Found: 20
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Serum MicroRNA profiles in chronic hepatitis C Egyptian patients before and after combined sofosbuvir and daclatasvir treatment.
- Published in:
- BMC Infectious Diseases, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12879-023-08016-2
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- Article
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis.
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- Middle East Journal of Medical Genetics, 2022, v. 11, n. 2, p. 58, doi. 10.21608/MXE.2023.287527
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- Article
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families.
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- Genes, 2023, v. 14, n. 4, p. 900, doi. 10.3390/genes14040900
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- Article
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.
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- Genes, 2021, v. 12, n. 9, p. 1389, doi. 10.3390/genes12091389
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- Article
Transforming growth factor-β1 gene polymorphism in psoriasis vulgaris.
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- Clinical, Cosmetic & Investigational Dermatology, 2018, v. 11, p. 415, doi. 10.2147/CCID.S171403
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- Article
Prediction of relapse after interferon therapy in hepatitis C virus-infected patients by the use of triple assay.
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- Journal of Gastroenterology & Hepatology, 2003, v. 18, n. 1, p. 68, doi. 10.1046/j.1440-1746.2003.02919.x
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- Article
Long interspersed nuclear element-1 (LINE1)-mediated deletion of EVC, EVC2, C4orf6, and STK32B in Ellis-van Creveld syndrome with borderline intelligence.
- Published in:
- Human Mutation, 2008, v. 29, n. 7, p. 931, doi. 10.1002/humu.20778
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- Article
Screening of dystrophin gene deletions in Egyptian patients with DMD/BMD muscular dystrophies.
- Published in:
- Disease Markers, 2000, v. 16, n. 3-4, p. 125, doi. 10.1155/2000/437372
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- Article
Corrigendum to "Defining the molecular pathology and consequent phenotypes in Egyptian HB patients" [J. Genet. Eng. Biotechnol. 19(1) (2021) 75].
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- Journal of Genetic Engineering & Biotechnology, 2024, v. 22, n. 2, p. N.PAG, doi. 10.1016/j.jgeb.2024.100374
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- Article
Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients.
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- Journal of Genetic Engineering & Biotechnology, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s43141-023-00585-8
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- Article
Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.
- Published in:
- 2022
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- Correction Notice
Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.
- Published in:
- Journal of Genetic Engineering & Biotechnology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s43141-022-00399-0
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- Publication type:
- Article
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?
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- Journal of Genetic Engineering & Biotechnology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s43141-021-00272-6
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- Article
Correlation of circulating miRNA-33a and miRNA-122 with lipid metabolism among Egyptian patients with metabolic syndrome.
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- Journal of Genetic Engineering & Biotechnology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s43141-021-00246-8
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- Article
Schistosoma hematobium soluble egg antigens induce proliferation of urothelial and endothelial cells.
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- World Journal of Urology, 2001, v. 19, n. 4, p. 263, doi. 10.1007/s003450100217
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- Article
Association of anti‐cyclic citrullinated peptide antibodies and rheumatoid factor isotypes with HLA‐DRB1 shared epitope alleles in Egyptian rheumatoid arthritis patients.
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- International Journal of Rheumatic Diseases, 2020, v. 23, n. 5, p. 647, doi. 10.1111/1756-185X.13819
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- Article
Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1.
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- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 12, p. 1, doi. 10.1002/mgg3.1631
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- Article
Genomic alterations in the F8 gene correlating with severe hemophilia A in Egyptian patients.
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- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 2, p. 1, doi. 10.1002/mgg3.1575
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- Publication type:
- Article
Defining the molecular pathology and consequent phenotypes in Egyptian HB patients.
- Published in:
- Journal of Genetic Engineering & Biotechnology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s43141-021-00165-8
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- Publication type:
- Article
Epigenetic effects toward new insights as potential therapeutic target in B-thalassemia.
- Published in:
- Journal of Genetic Engineering & Biotechnology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s43141-021-00138-x
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- Publication type:
- Article