Read more about the article Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy.
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Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy.

Abstract Inherited demyelinating peripheral neuropathies are progressive incurable diseases without effective treatment. To develop a gene therapy approach targeting myelinating Schwann cells that can be translatable, we delivered a lentiviral…

Continue ReadingIntrathecal gene therapy rescues a model of demyelinating peripheral neuropathy.
Read more about the article Assessing the Relationship between Neurocognitive Performance and Brain Volume in Chronic Moderate-Severe Traumatic Brain Injury.
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Assessing the Relationship between Neurocognitive Performance and Brain Volume in Chronic Moderate-Severe Traumatic Brain Injury.

Abstract Characterize the scale and pattern of long-term atrophy in gray matter (GM), white matter (WM), and cerebrospinal fluid (CSF) in chronic moderate-severe traumatic brain injury (TBI) and its relationship…

Continue ReadingAssessing the Relationship between Neurocognitive Performance and Brain Volume in Chronic Moderate-Severe Traumatic Brain Injury.
Read more about the article Geographical Distribution of MDR1 Expression in Leishmania Isolates, from Greece and Cyprus, Measured by the Rhodamine-123 Efflux Potential of the Isolates, Using Flow Cytometry.
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Geographical Distribution of MDR1 Expression in Leishmania Isolates, from Greece and Cyprus, Measured by the Rhodamine-123 Efflux Potential of the Isolates, Using Flow Cytometry.

Abstract Leishmaniasis, a neglected vector-borne disease caused by the protozoan parasite Leishmania, is encountered in 98 countries causing serious concerns to public health. The most alarming is the development of…

Continue ReadingGeographical Distribution of MDR1 Expression in Leishmania Isolates, from Greece and Cyprus, Measured by the Rhodamine-123 Efflux Potential of the Isolates, Using Flow Cytometry.
Read more about the article Circum-Mediterranean phylogeography of a bat coupled with past environmental niche modeling: A new paradigm for the recolonization of Europe?
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Circum-Mediterranean phylogeography of a bat coupled with past environmental niche modeling: A new paradigm for the recolonization of Europe?

Abstract The isolation of populations in the Iberian, Italian and Balkan peninsulas during the ice ages define four main paradigms that explain much of the known distribution of intraspecific genetic…

Continue ReadingCircum-Mediterranean phylogeography of a bat coupled with past environmental niche modeling: A new paradigm for the recolonization of Europe?
Read more about the article RAAS inhibition and the course of Alport syndrome.
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RAAS inhibition and the course of Alport syndrome.

Abstract Alport syndrome (AS) is a hereditary progressive glomerulonephritis with a high life-time risk for end-stage renal disease (ESRD). Most patients will reach ESRD before the age of 30 years,…

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Read more about the article A ligand-independent integrin β1 mechanosensory complex guides spindle orientation.
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A ligand-independent integrin β1 mechanosensory complex guides spindle orientation.

Abstract Control of spindle orientation is a fundamental process for embryonic development, morphogenesis and tissue homeostasis, while defects are associated with tumorigenesis and other diseases. Force sensing is one of…

Continue ReadingA ligand-independent integrin β1 mechanosensory complex guides spindle orientation.
Read more about the article Titin antibodies in "seronegative" myasthenia gravis–A new role for an old antigen.
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Titin antibodies in "seronegative" myasthenia gravis–A new role for an old antigen.

Abstract Myasthenia gravis (MG) is an autoimmune disease caused by antibodies targeting the neuromuscular junction of skeletal muscles. Triple-seronegative MG (tSN-MG, without detectable AChR, MuSK and LRP4 antibodies), which accounts…

Continue ReadingTitin antibodies in "seronegative" myasthenia gravis–A new role for an old antigen.
Read more about the article Sequence evidence for common ancestry of eukaryotic endomembrane coatomers.
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Sequence evidence for common ancestry of eukaryotic endomembrane coatomers.

Abstract Eukaryotic cells are defined by compartments through which the trafficking of macromolecules is mediated by large complexes, such as the nuclear pore, transport vesicles and intraflagellar transport. The assembly…

Continue ReadingSequence evidence for common ancestry of eukaryotic endomembrane coatomers.
Read more about the article No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
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No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.

Abstract BRCA1 interacting protein C-terminal helicase 1 (BRIP1) is one of the Fanconi Anaemia Complementation (FANC) group family of DNA repair proteins. Biallelic mutations in BRIP1 are responsible for FANC…

Continue ReadingNo evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
Read more about the article Transmembrane protein TMEM170A is a newly discovered regulator of ER and nuclear envelope morphogenesis in human cells.
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Transmembrane protein TMEM170A is a newly discovered regulator of ER and nuclear envelope morphogenesis in human cells.

Abstract The mechanism of endoplasmic reticulum (ER) morphogenesis is incompletely understood. ER tubules are shaped by the reticulons (RTNs) and DP1/Yop1p family members, but the mechanism of ER sheet formation…

Continue ReadingTransmembrane protein TMEM170A is a newly discovered regulator of ER and nuclear envelope morphogenesis in human cells.