共 200 条
Non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors: Past, present, and future perspectives
被引:127
作者:

Campiani, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy

Ramunno, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy

Maga, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy

Nacci, V
论文数: 0 引用数: 0
h-index: 0
机构: Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy

Fattorusso, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy

Catalanotti, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy

Morelli, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy

Novellino, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy
机构:
[1] Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy
[2] Univ Siena, Dipartimento Sci Farmaceut, I-53100 Siena, Italy
[3] CNR, Ist Genet Biochim & Evoluzionist, I-27100 Pavia, Italy
[4] Univ Naples Federico II, Dipartimento Chim Sostanze Nat, I-80131 Naples, Italy
[5] Univ Naples Federico II, Dipartimento Chim Farmaceut & Tossicol, I-80131 Naples, Italy
关键词:
D O I:
10.2174/1381612024607207
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Along with nucleoside reverse transcriptase inhibitors (NRTIs) and protease inhibitors (Pis), non-nucleoside reverse transcriptase inhibitors (NNRTIs) have gained a definitive and important place in the treatment of HIV-1 infections, and are in rapid development. These compounds can be grouped into two classes: the first generation NNRTIs, mainly discovered by random screening, and the second generation NNRTIs, developed as a result of comprehensive strategies involving molecular modelling, rationale-based drug synthesis, biological and pharmacokinetic evaluations. The recent boom of NNRTIs is mainly due to their antiviral potency, high specificity and low toxicity. The rapid emergence of drug-resistant HIV-1 strains induced by the first generation drugs is a disadvantage bypassed, in part, by the broad spectrum second generation NNRTIs. Starting from the first generation, this review will focus on the second generation NNRTIs dealing with the recent and most interesting published results, highlighting the guidelines for the development of a third generation of NNRT1s.
引用
收藏
页码:615 / 657
页数:43
相关论文
共 200 条
[1]
Efavirenz
[J].
Adkins, JC
;
Noble, S
.
DRUGS,
1998, 56 (06)
:1055-1064

Adkins, JC
论文数: 0 引用数: 0
h-index: 0
机构:
Adis Int Ltd, Auckland 10, New Zealand Adis Int Ltd, Auckland 10, New Zealand

Noble, S
论文数: 0 引用数: 0
h-index: 0
机构:
Adis Int Ltd, Auckland 10, New Zealand Adis Int Ltd, Auckland 10, New Zealand
[2]
THE PETT SERIES, A NEW CLASS OF POTENT NONNUCLEOSIDE INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE
[J].
AHGREN, C
;
BACKRO, K
;
BELL, FW
;
CANTRELL, AS
;
CLEMENS, M
;
COLACINO, JM
;
DEETER, JB
;
ENGELHARDT, JA
;
HOGBERG, M
;
JASKUNAS, SR
;
JOHANSSON, NG
;
JORDAN, CL
;
KASHER, JS
;
KINNICK, MD
;
LIND, P
;
LOPEZ, C
;
MORIN, JM
;
MUESING, MA
;
NOREEN, R
;
OBERG, B
;
PAGET, CJ
;
PALKOWITZ, JA
;
PARRISH, CA
;
PRANC, P
;
RIPPY, MK
;
RYDERGARD, C
;
SAHLBERG, C
;
SWANSON, S
;
TERNANSKY, RJ
;
UNGE, T
;
VASILEFF, RT
;
VRANG, L
;
WEST, SJ
;
ZHANG, H
;
XHOU, XX
.
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY,
1995, 39 (06)
:1329-1335

AHGREN, C
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

BACKRO, K
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

BELL, FW
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

CANTRELL, AS
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

CLEMENS, M
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

COLACINO, JM
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

DEETER, JB
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

ENGELHARDT, JA
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

HOGBERG, M
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

JASKUNAS, SR
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

JOHANSSON, NG
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

JORDAN, CL
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

KASHER, JS
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

KINNICK, MD
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

LIND, P
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

LOPEZ, C
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

MORIN, JM
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

MUESING, MA
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

NOREEN, R
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

OBERG, B
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

PAGET, CJ
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

PALKOWITZ, JA
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

PARRISH, CA
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

PRANC, P
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

RIPPY, MK
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

RYDERGARD, C
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

SAHLBERG, C
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

SWANSON, S
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

TERNANSKY, RJ
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

UNGE, T
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

VASILEFF, RT
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

VRANG, L
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

WEST, SJ
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

ZHANG, H
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN

XHOU, XX
论文数: 0 引用数: 0
h-index: 0
机构: MEDIVIR AB,HUDDINGE,SWEDEN
[3]
1,2,3-TRIAZOLE-[2',5'-BIS-O-(TERT-BUTYLDIMETHYLSILYL)-BETA-D-RIBOFURANOSYL]-3'-SPIRO-5''-(4''-AMINO-1'',2''-OXATHIOL 2'',2''-DIOXIDE) (TSAO) ANALOGS - SYNTHESIS AND ANTI-HIV-1 ACTIVITY
[J].
ALVAREZ, R
;
VELAZQUEZ, S
;
SANFELIX, A
;
AQUARO, S
;
DECLERCQ, E
;
PERNO, CF
;
KARLSSON, A
;
BALZARINI, J
;
CAMARASA, MJ
.
JOURNAL OF MEDICINAL CHEMISTRY,
1994, 37 (24)
:4185-4194

