Scopus وضعیت انتشارات مرکز در پایگاه<td style="width: 39px;
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Title |
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2024 |
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1 |
The emerging roles of long non-coding RNA (lncRNA) H19 in gynecologic |
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2 |
Investigation of GNB1 derivative circular RNAs hsa_circ_0009361 and hsa_circ_0009362 expressions in colorectal cancer patients: potential new diagnostic factors, Gastroenterology and Hepatology From Bed to Bench.
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3 |
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4 |
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5 |
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6 |
An update of the variant spectrum of the APC gene in Iranian familial adenomatous polyposis patients
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7 |
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8 |
Genetic change investigation in DOCK1 gene in an Iranian family with sign and symptoms of temporomandibular joint disorder (TMD).
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9 |
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases |
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10 |
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11 |
The Role of Laser and Microwave in Treatment of Endocrine Disorders: A Systematic Review. |
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12 |
NF-kappa B signaling pathway is associated with metformin resistance in type 2 diabetes patients |
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13 |
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14 |
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15 |
Evaluation of Laser Intensity Effect on Photodynamic Therapy Efficacy |
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16 |
Mycobacterium genavense infections in immunopromised patients with HIV: A clinical case report
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17 |
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18 |
The Role of Laser and Microwave in Treatment of Endocrine Disorders: A Systematic Review: Laser and microwave in endocrine disorders
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19 |
Breast Tuberculosis in Iran: A Comprehensive Review |
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20 |
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21 |
Novel BRAT1 variant associated with neurodevelopmental disorder with cerebellar atrophy and seizure: Case report and a literature review
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22 |
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23 |
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2023 |
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1 |
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2 |
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3 |
SBF2-AS1 and TreRNA: novel lncRNA players in triple-negative breast cancer pathogenesis |
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4 |
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5 |
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6 |
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7 |
BRAT1–related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients |
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8 |
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9 |
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10 |
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11 |
Fatal vanishing bile duct syndrome in Iranian patient with Hodgkin's lymphoma |
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12 |
An update of the variant spectrum of the APC gene in Iranian familial adenomatous polyposis patients |
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13 |
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14 |
Introducing Estrogen Metabolism as the Main Target of Wedelia chinensis in Prostate Cancer Cells, RJP Research Journal Pharmacognosy, Original Paper, doi: 10.22127/RJP.2023.376910.2026 |
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15 |
Mucormycosis, New Causative Agents, and New Susceptible Populations: Review of Cases in a Tertiary Care Hospital in Iran (2007-2021) |
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16 |
Association of Catechol-O-Methyl-Transferase and Estrogen Receptors polymorphism with Severity of Temporomandibular Disorder in Iranian Patients, Avicenna Journal of Medical Biotechnology Volume 15, Issue 4, 245-252, https://doi.org/10.18502/ajmb.v15i4.13498, Vol. 15, No. 4, October-December 2023 |
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17 |
Whole Exome Sequencing to Find Candidate Variants for the Prediction of Kidney Transplantation Efficacy, Genes 2023, 14, 1251. https://doi.org/10.3390/genes14061251, https://www.mdpi.com/journal/gene |
