Zobrazeno 1 - 10 of 48 pro vyhledávání: '"Abed, Abdalla A."'
1
Akademický článek
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2
Akademický článek
Relationship between ApoE gene polymorphism and coronary heart disease in Gaza Strip
Autor: Marrzoq, Lamia F.Abu. *, Sharif, Fadel A., Abed, Abdalla A.
Publikováno v: In Journal of Cardiovascular Disease Research January-March 2011 2(1):29-35
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5
Akademický článek
In vitro inhibition of human leukemia THP-1 cells by Origanum syriacum L. and Thymus vulgaris L. extracts.
Autor: Ayesh, Basim M.1 (AUTHOR), Abed, Abdalla A.2 (AUTHOR), Faris, Doa’a M.3 (AUTHOR) d_fariss@yahoo.com
Publikováno v: BMC Research Notes. 2014, Vol. 7 Issue 1, p612-617. 6p. 1 Chart, 2 Graphs.
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6
Single nucleotide polymorphism E23K of KCNJ11 gene and other risk factors associated with type-2 diabetes mellitus in Gaza
Autor: Abed, Abdalla, Ayesh, Basim M., Hamdona, Osama Mohammad
Type 2 diabetes mellitus (T2DM) is a multifactorial disease in which environmental triggers interact with genetic variants in predisposition to disease. The aim of this study was to evaluate (E23K) SNP in KCNJ11 gene as a possible contributor to T2DM
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______4294::777765ae422916fdb509d10fa2a0f87b
http://ijcls.com/index.php/ijcls/article/view/63
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8
Akademický článek
CHRNA5 and CHRNA3 polymorphism and lung cancer susceptibility in Palestinian population.
Autor: Ayesh, Basim Mohammad, Al‑Masri, Rami, Abed, Abdalla Assaf
Publikováno v: BMC Research Notes; 4/2/2018, Vol. 11 Issue 1, p1-6, 6p, 1 Black and White Photograph, 2 Charts
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9
HFE Gene Mutations Among β-Thalassemia Intermediate and β-Thalassemia Minor Individuals in Gaza Strip, Palestine
Autor: Harara, Zayed, Abed, Abdalla, Sharif, Fadel A.
Background: Hereditary hemochromatosis (HH) is an autosomal recessive disorder of iron metabolism caused by mutations in the HFE gene. Objectives: The aim of this study was to determine the occurrence of C282Y and H63D mutations among β–thalassemi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______4294::ce6e67250724ac6593083e5999383f20
http://books.google.com/books?hl=en&lr=&id=P72404FJjPIC&oi=fnd&pg=PA115&dq=info:0ukhKiYMGcgJ:scholar.google.com&ots=EAhXKYAy6B&sig=ifG-8qL6D7ERdWlO_PljSH_ypno
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10
Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz‐Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597 …
Autor: Abed, Abdalla, Günther, Klaus, Kraus, Cornelia, Hohenberger, Werner, Ballhausen, Wolfgang G
This study was intended to evaluate a diagnostic reverse transcriptase polymerase chain reaction based protein‐truncation test for the identification of germline mutations in the serine/threonine protein kinase 11 (STK11, also designated LKB1) gene
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______4294::9dc6128231e35b15dcec103ba26ac083
Wiley Online Library
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Plný text Recenzováno Digitální knihovna AV ČR
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