Molecular dissection of two human chromatin diseases, Rett syndrome and icf syndrome

Reference: GGP02308 Abstract: Failure of correct gene expression underlies many human genetic disorders. In monogenic disorders, altered expression of a single gene can result from loss of the gene and/or modification of regulative control of gene expression. A class of monogenic disorders presents mutations of factors which mediate gene regulation, that can regulate more target … Read more

Cell line and DNA bank of Rett syndrome and other x-linked mental retardation

Reference: GTF02006 Abstract: Mental retardation (MR) is the most frequent cause of serious handicap in humans with an estimated total prevalence of 1-1,5% in the general population. It is calculated that X-linked MR (XLMR) may account for about 20-25% of mentally retarded males. Up to now, 42 genes have been found involved in XLMR, comprising … Read more

na

Reference: Prof. Dr. Albena Todorova Abstract: n.a PROJECT DETAILS  beginning: 2004. end: 2005. Country of research: Germany Counry of funding source: Germany Funding organization: Humboldt Research Fellowship for Postdoctoral Researchers Financing: PRIVATE FUNDERS – 63 600 € hyperlink

Relationships between ghrelin concentration in blood and growth and physical activity in children

Reference: ETF6225ᅠ Abstract: The biochemical markers that influence the growth of children have not been investigated much. The main goal of the present study is to investigate the relationships between novel peptide hormone ghrelin and anthropometrical characteristics, body composition, physical activity and aerobic working capacity, also to examine the adaptation to aerobic work and weight … Read more

By continuing to use the site, you agree to the use of cookies. more information

The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.

Close