Functional characterization of a novel non-coding mutation “Ghent +49A > G” in the iron-responsive element of L-ferritin causing hereditary hyperferritinaemia-cataract syndrome | Scientific Reports
Ferritin light chain deficiency-induced ferroptosis is involved in preeclampsia pathophysiology by disturbing uterine spiral artery remodelling - ScienceDirect
FTL Gene - GeneCards | FRIL Protein | FRIL Antibody
Anti-Ferritin, Light Chain Antibody Clone FTL/1389 – enQuire BioReagents
Genetic analyses of the FTL gene in the proband. A. Analysis of PCR... | Download Scientific Diagram
Schematic diagram of the effect of FTL on the cell cycle. FTL may have... | Download Scientific Diagram
Human Ferritin light chain Lentiviral cDNA ORF Clone, C-GFPSpark® tag, HG16460-ACGLN | Sino Biological
Scheme of mutations on the FTL gene. Schematic representation of the... | Download Scientific Diagram
FTL Gene - GeneCards | FRIL Protein | FRIL Antibody
FTL Gene - GeneCards | FRIL Protein | FRIL Antibody
Anti-FTL Antibody (CAB1768) | WB, IHC, IF
Repression of ferritin light chain translation by human eIF3 | bioRxiv
Preferential Iron Trafficking Characterizes Glioblastoma Stem-like Cells - ScienceDirect
Systemic and Cerebral Iron Homeostasis in Ferritin Knock-Out Mice | PLOS ONE
FTL Gene - GeneCards | FRIL Protein | FRIL Antibody
Addgene: pMRX-IB-mGFP-FTL
FTL Gene - GeneCards | FRIL Protein | FRIL Antibody
Ferritin light chain - Wikipedia
Repression of ferritin light chain translation by human eIF3 | eLife
Hypoxia induced ferritin light chain (FTL) promoted epithelia mesenchymal transition and chemoresistance of glioma | Journal of Experimental & Clinical Cancer Research | Full Text
Hyperferritinemia-Cataract Syndrome | Hereditary Ocular Diseases
