Sirous Zeinali

Sirous Zeinali

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Sirous Zeinali

Publications by authors named "Sirous Zeinali"

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Biosimilar Gene Therapy: Investigational Assessment of Secukinumab Gene Therapy.

Cell J 2020 Jan 29;21(4):433-443. Epub 2019 Jul 29.

Cellular and Molecular Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.Electronic

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http://dx.doi.org/10.22074/cellj.2020.6309DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722441PMC
January 2020

Genetic testing of Mucopolysaccharidoses disease using multiplex PCR- based panels of STR markers: in silico analysis of novel mutations.

Metab Brain Dis 2019 Oct 24;34(5):1447-1455. Epub 2019 Jun 24.

Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Pasteur St, Tehran, Iran.

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http://dx.doi.org/10.1007/s11011-019-00434-zDOI Listing
October 2019

Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations.

J Hepatol 2019 Aug 4;71(2):366-370. Epub 2019 Apr 4.

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, and Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, PA, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S01688278193022
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http://dx.doi.org/10.1016/j.jhep.2019.03.026DOI Listing
August 2019

Improvement of K562 Cell Line Transduction by FBS Mediated Attachment to the Cell Culture Plate.

Biomed Res Int 2019 27;2019:9540702. Epub 2019 Mar 27.

Department of Virology, Pasteur Institute of Iran, Tehran 1316943551, Iran.

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http://dx.doi.org/10.1155/2019/9540702DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6457364PMC
August 2019

Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations.

Metab Brain Dis 2019 Aug 22;34(4):1145-1156. Epub 2019 May 22.

Dr. Zeinali's Medical Genetics Laboratory, Kawsar Human Genetics Research Center, No. 41 Majlesi St., Vali Asr St., Tehran, 1595645513, Iran.

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http://dx.doi.org/10.1007/s11011-019-00435-yDOI Listing
August 2019

Endometriotic Mesenchymal Stem Cells Epigenetic Pathogenesis: Deregulation of , , and in A Functional Imbalanced Epigenetic Disease.

Cell J 2019 Jul 20;21(2):179-185. Epub 2019 Feb 20.

Endometriosis Research Center, Iran University of Medical Science, Tehran, Iran.

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http://dx.doi.org/10.22074/cellj.2019.5903DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397607PMC
July 2019

Microsatellite Marker Analysis for Laboratory Mice Profiling.

Adv Biomed Res 2019 28;8:40. Epub 2019 Jun 28.

Department of Quality Control, Pasteur Institute of Iran, Tehran, Iran.

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http://dx.doi.org/10.4103/abr.abr_53_19DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6621418PMC
June 2019

A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis.

J Invest Dermatol 2019 May 29;139(5):1195-1198. Epub 2018 Nov 29.

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, and Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S0022202X183289
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http://dx.doi.org/10.1016/j.jid.2018.11.011DOI Listing
May 2019

Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families

Iran Biomed J 2019 05 24;23(3):228-34. Epub 2019 Feb 24.

Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462296PMC
May 2019

Factor XIII Deficiency in Western Afghanistan due to a Novel F13A Gene Mutation.

Int J Lab Hematol 2019 May 28. Epub 2019 May 28.

Department of Hematology and Blood Transfusion, School of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran.

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http://dx.doi.org/10.1111/ijlh.13050DOI Listing
May 2019

Therapeutic targeting of angiogenesis molecular pathways in angiogenesis-dependent diseases.

Biomed Pharmacother 2019 Feb 13;110:775-785. Epub 2018 Dec 13.

Biotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran; Molecular Medicine Research Centre, Tabriz University of Medical Sciences, Tabriz, Iran. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S07533322183635
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http://dx.doi.org/10.1016/j.biopha.2018.12.022DOI Listing
February 2019

Epidermodysplasia Verruciformis: Genetic Heterogeneity and EVER1 and EVER2 Mutations Revealed by Genome-Wide Analysis.

J Invest Dermatol 2019 Jan 20;139(1):241-244. Epub 2018 Jul 20.

