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Study of the relation between two common cyclooxygenase 2 gene polymorphisms with risk of developing and subtypes of vitiligo in Egyptian patients.
- Published in:
- Indian Journal of Dermatology, Venereology & Leprology, 2018, v. 84, n. 6, p. 696, doi. 10.4103/ijdvl.IJDVL_813_16
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- Publication type:
- Article
Study of the relation between two common cyclooxygenase 2 gene polymorphisms with risk of developing and subtypes of vitiligo in Egyptian patients.
- Published in:
- 2017
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- Publication type:
- journal article
Association of a novel Granulocyte‐Macrophage Colony‐Stimulating Factor (GM‐CSF)‐3928C/T and GM‐CSF(3606T⁄C) Promoter gene polymorphisms with the pathogenesis and severity of acne vulgaris: A case‐controlled study
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- Journal of Cosmetic Dermatology, 2021, v. 20, n. 11, p. 3679, doi. 10.1111/jocd.14481
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- Publication type:
- Article
Serum MicroRNA profiles in chronic hepatitis C Egyptian patients before and after combined sofosbuvir and daclatasvir treatment.
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- BMC Infectious Diseases, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12879-023-08016-2
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- Publication type:
- Article
Polymorphisms at IL28B Gene as Predictors of Viral Relapse in Genotype 4 Egyptian Hepatitis C Patients.
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- Journal of Medical Virology, 2016, v. 88, n. 3, p. 481, doi. 10.1002/jmv.24354
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- Publication type:
- Article
Screening of dystrophin gene deletions in Egyptian patients with DMD/BMD muscular dystrophies.
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- Disease Markers, 2000, v. 16, n. 3-4, p. 125, doi. 10.1155/2000/437372
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- Publication type:
- Article
Next‐generation sequencing in identification of pathogenic variants in primary hyperoxaluria among 21 Egyptian families: Identification of two novel AGXT gene mutations.
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- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 8, p. 1, doi. 10.1002/mgg3.1992
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- Publication type:
- 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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- Publication type:
- 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
Expression of B and T lymphocyte attenuator, retinoid‐related orphan receptor gamma‐isoform‐t and interleukin 7 in psoriasis vulgaris.
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- Australasian Journal of Dermatology, 2019, v. 60, n. 2, p. e132, doi. 10.1111/ajd.12965
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- Article
APOA2 Polymorphism in Relation to Obesity and Lipid Metabolism.
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- Cholesterol, 2013, p. 1, doi. 10.1155/2013/289481
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- Publication type:
- 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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- Publication type:
- Article
Clinical and molecular characterization in a cohort of patients with progressive pseudorheumatoid dysplasia.
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- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 9, p. 2329, doi. 10.1002/ajmg.a.63339
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- Publication type:
- Article
A novel variant in GNPNAT1 gene causing a spondylo‐epi‐metaphyseal dysplasia resembling PGM3—Desbuquois like dysplasia.
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- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 10, p. 2861, doi. 10.1002/ajmg.a.62933
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- Publication type:
- Article
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development.
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 6, p. 1666, doi. 10.1002/ajmg.a.62129
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- Publication type:
- Article
Clinical and Molecular Characterization of Seven Egyptian Families with Autosomal Recessive Robinow Syndrome: Identification of Four Novel ROR2 Gene Mutations.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3054, doi. 10.1002/ajmg.a.37287
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- Publication type:
- Article
Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype-phenotype correlations.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 6, p. 1354, doi. 10.1002/ajmg.a.35938
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- Publication type:
- Article
Expanding the phenotypic and mutational spectrum in microcephalic osteodysplastic primordial dwarfism type I.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 6, p. 1455, doi. 10.1002/ajmg.a.35356
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- Publication type:
- Article
Clinical, Biochemical, and Molecular Characterization of Metachromatic Leukodystrophy Among Egyptian Pediatric Patients: Expansion of the ARSA Mutational Spectrum.
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- Journal of Molecular Neuroscience, 2021, v. 71, n. 5, p. 1112, doi. 10.1007/s12031-020-01734-1
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- Publication type:
- Article
Cyclooxygenase-2 Gene Polymorphisms –765G>C and –1195A>G and Mycosis Fungoides Risk.
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- Dermatology (10188665), 2021, v. 237, n. 1, p. 17, doi. 10.1159/000504840
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- Publication type:
- Article
Is There a Link between Human Herpesvirus Infection and Toll-like Receptors in the Pathogenesis of Pityriasis Rosea? A Case-control Study.
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- Acta Dermatovenerologica Croatica, 2016, v. 24, n. 4, p. 282
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- Publication type:
- Article
The effect of insulin‐loaded gold and carboxymethyl chitosan nanoparticles on gene expression of glucokinase and pyruvate kinase in rats with diabetes type 1.
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- Journal of Food Biochemistry, 2022, v. 46, n. 12, p. 1, doi. 10.1111/jfbc.14447
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- Publication type:
- 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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- Publication type:
- Article
Genetic assessment of ten Egyptian patients with Sjögren–Larsson syndrome: expanding the clinical spectrum and reporting a novel ALDH3A2 mutation.
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- Archives of Dermatological Research, 2019, v. 311, n. 9, p. 721, doi. 10.1007/s00403-019-01953-6
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- Publication type:
- 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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- Publication type:
- Article
Quantification of hemoglobin peptides in Beta-thalassemia patients using tandem mass spectrometry for future national screening program.
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- Middle East Journal of Medical Genetics, 2020, v. 9, n. 1, p. 1
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- Publication type:
- Article
A novel frameshift mutation of COL7A1 in an Egyptian patient with autosomal recessive dystrophic epidermolysis bullosa.
