Browsing by Author "Department of Biochemistry and Molecular Genetics. Faculty of Medicine,"

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Antitumor effect and nanoparticle development of the Adamantyl Retinoid ST1926 in acute myeloid leukemia -

El-Houjeiri, Leeanna Ali, (2015)

Acute myeloid leukemia (AML) is a clinically and genetically heterogeneous disorder of hematopoietic progenitor cells, which have lost their normal ability to differentiate. AML represents one of the most complex types of ...
Differential expression of the Bradykinin and Retinoic Acid Receptors in human colorectal cancer cell lines

Khati, Celine Fouad, (2015)

Chronic inflammation is a major characteristic of the development and progression of several tumors, in particular colorectal cancer. The connection between inflammation and tumorigenesis has been well supported from ...
Genetic screening for mutations in patients with inherited cardiomyopathies using next generation sequencing -

Hassanieh, Sylvana, (2015)

Cardiomyopathy is a disease affecting the myocardium leading to its weakness and enlargement, consequently ending in heart failure or sudden cardiac death. Cardiomyopathy is classified to five types based on its manifestation ...
In vitro effect of Penicillamine on neuronal and gliomal cells : possible implications on Wilson Disease patients -

Katerji, Meghri Sarkis (2015)

Background: Copper is an essential trace element that acts as a cofactor for many cuproenzymes. Cu is also crucial for the brain development and function. However, due to its high redox potential when present in excess, ...
Insights into the deregulations of Rbm20 in Lamin A-C and emerin related cardiomyopathies -

Sedki, Dana MHD Hazem, (2015)

Cardiomyopathies are among the leading causes of premature sudden death. Their etiology is genetically heterogeneous with more than 50 genes linked to them. The most substantial mutations involved in the cardiac phenotypes ...
NFATC1 and PAX pathway in cardiac and ocular diseases -

Poladian, Sarin Nazar, (2015)

The cardiac valvular and septal malformations account for the majority of the congenital heart defects (CHD). Processes that govern the heart development have been studied thoroughly through the last decade, however little ...
The role of MBTPS2 in epidermal proliferation and differentiation -

Ballout, Farah Rabih, (2015)

Ichthyosis (“fish scales”) and ichthyosiform disorders are inherited skin disorders for which no ideal therapy exists. These disorders are mainly caused by disturbances in epidermal differentiation and can present either ...

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Browsing by Author "Department of Biochemistry and Molecular Genetics. Faculty of Medicine,"

Browsing by Author "Department of Biochemistry and Molecular Genetics. Faculty of Medicine,"

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Copyright Statement