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168.303  Articles
1 of 16.831 pages  |  10  records  |  more records»
Background: Breast cancer is the most common malignancy in women. In the countries of Central and Eastern Europe founder mutations in the BRCA1 and BRCA2 genes are responsible for a significant proportion of breast cancer cases; however, regional differen... see more

AbstractBackground: Azithromycin regimens have been considered first-line treatment for Mycoplasma genitalium (M. genitalium), a sexually transmitted infection (STI) associated with adverse pregnancy outcomes. However, recent years have seen rapid emergen... see more

Current clinical genetic and genomic testing involves genome-wide evaluation of chromosomal abnormalities, copy number variants (CNVs) and gene mutations. The major challenge facing genetic laboratory directors, physicians and counselors is to distinguish... see more

Multiple primary tumors are understudied cancer. Criteria multiplicity of primary tumor: a tumor should be located in different organs, their morphology must be unequal, and each tumorshould provide their own metastases. At the time of appearance there ar... see more

Background: Familial Mediterranean Fever (FMF) is a genetic disorder characterized by recurrent episodes of fever and abdominal pain. Mutations in the Mediterranean fever (MEFV) gene are localized on the p arm of chromosome 16. Over 333 MEFV sequence vari... see more

Colorectal carcinoma (CRC) represents a global health problem. The EGFR signaling pathway is very important in the initiation of different human epithelial cancers and plays a key role in colorectal carcinogenesis. Considering the role of EGFR as a mitoge... see more

BACKGROUND Retinoblastoma (RB) is an inherited disorder caused by the RB1 gene mutation in retinal cells or germline mutation. Identifying the specific mutation is crucial for prognosis, inheritance risk assessment, and treatment planning. This study aime... see more

 
The aim of this study is to determine the risk factors for retinopathy of prematurity (ROP), and also to screen Norrie Disease Pseudoglioma (NDP) gene mutation in order to determine if mutation in the NDP gene may play a role in the development of ROP amo... see more

1 of 16.831 pages  |  10  records  |  more records»