Seifi M - Search Results

1

Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.

Seifi M, Footz T, Taylor SA, Elhady GM, Abdalla EM, Walter MA. Seifi M, et al. Acta Ophthalmol. 2016 Nov;94(7):e571-e579. doi: 10.1111/aos.13030. Epub 2016 Mar 24. Acta Ophthalmol. 2016. PMID: 27009473 Free article.

2

Axenfeld-Rieger syndrome.

Seifi M, Walter MA. Seifi M, et al. Clin Genet. 2018 Jun;93(6):1123-1130. doi: 10.1111/cge.13148. Epub 2018 Jan 25. Clin Genet. 2018. PMID: 28972279 Review.

3

Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms.

Seifi M, Walter MA. Seifi M, et al. PLoS One. 2018 Apr 17;13(4):e0195971. doi: 10.1371/journal.pone.0195971. eCollection 2018. PLoS One. 2018. PMID: 29664915 Free PMC article.

4

Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld-Rieger Syndrome.

Seifi M, Footz T, Taylor SA, Walter MA. Seifi M, et al. Hum Mutat. 2017 Feb;38(2):169-179. doi: 10.1002/humu.23141. Epub 2016 Nov 21. Hum Mutat. 2017. PMID: 27804176

5

FOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25.

Rasnitsyn A, Doucette L, Seifi M, Footz T, Raymond V, Walter MA. Rasnitsyn A, et al. Among authors: seifi m. PLoS One. 2017 Jun 2;12(6):e0178518. doi: 10.1371/journal.pone.0178518. eCollection 2017. PLoS One. 2017. PMID: 28575017 Free PMC article.

6

The interactions of genes, age, and environment in glaucoma pathogenesis.

Doucette LP, Rasnitsyn A, Seifi M, Walter MA. Doucette LP, et al. Among authors: seifi m. Surv Ophthalmol. 2015 Jul-Aug;60(4):310-26. doi: 10.1016/j.survophthal.2015.01.004. Epub 2015 Feb 4. Surv Ophthalmol. 2015. PMID: 25907525 Review.

7

Mutation analysis of the CYP21A2 gene in congenital adrenal hyperplasia.

Forouzanfar K, Seifi M, Hashemi-Gorji F, Karimi N, Estiar MA, Karimoei M, Sakhinia E, Karimipour M, Ghergherehchi R. Forouzanfar K, et al. Among authors: seifi m. Cell Mol Biol (Noisy-le-grand). 2015 Aug 17;61(4):51-5. Cell Mol Biol (Noisy-le-grand). 2015. PMID: 26278268

8

MYCN gene amplification in patients with neuroblastic tumors.

Estiar MA, Fazilaty H, Aslanabadi S, Seifi M, Varghaei P, Rezamand A. Estiar MA, et al. Among authors: seifi m. Cell Mol Biol (Noisy-le-grand). 2014 Sep 16;60(3):23-8. Cell Mol Biol (Noisy-le-grand). 2014. PMID: 25231001

9

Mutations of the connexin 37 and 40 gap-junction genes in patients with acute myocardial infarction.

Seifi M, Fallah S, Ghasemi A, Aghajani H, Razaghi M, Danaei N. Seifi M, et al. Clin Lab. 2013;59(3-4):343-8. doi: 10.7754/clin.lab.2012.120305. Clin Lab. 2013. PMID: 23724624

10

Detection of immunoglobulin IGH gene rearrangements on formalin-fixed, paraffin embedded tissue in lymphoid malignancies.

Moharrami G, Ghorbian S, Seifi M, Estiar MA, Fakhrjoo A, Sakhinia M, Sakhinia E. Moharrami G, et al. Among authors: seifi m. Cell Mol Biol (Noisy-le-grand). 2014 Dec 8;60(4):43-7. Cell Mol Biol (Noisy-le-grand). 2014. PMID: 25481017

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