The ultrastructure of the adult and developing human myotendinous junction

Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study.

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Oppenheim's myatonia congenita.

Neuropediatrics·2001

Age-related morphological changes of the deltoid muscle from 50 to 79 years of age.

Acta neuropathologica·2001

Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene.

Neurology·2000

Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA.

Human molecular genetics·2000

Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.

Human molecular genetics·2000

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

Changes in five cerebrospinal fluid and three plasma Alzheimer's disease biomarkers across increasing brain amyloid-beta and tau pathology burden.

Acta neuropathologica·2026

Seeds from ALS patients homozygous for the SOD1 D90A mutation transmit two types of SOD1 aggregation and motor neuron disease.

Acta neuropathologica·2026

High levels of cell-free hemoglobin and iron in cerebral thrombi of pre-Omicron COVID-19 stroke patients: novel drivers of SARS-CoV-2-induced prothrombotic state.

Acta neuropathologica·2026

Anatomical Determinants of the Left Atrial Electrograms: Wall Thickness and Myocardial Fat Infiltration.

Journal of cardiovascular electrophysiology·2026

Bridging Temporal and Spatial Scales: Contemporary Advances in EEG-fMRI Integration With a Focus on Epilepsy.

Journal of medical imaging and radiation oncology·2026

Optimizing Electrical Stimulation Parameters to Enhance Viability of Dental Pulp Stem Cells in Graphene-Based Scaffolds.

ACS omega·2026

Impact of Total Protein and Triglycerides on the comparability of Sodium and Potassium Measurements by Direct and Indirect Ion-Selective Electrodes : An Experimental Analytical Study.

EJIFCC·2026

SLATE-PTP: A spine-leaf architecture timestamps and evaluation dataset for IEEE 1588 precision time protocol benchmarking.

Data in brief·2026

Feasibility of Neurological Prognostication After Pediatric Cardiac Arrest with a Reduced Number of EEG Electrodes.

Resuscitation·2026

Related Experiment Videos

The ultrastructure of the adult and developing human myotendinous junction

Related Concept Videos

Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study.

Oppenheim's myatonia congenita.

Age-related morphological changes of the deltoid muscle from 50 to 79 years of age.

Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene.

Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA.

Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.

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.

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High levels of cell-free hemoglobin and iron in cerebral thrombi of pre-Omicron COVID-19 stroke patients: novel drivers of SARS-CoV-2-induced prothrombotic state.

Anatomical Determinants of the Left Atrial Electrograms: Wall Thickness and Myocardial Fat Infiltration.

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The ultrastructure of the adult and developing human myotendinous junction

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