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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">9535</item><item key="factors"><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item><item><item key="GSE9918GSM251003"/></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">11</item><item key="summary_wrapped">retinal ganglion cells die after optic nerve injury, either crush or transection. The molecular causesunderlying this degeneration are...</item><item key="pubmed_id">18552980</item><item key="geo_gse_id">E-GEOD-9918</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">35</item><item key="tags"><item>ganglion</item><item>nerve</item><item>optic nerve</item><item>point</item></item><item key="lastmodified">Feb.09, 2015</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-9918_A-AFFY-43</item><item key="slug">transcription-profiling-of-rat-retina-after-iont-a</item><item key="geo_gds_id"/><item key="name">Transcription profiling of rat retina after IONT and IONC - time series</item><item key="created">Jan.12, 2015</item><item key="summary">retinal ganglion cells die after optic nerve injury, either crush or transection. The molecular causesunderlying this degeneration are largely unkwon; the purpose of this job is to find which  (if any) gene regulation triggers RGC death with the final goal of design neuroprotective protocols Experiment Overall Design: 3 groups: naive, IONT (intraorbital nerve transection) IONC (intraorbital nerve crush). IONT and IONC lesioned animals were kept the appropriate times postlesion (12h,. 24h, 48h, 3d, 7d, and 15d). For each time point 8-12 animals were used. RNA from 4 animals was pooled and extracted to hybridaze 1 array replica.  All replicas were pooled biological replicas: 5 for naive RNA (each replica 4 retinas, therefore  5 independent RNA extractions were done with a total of 20 retinas), IONT: 12h 3 replicas, 24h 2 replicas, 48h 3replicas, 3d 2 replicas, 7d 3 replicas, 15d 2 replicas. IONC: 3 replicas per time point: 12h, 24h, 48h, 3d and 7d)</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-9918</item><item key="species">rat</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-9918/samples/</item></data></biogps>