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18 |
Evaluation of the Cellular Resistance Process in Treated Cells Via Extracorporeal Photopheresis, Journal of Lasers, J Lasers Med Sci 2023;14:e46, doi 10.34172/jlms.2023.46 |
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19 |
Collagen Synthesis as a Prominent Process During the Interval between Two Laser Sessions, Journal of Lasers in Medical Sciences, J Lasers Med Sci 2023;14:e50, i 10.34172/jlms.2023.50 |
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20 |
The Accuracy of Diagnosis and Genotyping of Leishmania Species Based on Spliced Leader Mini-Exon Gene by Nuclear Magnetic Resonance and Sequencing Assays , Iran J Parasitol: Vol. 18, No. 3, Jul-Sep 2023, pp.331-341 |
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21 |
The Potential of Algae in Treating Celiac Disease, International Journal of Medical Toxicology and Forensic Medicine, Autumn 2023, Volume 13, Number 4 |
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22 |
The Maim Targets of Okadaic Acid Toxin in Human Intestinal Caco-2 Cells: An Investigation of Biological Systems, International Journal of Medical Toxicology and Forensic Medicine, Autumn 2023, Volume 13, Number 4 |
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23 |
Factors Affecting Post-Cesarean Pain Intensity in Patients at Taleghani Hospital in 2021, Journal of Obstetrics, Gynecology and Cancer Research, Volume 8, September – October 2023 |
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24 |
Role of rs9939506 polymorphism of FTO gene in resistance to eating in male adolescents, BMC Pediatrics, https://doi.org/10.1186/s12887-023-04310-9 |
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25 |
Stimulator of Interferon Genes, the Missing Link in the Pathogenesis of COVID‑19, Biomedical and Biotechnology Research Journal 7(4):p 649-651, Oct–Dec 2023. | DOI: 10.4103/bbrj.bbrj_233_23, letter to editor |
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26 |
Potential Molecular Mechanisms of Bisphenol A in Obesity Development |
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27 |
Investigating the Mechanism of Arsenic-induced Ferroptosis in the Skin |
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2022 |
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1 |
Autophagy ATG16L1 rs2241880 impacts the colorectal cancer risk: A case-control study |
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2 |
Determination of Changes in Interleukin-8 Gene Expression in Colorectal Cancer Tissues and Its Relationship with Pathological and Clinical Features of the Affected Patients, Changes of Interleukin-8 Gene Expression in Colorectal Cancer, گوارش/ دوره 27 ، شماره 3/ پاییز 1401 / 147 - 1 |
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3 |
Interactions dietary components with expression level of breast cancer-related genes |
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4 |
Neurodegenerative disorder and diffuse brain calcifications due to FARSB mutation in two siblings |
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5 |
The effect of FTO rs9939609 polymorphism on the association between colorectal cancer and dietary fiber |
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6 |
Unraveling the Complex Interactions between the Fat Mass and Obesity-Associated (FTO) Gene, Lifestyle, and Cancer |
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7 |
Integrated microfluidic system for efficient DNA extraction using on-disk magnetic stirrer micromixer, Sensors and Actuators: B. Chemical, Elsevier, Sensors & Actuators: B. Chemical 351 (2022) 130919, |
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8 |
Gnathodiaphyseal dysplasia with a novel genetic variant in a large family from Iran, Molecular, Genetics & Genomics Medicine |
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9 |
Analysis of Cytogenetic Abnormalities in Iranian Patients with Syndromic Autism Spectrum Disorder: A Case Series, CASE SERIES, Iran J Child Neurol. Spring 2022 Vol. 16 No. 2 |
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10 |
Global, regional, and national burden of colorectal cancer and its risk factors, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019, GBD 2019 Colorectal Cancer Collaborators*, www.thelancet.com/gastrohep Published online April 7, 2022 https://doi.org/10.1016/S2468-1253(22)00044-9 |
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11 |
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12 |
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13 |
The effects of FTO gene rs9939609 polymorphism on the association between breast cancer and dietary intake, ORIGINAL A RTICL E, DOI: 10.1111/jcmm.17595, J Cell Mol Med. 2022;26:5794–5806. |
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14 |
Identification of early diagnostic biomarkers via WGCNA in gastric cancer, Biomedicine & Pharmacotherapy, 145 (2022) 112477, |