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College and Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S0022202X183236
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http://dx.doi.org/10.1016/j.jid.2018.07.010DOI Listing
January 2019

Corrigendum to "Potential circulating miRNA signature for early detection of NSCLC" [Cancer Genetics 216-217 (2017) 150-158].

Cancer Genet 2018 12 15;228-229:127. Epub 2018 Jun 15.

Lung Transplantation Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

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http://dx.doi.org/10.1016/j.cancergen.2018.05.002DOI Listing
December 2018

Prevalence of factor VIII inhibitors among Afghan patients with hemophilia A: a first report.

Blood Coagul Fibrinolysis 2018 Dec;29(8):697-700

Department of Molecular Medicine, Biotechnology Research Centre, Pasteur Institute.

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http://dx.doi.org/10.1097/MBC.0000000000000780DOI Listing
December 2018

Transient expression of anti-VEFGR2 nanobody in .

3 Biotech 2018 Dec 15;8(12):484. Epub 2018 Nov 15.

1Department of Plant Breeding and Biotechnology, Faculty of Agriculture, Tarbiat Modares University, P.O. Box 14115-336, Tehran, Islamic Republic of Iran.

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http://dx.doi.org/10.1007/s13205-018-1500-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237708PMC
December 2018

Molecular genetic study of Calpainopathy in Iran.

Gene 2018 Nov 27;677:259-265. Epub 2018 Jul 27.

Kawsar Human Genetics Research Center, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2018.07.067DOI Listing
November 2018

The first successful application of preimplantation genetic diagnosis for hearing loss in Iran.

Cell Mol Biol (Noisy-le-grand) 2018 Jun 30;64(9):1718. Epub 2018 Jun 30.

Vali-e-Asr Reproductive Health Research Center, Tehran University of Medical Sciences, Tehran, Iran.

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June 2018

Expression of VGRNb-PE immunotoxin in transplastomic lettuce (Lactuca sativa L.).

Plant Mol Biol 2018 May 10;97(1-2):103-112. Epub 2018 Apr 10.

Biotechnology Research Center, Biotechnology Department, Venom & Biotherapeutics Molecules Lab., Pasteur Institute of Iran, Tehran, Iran.

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http://dx.doi.org/10.1007/s11103-018-0726-9DOI Listing
May 2018

The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series.

BMC Med Genet 2018 05 25;19(1):87. Epub 2018 May 25.

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, 233 S. 10th Street, Suite 450 BLSB, Philadelphia, PA, 19107, USA.

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http://dx.doi.org/10.1186/s12881-018-0581-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970508PMC
May 2018

High-Resolution HLA-A Typing in Normal Iranian Population

Iran Biomed J 2018 03 27;22(2):134-7. Epub 2017 Sep 27.

Kawsar Human Genetics Research Center, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786660PMC
March 2018

Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy.

Matrix Biol 2018 03 11;66:22-33. Epub 2017 Nov 11.

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA; Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, PA, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S0945053X173024
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http://dx.doi.org/10.1016/j.matbio.2017.11.003DOI Listing
March 2018

Molecular Basis of α-Thalassemia in Iran

Iran Biomed J 2018 01;22(1):6-14

Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712386PMC
January 2018

Rapid characterization of the CHO platform cell line and identification of pseudo attP sites for PhiC31 integrase.

Protein Expr Purif 2017 Dec 9;140:60-64. Epub 2017 Aug 9.

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran; Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran; Kawsar Genomics and Biotech Center, Tehran, Iran.

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http://dx.doi.org/10.1016/j.pep.2017.08.002DOI Listing
December 2017

Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications.

J Invest Dermatol 2017 12 19;137(12):2649-2652. Epub 2017 Aug 19.

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA; Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, USA. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2017.07.830DOI Listing
December 2017

A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome.

Orphanet J Rare Dis 2017 12 6;12(1):176. Epub 2017 Dec 6.

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, 233 S. 10th Street, Suite 450 BLSB, Philadelphia, PA, 19107, USA.

