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ArticlesPeer ReviewedFull Text
Breast cancer prediction with transcriptome profiling using feature selection and machine learning methods
Author / Creator:Taghizadeh, Eskandar ; Heydarheydari, Sahel ; Saberi, Alihossein ; JafarpoorNesheli, Shabnam ; Rezaeijo, Seyed Masoud
Publisher:London: BioMed Central Ltd
Journal title:BMC bioinformatics, 2022-10, Vol.23 (1), p.1-410, Article 410
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LncRNAs as putative biomarkers and therapeutic targets for Parkinson’s disease
Author / Creator:Taghizadeh, Eskandar ; Gheibihayat, Seyed Mohammad ; Taheri, Forough ; Afshani, Seyed Mohammadreza ; Farahani, Najmeh ; Saberi, Alihossein
Publisher:Cham: Springer International Publishing
Journal title:Neurological sciences, 2021-10, Vol.42 (10), p.4007-4015
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Genotype–phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran
Author / Creator:Hamid, Mohammad ; keikhaei, Bijan ; Galehdari, Hamid ; Saberi, Alihossein ; Sedaghat, Alireza ; Shariati, Gholamreza ; Mohammadi-Anaei, Marziye
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2022-03, Vol.12 (1), p.4856-4856, Article 4856
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Identification of a new mutation in the ACTL9 gene in men with unexplained infertility
Author / Creator:Sinaei, Roya ; Eslami, Maryam ; Dadfar, Mohammadreza ; Saberi, Alihossein
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2024-05, Vol.12 (5), p.e2448-n/a
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FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathway
Author / Creator:Ishiai, Masamichi ; Kitao, Hiroyuki ; Smogorzewska, Agata ; Tomida, Junya ; Kinomura, Aiko ; Uchida, Emi ; Saberi, Alihossein ; Kinoshita, Eiji ; Kinoshita-Kikuta, Emiko ; Koike, Tohru ; Tashiro, Satoshi ; Elledge, Stephen J ; Takata, Minoru
Publisher:New York: Nature Publishing Group US
Journal title:Nature structural & molecular biology, 2008-11, Vol.15 (11), p.1138-1146
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Association of rs1570360 and rs2010963 in VEGF and rs2279744 in MDM2 gene with Recurrent Implantation Failure in Iranian Women
Author / Creator:Elmi, Mehdi ; Ghandil, Pegah ; Hemadi, Masoud ; Birgani, Maryam Tahmasebi ; Saberi, Alihossein
Publisher:Brazil: Sociedade Brasileira de Reprodução Humana (Brazilian Society of Assisted Reproduction)
Journal title:JBRA assisted reproduction, 2023, Vol.27 (3), p.342-347
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Integrative bioinformatics analysis of miRNA and mRNA expression profiles identified some potential biomarkers for breast cancer
Author / Creator:Rezaeijo, Seyed Masoud ; Rezaei, Monireh ; Poursheikhani, Arash ; Mohammadkhani, Shima ; Goharifar, Naieme ; Shayankia, Ghazal ; Heydarheydari, Sahel
Publisher:Cairo: Springer
Journal title:The Egyptian journal of medical human genetics, 2023-12, Vol.24 (1), p.62
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Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual
Author / Creator:Hamid, Mohammad ; keikhaei, Bijan ; Galehdari, Hamid ; Saberi, Alihossein ; Sedaghat, Alireza ; Shariati, Gholamreza ; Mohammadi‐Anaei, Marziye
Publisher:United States: John Wiley & Sons, Inc
Journal title:EJHaem, 2021-08, Vol.2 (3), p.366-374
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Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran
Author / Creator:Papi, Atefe ; Zamani, Mina ; Shariati, Gholamreza ; Sedaghat, Alireza ; Seifi, Tahere ; Negahdari, Samira ; Sedighzadeh, Sahar Sadat ; Zeighami, Jawaher ; Saberi, Alihossein ; Hamid, Mohammad ; Galehdari, Hamid
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2023-02, Vol.11 (2), p.e2099-n/a
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Histone Deacetylase Inhibitors Selectively Target Homology Dependent DNA Repair Defective Cells and Elevate Non-Homologous Endjoining Activity
Author / Creator:Smith, Stephanie ; Fox, Jennifer ; Mejia, Marco ; Ruangpradit, Wanvipa ; Saberi, Alihossein ; Kim, Sunmi ; Choi, Yongjun ; Oh, Sehyun ; Wang, Yucai ; Choi, Kyungho ; Li, Lei ; Hendrickson, Eric A. ; Takeda, Shunichi ; Muller, Mark ; Myung, Kyungjae
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-01, Vol.9 (1), p.e87203
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Identification of three novel mutations in the FANCA, FANCC, and ,ITGA2B genes by whole exome sequencing
