A haplotype map of the human genome

Identification of putative kidney-derived proteins in plasma using nanoparticle enrichment.

Molecular omics·2026

Identification of metabolomic signatures of diabetic kidney disease in urine and plasma using untargeted gas chromatography-mass spectrometry.

Molecular omics·2026

A mass spectrometry-based approach identifies a putative plasma protein biomarker signature for early diabetic kidney disease diagnosis.

Molecular omics·2026

A human airway-on-a-chip microphysiological system for modeling chlorine gas toxicity.

Toxicological sciences : an official journal of the Society of Toxicology·2025

Liver molecular networks associated with drinking behavior in nonhuman primates.

Alcohol, clinical & experimental research·2025

Association of the HDL lipidome with HDL traits before and after exercise training: HERITAGE family study.

Metabolomics : Official journal of the Metabolomic Society·2025

Epigenomic patterns in fish with divergent cortisol reactivity.

Physiological genomics·2026

Transcriptome analysis reveals IGF-dependent and IGF-independent mechanisms affected by loss of IGF binding protein-2b in rainbow trout.

Physiological genomics·2026

Adaptation to chronic hypercapnia drives time- and region-dependent changes in brainstem cardiorespiratory nuclei.

Physiological genomics·2026

Multiomic characterization of DNA released after airway exposure to allergens and nanoparticles reveals selective export of repetitive and fragile site DNA.

Physiological genomics·2026

Transcriptomic Profiling Reveals Immunometabolic Gene Regulation during a 24-Hour Cold Exposure Survival Simulation in Humans.

Physiological genomics·2026

Maternal estradiol impacts fetal HPA axis and pulmonary transcriptomes in sheep.

Physiological genomics·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

The first 25 years of the NICHD Structural Birth Defects Initiative.

Developmental biology·2026

Related Experiment Videos

A haplotype map of the human genome

Related Concept Videos

Identification of putative kidney-derived proteins in plasma using nanoparticle enrichment.

Identification of metabolomic signatures of diabetic kidney disease in urine and plasma using untargeted gas chromatography-mass spectrometry.

A mass spectrometry-based approach identifies a putative plasma protein biomarker signature for early diabetic kidney disease diagnosis.

A human airway-on-a-chip microphysiological system for modeling chlorine gas toxicity.

Liver molecular networks associated with drinking behavior in nonhuman primates.

Association of the HDL lipidome with HDL traits before and after exercise training: HERITAGE family study.

Epigenomic patterns in fish with divergent cortisol reactivity.

Transcriptome analysis reveals IGF-dependent and IGF-independent mechanisms affected by loss of IGF binding protein-2b in rainbow trout.

Adaptation to chronic hypercapnia drives time- and region-dependent changes in brainstem cardiorespiratory nuclei.

Multiomic characterization of DNA released after airway exposure to allergens and nanoparticles reveals selective export of repetitive and fragile site DNA.

Transcriptomic Profiling Reveals Immunometabolic Gene Regulation during a 24-Hour Cold Exposure Survival Simulation in Humans.

Maternal estradiol impacts fetal HPA axis and pulmonary transcriptomes in sheep.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

The first 25 years of the NICHD Structural Birth Defects Initiative.

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A haplotype map of the human genome

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