<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item><item key="slug">transcription-profiling-of-human-ibs-patients-befo</item><item key="factor_count">0</item><item key="sample_count">14</item><item key="tags"><item>cell</item><item>diarrhea</item><item>genome</item><item>irritable bowel syndrome</item><item>syndrome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-14842</item><item key="id">3169</item><item key="name">Transcription profiling of human IBS patients before and after treatment</item></item><item><item key="slug">transcription-profiling-of-human-skeletal-muscle-o</item><item key="factor_count">0</item><item key="sample_count">29</item><item key="tags"><item>body</item><item>glucose</item><item>hyperinsulinemia</item><item>insulin</item><item>lipid</item><item>muscle</item><item>ovary</item><item>polycystic ovary syndrome</item><item>syndrome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-6798</item><item key="id">4861</item><item key="name">Transcription profiling of human skeletal muscle of women with PCOS reveals reduced expression of mitochondrial oxidative metabolism genes</item></item><item><item key="slug">transcription-profiling-of-hut-78-cells-sezary-snd</item><item key="factor_count">1</item><item key="sample_count">11</item><item key="tags"><item>cell</item><item>lymphoma</item><item>protein</item><item>sezary syndrome</item><item>syndrome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-14746</item><item key="id">3163</item><item key="name">Transcription profiling of Hut 78 cells (Sezary sndrome) with a stable knockdown of AHI-1 expression to identify mediators of the AHI-1.</item></item><item><item key="slug">transcription-profiling-of-primary-fibroblasts-fro</item><item key="factor_count">1</item><item key="sample_count">9</item><item key="tags"><item>genetic disorder</item><item>genome</item><item>hutchinson-gilford progeria syndrome</item><item>lamin a</item><item>nuclear lamina</item><item>skin</item><item>syndrome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-MEXP-3097</item><item key="id">5175</item><item key="name">Transcription profiling of primary fibroblasts from a family with autosomal recessive Hutchinson-Gilford Progeria Syndrome</item></item><item><item key="slug">whole-exome-sequencing-identifies-mutations-of-bco</item><item key="factor_count">1</item><item key="sample_count">24</item><item key="tags"><item>chromosome</item><item>protein</item><item>syndrome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-30442</item><item key="id">4155</item><item key="name">Whole-exome sequencing identifies mutations of BCOR in acute myeloid leukemia with normal karyotype</item></item><item><item key="slug">zmym2fgfr1-bcrfgfr1-or-bcrabl1-in-human-cord-blood</item><item key="factor_count">2</item><item key="sample_count">12</item><item key="tags"><item>cell</item><item>chronic myeloid leukemia</item><item>leukemia</item><item>lymphoma</item><item>myeloid leukemia</item><item>myeloproliferative disorder</item><item>stem cell</item><item>stem cell leukemia</item><item>syndrome</item><item>tyrosine</item><item>umbilical cord</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-15811</item><item key="id">3258</item><item key="name">ZMYM2/FGFR1, BCR/FGFR1 or BCR/ABL1 in human cord blood CD34+ cells reveals similar but distinct gene expression profiles</item></item><item><item key="slug">transcription-profiling-of-rat-low-and-high-capaci</item><item key="factor_count">0</item><item key="sample_count">16</item><item key="tags"><item>carbohydrate</item><item>fatty acid</item><item>genome</item><item>glucose</item><item>left</item><item>left ventricle</item><item>lipid</item><item>liquid</item><item>metabolic syndrome</item><item>protein</item><item>syndrome</item><item>ventricle</item></item><item key="species">rat</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-9445</item><item key="id">9405</item><item key="name">Transcription profiling of rat low and high capacity  - sedentary and trained: left ventricle</item></item><item><item key="slug">transcription-profiling-of-rat-soleus-muscle-from</item><item key="factor_count">0</item><item key="sample_count">16</item><item key="tags"><item>body</item><item>central</item><item>disease</item><item>fatty acid</item><item>genome</item><item>line</item><item>lipid</item><item>metabolic syndrome</item><item>muscle</item><item>soleus</item><item>syndrome</item></item><item key="species">rat</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-10527</item><item key="id">8977</item><item key="name">Transcription profiling of rat soleus muscle from animals artificially selected for high and low running capacity</item></item><item><item key="slug">transcription-profiling-of-liver-from-wistar-and-k</item><item key="factor_count">3</item><item key="sample_count">18</item><item key="tags"><item>disease</item><item>fatty liver disease</item><item>glucose</item><item>glycogen</item><item>liver</item><item>liver disease</item><item>metabolic syndrome</item><item>syndrome</item></item><item key="species">rat</item><item key="is_default">False</item><item key="geo_gse_id">E-BIID-1</item><item key="id">8883</item><item key="name">Transcription profiling of liver from wistar and kyoto rats exposed to orotic acid to investigate fatty liver disease</item></item><item><item key="slug">differential-gene-expression-and-mitochondrial-dys</item><item key="factor_count">2</item><item key="sample_count">14</item><item key="tags"><item>brain</item><item>chromosome</item><item>genetic disorder</item><item>genome</item><item>heart</item><item>hypogonadism</item><item>liver</item><item>morbid obesity</item><item>muscle</item><item>obesity</item><item>prader-willi syndrome</item><item>syndrome</item><item>vastus lateralis</item></item><item key="species">mouse</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-41759</item><item key="id">7051</item><item key="name">Differential Gene Expression and Mitochondrial Dysfunction in Imprinting center deletion (PWS- IC del) Mouse model of Prader-Willi Syndrome</item></item></data></biogps>
