Ultrastructure of human and experimental ependymomas. A comparative 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

Drug-induced autophagic myopathies: Exploring pathophysiology with immunolabelling and proteomics.

Journal of neuropathology and experimental neurology·2026

Neural stem cell-derived small extracellular vesicles ameliorate disease progression in the SOD1 G93A murine model of amyotrophic lateral sclerosis.

Journal of neuropathology and experimental neurology·2026

Mitochondrial alterations in pellagra-associated central chromatolysis: Comparison with ballooned achromatic neurons of other etiologies.

Journal of neuropathology and experimental neurology·2026

A phosphorylation‑independent monoclonal antibody improves detection of TDP‑43 pathology across frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and limbic predominant age related TDP‑43 encephalopathy neuropathological change.

Journal of neuropathology and experimental neurology·2026

Keratan sulfate proteoglycan is not expressed in human fetal cerebellar system except pontine nuclei and transitory vermal septa or in fasciculi caudal to the internal capsule.

Journal of neuropathology and experimental neurology·2026

Large amyloid plaques associate with early behavioral alterations in 6-month-old APPswe/PS1dE9 mice.

Journal of neuropathology and experimental neurology·2026

Dissemination along the hepatocaval ligament in a caudate-origin intrahepatic cholangiocarcinoma: a case report with video.

Journal of surgical case reports·2026

Alternative oncogenic drivers and sensitivity to BTK inhibition in CRISPR/Cas gene-edited human DLBCL cell models.

Blood neoplasia·2026

Real-world outcomes of T cell lymphoma in a tertiary cancer center in Saudi Arabia.

Annals of Saudi medicine·2026

mRNA-based immunotherapy improves the efficacy of adoptively transferred TCR transgenic T cells in a murine solid tumour model.

Scientific reports·2026

Integrative bioinformatic and experimental analyses identify the SPI1-NFE2L2/HMGB1 axis linking pyroptosis and immune dysregulation in non-obstructive azoospermia.

Reproductive biology·2026

Targeting a CDH1-TK1-dependent DNA Synthesis Pathway Overcomes Chemoresistance in Acute Myeloid Leukemia.

Hematological oncology·2026

Related Experiment Videos

Ultrastructure of human and experimental ependymomas. A comparative study

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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.

Drug-induced autophagic myopathies: Exploring pathophysiology with immunolabelling and proteomics.

Neural stem cell-derived small extracellular vesicles ameliorate disease progression in the SOD1 G93A murine model of amyotrophic lateral sclerosis.

Mitochondrial alterations in pellagra-associated central chromatolysis: Comparison with ballooned achromatic neurons of other etiologies.

A phosphorylation‑independent monoclonal antibody improves detection of TDP‑43 pathology across frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and limbic predominant age related TDP‑43 encephalopathy neuropathological change.

Keratan sulfate proteoglycan is not expressed in human fetal cerebellar system except pontine nuclei and transitory vermal septa or in fasciculi caudal to the internal capsule.

Large amyloid plaques associate with early behavioral alterations in 6-month-old APPswe/PS1dE9 mice.

Dissemination along the hepatocaval ligament in a caudate-origin intrahepatic cholangiocarcinoma: a case report with video.

Alternative oncogenic drivers and sensitivity to BTK inhibition in CRISPR/Cas gene-edited human DLBCL cell models.

Real-world outcomes of T cell lymphoma in a tertiary cancer center in Saudi Arabia.

mRNA-based immunotherapy improves the efficacy of adoptively transferred TCR transgenic T cells in a murine solid tumour model.

Integrative bioinformatic and experimental analyses identify the SPI1-NFE2L2/HMGB1 axis linking pyroptosis and immune dysregulation in non-obstructive azoospermia.

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Ultrastructure of human and experimental ependymomas. A comparative study

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