General report on the First International Workshop on Chromosomes in Leukemia

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

Cross-Regulation Between DNA Methylation and Circadian Clock Reprogramming in Ovarian Cancer: Mechanistic Insights, Biomarker Potential, and Therapeutic Implications.

International journal of cancer·2026

Spatially Resolved Metabolomics of Optimal Cutting Temperature (OCT) Compound-Embedded Tumors.

International journal of cancer·2026

Genomic and Transcriptomic Analysis of Sinonasal Mucosal Melanoma and Conjunctival Melanoma.

International journal of cancer·2026

Global Real-World Outcomes of Olaparib in Metastatic Castration-Resistant Prostate Cancer Patients With Homologous Recombination Repair Alterations.

International journal of cancer·2026

Anthracycline-Free Neoadjuvant Therapy With Nab-Paclitaxel and Carboplatin in Non-Luminal Breast Cancer: A Single-Arm Clinical Trial.

International journal of cancer·2026

Outcomes of Cisplatin, Gemcitabine, and Durvalumab According to TOPAZ-1 Study Eligibility: A Large Global Analysis in a Real-World Setting.

International journal of cancer·2026

A homozygous lamin B receptor variant resulting in Pelger-Huët anomaly without skeletal dysplasia.

Nucleus (Austin, Tex.)·2026

ZATELLITE: a toolkit to visualize and manipulate human centromeres in live cells using synthetic zinc fingers.

bioRxiv : the preprint server for biology·2026

Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease.

medRxiv : the preprint server for health sciences·2026

Structural determination of human nucleosomes reconstituted by the ExACT platform.

bioRxiv : the preprint server for biology·2026

The linker histone H1.4 condenses chromatin in maturing postmitotic neurons.

bioRxiv : the preprint server for biology·2026

dif-XerCD is Required for Chromosome Segregation During cSDR-Dependent Growth in Escherichia coli.

Molecular and cellular biology·2026

Related Experiment Videos

General report on the First International Workshop on Chromosomes in Leukemia

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.

Cross-Regulation Between DNA Methylation and Circadian Clock Reprogramming in Ovarian Cancer: Mechanistic Insights, Biomarker Potential, and Therapeutic Implications.

Spatially Resolved Metabolomics of Optimal Cutting Temperature (OCT) Compound-Embedded Tumors.

Genomic and Transcriptomic Analysis of Sinonasal Mucosal Melanoma and Conjunctival Melanoma.

Global Real-World Outcomes of Olaparib in Metastatic Castration-Resistant Prostate Cancer Patients With Homologous Recombination Repair Alterations.

Anthracycline-Free Neoadjuvant Therapy With Nab-Paclitaxel and Carboplatin in Non-Luminal Breast Cancer: A Single-Arm Clinical Trial.

Outcomes of Cisplatin, Gemcitabine, and Durvalumab According to TOPAZ-1 Study Eligibility: A Large Global Analysis in a Real-World Setting.

A homozygous lamin B receptor variant resulting in Pelger-Huët anomaly without skeletal dysplasia.

ZATELLITE: a toolkit to visualize and manipulate human centromeres in live cells using synthetic zinc fingers.

Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease.

Structural determination of human nucleosomes reconstituted by the ExACT platform.

The linker histone H1.4 condenses chromatin in maturing postmitotic neurons.

dif-XerCD is Required for Chromosome Segregation During cSDR-Dependent Growth in Escherichia coli.

Related Experiment Videos

General report on the First International Workshop on Chromosomes in Leukemia

Related Concept Videos

Related Articles