ALVAREZ, R
论文数: 0 引用数: 0
h-index: 0
机构: CSIC,INST QUIM MED,E-28006 MADRID,SPAIN

VELAZQUEZ, S
论文数: 0 引用数: 0
h-index: 0
机构: CSIC,INST QUIM MED,E-28006 MADRID,SPAIN

SANFELIX, A
论文数: 0 引用数: 0
h-index: 0
机构: CSIC,INST QUIM MED,E-28006 MADRID,SPAIN

AQUARO, S
论文数: 0 引用数: 0
h-index: 0
机构: CSIC,INST QUIM MED,E-28006 MADRID,SPAIN

DECLERCQ, E
论文数: 0 引用数: 0
h-index: 0
机构: CSIC,INST QUIM MED,E-28006 MADRID,SPAIN

PERNO, CF
论文数: 0 引用数: 0
h-index: 0
机构: CSIC,INST QUIM MED,E-28006 MADRID,SPAIN

论文数: 引用数:
h-index:
机构:

BALZARINI, J
论文数: 0 引用数: 0
h-index: 0
机构: CSIC,INST QUIM MED,E-28006 MADRID,SPAIN

CAMARASA, MJ
论文数: 0 引用数: 0
h-index: 0
机构: CSIC,INST QUIM MED,E-28006 MADRID,SPAIN
[4]
Synthesis and anti-human immunodeficiency virus type 1 activity of novel 3'-spiro nucleoside analogues of TSAO-T
[J].
Alvarez, R
;
Jimeno, ML
;
PerezPerez, MJ
;
DeClercq, E
;
Balzarini, J
;
Camarasa, MJ
.
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY,
1997, 8 (06)
:507-517

Alvarez, R
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, INST QUIM MED, E-28006 MADRID, SPAIN

Jimeno, ML
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, INST QUIM MED, E-28006 MADRID, SPAIN

PerezPerez, MJ
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, INST QUIM MED, E-28006 MADRID, SPAIN

DeClercq, E
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, INST QUIM MED, E-28006 MADRID, SPAIN

Balzarini, J
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, INST QUIM MED, E-28006 MADRID, SPAIN

Camarasa, MJ
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, INST QUIM MED, E-28006 MADRID, SPAIN
[5]
Novel 1,1,3-trioxo-2H,4H-thieno [3,4-e][1,2,4] thiadiazine derivatives as non-nucleoside reverse transcriptase inhibitors that inhibit human immunodeficiency virus type 1 replication
[J].
Arranz, E
;
Díaz, JA
;
Ingate, ST
;
Witvrouw, M
;
Pannecouque, C
;
Balzarini, J
;
De Clercq, E
;
Vega, S
.
JOURNAL OF MEDICINAL CHEMISTRY,
1998, 41 (21)
:4109-4117

Arranz, E
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, Inst Quim Med, E-28006 Madrid, Spain

Díaz, JA
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, Inst Quim Med, E-28006 Madrid, Spain

Ingate, ST
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, Inst Quim Med, E-28006 Madrid, Spain

Witvrouw, M
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, Inst Quim Med, E-28006 Madrid, Spain

Pannecouque, C
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, Inst Quim Med, E-28006 Madrid, Spain

Balzarini, J
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, Inst Quim Med, E-28006 Madrid, Spain

De Clercq, E
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, Inst Quim Med, E-28006 Madrid, Spain

Vega, S
论文数: 0 引用数: 0
h-index: 0
机构: CSIC, Inst Quim Med, E-28006 Madrid, Spain
[6]
5H-Pyrrolo[1,2-b][1,2,5]benzothiadiazepines (PBTDs): A novel class of non-nucleoside reverse transcriptase inhibitors
[J].
Artico, M
;
Silvestri, R
;
Pagnozzi, E
;
Stefancich, G
;
Massa, S
;
Loi, AG
;
Putzolu, M
;
Corrias, S
;
Spiga, MG
;
LaColla, P
.
BIOORGANIC & MEDICINAL CHEMISTRY,
1996, 4 (06)
:837-850

