Repetitious DNA in mammalian chromosomes

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Leukemia·2017

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

Leukemia·2016

MicroRNA-related sequence variations in human cancers.

Human genetics·2013

Recurrent and founder mutations in the PMS2 gene.

Clinical genetics·2012

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

Clinical genetics·2011

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Gut·2010

miR-335-3p acts as a tumor suppressor in esophageal squamous cell carcinoma and predicts favorable prognosis.

Hereditas·2026

SNP rs7430456 mediated LINC00578 drives triple negative breast cancer through regulating miR-143-5p expression.

Hereditas·2026

BFLF1 gene polymorphisms are associated with increased mortality in patients with EBV-associated diseases.

Hereditas·2026

miR-1-3p, as a novel diagnostic and prognostic biomarker, aggravates pancreatic acinar cell injury in acute pancreatitis by targeting GNPTAB.

Hereditas·2026

Identification of FOXK1 and SEMA7A as key genes associated with m6A-related programmed cell death in diabetic retinopathy.

Hereditas·2026

miR-146b-5p serves as a novel biomarker for acute myocardial infarction and is involved in regulating oxidized low-density lipoprotein-induced endothelial injury through targeting PRKAR2A.

Hereditas·2026

Natural transformation drives large-scale genome mosaicism in human gut bifidobacteria.

The ISME journal·2026

Strategic enhancement of Cas9 nickase-driven gene amplification.

Cell reports methods·2026

Evolution-guided yeast complementation reveals functional differences in human PSPH variants.

FEBS open bio·2026

Cell villages and Dirichlet modeling map human cell fitness genetics.

American journal of human genetics·2026

Haplotype and diversity signatures of ultra-soft selective sweeps in HIV-1.

bioRxiv : the preprint server for biology·2026

A NHEJ1 mutator allele influencing germline mutation rates sex-specifically in humans.

Science advances·2026

Related Experiment Videos

Repetitious DNA in mammalian chromosomes

Related Concept Videos

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

MicroRNA-related sequence variations in human cancers.

Recurrent and founder mutations in the PMS2 gene.

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

miR-335-3p acts as a tumor suppressor in esophageal squamous cell carcinoma and predicts favorable prognosis.

SNP rs7430456 mediated LINC00578 drives triple negative breast cancer through regulating miR-143-5p expression.

BFLF1 gene polymorphisms are associated with increased mortality in patients with EBV-associated diseases.

miR-1-3p, as a novel diagnostic and prognostic biomarker, aggravates pancreatic acinar cell injury in acute pancreatitis by targeting GNPTAB.

Identification of FOXK1 and SEMA7A as key genes associated with m6A-related programmed cell death in diabetic retinopathy.

miR-146b-5p serves as a novel biomarker for acute myocardial infarction and is involved in regulating oxidized low-density lipoprotein-induced endothelial injury through targeting PRKAR2A.

Natural transformation drives large-scale genome mosaicism in human gut bifidobacteria.

Strategic enhancement of Cas9 nickase-driven gene amplification.

Evolution-guided yeast complementation reveals functional differences in human PSPH variants.

Cell villages and Dirichlet modeling map human cell fitness genetics.

Haplotype and diversity signatures of ultra-soft selective sweeps in HIV-1.

A NHEJ1 mutator allele influencing germline mutation rates sex-specifically in humans.

Related Experiment Videos

Repetitious DNA in mammalian chromosomes

Related Concept Videos

Related Articles