(Q33267847)

24 July 2017

Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery (English)

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24 July 2017

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Houghten RA

1

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24 July 2017

Pinilla C

2

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24 July 2017

Blondelle SE

3

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24 July 2017

Appel JR

4

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24 July 2017

Dooley CT

5

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24 July 2017

Cuervo JH

6

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24 July 2017

language of work or name

English

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publication date

1 November 1991

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24 July 2017

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24 July 2017

354

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24 July 2017

84-86

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24 July 2017

6348

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https://scigraph.springernature.com/pub.10.1038/354084a0

24 July 2017

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cites work

Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide

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7 January 2021

Use of peptide synthesis to probe viral antigens for epitopes to a resolution of a single amino acid

1 reference

7 January 2021

General method for the rapid solid-phase synthesis of large numbers of peptides: specificity of antigen-antibody interaction at the level of individual amino acids

1 reference

7 January 2021

Light-directed, spatially addressable parallel chemical synthesis

1 reference

7 January 2021

A priori delineation of a peptide which mimics a discontinuous antigenic determinant

1 reference

7 January 2021

Searching for Peptide Ligands with an Epitope Library

1 reference

7 January 2021

Random peptide libraries: a source of specific protein binding molecules

1 reference

7 January 2021

Peptides on phage: a vast library of peptides for identifying ligands

1 reference

7 January 2021

Cell-free immunity in insects

1 reference

7 January 2021

Magainins, a class of antimicrobial peptides from Xenopus skin: isolation, characterization of two active forms, and partial cDNA sequence of a precursor

1 reference

7 January 2021

Hemolytic and antimicrobial activities of the twenty-four individual omission analogues of melittin

1 reference

7 January 2021

The structure of an antigenic determinant in a protein

1 reference

7 January 2021

The monitoring of reactions in solid-phase peptide synthesis with picric acid

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7 January 2021

Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides

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7 January 2021

Simplified procedure for carrying out simultaneous multiple hydrogen fluoride cleavages of protected peptide resins

1 reference

7 January 2021

Identifiers

DOI

10.1038/354084A0

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Dimensions Publication ID

24 July 2017

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