Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Amany H. AbdelRahman"'
Autor:
Ghada A. Elshaarawy, Iman I. Salama, Somaia I. Salama, Amany H. Abdelrahman, Mirhane Hassan, Eman Eissa, Sherif Ismail, Sherif E. Eldeeb, Doaa E. Ahmed, Hazem Elhariri, Rasmia Elgohary, Aida M. Abdelmohsen, Walaa A. Fouad, Hala M. Raslan
Publikováno v:
BMC Musculoskeletal Disorders, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Knee osteoarthritis (KOA) is an important cause of disability in the world and it denotes a public health defiance of the upcoming years. Aim To examine the connection between ADAMTS14 gene rs4747096 polymorphism and KOA and to assess risk f
Externí odkaz:
https://doaj.org/article/4a46da30dbda45b090ab492b25049d18
Autor:
Amany H. Abdelrahman, Ola M. Eid, Mona H. Ibrahim, Safa N. Abd El-Fattah, Maha M. Eid, Nagwa A. Meguid
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-10 (2021)
Abstract Background Autism spectrum disorder is a condition related to brain development that affects a person’s perception and socialization, resulting in problems in social interaction and communication. It has no single known cause, yet several
Externí odkaz:
https://doaj.org/article/365daf5ec31448868cc9d888d4f31d50
Autor:
Ola M. Eid, Rania M. A. Abdel Kader, Lamiaa A. Fathalla, Amany H. Abdelrahman, Ahmed Rabea, Rana Mahrous, Maha M. Eid
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 19, Iss 1, Pp 1-7 (2021)
Abstract Background Chronic lymphocytic leukemia (CLL) is the most common form of adult leukemia. This disease is genetically heterogeneous, and approximately 85% of patients with CLL harbor chromosomal aberrations that are considered effective progn
Externí odkaz:
https://doaj.org/article/322180fe4c714588bc0467a10ce458ce
Autor:
Ola M. Eid, Maha M. Eid, Amany H. Abdelrahman, Rania M. A. Abdel kader, Marwa Farid, Rana Mahrous, Mona K. Mekkawy, Alaa K. Kamel, Inas Mazen, Hala T. El-Bassyouni
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background Short stature is defined as a body height below the third percentile, based on chronological age, or 2 standard deviations (SD) below the national height standard. The prevalence of short stature is around 2% of children worldwide
Externí odkaz:
https://doaj.org/article/1c67282c8740459d9ef6171ea075d21b
Autor:
Amany H. Abdelrahman, Maha M. Eid, Mirhane Hassan, Ola M. Eid, Rania M. A. AbdelKader, Nevin M. AlAzhary, Rasha Y. Shahin, Mohamed T. Sallam
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 20, Iss 1, Pp 1-9 (2019)
Abstract Background Telomere is a complex DNA–protein structure located at the end of all eukaryotic chromosomes. The major role of human telomerase is to catalyze the addition of telomeric repeat sequences TTAGGG onto chromosome ends for stabiliza
Externí odkaz:
https://doaj.org/article/b1c931eba7ff4aac894bcab8eb417a7d
Autor:
Omneya Moguib, Hala M. Raslan, Inas Abdel Rasheed, Laila Effat, Nadia Mohamed, Safaa El Serougy, Ghada Hussein, Salwa Tawfeek, Amany H. AbdelRahman, Khalda Omar
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 15, Iss 2, Pp 431-436 (2017)
Background: Genetic factors play important role in the development of type 2 diabetes and diabetic nephropathy. Endothelial nitric oxide synthase (eNOS) gene is responsible for the bioavailability of nitric oxide and endothelial function. Aim: To ass
Externí odkaz:
https://doaj.org/article/211808e2680341739c6e31d80031d2c9
Autor:
Amany H. Abdelrahman, Alshaymaa A. Ibrahim, Ola M. Eid, Mirhane Hassan, Maha M. Eid, Abeer M. Nour El Din Abd El Baky, Mervat Ismail, Maha Abou-Zekri, Safa N. Abd El-Fattah
Publikováno v:
Human Gene. 36:201180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3bd8d32fb33769245cbfacefa60bf97
https://doi.org/10.1016/j.humgen.2023.201180
https://doi.org/10.1016/j.humgen.2023.201180
Autor:
Rania M. A. Abdel kader, Marwa Farid, Maha M. Eid, Mona K. Mekkawy, Inas Mazen, Amany H. Abdelrahman, Ola M. Eid, Hala T. El-Bassyouni, Alaa K. Kamel, Rana Mahrous
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-8 (2020)
Background Short stature is defined as a body height below the third percentile, based on chronological age, or 2 standard deviations (SD) below the national height standard. The prevalence of short stature is around 2% of children worldwide. Several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93c813177d98ad4a540a3476dd59aa3c
http://link.springer.com/article/10.1186/s43042-020-00090-4
http://link.springer.com/article/10.1186/s43042-020-00090-4
Autor:
Maha M. Eid, Amany H. Abdelrahman, Mona Hamed Ibrahim, Safa N. Abd El-Fattah, Nagwa A. Meguid, Ola M. Eid
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-10 (2021)
Background Autism spectrum disorder is a condition related to brain development that affects a person’s perception and socialization, resulting in problems in social interaction and communication. It has no single known cause, yet several different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1742e758fa22de8f1d2ebc61d76430a7
https://doi.org/10.1186/s43042-021-00202-8
https://doi.org/10.1186/s43042-021-00202-8
Autor:
Maha M. Eid, Rania M. A. Abdel kader, Ola M. Eid, Amany H. Abdelrahman, Lamiaa A. Fathalla, Rana Mahrous, Ahmed Rabea
Publikováno v:
Journal of Genetic Engineering & Biotechnology
Journal of Genetic Engineering and Biotechnology, Vol 19, Iss 1, Pp 1-7 (2021)
Journal of Genetic Engineering and Biotechnology, Vol 19, Iss 1, Pp 1-7 (2021)
Background Chronic lymphocytic leukemia (CLL) is the most common form of adult leukemia. This disease is genetically heterogeneous, and approximately 85% of patients with CLL harbor chromosomal aberrations that are considered effective prognostic bio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1678bc42d958823771438a2e9396fd6
https://doi.org/10.1186/s43141-021-00198-z
https://doi.org/10.1186/s43141-021-00198-z