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Showing 41-60 of 143 results
  1. Chronic stress impairs the aquaporin-4-mediated glymphatic transport through glucocorticoid signaling

    Background

    The glymphatic system has recently been proposed to function as a brain-wide macroscopic system for the clearance of potentially harmful...

    Fang Wei, Jian Song, ... Lin-Hui Wang in Psychopharmacology
    Article 03 January 2019
  2. Myelination is delayed during postnatal brain development in the mdx mouse model of Duchenne muscular dystrophy

    Background

    In Duchenne muscular dystrophy (DMD), the loss of the dystrophin component of the dystrophin-glycoprotein complex (DGC) compromises plasma...

    Azeez Aranmolate, Nathaniel Tse, Holly Colognato in BMC Neuroscience
    Article Open access 14 August 2017
  3. Long and Short QT Syndromes

    The long and short QT syndromes are genetically transmitted arrhythmogenic diseases characterized by an abnormal QTc on the basal ECG and by an...
    Lia Crotti, Maria-Christina Kotta, Silvia Castelletti in Channelopathies in Heart Disease
    Chapter 2018
  4. Progress of Genomics in Cardiac Conduction and Rhythm Disorders

    Genes and genetic loci linked thus far to cardiac electrical function and arrhythmia have been primarily uncovered through numerous studies. The...
    Zhenyan Xu, Qinmei **ong, ... Kui Hong in Heart Genomics
    Chapter 2018
  5. Tumor analysis: freeze–thawing cycle of triple-negative breast cancer cells alters tumor CD24/CD44 profiles and the percentage of tumor-infiltrating immune cells

    Objective

    The use of novel methods to characterize living tumor cells relies on well-conceived biobanks. Herein, we raised the question of whether the...

    Matthieu Le Gallo, Thibault de la Motte Rouge, ... Patrick Legembre in BMC Research Notes
    Article Open access 20 June 2018
  6. Genetic Testing for Inheritable Cardiac Channelopathies

    Inheritable cardiac channelopathies (ICC) are defined as primary electrical disorders without identifiable cardiac structural abnormalities and are...
    Florence Kyndt, Jean-Baptiste Gourraud, Julien Barc in Channelopathies in Heart Disease
    Chapter 2018
  7. The Cardiac Sodium Channel and Its Protein Partners

    Activation of the electrical signal and its transmission as a depolarizing wave in the whole heart requires highly organized myocyte architecture and...
    Chapter 2017
  8. Actin depolymerization mediated loss of SNTA1 phosphorylation and Rac1 activity has implications on ROS production, cell migration and apoptosis

    Alpha-1-syntrophin (SNTA1) and Rac1 are part of a signaling pathway via the dystrophin glycoprotein complex (DGC). Both SNTA1 and Rac1 proteins are...

    Sehar Saleem Bhat, Arif Ali Parray, ... Firdous Ahmad Khanday in Apoptosis
    Article 05 April 2016
  9. Protein Biomarkers and Neuroproteomics Characterization of Microvesicles/Exosomes from Human Cerebrospinal Fluid Following Traumatic Brain Injury

    Recently, there have been emerging interests in the area of microvesicles and exosome (MV/E) released from brain cells in relation to...

    Rachna Manek, Ahmed Moghieb, ... Kevin K.W. Wang in Molecular Neurobiology
    Article 29 November 2017
  10. A meta-analysis of public microarray data identifies biological regulatory networks in Parkinson’s disease

    Background

    Parkinson’s disease (PD) is a long-term degenerative disease that is caused by environmental and genetic factors. The networks of genes and...

    Lining Su, Chunjie Wang, ... **aoqing Song in BMC Medical Genomics
    Article Open access 13 April 2018
  11. Sarcoglycanopathies: Clinical, Molecular and Genetic Characteristics, Epidemiology, Diagnostics and Treatment Options

    Sarcoglycanopathies are a group of autosomal recessive limb-girdle muscular dystrophies (LGMD) caused by mutations in sarcoglycan genes: SGCA (LGMD...

    M. V. Bulakh, O. P. Ryzhkova, A. V. Polyakov in Russian Journal of Genetics
    Article 01 February 2018
  12. GRMD cardiac and skeletal muscle metabolism gene profiles are distinct

    Background

    Duchenne muscular dystrophy (DMD) is caused by mutations in the DMD gene, which codes for the dystrophin protein. While progress has been...

    Larry W. Markham, Candice L. Brinkmeyer-Langford, ... Cristi L. Galindo in BMC Medical Genomics
    Article Open access 08 April 2017
  13. Discovery and replication of a peripheral tissue DNA methylation biosignature to augment a suicide prediction model

    Background

    Suicide is the second leading cause of death among adolescents in the USA, and rates are rising. Methods to identify individuals at risk...

    Makena L. Clive, Marco P. Boks, ... Zachary Kaminsky in Clinical Epigenetics
    Article Open access 03 November 2016
  14. A Novel Relationship for Schizophrenia, Bipolar, and Major Depressive Disorder. Part 8: a Hint from Chromosome 8 High Density Association Screen

    Convergent evidence from genetics, symptomatology, and psychopharmacology implies that there are intrinsic connections between schizophrenia (SCZ),...

    **ng Chen, Feng Long, ... Gang Chen in Molecular Neurobiology
    Article 22 September 2016
  15. Cardiac Arrhythmias Related to Sodium Channel Dysfunction

    The voltage-gated cardiac sodium channel (Nav1.5) is a mega-complex comprised of a pore-forming α subunit and 4 ancillary β-subunits together with...
    Eleonora Savio-Galimberti, Mariana Argenziano, Charles Antzelevitch in Voltage-gated Sodium Channels: Structure, Function and Channelopathies
    Chapter 2017
  16. Plasma Membrane Calcium-Transporting ATPase

    Emanuel E. Strehler in Encyclopedia of Signaling Molecules
    Living reference work entry 2016
  17. Targeted Gene Resequencing (Astrochip) to Explore the Tripartite Synapse in Autism–Epilepsy Phenotype with Macrocephaly

    The frequent co-occurrence of autism spectrum disorders (ASD) and epilepsy, or paroxysmal EEG abnormalities, defines a condition termed...

    Maria Marchese, Giulia Valvo, ... Filippo M. Santorelli in NeuroMolecular Medicine
    Article 04 November 2015
  18. Molecular Pathways and Animal Models of Cardiomyopathies

    Cardiomyopathies are a heterogeneous group of disorders of heart muscle that ultimately result in congestive heart failure (CHF), sudden cardiac...
    Chapter 2016
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