Nucleotide sequence of human muscle acetylcholine receptor beta-subunit

Molecular characterization of congenital myasthenic syndromes in Spain.

Neuromuscular disorders : NMD·2017

RYR1-related congenital myopathy with fatigable weakness, responding to pyridostigimine.

Neuromuscular disorders : NMD·2014

A mouse model of the slow channel myasthenic syndrome: Neuromuscular physiology and effects of ephedrine treatment.

Experimental neurology·2013

Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myasthenia.

Neuromuscular disorders : NMD·2010

Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7.

Neurology·2010

A human recombinant autoantibody-based immunotoxin specific for the fetal acetylcholine receptor inhibits rhabdomyosarcoma growth in vitro and in a murine transplantation model.

Journal of biomedicine & biotechnology·2010

Nuclear receptor Nur77 resolves the inflammatory response of macrophages primarily by regulating expression of AP-1 transcription factors and their target genes.

Nucleic acids research·2026

When circular RNAs meet the genome: CiR-loops as chromatin regulators and disease drivers.

Nucleic acids research·2026

SpliceImpactR maps alternative RNA processing events driving protein functional diversity.

Nucleic acids research·2026

The leading region of many plasmids is adapted for translational efficiency.

Nucleic acids research·2026

Binary-SPA: a reference-free method for cell annotation in high-resolution spatial transcriptomics.

Nucleic acids research·2026

DeepPNI: a language- and graph-based model for mutation-driven protein-nucleic acid binding energetics.

Nucleic acids research·2026

DDX3x Regulates NINJ1 Transcription via Histone Lactylation in Sepsis Associated-Acute Kidney Injury.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Persistent Cognitive Dysfunction in Postural Orthostatic Tachycardia Syndrome: A Scoping Review of Neural Mechanisms, Interventions, and Critical Research Gaps.

Cureus·2026

Assessment of Inflammation Control in Allergic Rhinitis and Chronic Rhinosinusitis.

Journal of inflammation research·2026

Vagus Nerve Modulation of the Gut-Brain Axis: Implications for Mental Health and Cognitive Function.

The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry·2026

Written in the Stars: Astrocyte Biology From Evolution to Disease.

Acta physiologica (Oxford, England)·2026

[Hereditary sensory and autonomic neuropathy type IV].

Medicina·2026

Related Experiment Videos

Nucleotide sequence of human muscle acetylcholine receptor beta-subunit

Related Concept Videos

Molecular characterization of congenital myasthenic syndromes in Spain.

RYR1-related congenital myopathy with fatigable weakness, responding to pyridostigimine.

A mouse model of the slow channel myasthenic syndrome: Neuromuscular physiology and effects of ephedrine treatment.

Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myasthenia.

Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7.

A human recombinant autoantibody-based immunotoxin specific for the fetal acetylcholine receptor inhibits rhabdomyosarcoma growth in vitro and in a murine transplantation model.

Nuclear receptor Nur77 resolves the inflammatory response of macrophages primarily by regulating expression of AP-1 transcription factors and their target genes.

When circular RNAs meet the genome: CiR-loops as chromatin regulators and disease drivers.

SpliceImpactR maps alternative RNA processing events driving protein functional diversity.

The leading region of many plasmids is adapted for translational efficiency.

Binary-SPA: a reference-free method for cell annotation in high-resolution spatial transcriptomics.

DeepPNI: a language- and graph-based model for mutation-driven protein-nucleic acid binding energetics.

DDX3x Regulates NINJ1 Transcription via Histone Lactylation in Sepsis Associated-Acute Kidney Injury.

Persistent Cognitive Dysfunction in Postural Orthostatic Tachycardia Syndrome: A Scoping Review of Neural Mechanisms, Interventions, and Critical Research Gaps.

Assessment of Inflammation Control in Allergic Rhinitis and Chronic Rhinosinusitis.

Vagus Nerve Modulation of the Gut-Brain Axis: Implications for Mental Health and Cognitive Function.

Written in the Stars: Astrocyte Biology From Evolution to Disease.

[Hereditary sensory and autonomic neuropathy type IV].

Related Experiment Videos

Nucleotide sequence of human muscle acetylcholine receptor beta-subunit

Related Concept Videos

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