J. F. Hernández

发表

JLK isocoumarin inhibitors: Selective γ‐secretase inhibitors that do not interfere with notch pathway in vitro or in vivo

F. Checler, C. A. D. Alves da Costa, P. Marambaud, 2003, Journal of neuroscience research.

Galactomannan from Caesalpinia spinosa induces phenotypic and functional maturation of human dendritic cells.

N. Mooney, M. Aoki, H. Moins-Teisserenc, 2011, International immunopharmacology.

Solution structure of the epidermal growth factor (EGF)-like module of human complement protease C1r, an atypical member of the EGF family.

D. Marion, G. Arlaud, J. F. Hernández, 1998, Biochemistry.

Grafting an RGD motif onto an epidermal growth factor-like module: chemical synthesis and functional characterization of the chimeric molecule.

G. Arlaud, M. Block, A. Molla, 1999, The journal of peptide research : official journal of the American Peptide Society.

Structural insights into the design of inhibitors for the L1 metallo-beta-lactamase from Stenotrophomonas maltophilia.

O. Dideberg, R. Kahn, J. F. Hernández, 2008, Journal of molecular biology.

Squash trypsin inhibitors from Momordica cochinchinensis exhibit an atypical macrocyclic structure.

L. Chiche, A. Heitz, J. Gagnon, 2000, Biochemistry.

Structure and functions of the interaction domains of C1r and C1s: keystones of the architecture of the C1 complex.

N. Thielens, G. Arlaud, J. F. Hernández, 1999, Immunopharmacology.

Structural and functional studies on C1r and C1s: new insights into the mechanisms involved in C1 activity and assembly.

N. Thielens, G. Arlaud, C. Gaboriaud, 1998, Immunobiology.

Solution structure of the squash trypsin inhibitor MCoTI-II. A new family for cyclic knottins.

L. Chiche, A. Heitz, D. Le-Nguyen, 2001, Biochemistry.

Functional determinants of the Epstein-Barr virus protease.

F. Baudin, R. Ruigrok, G. Arlaud, 2001, Journal of molecular biology.

Enkephalin-degrading enzyme inhibitors. Crucial role of the C-terminal residue on the inhibitory potencies of retro-hydroxamate dipeptides.

B. Roques, M. Fournié-Zaluski, J. F. Hernández, 2009, International journal of peptide and protein research.

Chemical synthesis and characterization of the epidermal growth factor-like module of human complement protease C1r.

G. Arlaud, Y. Pétillot, J. Gagnon, 2009 .

A coil-helix instead of a helix-coil motif can be induced in a chloroplast transit peptide from Chlamydomonas reinhardtii.

P. Gans, G. Arlaud, J. Lancelin, 1999, European journal of biochemistry.

Alanine series of ovine corticotropin releasing factor (oCRF): a structure-activity relationship study.

C. Donaldson, W. Vale, J. Rivier, 1992, Journal of medicinal chemistry.

Functional cooperation of the mitochondrial processing peptidase subunits.

V. Géli, J. F. Hernández, A. Brandt, 1997, Journal of molecular biology.

Retro-inverso concept applied to the complete inhibitors of enkephalin-degrading enzymes.

B. Roques, M. Fournié-Zaluski, J. F. Hernández, 1988, Journal of medicinal chemistry.

In vitro analysis of complement-dependent HIV-1 cell infection using a model system.

Robert B Sim, N. Thielens, P. Tacnet-Delorme, 1999, Journal of immunology.

Synthesis and relative potencies of new constrained CRF antagonists.

Y. Taché, W. Vale, J. Rivier, 1993, Journal of medicinal chemistry.

Mapping of the interaction between the immunodominant loop of the ectodomain of HIV-1 gp41 and human complement protein C1q.

T. Vernet, G. Arlaud, J. F. Hernández, 1999, European journal of biochemistry.