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Showing 41-60 of 84 results
  1. Molekulare Netzwerke von Hypoxie und neuronaler Apoptose in der Cochlea

    Background

    In organotypic cultures, the modiolus (MOD) region of newborn rats shows a fourfold higher rate of cell death than the organ of Corti (OC)....

    J. Gross, H. Olze, B. Mazurek in HNO
    Article 24 July 2018
  2. PsychENCODE and beyond: transcriptomics and epigenomics of brain development and organoids

    Crucial decisions involving cell fate and connectivity that shape the distinctive development of the human brain occur in the embryonic and fetal...

    Alexandre Jourdon, Soraya Scuderi, ... Flora M. Vaccarino in Neuropsychopharmacology
    Article 13 July 2020
  3. Pianp deficiency links GABAB receptor signaling and hippocampal and cerebellar neuronal cell composition to autism-like behavior

    Pianp (also known as Leda-1) is a type I transmembrane protein with preferential expression in the mammalian CNS. Its processing is characterized by...

    Manuel Winkler, Siladitta Biswas, ... Cyrill Géraud in Molecular Psychiatry
    Article Open access 11 September 2019
  4. Gene and environmental interactions according to the components of lifestyle modifications in hypertension guidelines

    Risk factors for hypertension consist of lifestyle and genetic factors. Family history and twin studies have yielded heritability estimates of BP in...

    Yoshihiro Kokubo, Sandosh Padmanabhan, ... Atsushi Goto in Environmental Health and Preventive Medicine
    Article Open access 11 March 2019
  5. Barriers and facilitators for the management of vertigo: a qualitative study with primary care providers

    Background

    Although the management of patients presenting with vertigo and dizziness in primary care has been reported to be inefficient, little is...

    Anna-Janina Stephan, Eva Kovacs, ... Eva Grill in Implementation Science
    Article Open access 08 February 2018
  6. Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP

    Mutations in the microtubule-associated protein tau ( MAPT ) gene cause autosomal dominant frontotemporal lobar degeneration with tau inclusions...

    Shan Jiang, Natalie Wen, ... Celeste M. Karch in Translational Psychiatry
    Article Open access 13 December 2018
  7. Transcriptome level analysis in Rett syndrome using human samples from different tissues

    The mechanisms of neuro-genetic disorders have been mostly investigated in the brain, however, for some pathologies, transcriptomic analysis in...

    Stephen Shovlin, Daniela Tropea in Orphanet Journal of Rare Diseases
    Article Open access 11 July 2018
  8. Barriers to and Facilitators of Alcohol Use Disorder Pharmacotherapy in Primary Care: A Qualitative Study in Five VA Clinics

    Background

    Three medications are FDA-approved and recommended for treating alcohol use disorders (AUD) but they are not offered to most patients with...

    Emily C. Williams, Carol E. Achtmeyer, ... Alex H. S. Harris in Journal of General Internal Medicine
    Article 30 October 2017
  9. Interactome analysis reveals ZNF804A, a schizophrenia risk gene, as a novel component of protein translational machinery critical for embryonic neurodevelopment

    Recent genome-wide association studies identified over 100 genetic loci that significantly associate with schizophrenia (SZ). A top candidate gene, ZNF804A...

    Y Zhou, F Dong, ... Y Mao in Molecular Psychiatry
    Article Open access 19 September 2017
  10. Pre-B Lymphocyte Protein 3 (VPREB3) Expression in the Adrenal Cortex: Precedent for non-Immunological Roles in Normal and Neoplastic Human Tissues

    The pre-B lymphocyte protein 3 (VPREB3) is expressed during B cell differentiation and in subsets of mature B lymphocytes and is mainly found in bone...

    Saulo J. A. Felizola, Koshin Katsu, ... Hironobu Sasano in Endocrine Pathology
    Article 10 April 2015
  11. DNA hypermethylation of CD3+ T cells from cord blood of infants exposed to intrauterine growth restriction

    Aims/hypothesis

    Intrauterine growth restriction (IUGR) is associated with increased susceptibility to obesity, metabolic syndrome and type 2 diabetes....

    Lyda Williams, Yoshinori Seki, ... Maureen J. Charron in Diabetologia
    Article 17 May 2016
  12. Resuscitation of a dead cardiomyocyte

    Although cardiac resuscitation can revive the whole body, the mechanisms are unclear. To this end, we propose that reviving a dead/dysfunctional...

    George H. Kunkel, Pankaj Chaturvedi, Suresh C. Tyagi in Heart Failure Reviews
    Article 27 August 2015
  13. Pan-cancer transcriptome analysis reveals a gene expression signature for the identification of tumor tissue origin

    Carcinoma of unknown primary, wherein metastatic disease is present without an identifiable primary site, accounts for ~3–5% of all cancer diagnoses....

    Qinghua Xu, **ying Chen, ... **ang Du in Modern Pathology
    Article 18 March 2016
  14. SPON2, a newly identified target gene of MACC1, drives colorectal cancer metastasis in mice and is prognostic for colorectal cancer patient survival

    MACC1 (metastasis associated in colon cancer 1) is a prognostic biomarker for tumor progression, metastasis and survival of a variety of solid...

    F Schmid, Q Wang, ... U Stein in Oncogene
    Article 21 December 2015
  15. Generation of functional human serotonergic neurons from fibroblasts

    The brain’s serotonergic system centrally regulates several physiological processes and its dysfunction has been implicated in the pathophysiology of...

    K C Vadodaria, J Mertens, ... F H Gage in Molecular Psychiatry
    Article 27 October 2015
  16. Spatial regulation of gene expression during growth of articular cartilage in juvenile mice

    Background:

    In juvenile mammals, the epiphyses of long bones grow by chondrogenesis within the articular cartilage. A better understanding of the...

    Julian C. Lui, Michael Chau, ... Jeffrey Baron in Pediatric Research
    Article 18 December 2014
  17. Genomic structural variants are linked with intellectual disability

    Mutations in more than 500 genes have been associated with intellectual disability (ID) and related disorders of cognitive function, such as autism...

    Kazima Bulayeva, Klaus-Peter Lesch, ... Paul M. Thompson in Journal of Neural Transmission
    Article 28 January 2015
  18. Modulation of behavioral networks by selective interneuronal inactivation

    Gamma-aminobutyric acid (GABA)-ergic disturbances are hallmark features of schizophrenia and other neuropsychiatric disorders and encompass multiple...

    M J Schmidt, S Horvath, ... K Mirnics in Molecular Psychiatry
    Article 10 December 2013
  19. Altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia

    The underlying pathology of schizophrenia (SZ) is likely as heterogeneous as its symptomatology. A variety of cortical and subcortical regions,...

    A L Guillozet-Bongaarts, T M Hyde, ... J E Kleinman in Molecular Psychiatry
    Article Open access 26 March 2013
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