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Displaying 20 of 28 results for "ASPN"
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  1. Hs_Phospho_AspN_CID OmicsDI

    ID: PAe005276

    Date Released: 12-31-2015

    Description: Multiple protease based human phosphopeptide, AspN, CID

  2. SHR_AspN_Velos OmicsDI

    ID: PAe004320

    Date Released: 12-31-2013

    Description: SHR_liver, AspN, LTQ Orbi Velos

  3. BN_AspN_Velos OmicsDI

    ID: PAe004324

    Date Released: 12-31-2013

    Description: BN-Lx_liver, AspN, LTQ Orbi Velos

  4. SHR_AspN_TTOF OmicsDI

    ID: PAe004330

    Date Released: 12-31-2013

    Description: SHR_liver, AspN, ABI TripleTOF

  5. Hs_Hela_AspN_CID OmicsDI

    ID: PAe005008

    Date Released: 12-31-2014

    Description: Human hela proteome, AspN CID

  6. Hs_Phospho_AspN_ETD OmicsDI

    ID: PAe005250

    Date Released: 12-31-2015

    Description: Multiple protease based human phosphopeptide, AspN, ETD

  7. BN_AspN_TTOF OmicsDI

    ID: PAe004329

    Date Released: 12-31-2013

    Description: BN-Lx_liver, AspN, ABI TripleTOF

  8. ASPN_BOVIN UniProt:Swiss-Prot

    ID: Q3ZBN5

    Description: Asporin LRRNT LRR 1 LRR 2 LRR 3 LRR 4 LRR 5 LRR 6 LRR 7 LRR 8 LRR 9 LRR 10 LRR 11 Cys-rich O-linked (GalNAc...) N-linked (GlcNAc...)

    gene.name: ASPN
  9. Hs_Hela_AspN_HCD OmicsDI

    ID: PAe005048

    Date Released: 12-31-2014

    Description: Human hela proteome, AspN HCD

  10. Gene Expression Profiling of Peri-implant Healing of PLGA-Li+ Implants Suggests an Activated Wnt Signaling Pathway in vivo ArrayExpress

    ID: E-GEOD-54294

    Description: SL1, and the extracellular protein-encoding gene, ASPN, were significantly upregulated by Li+ compared with Ctrl. The presence of β-catenin, FOSL1 and ASPN positive cells was confirmed around implants of both groups. Interestingly, a significantly reduced bone area was observed over time around both implant groups. The presence of periostin and calcitonin receptor-positive cells was observed at both time points. This study is to the best of the authors’ knowledge the first report evaluating the effect of a local release of Li+ from PLGA at the fracture site. The present study shows that during the current time frame and with the present dose of Li+ in PLGA implants, Li+ is not an enhancer of early bone growth, although it affects the Wnt signaling pathway. PLGA implants with +/- incorporated Li were inserted in rat tibia for 7 or 28 days, peri-implant bone was harvested and RNA extracted using Qiazol lysis reagent and TissueLyser followed by Qiagen's Rneasy Micro Kit. The microarray experiment was conducted at SCIBLU Genomics (www.lu.se/sciblu) according to Affymetrix guidelines (n=6)....

  11. Gene Expression Analyses of Subchondral Bone in Early Experimental Osteoarthritis by Microarray ArrayExpress

    ID: E-GEOD-30322

    Description: Igf1, Tgf β1, Postn, Mmp3, Tnfsf11, Acp5, Bmp5, Aspn and Ihh, were confirmed by real-time PCR, and results indicated that our microarray data could accurately reflect gene expression patterns of early OA. Subsequently, to validate the results of our microarray analysis at protein level, immunohistochemistry staining was introduced to investigate the translational level of genes Mmp3 and Aspn in tissue sections, and results showed that the level of Mmp3 protein expression was totally matched the results of microarray and real-time PCR analysis. Nevertheless, the expression of Aspn protein was not observed differentially expressed at any time point. Ninety 10-week-old male Sprague-Dawley rats, weighing 300-325g, were used in the study. Animals were equally divided into two groups: experimental group (E-Group) and sham-operated group (S-Group). The E-Group rats underwent open surgery, involved in both medial meniscectomy and medial collateral ligament (MCL)...

  12. Gene Expression Analyses of Subchondral Bone in Early Experimental Osteoarthritis by Microarray OmicsDI

    ID: E-GEOD-30322

    Date Released: 06-02-2014

    Description: Igf1, Tgf β1, Postn, Mmp3, Tnfsf11, Acp5, Bmp5, Aspn and Ihh, were confirmed by real-time PCR, and results indicated that our microarray data could accurately reflect gene expression patterns of early OA. Subsequently, to validate the results of our microarray analysis at protein level, immunohistochemistry staining was introduced to investigate the translational level of genes Mmp3 and Aspn in tissue sections, and results showed that the level of Mmp3 protein expression was totally matched the results of microarray and real-time PCR analysis. Nevertheless, the expression of Aspn protein was not observed differentially expressed at any time point. Ninety 10-week-old male Sprague-Dawley rats, weighing 300-325g, were used in the study. Animals were equally divided into two groups: experimental group (E-Group) and sham-operated group (S-Group). The E-Group rats underwent open surgery, involved in both medial meniscectomy and medial collateral ligament (MCL)...

  13. Gene Expression Profiling of Peri-implant Healing of PLGA-Li+ Implants Suggests an Activated Wnt Signaling Pathway in vivo BioProject

    ID: PRJNA236109

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: SL1, and the extracellular protein-encoding gene, ASPN, were significantly upregulated by Li+ compared with Ctrl. The presence of β-catenin, FOSL1 and ASPN positive cells was confirmed around implants of both groups. Interestingly, a significantly reduced bone area was observed over time around both implant groups. The presence of periostin and calcitonin receptor-positive cells was observed at both time points. This study is to the best of the authors’ knowledge the first report evaluating the effect of a local release of Li+ from PLGA at the fracture site. The present study shows that during the current time frame and with the present dose of Li+ in PLGA implants, Li+ is not an enhancer of early bone growth, although it affects the Wnt signaling pathway. Overall design: PLGA implants with +/- incorporated Li were inserted in rat tibia for 7 or 28 days, peri-implant bone was harvested and RNA extracted using Qiazol lysis reagent and TissueLyser followed by Qiagen's Rneasy Micro Kit. The microarray experiment was conducted at SCIBLU Genomics (www.lu.se/sciblu) according to Affymetrix guidelines (n=6)....
  14. Gene Expression Analyses of Subchondral Bone in Early Experimental Osteoarthritis by Microarray BioProject

    ID: PRJNA143609

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: Igf1, Tgf β1, Postn, Mmp3, Tnfsf11, Acp5, Bmp5, Aspn and Ihh, were confirmed by real-time PCR, and results indicated that our microarray data could accurately reflect gene expression patterns of early OA. Subsequently, to validate the results of our microarray analysis at protein level, immunohistochemistry staining was introduced to investigate the translational level of genes Mmp3 and Aspn in tissue sections, and results showed that the level of Mmp3 protein expression was totally matched the results of microarray and real-time PCR analysis. Nevertheless, the expression of Aspn protein was not observed differentially expressed at any time point. Overall design: Ninety 10-week-old male Sprague-Dawley rats, weighing 300-325g, were used in the study. Animals were equally divided into two groups: experimental group (E-Group) and sham-operated group (S-Group). The E-Group rats underwent open surgery, involved in both medial meniscectomy and medial collatera...
  15. Gene Expression Profiling of Peri-implant Healing of PLGA-Li+ Implants Suggests an Activated Wnt Signaling Pathway in vivo. OmicsDI

    ID: E-GEOD-54294

    Date Released: 07-26-2014

    Description: SL1, and the extracellular protein-encoding gene, ASPN, were significantly upregulated by Li+ compared with Ctrl. The presence of β-catenin, FOSL1 and ASPN positive cells was confirmed around implants of both groups. Interestingly, a significantly reduced bone area was observed over time around both implant groups. The presence of periostin and calcitonin receptor-positive cells was observed at both time points. This study is to the best of the authors’ knowledge the first report evaluating the effect of a local release of Li+ from PLGA at the fracture site. The present study shows that during the current time frame and with the present dose of Li+ in PLGA implants, Li+ is not an enhancer of early bone growth, although it affects the Wnt signaling pathway. PLGA implants with +/- incorporated Li were inserted in rat tibia for 7 or 28 days, peri-implant bone was harvested and RNA extracted using Qiazol lysis reagent and TissueLyser followed by Qiagen's Rneasy Micro Kit. The microarray experiment was conducted at SCIBLU Genomics (www.lu.se/sciblu) according to Affymetrix guidelines (n=6)....

  16. Proteogenomic analysis of Helicobacter pylori strain 26695 OmicsDI

    ID: PXD000054

    Date Released: 08-01-2013

    Description: SEC fractionation of LMW proteins and subsequent AspN digestion, replicate 1 A2: SEC fractionation of LMW proteins and subsequent AspN digestion, replicate 2 L1: SEC fractionation of LMW proteins and subsequent LysC digestion, replicate 1 L2: SEC fractionation of LMW proteins and subsequent LysC digestion, replicate 2 In our proteogenomics approach, we could identify four previously missing protein annotations and were able to correct sequences of six protein coding regions. Furthermore we identified signal peptidase cleavage sites for 72 different proteins. MGFs were generated by Maxquant 1.1 [1] using recalibration of peptide parent masses. For PRIDE (http://www.e...

  17. Gene expression changes in NFAT5/TonEBP under isotonic and hypertonic conditions ArrayExpress

    ID: E-GEOD-25816

    Description: TonEBP is a transcription factor that promotes cellular accumulation of organic osmolytes in the hypertonic renal medulla by stimulating expression of...

  18. Combining solid phase extraction with ultra-short gradients in LC-MS/MS substantially improves protein identification per unit of time OmicsDI

    ID: PXD001111

    Date Released: 12-12-2014

    Description: mics experiment, involving 36 SCX fractions of an AspN digested cell lysate, lead to the detection of over 3600 protein groups in only 3h cumulative gradient time when using a QExactive mass analyser. Application to typical various proteomics experiments such as samples from pull-downs allowed the detection of hundreds of proteins whereby a given protein’s interactome could be determined in less than 1h of accumulated gradient time. This new LC system diminishes proteome analysis time considerably, whole providing sufficient proteomic detail, and may thus also aid in bringing proteomics into the clinic where fast turn-over times are essential....

  19. Gene expression changes in NFAT5/TonEBP under isotonic and hypertonic conditions BioProject

    ID: PRJNA135623

    Keywords: Transcriptome or Gene expression

    Access Type: download

  20. Transcription profiling of mouse E12.5 AV cushion and E17.5 AV valve from wild-type FVB/N mice and in vitro cultured MC3T3 cells ArrayExpress

    ID: E-GEOD-11040

    Description: E12.5 AV cushion and E17.5 AV valve from wild-type FVB/N mice and in vitro cultured MC3T3 cells; In the study we demonstrated shared gene expression i...


Displaying 20 of 28 results for "ASPN"