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http://dx.doi.org/10.1186/s13023-017-0728-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717823PMC
December 2017

Potential circulating miRNA signature for early detection of NSCLC.

Cancer Genet 2017 Oct 7;216-217:150-158. Epub 2017 Aug 7.

Lung Transplantation Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

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http://dx.doi.org/10.1016/j.cancergen.2017.07.006DOI Listing
October 2017

MiR-377 reverses cancerous phenotypes of pancreatic cells via suppressing DNMT1 and demethylating tumor suppressor genes.

Epigenomics 2017 08 31;9(8):1059-1075. Epub 2017 Jul 31.

Molecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.

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https://www.futuremedicine.com/doi/10.2217/epi-2016-0175
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http://dx.doi.org/10.2217/epi-2016-0175DOI Listing
August 2017

Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinity.

J Invest Dermatol 2017 03 21;137(3):678-685. Epub 2016 Nov 21.

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA; Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, USA. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2016.11.012DOI Listing
March 2017

Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages.

J Invest Dermatol 2017 03 27;137(3):660-669. Epub 2016 Oct 27.

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA; Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, USA. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2016.10.023DOI Listing
March 2017

In silico analysis of novel mutations in maple syrup urine disease patients from Iran.

Metab Brain Dis 2017 02 10;32(1):105-113. Epub 2016 Aug 10.

Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.

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http://link.springer.com/10.1007/s11011-016-9867-1
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http://dx.doi.org/10.1007/s11011-016-9867-1DOI Listing
February 2017

Molecular Dynamics Simulation of the Consequences of a PYCR1 Mutation (p.Ala189Val) in Patients with Complex Connective Tissue Disorder and Severe Intellectual Disability.

J Invest Dermatol 2017 02 15;137(2):525-528. Epub 2016 Oct 15.

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, USA. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2016.10.007DOI Listing
February 2017

Gene-Targeted Next-Generation Sequencing Identifies a Novel CLDN1 Mutation in a Consanguineous Family With NISCH Syndrome.

Am J Gastroenterol 2017 Feb;112(2):396-398

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College and Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

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http://dx.doi.org/10.1038/ajg.2016.533DOI Listing
February 2017

Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene.

Acta Derm Venereol 2017 01;97(1):108-109

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, 233 S. 10th Street, Suite 450 BLSB, Philadelphia, PA 19107, Pennsylvania, USA.

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http://dx.doi.org/10.2340/00015555-2459DOI Listing
January 2017

Revisiting a Complex Rearrangement Involving a 619 Base Pairs Deletion, 6 Nucleotide Insertion Followed by a A > G Substitution Causing β°-Thalassemia.

Indian J Hematol Blood Transfus 2016 Dec 26;32(4):500-503. Epub 2016 May 26.

Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Pasteur St., Tehran, Iran ; Medical Genetics Lab, Kawsar Human Genetics Research Center, No. 41 Majlesi St., ValiAsr St., Tehran, Iran.

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http://link.springer.com/10.1007/s12288-016-0682-y
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http://dx.doi.org/10.1007/s12288-016-0682-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074969PMC
December 2016

Molecular Characterization of δ-Thalassemia in Iran.

Hemoglobin 2016 ;40(1):44-7

a Department of Molecular Medicine , Biotechnology Research Centre, Pasteur Institute of Iran , Tehran , Iran.

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http://dx.doi.org/10.3109/03630269.2015.1092982DOI Listing
October 2016

Identification and characterization of a novel nanobody against human placental growth factor to modulate angiogenesis.

Mol Immunol 2016 10 17;78:183-192. Epub 2016 Sep 17.

Vrije University Brussel, Research group Cellular & Molecular Immunology, Brussels, Belgium; VIB, Department of Structural Biology, Vrije University Brussel, Belgium.

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http://dx.doi.org/10.1016/j.molimm.2016.09.012DOI Listing
October 2016

KRT5 and KRT14 Mutations in Epidermolysis Bullosa Simplex with Phenotypic Heterogeneity, and Evidence of Semidominant Inheritance in a Multiplex Family.

