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Characterization of a 78-residue fragment of c-Raf-1 that comprises a minimal binding domain for the interaction with Ras-GTP

The Journal of biological chemistry, 1994-09, Vol.269 (35), p.22340-22346

1994

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Solution structure of an analog of vasoactive intestinal peptide as determined by two-dimensional NMR and circular dichroism spectroscopies and constrained molecular dynamics

Biochemistry (Easton), 1989-03, Vol.28 (6), p.2399-2409

1989

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Synthesis, biological activity and conformational analysis of cyclic GRF analogs

International Journal of Peptide and Protein Research, 1988-12, Vol.32 (6), p.441-454

1988

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Solution structures of cyclic and dicyclic analogues of growth hormone releasing factor as determined by two-dimensional NMR and CD spectroscopies and constrained molecular dynamics

Biopolymers, 1992-06, Vol.32 (6), p.649-666

1992

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A fast and simplein situ method for the determination of the absolute configuration of amino acid esters using the chiroptical properties of their Eu(FOD)3 complexes

Amino acids, 1992-06, Vol.3 (2), p.195-203

1992

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Purification and Characterization of Recombinant Rev Protein of Human Immunodeficiency Virus Type 1

Proceedings of the National Academy of Sciences - PNAS, 1990-10, Vol.87 (19), p.7593-7597

1990

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Application of MDPF and fluorescamine XV chiroptical properties of MDPF condensation compounds with dipeptides in situ

Biochemical and biophysical research communications, 1983-07, Vol.114 (2), p.433-439

1983

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Application of fluorescamine XII. Chiroptical properties of fluorescamine condensation compounds with some less common α-amino acids

Biochemical and biophysical research communications, 1980-01, Vol.92 (2), p.447-451

1980

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Chiroptical properties of fluorescamine condensation compounds with amino acid esters in situ. Pyrrolinone chirality rule

Biochemical and biophysical research communications, 1978-12, Vol.85 (4), p.1496-1502

1978

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Chiroptical properties of fluorescamine condensation compounds with α-amino acids in situ

Biochemical and biophysical research communications, 1976-03, Vol.69 (1), p.206-211

1976

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Chiroptical properties of fluorescamine condensation compounds with dipeptides in situ

Biochemical and biophysical research communications, 1977-01, Vol.74 (2), p.825-830

1977

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Chiroptical properties of fluorescamine condensation compounds with secondary amino acids in situ

Biochemical and biophysical research communications, 1976-07, Vol.71 (2), p.598-602

1976

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Chiroptical properties of fluorescamine condensation compounds with secondary amino acids insitu

Biochemical and biophysical research communications, 1976-07, Vol.71 (2), p.598-602

1976

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Characterization of recombinant HIV-1 Tat and its interaction with TAR RNA

Biochemistry (Easton), 1992-12, Vol.31 (48), p.12062-12068

1992

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aS,7S-absolute configuration of natural (−)-colchicine and allocongeners

FEBS letters, 1990-03, Vol.262 (1), p.5-7

1990

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A Fast and Simple in Situ Method for the Determination of the Absolute Configuration of 2-and 3-Hydroxycarboxylic Acids, Esters and Ethers Using the Chiroptical Properties of Their Eu(Fod)3 Complexes. A Preliminary Report

Analytical letters, 1991-02, Vol.24 (2), p.317-326

1991

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Chiroptical properties of fluorescamine condensation compounds with amino acid esters [formula omitted]. Pyrrolinone chirality rule

Biochemical and biophysical research communications, 1978, Vol.85 (4), p.1496-1502

1978

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Application Of Fluorescamine Xiv 1 . Determination Of Optical Purity Of A Small Amount Of Amino Acids By The Fluorescamine Method

Analytical letters, 1981-01, Vol.14 (20), p.1725-1733

1981

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Application Of Fluorescamine Xiv1. Determination Of Optical Purity Of A Small Amount Of Amino Acids By The Fluorescamine Method

Analytical letters, 1981-01, Vol.14 (20), p.1725-1733

1981

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aS,7S-absolute configuration of natural (-)-colchicine and allo-congeners

FEBS letters, 1990-03, Vol.262 (1), p.5-7

1990

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Chiroptical properties of fluorescamine condensation compounds with dipeptides [formula omitted]

