Emerging molecular mechanism for cerebral small vessel disease: Lessons from hereditary small vessel disease
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چکیده
Emerging molecular mechanism for cerebral small vessel disease: Lessons from hereditary small vessel disease Osamu Onodera, Yumi Sekine, Taisuke Kato, Akihide Koyama, Hiroaki Nozaki and Masatoyo Nishizawa Department of Molecular Neuroscience, Resource Branch for Brain Disease Research, Center for Bioresource-based Research, Department of Neurology, Clinical Neuroscience Branch, Brain Research Institute, Center for Transdisciplinary Research, and School of Health Sciences, Faculty
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Cerebral small-vessel disease protein HTRA1 controls the amount of TGF-β1 via cleavage of proTGF-β1.
Cerebral small-vessel disease is a common disorder in elderly populations; however, its molecular basis is not well understood. We recently demonstrated that mutations in the high-temperature requirement A (HTRA) serine peptidase 1 (HTRA1) gene cause a hereditary cerebral small-vessel disease, cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)....
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