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15 |
Evaluation the relationship between polymorphism of galactose mutarotase gene by creating jaw sound in patients with temporomandibular disorder (TMD), Journal of Craniomaxillofacial Research, Vol. 9, No. 1, J Craniomax Res 2022; 9(1) : 31-39 |
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16 |
Temporomandibular disorders is associated with genetic factors: A review, Journal of Craniomaxillofacial Research, Vol. 9, No. 2, J Craniomax Res 2022; 9(2) : 69-80 |
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17 |
Circulating tumor cells and DNAs in prostate tumors |
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18 |
Liquid biopsy in female genital tract (ovarian cancer, endometrial tumor, and cervical tumor) |
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2021 |
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1 |
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2 |
Can hypoxia-inducible factor-1α overexpression discriminate human colorectal cancers with different microsatellite instability? Genes Genet. Syst. (2021) 96, p. 1–6, published date: 21 August 2021 |
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3 |
Long noncoding RNA LINC00978 acts as a potential diagnostic biomarker in patients with colorectal cancer, Experimental and Molecular Pathology 122 (2021) 104666, Experimental and Molecular Pathology |
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4 |
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5 |
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6 |
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7 |
Emerging Roles of Long Non-coding RNAs in Uterine Leiomyoma Pathogenesis: a Review |
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8 |
Convalescent Blood: Current Perspective on the Efficacy of a Legacy Approach in COVID-19 Treatment |
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9 |
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10 |
A randomized, double-blind, placebo-controlled trial of acommercial Aloe vera gel for mitigation of phototherapy side-effects in vitiligo patients, Journal of Herbal Medicine, Available online 3 March 2021, 100442, https://doi.org/10.1016/j.hermed.2021.100442 |
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11 |
Differential expression of Hsa-miR-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia, Original Investigation, 29 July, 2021, DOI: 10.4274/jtgga.galenos.2021.2021.0062 |
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12 |
The paradoxical reaction to rituximab in six granulomatosis with polyangiitis patients: How could it be explained and managed?, 2021 Feb 19. doi: 10.2174/1573397117666210219121659., PMID: 33605863 |
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13 |
Autophagy ATG16L1 rs2241880 impacts the colorectal cancer risk: A case-control study, RE S E ARCH A RT ICL E, wileyonlinelibrary.com/journal/jcla, DOI: 10.1002/jcla.24169, 9 November 2021 |
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14 |
Interactions of anthropometric indices, rs9939609 FTO gene polymorphism and breast cancer: A case-control study, ORIGINAL A RTICL E, DOI: 10.1111/jcmm.16394,J Cell Mol Med.2021;25:3252–3257. |
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15 |
Overexpression of GABRP Gene in Triple Negative Breast Cancer: Molecular Mechanisms and Interpretation, Published online 2021 November 29., doi: 10.5812/ijcm.119130, Int J Cancer Manag. 2021 November; 14(11):e119130. |
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16 |
Sniffer dogs as a screening/diagnostic tool for COVID-19: a proof of concept study, Eskandari et al. BMC Infectious Diseases (2021) 21:243, https://doi.org/10.1186/s12879-021-05939-6 |
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2020 |
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1 |
Pathogenic and protective roles of cytokines in pemphigus: A systematic Review, Cytokine, Contents lists available at ScienceDirect, Cytokine 129 (2020) 155026, |
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2 |
*CYP24A1 expression analysis in uterine leiomyoma regarding MED12 mutation profile, Archives of Gynecology and Obstetrics, https://doi.org/10.1007/s00404-020-05825-7, GYNECOLOGIC ONCOLOGY |
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3 |
*Dysregulation of vitamin D synthesis pathway genes in colorectal cancer: A case-control study DOI: 10.1002/jcla.23617, Accepted: 19 September 2020, J Clin Lab Anal. 2020;00:e23617. https://doi.org/10.1002/jcla.23617 |
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4 |
Identification of a stool long non-coding RNAs panel as a potential biomarker for early detection of colorectal cancer, DOI: 10.1002/jcla.23601, J Clin Lab Anal. 2020;00:e23601. https://doi.org/10.1002/jcla.23601 |
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5 |
