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Establishment and characterization of BHD-F59RSVT, an immortalized cell  line derived from a renal cell carcinoma in a patient with Birt–Hogg–Dubé  syndrome | Laboratory Investigation
Establishment and characterization of BHD-F59RSVT, an immortalized cell line derived from a renal cell carcinoma in a patient with Birt–Hogg–Dubé syndrome | Laboratory Investigation

FLCN-regulated miRNAs suppressed reparative response in cells and pulmonary  lesions of Birt-Hogg-Dubé syndrome | Thorax
FLCN-regulated miRNAs suppressed reparative response in cells and pulmonary lesions of Birt-Hogg-Dubé syndrome | Thorax

FLCN: The causative gene for Birt-Hogg-Dubé syndrome - ScienceDirect
FLCN: The causative gene for Birt-Hogg-Dubé syndrome - ScienceDirect

Brit-Hogg-Dube syndrome. (A) Folliculin (FLCN) gene analysis showing a... |  Download Scientific Diagram
Brit-Hogg-Dube syndrome. (A) Folliculin (FLCN) gene analysis showing a... | Download Scientific Diagram

A FLCN-TFE3 Feedback Loop Prevents Excessive Glycogenesis and Phagocyte  Activation by Regulating Lysosome Activity - ScienceDirect
A FLCN-TFE3 Feedback Loop Prevents Excessive Glycogenesis and Phagocyte Activation by Regulating Lysosome Activity - ScienceDirect

EN Birt Hogg Dubé syndrome - YouTube
EN Birt Hogg Dubé syndrome - YouTube

Frontiers | Folliculin: A Regulator of Transcription Through AMPK and mTOR  Signaling Pathways
Frontiers | Folliculin: A Regulator of Transcription Through AMPK and mTOR Signaling Pathways

Mutation spectrum of the FLCN gene responsible for BHD syndrome. Top of...  | Download Scientific Diagram
Mutation spectrum of the FLCN gene responsible for BHD syndrome. Top of... | Download Scientific Diagram

Mutation analysis of the FLCN gene. Sequencing of exon 12 of the FLCN... |  Download Scientific Diagram
Mutation analysis of the FLCN gene. Sequencing of exon 12 of the FLCN... | Download Scientific Diagram

Genotypic characteristics of Chinese patients with BHD syndrome and  functional analysis of FLCN variants | Orphanet Journal of Rare Diseases |  Full Text
Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variants | Orphanet Journal of Rare Diseases | Full Text

Genotypic characteristics of Chinese patients with BHD syndrome and  functional analysis of FLCN variants | Orphanet Journal of Rare Diseases |  Full Text
Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variants | Orphanet Journal of Rare Diseases | Full Text

Frontiers | Folliculin: A Regulator of Transcription Through AMPK and mTOR  Signaling Pathways
Frontiers | Folliculin: A Regulator of Transcription Through AMPK and mTOR Signaling Pathways

Genomic structure of FLCN gene and the mutation identified in the... |  Download Scientific Diagram
Genomic structure of FLCN gene and the mutation identified in the... | Download Scientific Diagram

PRISMS - Birt-Hogg-Dubé and Smith-Magenis Syndromes: Separate Disorders  Linked through 17p11.2
PRISMS - Birt-Hogg-Dubé and Smith-Magenis Syndromes: Separate Disorders Linked through 17p11.2

The genetics of BHD – Birt-Hogg-Dubé Syndrome
The genetics of BHD – Birt-Hogg-Dubé Syndrome

PDF] Birt-Hogg-Dubé syndrome: diagnosis and management. | Semantic Scholar
PDF] Birt-Hogg-Dubé syndrome: diagnosis and management. | Semantic Scholar

Figure 4 from A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel  Folliculin (FLCN) Gene Mutation | Semantic Scholar
Figure 4 from A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel Folliculin (FLCN) Gene Mutation | Semantic Scholar

Frontiers | Nutrient Signaling and Lysosome Positioning Crosstalk Through a  Multifunctional Protein, Folliculin
Frontiers | Nutrient Signaling and Lysosome Positioning Crosstalk Through a Multifunctional Protein, Folliculin

The FLCN pathway. a FLCN is the gene for the Birt-Hogg-Dubé (BHD)... |  Download Scientific Diagram
The FLCN pathway. a FLCN is the gene for the Birt-Hogg-Dubé (BHD)... | Download Scientific Diagram

Recurrent primary spontaneous pneumothorax in a large Chinese family: a  clinical and genetic investigation | Chinese Medical Journal
Recurrent primary spontaneous pneumothorax in a large Chinese family: a clinical and genetic investigation | Chinese Medical Journal

Schemes of the FLCN/FNIP1/FNIP2 pathway. Yellow and light blue show... |  Download Scientific Diagram
Schemes of the FLCN/FNIP1/FNIP2 pathway. Yellow and light blue show... | Download Scientific Diagram

Splice-site mutation causing partial retention of intron in the FLCN gene  in Birt-Hogg-Dubé syndrome: a case report | BMC Medical Genomics | Full Text
Splice-site mutation causing partial retention of intron in the FLCN gene in Birt-Hogg-Dubé syndrome: a case report | BMC Medical Genomics | Full Text

FLCN Gene - GeneCards | FLCN Protein | FLCN Antibody
FLCN Gene - GeneCards | FLCN Protein | FLCN Antibody

Frontiers | A Novel FLCN Intragenic Deletion Identified by NGS in a BHDS  Family and Literature Review
Frontiers | A Novel FLCN Intragenic Deletion Identified by NGS in a BHDS Family and Literature Review

JCI - Folliculin impairs breast tumor growth by repressing TFE3-dependent  induction of the Warburg effect and angiogenesis
JCI - Folliculin impairs breast tumor growth by repressing TFE3-dependent induction of the Warburg effect and angiogenesis

Genetic screening of the FLCN gene identify six novel variants and a Danish  founder mutation | Journal of Human Genetics
Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation | Journal of Human Genetics

Kidney Cancer | Oncohema Key
Kidney Cancer | Oncohema Key