Can complex genetic diseases be solved? (and a PS on PXE)

Erythropoietin and arterial hypertension.

Clinical nephrology·2000

Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families.

Clinical genetics·2000

Angiotensinogen concentrations and renin clearance : implications for blood pressure regulation.

Hypertension (Dallas, Tex. : 1979)·2000

beta-2 adrenergic receptor gene variations, blood pressure, and heart size in normal twins.

Hypertension (Dallas, Tex. : 1979)·2000

Blood pressure-independent effects in rats with human renin and angiotensinogen genes.

Hypertension (Dallas, Tex. : 1979)·2000

Cardiopulmonary auscultation: duo for strings--Opus 99.

Archives of internal medicine·2000

Non-transferrin-bound iron uptake by cardiomyocytes.

Journal of molecular medicine (Berlin, Germany)·2026

Beyond the target: implications of Wnt pathway inhibitors on bone health.

Journal of molecular medicine (Berlin, Germany)·2026

Proteomic analysis reveals divergent inflammatory mechanisms of COVID-associated Guillain-Barré syndrome.

Journal of molecular medicine (Berlin, Germany)·2026

Integrative genetic and functional analysis of autosomal dominant hearing loss in 108 multigenerational families.

Journal of molecular medicine (Berlin, Germany)·2026

Preclinical evaluation of cysteine protease-inhibitor aloxistatin (E64d) for heart failure therapy.

Journal of molecular medicine (Berlin, Germany)·2026

Zinc-binding protein metallothionein 3 protects vascular smooth muscle cells from ferroptosis via blocking lysosomal degradation of GPX4.

Journal of molecular medicine (Berlin, Germany)·2026

A generalized test of genotype-phenotype causality in population-sampled nuclear families.

PLoS genetics·2026

Defining Haplosufficiency in Autosomal Recessive Limb-Girdle Muscular Dystrophy Using Molecular Markers in Disease Carriers.

Neurology. Genetics·2026

Low-Coverage Whole-Genome Sequencing Identifies Loci Associated with Birth Weight in East Friesian × Hu Crossbred Sheep.

Animals : an open access journal from MDPI·2026

Integrative MRI and Genomics Analyses Prioritize PACSIN1 as a Candidate Gene for Cerebellar Ataxia in Border Collies.

Animals : an open access journal from MDPI·2026

Bayesian Population-Based Prevalence Estimation of KCNV2-Associated Retinopathy: A Comparative Analysis of Disease-Associated Variant Frequencies in Russian and Global Populations.

International journal of molecular sciences·2026

Translatable electrophysiological and behavioral abnormalities in a humanized model of SYNGAP1-disorder.

Molecular psychiatry·2026

Related Experiment Videos

Can complex genetic diseases be solved? (and a PS on PXE)

Related Concept Videos

Erythropoietin and arterial hypertension.

Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families.

Angiotensinogen concentrations and renin clearance : implications for blood pressure regulation.

beta-2 adrenergic receptor gene variations, blood pressure, and heart size in normal twins.

Blood pressure-independent effects in rats with human renin and angiotensinogen genes.

Cardiopulmonary auscultation: duo for strings--Opus 99.

Non-transferrin-bound iron uptake by cardiomyocytes.

Beyond the target: implications of Wnt pathway inhibitors on bone health.

Proteomic analysis reveals divergent inflammatory mechanisms of COVID-associated Guillain-Barré syndrome.

Integrative genetic and functional analysis of autosomal dominant hearing loss in 108 multigenerational families.

Preclinical evaluation of cysteine protease-inhibitor aloxistatin (E64d) for heart failure therapy.

Zinc-binding protein metallothionein 3 protects vascular smooth muscle cells from ferroptosis via blocking lysosomal degradation of GPX4.

A generalized test of genotype-phenotype causality in population-sampled nuclear families.

Defining Haplosufficiency in Autosomal Recessive Limb-Girdle Muscular Dystrophy Using Molecular Markers in Disease Carriers.

Low-Coverage Whole-Genome Sequencing Identifies Loci Associated with Birth Weight in East Friesian × Hu Crossbred Sheep.

Integrative MRI and Genomics Analyses Prioritize PACSIN1 as a Candidate Gene for Cerebellar Ataxia in Border Collies.

Bayesian Population-Based Prevalence Estimation of KCNV2-Associated Retinopathy: A Comparative Analysis of Disease-Associated Variant Frequencies in Russian and Global Populations.

Translatable electrophysiological and behavioral abnormalities in a humanized model of SYNGAP1-disorder.

Related Experiment Videos

Can complex genetic diseases be solved? (and a PS on PXE)

Related Concept Videos

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