laser Microdissection for Species-Agnostic Single-Tissue Applications

Published on: March 31, 2022

2.2K

Related Concept Videos

In-vitro Mutagenesis01:16

In-vitro Mutagenesis

13.9K
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
13.9K

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

Research agenda and related workforce requirements inspired by Lived Experience Experts and grounded in health equity for the Bleeding Disorders Research Collaborative.

Expert review of hematology·2026

DNA Methylation Variation in Blood Cells may Impact Platelet Function.

TH open : companion journal to thrombosis and haemostasis·2026

Co-occurring clonal hematopoiesis exhibits strong selection and high leukemia risk.

Nature communications·2026

Molecular determinants of thrombosis recurrence risk across venous thromboembolism subtypes.

Blood·2025

Multipopulation GWAS for venous thromboembolism identifies novel loci followed by experimental validation in zebrafish.

Blood advances·2025

Genome-wide meta-analysis of heavy menstrual bleeding reveals 36 risk loci.

Blood·2025

Genome-wide detection of genotype-environment interactions at biobank scale with fastGxE.

Nature genetics·2026

Leveraging genomic deep learning models for the prediction of noncoding variant effects.

Nature genetics·2026

Genome-wide analyses identify 60 loci associated with liver triglyceride content.

Nature genetics·2026

The landscape of gene loss and missense variation across the mammalian tree informs on gene essentiality.

Nature genetics·2026

A systems perspective on monoallelic inborn errors of immunity.

Nature genetics·2026

Multiancestry conditional and joint analysis applied to GWAS summary statistics.

Nature genetics·2026

Characterisation of the Novel HLA-DRB1*12:02:14 and HLA-DRB1*12:02:15 Alleles by Next-Generation Sequencing.

HLA·2026

Small variant calling in the era of long-read sequencing.

Nature reviews. Genetics·2026

Sequence diversity and forensic efficiency of Y-STRs in the Han population of Yunnan Province, Southwest China.

International journal of legal medicine·2026

A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review.

American journal of medical genetics. Part A·2026

Repeat-length variation generates stable TTGGG-family G-quadruplex motifs in plant mitochondrial genomes.

Planta·2026

A KIAA0586 c.1815G>A Founder Allele Associated with Short-Rib Polydactyly Syndrome Type IV in Romani Families.

medRxiv : the preprint server for health sciences·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