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Results: 1 to 20 of 23

1.

Significant expressivity of Wolfram syndrome: phenotypic assessment of two known and one novel mutation in the WFS1 gene in three Iranian families.

Sobhani M, Tabatabaiefar MA, Rajab A, Kajbafzadeh AM, Noori-Daloii MR.

Mol Biol Rep. 2014 Aug 31. [Epub ahead of print]

PMID:
25173644
[PubMed - as supplied by publisher]
2.

Characterization of wild-type and mutated RET proto- oncogene associated with familial medullary thyroid cancer.

Masbi MH, Mohammadiasl J, Galehdari H, Ahmadzadeh A, Tabatabaiefar MA, Golchin N, Haghpanah V, Rahim F.

Asian Pac J Cancer Prev. 2014;15(5):2027-33.

PMID:
24716929
[PubMed - in process]
Free Article
3.

Identification of Xq22.1-23 as a region linked with hereditary recurrent spontaneous abortion in a family.

Shekouhi S, Baghbani F, Hasanzadeh Nazar-Abadi M, Hamzehloie T, Abbaszadegan MR, Saghafi N, Raoofian R, Zavar Reza J, Ahmadzadeh S, Tabatabaiefar MA, Mojarrad M.

Iran J Reprod Med. 2013 Aug;11(8):659-64.

PMID:
24639804
[PubMed]
Free PMC Article
4.

Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent.

Taghizade Mortezaee F, Tabatabaiefar MA, Hashemzadeh Chaleshtori M, Miraj S.

Cell J. 2014 Summer;16(2):225-30. Epub 2014 May 25.

PMID:
24567938
[PubMed]
Free PMC Article
5.

The role of epigenetics in the induction of fetal hemoglobin: a combination therapy approach.

Ahmadvand M, Noruzinia M, Fard AD, Zohour MM, Tabatabaiefar MA, Soleimani M, Kaviani S, Abroun S, Beiranvand S, Saki N.

Int J Hematol Oncol Stem Cell Res. 2014;8(1):9-14.

PMID:
24505546
[PubMed]
Free PMC Article
6.

Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome.

Yazdanpanahi N, Tabatabaiefar MA, Farrokhi E, Abdian N, Bagheri N, Shahbazi S, Noormohammadi Z, Chaleshtori MH.

Clin Exp Otorhinolaryngol. 2013 Dec;6(4):201-8. doi: 10.3342/ceo.2013.6.4.201. Epub 2013 Nov 29.

PMID:
24353858
[PubMed]
Free PMC Article
7.

UGT1A1 gene mutation due to Crigler-Najjar syndrome in Iranian patients: identification of a novel mutation.

Mohammadi Asl J, Tabatabaiefar MA, Galehdari H, Riahi K, Masbi MH, Zargar Shoshtari Z, Rahim F.

Biomed Res Int. 2013;2013:342371. doi: 10.1155/2013/342371. Epub 2013 Oct 28.

PMID:
24286076
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Study of VSX1 mutations in patients with keratoconus in southwest Iran using PCR-single-strand conformation polymorphism/heteroduplex analysis and sequencing method.

Dehkordi FA, Rashki A, Bagheri N, Chaleshtori MH, Memarzadeh E, Salehi A, Ghatreh H, Zandi F, Yazdanpanahi N, Tabatabaiefar MA, Chaleshtori MH.

Acta Cytol. 2013;57(6):646-51. doi: 10.1159/000353297. Epub 2013 Oct 1.

PMID:
24107477
[PubMed - indexed for MEDLINE]
9.

Is the IL-10 -819 polymorphism associated with visceral leishmaniasis?

Hajilooi M, Sardarian K, Dadmanesh M, Matini M, Lotfi P, Bazmani A, Tabatabaiefar MA, Arababadi MK, Momeni M.

Inflammation. 2013 Dec;36(6):1513-8. doi: 10.1007/s10753-013-9693-0.

PMID:
23912644
[PubMed - indexed for MEDLINE]
10.

Molecular characterization of WFS1 in an Iranian family with Wolfram syndrome reveals a novel frameshift mutation associated with early symptoms.

Sobhani M, Tabatabaiefar MA, Rajab A, Kajbafzadeh AM, Noori-Daloii MR.

Gene. 2013 Oct 10;528(2):309-13. doi: 10.1016/j.gene.2013.06.040. Epub 2013 Jul 8.

PMID:
23845777
[PubMed - indexed for MEDLINE]
11.

