sta sârguință sosire flcn gene mutation anafură invenţie posibilitate
PDF] Birt-Hogg-Dubé syndrome: diagnosis and management. | Semantic Scholar
FLCN | JCGA
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
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
Frontiers | Nutrient Signaling and Lysosome Positioning Crosstalk Through a Multifunctional Protein, Folliculin
Mutation spectrum of the FLCN gene responsible for BHD syndrome. Top of... | Download Scientific Diagram
Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variants | Orphanet Journal of Rare Diseases | Full Text
Recurrent primary spontaneous pneumothorax in a large Chinese family: a clinical and genetic investigation | Chinese Medical Journal
EN Birt Hogg Dubé syndrome - YouTube
PRISMS - Birt-Hogg-Dubé and Smith-Magenis Syndromes: Separate Disorders Linked through 17p11.2
A FLCN-TFE3 Feedback Loop Prevents Excessive Glycogenesis and Phagocyte Activation by Regulating Lysosome Activity - ScienceDirect
The FLCN pathway. A) FLCN is the gene for the Birt-Hogg-Dubé (BHD)... | Download Scientific Diagram
FLCN-regulated miRNAs suppressed reparative response in cells and pulmonary lesions of Birt-Hogg-Dubé syndrome | Thorax
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
Kidney Cancer | Oncohema Key
The Folliculin Tumor Suppressor Is a GAP for the RagC/D GTPases That Signal Amino Acid Levels to mTORC1 - ScienceDirect
The genetics of BHD – Birt-Hogg-Dubé Syndrome
Differential mTORC1 pathways in BHD | Nature Reviews Urology
Late Onset of Skin Manifestations in Birt-Hogg-Dubé Syndrome with FLCN Mutation p.W260X | HTML | Acta Dermato-Venereologica
Identification of a novel frameshift mutation of the FLCN gene in the... | Download Scientific Diagram
Frontiers | A Novel FLCN Intragenic Deletion Identified by NGS in a BHDS Family and Literature Review