<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">4616</item><item key="factors"><item><item key="GSM1050260"><item key="DISEASE STATE">tibial muscular dystrophy (TMD)</item><item key="AGE AT BIOPSY">53</item><item key="INDIVIDUAL IDENTIFIER">not specified</item><item key="ORGANISM PART">extensor digitorum longus</item></item></item><item><item key="GSM105026"><item key="DISEASE STATE">tibial muscular dystrophy (TMD)</item><item key="AGE AT BIOPSY">62</item><item key="INDIVIDUAL IDENTIFIER">not specified</item><item key="ORGANISM PART">gastrocnemius medialis</item></item></item><item><item key="GSM1050262"><item key="DISEASE STATE">tibial muscular dystrophy (TMD)</item><item key="AGE AT BIOPSY">48</item><item key="INDIVIDUAL IDENTIFIER">not specified</item><item key="ORGANISM PART">tibialis anterior</item></item></item><item><item key="GSM1050263"><item key="DISEASE STATE">tibial muscular dystrophy (TMD)</item><item key="AGE AT BIOPSY">65</item><item key="INDIVIDUAL IDENTIFIER">not specified</item><item key="ORGANISM PART">extensor digitorum longus</item></item></item><item><item key="GSM1050264"><item key="DISEASE STATE">tibial muscular dystrophy (TMD)</item><item key="AGE AT BIOPSY">52</item><item key="INDIVIDUAL IDENTIFIER">not specified</item><item key="ORGANISM PART">soleus</item></item></item><item><item key="GSM1050265"><item key="DISEASE STATE">tibial muscular dystrophy (TMD)</item><item key="AGE AT BIOPSY">52</item><item key="INDIVIDUAL IDENTIFIER">not specified</item><item key="ORGANISM PART">tibialis posterior</item></item></item><item><item key="GSM1050266"><item key="DISEASE STATE">tibial muscular dystrophy (TMD)</item><item key="AGE AT BIOPSY">52</item><item key="INDIVIDUAL IDENTIFIER">not specified</item><item key="ORGANISM PART">tibialis anterior</item></item></item><item><item key="GSM1050270"><item key="DISEASE STATE">healthy</item><item key="AGE AT BIOPSY">76</item><item key="INDIVIDUAL IDENTIFIER">1</item><item key="ORGANISM PART">tibialis posterior</item></item></item><item><item key="GSM105027"><item key="DISEASE STATE">healthy</item><item key="AGE AT BIOPSY">76</item><item key="INDIVIDUAL IDENTIFIER">1</item><item key="ORGANISM PART">extensor digitorum longus</item></item></item><item><item key="GSM1050272"><item key="DISEASE STATE">healthy</item><item key="AGE AT BIOPSY">80</item><item key="INDIVIDUAL IDENTIFIER">2</item><item key="ORGANISM PART">tibialis anterior</item></item></item><item><item key="GSM1050273"><item key="DISEASE STATE">healthy</item><item key="AGE AT BIOPSY">80</item><item key="INDIVIDUAL IDENTIFIER">2</item><item key="ORGANISM PART">extensor digitorum longus</item></item></item><item><item key="GSM1050274"><item key="DISEASE STATE">healthy</item><item key="AGE AT BIOPSY">76</item><item key="INDIVIDUAL IDENTIFIER">1</item><item key="ORGANISM PART">soleus</item></item></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">Tibial muscular dystrophy (TMD) is a late onset, autosomal dominant distal myopathy that results from mutations in the two last domains...</item><item key="pubmed_id">24618559</item><item key="geo_gse_id">E-GEOD-42806</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">4</item><item key="sample_count">12</item><item key="tags"><item>distal</item><item>distal myopathy</item><item>muscle</item><item>muscular dystrophy</item><item>myopathy</item><item>tibial</item><item>titin</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">gene-expression-profiling-in-tibial-muscular-dystr</item><item key="geo_id_plat">E-GEOD-42806_A-AFFY-44</item><item key="name">Gene expression profiling in tibial muscular dystrophy and control skeletal muscle</item><item key="created">Sep.19, 2014</item><item key="summary">Tibial muscular dystrophy (TMD) is a late onset, autosomal dominant distal myopathy that results from mutations in the two last domains of titin. The cascade of molecular events leading from the causative Titin mutations to the preterm death of muscle cells in TMD is largely unknown. To identify these components, we used gene expression profiling of muscle biopsies from TMD patients and healthy controls. 5 muscle samples from 2 normal control subjects and muscle samples from 7 TMD subjects.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-42806</item><item key="species">human</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-42806/samples/</item></data></biogps>
