Clinical and <i>FLCN</i> gene characteristics in BHD group.

NIAID Data Ecosystem2026-03-10 收录

Birt-Hogg-Dubé综合征

FLCN基因

数据链接：

https://figshare.com/articles/dataset/Clinical_and_i_FLCN_i_gene_characteristics_in_BHD_group_/4611829 数据链接链接失效反馈

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Clinical and FLCN gene characteristics in BHD group.

创建时间：

2017-02-03

RNAseq raw counts FLCN positive vs. FLCN negative renal proximal tubular epithelial cells (RPTEC)

肾脏研究

FLCN基因

Germline inactivating mutations in Folliculin (FLCN) cause BirtâHoggâDubÃ© (BHD) syndrome, a rare autosomal dominant disorder predisposing to kidney tumors. FLCN is a conserved, essential gene lin

DataONE2021-01-25 更新90

Birt-Hogg-Dubé Syndrome in Skin of Color: Literature Review

Birt-Hogg-Dubé综合征

有色人种皮肤表现

Supplementary Figure 1. Flowchart summarizes our systemic review following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines to characterize the epidemiologica

NIAID Data Ecosystem40

Data from: Renal imaging in 199 Dutch patients with Birt-Hogg-Dubé syndrome: screening compliance and outcome

Birt-Hogg-Dubé综合征

肾脏研究

Birt-Hogg-Dubé syndrome is associated with an increased risk for renal cell carcinoma. Surveillance is recommended, but the optimal imaging method and screening interval remain to be defined. The ma

DataCite Commons2025-06-01 更新30

Birt-Hogg-Dubé Syndrome in Skin of Color: Literature Review

Birt-Hogg-Dubé综合征

有色皮肤人群

Mendeley Data2024-01-31 更新80

Birt-Hogg-Dubé syndrome associated with chorioretinopathy and nyctalopia: a case report and review of the literature

Birt-Hogg-Dubé综合征

眼科疾病

To report a rare case of Birt-Hogg-Dubé Syndrome (BHD) with progressive chorioretinopathy. Case report. A 55-year-old woman presented with longstanding nyctalopia attributed to a congenital retinal dy

DataCite Commons2023-04-05 更新40

Clinical and <i>FLCN</i> gene characteristics in BHD group.

资源简介：

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