Keramatipour M - Search Results

1

Saberi M, Golchehre Z, Karamzade A, Entezam M, Eshaghkhani Y, Alavinejad E, Khojasteh Jafari H, Keramatipour M. Saberi M, et al. Among authors: keramatipour m. Iran Biomed J. 2019 Sep;23(5):362-8. doi: 10.29252/.23.5.362. Epub 2019 May 19. Iran Biomed J. 2019. PMID: 31103025 Free PMC article. Review.

2

Genetic analysis of Iranian autosomal dominant polycystic kidney disease: new insight to haplotype analysis.

Entezam M, Khatami MR, Saddadi F, Ayati M, Roozbeh J, Saghafi H, Keramatipour M. Entezam M, et al. Among authors: keramatipour m. Cell Mol Biol (Noisy-le-grand). 2016 Feb 4;62(2):15-20. Cell Mol Biol (Noisy-le-grand). 2016. PMID: 26950445

3

The individual or combinational effects of Hesperetin and Letrozole on the activity and expression of aromatase in MCF-7 cells.

Rahideh ST, Shidfar F, Nourbakhsh M, Hoseini M, Koohdani F, Entezam M, Keramatipour M. Rahideh ST, et al. Among authors: keramatipour m. Cell Mol Biol (Noisy-le-grand). 2016 May 30;62(6):38-43. Cell Mol Biol (Noisy-le-grand). 2016. PMID: 27262800

4

PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data.

Entezam M, Khatami MR, Saddadi F, Ayati M, Roozbeh J, Keramatipour M. Entezam M, et al. Among authors: keramatipour m. Kidney Res Clin Pract. 2016 Jun;35(2):96-101. doi: 10.1016/j.krcp.2016.02.003. Epub 2016 Feb 27. Kidney Res Clin Pract. 2016. PMID: 27366664 Free PMC article.

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: keramatipour m. 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

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. Among authors: keramatipour m. 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.

7

Comparison of Two Different PCR-based Methods for Detection of GAA Expansions in Frataxin Gene.

Entezam M, Amirfiroozi A, Togha M, Keramatipour M. Entezam M, et al. Among authors: keramatipour m. Iran J Public Health. 2017 Feb;46(2):222-228. Iran J Public Health. 2017. PMID: 28451558 Free PMC article.

8

Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration Families.

Ghofrani M, Yahyaei M, Brunner HG, Cremers FP, Movasat M, Imran Khan M, Keramatipour M. Ghofrani M, et al. Among authors: keramatipour m. Iran Biomed J. 2017 Sep;21(5):294-302. doi: 10.18869/acadpub.ibj.21.5.294. Epub 2017 May 2. Iran Biomed J. 2017. PMID: 28460491 Free PMC article.

9

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: keramatipour m. Iran J Public Health. 2017 Apr;46(4):560-564. Iran J Public Health. 2017. PMID: 28540274 Free PMC article.

10

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: keramatipour m. 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

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