Biochemical and biophysical research communications, 1977, Vol.74 (2), p.825-830

1977

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Chiroptical properties of fluorescamine condensation compounds with secondary amino acids [formula omitted]

Biochemical and biophysical research communications, 1976, Vol.71 (2), p.598-602

1976

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Precursors of the mammalian synthesis of morphine: (+)‐salutaridine and (−)‐thebaine from (+)‐6‐demethylsalutaridine, and (−)‐N‐13CH3‐thebaine from (−)‐northebaine

FEBS letters, 1986-09, Vol.206 (1), p.125-129

1986

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Chiroptical Properties of Fluorescamine Derivatives of Chiral Primary Amines in situ

Spectroscopy letters, 1977-01, Vol.10 (9), p.747-756

1977

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ChemInform Abstract: Natural Products. Antitubulin Effect of Congeners of N-Acetylcolchinyl Methyl Ether: Synthesis of Optically Active 5- Acetamidodeaminocolchinyl Methyl Ether and of Demethoxy Analogues of Deaminocolchinyl Methyl Ether

ChemInform, 1993-01, Vol.24 (4), p.no-no

1993

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Characterization of a 78-residue fragment of c-Raf-1 that comprises a minimal binding domain for the interaction with Ras-GTP

Solution structure of an analog of vasoactive intestinal peptide as determined by two-dimensional NMR and circular dichroism spectroscopies and constrained molecular dynamics

Synthesis, biological activity and conformational analysis of cyclic GRF analogs

Solution structures of cyclic and dicyclic analogues of growth hormone releasing factor as determined by two-dimensional NMR and CD spectroscopies and constrained molecular dynamics

A fast and simplein situ method for the determination of the absolute configuration of amino acid esters using the chiroptical properties of their Eu(FOD)3 complexes

Purification and Characterization of Recombinant Rev Protein of Human Immunodeficiency Virus Type 1

Application of MDPF and fluorescamine XV chiroptical properties of MDPF condensation compounds with dipeptides in situ

Application of fluorescamine XII. Chiroptical properties of fluorescamine condensation compounds with some less common α-amino acids

Chiroptical properties of fluorescamine condensation compounds with amino acid esters in situ. Pyrrolinone chirality rule

Chiroptical properties of fluorescamine condensation compounds with α-amino acids in situ

Chiroptical properties of fluorescamine condensation compounds with dipeptides in situ

Chiroptical properties of fluorescamine condensation compounds with secondary amino acids in situ

Chiroptical properties of fluorescamine condensation compounds with secondary amino acids insitu

Characterization of recombinant HIV-1 Tat and its interaction with TAR RNA

aS,7S-absolute configuration of natural (−)-colchicine and allocongeners

A Fast and Simple in Situ Method for the Determination of the Absolute Configuration of 2-and 3-Hydroxycarboxylic Acids, Esters and Ethers Using the Chiroptical Properties of Their Eu(Fod)3 Complexes. A Preliminary Report

Chiroptical properties of fluorescamine condensation compounds with amino acid esters [formula omitted]. Pyrrolinone chirality rule

Application Of Fluorescamine Xiv 1 . Determination Of Optical Purity Of A Small Amount Of Amino Acids By The Fluorescamine Method

Application Of Fluorescamine Xiv1. Determination Of Optical Purity Of A Small Amount Of Amino Acids By The Fluorescamine Method

aS,7S-absolute configuration of natural (-)-colchicine and allo-congeners

Chiroptical properties of fluorescamine condensation compounds with dipeptides [formula omitted]

Chiroptical properties of fluorescamine condensation compounds with secondary amino acids [formula omitted]

Precursors of the mammalian synthesis of morphine: (+)‐salutaridine and (−)‐thebaine from (+)‐6‐demethylsalutaridine, and (−)‐N‐13CH3‐thebaine from (−)‐northebaine

Chiroptical Properties of Fluorescamine Derivatives of Chiral Primary Amines in situ

ChemInform Abstract: Natural Products. Antitubulin Effect of Congeners of N-Acetylcolchinyl Methyl Ether: Synthesis of Optically Active 5- Acetamidodeaminocolchinyl Methyl Ether and of Demethoxy Analogues of Deaminocolchinyl Methyl Ether

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