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- Middle East Journal of Medical Genetics, 2019, v. 8, n. 2, p. 83, doi. 10.4103/MXE.MXE_3_19
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- Publication type:
- Article
IL-6 - 174G/C polymorphism in obese adolescents with nonalcoholic fatty liver disease and its relation to metabolic and biochemical markers.
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- Middle East Journal of Medical Genetics, 2016, v. 5, n. 1, p. 20, doi. 10.1097/01.MXE.0000475219.52150.ca
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- Publication type:
- Article
Definition of the phenotypic spectrum of Temtamy preaxial brachydactyly syndrome associated with autosomal recessive CHYS1 mutations.
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- Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 64, doi. 10.1097/01.MXE.0000414918.78299.94
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- Publication type:
- Article
A clinical and genetic study of childhood and adolescent obesity.
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- Middle East Journal of Medical Genetics, 2012, v. 1, n. 1, p. 18, doi. 10.1097/01.MXE.0000407741.35881.c2
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- Publication type:
- Article
Evaluation of the correlation between serum levels of vitamin D and vitamin D receptor gene polymorphisms in an Egyptian population.
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- International Journal of Dermatology, 2016, v. 55, n. 12, p. 1329, doi. 10.1111/ijd.13363
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- Publication type:
- Article
Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 873, doi. 10.1515/jpem-2013-0443
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- Publication type:
- 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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- Publication type:
- Article
Immunomodulatory Functions of Adipose Mesenchymal Stromal/Stem Cell Derived From Donors With Type 2 Diabetes and Obesity on CD4 T Cells.
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- Stem Cells, 2023, v. 41, n. 5, p. 505, doi. 10.1093/stmcls/sxad021
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- Publication type:
- Article
C242T polymorphism of NADPH oxidase p22phox gene reduces the risk of coronary artery disease in a random sample of Egyptian population.
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- Molecular Biology Reports, 2014, v. 41, n. 4, p. 2281, doi. 10.1007/s11033-014-3081-1
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- Publication type:
- Article
Craniofacial anthropometric measurements of the cohort of Egyptian male school children and their utility in detection of abnormalities.
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- Bulletin of the National Research Centre, 2024, v. 48, n. 1, p. 1, doi. 10.1186/s42269-024-01184-4
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- Publication type:
- Article
Study the association of microRNA polymorphisms (miR‐146a, miR‐4513) with the risk of coronary heart diseases in Egyptian population.
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- Journal of Biochemical & Molecular Toxicology, 2023, v. 37, n. 3, p. 1, doi. 10.1002/jbt.23284
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- Publication type:
- Article
Whole exome sequencing identifies a new mutation in the SLC19A2 gene leading to thiamine‐responsive megaloblastic anemia in an Egyptian family.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 7, p. N.PAG, doi. 10.1002/mgg3.777
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- Publication type:
- Article
Study of DYRK1B gene expression and its association with metabolic syndrome in a small cohort of Egyptians.
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- Molecular Biology Reports, 2021, v. 48, n. 7, p. 5497, doi. 10.1007/s11033-021-06560-1
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- Publication type:
- Article
Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum.
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- Human Mutation, 2012, v. 33, n. 10, p. 1444, doi. 10.1002/humu.22133
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- Publication type:
- Article
Long interspersed nuclear element-1 (LINE1)-mediated deletion of EVC, EVC2, C4orf6, and STK32B in Ellis-van Creveld syndrome with borderline intelligence.
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- Human Mutation, 2008, v. 29, n. 7, p. 931, doi. 10.1002/humu.20778
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- Publication type:
- 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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- Publication type:
- Article
Confirmation of a Phenotypic Entity for TSPEAR Variants in Egyptian Ectodermal Dysplasia Patients and Role of Ethnicity.
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- Genes, 2022, v. 13, n. 6, p. 1056, doi. 10.3390/genes13061056
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- Publication type:
- Article
Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease.
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- Genes, 2021, v. 12, n. 10, p. 1552, doi. 10.3390/genes12101552
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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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- Publication type:
- Article
Clinical and Mutational Spectrum of Xeroderma Pigmentosum in Egypt: Identification of Six Novel Mutations and Implications for Ancestral Origins.
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- Genes, 2021, v. 12, n. 2, p. 295, doi. 10.3390/genes12020295
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- Publication type:
- Article
JAK1 rs310241 and JAK3 rs3008 Genotypes May Increase Susceptibility to Psoriasis: A Case Control Study.
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- Skin Pharmacology & Physiology, 2020, v. 33, n. 4, p. 207, doi. 10.1159/000509880
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- Publication type:
- Article
Primary hyperoxaluria type 1 in children: Clinical classification, renal replacement therapy, and outcome in a single centre experience.
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- Therapeutic Apheresis & Dialysis, 2022, v. 26, n. 1, p. 162, doi. 10.1111/1744-9987.13666
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- Publication type:
- Article
The role of microRNA-31 and microRNA-21 as regulatory biomarkers in the activation of T lymphocytes of Egyptian lupus patients.
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- Rheumatology International, 2016, v. 36, n. 11, p. 1617, doi. 10.1007/s00296-016-3550-z
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- Publication type:
- Article
Association of PTPN22 1858C→T polymorphism, HLA-DRB1 shared epitope and autoantibodies with rheumatoid arthritis.
- Published in:
- Rheumatology International, 2016, v. 36, n. 8, p. 1167, doi. 10.1007/s00296-016-3511-6
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- Publication type:
- Article