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6 |
Mutations in the VPS13B Gene in Iranian Patients with Different Phenotypes of Cohen Syndrome, Journal of Molecular Neuroscience (2020) 70:21–25, https://doi.org/10.1007/s12031-019-01394-w |
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7 |
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8 |
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9 |
TINCR: An lncRNA with dual functions in the carcinogenesis process, Non-coding RNA Research, 5 (2020) 109–115journal homepage: http://www.keaipublishing.com/ncrna, Available online 09 July 2020 |
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10 |
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11 |
Could CYP24A1 promoter methylation status affect the gene expression in the colorectal cancer patients? Meta Gene, Elsevier, Volume 24, June 2020, 100656 |
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12 |
Investigation of circRNA-miRNA-mRNA network in colorectal cancer using an integrative bioinformatics approach, Gastroenterology and Hepatology From Bed to Bench, Original Received: 24 June 2020 Accepted: 29 August 2020 |
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13 |
Determination of mutation in the coding regions of FAM83H and ENAM genes in patients with imperfect enamel (Amelogenesis Imperfecta), Journal of Craniomaxillofacial Research, Vol. 7, No. 3, J Craniomax Res 2020; 7(3) : 126-131 |
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14 |
The Impact of OPIUM and Its Derivatives on Cell Apoptosis and Angiogenesis, Translational Research in Urology, 2(4): 110-117 Autumn 2020 |
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15 |
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16 |
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17 |
Hereditary factors of bruxism, Journal of |
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2019 |
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1 |
Ectopic expression of CYP24A1 circular RNA hsa_circ_0060927 in uterine leiomyomas, J Clin Lab Anal. 2019;00:e23114, DOI: 10.1002/jcla.23114 |
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2 |
Mutations in the VPS13B Gene in Iranian Patients with Different Phenotypes of Cohen Syndrome. J Mol Neurosci, 2019, p1-p5. PMID:31444703, https://doi.org/10.1007/s12031-019-01394-w |
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3 |
Next generation sequencing elucidated a clinically undiagnosed metabolic disorder - An Iranian family with hereditary orotic aciduria, Gene Reports, Volume 16, September 2019, 100457, https://doi.org/10.1016/j.genrep.2019.100457 |
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4 |
Investigation of CEBPA and CEBPA-AS Genes Expression in Acute Myeloid Leukemia. Reports of Biochemistry & Molecular Biology, Vol.7, No.2, Jan 2019. Reports of Biochemistry and Molecular Biology 2019;(7). |
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5 |
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6 |
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7 |
LncRNASRA1mayplayaroleintheuterine leiomyoma tumor growth regarding the MED12 mutationpattern, InternationalJournalofWomen'sHealth, |
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8 |
MED12 Exon 1 Mutational Screening in Iranian Patients with Uterine Leiomyoma, Reports of Biochemistry & Molecular Biology , Vol.8, No.1, Apr 2019 |
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2018 |
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1 |
Novel LAMA2 gene mutations associated with merosin-deficient congenital muscular dystrophy, Iranian Biomedical Journal, 22 (6): 408-414 November 2018 |
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2 |
A new mutation in steroidogenic acute regulatory protein (StAR) is segregated in an Iranian family. Meta Gene. 2018;(16)196-198. 10.1016/j.mgene.2018.03.005 |
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3 |
A study of CAG repeat instability of HTT gene following spermatogenesis, by single sperm analysis. Gene Reports. 2018;(12)294-298. 10.1016/j.genrep.2018.07.013 |
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4 |
ACE gene rs4343 polymorphism elevates the risk of preeclampsia in pregnant women. Journal of Human Hypertension. 2018 10.1038/s41371-018-0096-4 |
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5 |
Association of the Risk of Dental Caries and Polymorphism of MBL2 rs11003125 Gene in Iranian Adults. Caries Research. 2018;(14)60-64. 10.1159/000489572 |
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6 |
Comparing the short-term therapeutic effects and safety profiles of rituximab therapy in pemphigus vulgaris patients either early treated or later than six months. Journal of Dermatological Treatment. 2018;(12)1-4. |
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7 |
