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124 related items for PubMed ID: 11104773

  • 1. The role of dibasic residues in prohormone sorting to the regulated secretory pathway. A study with proneurotensin.
    Feliciangeli S, Kitabgi P, Bidard JN.
    J Biol Chem; 2001 Mar 02; 276(9):6140-50. PubMed ID: 11104773
    [Abstract] [Full Text] [Related]

  • 2. Immunological and biochemical characterization of processing products from the neurotensin/neuromedin N precursor in the rat medullary thyroid carcinoma 6-23 cell line.
    Bidard JN, de Nadai F, Rovere C, Moinier D, Laur J, Martinez J, Cuber JC, Kitabgi P.
    Biochem J; 1993 Apr 01; 291 ( Pt 1)(Pt 1):225-33. PubMed ID: 8471039
    [Abstract] [Full Text] [Related]

  • 3. Insertion of dibasic residues directs a constitutive protein to the regulated secretory pathway.
    Féliciangéli S, Kitabgi P.
    Biochem Biophys Res Commun; 2002 Jan 11; 290(1):191-6. PubMed ID: 11779152
    [Abstract] [Full Text] [Related]

  • 4. Isolation and quantitation of several new peptides from the canine neurotensin/neuromedin N precursor.
    Carraway RE, Mitra SP, Salmonsen R.
    Peptides; 1992 Jan 11; 13(6):1039-47. PubMed ID: 1494486
    [Abstract] [Full Text] [Related]

  • 5. Differential processing of pro-neurotensin/neuromedin N and relationship to pro-hormone convertases.
    Kitabgi P.
    Peptides; 2006 Oct 11; 27(10):2508-14. PubMed ID: 16904237
    [Abstract] [Full Text] [Related]

  • 6. Post-translational processing of the neurotensin/neuromedin N precursor in the central nervous system of the rat--I. Biochemical characterization of maturation products.
    de Nadai F, Rovère C, Bidard JN, Cuber JC, Beaudet A, Kitabgi P.
    Neuroscience; 1994 May 11; 60(1):159-66. PubMed ID: 8052409
    [Abstract] [Full Text] [Related]

  • 7. Progastrin is directed to the regulated secretory pathway by synergistically acting basic and acidic motifs.
    Bundgaard JR, Birkedal H, Rehfeld JF.
    J Biol Chem; 2004 Feb 13; 279(7):5488-93. PubMed ID: 14660571
    [Abstract] [Full Text] [Related]

  • 8. Prohormone convertases differentially process pro-neurotensin/neuromedin N in tissues and cell lines.
    Kitabgi P.
    J Mol Med (Berl); 2006 Aug 13; 84(8):628-34. PubMed ID: 16688434
    [Abstract] [Full Text] [Related]

  • 9. Impaired processing of brain proneurotensin and promelanin-concentrating hormone in obese fat/fat mice.
    Rovere C, Viale A, Nahon J, Kitabgi P.
    Endocrinology; 1996 Jul 13; 137(7):2954-8. PubMed ID: 8770919
    [Abstract] [Full Text] [Related]

  • 10. Arg-X-Lys/Arg-Arg motif as a signal for precursor cleavage catalyzed by furin within the constitutive secretory pathway.
    Hosaka M, Nagahama M, Kim WS, Watanabe T, Hatsuzawa K, Ikemizu J, Murakami K, Nakayama K.
    J Biol Chem; 1991 Jul 05; 266(19):12127-30. PubMed ID: 1905715
    [Abstract] [Full Text] [Related]

  • 11. Tissue-specific processing of neurotensin/neuromedin-N precursor in cat.
    Carraway RE, Mitra SP, Joyce TJ.
    Regul Pept; 1993 Jan 22; 43(1-2):97-106. PubMed ID: 8426913
    [Abstract] [Full Text] [Related]

  • 12. Neurotensin and neuromedin N are differentially processed from a common precursor by prohormone convertases in tissues and cell lines.
    Kitabgi P.
    Results Probl Cell Differ; 2010 Jan 22; 50():85-96. PubMed ID: 19862492
    [Abstract] [Full Text] [Related]

  • 13. Prohormone thiol protease and enkephalin precursor processing: cleavage at dibasic and monobasic sites.
    Krieger TJ, Mende-Mueller L, Hook VY.
    J Neurochem; 1992 Jul 22; 59(1):26-31. PubMed ID: 1613503
    [Abstract] [Full Text] [Related]

  • 14. Mono- and dibasic proteolytic cleavage sites in insect neuroendocrine peptide precursors.
    Veenstra JA.
    Arch Insect Biochem Physiol; 2000 Feb 22; 43(2):49-63. PubMed ID: 10644969
    [Abstract] [Full Text] [Related]

  • 15. Secretory granule biogenesis and neuropeptide sorting to the regulated secretory pathway in neuroendocrine cells.
    Loh YP, Kim T, Rodriguez YM, Cawley NX.
    J Mol Neurosci; 2004 Feb 22; 22(1-2):63-71. PubMed ID: 14742911
    [Abstract] [Full Text] [Related]

  • 16. Dibasic cleavage site is required for sorting to the regulated secretory pathway for both pro- and neuropeptide Y.
    Brakch N, Allemandou F, Cavadas C, Grouzmann E, Brunner HR.
    J Neurochem; 2002 Jun 22; 81(6):1166-75. PubMed ID: 12068065
    [Abstract] [Full Text] [Related]

  • 17. A prohormone convertase cleavage site within a predicted alpha-helix mediates sorting of the neuronal and endocrine polypeptide VGF into the regulated secretory pathway.
    Garcia AL, Han SK, Janssen WG, Khaing ZZ, Ito T, Glucksman MJ, Benson DL, Salton SR.
    J Biol Chem; 2005 Dec 16; 280(50):41595-608. PubMed ID: 16221685
    [Abstract] [Full Text] [Related]

  • 18. BON cells display the intestinal pattern of neurotensin/neuromedin N precursor processing.
    Carraway RE, Mitra SP, Evers BM, Townsend CM.
    Regul Pept; 1994 Aug 31; 53(1):17-29. PubMed ID: 7800856
    [Abstract] [Full Text] [Related]

  • 19. Biosynthesis and posttranslational processing of the neurotensin/neuromedin N precursor in the rat medullary thyroid carcinoma 6-23 cell line. Effect of dexamethasone.
    de Nadai F, Rovere C, Bidard JN, Laur J, Martinez J, Cuber JC, Kitabgi P.
    Endocrinology; 1993 Apr 31; 132(4):1614-20. PubMed ID: 8462460
    [Abstract] [Full Text] [Related]

  • 20. The somatostatin-28(1-12)-NPAMAP sequence: an essential helical-promoting motif governing prosomatostatin processing at mono- and dibasic sites.
    Brakch N, Lazar N, Panchal M, Allemandou F, Boileau G, Cohen P, Rholam M.
    Biochemistry; 2002 Feb 05; 41(5):1630-9. PubMed ID: 11814357
    [Abstract] [Full Text] [Related]

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