Silent mutation at codon 15 interferes with the detection of a mutated N-ras codon 12 allele by oligonucleotide hybridization

A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.

Leukemia·2016

Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline.

Molecular and cellular probes·2015

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

JAMA·2015

Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients.

Leukemia·2014

[Molecular genetic detection of minimal residual disease (MRD) in children with acute lymphoblastic leukemia].

Klinische Padiatrie·2013

Very early/early relapses of acute lymphoblastic leukemia show unexpected changes of clonal markers and high heterogeneity in response to initial and relapse treatment.

Leukemia·2011

Circulating tumor cells identify a disseminated genomic high-risk phenotype within IMS-IMWG 2025 staging in newly diagnosed multiple myeloma.

Leukemia·2026

Functional characterization of snoRNA-derived RNA (sdRNA) expression in healthy hematopoiesis and acute myeloid leukemia.

Leukemia·2026

Csnk1a1 E98 mutations rewire signaling and metabolism in del(5q) myelodysplastic neoplasms.

Leukemia·2026

Patterns of clonal hematopoiesis in aplastic anemia under immunosuppressive therapy.

Leukemia·2026

KLF4/MLL3 complex axis drives NRBP2 transcription to eliminate acute myeloid leukemia cells.

Leukemia·2026

Choice of hypomethylating agent for newly diagnosed TP53-mutant acute myeloid Leukemia: a COMMAND registry study.

Leukemia·2026

Carcinoembryonic Antigen Elevation in Bronchial Foreign Body Patients Initially Misdiagnosed as Lung Cancer.

Clinical laboratory·2026

A Case of De Novo Neuroendocrine Prostate Cancer Presenting With Elevated Carcinoembryonic Antigen (CEA) Levels.

Cureus·2026

Non-Invasive and AI-Enabled Diagnostic Approaches for Polycystic Ovary Syndrome: A PRISMA-Guided Narrative Review.

International journal of women's health·2026

An immunocompetent transplantable mouse model of basal cell carcinoma.

JID innovations : skin science from molecules to population health·2026

The Role of Mitochondrial Dysfunction in Hepatocellular Carcinoma: From Pathogenesis and Drug Resistance to Targeted Therapeutic Strategies.

Journal of hepatocellular carcinoma·2026

Imaging transcriptomics in basal cell carcinoma: Coupling in vivo tumor morphology with gene expression.

JID innovations : skin science from molecules to population health·2026

Related Experiment Videos

Silent mutation at codon 15 interferes with the detection of a mutated N-ras codon 12 allele by oligonucleotide

Related Concept Videos

A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.

Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline.

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients.

[Molecular genetic detection of minimal residual disease (MRD) in children with acute lymphoblastic leukemia].

Very early/early relapses of acute lymphoblastic leukemia show unexpected changes of clonal markers and high heterogeneity in response to initial and relapse treatment.

Circulating tumor cells identify a disseminated genomic high-risk phenotype within IMS-IMWG 2025 staging in newly diagnosed multiple myeloma.

Functional characterization of snoRNA-derived RNA (sdRNA) expression in healthy hematopoiesis and acute myeloid leukemia.

Csnk1a1 E98 mutations rewire signaling and metabolism in del(5q) myelodysplastic neoplasms.

Patterns of clonal hematopoiesis in aplastic anemia under immunosuppressive therapy.

KLF4/MLL3 complex axis drives NRBP2 transcription to eliminate acute myeloid leukemia cells.

Choice of hypomethylating agent for newly diagnosed TP53-mutant acute myeloid Leukemia: a COMMAND registry study.

Carcinoembryonic Antigen Elevation in Bronchial Foreign Body Patients Initially Misdiagnosed as Lung Cancer.

A Case of De Novo Neuroendocrine Prostate Cancer Presenting With Elevated Carcinoembryonic Antigen (CEA) Levels.

Non-Invasive and AI-Enabled Diagnostic Approaches for Polycystic Ovary Syndrome: A PRISMA-Guided Narrative Review.

An immunocompetent transplantable mouse model of basal cell carcinoma.

The Role of Mitochondrial Dysfunction in Hepatocellular Carcinoma: From Pathogenesis and Drug Resistance to Targeted Therapeutic Strategies.

Imaging transcriptomics in basal cell carcinoma: Coupling in vivo tumor morphology with gene expression.

Related Experiment Videos

Silent mutation at codon 15 interferes with the detection of a mutated N-ras codon 12 allele by oligonucleotide...

Related Concept Videos

Related Articles

Silent mutation at codon 15 interferes with the detection of a mutated N-ras codon 12 allele by oligonucleotide