[The genetic mechanisms of lysosomal enzymopathies]

Widespread distribution of beta-hexosaminidase activity in the brain of a Sandhoff mouse model after coinjection of adenoviral vector and mannitol.

Gene therapy·2003

Endothelial nitric oxide synthase gene polymorphisms in Fabry's disease.

Clinical genetics·2002

Muscle as a putative producer of acid alpha-glucosidase for glycogenosis type II gene therapy.

Human molecular genetics·2002

From gene transfer to gene therapy in lysosomal storage diseases affecting the central nervous system.

Annals of medicine·2001

Gene therapy in lysosomal diseases.

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie·2000

Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlation.

Neurology·2000

Changes in the iodine content of vegetables following the Chernobyl accident.

Endocrinologie·1991

Epidemiological surveillance of iodine deficiency in Romania by urinary iodine determinations in children aged 6-16 years from 30 counties.

Endocrinologie·1991

Cardiac disturbances in thyrotoxicosis: diagnosis, incidence, clinical features and management.

Endocrinologie·1991

Melatonin involvement in oxidative processes.

Endocrinologie·1991

Influence of sex and glucocorticoid hormones on 3H cholesterol uptake in the aortic wall and 3H adrenaline in the brain.

Endocrinologie·1991

Cardiothyreosis.

Endocrinologie·1991

Association of miR-499, miR-27a, and miR-34a Gene Polymorphisms With Susceptibility to Type 2 Diabetes Mellitus in an Iranian Population: A Case-Control Study.

BioMed research international·2026

Atherosclerotic plaque fibroblasts derive from adventitial and medial Pdgfra-lineage-positive cells and predominantly maintain fibroblast identity.

Cardiovascular research·2026

Revealing Causal Proteomic Signatures of Hypertension: Systematic Insights From Proteome-Wide Mendelian Randomization.

Hypertension (Dallas, Tex. : 1979)·2026

Inheritance entropy: A model-independent method to probe the hereditary structure of cell lineage trees.

PRX life·2026

Early life high-fat diet exposure modulates adult metabolic phenotypes in Drosophila.

iScience·2026

Decoding the Link: Exploring FMO3 Gene Variations as a Key to Understanding Type Two Diabetes Through Bioinformatics and Case-Control Analyses.

Indian journal of clinical biochemistry : IJCB·2026

Related Experiment Videos

[The genetic mechanisms of lysosomal enzymopathies]

Related Concept Videos

Widespread distribution of beta-hexosaminidase activity in the brain of a Sandhoff mouse model after coinjection of adenoviral vector and mannitol.

Endothelial nitric oxide synthase gene polymorphisms in Fabry's disease.

Muscle as a putative producer of acid alpha-glucosidase for glycogenosis type II gene therapy.

From gene transfer to gene therapy in lysosomal storage diseases affecting the central nervous system.

Gene therapy in lysosomal diseases.

Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlation.

Changes in the iodine content of vegetables following the Chernobyl accident.

Epidemiological surveillance of iodine deficiency in Romania by urinary iodine determinations in children aged 6-16 years from 30 counties.

Cardiac disturbances in thyrotoxicosis: diagnosis, incidence, clinical features and management.

Melatonin involvement in oxidative processes.

Influence of sex and glucocorticoid hormones on 3H cholesterol uptake in the aortic wall and 3H adrenaline in the brain.

Cardiothyreosis.

Association of miR-499, miR-27a, and miR-34a Gene Polymorphisms With Susceptibility to Type 2 Diabetes Mellitus in an Iranian Population: A Case-Control Study.

Atherosclerotic plaque fibroblasts derive from adventitial and medial Pdgfra-lineage-positive cells and predominantly maintain fibroblast identity.

Revealing Causal Proteomic Signatures of Hypertension: Systematic Insights From Proteome-Wide Mendelian Randomization.

Inheritance entropy: A model-independent method to probe the hereditary structure of cell lineage trees.

Early life high-fat diet exposure modulates adult metabolic phenotypes in Drosophila.

Decoding the Link: Exploring FMO3 Gene Variations as a Key to Understanding Type Two Diabetes Through Bioinformatics and Case-Control Analyses.

Related Experiment Videos

[The genetic mechanisms of lysosomal enzymopathies]

Related Concept Videos

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