A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect.

Davoudi-Dehaghani E, Zeinali S, Mahdieh N, Shirkavand A, Bagherian H, Tabatabaiefar MA.

Int J Pediatr Otorhinolaryngol. 2013 May;77(5):821-6. doi: 10.1016/j.ijporl.2013.02.021. Epub 2013 Mar 21.

PMID:
23523375
[PubMed - indexed for MEDLINE]
12.

Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: assessment of GJB4, GJA1, and GJC3.

Kooshavar D, Tabatabaiefar MA, Farrokhi E, Abolhasani M, Noori-Daloii MR, Hashemzadeh-Chaleshtori M.

Int J Pediatr Otorhinolaryngol. 2013 Feb;77(2):189-93. doi: 10.1016/j.ijporl.2012.10.015. Epub 2012 Nov 8.

PMID:
23141803
[PubMed - indexed for MEDLINE]
13.

A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment.

Schrauwen I, Helfmann S, Inagaki A, Predoehl F, Tabatabaiefar MA, Picher MM, Sommen M, Seco CZ, Oostrik J, Kremer H, Dheedene A, Claes C, Fransen E, Chaleshtori MH, Coucke P, Lee A, Moser T, Van Camp G.

Am J Hum Genet. 2012 Oct 5;91(4):636-45. doi: 10.1016/j.ajhg.2012.08.018. Epub 2012 Sep 13.

PMID:
22981119
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Association of the TCF7L2 rs12255372 (G/T) variant with type 2 diabetes mellitus in an Iranian population.

Alami FM, Ahmadi M, Bazrafshan H, Tabarraei A, Khosravi A, Tabatabaiefar MA, Samaei NM.

Genet Mol Biol. 2012 Apr;35(2):413-7. doi: 10.1590/S1415-47572012005000029. Epub 2012 May 17.

PMID:
22888288
[PubMed]
Free PMC Article
15.

Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform.

De Keulenaer S, Hellemans J, Lefever S, Renard JP, De Schrijver J, Van de Voorde H, Tabatabaiefar MA, Van Nieuwerburgh F, Flamez D, Pattyn F, Scharlaken B, Deforce D, Bekaert S, Van Criekinge W, Vandesompele J, Van Camp G, Coucke P.

BMC Med Genomics. 2012 May 18;5:17. doi: 10.1186/1755-8794-5-17.

PMID:
22607986
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss.

Yazdanpanahi N, Chaleshtori MH, Tabatabaiefar MA, Noormohammadi Z, Farrokhi E, Najmabadi H, Shahbazi S, Hosseinipour A.

Int J Pediatr Otorhinolaryngol. 2012 Jun;76(6):845-50. doi: 10.1016/j.ijporl.2012.02.056. Epub 2012 Mar 23.

PMID:
22444735
[PubMed - indexed for MEDLINE]
17.

Bilateral dislocation of temporomandibular joint induced by haloperidol following suicide attempt: a case report.

Zakariaei Z, Taslimi S, Tabatabaiefar MA, Arghand Dargahi M.

Acta Med Iran. 2012;50(3):213-5.

PMID:
22418992
[PubMed - indexed for MEDLINE]
Free Article
18.

Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.

Montazer Zohour M, Tabatabaiefar MA, Dehkordi FA, Farrokhi E, Akbari MT, Chaleshtori MH.

Genet Test Mol Biomarkers. 2012 Apr;16(4):271-8. doi: 10.1089/gtmb.2011.0176. Epub 2011 Nov 11.

PMID:
22077646
[PubMed - indexed for MEDLINE]
19.

Estrogen receptor alpha gene polymorphisms are associated with type 2 diabetes and fasting glucose in male subjects.

Meshkani R, Saberi H, MohammadTaghvaei N, Tabatabaiefar MA.

Mol Cell Biochem. 2012 Jan;359(1-2):225-33. doi: 10.1007/s11010-011-1017-9. Epub 2011 Aug 12.

PMID:
21837403
[PubMed - indexed for MEDLINE]
20.

DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment.

Tabatabaiefar MA, Alasti F, Shariati L, Farrokhi E, Fransen E, Nooridaloii MR, Chaleshtori MH, Van Camp G.

Clin Genet. 2011 Jun;79(6):594-8. doi: 10.1111/j.1399-0004.2010.01593.x. No abstract available.

PMID:
21542834
[PubMed - indexed for MEDLINE]

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