Akbari MT - Search Results

1

Transient expression assay of Agamma-588 (A/G) mutations in the K562 cell line.

Hamid M, Mahjoubi F, Akbari MT, Khanahmad H, Jamshidi F, Zeinali S, Karimipoor M. Hamid M, et al. Among authors: akbari mt. Iran Biomed J. 2011;15(1-2):15-21. Iran Biomed J. 2011. PMID: 21725495 Free PMC article.

2

Globin chain synthesis is a useful complementary tool in the differential diagnosis of thalassemias.

Khatami S, Dehboneh SR, Sadeghi S, Mirzazadeh R, Saeedi P, Bayat P, Najmabadi H, Zeinali S, Akbari MT, Ardjmand M, Amirkhani A. Khatami S, et al. Among authors: akbari mt. Hemoglobin. 2007;31(3):333-41. doi: 10.1080/03630260701462006. Hemoglobin. 2007. PMID: 17654070

3

The Cretan type of nondeletional hereditary persistence of fetal hemoglobin in an Iranian family.

Hamid M, Mahjoubi F, Akbari MT, Zeinali S, Karimipoor M. Hamid M, et al. Among authors: akbari mt. Ann Hematol. 2009 Dec;88(12):1267-8. doi: 10.1007/s00277-009-0756-0. Epub 2009 May 26. Ann Hematol. 2009. PMID: 19468729 No abstract available.

4

A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients.

Hamid M, Karimipoor M, Chaleshtori MH, Akbari MT. Hamid M, et al. Among authors: akbari mt. J Genet. 2009 Dec;88(3):359-62. doi: 10.1007/s12041-009-0054-6. J Genet. 2009. PMID: 20086306 No abstract available.

5

Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family.

Akbari MT, Hamid M, Izadyar M. Akbari MT, et al. Ann Hematol. 2011 Mar;90(3):349-51. doi: 10.1007/s00277-010-1003-4. Epub 2010 Jun 3. Ann Hematol. 2011. PMID: 20521148 Free article. No abstract available.

6

Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.

Mahdieh N, Rabbani B, Wiley S, Akbari MT, Zeinali S. Mahdieh N, et al. Among authors: akbari mt. J Hum Genet. 2010 Oct;55(10):639-48. doi: 10.1038/jhg.2010.96. Epub 2010 Aug 26. J Hum Genet. 2010. PMID: 20739942 Review.

7

Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling.

Mahdieh N, Shirkavand A, Raeisi M, Akbari MT, Tekin M, Zeinali S. Mahdieh N, et al. Among authors: akbari mt. Biochem Biophys Res Commun. 2010 Nov 12;402(2):305-7. doi: 10.1016/j.bbrc.2010.10.021. Epub 2010 Oct 19. Biochem Biophys Res Commun. 2010. PMID: 20937258

8

Investigation of GJB6 large deletions in Iranian patients using quantitative real-time PCR.

Mahdieh N, Raeisi M, Shirkavand A, Bagherian H, Akbari MT, Zeinali S. Mahdieh N, et al. Among authors: akbari mt. Clin Lab. 2010;56(9-10):467-71. Clin Lab. 2010. PMID: 21086793

9

Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variant.

Mahdieh N, Rabbani B, Shirkavand A, Bagherian H, Movahed ZS, Fouladi P, Rahiminejad F, Masoudifard M, Akbari MT, Zeinali S. Mahdieh N, et al. Among authors: akbari mt. Genet Test Mol Biomarkers. 2011 Jul-Aug;15(7-8):489-93. doi: 10.1089/gtmb.2010.0145. Epub 2011 Mar 9. Genet Test Mol Biomarkers. 2011. PMID: 21388256

10

Determination of exon 7 SMN1 deletion in Iranian patients and heterozygous carriers by quantitative real-time PCR.

Akbari MT, Noruzinia M, Mozdarani H, Hamid M. Akbari MT, et al. J Genet. 2011 Apr;90(1):133-6. doi: 10.1007/s12041-011-0038-1. J Genet. 2011. PMID: 21677399 Free article. No abstract available.

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