Early lesion of Pelizaeus-Merzbacher disease: electron microscopic and biochemical study

Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog.

Molecular genetics and metabolism·2016

Protein aggregation in inclusion body myositis, a sporadic form among protein aggregate myopathies, and in myofibrillar myopathies--a comparative study.

Romanian journal of internal medicine = Revue roumaine de medecine interne·2011

Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1.

Neuropediatrics·2010

CLN5 mutations are frequent in juvenile and late-onset non-Finnish patients with NCL.

Neurology·2010

Macrophagic myofasciitis plus (distinct types of muscular dystrophy).

Neuropediatrics·2010

Consequences of mutations within the C terminus of the FHL1 gene.

Neurology·2009

HOXD12 as an oncofetal protein expressed in WNT-activated medulloblastomas.

Journal of neuropathology and experimental neurology·2026

Cardiovascular risk factors and regional neuropathology in autopsy-confirmed Alzheimer disease.

Journal of neuropathology and experimental neurology·2026

CDKN2A/B status can be assessed by p16/MTAP immunohistochemistry as a practical surrogate in pleomorphic xanthoastrocytoma and high-grade astrocytoma with piloid features.

Journal of neuropathology and experimental neurology·2026

Epigenetic deregulation in adult gliomas: A key driver of molecular heterogeneity and precision oncology.

Journal of neuropathology and experimental neurology·2026

MyD88 deficiency modestly attenuates disease in a Leigh syndrome mouse model while enrofloxacin accelerates disease.

Journal of neuropathology and experimental neurology·2026

Molecular mechanisms of maturation in neurogenic embryonal tumors of peripheral and central localization.

Journal of neuropathology and experimental neurology·2026

Genomic and phenotypic characterization of Antarctic Pseudomonas/Aquipseudomonas sp. strains with cold-active antifungal activity against Botrytis cinerea.

Frontiers in microbiology·2026

Quantity down, quality preserved: a continuous HOMA-IR analysis of IVF/ICSI outcomes in PMOS patients.

Frontiers in endocrinology·2026

NDM-Producing Escherichia coli subdural empyema mimicking chronic subdural hematoma: a case report.

Frontiers in medicine·2026

Biological characterization of a clinical human adenovirus type 3 isolate with oncolytic potential.

Frontiers in microbiology·2026

Case Report: Fulminant meningococcus-meningitis under treatment with ravulizumab despite complete vaccination-a rare but severe complication.

Frontiers in medicine·2026

Dynamic effects of microglial NLRP3 on transcriptional alterations post-traumatic brain injury.

Frontiers in neuroscience·2026

Related Experiment Videos

Early lesion of Pelizaeus-Merzbacher disease: electron microscopic and biochemical study

Related Concept Videos

Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog.

Protein aggregation in inclusion body myositis, a sporadic form among protein aggregate myopathies, and in myofibrillar myopathies--a comparative study.

Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1.

CLN5 mutations are frequent in juvenile and late-onset non-Finnish patients with NCL.

Macrophagic myofasciitis plus (distinct types of muscular dystrophy).

Consequences of mutations within the C terminus of the FHL1 gene.

HOXD12 as an oncofetal protein expressed in WNT-activated medulloblastomas.

Cardiovascular risk factors and regional neuropathology in autopsy-confirmed Alzheimer disease.

CDKN2A/B status can be assessed by p16/MTAP immunohistochemistry as a practical surrogate in pleomorphic xanthoastrocytoma and high-grade astrocytoma with piloid features.

Epigenetic deregulation in adult gliomas: A key driver of molecular heterogeneity and precision oncology.

MyD88 deficiency modestly attenuates disease in a Leigh syndrome mouse model while enrofloxacin accelerates disease.

Molecular mechanisms of maturation in neurogenic embryonal tumors of peripheral and central localization.

Genomic and phenotypic characterization of Antarctic Pseudomonas/Aquipseudomonas sp. strains with cold-active antifungal activity against Botrytis cinerea.

Quantity down, quality preserved: a continuous HOMA-IR analysis of IVF/ICSI outcomes in PMOS patients.

NDM-Producing Escherichia coli subdural empyema mimicking chronic subdural hematoma: a case report.

Biological characterization of a clinical human adenovirus type 3 isolate with oncolytic potential.

Case Report: Fulminant meningococcus-meningitis under treatment with ravulizumab despite complete vaccination-a rare but severe complication.

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Related Experiment Videos

Early lesion of Pelizaeus-Merzbacher disease: electron microscopic and biochemical study

Related Concept Videos

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