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Analysis of Ftl-/- mice revealed systemic and brain iron dyshomeostasis, without any noticeable signs of neurodegeneration.
Noncoding G-to-T transversion (c.-168G>T) located in the iron response element (IRE) of the gene coding for ferritin light chain (FTL) cosegregated with cataract in the family.
Ferritin H subunit (show FTH1 Proteins) gene is specifically expressed in melanophore precursor-derived white pigment cells
fumarate increases ferritin gene transcription by activating the NRF2 (show GABPA Proteins) (nuclear factor [erythroid-derived 2]-like 2) transcription factor.
there is no significant relationship between serum ferritin concentrations and depressive symptoms among Chinese adults.
Data suggest that, in homopolymeric H-subunit ferritin (HuHF), iron oxidation proceeds with a 2:1 Fe(II):O(2) stoichiometry at iron level of 2 Fe(II) atoms/H-subunit with generation of H2O2; L-subunit-rich heteropolymeric ferritin also facilitates iron oxidation at the ferroxidase (show CP Proteins) center and additionally promotes oxidation at the mineral surface once iron-binding capacity has been exceeded.
Baseline serum ferritin (SF) did not influence bloodstream infections (BSIs), but higher levels resulted in more invasive fungal infections (IFIs)
High serum ferritin expression is associated with metabolic syndrome.
Hepatitis E virus ORF1 (show NCKIPSD Proteins) encoded macro domain protein interacts with light chain subunit of human ferritin and inhibits its secretion.
Ferritin light chain and ferritin heavy chain (show FTH1 Proteins) are required for the neural differentiation of bone marrow-derived mesenchymal stem cells under extremely low-frequency electromagnetic field.
This study demostrated that FTL mutation progressive brain iron dysregulation, morphological signs of early neurodegeneration and motor coordination deficits show
FTL expression was higher in glioblastoma than in low-grade glioma, and decreased expression of FTL correlated with increased survival in glioblastoma patients.
FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy
Transmission electron microscopy shows a clear selectivity of alkylated ferritin adsorption onto the PCL (show PKD2L1 Proteins) phase while wild ferritin predominantly adsorbs onto the PDTD phase.
This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in this light chain ferritin gene are associated with several neurodegenerative diseases and hyperferritinemia-cataract syndrome. This gene has multiple pseudogenes.
ferritin, light polypeptide
, ferritin L subunit 1
, ferritin H subunit A
, ferritin heavy chain 2
, ferritin heavy chain A
, ferritin light-chain
, ferritin L subunit
, ferritin light chain
, ferritin L-chain
, ferritin light polypeptide-like 3
, ferritin light chain 2
, ferritin light chain 1