J Invest Dermatol 2016 09 7;136(9):1897-1901. Epub 2016 Jun 7.

Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2016.05.106DOI Listing
September 2016

Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group.

J Mol Neurosci 2016 Jul 4;59(3):392-6. Epub 2016 Jun 4.

Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Pasteur St., Tehran, Iran.

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http://link.springer.com/10.1007/s12031-016-0772-1
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http://dx.doi.org/10.1007/s12031-016-0772-1DOI Listing
July 2016

Identification of six novel mutations in Iranian patients with maple syrup urine disease and their in silico analysis.

Mutat Res 2016 Apr 25;786:34-40. Epub 2016 Jan 25.

Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran; Dr. Zeinali's Medical Genetics Laboratory, Kawsar Human Genetics Research Center, Tehran, Iran. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00275107163000
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http://dx.doi.org/10.1016/j.mrfmmm.2016.01.005DOI Listing
April 2016

A novel mutation in alpha sarcoglycan gene in an Iranian family with limb girdle muscular dystrophy 2D.

Neurol Res 2016 Mar 19;38(3):220-3. Epub 2016 Apr 19.

a Department of Molecular Medicine , Biotechnology Research Center, Pasteur Institute of Iran , Tehran , Iran.

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http://dx.doi.org/10.1080/01616412.2015.1105625DOI Listing
March 2016

NPM1 Mutation Detection in Acute Myeloid Leukemia: A Method Comparison Study.

Genet Test Mol Biomarkers 2016 Feb 14;20(2):63-6. Epub 2015 Dec 14.

2 Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran , Tehran, Iran .

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http://www.liebertpub.com/doi/10.1089/gtmb.2015.0184
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http://dx.doi.org/10.1089/gtmb.2015.0184DOI Listing
February 2016

A Large Cohort Study of Genotype and Phenotype Correlations of Beta- Thalassemia in Iranian Population.

Int J Hematol Oncol Stem Cell Res 2015 Oct;9(4):198-202

Biotechnology Research Center, Department of Molecular Medicine, Pasteur Institute of Iran, Tehran, Iran; Kawsar Human Genetics Research Center, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748687PMC
October 2015

GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.

Eur Arch Otorhinolaryngol 2015 Sep 11;272(9):2255-9. Epub 2014 Jul 11.

Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Pasteur St., Tehran, Iran,

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http://dx.doi.org/10.1007/s00405-014-3171-7DOI Listing
September 2015

TCF4 silencing sensitizes the colon cancer cell line to oxaliplatin as a common chemotherapeutic drug.

Anticancer Drugs 2014 Sep;25(8):908-16

aDepartment of Biotechnology, College of Science, University of Tehran bMolecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.

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https://insights.ovid.com/crossref?an=00001813-201409000-000
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http://dx.doi.org/10.1097/CAD.0000000000000118DOI Listing
September 2014

MicroRNA-148b and microRNA-152 reactivate tumor suppressor genes through suppression of DNA methyltransferase-1 gene in pancreatic cancer cell lines.

Cancer Biol Ther 2014 Apr 21;15(4):419-27. Epub 2014 Jan 21.

Department of Molecular Medicine; Biotechnology Research Center; Pasteur Institute of Iran; Tehran, Iran.

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http://dx.doi.org/10.4161/cbt.27630DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979819PMC
April 2014

Reporting the presence of three different diseases causing GJB2 mutations in a consanguineous deaf family.

Int J Audiol 2014 Feb 13;53(2):128-31. Epub 2013 Nov 13.

* Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences , Tehran , Iran.

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http://dx.doi.org/10.3109/14992027.2013.850748DOI Listing
February 2014

A novel PCBD gene mutation in an Iranian patient with hyperphenylalaninemia.

Clin Lab 2013 ;59(7-8):925-8

Medical Genetics Lab. of Dr. Zeinali, Kawsar's Human Genetic Research Center, Tehran, Iran.

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November 2013

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.

