Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sarah Okashah"'
Autor:
Shaza Alkhidir, Karen El-Akouri, Nader Al-Dewik, Houssein Khodjet-El-khil, Sarah Okashah, Nazmul Islam, Tawfeg Ben-Omran, Mashael Al-Shafai
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract Hearing loss is the most predominant sensory defect occurring in pediatrics, of which, 66% cases are attributed to genetic factors. The prevalence of hereditary hearing loss increases in consanguineous populations, and the prevalence of hear
Externí odkaz:
https://doaj.org/article/a5b78ae7fd3746b39dd5edc2d75c9ff8
Autor:
Sarah Okashah, Dhanya Vasudeva, Aya El Jerbi, Houssein Khodjet-El-khil, Mashael Al-Shafai, Najeeb Syed, Marios Kambouris, Sharda Udassi, Luis R. Saraiva, Hesham Al-Saloos, Jai Udassi, Kholoud N. Al-Shafai
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1369
Congenital heart disease (CHD) is one of the most common forms of birth defects worldwide, with a prevalence of 1–2% in newborns. CHD is a multifactorial disease partially caused by genetic defects, including chromosomal abnormalities and single ge
Publikováno v:
Ophthalmic Epidemiology. 29:1-12
Primary congenital glaucoma (PCG) is a rare glaucoma type that develops in early infantile period and contributes to an elevated pressure on ocular cavity. Variants in gene are the most encountered in PCG cases. The prevalence of PCG is relatively hi
Publikováno v:
Reproduction, fertility, and development. 34(14)
Although Male Infertility (MI) in Arabs is fairly common, there is a dearth in published reports of genetic epidemiology of MI among Arabs. This study aimed to review the existing literature reporting the variants that are associated with MI in the 2
Autor:
Hatem Zayed, Anu Preethi, Bithia Rajan, Selvarajan Ethiraj, S. Udhaya Kumar, Salma Younes, Thirumal Kumar D, George Priya Doss C, Sarah Okashah, Taghreed Abunada
Publikováno v:
Genes
Volume 11
Issue 11
Genes, Vol 11, Iss 1256, p 1256 (2020)
Volume 11
Issue 11
Genes, Vol 11, Iss 1256, p 1256 (2020)
(1) Aims: Diabesity, defined as diabetes occurring in the context of obesity, is a serious health problem that is associated with an increased risk of premature heart attack, stroke, and death. To date, a key challenge has been to understand the mole
Autor:
Thirumal Kumar D, George Priya Doss C, Srivarshini Sankar, S. Udhaya Kumar, Abeer M. Al-Subaie, Hatem Zayed, Balu Kamaraj, Muneera Naseer Ahmad, Salma Younes, Sarah Okashah
Publikováno v:
Molecules
Volume 25
Issue 23
Molecules, Vol 25, Iss 5543, p 5543 (2020)
Volume 25
Issue 23
Molecules, Vol 25, Iss 5543, p 5543 (2020)
Filamins (FLN) are a family of actin-binding proteins involved in regulating the cytoskeleton and signaling phenomenon by developing a network with F-actin and FLN-binding partners. The FLN family comprises three conserved isoforms in mammals: FLNA,