Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Khalda S. Amr"'
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 22, Iss 2, Pp 100374- (2024)
Externí odkaz:
https://doaj.org/article/e50bd9c9c6bf43038bd79266a8b5f3b2
Autor:
Wafaa M. Ezzat, Khalda S. Amr, Salwa Tawfeek, Hassan Elbatae, Eman A. Bayomi, Ahmed Heiba, Yasser Elhosary
Publikováno v:
BMC Infectious Diseases, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background MicroRNAs (miR) are small sequence of nucleotides that can affect multiple genes involved in the hepatitis C virus (HCV) life cycle and disease development. The purpose of the present study was to investigate the clinical signific
Externí odkaz:
https://doaj.org/article/15a60f3433c846ae9ee3a90057d72c63
Autor:
Azza K. Abdel Megeid, Miral M. Refeat, Engy A. Ashaat, Ghada El-Kamah, Sonia A. El-Saiedi, Mona M. Elfalaki, Mona O. El Ruby, Khalda S. Amr
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 20, Iss 1, Pp 1-9 (2022)
Abstract Background Interstitial lung disease (ILD) is a broad heterogeneous group of lung disorders that is characterized by inflammation of the lungs. Surfactant dysfunction disorders are a rare form of ILD diseases that result from mutations in su
Externí odkaz:
https://doaj.org/article/eb51ec2af8c04083a14fe99944b51368
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 19, Iss 1, Pp 1-8 (2021)
Abstract Background Genetic variants in the transcription factor 7-like 2 (TCF7L2) gene are related with type 2 diabetes (T2D) and gestational diabetes mellitus (GDM) in various populations, but there are not enough statistics regarding GDM among Egy
Externí odkaz:
https://doaj.org/article/78fec45a05894abc92d5d02d3686f96c
Autor:
Miral M. Refeat, Naglaa Abu-Mandil Hassan, Inass Hassan Ahmad, Eman Roshdy Mohamed Mostafa, Khalda S. Amr
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 19, Iss 1, Pp 1-8 (2021)
Abstract Background Metabolic syndrome is defined as a group of interrelated biochemical, clinical, and metabolic factors that directly increase the risk of cardiovascular disease, obesity, and type 2 diabetes mellitus. MicroRNA-33a (miR-33a) and Mic
Externí odkaz:
https://doaj.org/article/b735e6cda9264ed0989027935ff821ad
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 19, Iss 1, Pp 1-6 (2021)
Abstract Background Hemophilia B (HB) (also known as Christmas disease) is a rare X-linked recessive disorder characterized by spontaneous or prolonged hemorrhages caused by mutations in Factor 9 (F9) gene leading to deficient or defective coagulatio
Externí odkaz:
https://doaj.org/article/6fb8025af1934b8da22d920a0c6fd9de
Autor:
Noha Hamdy Eltaweel, Ghada Youssef ElKamah, Rabab Khairat, Hanan Abd Elmawgoud Atia, Khalda S. Amr
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 19, Iss 1, Pp 1-12 (2021)
Abstract Background Fetal hemoglobin (HbF) induction has shown promise for the treatment of β-hemoglobinopathies. HbF induction in β-thalassemia could overcome ineffective hematopoiesis and thus terminate transfusion dependency for formerly transfu
Externí odkaz:
https://doaj.org/article/00819864096e44f385d25859494fe326
Autor:
Nahla N.Abdel‐Aziz, Ghada Y.El‐Kamah, Rabab A.Khairat, Hanan R.Mohamed, Yehia Z.Gad, Akmal M. El‐Ghor, Khalda S. Amr
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 12, Pp n/a-n/a (2021)
Abstract Background Neurofibromatosis 1 (NF1; OMIM# 162200) is a common autosomal dominant genetic disease [incidence: ~1:3500]. In 95% of cases, clinical diagnosis of the disease is based on the presence of at least two of the seven National Institu
Externí odkaz:
https://doaj.org/article/6aeb6dc9008349d5b9108c271055f656
Autor:
Azza K. Abdel Megeid, Miral M. Refeat, Engy A. Ashaat, Ghada El-Kamah, Sonia A. El-Saiedi, Mona M. Elfalaki, Mona O. El Ruby, Khalda S. Amr
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 20, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/bf19b7f959e24bafaa102528c90762f5
Autor:
Rehab M. Mosaad, Khalda S. Amr, Eman A. Rabie, Naglaa O. Mostafa, Sonia A. Habib, Ghada Y. El‐Kamah
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Abstract Background Hemophilia A (HA) is an inherited X‐linked recessive coagulation disorder caused by factor VIII (F8) deficiency. F8 rearrangements involving intron 22 (int22) and intron 1 (int1) account for almost half of severe HA phenotype al
Externí odkaz:
https://doaj.org/article/52f5c1ffa7df41dc9263349910215ee5