Combinative oligonucleotide-directed large deletions as a strategy for surveying the regulatory region of a gene

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Clinical genetics·2016

Unresolved questions regarding human hereditary deafness.

Oral diseases·2016

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.

Clinical genetics·2009

Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.

Clinical genetics·2009

USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.

Clinical genetics·2008

A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.

Clinical genetics·2008

Performance of microarray genotyping and massively parallel sequencing for dense SNP profiling of challenged skeletal remains.

BioTechniques·2026

Removal of antibiotic resistance genes in wastewater treatment plants and their distribution in selected Asian communities.

BioTechniques·2026

Recent advances in deep learning for biological microscopy image analysis beyond segmentation.

BioTechniques·2026

A refined qPCR duplexing method for the molecular sex determination of sturgeon (Acipenser genus), providing a validating, endogenous control.

BioTechniques·2026

A QC-guided framework for performance assessment in plate-based RNAi screening with fluorescence and metabolic readouts.

BioTechniques·2026

Detection of antisense oligonucleotides from biological samples by ligase detection reaction using T4 RNA ligase 2.

BioTechniques·2026

Trait-Informed Machine Learning Improves Precise Genomic Selection and Hybrid Design in Wheat.

Plant communications·2026

Spatial multi-omics analyses of the tumor immune microenvironment: advances and novel therapeutic avenues.

Molecular cancer·2026

Link between C-reactive protein-triglyceride glucose index and cardiovascular disease risk in diverse glycemic statuses: a nationwide prospective cohort study.

BMC cardiovascular disorders·2026

Single-oocyte proteome-transcriptome co-profiling reveals a role of dysregulated lactate metabolism in oocyte aging.

Nature communications·2026

BEAR-GRN: Systematic assessment of single-cell multi-omics-based gene regulatory network inference methods.

Nature communications·2026

PEAK: a phenotype-based classification of genetic variants.

Trends in genetics : TIG·2026

Related Experiment Videos

Combinative oligonucleotide-directed large deletions as a strategy for surveying the regulatory region of a gene

Related Concept Videos

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Unresolved questions regarding human hereditary deafness.

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.

Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.

USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.

A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.

Performance of microarray genotyping and massively parallel sequencing for dense SNP profiling of challenged skeletal remains.

Removal of antibiotic resistance genes in wastewater treatment plants and their distribution in selected Asian communities.

Recent advances in deep learning for biological microscopy image analysis beyond segmentation.

A refined qPCR duplexing method for the molecular sex determination of sturgeon (Acipenser genus), providing a validating, endogenous control.

A QC-guided framework for performance assessment in plate-based RNAi screening with fluorescence and metabolic readouts.

Detection of antisense oligonucleotides from biological samples by ligase detection reaction using T4 RNA ligase 2.

Trait-Informed Machine Learning Improves Precise Genomic Selection and Hybrid Design in Wheat.

Spatial multi-omics analyses of the tumor immune microenvironment: advances and novel therapeutic avenues.

Link between C-reactive protein-triglyceride glucose index and cardiovascular disease risk in diverse glycemic statuses: a nationwide prospective cohort study.

Single-oocyte proteome-transcriptome co-profiling reveals a role of dysregulated lactate metabolism in oocyte aging.

BEAR-GRN: Systematic assessment of single-cell multi-omics-based gene regulatory network inference methods.

PEAK: a phenotype-based classification of genetic variants.

Related Experiment Videos

Combinative oligonucleotide-directed large deletions as a strategy for surveying the regulatory region of a gene

Related Concept Videos

Related Articles