Assignment of human asialoglycoprotein receptor gene (ASGR1) to chromosome 17p11-13

Dual-Baseline Search for Active-to-Sterile Neutrino Oscillations in NOvA.

Physical review letters·2025

Search for CP-Violating Neutrino Nonstandard Interactions with the NOvA Experiment.

Physical review letters·2024

Measurement of the ν_{e}-Nucleus Charged-Current Double-Differential Cross Section at ⟨E_{ν}⟩=2.4 GeV Using NOvA.

Physical review letters·2023

Spontaneous Escherichia coli Meningitis and Pyogenic Ventriculitis in an Adult Receiving Anti-Tumour Necrosis Factor Alpha Therapy.

Irish medical journal·2022

Transport and Barrier Functions in Rainbow Trout Trunk Skin Are Regulated by Environmental Salinity.

Frontiers in physiology·2022

Cognitive performance of military men and women during prolonged load carriage.

BMJ military health·2022

A novel tRNA-derived fragment, tRF-16-WSNKP9D promotes malignant progression of colorectal carcinoma through mediating PFN1.

Genomics·2026

Integrative profiling of multi-modal plasma cfRNA signatures enables detection and prognostic risk stratification in breast cancer.

Genomics·2026

Metabolomics and network pharmacology identify three key bioactive organic acid metabolites in Amomum tsao-ko.

Genomics·2026

New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae.

Genomics·2026

Comprehensive evaluation of new sequencer T20 and well-established T7 with 507 human samples.

Genomics·2026

A chromosome-level genome assembly and developmental transcriptome profiling reveal stage-specific remodeling of the molecular chaperone system in Helicoverpa armigera.

Genomics·2026

Founder mutations in movement disorders: global distribution, molecular mechanisms, and clinical consequences-a scoping review.

Neurogenetics·2026

Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.

Vavilovskii zhurnal genetiki i selektsii·2026

Case Report: A novel 1, 171 bp GCK promoter/exon 1 deletion in a Chinese pedigree: correcting a misdiagnosis of MODY10 based on an incidental INS variant.

Frontiers in endocrinology·2026

A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.

Vavilovskii zhurnal genetiki i selektsii·2026

Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissue.

Genome research·2026

Genetic Susceptibility in Relative Maternal Protection From Type 1 Diabetes.

Diabetes care·2026

Related Experiment Videos

Assignment of human asialoglycoprotein receptor gene (ASGR1) to chromosome 17p11-13

Related Concept Videos

Dual-Baseline Search for Active-to-Sterile Neutrino Oscillations in NOvA.

Search for CP-Violating Neutrino Nonstandard Interactions with the NOvA Experiment.

Measurement of the ν_{e}-Nucleus Charged-Current Double-Differential Cross Section at ⟨E_{ν}⟩=2.4 GeV Using NOvA.

Spontaneous Escherichia coli Meningitis and Pyogenic Ventriculitis in an Adult Receiving Anti-Tumour Necrosis Factor Alpha Therapy.

Transport and Barrier Functions in Rainbow Trout Trunk Skin Are Regulated by Environmental Salinity.

Cognitive performance of military men and women during prolonged load carriage.

A novel tRNA-derived fragment, tRF-16-WSNKP9D promotes malignant progression of colorectal carcinoma through mediating PFN1.

Integrative profiling of multi-modal plasma cfRNA signatures enables detection and prognostic risk stratification in breast cancer.

Metabolomics and network pharmacology identify three key bioactive organic acid metabolites in Amomum tsao-ko.

New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae.

Comprehensive evaluation of new sequencer T20 and well-established T7 with 507 human samples.

A chromosome-level genome assembly and developmental transcriptome profiling reveal stage-specific remodeling of the molecular chaperone system in Helicoverpa armigera.

Founder mutations in movement disorders: global distribution, molecular mechanisms, and clinical consequences-a scoping review.

Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.

Case Report: A novel 1, 171 bp GCK promoter/exon 1 deletion in a Chinese pedigree: correcting a misdiagnosis of MODY10 based on an incidental INS variant.

A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.

Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissue.

Genetic Susceptibility in Relative Maternal Protection From Type 1 Diabetes.

Related Experiment Videos

Assignment of human asialoglycoprotein receptor gene (ASGR1) to chromosome 17p11-13

Related Concept Videos

Related Articles