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1.067  Articles
1 of 108 pages  |  10  records  |  more records»
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

The research objective is specifically to obtain the results of the analysis of the effect of mutation variables, incentives, and leadership styles on employee performance partially or simultaneously. The research method uses descriptive and verification ... see more

Previous studies showed that mutations in the SARS-CoV-2 ORF3a protein can influence viral pathogenesis. Therefore, it is necessary to observe mutations, especially in the functional domain of the protein. We observed the presence of mutations in the ORF3... see more

Induced mutagenesis opens great perspectives for radical genetic improvement of cultivated plants. Scientists seeking new sources and methodological approaches to improve the frequency and extend the range of mutations have drawn attention to the Zone of ... see more

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

Women who carry a pathogenic mutation in the breast cancer susceptibility genes BRCA1 or BRCA2 (BRCA) have markedly increased risks of developing breast and ovarian cancers during their lifetime. It has been estimated that their breast and ovarian cancer ... 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

L’absence ou l’atrésie bilatéraledes canaux déférents ABCD est une affection congénitale et héréditaire de transmission autosomique récessive : Elle représente 1 – 2% des causes d’infertilité masculine et 9 à 25 % des azoospermies obstructives. De nombreu... 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

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