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Site-specific ubiquitination of pathogenic huntingtin attenuates its deleterious effects

Proceedings of the National Academy of Sciences - PNAS, 2020-08, Vol.117 (31), p.18661-18669

2020

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Huntington-Erkrankung

Medizinische Genetik, 2018-06, Vol.30 (2), p.246-251

2018

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SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2

The Journal of neuroscience, 2021-06, Vol.41 (22), p.4910-4936

2021

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Dysregulation of gene expression in the striatum of BACHD rats expressing full-length mutant huntingtin and associated abnormalities on molecular and protein levels

Neuropharmacology, 2017-05, Vol.117, p.260-272

2017

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Intravenous MSC-Treatment Improves Impaired Brain Functions in the R6/2 Mouse Model of Huntington's Disease via Recovered Hepatic Pathological Changes

Cells (Basel, Switzerland), 2024-03, Vol.13 (6), p.469

2024

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Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene

International journal of molecular sciences, 2023-09, Vol.24 (19), p.14716

2023

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Intranasal Administration of Mesenchymal Stem Cells Ameliorates the Abnormal Dopamine Transmission System and Inflammatory Reaction in the R6/2 Mouse Model of Huntington Disease

Cells (Basel, Switzerland), 2019-06, Vol.8 (6), p.595

2019

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Broad genomic workup including optical genome mapping uncovers a DDX3X: MLLT10 gene fusion in acute myeloid leukemia

Frontiers in oncology, 2022-09, Vol.12, p.959243-959243

2022

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Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy

Genes, 2022-09, Vol.13 (10), p.1752

2022

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Loss-of-function of GNAL dystonia gene impairs striatal dopamine receptors-mediated adenylyl cyclase/ cyclic AMP signaling pathway

Neurobiology of disease, 2024-02, Vol.191, p.106403-106403, Article 106403

2024

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Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the IDMD/I Gene

International journal of molecular sciences, 2023-09, Vol.24 (19)

2023

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C8 Metabolic properties of hypothalamic primary neuron cultures from bachd rats

Journal of neurology, neurosurgery and psychiatry, 2016-09, Vol.87 (Suppl 1), p.A29-A29

2016

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Preface by the editors

Current topics in behavioral neurosciences, 2015, Vol.22, p.v

2015

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A Trial of Itraconazole or Amphotericin B for HIV-Associated Talaromycosis

The New England journal of medicine, 2017-06, Vol.376 (24), p.2329-2340

2017

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Empowering Intelligent Surfaces and User Pairing for IoT Relaying Systems: Outage Probability and Ergodic Capacity Performance

Sensors (Basel, Switzerland), 2022-08, Vol.22 (17), p.6576

2022

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Automatic Polyp Segmentation Using Modified Recurrent Residual Unet Network

IEEE access, 2022, Vol.10, p.65951-65961

2022

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Actionable Mutation Profiles of Non-Small Cell Lung Cancer patients from Vietnamese population

Scientific reports, 2020-02, Vol.10 (1), p.2707-2707, Article 2707

2020

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How can CSR in demarketing trigger brand advocacy and mindful consumption? Mediating roles of perceived corporate hypocrisy and brand credibility

Journal of fashion marketing and management, 2023-11, Vol.27 (5), p.851-869

2023

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Pathogenic Variant Profile of Hereditary Cancer Syndromes in a Vietnamese Cohort

Frontiers in oncology, 2022-01, Vol.11, p.789659-789659

2022

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Clinical validation of a ctDNA-Based Assay for Multi-Cancer Detection: An Interim Report from a Vietnamese Longitudinal Prospective Cohort Study of 2795 Participants

Cancer investigation, 2023-03, Vol.41 (3), p.232-248

2023

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Characterization of single nucleotide polymorphism in IGF1 and IGF1R genes associated with growth traits in striped catfish (Pangasianodon hypophthalmus Sauvage, 1878)

Aquaculture, 2021-05, Vol.538, p.736542, Article 736542

2021

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Subtotal Laryngectomy with Epiglottic Reconstruction for Glottic Carcinoma: A Single Institutional Experience

International journal of general medicine, 2022-01, Vol.15, p.2321-2328

2022

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Improvement in neoantigen prediction via integration of RNA sequencing data for variant calling

Frontiers in immunology, 2023-09, Vol.14, p.1251603-1251603

2023

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Site-specific ubiquitination of pathogenic huntingtin attenuates its deleterious effects

Huntington-Erkrankung

SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2

Dysregulation of gene expression in the striatum of BACHD rats expressing full-length mutant huntingtin and associated abnormalities on molecular and protein levels

Intravenous MSC-Treatment Improves Impaired Brain Functions in the R6/2 Mouse Model of Huntington's Disease via Recovered Hepatic Pathological Changes

Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene

Intranasal Administration of Mesenchymal Stem Cells Ameliorates the Abnormal Dopamine Transmission System and Inflammatory Reaction in the R6/2 Mouse Model of Huntington Disease

Broad genomic workup including optical genome mapping uncovers a DDX3X: MLLT10 gene fusion in acute myeloid leukemia

Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy

Loss-of-function of GNAL dystonia gene impairs striatal dopamine receptors-mediated adenylyl cyclase/ cyclic AMP signaling pathway

Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the IDMD/I Gene

C8 Metabolic properties of hypothalamic primary neuron cultures from bachd rats

Preface by the editors

A Trial of Itraconazole or Amphotericin B for HIV-Associated Talaromycosis

Empowering Intelligent Surfaces and User Pairing for IoT Relaying Systems: Outage Probability and Ergodic Capacity Performance

Genetic landscape of recessive diseases in the Vietnamese population from large‐scale clinical exome sequencing

SketchANIMAR: Sketch-based 3D animal fine-grained retrieval

Automatic Polyp Segmentation Using Modified Recurrent Residual Unet Network

Actionable Mutation Profiles of Non-Small Cell Lung Cancer patients from Vietnamese population

How can CSR in demarketing trigger brand advocacy and mindful consumption? Mediating roles of perceived corporate hypocrisy and brand credibility

Pathogenic Variant Profile of Hereditary Cancer Syndromes in a Vietnamese Cohort

Clinical validation of a ctDNA-Based Assay for Multi-Cancer Detection: An Interim Report from a Vietnamese Longitudinal Prospective Cohort Study of 2795 Participants

Characterization of single nucleotide polymorphism in IGF1 and IGF1R genes associated with growth traits in striped catfish (Pangasianodon hypophthalmus Sauvage, 1878)

Subtotal Laryngectomy with Epiglottic Reconstruction for Glottic Carcinoma: A Single Institutional Experience

Improvement in neoantigen prediction via integration of RNA sequencing data for variant calling

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