منابع مشابه
Fragile States
Fragile States Fragile States T UNU-WIDER PROJECT ON “FRAGILITY AND development’’ began with the premise that dealing simultaneously with household vulnerability and state fragility is probably one of the most urgent development challenges of our time. Consequently, the project explored the dimensions of household vulnerability and state fragility in development. This research brief is about th...
متن کاملFragile X syndrome and fragile X-associated disorders
Fragile X syndrome (FXS) is caused by a full mutation on the FMR1 gene and a subsequent lack of FMRP, the protein product of FMR1. FMRP plays a key role in regulating the translation of many proteins involved in maintaining neuronal synaptic connections; its deficiency may result in a range of intellectual disabilities, social deficits, psychiatric problems, and dysmorphic physical features. A ...
متن کاملFRAGILE and SEMI - FRAGILE WATERMARKING TECHNIQUES for IMAGE AUTHENTICATION
Techniques to establish the authenticity and integrity of digital images are becoming increasly essential over the Intermet. The authentication algorithm should distinguish malicious manipulations from the original watermarked image[1]. Fragile watermarking is recomended for a very sensible image authentication scheme, able to localize the slightest changes occured to the marked image. The frag...
متن کاملIncreased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives.
Fragile X premutations are known to be a risk factor for diminished ovarian function at a relatively young age. We studied endocrine profiles of female fragile X family members (n = 79) at risk of premature ovarian failure (POF). Of these 79 women aged <40 years, 45 had menstrual cycles, and 34 were using oral contraceptives. Of the women with menstrual cycles, the premutation carriers had high...
متن کاملThe drosophila fragile X protein dFMR1 is required during early embryogenesis for pole cell formation and rapid nuclear division cycles.
The FMR family of KH domain RNA-binding proteins is conserved from invertebrates to humans. In humans, inactivation of the X-linked FMR gene fragile X is the most common cause of mental retardation and leads to defects in neuronal architecture. While there are three FMR family members in humans, there is only a single gene, dfmr1, in flies. As in humans, inactivation of dfmr1 causes defects in ...
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ژورنال
عنوان ژورنال: Journal of Differential Equations
سال: 2012
ISSN: 0022-0396
DOI: 10.1016/j.jde.2011.12.002