Author / Creator:Negahdari, Samira ; Zamani, Mina ; Seifi, Tahereh ; Sedighzadeh, Sahar ; Mazaheri, Neda ; Zeighami, Jawaher ; Sedaghat, Alireza ; Saberi, Alihossein ; Hamid, Mohammad ; keikhaei, Bijan ; Radpour, Ramin ; Shariati, Gholamreza ; Galehdari, Hamid
Publisher:Iran: Medknow Publications & Media Pvt. Ltd
Journal title:International journal of preventive medicine, 2020, Vol.11 (1), p.117-117
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Culturing in serum-free culture medium on collagen type-I-coated plate increases expression of CD133 and retains original phenotype of HT-29 cancer stem cell
Author / Creator:Arab-Bafrani, Zahra ; Shahbazi-Gahrouei, Daryoush ; Abbasian, Mehdi ; Saberi, Alihossein ; Fesharaki, Mehrafarin ; Hejazi, Seyed ; Manshaee, Samira
Publisher:India: Wolters Kluwer - Medknow Publications
Journal title:Advanced biomedical research, 2016-01, Vol.5 (1), p.59-59
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The Effect of CYP2C9 Genotype Variants in Type 2 Diabetes on the Pharmacological Effectiveness of Sulfonylureas, Diabetic Retinopathy, and Nephropathy
Author / Creator:Saberi, Meisam ; Ramazani, Zahra ; Rashidi, Homeira ; Saberi, Alihossein
Publisher:New Zealand: Taylor & Francis Ltd
Journal title:Vascular health and risk management, 2020-01, Vol.16, p.241-248
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KCNQ1 rs2237895 polymorphism is associated with the therapeutic response to sulfonylureas in Iranian type 2 diabetes mellitus patients
Author / Creator:Shakerian, Siavash ; Rashidi, Homeira ; Birgani, Maryam Tahmasebi ; Saberi, Alihossein
Publisher:Cham: Springer International Publishing
Journal title:Journal of diabetes and metabolic disorders, 2022-06, Vol.21 (1), p.33-41
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Hb Narges Lab, a Novel Hemoglobin Variant of the β-Globin Gene
Author / Creator:Hamid, Mohammad ; Shahbazi, Zahra ; Keikhaei, Bijan ; Galehdari, Hamid ; Saberi, Alihossein ; Sedaghat, Alireza ; Shariati, Gholamreza ; Mohammadi-Anaei, Marziye
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2022-05, Vol.25 (5), p.339-342
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Genotypic variants of the tetrahydrobiopterin (BH4) biosynthesis genes in patients with hyperphenylalaninemia from different regions of Iran
Author / Creator:Nezhad, Seyed Reza Kazemi ; Aligoodarzi, Pegah Namdar ; Rostami, Golale ; Shariati, Gholamreza ; Galehdari, Hamid ; Saberi, Alihossein ; Sedaghat, Alireza ; Hamid, Mohammad
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2024-01, Vol.12 (1), p.e2294-n/a
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Identification of Cytochrome b‐245, beta‐chain gene mutations, and clinical presentations in Iranian patients with X‐linked chronic granulomatous disease
Author / Creator:Heydari, Atefeh ; Abolnezhadian, Farhad ; Sadeghi‐Shabestari, Mahnaz ; Saberi, Alihossein ; Shamsizadeh, Ahmad ; Ghadiri, Ata A. ; Ghandil, Pegah
Publisher:United States: John Wiley & Sons, Inc
Journal title:Journal of clinical laboratory analysis, 2021-02, Vol.35 (2), p.e23637-n/a
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Parp-1 protects homologous recombination from interference by Ku and Ligase IV in vertebrate cells
Author / Creator:Hochegger, Helfrid ; Dejsuphong, Donniphat ; Fukushima, Toru ; Morrison, Ciaran ; Sonoda, Eiichiro ; Schreiber, Valérie ; Zhao, Guang Yu ; Saberi, Alihossein ; Masutani, Mitsuko ; Adachi, Noritaka ; Koyama, Hideki ; de Murcia, Gilbert ; Takeda, Shunichi
Publisher:Chichester, UK: John Wiley & Sons, Ltd
Journal title:The EMBO journal, 2006-03, Vol.25 (6), p.1305-1314
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A First Report of Hb Alesha [β67(E11)Val>Met, GTG>ATG] in an Iranian Patient
Author / Creator:Hamid, Mohammad ; Zargan Nezhad, Ebtesam ; Galehdari, Hamid ; Saberi, Alihossein ; Shariati, Gholamreza ; Sedaghat, Alireza
Publisher:Iran: Pasteur Institute of Iran
Journal title:Iranian biomedical journal, 2019-11, Vol.23 (6), p.429-431
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Wolf-Hirschhorn Syndrome: A Case with Normal Karyotype, Demonstrated by Array CGH (aCGH)
Author / Creator:Saberi, Alihossein ; Shariati, Gholamreza ; Hamid, Mohammad ; Galehdari, Hamid ; Abdorasouli, Nehzat
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2014-09, Vol.17 (9), p.642
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Showing 1 to 20 of 30 results