Int J Pediatr Otorhinolaryngol 2013 May 21;77(5):821-6. Epub 2013 Mar 21.

Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Pasteur St., Tehran, Iran.

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http://dx.doi.org/10.1016/j.ijporl.2013.02.021DOI Listing
May 2013

Expression Enhancement in Trastuzumab Therapeutic Monoclonal Antibody Production using Genomic Amplification with Methotrexate.

Avicenna J Med Biotechnol 2013 Apr;5(2):87-95

Department of Industrial and Environmental Biotechnology, National Institute for Genetic Engineering and Biotechnology, (NIGEB), Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689561PMC
April 2013

In silico design, construction and cloning of Trastuzumab humanized monoclonal antibody: A possible biosimilar for Herceptin.

Adv Biomed Res 2012 6;1:21. Epub 2012 Jul 6.

Department of Industrial and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran ; Molecular Medical, Kawsar Genomics and Biotech Complex, Tehran, Iran.

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http://dx.doi.org/10.4103/2277-9175.98122DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507020PMC
December 2012

Screening of OTOF mutations in Iran: a novel mutation and review.

Int J Pediatr Otorhinolaryngol 2012 Nov 18;76(11):1610-5. Epub 2012 Aug 18.

Medical Genetic Group, Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran.

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http://linkinghub.elsevier.com/retrieve/pii/S016558761200432
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http://dx.doi.org/10.1016/j.ijporl.2012.07.030DOI Listing
November 2012

Design of a biological method for rapid detection of presence of PCR inhibitors in aged bone DNA.

Clin Lab 2012 ;58(7-8):681-6

Human Genetics Research Center, Baqyatallah University of Medical Sciences, Tehran, Iran.

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October 2012

BRCA1 and BRCA2 germline mutations in 85 Iranian breast cancer patients.

Fam Cancer 2012 Mar;11(1):57-67

Department of Biology, Sanandaj Branch, Islamic Azad University, Sanandaj, Iran.

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http://dx.doi.org/10.1007/s10689-011-9477-3DOI Listing
March 2012

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

Iran Biomed J 2011 ;15(1-2):15-21

Molecular Medicine Division, Biotechnology Research Center, Pasteur Institute of Iran, Tehran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639736PMC
February 2012

The carrier frequency of α-globin gene triplication in an Iranian population with normal or borderline hematological parameters.

Hemoglobin 2011 ;35(4):323-30

Molecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.

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http://dx.doi.org/10.3109/03630269.2011.571527DOI Listing
December 2011

β-Thalassemia mutations found during 1 year of prenatal diagnoses in Fars Province, Iran.

Hemoglobin 2011 ;35(4):331-7

Division of Pediatric Hematology Oncology, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.

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http://dx.doi.org/10.3109/03630269.2011.601385DOI Listing
December 2011

Molecular characterization of β-thalassemia intermedia: a report from Iran.

Mol Biol Rep 2011 Oct 1;38(7):4321-6. Epub 2010 Dec 1.

Molecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran, Pasteur Street, 13164 Tehran, Iran.

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http://dx.doi.org/10.1007/s11033-010-0557-5DOI Listing
October 2011

8q24.3 and 11q25 chromosomal loci association with low HDL-C in metabolic syndrome.

Eur J Clin Invest 2011 Oct 28;41(10):1105-12. Epub 2011 Mar 28.

Obesity Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti MC, Tehran, Iran.

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http://dx.doi.org/10.1111/j.1365-2362.2011.02516.xDOI Listing
October 2011

Heterogeneity of hemoglobin h disease in childhood.

N Engl J Med 2011 05;364(21):2070-1; author reply 2071

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http://dx.doi.org/10.1056/NEJMc1103406DOI Listing
May 2011

Co-inheritance of hemoglobin D and β-thalassemia traits in three Iranian families: clinical relevance.

Arch Iran Med 2011 Jan;14(1):61-3

Molecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.

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http://dx.doi.org/011141/AIM.0014DOI Listing
January 2011