Evaluation of caries experience in two genders and ENAM polymorphism in Iranian adults. Meta Gene. 2018;(17)78-81. 10.1016/j.mgene.2018.05.002 |
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8 |
Genetic analysis of Iranian patients with familial hypercholesterolemia. Iranian Biomedical Journal. 2018;(22)117-122. 10.22034/ibj.22.2.117 |
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9 |
Investigation of piwi-interacting RNA pathway genes role in idiopathic non-obstructive azoospermia. Scientific Reports. 2018;(8). 10.1038/s41598-017-17518-4 |
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10 |
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population. Journal of Inherited Metabolic Disease . 2018 10.1007/s10545-018-0228-6 |
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11 |
Neurodegeneration with brain iron accumulation 2A: Report of four independent cases. Meta Gene. 2018;(15)87-89. 10.1016/j.mgene.2017.12.006 |
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12 |
Pharmacogenetics: A strategy for personalized medicine for autoimmune diseases. Clinical Genetics. 2018;(93)481-497. 10.1111/cge.13186 |
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13 |
Report of three cases with hereditary spastic paraplegia and investigation of the mutations. Meta Gene. 2018;(16)105-107. 10.1016/j.mgene.2018.02.009 |
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14 |
Sixteen-year history of rituximab therapy for 1085 pemphigus vulgaris patients: A systematic review. International Immunopharmacology. 2018;(54)131-138. 10.1016/j.intimp.2017.11.005 |
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15 |
The rs4846049 polymorphism in the 3?UTR region of the MTHFR gene increases the migraine susceptibility in an Iranian population. Journal of Pain Research. 2018;(11)145-149. 10.2147/JPR.S152930 |
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16 |
Tofacitinib as the potent treatment for refractory pemphigus: A possible alternative treatment for pemphigus. Dermatologic therapy. 2018;(11)1-3. 10.1111/dth.12696 |
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17 |
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2017 |
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1 |
A new mutation in WT1 gene associated with wilms tumor with reduced penetrance in an Iranian family. International Journal of Cancer Management. 2017;(10). 10.5812/ijcm.7500 |
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2 |
Association of a novel nonsense mutation in KIAA1279 with Goldberg-Shprintzen syndrome. Iranian Journal of Child Neurology. 2017;(11)70-74. |
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3 |
Autosomal recessive polycystic kidney disorder due to two novel compound heterozygote mutations in PKHD1 gene: Case report. Tehran University Medical Journal. 2017;(74)746-749. |
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4 |
Clinical, biochemical and molecular features of Iranian families with mucopolysaccharidosis: A case series. Clinica Chimica Acta. 2017;(474)88-95. 10.1016/j.cca.2017.08.017 |
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5 |
Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian Patients. Journal of inherited metabolic disorders reports. 2017;(32)7-14. 10.1007/8904_2016_572 |
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6 |
Green tea in non-alcoholic fatty liver disease: A double blind randomized clinical trial. Hepatitis Monthly. 2017;(17). 10.5812/hepatmon.14993 |
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7 |
Limb girdle muscular dystrophy type 2E due to a novel large deletion in SGCB gene. Iranian Journal of Child Neurology. 2017;(11)57-60. 10.22037/ijcn.v11i3.10521 |
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8 |
Mental retardation due to chromosomal translocation in an Iranian consanguineous family: Report of three cases. Tehran University Medical Journal. 2017;(74)817-822. |
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9 |
Multidisciplinary management of a patient with van der Woude syndrome: A case report. International Journal of Surgery Case Reports. 2017;(30)142-147. 10.1016/j.ijscr.2016.11.032 |
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10 |
10- SOCS gene family expression profile in the blood of multiple sclerosis patients. Journal of the Neurological Sciences. 2017;(375)481-485. 10.1016/j.jns.2017.02.015 |
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11 |
The role of parental microRNA alleles in recurrent pregnancy loss: an association study. Reproductive BioMedicine Online. 2017;(34)325-330. 10.1016/j.rbmo.2016.12.004 |
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12 |
Towards personalized medicine for patients with autoimmune diseases: Opportunities and challenges. Immunology Letters. 2017;(190)130-138. 10.1016/j.imlet.2017.08.002 |
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13 |
