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Diabetes / Chromosomal abnormalities / Cytogenetics / 1p36 deletion syndrome / Prader–Willi syndrome / Monosomy / Hyperinsulinism / Contiguous gene syndrome / Metabolic syndrome / Health / Syndromes / Genodermatoses


The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro
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City

Osaka / Chieti / Rüschendorf / Florence / /

Company

Berry SA / LG / Santorico SA / Weder AB / Proc Natl Acad Sci U S A / Agilent / Genzyme / Cox / Monaghan KG / Case / BioMed Central Ltd. / Creative Commons / /

Country

Germany / Italy / /

Currency

pence / /

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Event

Product Issues / /

Facility

Anna Meyer Children’s University Hospital / University of Chieti / University of Florence / /

IndustryTerm

midi-satellite probe / /

MedicalCondition

Microcephaly / PDA / neoplasms / common chromosomal syndrome / severe obesity / Del 1p36 syndrome / mild learning disability / neuroblastoma maps / Seizures / congenital abnormalities / arterial hypertension / both systolic and diastolic hypertension / common deletion syndrome / Monosomy 1p36 deletion syndrome / deletion 1p36 syndrome / monosomy 1p36 syndrome / Prader-Willi syndrome / 1p36 deletion syndrome / sensorineural hearing loss / X syndrome / Prader-Willi-like syndrome / newly delineated syndrome / deafness / cortical dysplasia / obesity / particular deletion syndrome / glucose metabolism disorders / 6q deletion syndrome / disorder / systolic and diastolic hypertension / severe hyperinsulinism / both obesity / scoliosis / hearing impairment / II diabetes / ovarian carcinoma / substantial truncular obesity / hyperinsulinism / premature myocardial infarction / marked insulin resistance / insulin resistance / thyroid nodules / Mental retardation / hypertension / cardiomyopathy / Cancer / hypotonia / developmental delay / patent ductus arteriosus / considerable basal hyperinsulinism / congenital hypothyroidism / respiratory infections / diabetes / pulmonary hypertension / metabolic syndrome / coeliac disease / Angelman syndrome / diabetes mellitus / marked hyperinsulinism / II diabetes mellitus / Cantu syndrome / Epilepsy / Strabismus / hypotonia / neonatal hypotonia / Heart abnormalities / tetralogy of Fallot / glucose metabolism deficiency / atrial septal defect / syndrome / /

MusicGroup

Nelson / /

Organization

4Paediatric Endocrinology Unit / Paediatric Endocrinology Unit / University of Chieti / ND ND / national heart / lung and blood institute / Molecular Medicine Unit / Health’s Sciences Department / University of Florence / Anna Meyer Children’s University Hospital / Genetics and Molecular Medicine Unit / ND ND ND / /

Person

Angelo Eugster / D'Angelo / /

Position

MP / Zori RT / author / representative / Marshall / /

Product

ACTH / glucose tolerance / /

ProgrammingLanguage

DC / /

ProvinceOrState

Massachusetts / /

Technology

udp / Human Genome / DNA Chip / genotype / PDA / midi / /

URL

http /

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