Anna Cozzi Selected Research

Apoferritins

4/2021	Pathogenic mechanism and modeling of neuroferritinopathy.
11/2019	Stem Cell Modeling of Neuroferritinopathy Reveals Iron as a Determinant of Senescence and Ferroptosis during Neuronal Aging.
9/2015	A novel neuroferritinopathy mouse model (FTL 498InsTC) shows progressive brain iron dysregulation, morphological signs of early neurodegeneration and motor coordination deficits.
8/2013	Human L-ferritin deficiency is characterized by idiopathic generalized seizures and atypical restless leg syndrome.
4/2010	Mutant ferritin L-chains that cause neurodegeneration act in a dominant-negative manner to reduce ferritin iron incorporation.
1/2010	Oxidative stress and cell death in cells expressing L-ferritin variants causing neuroferritinopathy.
9/2006	Characterization of the l-ferritin variant 460InsA responsible of a hereditary ferritinopathy disorder.
6/2005	Characterization of nuclear ferritin and mechanism of translocation.
6/2005	Neuroferritinopathy: a neurodegenerative disorder associated with L-ferritin mutation.
10/2003	Identification of two novel mutations in the 5'-untranslated region of H-ferritin using denaturing high performance liquid chromatography scanning.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.

Realize the full power of the drug-disease research graph!

Anna Cozzi Research Topics

Disease

6	Movement Disorders (Movement Disorder) 04/2021 - 06/2005
6	Neuroferritinopathy 04/2021 - 06/2005
4	Pantothenate Kinase-Associated Neurodegeneration (Hallervorden-Spatz Disease) 05/2020 - 09/2012
4	Neurodegenerative Diseases (Neurodegenerative Disease) 10/2016 - 06/2005
3	Iron Overload 01/2022 - 10/2003
3	Neurodegeneration with brain iron accumulation (NBIA) 04/2021 - 12/2012
2	Sideroblastic Anemia 10/2011 - 10/2004
2	Friedreich Ataxia (Friedreich's Ataxia) 01/2009 - 10/2004
1	Hemolysis 01/2018
1	Thalassemia 01/2018
1	Mitochondrial Diseases (Mitochondrial Disease) 10/2016
1	Inborn Genetic Diseases (Disease, Hereditary) 09/2015
1	Seizures (Absence Seizure) 08/2013
1	Restless Legs Syndrome (Restless Legs) 08/2013
1	Starvation 10/2011
1	Refractory Anemia 10/2011
1	Neuroblastoma 01/2010
1	Astrocytoma (Pilocytic Astrocytoma) 06/2005
1	Basal Ganglia Diseases (Basal Ganglia Disease) 06/2005
1	Hyperferritinemia 10/2003
1	hereditary Hyperferritinemia with congenital cataracts 10/2003

Drug/Important Bio-Agent (IBA)

14	IronIBA 04/2021 - 10/2003
10	ApoferritinsIBA 04/2021 - 10/2003
5	Ferritins (Ferritin)IBA 04/2021 - 10/2003
4	NucleotidesIBA 04/2010 - 06/2005
2	Coenzyme A (CoA)IBA 01/2022 - 12/2012
2	FrataxinIBA 01/2009 - 10/2004
2	Messenger RNA (mRNA)IBA 06/2005 - 10/2003
1	CalciumIBA 05/2020
1	pantothenate kinaseIBA 12/2012
1	Reactive Oxygen Species (Oxygen Radicals)IBA 10/2011
1	Proteins (Proteins, Gene)FDA Link 10/2011
1	Protein SIBA 01/2010
1	EnzymesIBA 01/2009
1	Peptides (Polypeptides)IBA 09/2006
1	Amino Acids FDA Link 06/2005
1	Mitochondrial DNA (mtDNA)IBA 10/2004
1	Mitochondrial Proteins (Mitochondrial Protein)IBA 10/2004
1	5' Untranslated Regions (5' UTR)IBA 10/2003

Therapy/Procedure

1	Therapeutics 10/2016