CTG trinucleotide repeat variability in identical twins with myotonic dystrophy

Involvement of autoantibodies against G protein-coupled receptors in post-COVID condition and Chronic Fatigue Syndrome.

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Understanding the olfactory role in post-COVID cognitive and neuropsychiatric manifestations.

Frontiers in psychology·2024

Dysautonomia and small fiber neuropathy in post-COVID condition and Chronic Fatigue Syndrome.

Journal of translational medicine·2023

Epidemiology of ataxia and hereditary spastic paraplegia in Spain: A cross-sectional study.

Neurologia·2023

Brain fog of post-COVID-19 condition and Chronic Fatigue Syndrome, same medical disorder?

Journal of translational medicine·2022

[Understanding the evolution of polydnaviruses].

Virologie (Montrouge, France)·2021

Outcomes of Intra-Arterial Tenecteplase after Endovascular Reperfusion for Acute Ischemic Stroke Due to Cardioembolism and Non-Cardioembolism: A Secondary Analysis of the POST-TNK Trial.

Annals of neurology·2026

A Human Gait Circuit Derived from Brain Lesions and Deep Brain Stimulation.

Annals of neurology·2026

Genetic Modifiers of ABCA1 Activity Interact with APOE Isoforms to Mediate Alzheimer's Disease Risk.

Annals of neurology·2026

Establishing Sensory Neurons as Therapeutic Targets in Peripheral Neuropathy Driven by Polyglutamine Expanded Murine ATXN3.

Annals of neurology·2026

Two Years of Ocrelizumab Treatment in Black and Hispanic People with Multiple Sclerosis in CHIMES: A Single-Arm Clinical Trial.

Annals of neurology·2026

Toward a Behavioral Reserve Model in Amyotrophic Lateral Sclerosis.

Annals of neurology·2026

Ctf18-dependent localization of interstitial telomeric sequence to nuclear pore complexes prevents chromosome fragility.

Nucleic acids research·2026

Nuclear compartmentalization at the G1/S transition plays a key role in DNA replication control.

Nature communications·2026

SOAT1 Nonsense Variant in a Cat With Sebaceous Gland Dysplasia.

Animal genetics·2026

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Human molecular genetics·2026

Type, Location and Zygosity of KCNJ16 Variants May Determine the Clinical Severity of Hypokalemia Tubulopathy and Deafness (HkTD).

Kidney360·2026

Differential contributions of β-tubulin isotypes to acentrosomal oocyte meiosis in C. elegans.

The Journal of cell biology·2026

Related Experiment Videos

CTG trinucleotide repeat variability in identical twins with myotonic dystrophy

Related Concept Videos

Involvement of autoantibodies against G protein-coupled receptors in post-COVID condition and Chronic Fatigue Syndrome.

Understanding the olfactory role in post-COVID cognitive and neuropsychiatric manifestations.

Dysautonomia and small fiber neuropathy in post-COVID condition and Chronic Fatigue Syndrome.

Epidemiology of ataxia and hereditary spastic paraplegia in Spain: A cross-sectional study.

Brain fog of post-COVID-19 condition and Chronic Fatigue Syndrome, same medical disorder?

[Understanding the evolution of polydnaviruses].

Outcomes of Intra-Arterial Tenecteplase after Endovascular Reperfusion for Acute Ischemic Stroke Due to Cardioembolism and Non-Cardioembolism: A Secondary Analysis of the POST-TNK Trial.

A Human Gait Circuit Derived from Brain Lesions and Deep Brain Stimulation.

Genetic Modifiers of ABCA1 Activity Interact with APOE Isoforms to Mediate Alzheimer's Disease Risk.

Establishing Sensory Neurons as Therapeutic Targets in Peripheral Neuropathy Driven by Polyglutamine Expanded Murine ATXN3.

Two Years of Ocrelizumab Treatment in Black and Hispanic People with Multiple Sclerosis in CHIMES: A Single-Arm Clinical Trial.

Toward a Behavioral Reserve Model in Amyotrophic Lateral Sclerosis.

Ctf18-dependent localization of interstitial telomeric sequence to nuclear pore complexes prevents chromosome fragility.

Nuclear compartmentalization at the G1/S transition plays a key role in DNA replication control.

SOAT1 Nonsense Variant in a Cat With Sebaceous Gland Dysplasia.

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Type, Location and Zygosity of KCNJ16 Variants May Determine the Clinical Severity of Hypokalemia Tubulopathy and Deafness (HkTD).

Differential contributions of β-tubulin isotypes to acentrosomal oocyte meiosis in C. elegans.

Related Experiment Videos

CTG trinucleotide repeat variability in identical twins with myotonic dystrophy

Related Concept Videos

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