Talebi S - Search Results

1

An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria.

Talebi S, Entezam M, Mohajer N, Kazemi-Sefat GE, Razipour M, Ahmadloo S, Setoodeh A, Keramatipour M. Talebi S, et al. Cell J. 2016 Jul-Sep;18(2):229-36. doi: 10.22074/cellj.2016.4318. Epub 2016 May 30. Cell J. 2016. PMID: 27540528 Free PMC article.

2

Impact of vitamin A supplementation on RAR gene expression in multiple sclerosis patients.

Bitarafan S, Harirchian MH, Sahraian MA, Keramatipour M, Beladi Moghadam N, Togha M, Nafissi S, Siassi F, Eshraghian MR, Mohammadzadeh Honarvar N, Ansar H, Talebi S, Saboor-Yarghi AA. Bitarafan S, et al. Among authors: talebi s. J Mol Neurosci. 2013 Oct;51(2):478-84. doi: 10.1007/s12031-013-0090-9. Epub 2013 Aug 17. J Mol Neurosci. 2013. PMID: 23955709 Clinical Trial.

3

Investigating the Effect of rs3783605 Single-nucleotide Polymorphism on the Activity of VCAM-1 Promoter in Human Umbilical Vein Endohelial Cells.

Dadgar Pakdel F, Keramatipour M, Noorbakhsh F, Talebi S, Vodjgani M. Dadgar Pakdel F, et al. Among authors: talebi s. Iran J Allergy Asthma Immunol. 2015 Apr;14(2):179-87. Iran J Allergy Asthma Immunol. 2015. PMID: 25780884 Free article.

4

Comparable vitamin D3 metabolism in the endometrium of patients with recurrent spontaneous abortion and fertile controls.

Tavakoli M, Salek-Moghaddam A, Jeddi-Tehrani M, Talebi S, Kazemi-Sefat GE, Vafaei S, Mohammadzadeh A, Sheikhhassani S, Zarnani AH. Tavakoli M, et al. Among authors: talebi s. Mol Reprod Dev. 2015 May;82(5):356-64. doi: 10.1002/mrd.22486. Epub 2015 Apr 23. Mol Reprod Dev. 2015. PMID: 25914243

5

Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient.

Alaei MR, Talebi S, Ghofrani M, Taghizadeh M, Keramatipour M. Alaei MR, et al. Among authors: talebi s. Iran Biomed J. 2016 Nov;20(5):295-301. doi: 10.22045/ibj.2016.07. Epub 2016 Jul 25. Iran Biomed J. 2016. PMID: 27452399 Free PMC article.

6

Functional Analysis of A Novel Splicing Mutation in The Mutase Gene of Two Unrelated Pedigrees.

Ahmadloo S, Talebi S, Miryounesi M, Pasalar P, Keramatipour M. Ahmadloo S, et al. Among authors: talebi s. Cell J. 2016 Fall;18(3):397-404. doi: 10.22074/cellj.2016.4568. Epub 2016 Aug 24. Cell J. 2016. PMID: 27602322 Free PMC article.

7

Comparison of the effects of nobiletin and letrozole on the activity and expression of aromatase in the MCF-7 breast cancer cell line.

Rahideh ST, Keramatipour M, Nourbakhsh M, Koohdani F, Hoseini M, Talebi S, Shidfar F. Rahideh ST, et al. Among authors: talebi s. Biochem Cell Biol. 2017 Aug;95(4):468-473. doi: 10.1139/bcb-2016-0206. Epub 2017 Feb 1. Biochem Cell Biol. 2017. PMID: 28177754

8

Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report.

Razipour M, Kooshavar D, Alavinejad E, Sajedi SZ, Mohajer N, Setoodeh A, Talebi S, Keramatipour M. Razipour M, et al. Among authors: talebi s. Iran J Public Health. 2017 Apr;46(4):560-564. Iran J Public Health. 2017. PMID: 28540274 Free PMC article.

9

Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes.

Razipour M, Alavinejad E, Sajedi SZ, Talebi S, Entezam M, Mohajer N, Kazemi-Sefat GE, Gharesouran J, Setoodeh A, Mohaddes Ardebili SM, Keramatipour M. Razipour M, et al. Among authors: talebi s. Metab Brain Dis. 2017 Oct;32(5):1685-1691. doi: 10.1007/s11011-017-0048-7. Epub 2017 Jul 4. Metab Brain Dis. 2017. PMID: 28676969

10

A Novel Variant in the PAH Gene Causing Phenylketonuria in an Iranian Pedigree.

Alavinejad E, Sajedi SZ, Razipour M, Entezam M, Mohajer N, Setoodeh A, Talebi S, Keramatipour M. Alavinejad E, et al. Among authors: talebi s. Avicenna J Med Biotechnol. 2017 Jul-Sep;9(3):146-149. Avicenna J Med Biotechnol. 2017. PMID: 28706611 Free PMC article.

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