Gharesouran J - Search Results

1

First Report of Congenital Short Bowel Syndrome in an Iranian Patient Caused by a Mutation in the CLMP Gene.

Gharesouran J, Esfahani BS, Valilou SF, Moradi M, Mousavi MH, Rezazadeh M. Gharesouran J, et al. J Pediatr Genet. 2019 Jun;8(2):73-80. doi: 10.1055/s-0038-1675339. Epub 2018 Oct 26. J Pediatr Genet. 2019. PMID: 31061750 Free PMC article.

2

Genetic association of TNF-α-308 G/A and -863 C/A polymorphisms with late onset Alzheimer's disease in Azeri Turk population of Iran.

Ardebili SM, Yeghaneh T, Gharesouran J, Rezazadeh M, Farhoudi M, Ayromlou H, Talebi M, Ghojazadeh M. Ardebili SM, et al. Among authors: gharesouran j. J Res Med Sci. 2011 Aug;16(8):1006-13. J Res Med Sci. 2011. PMID: 22279475 Free PMC article.

3

Genetic evidence for the involvement of variants at APOE, BIN1, CR1, and PICALM loci in risk of late-onset Alzheimer's disease and evaluation for interactions with APOE genotypes.

Gharesouran J, Rezazadeh M, Khorrami A, Ghojazadeh M, Talebi M. Gharesouran J, et al. J Mol Neurosci. 2014 Dec;54(4):780-6. doi: 10.1007/s12031-014-0377-5. Epub 2014 Jul 15. J Mol Neurosci. 2014. PMID: 25022885

4

A primate-specific functional GTTT-repeat in the core promoter of CYTH4 is linked to bipolar disorder in human.

Rezazadeh M, Gharesouran J, Mirabzadeh A, Khorram Khorshid HR, Biglarian A, Ohadi M. Rezazadeh M, et al. Among authors: gharesouran j. Prog Neuropsychopharmacol Biol Psychiatry. 2015 Jan 2;56:161-7. doi: 10.1016/j.pnpbp.2014.09.001. Epub 2014 Sep 18. Prog Neuropsychopharmacol Biol Psychiatry. 2015. PMID: 25240857

5

Dominant and Protective Role of the CYTH4 Primate-Specific GTTT-Repeat Longer Alleles Against Neurodegeneration.

Rezazadeh M, Gharesouran J, Movafagh A, Taheri M, Darvish H, Emamalizadeh B, Shahmohammadibeni N, Khorram Khorshid HR, Behmanesh M, Sahraian MA, Ohadi M. Rezazadeh M, et al. Among authors: gharesouran j. J Mol Neurosci. 2015 Jul;56(3):593-6. doi: 10.1007/s12031-015-0542-5. Epub 2015 Apr 1. J Mol Neurosci. 2015. PMID: 25823437

6

Genetic Factors Affecting Late-Onset Alzheimer's Disease Susceptibility.

Rezazadeh M, Khorrami A, Yeghaneh T, Talebi M, Kiani SJ, Heshmati Y, Gharesouran J. Rezazadeh M, et al. Among authors: gharesouran j. Neuromolecular Med. 2016 Mar;18(1):37-49. doi: 10.1007/s12017-015-8376-4. Epub 2015 Nov 9. Neuromolecular Med. 2016. PMID: 26553058

7

Association Study of ANRIL Genetic Variants and Multiple Sclerosis.

Rezazadeh M, Gharesouran J, Moradi M, Noroozi R, Omrani MD, Taheri M, Ghafouri-Fard S. Rezazadeh M, et al. Among authors: gharesouran j. J Mol Neurosci. 2018 May;65(1):54-59. doi: 10.1007/s12031-018-1069-3. Epub 2018 Apr 30. J Mol Neurosci. 2018. PMID: 29713948

8

Assessment of expression of RELN signaling pathway in multiple sclerosis patients.

Talebian S, Gharesouran J, Ghafouri-Fard S, Esfahani BS, Arsang-Jang S, Omrani MD, Taheri M, Rezazadeh M. Talebian S, et al. Among authors: gharesouran j. Immunobiology. 2019 May;224(3):402-407. doi: 10.1016/j.imbio.2019.02.007. Epub 2019 Feb 12. Immunobiology. 2019. PMID: 30777599

9

Genetic discoveries and advances in late-onset Alzheimer's disease.

Rezazadeh M, Hosseinzadeh H, Moradi M, Salek Esfahani B, Talebian S, Parvin S, Gharesouran J. Rezazadeh M, et al. Among authors: gharesouran j. J Cell Physiol. 2019 Aug;234(10):16873-16884. doi: 10.1002/jcp.28372. Epub 2019 Feb 20. J Cell Physiol. 2019. PMID: 30790294 Review.

10

The Neuronal Ceroid Lipofuscinoses-Linked Loss of Function CLN5 and CLN8 Variants Disrupt Normal Lysosomal Function.

Parvin S, Rezazadeh M, Hosseinzadeh H, Moradi M, Shiva S, Gharesouran J. Parvin S, et al. Among authors: gharesouran j. Neuromolecular Med. 2019 Jun;21(2):160-169. doi: 10.1007/s12017-019-08529-7. Epub 2019 Mar 27. Neuromolecular Med. 2019. PMID: 30919163

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