Choline acetyltransferase: a molecular genetic approach

Genetic variation and pesticide exposure influence blood DNA methylation signatures in females with early-stage Parkinson's disease.

NPJ Parkinson's disease·2024

The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells.

Scientific reports·2019

The genetic landscape of Parkinson's disease.

Revue neurologique·2018

Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein.

Scientific reports·2017

Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease.

European journal of neurology·2017

Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease.

Neurobiology of aging·2016

Mindfulness and meditation: Promoting emotional and cognitive health.

Progress in brain research·2025

Cognitive stimulation enhancing memory and mental function.

Progress in brain research·2025

The science behind non-pharmacological interventions.

Progress in brain research·2025

Technology-assisted interventions for neuropsychiatric disorders.

Progress in brain research·2025

Ethical consideration in non-pharmacological treatments for neuropsychiatric disorders.

Progress in brain research·2025

The role of caregivers: Providing compassionate and effective care.

Progress in brain research·2025

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

Related Experiment Videos

Choline acetyltransferase: a molecular genetic approach

Related Concept Videos

Genetic variation and pesticide exposure influence blood DNA methylation signatures in females with early-stage Parkinson's disease.

The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells.

The genetic landscape of Parkinson's disease.

Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein.

Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease.

Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease.

Mindfulness and meditation: Promoting emotional and cognitive health.

Cognitive stimulation enhancing memory and mental function.

The science behind non-pharmacological interventions.

Technology-assisted interventions for neuropsychiatric disorders.

Ethical consideration in non-pharmacological treatments for neuropsychiatric disorders.

The role of caregivers: Providing compassionate and effective care.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

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Choline acetyltransferase: a molecular genetic approach

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