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Article title matches

  1. Category:Egln (35 bytes)
    1: List of pages with the keyword Egln

Page text matches

  1. 2hbt (4,206 bytes)
    2: ==Crystal structure of HIF prolyl hydroxylase EGLN-1 in complex with a biologically active inhibitor...
    11: ...t.org/uniprot/EGLN1_HUMAN EGLN1_HUMAN] Defects in EGLN1 are the cause of familial erythrocytosis type 3 ...
    13: ...d increased expression of hypoxy-inducible genes. EGLN1 is the most important isozyme under normoxia and...
  2. 2hbu (4,181 bytes)
    2: ==Crystal structure of HIF prolyl hydroxylase EGLN-1 in complex with a biologically active inhibitor...
    11: ...t.org/uniprot/EGLN1_HUMAN EGLN1_HUMAN] Defects in EGLN1 are the cause of familial erythrocytosis type 3 ...
    13: ...d increased expression of hypoxy-inducible genes. EGLN1 is the most important isozyme under normoxia and...
  3. Category:Egln (35 bytes)
    1: List of pages with the keyword Egln
  4. 4bqy (4,703 bytes)
    2: ==HIF prolyl hydroxylase 2 (PHD2/ EGLN1) in complex with Fe(II) and N-[(1-chloro-4-hydro...
    11: ...t.org/uniprot/EGLN1_HUMAN EGLN1_HUMAN] Defects in EGLN1 are the cause of familial erythrocytosis type 3 ...
    13: ...d increased expression of hypoxy-inducible genes. EGLN1 is the most important isozyme under normoxia and...
    16: ...e activity of the HIF prolyl-hydroxylases (PHD or EGLN enzymes), which are Fe(II) and 2-oxoglutarate (2O...
  5. 4bqx (4,651 bytes)
    2: ==HIF prolyl hydroxylase 2 (PHD2/ EGLN1) in complex with Mn(II) and N-[(1-chloro-4-hydro...
    11: ...t.org/uniprot/EGLN1_HUMAN EGLN1_HUMAN] Defects in EGLN1 are the cause of familial erythrocytosis type 3 ...
    13: ...d increased expression of hypoxy-inducible genes. EGLN1 is the most important isozyme under normoxia and...
    16: ...e activity of the HIF prolyl-hydroxylases (PHD or EGLN enzymes), which are Fe(II) and 2-oxoglutarate (2O...
  6. 4bqw (4,676 bytes)
    2: ==HIF prolyl hydroxylase 2 (PHD2/ EGLN1) in complex with Mn(II) and 2-(4-hydroxy-2-oxo-1...
    11: ...t.org/uniprot/EGLN1_HUMAN EGLN1_HUMAN] Defects in EGLN1 are the cause of familial erythrocytosis type 3 ...
    13: ...d increased expression of hypoxy-inducible genes. EGLN1 is the most important isozyme under normoxia and...
    16: ...e activity of the HIF prolyl-hydroxylases (PHD or EGLN enzymes), which are Fe(II) and 2-oxoglutarate (2O...

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