Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Nadia I Sewelam"'
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 68, Iss 1, Pp 1-7 (2020)
Background Sickle cell disease (SCD) is a disorder characterized by a heterogeneous clinical outcome. Interleukin-1β (IL-1β) and interleukin-6 (IL-6) are important mediators of inflammatory response. Genetic modifiers that alter cytokine levels may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67acc3afaff0b93d5ff94debc99f8cc0
https://doi.org/10.1186/s43054-020-00025-z
https://doi.org/10.1186/s43054-020-00025-z
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 4, Pp 325-331 (2018)
Background: Many genetic factors, including polymorphisms in the genes regulating blood coagulation and fibrinolysis have been proposed as risk factors for coronary artery disease (CAD). PAI-1 is the chief inhibitor of tissue plasminogen activator an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6660a70cd9cd1cd776fdc53a26a218b1
http://www.sciencedirect.com/science/article/pii/S1110863018300648
http://www.sciencedirect.com/science/article/pii/S1110863018300648
Publikováno v:
Life Sciences. 196:38-47
Human induced pluripotent stem cells (hiPSCs) act as a promising therapeutic alternative for cardiovascular diseases. They yield a large number of functional cardiomyocytes (CMs) from autologous cell sources without ethical or immunological problems.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79020f2144838fac7c659398de08e847
https://doi.org/10.1016/j.lfs.2018.01.009
https://doi.org/10.1016/j.lfs.2018.01.009
Publikováno v:
Electronic Physician, Vol 8, Iss 9, Pp 2897-2903 (2016)
Electronic Physician
Electronic Physician
Aim The purpose of present study was to access the prevalence of anti-cyclic citrullinated peptide (anti-CCP) antibodies in children with Juvenile Idiopathic Arthritis (JIA), and to investigate the clinical significance and diagnostic value of the an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07a6b52b3737cad04fc77fd10e2da8e5
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074747/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074747/
Publikováno v:
Rheumatology. 56
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5bd3cd158422a47352e8248875d8727
https://doi.org/10.1093/rheumatology/kex390.044
https://doi.org/10.1093/rheumatology/kex390.044
Publikováno v:
Egyptian Journal of Neurology, Psychiatry & Neurosurgery. Jul2013, Vol. 50 Issue 3, p315-321. 7p.
Publikováno v:
Comparative Clinical Pathology. 23:933-939
The T-cell immunoglobulin- and mucin-domain-containing molecules (TIMs) influence immune regulation. TIM-3, a transmembrane protein expressed on terminally differentiated Th1 cells, is a central regulator of T-cell responses. Dysfunctional T-lymphocy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbe37ab2acf7a82bd1e5f6b94358f90a
https://doi.org/10.1007/s00580-013-1716-6
https://doi.org/10.1007/s00580-013-1716-6
Publikováno v:
The Egyptian Journal of Haematology. 43:119
Background Immune thrombocytopenia (ITP) is an acquired immune disorder. Chemokines have complicated role in different autoimmune disorders including ITP. C-C motif chemokine ligand 2 (CCL2) chemokine represents a T helper (Th)2 polarizing chemokine,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f61693cfacb90664c77b4bec254b8901
https://doi.org/10.4103/ejh.ejh_12_18
https://doi.org/10.4103/ejh.ejh_12_18
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 14, No 2 (2013)
The present study investigated the relationship between the genetic polymorphisms in MMP-9 and MMP-3 genes and acute myocardial infarction (AMI). We examined 40 patients with acute myocardial infarction and 40 age and sex matched controls for MMP-9 f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef67bfa2da2f147e9e257a4efcddf695
https://www.ajol.info/index.php/ejhg/article/view/87406
https://www.ajol.info/index.php/ejhg/article/view/87406
Publikováno v:
The Egyptian Journal of Haematology. 39:98
Background Coronary artery diseases (CAD) are complex disorders resulting from interactions of different predisposing factors. Aim to evaluate the role of -455 G/A Fibrinogen polymorphism (rs1800790) in Egyptian patients with CAD. Subjects and Method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d03345b127df3a3d8f873b8f15349364
https://doi.org/10.4103/1110-1067.148225
https://doi.org/10.4103/1110-1067.148225