Inheritance of two types of deficiency of human serum cholinesterase

Early risk factors for metabolic dysfunction in young people with major mood disorders: Longitudinal path analysis of a prospective birth cohort using structural equation modelling.

Journal of affective disorders·2026

Systemic Anti-Inflammatory Therapy Aided by Curcumin-Laden Double-Headed Nanoparticles Combined with Injectable Long-Acting Insulin in a Rodent Model of Diabetes Eye Disease.

ACS nano·2023

First Precision Measurement of the Parity Violating Asymmetry in Cold Neutron Capture on ^{3}He.

Physical review letters·2020

Systemic anti-inflammatory therapy aided by double-headed nanoparticles in a canine model of acute intraocular inflammation.

Science advances·2020

Approaches to screening for hyperglycaemia in pregnant women during and after the COVID-19 pandemic.

Diabetic medicine : a journal of the British Diabetic Association·2020

Risk factors and patterns of household clusters of respiratory viruses in rural Nepal.

Epidemiology and infection·2019

Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses.

Annals of human genetics·2026

What Uniparental Lineages Tell Us About the Prehistoric Human Colonization of the Americas.

Annals of human genetics·2026

Genomic Structural Equation Modeling Identifies a Shared Inflammatory Genetic Dimension Across Inflammatory Arthritis Phenotypes and Biomarkers.

Annals of human genetics·2026

Genetically Proxied Leukocyte Telomere Length and Epigenetic Age Acceleration in Relation to Healthspan: A Mendelian Randomization Study.

Annals of human genetics·2026

Decoding the Genetic and Phenotypic Spectrum of MT-TI Mitochondrial Diseases.

Annals of human genetics·2026

Ancestry-Stratified Variant Classification in Monogenic Diabetes Genes: Annotation Coverage and Differential Curation Burden.

Annals of human genetics·2026

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

International journal of reproductive biomedicine·2026

Whole-Exome Sequencing Reveals the Genetic Landscape and Genotype-Phenotype Spectrum of Dystonia in a Chinese Cohort.

CNS neuroscience & therapeutics·2026

Genome-wide analysis of 439 mass spectrometry-based proteomic profiles in a population of 15,035 Scottish individuals.

Nature communications·2026

Generation of a human induced pluripotent stem cell line (PNUYHi004-A) from a patient with hereditary spastic paraplegia type 46 (SPG46) carrying compound heterozygous GBA2 variants.

Stem cell research·2026

Polygenic Risk Scores for Islet Autoantibody Positive Early-Stage Type 1 Diabetes Pre-Screening.

Diabetes, obesity & metabolism·2026

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

Clinical genetics·2026

Related Experiment Videos

Inheritance of two types of deficiency of human serum cholinesterase

Related Concept Videos

Early risk factors for metabolic dysfunction in young people with major mood disorders: Longitudinal path analysis of a prospective birth cohort using structural equation modelling.

Systemic Anti-Inflammatory Therapy Aided by Curcumin-Laden Double-Headed Nanoparticles Combined with Injectable Long-Acting Insulin in a Rodent Model of Diabetes Eye Disease.

First Precision Measurement of the Parity Violating Asymmetry in Cold Neutron Capture on ^{3}He.

Systemic anti-inflammatory therapy aided by double-headed nanoparticles in a canine model of acute intraocular inflammation.

Approaches to screening for hyperglycaemia in pregnant women during and after the COVID-19 pandemic.

Risk factors and patterns of household clusters of respiratory viruses in rural Nepal.

Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses.

What Uniparental Lineages Tell Us About the Prehistoric Human Colonization of the Americas.

Genomic Structural Equation Modeling Identifies a Shared Inflammatory Genetic Dimension Across Inflammatory Arthritis Phenotypes and Biomarkers.

Genetically Proxied Leukocyte Telomere Length and Epigenetic Age Acceleration in Relation to Healthspan: A Mendelian Randomization Study.

Decoding the Genetic and Phenotypic Spectrum of MT-TI Mitochondrial Diseases.

Ancestry-Stratified Variant Classification in Monogenic Diabetes Genes: Annotation Coverage and Differential Curation Burden.

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

Whole-Exome Sequencing Reveals the Genetic Landscape and Genotype-Phenotype Spectrum of Dystonia in a Chinese Cohort.

Genome-wide analysis of 439 mass spectrometry-based proteomic profiles in a population of 15,035 Scottish individuals.

Generation of a human induced pluripotent stem cell line (PNUYHi004-A) from a patient with hereditary spastic paraplegia type 46 (SPG46) carrying compound heterozygous GBA2 variants.

Polygenic Risk Scores for Islet Autoantibody Positive Early-Stage Type 1 Diabetes Pre-Screening.

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

Related Experiment Videos

Inheritance of two types of deficiency of human serum cholinesterase

Related Concept Videos

Related Articles