Mutation research genomics: a blending two of disciplines

Sequence-specific identification of 18 pathogenic microorganisms using microarray technology.

Molecular and cellular probes·2002

High-resolution cartography of recently integrated human chromosome 19-specific Alu fossils.

Journal of molecular biology·1998

Identification and characterization of two polymorphic Ya5 Alu repeats.

Mutation research·1997

Alu fossil relics--distribution and insertion polymorphism.

Genome research·1996

Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes.

Genomics·1996

Assembly of a 1-Mb restriction-mapped cosmid contig spanning the candidate region for Finnish congenital nephrosis (NPHS1) in 19q13.1.

Genomics·1996

The role of KIT mutations in oral melanoma and disease progression: A literature review on early detection and targeted therapy.

Mutation research·2026

Mothers against decapentaplegic homolog 3-activated FAT atypical cadherin 2 regulates programmed death ligand-1 to mediate immune evasion in lung squamous cell carcinoma.

Mutation research·2026

Potential targets and molecular mechanisms of curcumin in treating Laryngeal and Pharyngeal Carcinoma throat cancer based on network pharmacology and bioinformatics analysis.

Mutation research·2026

Non-clonal interphase markers of chromosomal instability in malignancy acquisition and cancer progression.

Mutation research·2026

miR-145-5p induces ferroptosis by targeting Notch2 to suppress melanoma progression.

Mutation research·2026

Monoallelic germline RAD51C, RAD51D, and BRIP1 variants in hereditary cancer testing: Variant spectrum and clinical counselling implications.

Mutation research·2026

[Recent Advances in the Classification and Treatment of Pediatric Gliomas].

No shinkei geka. Neurological surgery·2026

Integrated Analysis of SNPs and Structural Variations via High-depth Whole-genome Sequencing Reveals the Genetic Architecture and Optimizes Genomic Prediction in Chickens.

Poultry science·2026

Therapeutic challenge in a 5-year-old girl with Gorlin-Goltz syndrome and cardiac fibroma.

Annals of pediatric cardiology·2026

Integrative genomic and proteomic analyses identify candidate genetic loci and genetically supported proteins in age-related macular degeneration.

Eye and vision (London, England)·2026

Integrative Multi-omics Analysis for Prioritization of Candidate Genes in Polycystic Ovary Syndrome.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2026

Sequence analyses to accelerate the development of rapid resistance assays targeting the Neisseria gonorrhoeae gyrA gene.

European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology·2026

Related Experiment Videos

Mutation research genomics: a blending two of disciplines

Related Concept Videos

Sequence-specific identification of 18 pathogenic microorganisms using microarray technology.

High-resolution cartography of recently integrated human chromosome 19-specific Alu fossils.

Identification and characterization of two polymorphic Ya5 Alu repeats.

Alu fossil relics--distribution and insertion polymorphism.

Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes.

Assembly of a 1-Mb restriction-mapped cosmid contig spanning the candidate region for Finnish congenital nephrosis (NPHS1) in 19q13.1.

The role of KIT mutations in oral melanoma and disease progression: A literature review on early detection and targeted therapy.

Mothers against decapentaplegic homolog 3-activated FAT atypical cadherin 2 regulates programmed death ligand-1 to mediate immune evasion in lung squamous cell carcinoma.

Potential targets and molecular mechanisms of curcumin in treating Laryngeal and Pharyngeal Carcinoma throat cancer based on network pharmacology and bioinformatics analysis.

Non-clonal interphase markers of chromosomal instability in malignancy acquisition and cancer progression.

miR-145-5p induces ferroptosis by targeting Notch2 to suppress melanoma progression.

Monoallelic germline RAD51C, RAD51D, and BRIP1 variants in hereditary cancer testing: Variant spectrum and clinical counselling implications.

[Recent Advances in the Classification and Treatment of Pediatric Gliomas].

Integrated Analysis of SNPs and Structural Variations via High-depth Whole-genome Sequencing Reveals the Genetic Architecture and Optimizes Genomic Prediction in Chickens.

Therapeutic challenge in a 5-year-old girl with Gorlin-Goltz syndrome and cardiac fibroma.

Integrative genomic and proteomic analyses identify candidate genetic loci and genetically supported proteins in age-related macular degeneration.

Integrative Multi-omics Analysis for Prioritization of Candidate Genes in Polycystic Ovary Syndrome.

Sequence analyses to accelerate the development of rapid resistance assays targeting the Neisseria gonorrhoeae gyrA gene.

Related Experiment Videos

Mutation research genomics: a blending two of disciplines

Related Concept Videos

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