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Upregulation of the double-stranded RNA binding protein DGCR8 in invasive ductal breast carcinoma

Gene, 2016-05, Vol.581 (2), p.146-151

2016

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Mitochondrial complex I gene variations; as a potential genetic risk factor in pathogenesis of multiple sclerosis

Journal of the neurological sciences, 2014-10, Vol.345 (1), p.220-223

2014

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Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran

Journal of research in medical sciences, 2017-01, Vol.22 (1), p.99-99

2017

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Dysregulated expression of Dicer in invasive ductal breast carcinoma

Medical oncology (Northwood, London, England), 2015-07, Vol.32 (7), p.203-203, Article 203

2015

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The expression of Drosha, DGCR8, Dicer and Ago-2 genes are upregulated in human umbilical vein endothelial cells under hyperglycemic condition

Endocrine regulations (Bratislava), 2018-07, Vol.52 (3), p.123-127

2018

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Cell-free fetal DNA: new perspective and clinical implication in diagnosis of polycystic kidney diseases

Renal failure, 2014-05, Vol.36 (4), p.661-661

2014

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Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss

Iranian journal of public health, 2016-05, Vol.45 (5), p.680-687

2016

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Congenital heart defects among Down syndrome patients: a clinical profiling

Journal of public health, 2016-02, Vol.24 (1), p.57-63

2016

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Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A Case-Control Study with Haplotype and in silico Analysis

European journal of obstetrics & gynecology and reproductive biology, 2017-08, Vol.215, p.93-100

2017

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Genetic susceptibility to deep venous thromboembolism: the roles of inherited thrombophilia polymorphisms

Blood coagulation & fibrinolysis, 2016-04, Vol.27 (3), p.308-312

2016

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Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations

Iranian journal of public health, 2017-12, Vol.47 (1)

2017

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Effect of Platelet-Rich Plasma on Differentiation of Osteoblasts and Osteoclasts in the Presence of Three-Dimensional Scaffold

Pharmaceutical Sciences, 2018-06, Vol.24 (2), p.124-130

2018

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Computational studies on the conformational preference of N‐(Thiazol‐2‐yl) benzamide

Journal of the Chinese Chemical Society (Taipei), 2020-10, Vol.67 (10), p.1800-1806

2020

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Second-Order Nonlinear Analysis of Steel Tapered Beams Subjected to Span Loading

Advances in mechanical engineering, 2014-01, Vol.6, p.237983

2014

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Evaluation of the effect of blood contamination on the compressive strength of MTA modified with hydration accelerators

Restorative Dentistry and Endodontics, 2013, 38(3), , pp.128-133

2013

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Evaluation of the effect of blood contamination on the compressive strength of MTA modified with hydration accelerators

Restorative dentistry & endodontics, 2013, Vol.38 (3), p.128-133

2013

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Upregulation of the double-stranded RNA binding protein DGCR8 in invasive ductal breast carcinoma

Mitochondrial complex I gene variations; as a potential genetic risk factor in pathogenesis of multiple sclerosis

Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran

Dysregulated expression of Dicer in invasive ductal breast carcinoma

The expression of Drosha, DGCR8, Dicer and Ago-2 genes are upregulated in human umbilical vein endothelial cells under hyperglycemic condition

Cell-free fetal DNA: new perspective and clinical implication in diagnosis of polycystic kidney diseases

Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss

Congenital heart defects among Down syndrome patients: a clinical profiling

Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A Case-Control Study with Haplotype and in silico Analysis

Genetic susceptibility to deep venous thromboembolism: the roles of inherited thrombophilia polymorphisms

Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations

Effect of Platelet-Rich Plasma on Differentiation of Osteoblasts and Osteoclasts in the Presence of Three-Dimensional Scaffold

Computational studies on the conformational preference of N‐(Thiazol‐2‐yl) benzamide

Second-Order Nonlinear Analysis of Steel Tapered Beams Subjected to Span Loading

Evaluation of the effect of blood contamination on the compressive strength of MTA modified with hydration accelerators

Evaluation of the effect of blood contamination on the compressive strength of MTA modified with hydration accelerators

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