A histochemical study of the enzyme profile of Krabbe's cells

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Danon disease: a focus on processing of the novel LAMP2 mutation and comments on the beneficial use of peripheral white blood cells in the diagnosis of LAMP2 deficiency.

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Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone.

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Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis.

Human molecular genetics·2010

Oligodendroglia from ADSL-deficient patient produce SAICAribotide and SAMP.

Molecular genetics and metabolism·2010

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Complementary use of the DNA methylation-based tumor classification by the Bethesda v3 classifier in routine diagnostics: evaluation in a series of 516 cases.

Acta neuropathologica·2026

Molecular programs in human locus coeruleus link APOE and neuromelanin to Alzheimer's vulnerability.

Acta neuropathologica·2026

Oligodendroglial somatic SNCA copy number gains are associated with inclusions and disease onset in multiple system atrophy.

Acta neuropathologica·2026

Familial, neuropathological and cellular analysis identify ARPP21 as a major amyotrophic lateral sclerosis associated gene in French cohorts.

Acta neuropathologica·2026

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Nano letters·2026

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Chemical reviews·2026

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Angewandte Chemie (International ed. in English)·2026

Light- and H2O2-Switchable Dual-Enzyme Carbon Dot Nanozymes with Fe-Pyrrolic N Dual Sites for Orthogonally Activated Multimodal Detection of Glutathione and Hydrogen Peroxide.

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Biochemical characterization of serine racemases from major mammalian lineages.

Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology·2026

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Related Experiment Videos

A histochemical study of the enzyme profile of Krabbe's cells

Related Concept Videos

[Prenatal diagnosis of lysosomal enzymopathies in the Czech Republic].

[The role of PET-CT in decision making on the treatment of localized nodular form of pulmonary AL-amyloidosis].

Danon disease: a focus on processing of the novel LAMP2 mutation and comments on the beneficial use of peripheral white blood cells in the diagnosis of LAMP2 deficiency.

Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone.

Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis.

Oligodendroglia from ADSL-deficient patient produce SAICAribotide and SAMP.

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A new era of genome-wide association studies in the field of Alzheimer's disease and overlapping co-pathologies: lessons learned from a neuropathology-centered approach.

Complementary use of the DNA methylation-based tumor classification by the Bethesda v3 classifier in routine diagnostics: evaluation in a series of 516 cases.

Molecular programs in human locus coeruleus link APOE and neuromelanin to Alzheimer's vulnerability.

Oligodendroglial somatic SNCA copy number gains are associated with inclusions and disease onset in multiple system atrophy.

Familial, neuropathological and cellular analysis identify ARPP21 as a major amyotrophic lateral sclerosis associated gene in French cohorts.

Spatiotemporal Sequential Fluorescence and Electrochemistry Bimodal Quantitation of Enzyme Activity in a Living Cell.

Milestones in the Elucidation of Heme Biosynthesis.

Heme Peroxo Reaction Intermediates: Mimicking Biological Structure and Reactivity With Synthetic Model Systems.

Light- and H2O2-Switchable Dual-Enzyme Carbon Dot Nanozymes with Fe-Pyrrolic N Dual Sites for Orthogonally Activated Multimodal Detection of Glutathione and Hydrogen Peroxide.

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Related Experiment Videos

A histochemical study of the enzyme profile of Krabbe's cells

Abstract:

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