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<biogps><data><item><item key="slug">a-whole-genome-approach-to-characterising-a-novel</item><item key="factor_count">1</item><item key="sample_count">2</item><item key="tags"><item>genome</item><item>nucleotide</item><item>peripheral</item><item>syndrome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-14845</item><item key="id">3171</item><item key="name">A Whole Genome Approach to Characterising a Novel Immunodeficiency Disorder</item></item><item><item key="slug">bcor-regulated-genes-in-human-oculo-facio-cardio-d</item><item key="factor_count">0</item><item key="sample_count">2</item><item key="tags"><item>apical</item><item>eye</item><item>genetic disorder</item><item>syndrome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-15214</item><item key="id">3211</item><item key="name">BCOR-regulated genes in human oculo-facio-cardio-dental syndrome</item></item><item><item key="slug">common-gene-expression-profile-in-the-mitochondria</item><item key="factor_count">5</item><item key="sample_count">15</item><item key="tags"><item>disease</item><item>fibroblast</item><item>lipid</item><item>syndrome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-33769</item><item key="id">2475</item><item key="name">Common gene expression profile in the mitochondrial syndrome of coenzyme Q deficiency</item></item><item><item key="slug">common-gene-transcriptional-patterns-following-imm</item><item key="factor_count">1</item><item key="sample_count">20</item><item key="tags"><item>autoimmune disease</item><item>brain</item><item>compartment</item><item>compartment syndrome</item><item>disease</item><item>liquid</item><item>muscle</item><item>protein</item><item>spinal cord</item><item>syndrome</item><item>vastus lateralis</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-21497</item><item key="id">3642</item><item key="name">Common Gene Transcriptional Patterns Following Immobilization, Spinal Cord Injury, and Unloading in Human Skeletal Muscle</item></item><item><item key="slug">correlated-alterations-in-genome-organization-hist</item><item key="factor_count">4</item><item key="sample_count">6</item><item key="tags"><item>chromatin</item><item>chromosome</item><item>disease</item><item>exon</item><item>genome</item><item>heterochromatin</item><item>hutchinson-gilford progeria syndrome</item><item>lamin a</item><item>nuclear lamin</item><item>nuclear lamina</item><item>point</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-41751</item><item key="id">4601</item><item key="name">Correlated alterations in genome organization, histone methylation, and DNA-lamina interactions in Hutchinson-Gilford progeria syndrome (expression)</item></item><item><item key="slug">differential-gene-expression-in-granulosa-cells-fr</item><item key="factor_count">1</item><item key="sample_count">10</item><item key="tags"><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-34526</item><item key="id">2699</item><item key="name">Differential Gene Expression in Granulosa Cells from Polycystic Ovary Syndrome Patients with and without Insulin Resistance:  Identification of Susceptibility Gene Sets through Network Analysis</item></item><item><item key="slug">expression-data-of-ribosomal-proteins-from-sorted</item><item key="factor_count">2</item><item key="sample_count">19</item><item key="tags"><item>myelodysplastic syndrome</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-30201</item><item key="id">4144</item><item key="name">Expression data of ribosomal proteins from sorted hematopoietic stems cells from patients with low risk MDS.</item></item><item><item key="slug">expression-data-of-the-ipscs-derived-from-foreskin</item><item key="factor_count">3</item><item key="sample_count">18</item><item key="tags"><item>chromosome</item><item>disease</item><item>fibroblast</item><item>line</item><item>syndrome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-37258</item><item key="id">4465</item><item key="name">Expression data of the iPSCs derived from foreskin fibroblast cells of normal person and KS patient</item></item><item><item key="slug">expression-profiles-of-amniotic-fluid-from-human-f</item><item key="factor_count">3</item><item key="sample_count">14</item><item key="tags"><item>chromosome</item><item>down syndrome</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-16176</item><item key="id">3286</item><item key="name">Expression profiles of amniotic fluid from human fetuses with Down syndrome and euploid controls</item></item><item><item key="slug">expression-profiling-in-williams-beuren-syndrome-p</item><item key="factor_count">2</item><item key="sample_count">17</item><item key="tags"><item>cell</item><item>chromosome</item><item>disease</item><item>fibroblast</item><item>serum</item><item>skin</item><item>syndrome</item><item>williams-beuren syndrome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-16715</item><item key="id">3327</item><item key="name">Expression profiling in Williams-Beuren Syndrome patient fibroblast cell lines</item></item></data></biogps>
