Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery

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Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery

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The relationship between monogenic and polygenic forms of epilepsy is poorly understood and the extent to which the genetic and acquired epilepsies share common pathways is unclear. Here, we use an integrated systems-level analysis of brain gene expression data to identify molecular networks disrupted in epilepsy |

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Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery

Descriptive epidemiological study of rare, less common and common cancers in Western Australia

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Đang chuẩn bị liên kết để tải về tài liệu: Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery

Descriptive epidemiological study of rare, less common and common cancers in Western Australia

báo cáo khoa học: "A rare combination of an endocrine tumour of the common bile duct and a follicular lymphoma of the ampulla of Vater: a case report and review of the literature"

Báo cáo y học: "Bench-to-bedside review: Rare and common viral infections in the intensive care unit – linking pathophysiology to clinical presentatio"

Báo cáo y học: " Transient antiretroviral therapy selecting for common HIV-1 mutations substantially accelerates the appearance of rare mutations"

Báo cáo y học: "Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level"

Ebook Tropical diseases - A practical guide for medical practitioners and students: Part 2

Protein–protein and protein‑nucleic acid binding residues important for common and rare sequence variants in human

Diagnostic delay is common among patients with hypophosphatasia: Initial findings from a longitudinal, prospective, global registry

Correction for both common and rare cell types in blood is important to identify genes that correlate with age

Understanding rare and common diseases in the context of human evolution

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Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery