Expressed sequence tags from testis and placenta tissue: Analysis, annotation, and utility for mapping-2

<p><b>Copyright information:</b></p><p>Taken from "Expressed sequence tags from testis and placenta tissue: Analysis, annotation, and utility for mapping"</p><p>http://www.biomedcentral.com/1471-2164/9/300</p><p>BMC Genomics 2008;9():300-300.</p><p>Published online 24 Jun 2008</p><p>PMCID:PMC2443383.</p><p></p

Expressed sequence tags from testis and placenta tissue: Analysis, annotation, and utility for mapping-1

Ed using homologs. GO terms were obtained using the online tool, FatiGO []. The 'n' denotes the number of genes containing the same GO term, and the percentage represents the ratio of the number of genes annotated with the same GO term versus the total number of genes with GO annotation (some genes do not have GO information and many genes have multiple GO annotations).<p><b>Copyright information:</b></p><p>Taken from "Expressed sequence tags from testis and placenta tissue: Analysis, annotation, and utility for mapping"</p><p>http://www.biomedcentral.com/1471-2164/9/300</p><p>BMC Genomics 2008;9():300-300.</p><p>Published online 24 Jun 2008</p><p>PMCID:PMC2443383.</p><p></p

The release profile of ketorolac <i>in vitro</i> and <i>in vivo</i>.

<p>(A) <i>In vitro</i> assessment of cumulative ketorolac drug release from keto-hydrogel for 28 days. Inset shows the detail of ketorolac release for the initial 48 hours. (B) <i>In vivo</i> ketorolac concentration in tissue fluid at various time points (ketorolac solution versus keto-hydrogel; n = 3). Ketorolac concentrations are expressed as mean ± SD. *<i>P</i> < 0.05, **<i>P</i> < 0.001.</p

Evaluation of a novel biodegradable thermosensitive keto-hydrogel for improving postoperative pain in a rat model - Fig 1

<p>(A) Synthesis of BOX linking mPEG-PLGA diblock copolymer (BOX copolymer). (B) ¹H NMR spectrum of mPEG-PLGA diblock copolymer (BOX copolymer). # and * denote deuterated chloroform (CDCl₃) and H₂O respectively.</p

Postoperative pain and sensory assessment in rat hind-paw incisional model.

<p>(A) Pain threshold (mechanical hyperalgesia), (B) sensory threshold (tactile allodynia), and (C) pain score (relative to % body weight) of control, direct application of ketorolac solution, hydrogel, and keto-hydrogel treated rats after hind-paw incision. n = 8 per group. *<i>P</i> < 0.05, **<i>P</i> < 0.001 compared to control.</p

Number of tested animals in sham, control, ketorolac, keto-hydrogel and hydrogel group among various experimental methods.

<p>Number of tested animals in sham, control, ketorolac, keto-hydrogel and hydrogel group among various experimental methods.</p

Temperature-viscosity diagram for BOX copolymer aqueous solutions of different concentrations embedded with various amounts of ketorolac from 10 mg/mL to 30 mg/mL.

<p>Temperature-viscosity diagram for BOX copolymer aqueous solutions of different concentrations embedded with various amounts of ketorolac from 10 mg/mL to 30 mg/mL.</p

Effects of hind-paw incision on pro-inflammatory and angiogenic cytokine levels.

<p>The levels of TNF-α (A), IL-6 (B), VEGF (C), and IL-1β (D), were measured at day 3 (D3) and day 7 (D7) after incision. (N = 5 per group). Control indicates normal saline treatment, while sham indicates no surgical manipulation. * <i>P</i> < 0.05, **<i>P</i> < 0.001 compared between each group, # <i>P</i> < 0.05 compared between D3 and D7.</p

The sol-gel phase transition characteristics of keto-hydrogel by rheometer and tube inversion test at 37°C.

<p>S: solution, G: gel.</p