Výsledky vyhledávání - "Manal A. Fadl"

Akademický článek

IL1 β exon5 3954 C/T Polymorphism: A Potential Genetic Risk Factor of Heart Diseases' predisposition in Sudanese Patients

Autor: Manal A. Fadl, Sahar S. Noor algalil

Publikováno v: Sudan Journal of Medical Sciences, Vol 15, Pp 399-407 (2020)

Background: IL-1β was known to cause an inflammation in heart tissue leading to progressive loss of contractile tissues. The aim of this study was to evaluate “for the first time” the relationship between IL-1β polymorphism (rs1143634) and the

Externí odkaz: https://doaj.org/article/77527f7c1821429c896048eed570f169

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The association of the Fok1(rs2228570)vitamin D receptor (VDR) polymorphism with cardiovascular diseases predisposition in Sudanese patients

Autor: Hadeel M.M. Hassan, Manal A Fadl

Publikováno v: Journal of The Faculty of Science and Technology. :33-39

Cardiovascular diseases (CVDs) are public health concerns globally. The role of genetics in CVDs predisposition was evidenced in previous studies. The nuclear vitamin D receptor (VDR)regulates the transcription of a number of different genes implicat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::569708b668b5ce4715956d0942956412
https://doi.org/10.52981/jfst.vi6.601

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Prevalence of the elevated urea and creatinine level among hypertensives: Perspective to raise the awareness about disease complications

Autor: Manal A. Fadl, Huda A. Fadlalmula, Hisham AbdAllah Hussien

Publikováno v: Brazilian Journal of Biological Sciences. 8:13-23

An increasing prevalence of hypertension and mortality rate from hypertension complications especially the end stage kidney disease; urge the establishment of routine test for early detection of kidney disease. The aim of this study is to assess the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d8af0607ad07af1e5c837a0acc58a7aa
https://doi.org/10.21472/bjbs(2021)081803

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T594M mutation of the epithelial sodium channel beta subunit: No association with essential hypertension in Sudanese hypertensive

Autor: Huda A Fadlalmula, Elsadig E Elmahdi, Manal A Fadl

Publikováno v: Khartoum Medical Journal. 14

Background Hypertension is a multi-factorial disease, results from interplay between genetic and environmental factors. The epithelial sodium channel gene (SCNN1β) was known to regulate sodium absorption in the distal renal tubule. The T594M mutatio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::52a93cde75e42c783a78c1a90c3818f5
https://doi.org/10.53332/kmj.v14i2.26

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Wavelet Decomposition–Based Speckle Reduction Method for Ultrasound Images by Using Speckle-Reducing Anisotropic Diffusion and Hybrid Median

Autor: Manal M. Fadl allah, Razan I. Elsharif, Zeinab A. Mustafa, Sahar K. Abass, Banazier A. Ibraheem

Publikováno v: Journal of Clinical Engineering. 43:163-170

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::53bba0a3764b9add2af2ae0b9d5ce71f
https://doi.org/10.1097/jce.0000000000000300

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NOS3 894G > T Gene Polymorphism: A Potential Risk Factor of Stroke in Bahraini Patients

Autor: Moiz Bakhiet, Safa Taha, Manal A. Fadl, Adel A. AlJishi

Publikováno v: World Journal of Neuroscience. :98-107

The endothelial nitric oxide synthase (eNOS) encoded by the NOS3 gene is responsible for the synthesis of a vasoactive endothelium-derived nitric oxide (NO). The genetic polymorphism of this gene explains, in part, why some people are prone to develo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::98a5abce85a6fde402a9038e40539b57
https://doi.org/10.4236/wjns.2018.81009

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