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302.133  Articles
1 of 30.214 pages  |  10  records  |  more records»
A disorder of copper metabolism at Wilson’s disease (WD), conditioned by a mutation of adenosine thriphospate P-type gene (ATP7B), results in irreversible changes in the liver and in the nervous system. Mortality is high at WD, but it is one of hereditary... see more

A disorder of copper metabolism at Wilson’s disease (WD), conditioned by a mutation of adenosine thriphospate P-type gene (ATP7B), results in irreversible changes in the liver and in the nervous system. Mortality is high at WD, but it is one of hereditary... see more

Radio Frequency Identification (RFID) is a technology that is very popular due to the simplicity in its technology and high adaptability in a variety of areas. The simplicity in the technology, however, comes with a caveat – RFID tags have severe resource... see more

Follicle-stimulating hormone (FSH) plays a significant role in folliculogenesis by binding to its receptors located on the surface of the granulosa cells.Molecular effects of FSH receptor mutation are following. FSH receptor activity is reduced at variant... see more

The BADH2 gene acts as suppressor of 2-acetyl-1-pyrolline (2AP) biosynthesis in plants. 2AP is the volatile compound which provides fragrance in rice. Biosynthesis of 2AP occurs when BADH2 loses its function as suppressor gene. Aromatic rice cultivars nat... see more

Gastroesophageal disease (GERD) is the one of most spread diseases that injures an esophagus. Taking into account the large number of factors that can cause GERD development already in child age, including genetic predisposition, it is necessary to analyz... see more

Context. The problem of automation synthesis of artificial neural networks for further use in diagnosing, forecasting and patternrecognition is solved. The object of the study was the process of synthesis of ANN using a modified genetic algorithm.Objectiv... see more

Maternally inherited diabetes and deafness is a rare form of diabetes caused by a mitochondrial DNA mutation. The index case is a 55-year-old woman who was admitted with hypertrophic cardiomyopathy. She had a history of diabetes mellitus and hearing ... see more

Cystic fibrosis (CF) is the most frequent lethal autosomal recessive disorder among Caucasians (incidence: 1:2,500 newborn). In the last two decades CF prognosis considerably improved and many patients well survive into their adulthood. Furthermore, milde... see more

1 of 30.214 pages  |  10  records  |  more records»