Profound changes in cerebrospinal fluid proteome and metabolic profile are associated with congenital hydrocephalus

The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research*

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Proteomics and Metabolomics Approaches towards a Functional Insight onto AUTISM Spectrum Disorders: Phenotype Stratification and Biomarker Discovery

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Effects of minocycline on epiplexus macrophage activation, choroid plexus injury and hydrocephalus development in spontaneous hypertensive rats

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Delayed clearance of cerebrospinal fluid tracer from choroid plexus in idiopathic normal pressure hydrocephalus

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HDAC1 regulates the stability of glutamate carboxypeptidase II protein by modulating acetylation status of lysine 479 residue

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Delayed clearance of cerebrospinal fluid tracer from entorhinal cortex in idiopathic normal pressure hydrocephalus: A glymphatic magnetic resonance imaging study

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CHIP E3 ligase mediates proteasomal degradation of the proliferation regulatory protein ALDH1L1 during the transition of NIH3T3 fibroblasts from G0/G1 to S-phase

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Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells

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Acetylation takes aim at mRNA

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Protein Quality Control by Molecular Chaperones in Neurodegeneration

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Protein aggregation and neurodegenerative diseases: From theory to therapy

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Neonatal hydrocephalus is a result of a block in folate handling and metabolism involving 10-formyltetrahydrofolate dehydrogenase

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A HIF-1α-driven feed-forward loop augments HIF signalling in Hep3B cells by upregulation of ARNT

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Mice lacking glutamate carboxypeptidase II develop normally, but are less susceptible to traumatic brain injury

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Acetylation regulates the stability of glutamate carboxypeptidase II protein in human astrocytes

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Rsp5/Nedd4 is the main ubiquitin ligase that targets cytosolic misfolded proteins following heat stress

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Glutamate Carboxypeptidase II in Diagnosis and Treatment of Neurologic Disorders and Prostate Cancer

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Pathophysiology of congenital and neonatal hydrocephalus

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Glutamate carboxypeptidase II and folate deficiencies result in reciprocal protection against cognitive and social deficits in mice: Implications for neurodevelopmental disorders

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The impact of acetylation and deacetylation on the p53 pathway

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HSP90 at the hub of protein homeostasis: emerging mechanistic insights

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Cerebrospinal fluid and plasma biomarkers in Alzheimer disease

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The Role of Human Aldehyde Dehydrogenase in Normal and Cancer Stem Cells

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Folate Receptor Alpha Defect Causes Cerebral Folate Transport Deficiency: A Treatable Neurodegenerative Disorder Associated with Disturbed Myelin Metabolism

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Congenital hydrocephalus – prevalence, prenatal diagnosis and outcome of pregnancy in four European regions

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Addressing a Folate Imbalance in Fetal Cerebrospinal Fluid Can Decrease the Incidence of Congenital Hydrocephalus

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Evaluation of the Variation in Sample Preparation for Comparative Proteomics Using Stable Isotope Labeling by Amino Acids in Cell Culture

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Repeatability and Reproducibility in Proteomic Identifications by Liquid Chromatography−Tandem Mass Spectrometry

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