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Impact of miRNAs expression modulation on the methylation status of breast cancer stem cell-related genes

Autor: Heba H. Elosaily, M L Essawi, Iman Hassan Ibrahim, S M Salem

Publikováno v: Clinical and Translational Oncology. 23:1440-1451

Altered miRNAs play a crucial role in the emergence of the breast cancer stem cell (BCSC) phenotype. The interplay between miRNAs and methylation enzymes has been documented. One of the most aggressive breast cancer cell lines, MDA-MB-231, has expres

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5dd17a62eda19891a73298b4940b5c4e
https://doi.org/10.1007/s12094-020-02542-0

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Impact of miRNAs expression modulation on the methylation status of breast cancer stem cell-related genes

Autor: H H, El-Osaily, I H, Ibrahim, M L, Essawi, S M, Salem

Publikováno v: Clinicaltranslational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico. 23(7)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7f425d534e7a02c2ed7a8a34293d7bcc
https://pubmed.ncbi.nlm.nih.gov/33433838

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A novel nonsense mutation in exon 1 of HSD17B3 gene in an Egyptian 46,XY adult female presenting with primary amenorrhea

Autor: H A, Hassan, I, Mazen, Y Z, Gad, O S M, Ali, M, Mekkawy, M L, Essawi

Publikováno v: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation. 7(6)

17-β-Hydroxysteroid dehydrogenase type 3 deficiency is a rare autosomal recessive cause of 46,XY disorder of sex development. Worldwide, about 30 mutations in the hydroxysteroid (17-beta) dehydrogenase 3 (HSD17B3) gene have been reported, involving

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b0506e7b817902077725194f0c116898
https://pubmed.ncbi.nlm.nih.gov/23796702

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ACE gene polymorphism in Egyptian children with idiopathic nephrotic syndrome

Autor: M E, Fahmy, A M, Fattouh, R A, Hegazy, M L, Essawi

Publikováno v: Bratislavske lekarske listy. 109(7)

Idiopathic nephrotic syndrome is a common renal disease in children. ACE gene insertion/deletion (I/D) polymorphism has been studied as a predictor of clinical response to steroid therapy.To investigate the distribution of angiotensin-converting enzy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::90be74ef7578c311f4d01c631e6d6b86
https://pubmed.ncbi.nlm.nih.gov/18792483

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Screening for six Mediterranean mutations in 90 Egyptian patients with phenylketonuria

Autor: L K, Effat, M L, Essawi, M S, Abd El Hamid, N, Hawari, Y Z, Gad

Publikováno v: Bratislavske lekarske listy. 109(1)

The aim of this study is to assess the prevalence of six common mutations in the Mediterranean basin and Turkey among a large group of Egyptian PKU casesPhenylketonuria (PKU) is one of the most common inborn errors of amino acid metabolism that is ca

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::83bb03553fefd80b42c733ddffc1850a
https://pubmed.ncbi.nlm.nih.gov/18447256

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Molecular analysis of SMN1 and NAIP genes in Egyptian patients with spinal muscular atrophy

Autor: M L, Essawi, L K, Effat, G M L, Shanab, G M M, Al-Ettribi, A A, El-Haronui, A M, Karim

Publikováno v: Bratislavske lekarske listy. 108(3)

The aim of this study is to provide preliminary molecular data on spinal muscular atrophy in Egyptian patients thus facilitating a rapid and conventional molecular assay for accurate diagnosis of SMA.Childhood spinal muscular atrophy (SMA) is one of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b8afa1889a4bfb161dbda099510f205f
https://pubmed.ncbi.nlm.nih.gov/17682539

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