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Breast cancer prediction with transcriptome profiling using feature selection and machine learning methods

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LncRNAs as putative biomarkers and therapeutic targets for Parkinson’s disease

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Genotype–phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran

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Identification of a new mutation in the ACTL9 gene in men with unexplained infertility

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FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathway

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Association of rs1570360 and rs2010963 in VEGF and rs2279744 in MDM2 gene with Recurrent Implantation Failure in Iranian Women

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Integrative bioinformatics analysis of miRNA and mRNA expression profiles identified some potential biomarkers for breast cancer

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Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual

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Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran

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Histone Deacetylase Inhibitors Selectively Target Homology Dependent DNA Repair Defective Cells and Elevate Non-Homologous Endjoining Activity

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Identification of three novel mutations in the FANCA, FANCC, and ,ITGA2B genes by whole exome sequencing

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Culturing in serum-free culture medium on collagen type-I-coated plate increases expression of CD133 and retains original phenotype of HT-29 cancer stem cell

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The Effect of CYP2C9 Genotype Variants in Type 2 Diabetes on the Pharmacological Effectiveness of Sulfonylureas, Diabetic Retinopathy, and Nephropathy

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KCNQ1 rs2237895 polymorphism is associated with the therapeutic response to sulfonylureas in Iranian type 2 diabetes mellitus patients

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Hb Narges Lab, a Novel Hemoglobin Variant of the β-Globin Gene

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Genotypic variants of the tetrahydrobiopterin (BH4) biosynthesis genes in patients with hyperphenylalaninemia from different regions of Iran

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Identification of Cytochrome b‐245, beta‐chain gene mutations, and clinical presentations in Iranian patients with X‐linked chronic granulomatous disease

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Parp-1 protects homologous recombination from interference by Ku and Ligase IV in vertebrate cells

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A First Report of Hb Alesha [β67(E11)Val>Met, GTG>ATG] in an Iranian Patient

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Wolf-Hirschhorn Syndrome: A Case with Normal Karyotype, Demonstrated by Array CGH (aCGH)

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