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FTL gene

Known as: FERRITIN LIGHT CHAIN, NBIA3, ferritin light polypeptide-like 3 
National Institutes of Health

Related topics

Related topics

3 relations
FTH1 geneFerritin Light ChainNeuroferritinopathy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Genome-wide investigation of the clinical implications and molecular mechanism of long noncoding RNA LINC00668 and protein-coding genes in hepatocellular carcinoma
Hepatocellular carcinoma (HCC) is one of the leading causes of tumor-related mortalities worldwide. Long noncoding RNAs have been… 
2018
2018
FTL c.-168G>C Mutation in Hereditary Hyperferritinemia Cataract Syndrome: A New Italian Family
We describe a new Italian family with 7 members affected by hereditary hyperferritinemia cataract syndrome (HHCS), an uncommon… 
2013
2013
Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract
Purpose Cataract is a clinically and genetically heterogeneous disorder of the ocular lens and an important cause of visual… 
Highly Cited
2012
Highly Cited
2012
Ehrlichia chaffeensis TRP32 Interacts with Host Cell Targets That Influence Intracellular Survival
ABSTRACT Ehrlichia chaffeensis is an obligately intracellular bacterium that exhibits tropism for mononuclear phagocytes and… 
Review
2009
Review
2009
[Clinical features of neuroferritinopathy].
Neuroferritinopathy is an autosomal dominant basal ganglia disease with iron accumulation caused by a mutation of the gene… 
2006
2006
A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.
PURPOSE To map and identify the mutated gene for autosomal dominant cataract (ADC) in family ADC4. METHODS Ophthalmic… 
2003
2003
A high-throughput screening system for genes extending life-span
Highly Cited
2002
Highly Cited
2002
Neuroferritinopathy: a window on the role of iron in neurodegeneration.
Neuroferritinopathy is a recently recognised genetic disease resulting in a dominantly inherited movement disorder. The condition… 
2002
2002
Alterations in cellular Ca(2+) and free iron pool by sulfur amino acid deprivation: the role of ferritin light chain down-regulation in prooxidant production.
2002
2002
Screening of ferritin light polypeptide 460–461InsA mutation in Parkinson's disease patients in North America
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