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Items: 1 to 20 of 35

1.

A novel splicing variant in FLNC gene responsible for a highly penetrant familial dilated cardiomyopathy in an extended Iranian family.

Nozari A, Aghaei-Moghadam E, Zeinaloo A, Mollazadeh R, Majnoon MT, Alavi A, Ghasemi Firouzabadi S, Mohammadzadeh A, Banihashemi S, Nikzaban M, Najmabadi H, Behjati F.

Gene. 2018 Jun 15;659:160-167. doi: 10.1016/j.gene.2018.03.044. Epub 2018 Mar 15.

PMID:
29551499
2.

Improvement of hepatogenic differentiation of iPS cells on an aligned polyethersulfone compared to random nanofibers.

Mahmoodinia Maymand M, Soleimanpour-Lichaei HR, Ardeshirylajimi A, Soleimani M, Enderami SE, Nojehdehi S, Behjati F, Kabir Salmani M.

Artif Cells Nanomed Biotechnol. 2018 Jun;46(4):853-860. doi: 10.1080/21691401.2017.1345929. Epub 2017 Jul 11.

PMID:
28695746
3.

miRNA-Related Polymorphisms in miR-423 (rs6505162) and PEX6 (rs1129186) and Risk of Esophageal Squamous Cell Carcinoma in an Iranian Cohort.

Nariman-Saleh-Fam Z, Bastami M, Somi MH, Behjati F, Mansoori Y, Daraei A, Saadatian Z, Nariman-Saleh-Fam L, Mahmoodzadeh H, Makhdoumi Y, Tabrizi FV, Ebrahimi-Sharif B, Hezarian A, Naghashi S, Abbaszadegan MR, Tavakkoly-Bazzaz J.

Genet Test Mol Biomarkers. 2017 Jun;21(6):382-390. doi: 10.1089/gtmb.2016.0346. Epub 2017 Apr 21.

PMID:
28430524
4.

Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications.

Ghasemi Firouzabadi S, Vameghi R, Kariminejad R, Darvish H, Banihashemi S, Firouzkouhi Moghaddam M, Jamali P, Farbod Mofidi Tehrani H, Dehghani H, Raeisoon MR, Narooie-Nejad M, Jamshidi J, Tafakhori A, Sadabadi S, Behjati F.

Int J Mol Cell Med. 2016 Fall;5(4):236-245. Epub 2016 Dec 5.

5.

Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing.

Aristidou C, Koufaris C, Theodosiou A, Bak M, Mehrjouy MM, Behjati F, Tanteles G, Christophidou-Anastasiadou V, Tommerup N, Sismani C.

PLoS One. 2017 Jan 10;12(1):e0169935. doi: 10.1371/journal.pone.0169935. eCollection 2017. Erratum in: PLoS One. 2017 Mar 15;12 (3):e0174190.

6.

Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome.

Firouzabadi SG, Kariminejad R, Vameghi R, Darvish H, Ghaedi H, Banihashemi S, Firouzkouhi Moghaddam M, Jamali P, Mofidi Tehrani HF, Dehghani H, Narooie-Nejad M, Jamshidi J, Tafakhori A, Sadabadi S, Najmabadi H, Behjati F.

Mol Neurobiol. 2017 Nov;54(9):7019-7027. doi: 10.1007/s12035-016-0202-y. Epub 2016 Oct 28.

PMID:
27796743
7.

In silico dissection of miRNA targetome polymorphisms and their role in regulating miRNA-mediated gene expression in esophageal cancer.

Nariman-Saleh-Fam Z, Bastami M, Somi MH, Samadi N, Abbaszadegan MR, Behjati F, Ghaedi H, Tavakkoly-Bazzaz J, Masotti A.

Cell Biochem Biophys. 2016 Dec;74(4):483-497. Epub 2016 Aug 12.

PMID:
27518186
8.

Mutation Screening of BRCA Genes in 10 Iranian Males with Breast Cancer.

Zorrieh Zahra A, Kadkhoda S, Behjati F, Aghakhani Moghaddam F, Badiei A, Sirati F, Afshin Alavi H, Atri M, Omranipour R, Keyhani E.

Int J Mol Cell Med. 2016 Spring;5(2):114-22. Epub 2016 May 9.

9.

The Genotoxic and Cytotoxic Effects of Bisphenol-A (BPA) in MCF-7 Cell Line and Amniocytes.

Aghajanpour-Mir SM, Zabihi E, Akhavan-Niaki H, Keyhani E, Bagherizadeh I, Biglari S, Behjati F.

Int J Mol Cell Med. 2016 Winter;5(1):19-29.

10.