Association of a Novel Nonsense Mutation in KIAA1279 with Goldberg-Shprintzen Syndrome, Iran J Child Neurol. WINTER, 2017; 11(1):70-74. |
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2016 |
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1 |
A new nonsense mutation in CDKL5 gene in a male patient with early onset refractory epilepsy: A case report. International Journal of Pediatrics. 2016;(4)1315-1318. 10.22038/ijp.2016.6394 |
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2 |
A novel 5 nucleotide deletion in XPA gene is associated with severe neurological abnormalities. Gene. 2016;(576)379-380. 10.1016/j.gene.2015.08.039 |
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3 |
A novel homozygous LMNA mutation (p.Met540Ile) causes mandibuloacral dysplasia type A. Gene. 2016;(577)8-13. 10.1016/j.gene.2015.08.071 |
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4 |
A novel missense mutation in CLCN1 gene in a family with autosomal recessive congenital myotonia. Iranian Journal of Medical Sciences. 2016;(41)456-458. |
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5 |
A novel nonsense mutation in PANK2 gene in two patients with pantothenate kinase-associated neurodegeneration. International Journal of Molecular and Cellular Medicine. 2016;(5)255-259. 10.22088/acadpub.BUMS.5.4.255 |
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6 |
A novel splice site mutation in HPS1 gene is associated with Hermansky-Pudlak syndrome-1 (HPS1) in an Iranian family. International Journal of Molecular and Cellular Medicine. 2016;(5)192-195. |
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7 |
A novel splice site mutation in the GNPTAB gene in an Iranian patient with mucolipidosis II α/β. Journal of Pediatric Endocrinology and Metabolism. 2016;(29)991-993. 10.1515/jpem-2016-0032 |
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8 |
Analysis of the androgen receptor CAG repeats length in Iranian patients with idiopathic non-obstructive azoospermia. Asian Pacific Journal of Reproduction. 2016;(5)71-74. 10.1016/j.apjr.2015.12.013 |
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9 |
Co-existence of phenylketonuria either with maple syrup urine disease or Sandhoff disease in two patients from Iran: Emphasizing the role of consanguinity. Journal of Pediatric Endocrinology and Metabolism. 2016;(29)1215-1219. 10.1515/jpem-2016-0096 |
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10 |
First case report of EX3del4765 mutation in PAH gene in Asian population. Iranian Red Crescent Medical Journal. 2016;(18). 10.5812/ircmj.21633 |
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11 |
Functional analysis of a novel splicing mutation in the mutase gene of two unrelated pedigrees. Cell Journal. 2016;(18)397-404. |
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12 |
Gene expression profiling of the 8q22-24 position in human breast cancer: TSPYL5, MTDH, ATAD2 and CCNE2 genes are implicated in oncogenesis, while WISP1 and EXT1 genes may predict a risk of metastasis. Oncology Letters. 2016;(12)3845-3855. 10.3892/ol.2016.5218 |
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13 |
Homozygosity for a Robertsonian translocation (13q;14q) In a phenotypically normal 44, XX female with a history of recurrent abortion and a normal pregnancy outcome. Journal of Reproduction and Infertility. 2016;(17)184-187. |
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14 |
Leigh syndrome associated with a novel mutation in the COX15 gene. Journal of Pediatric Endocrinology and Metabolism. 2016;(29)741-744. 10.1515/jpem-2015-0396 |
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15 |
Mutation spectra of BRCA genes in Iranian women with early onset breast cancer - 15 years experience. Asian Pacific Journal of Cancer Prevention. 2016;(17)149-153. 10.7314/APJCP.2016.17.S3.149 |
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16 |
Mutation spectra of the ITGB2 gene in Iranian families with leukocyte adhesion deficiency type 1. Human Immunology. 2016;(77)191-195. 10.1016/j.humimm.2015.11.019 |
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17 |
New gene profiling in determination of breast cancer recurrence and prognosis in Iranian women. Asian Pacific Journal of Cancer Prevention. 2016;(17)155-160. 10.7314/APJCP.2016.17.S3.155 |
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18 |
Novel FKBP10 Mutation in a Patient with Osteogenesis Imperfecta Type XI. Fetal and Pediatric Pathology. 2016;(35)353-358. 10.1080/15513815.2016.1191567 |
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19 |
RAR-related orphan receptor A (RORA): A new susceptibility gene for multiple sclerosis. Journal of the Neurological Sciences. 2016;(369)259-262. 10.1016/j.jns.2016.08.045 |
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20 |
Report of a case with trisomy 9 mosaicism. Iranian Journal of Medical Sciences. 2016;(41)249-252. |
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21 |
