Seyyedmohsen Hosseinibarkooie Selected Research

cyclic hexapeptide(Phe-Phe-Trp-Lys-Thr-Phe)- somatostatin (CHP1)

1/2019	PLS3 Overexpression Delays Ataxia in Chp1 Mutant Mice.
2/2018	Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function.
1/2018	CHP1 reduction ameliorates spinal muscular atrophy pathology by restoring calcineurin activity and endocytosis.

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Seyyedmohsen Hosseinibarkooie Research Topics

Disease

7	Spinal Muscular Atrophy (Progressive Muscular Atrophy) 01/2020 - 01/2017
2	Ataxia (Dyssynergia) 01/2019 - 02/2018
2	Neurodegenerative Diseases (Neurodegenerative Disease) 01/2019 - 01/2017
1	Motor Neuron Disease (Primary Lateral Sclerosis) 01/2020
1	Osteoporosis 12/2018
1	Deafness (Deaf Mutism) 02/2018

Drug/Important Bio-Agent (IBA)

6	Proteins (Proteins, Gene)FDA Link 01/2020 - 01/2017
4	plastinIBA 01/2020 - 01/2018
3	cyclic hexapeptide(Phe-Phe-Trp-Lys-Thr-Phe)- somatostatin (CHP1)IBA 01/2019 - 01/2018
2	NeurocalcinIBA 01/2019 - 01/2017
2	CalcineurinIBA 01/2019 - 01/2018
1	CalciumIBA 01/2019
1	Actins (F Actin)IBA 12/2018
1	Biomarkers (Surrogate Marker)IBA 01/2018
1	Antisense OligonucleotidesIBA 01/2018