نتایج جستجو برای: fragile control

تعداد نتایج: 1341839  

Journal: :Somatic cell and molecular genetics 1984
S T Warren R L Davidson

The fragile X chromosome, associated with a common form of X-linked mental retardation, is cytologically observed most often as a gap or fragile site near the distal end of the long arm in band Xq28. Expression of this site is variable and dependent upon lowered thymidylate pools. In order to examine the behavior of this fragile site in a foreign genetic background, interspecific somatic cell h...

2008
Mark McGillivray Mina Baliamoune-Lutz

The international donor community has grave concerns about the prospects for poverty reduction in what it terms fragile states. A state is classified as fragile if its country policy and institutional assessment (CPIA) score falls below a particular threshold. Recognizing that all states are fragile to varying degrees, this paper questions the method used by the international community to deem ...

2008
Mark McGillivray Mina Baliamoune-Lutz

The international donor community has grave concerns about the prospects for poverty reduction in what it terms fragile states. A state is classified as fragile if its country policy and institutional assessment (CPIA) score falls below a particular threshold. Recognizing that all states are fragile to varying degrees, this paper questions the method used by the international community to deem ...

Journal: رستنیها 2012
R. Siahbalaei, S. Afsharzadeh Sh. Nekouei Sh. Shokravi

Cyanophyta of some paddy-fields of Golestan province (North of Iran, near the Caspian Sea) have been studied during 2006–07. Phormidium subinerusatum, P. tenue, P. jadinianum, P. purpurascens, P. lucidum, P. fragile, Microcoleus palaodus, M. lacustris are new records for Golestan province and Iran. Results showed that  P. subinerusatum, P. tenue were dominant in all stations. P. fragile, in spr...

2008

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...

Journal: :Cell 1991
M Pieretti F P Zhang Y H Fu S T Warren B A Oostra C T Caskey D L Nelson

We previously reported the isolation of a gene (FMR-1) expressed in brain at the fragile X locus. One exon of this gene lies within an EcoRI fragment that exhibits length variation in fragile X patients. This exon also contains the CGG repeat within the CpG island hypermethylated in fragile X patients. To study the involvement of the FMR-1 gene in the fragile X syndrome, its expression was stud...

2015
Daniela Neuhofer Christopher M. Henstridge Barna Dudok Marja Sepers Olivier Lassalle István Katona Olivier J. Manzoni

Fragile X is the most common cause of inherited intellectual disability and a leading cause of autism. The disease is caused by mutation of a single X-linked gene called fmr1 that codes for the Fragile X mental retardation protein (FMRP), a 71 kDa protein, which acts mainly as a translation inhibitor. Fragile X patients suffer from cognitive and emotional deficits that coincide with abnormaliti...

2015
Casey M Graves Annie Haakenstad Joseph L Dieleman

BACKGROUND Development assistance for health (DAH) has grown substantially, totaling more than $31.3 billion in 2013. However, the degree that countries with high concentrations of armed conflict, ethnic violence, inequality, debt, and corruption have received this health aid and how that assistance might be different from the funding provided to other countries has not been assessed. METHODS...

Journal: :Journal of neurophysiology 2013
Virginia Conde Francisco J Palomar María José Lama Raquel Martínez Fátima Carrillo Elizabeth Pintado Pablo Mir

The fragile X syndrome is a mutation-driven developmental disorder caused by a repetition over 200 times of the CGG trinucleotide situated in the 5'-untranslated region of the fragile X mental retardation 1 gene (FMR1). The interval between 55 and 199 CGG repeats, which is over the normal range but below full mutation, is named fragile X premutation. Recent studies have focused on the asymptoma...

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