Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników

Znaleziono wyników: 39

Liczba wyników na stronie
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 2 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników

Wyniki wyszukiwania

help Sortuj według:

help Ogranicz wyniki do:
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 2 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników
Epigenetic modifications, apart from affecting gene expression, play an important role in the chromatin structure stabilization, embryonic development and the genomic imprinting. Recent studies have shown that they also play a vital role in other biological processes, including silencing of the expression and mobility of transposable elements and resistance to viral infections by blocking the expression of viral genes. The stability of the genome and the expression of genes in normal cells are strongly dependent on the DNA methylation pattern, which is visibly disturbed in tumor cells. These alterations may be a consequence of the attachment of methyl groups to cytosines in unmethylated DNA sequences, resulting in an increase in the degree of methylation or can be a result of demethylation, i.e. a reduction in the level of DNA methylation. Currently, many techniques are available to determine the level of methylcytosine in DNA, both at the level of single genes and the whole genome. However, each method has its advantages and disadvantages, not being universal in relation to the type of research material and the purpose of planned analyses.
Dwarfism is a frequently occurring congenital disorder in human and farm animals. Defects in endochondral ossification lead to disproportionate dwarfism with abnormal length of the limbs in relation to the size of the trunk. Based on observed skeleton abnormities in general, a short- and long-limbed achondroplasia can be recognized. Short-headed dwarfism often relates to the latter ACH form and comprises a number of head deformities with a characteristic craniofacial shortening. Lethal cases with severe skeleton malformations occur when ACH is inherited in the homozygous recessive mode. A number of different ACH forms were described in Dexter, Holstein Fresian, Jersey, Aberdeen Angus, Hereford, Shorthorn and Japanese brown cattle. Only in the last mentioned breed two causative mutations have been detected causing ACH phenotype in the appendicular skeleton. Extensive efforts are being made to find mutations determining achondroplasia in other cattle breeds.
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 2 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.