Judy King Man Ng

ORCID: 0000-0002-4741-4652
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About
Contact & Profiles
Research Areas
  • Peripheral Neuropathies and Disorders
  • Hereditary Neurological Disorders
  • Virus-based gene therapy research
  • Viral Infectious Diseases and Gene Expression in Insects
  • Cellular Mechanics and Interactions
  • Cardiac Fibrosis and Remodeling
  • Bacteriophages and microbial interactions
  • Monoclonal and Polyclonal Antibodies Research
  • Cardiovascular Function and Risk Factors
  • Myasthenia Gravis and Thymoma
  • Virology and Viral Diseases
  • Cardiac Ischemia and Reperfusion
  • Nerve injury and regeneration
  • Animal Disease Management and Epidemiology
  • Cell Adhesion Molecules Research
  • Clusterin in disease pathology
  • Immune Response and Inflammation
  • Pluripotent Stem Cells Research
  • Heme Oxygenase-1 and Carbon Monoxide
  • Neuroinflammation and Neurodegeneration Mechanisms
  • CRISPR and Genetic Engineering
  • Neuroscience and Neural Engineering
  • Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Immune Cell Function and Interaction
  • Hemoglobinopathies and Related Disorders

Boehringer Ingelheim (Austria)
2023-2025

Ludwig-Maximilians-Universität München
2012-2018

Technical University of Munich
2015-2017

Klinikum rechts der Isar
2016-2017

German Centre for Cardiovascular Research
2014-2015

Max Planck Institute of Neurobiology
2012-2015

Max Planck Institute of Biochemistry
2015

Munich Cluster for Systems Neurology
2015

Harvard University
2015

German Center for Neurodegenerative Diseases
2015

We asked whether autoantibodies against neurofascin (NF)186 or NF155, both localized at the nodes of Ranvier, are present in serum patients with inflammatory neuropathy, and NF-specific monoclonal antibodies pathogenic vivo.We cloned human NF155 NF186, developed an ELISA cell-based assay to screen for NF a total 434 donors including 294 Guillain-Barré syndrome variants acute demyelinating polyneuropathy (AIDP), motor axonal chronic (CIDP). characterized reactive samples by isotyping, tissue...

10.1212/wnl.0b013e31827689ad article EN Neurology 2012-10-26

Cardiomyocytes (CMs) generated from human induced pluripotent stem cells (hiPSCs) are increasingly used in disease modelling and drug evaluation. However, they typically a heterogeneous mix of ventricular-, atrial-, nodal-like based on action potentials (APs) gene expression. This heterogeneity the paucity methods for high-throughput functional phenotyping hinder full exploitation their potential. We aimed at developing method rapid, sequential, subtype-specific hiPSC-CMs with respect to AP...

10.1093/eurheartj/ehw189 article EN cc-by-nc European Heart Journal 2016-06-16

To characterize phenotypes of T cells that accumulated in multiple sclerosis (MS) lesions, to compare the lesional T-cell receptor (TCR) repertoire subsets peripheral blood, and identify paired α β chains from single CD8(+) an index patient who we followed for 18 years.We combined immunohistochemistry, laser microdissection, single-cell multiplex PCR subtypes TCRα TCRβ individual brain-infiltrating frozen brain sections. The TCR repertoires were analyzed by pyrosequencing.We found a Vβ1(+)...

10.1212/nxi.0000000000000107 article EN cc-by-nc-nd Neurology Neuroimmunology & Neuroinflammation 2015-05-08

Recently, IgG autoantibodies against different paranodal proteins have been detected and this has led to important advances in the management of inflammatory neuropathies. In contrast, not much is known on IgM proteins.In present study, we screened a large cohort patients (n=140) with neuropathies for neurofascin-155, neurofascin-186 or contactin-1.IgM neurofascin-155 were by ELISA five patients, four demyelinating polyradiculoneuropathy (CIDP) one Guillain-Barré syndrome (GBS), confirmed...

10.1136/jnnp-2018-318170 article EN Journal of Neurology Neurosurgery & Psychiatry 2018-06-26

Multifocal motor neuropathy is an immune mediated disease presenting with multifocal muscle weakness and conduction block. IgM auto-antibodies against the ganglioside GM1 are detectable in about 50% of patients. Auto-antibodies paranodal proteins contactin-1 neurofascin-155 nodal protein neurofascin-186 have been detected subgroups patients chronic inflammatory demyelinating polyneuropathy. Recently, gliomedin were described more than 60% neuropathy. In current study, we aimed to validate...

10.1371/journal.pone.0134274 article EN cc-by PLoS ONE 2015-07-28

Objective: The actin polymerization regulator Thymosin β4 (Tβ4) has been shown to be involved in angiogenesis, wound healing, cell survival and anti-inflammatory responses. We have previously that Tβ4 is capable of recruiting pericytes, thus stabilizing the endothelial barrier function. Here, we analyzed whether treatment with able reduce pericytes loss lipopolysaccharides (LPS)-induced sepsis improve hemodynamic function C57BL/6 mice.Methods: Fourteen days before LPS injection, mice were...

10.1517/14712598.2015.1006193 article EN Expert Opinion on Biological Therapy 2015-01-21

Summary Advanced glycation end-products (AGEs) interact with their receptor RAGE, leading to an inflammatory state. We investigated the role of RAGE in postischaemic leukocyte adhesion after myocardial infarction and its effect on function. Wildtype (WT), ICAM-1-/-, RAGE-/- or ICAM-1/RAGE-/- mice underwent 20 minutes (min) LAD-occlusion followed by 15 min reperfusion. applied vivo fluorescence microscopy visualising Rhodamine-6G labelled leukocytes. To differentiate between endothelial we...

10.1160/th15-11-0898 article EN Thrombosis and Haemostasis 2016-03-01

Virus particle (VP) quantification plays a pivotal role in the development of production processes VPs for virus-based therapies. The yield based on total VP count serves as process performance indicator evaluating efficiency and consistency. Here, label-free method enveloped was developed, with potential applications oncolytic virotherapy, vaccine development, gene therapy. comprises size-exclusion chromatography (SEC) separation using high-performance liquid (HPLC) instruments. Ultraviolet...

10.1016/j.omtm.2024.101252 article EN cc-by-nc-nd Molecular Therapy — Methods & Clinical Development 2024-04-24

Abstract A new β°‐ halassemia mutation, a frameshift mutation with an insertion of single cytosine nucleotide in codon 27–28, is described. The propositus, who compound heterozygous for this and the IVSII‐654 C→T β°‐thalassemia has phenotype severe β‐thalassemia major.

10.1002/ajh.2830370103 article EN American Journal of Hematology 1991-05-01
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