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Distribution of Shagreen Patches and Fibrous Cephalic Plaques in Patients with Tuberous Sclerosis Complex: A Retrospective Cohort Study

NIAID Data Ecosystem2026-05-01 收录

结节性硬化症病理机制

皮肤病征分布分析

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supplemental materials 23.12.12

应用场景：

创建时间：

2023-12-12

结节性硬化症病理机制

mTOR抑制剂反应

Tuberous sclerosis complex (TSC) is a rare genetic disease characterized by mTOR hyperfunction induced benign tumor growths in multiple organs and neurological symptoms. Because the molecular patholog

NIAID Data Ecosystem90

Structure of the TSC2 N-terminus

蛋白质结构解析

结节性硬化症病理机制

Structure of the TSC2 N-terminus Descriptor: GTPase activator-like protein Authors: Zech, R, Kiontke, S, Kummel, D. Deposit date: 2016-01-12 Release date: 2016-08-10 Last modified: 2024-05-08 Method:

Protein Data Bank Japan2024-05-08 更新80

Additional file 4: Table S2. of Genomic analysis of the molecular neuropathology of tuberous sclerosis using a human stem cell model

结节性硬化症病理机制

RNA-seq基因分析

Gene set enrichment analysis of RNA-Seq data (related to Additional file 2: Figure S2B and E). (XLSX 22.2 kb)

Figshare2016-12-14 更新50

Mitochondrial DNA Sequencing by aMPS in patients with Tuberous Sclerosis Complex

线粒体基因组学

结节性硬化症病理机制

Tuberous Sclerosis Complex (TSC) is a tumor suppressor syndrome characterized by high phenotypic heterogeneity. TSC is caused by loss of function mutations in either the TSC1 or TSC2 gene resulting in

NIAID Data Ecosystem80

Profiling the Microenvironment in Tuberous Sclerosis Complex-Associated Angiomyolipoma: Insights from Spatial Gene Expression Analysis

肿瘤微环境空间转录组

结节性硬化症病理机制

Tuberous sclerosis complex (TSC) is a multisystem genetic disorder caused by mutations in TSC1 or TSC2, leading to constitutive activation of the mTORC1 pathway. Among its manifestations, renal angiom

NIAID Data Ecosystem50

Distribution of Shagreen Patches and Fibrous Cephalic Plaques in Patients with Tuberous Sclerosis Complex: A Retrospective Cohort Study

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