MUTATION ANALYSES OF COL7A1 GENE IN THREE TAIWANESE PATIENTS WITH SEVERE RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA

Mutation Analyses of COL7A1 Gene in Three Taiwanese Patients with Severe Recessive Dystrophic Epidermolysis Bullosa

Dystrophic epidermolysis bullosa (DEB) is a hereditary mechanobullous disorder characterized by fragility of the skin and mucous membranes caused by abnormal anchoring fibrils.Both dominant and recessive DEB are caused by mutations in COL7A1, the gene encoding type VII collagen, the major component of anchoring fibrils.We performed mutation analysi

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Current approaches to treatment of pain in the low part of back

We described the modern point Collections of view in the pathogenesis of the acute and chronicle low back pain, conception of the tree components formation of the chronicle pain: nociceptive, neuropathic and psychogenetic.Whereby, it was offered the ways of the pathogenetic treatment.We described and substantiated the modern way of treatment of the

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In Silico analysis unveils rs2109069 of DPP9 as a potential catalyst for COVID-19 severity and risk of inflammatory symptoms

Background: During the COVID-19 pandemic, the viral illness caused by SARS-CoV-2 spread through respiratory droplets, resulting in a global pandemic with a range of symptoms from mild to severe.Pathological inflammation posed a critical issue, yet Low Leg Power Recliner the genetic mechanisms behind the excessive activation of inflammatory response

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