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Publisher : egyptian society of human genetics

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Academic Journal

Association between miR-138-5p, miR-132-3p, SIRT1, STAT3, and CD36 and atherogenic indices in blood mononuclear cells from patients with atherosclerosis.

Authors : Ehsani, Samira^1,2 (AUTHOR); Mard‑Soltani, Maysam³ (AUTHOR); Ahmadpour, Fatemeh⁴ (AUTHOR)

Source: Egyptian Journal of Medical Human Genetics. 12/16/2023, Vol. 24 Issue 1, p1-9. 9p.

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Academic Journal

A novel pathogenic splice-site variant in the PTCH1 gene c.3549+1G>T, associated with Gorlin syndrome: a case report.

Authors : Conde-Rubio, Paula¹ (AUTHOR) ; García-Malinis, Ana Julia² (AUTHOR); Salvador-Rupérez, Elvira³ (AUTHOR)

Source: Egyptian Journal of Medical Human Genetics. 12/13/2023, Vol. 24 Issue 1, p1-8. 8p.

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Academic Journal

A novel mutation in the SOX5 gene c.1627del; p.(Tyr543IlefsTer14) is associated to Lamb–Shaffer syndrome: a case report.

Authors : Cuenca Alcocel, Jose¹ (AUTHOR) ; Criado Álamo, Elena¹ (AUTHOR); Salvador-Rupérez, Elvira¹ (AUTHOR)

Source: Egyptian Journal of Medical Human Genetics. 4/21/2023, Vol. 24 Issue 1, p1-6. 6p.

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Academic Journal

Association of methylation status of ABCA1/G1 genes with the risk of coronary artery disease.

Authors : Mansouri, Elaheh¹ (AUTHOR); Esmaeili, Fataneh^1,2 (AUTHOR); Montaseri, Maryam³ (AUTHOR)

Source: Egyptian Journal of Medical Human Genetics. 12/31/2022, Vol. 23 Issue 1, p1-10. 10p.

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Academic Journal

Association of Keap1 (rs11085735) polymorphism and lncRNA MEG3 hypermethylation status with the risk of preeclampsia.

Authors : Zangeneh, Maryam¹ (AUTHOR); Heydarian, Sara¹ (AUTHOR); Seifi, Zahra¹ (AUTHOR)

Source: Egyptian Journal of Medical Human Genetics. 3/23/2022, Vol. 23 Issue 1, p1-7. 7p.

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Academic Journal

Three novel variants in SOX10 gene: Waardenburg and PCWH syndromes.

Authors : Sienes Bailo, Paula¹ (AUTHOR); Goñi-Ros, Nuria¹ (AUTHOR) ; Gazulla, José² (AUTHOR)

Source: Egyptian Journal of Medical Human Genetics. 3/6/2022, Vol. 23 Issue 1, p1-7. 7p.

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Academic Journal

A novel likely pathogenic variant in the H1‑4 gene c.139G>C p.(Ala47Pro) associated with Rahman syndrome: a clinical report.

Authors : González‑Tarancón, R.¹; Salvador‑Rupérez, E.¹; Goñi‑Ros, N.¹

Source: Egyptian Journal of Medical Human Genetics. 3/5/2022, Vol. 23, p1-5. 5p.

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Academic Journal

Significance of promoter methylation of multiple tumor suppressor genes in hepatocellular carcinoma.

Authors : Tahoon, Alaa¹ (AUTHOR); El-Khateeb, Doaa² (AUTHOR); Mosbeh, Asmaa³ (AUTHOR)

Source: Egyptian Journal of Medical Human Genetics. 2/18/2022, Vol. 23 Issue 1, p1-9. 9p.

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Academic Journal

Correction: Association between miR-138-5p, miR-132-3p, SIRT1, STAT3, and CD36 and atherogenic indices in blood mononuclear cells from patients with atherosclerosis.

Authors : Ehsani, Samira^1,2 (AUTHOR); Mard-Soltani, Maysam³ (AUTHOR); Ahmadpour, Fatemeh⁴ (AUTHOR)

Source: Egyptian Journal of Medical Human Genetics. 1/31/2024, Vol. 25 Issue 1, p1-1. 1p.

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Academic Journal

Circulating MiRNA-21 and programed cell death (PDCD) 4 gene expression in hepatocellular carcinoma (HCC) in Egyptian patients.

Authors : El Gedawy, Gamalat¹; Obada, Manar¹ ; Kelani, Ayman²

Source: Egyptian Journal of Medical Human Genetics. Apr2017, Vol. 18 Issue 2, p137-145. 9p.

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نتائج البحث

فلترة النتائج

Association between miR-138-5p, miR-132-3p, SIRT1, STAT3, and CD36 and atherogenic indices in blood mononuclear cells from patients with atherosclerosis.

A novel pathogenic splice-site variant in the PTCH1 gene c.3549+1G>T, associated with Gorlin syndrome: a case report.

A novel mutation in the SOX5 gene c.1627del; p.(Tyr543IlefsTer14) is associated to Lamb–Shaffer syndrome: a case report.

Association of methylation status of ABCA1/G1 genes with the risk of coronary artery disease.

Association of Keap1 (rs11085735) polymorphism and lncRNA MEG3 hypermethylation status with the risk of preeclampsia.

Three novel variants in SOX10 gene: Waardenburg and PCWH syndromes.

A novel likely pathogenic variant in the H1‑4 gene c.139G>C p.(Ala47Pro) associated with Rahman syndrome: a clinical report.

Significance of promoter methylation of multiple tumor suppressor genes in hepatocellular carcinoma.

Correction: Association between miR-138-5p, miR-132-3p, SIRT1, STAT3, and CD36 and atherogenic indices in blood mononuclear cells from patients with atherosclerosis.

Circulating MiRNA-21 and programed cell death (PDCD) 4 gene expression in hepatocellular carcinoma (HCC) in Egyptian patients.

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