The study of MED12 gene mutations in uterine leiomyomas from Iranian patients. Tumor Biology. 2016;(37)1567-1571. 10.1007/s13277-015-3943-8 |
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22 |
Prognosticating Metastasis Risk In Early Breast Cancer WITH EXT1 and WISP1 Genes in 8q22-24 Position. International Journal of Biology, Pharmacy and Allied Sciences (IJBPAS). 2016;(5)19962007. |
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2015 |
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1 |
A case report: Autosomal recessive microcephaly caused by a novel mutation in MCPH1 gene. Gene. 2015;(571)149-150. 10.1016/j.gene.2015.07.058 |
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2 |
A mutational and expressional analysis of DNMT3A in acute myeloid leukemia cytogenetic subgroups. Hematology. 2015;(20)397-404. 10.1179/1607845415Y.0000000001 |
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3 |
A new missense mutation in the BCKDHB gene causes the classic form of maple syrup urine disease (MSUD). Journal of Pediatric Endocrinology and Metabolism. 2015;(28)673-675. 10.1515/jpem-2014-0341 |
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4 |
Expression analysis of Tsga10 during in vitro differentiation of germ cells from mouse embryonic stem cell. Tehran University Medical Journal. 2015;(72)748-754. |
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5 |
Inequality in utilization of in-patients health services in Iran. International Journal of Preventive Medicine. 2015;(2015-June)-. 10.4103/2008-7802.158169 |
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6 |
MicroRNA profiling during germline differentiation of mouse embryonic stem cells. Cellular and Molecular Biology. 2015;(61)84-91. 10.14715/cmb/2015.61.3.16 |
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7 |
Mutation analysis of the CYP21A2 gene in congenital adrenal hyperplasia. Cellular and Molecular Biology. 2015;(61)51-55. 10.14715/cmb/2015.61.4.9 |
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8 |
Novel missense mutation in the GALNS gene in an affected patient with severe form of mucopolysaccharidosis type IVA. Clinica Chimica Acta. 2015;(450)121-124. 10.1016/j.cca.2015.08.006 |
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9 |
Segregation of a novel MLH1 mutation in an Iranian Lynch syndrome family. Gene. 2015;(570)304-305. 10.1016/j.gene.2015.07.005 |
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2014 |
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1 |
A new approach for molecular diagnosis of TAR syndrome. Clinical Biochemistry. 2014;(47)835-839. 10.1016/j.clinbiochem.2014.04.018 |
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2 |
A vector-based system for the differentiation of mouse embryonic stem cells toward germ-line cells. Iranian Journal of Basic Medical Sciences. 2014;(17)566-570. |
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3 |
Cloning and expression of influenza H1N1 NS1 protein in Escherichia Coli BL21. Iranian Journal of Biotechnology. 2014;(12). 10.5812/ijb.12625 |
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4 |
Evaluation of in vitro spermatogenesis system effectiveness to study genes behavior: Monitoring the expression of the testis specific 10 (Tsga10) gene as a model. Archives of Iranian Medicine. 2014;(17)692-697. |
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5 |
Expression analysis of PAWP during mouse embryonic stem cell-based spermatogenesis in vitro. In Vitro Cellular and Developmental Biology - Animal. 2014;(50)475-481. 10.1007/s11626-013-9722-1 |
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6 |
Identifying ubiquitin D in paraffin-embedded tissues in patients with colorectal cancer. Journal of Isfahan Medical School. 2014;(32)972-981. |
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7 |
Prevalence of subclinical hypothyroidism in pregnant women in Tehran-Iran. International Journal of Fertility and Sterility. 2014;(8)163-166. |
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8 |
Single-nucleotide polymorphisms within microRNAs sequences and their 3 UTR target sites may regulate gene expression in gastrointestinal tract cancers. Iranian Red Crescent Medical Journal. 2014;(16). 10.5812/ircmj.16659 |
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9 |
The effect of progesterone suppositories on threatened abortion: A randomized clinical trial. Journal of Reproduction and Infertility. 2014;(15)147-151. |
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10 |
Tuboplasty as a reversal macrosurgery for tubal ligation, is pregnancy possible? A case series. Iranian Journal of Reproductive Medicine. 2014;(12)361-364. |
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11 |
Association between SLC4A7 and COX11variants and breast cancer in an iranian population. European Journal of Cancer. 2014;()e45. |
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2013 |