BOD1 Is Required for Cognitive Function in Humans and Drosophila.

Esmaeeli-Nieh S, Fenckova M, Porter IM, Motazacker MM, Nijhof B, Castells-Nobau A, Asztalos Z, WeiƟmann R, Behjati F, Tzschach A, Felbor U, Scherthan H, Sayfati SM, Ropers HH, Kahrizi K, Najmabadi H, Swedlow JR, Schenck A, Kuss AW.

PLoS Genet. 2016 May 11;12(5):e1006022. doi: 10.1371/journal.pgen.1006022. eCollection 2016 May.

11.

Evaluation of chromosomal aberrations caused by air pollutants in some taxi drivers from two polluted districts of urban Tehran and its comparison with drivers from rural areas of Lahijan: a pilot study.

Taghizadeh S, Najmabadi H, Kamali K, Behjati F.

J Environ Health Sci Eng. 2014 Dec 19;12(1):144. doi: 10.1186/s40201-014-0144-0. eCollection 2014.

12.

Phenotypical characterization of 13q deletion syndrome: Report of two cases.

Bagherizadeh E, Shafaghati Y, Hadipour F, Behjati F.

Indian J Hum Genet. 2014 Apr;20(2):203-5. doi: 10.4103/0971-6866.142912.

13.

Mutation analysis of androgen receptor gene: multiple uses for a single test.

Shojaei A, Behjati F, Ebrahimzadeh-Vesal R, Razzaghy-Azar M, Derakhshandeh-Peykar P, Izadi P, Kajbafzadeh AM, Dowlatih MA, Karami F, Tavakkoly-Bazzaz J.

Gene. 2014 Dec 1;552(2):234-8. doi: 10.1016/j.gene.2014.09.038. Epub 2014 Sep 18.

PMID:
25241384
14.

Identification of Chromosome Abnormalities in Subtelomeric Regions Using Multiplex Ligation Dependent Probe Amplification (MLPA) Technique in 100 Iranian Patients With Idiopathic Mental Retardation.

Behjati F, Ghasemi Firouzabadi S, Sajedi F, Kahrizi K, Najafi M, Ebrahimizade Ghasemlou B, Shafeghati Y, Behnia F, Mohammadi Arya AR, Karimi H, Hadipour F, Hadipour Z, Jamali P, Kariminejad R, Darvish H, Bahman I, Bagherizadeh E, Najmabadi H, Vameghi R.

Iran Red Crescent Med J. 2013 Oct;15(10):e8221. doi: 10.5812/ircmj.8221. Epub 2013 Oct 5.

15.

Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization.

Behjati F, Firouzabadi SG, Kariminejad R, Vameghi R, Sajedi F, Shafaghati Y, Ghasemlou BE, Shojaei A, Jamali P, Bahman I, Najmabadi H.

Indian J Hum Genet. 2013 Oct;19(4):443-8. doi: 10.4103/0971-6866.124373.

16.

Angiogenesis markers in breast cancer--potentially useful tools for priority setting of anti-angiogenic agents.

Keyhani E, Muhammadnejad A, Behjati F, Sirati F, Khodadadi F, Karimlou M, Moghaddam FA, Pazhoomand R.

Asian Pac J Cancer Prev. 2013;14(12):7651-6.

17.

Detection of HER2 status in breast cancer: comparison of current methods with MLPA and real-time RT-PCR.

Pazhoomand R, Keyhani E, Banan M, Najmabadi H, Khodadadi F, Iraniparast A, Feiz F, Majidzadeh K, Bahman I, Moghadam FA, Sobhani AM, Muhammadnejad A, Abedini SS, Behjati F.

Asian Pac J Cancer Prev. 2013;14(12):7621-8.

18.

Fraccaro syndrome: report of two Iranian cases: an infant and an adult in a family.

Hadipour F, Shafeghati Y, Bagherizadeh E, Behjati F, Hadipour Z.

Acta Med Iran. 2013;51(12):907-9.

19.

A novel mutation in MCPH1 gene in an Iranian family with primary microcephaly.

Hosseini MM, Tonekaboni SH, Papari E, Bahman I, Behjati F, Kahrizi K, Najmabadi H.

J Pak Med Assoc. 2012 Nov;62(11):1244-7.

20.

Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings.

Shojaei A, Behjati F, Derakhshandeh-Peykar P, Razzaghy-Azar M, Otukesh H, Kariminejad R, Dowlati MA, Rashidi-Nezhad A, Tavakkoly-Bazzaz J.

Gene. 2013 Mar 15;517(1):137-45. doi: 10.1016/j.gene.2012.11.013. Epub 2012 Nov 30.

PMID:
23201896

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