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Serum MicroRNA profiles in chronic hepatitis C Egyptian patients before and after combined sofosbuvir and daclatasvir treatment

BMC infectious diseases, 2024-01, Vol.24 (1), p.67-67, Article 67

2024

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Early diagnostic evaluation of miR-122 and miR-224 as biomarkers for hepatocellular carcinoma

Genes & diseases, 2017-12, Vol.4 (4), p.215-221

2017

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Corrigendum to “Defining the molecular pathology and consequent phenotypes in Egyptian HB patients” [J. Genet. Eng. Biotechnol. 19(1) (2021) 75]

Journal of Genetic Engineering and Biotechnology, 2024-06, Vol.22 (2), p.100374, Article 100374

2024

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Are single nucleotide polymorphisms rs7903146 and rs12255372 in transcription factor 7-like 2 gene associated with an increased risk for gestational diabetes mellitus in Egyptian women?

Journal of Genetic Engineering and Biotechnology, 2021-11, Vol.19 (1), p.169, Article 169

2021

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Epigenetic effects toward new insights as potential therapeutic target in B-thalassemia

Journal of Genetic Engineering and Biotechnology, 2021-03, Vol.19 (1), p.51, Article 51

2021

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Correlation of circulating miRNA-33a and miRNA-122 with lipid metabolism among Egyptian patients with metabolic syndrome

Journal of Genetic Engineering and Biotechnology, 2021-10, Vol.19 (1), p.147, Article 147

2021

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Gene Mutations of the Three Ectodysplasin Pathway Key Players ( EDA , EDAR , and EDARADD ) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations

Genes, 2021-09, Vol.12 (9), p.1389

2021

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Defining the molecular pathology and consequent phenotypes in Egyptian HB patients

Journal of Genetic Engineering and Biotechnology, 2021-05, Vol.19 (1), p.75, Article 75

2021

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Correlating SFTPC gene variants to interstitial lung disease in Egyptian children

Journal of Genetic Engineering and Biotechnology, 2022-12, Vol.20 (1), p.117, Article 117

2022

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Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children

Journal of Genetic Engineering and Biotechnology, 2022-12, Vol.20 (1), p.137, Article 137

2022

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Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1

Molecular genetics & genomic medicine, 2021-12, Vol.9 (12), p.e1631-n/a

2021

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Genomic alterations in the F8 gene correlating with severe hemophilia A in Egyptian patients

Molecular genetics & genomic medicine, 2021-02, Vol.9 (2), p.e1575-n/a

2021

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C242T polymorphism of NADPH oxidase p22phox gene reduces the risk of coronary artery disease in a random sample of Egyptian population

Molecular biology reports, 2014, Vol.41 (4), p.2281-2286

2014

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Reduction of RANTES expression in lesional psoriatic skin after narrow band ultraviolet therapy: a possible marker of therapeutic efficacy

EJD. European journal of dermatology, 2012-07, Vol.22 (4), p.481-487

2012

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Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients

Biochemical genetics, 2024-07

2024

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Role of nanoparticles in osteogenic differentiation of bone marrow mesenchymal stem cells

Cytotechnology (Dordrecht), 2020-02, Vol.72 (1), p.1-22

2020

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Nanomaterial-induced mesenchymal stem cell differentiation into osteoblast for counteracting bone resorption in the osteoporotic rats

Tissue & cell, 2021-12, Vol.73, p.101645, Article 101645

2021

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Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients

Journal of Genetic Engineering and Biotechnology, 2023-12, Vol.21 (1), p.149, Article 149

2023

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Lipoid proteinosis: A clinical and molecular study in Egyptian patients

Gene, 2017-09, Vol.628, p.308-314

2017

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Association of anti‐cyclic citrullinated peptide antibodies and rheumatoid factor isotypes with HLA‐DRB1 shared epitope alleles in Egyptian rheumatoid arthritis patients

International journal of rheumatic diseases, 2020-05, Vol.23 (5), p.647-653

2020

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Association of PTPN22 1858C→T polymorphism, HLA-DRB1 shared epitope and autoantibodies with rheumatoid arthritis

Rheumatology international, 2016-08, Vol.36 (8), p.1167-1175

2016

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Transforming growth factor-β1 gene polymorphism in psoriasis vulgaris

Clinical, cosmetic and investigational dermatology, 2018, Vol.11, p.415-419

2018

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Long interspersed nuclear element-1 (LINE1)-mediated deletion of EVC, EVC2, C4orf6, and STK32B in Ellis-van Creveld syndrome with borderline intelligence

Human mutation, 2008-07, Vol.29 (7), p.931-938

2008

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Possible role of angiotensin-converting enzyme polymorphism on progression of hepatic fibrosis in chronic hepatitis C virus infection

Transactions of the Royal Society of Tropical Medicine and Hygiene, 2011-07, Vol.105 (7), p.396-400

2011

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Outlining the Clinical Profile of ITCIRG1 14 Variants/I including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families

Genes, 2023-04, Vol.14 (4)

2023

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Serum MicroRNA profiles in chronic hepatitis C Egyptian patients before and after combined sofosbuvir and daclatasvir treatment

Early diagnostic evaluation of miR-122 and miR-224 as biomarkers for hepatocellular carcinoma

Corrigendum to “Defining the molecular pathology and consequent phenotypes in Egyptian HB patients” [J. Genet. Eng. Biotechnol. 19(1) (2021) 75]

Are single nucleotide polymorphisms rs7903146 and rs12255372 in transcription factor 7-like 2 gene associated with an increased risk for gestational diabetes mellitus in Egyptian women?

Epigenetic effects toward new insights as potential therapeutic target in B-thalassemia

Correlation of circulating miRNA-33a and miRNA-122 with lipid metabolism among Egyptian patients with metabolic syndrome

Gene Mutations of the Three Ectodysplasin Pathway Key Players ( EDA , EDAR , and EDARADD ) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations

Defining the molecular pathology and consequent phenotypes in Egyptian HB patients

Correlating SFTPC gene variants to interstitial lung disease in Egyptian children

Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children

Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1

Genomic alterations in the F8 gene correlating with severe hemophilia A in Egyptian patients

C242T polymorphism of NADPH oxidase p22phox gene reduces the risk of coronary artery disease in a random sample of Egyptian population

Reduction of RANTES expression in lesional psoriatic skin after narrow band ultraviolet therapy: a possible marker of therapeutic efficacy

Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients

Role of nanoparticles in osteogenic differentiation of bone marrow mesenchymal stem cells

Nanomaterial-induced mesenchymal stem cell differentiation into osteoblast for counteracting bone resorption in the osteoporotic rats

Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients

Lipoid proteinosis: A clinical and molecular study in Egyptian patients

Association of anti‐cyclic citrullinated peptide antibodies and rheumatoid factor isotypes with HLA‐DRB1 shared epitope alleles in Egyptian rheumatoid arthritis patients

Association of PTPN22 1858C→T polymorphism, HLA-DRB1 shared epitope and autoantibodies with rheumatoid arthritis

Transforming growth factor-β1 gene polymorphism in psoriasis vulgaris

Long interspersed nuclear element-1 (LINE1)-mediated deletion of EVC, EVC2, C4orf6, and STK32B in Ellis-van Creveld syndrome with borderline intelligence

Possible role of angiotensin-converting enzyme polymorphism on progression of hepatic fibrosis in chronic hepatitis C virus infection

Outlining the Clinical Profile of ITCIRG1 14 Variants/I including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families

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