Literature DB >> 369296

The predominating molecular form of gastrin and cholecystokinin in the gut is a small peptide corresponding to their COOH-terminal tetrapeptide amide.

J F Rehfeld, L I Larsson.   

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Year:  1979        PMID: 369296     DOI: 10.1111/j.1748-1716.1979.tb06320.x

Source DB:  PubMed          Journal:  Acta Physiol Scand        ISSN: 0001-6772


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  6 in total

1.  Structure of a human gastrin gene.

Authors:  O Wiborg; L Berglund; E Boel; F Norris; K Norris; J F Rehfeld; K A Marcker; J Vuust
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

2.  Molecular cloning of human gastrin cDNA: evidence for evolution of gastrin by gene duplication.

Authors:  E Boel; J Vuust; F Norris; K Norris; A Wind; J F Rehfeld; K A Marcker
Journal:  Proc Natl Acad Sci U S A       Date:  1983-05       Impact factor: 11.205

3.  Light- and electron-microscopic immunochemical analysis of nerve fibre types innervating the taenia of the guinea-pig caecum.

Authors:  J B Furness; S Pompolo; C W Shuttleworth; D E Burleigh
Journal:  Cell Tissue Res       Date:  1992-10       Impact factor: 5.249

4.  Isolation of a large cholecystokinin precursor from canine brain.

Authors:  V E Eysselein; J R Reeve; J E Shively; C Miller; J H Walsh
Journal:  Proc Natl Acad Sci U S A       Date:  1984-11       Impact factor: 11.205

5.  Post-translational processing of cholecystokinin in pig brain and gut.

Authors:  J Eng; Y Shiina; E Straus; R S Yalow
Journal:  Proc Natl Acad Sci U S A       Date:  1982-10       Impact factor: 11.205

6.  Post-poly(Glu) cleavage and degradation modified by O-sulfated tyrosine: a novel post-translational processing mechanism.

Authors:  J F Rehfeld; C P Hansen; A H Johnsen
Journal:  EMBO J       Date:  1995-01-16       Impact factor: 11.598

  6 in total

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