Artico, M
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ROMA LA SAPIENZA,DIPARTIMENTO STUDI FARMACEUT,I-00185 ROME,ITALY

论文数: 引用数:
h-index:
机构:

Pagnozzi, E
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ROMA LA SAPIENZA,DIPARTIMENTO STUDI FARMACEUT,I-00185 ROME,ITALY

Stefancich, G
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ROMA LA SAPIENZA,DIPARTIMENTO STUDI FARMACEUT,I-00185 ROME,ITALY

论文数: 引用数:
h-index:
机构:

Loi, AG
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ROMA LA SAPIENZA,DIPARTIMENTO STUDI FARMACEUT,I-00185 ROME,ITALY

Putzolu, M
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ROMA LA SAPIENZA,DIPARTIMENTO STUDI FARMACEUT,I-00185 ROME,ITALY

Corrias, S
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ROMA LA SAPIENZA,DIPARTIMENTO STUDI FARMACEUT,I-00185 ROME,ITALY

Spiga, MG
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ROMA LA SAPIENZA,DIPARTIMENTO STUDI FARMACEUT,I-00185 ROME,ITALY

LaColla, P
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ROMA LA SAPIENZA,DIPARTIMENTO STUDI FARMACEUT,I-00185 ROME,ITALY
[7]
3,4-DIHYDRO-2-ALKOXY-6-BENZYL-4-OXOPYRIMIDINES (DABOS) - A NEW CLASS OF SPECIFIC INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1
[J].
ARTICO, M
;
MASSA, S
;
MAI, A
;
MARONGIU, ME
;
PIRAS, G
;
TRAMONTANO, E
;
LACOLLA, P
.
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY,
1993, 4 (06)
:361-368

ARTICO, M
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV CAGLIARI,DIPARTIMENTO BIOL SPERIMENTALE,I-09124 CAGLIARI,ITALY UNIV CAGLIARI,DIPARTIMENTO BIOL SPERIMENTALE,I-09124 CAGLIARI,ITALY

论文数: 引用数:
h-index:
机构:

MAI, A
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV CAGLIARI,DIPARTIMENTO BIOL SPERIMENTALE,I-09124 CAGLIARI,ITALY UNIV CAGLIARI,DIPARTIMENTO BIOL SPERIMENTALE,I-09124 CAGLIARI,ITALY

MARONGIU, ME
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV CAGLIARI,DIPARTIMENTO BIOL SPERIMENTALE,I-09124 CAGLIARI,ITALY UNIV CAGLIARI,DIPARTIMENTO BIOL SPERIMENTALE,I-09124 CAGLIARI,ITALY

论文数: 引用数:
h-index:
机构:

论文数: 引用数:
h-index:
机构:

LACOLLA, P
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV CAGLIARI,DIPARTIMENTO BIOL SPERIMENTALE,I-09124 CAGLIARI,ITALY UNIV CAGLIARI,DIPARTIMENTO BIOL SPERIMENTALE,I-09124 CAGLIARI,ITALY
[8]
Structure-based design, synthesis, and biological evaluation of navel pyrrolyl aryl sulfones: HIV-1 non-nucleoside reverse transcriptase inhibitors active at nanomolar concentrations
[J].
Artico, M
;
Silvestri, R
;
Pagnozzi, E
;
Bruno, B
;
Novellino, E
;
Greco, G
;
Massa, S
;
Ettorre, A
;
Loi, AG
;
Scintu, F
;
La Colla, P
.
JOURNAL OF MEDICINAL CHEMISTRY,
2000, 43 (09)
:1886-1891

Artico, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Roma La Sapienza, Dipartimento Studi Farmaceut, Ist Pasteur Fdn Cenci Bolognetti, I-00185 Rome, Italy

论文数: 引用数:
h-index:
机构:

Pagnozzi, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Roma La Sapienza, Dipartimento Studi Farmaceut, Ist Pasteur Fdn Cenci Bolognetti, I-00185 Rome, Italy

Bruno, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Roma La Sapienza, Dipartimento Studi Farmaceut, Ist Pasteur Fdn Cenci Bolognetti, I-00185 Rome, Italy

论文数: 引用数:
h-index:
机构:

论文数: 引用数:
h-index:
机构:

Massa, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Roma La Sapienza, Dipartimento Studi Farmaceut, Ist Pasteur Fdn Cenci Bolognetti, I-00185 Rome, Italy

Ettorre, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Roma La Sapienza, Dipartimento Studi Farmaceut, Ist Pasteur Fdn Cenci Bolognetti, I-00185 Rome, Italy

Loi, AG
论文数: 0 引用数: 0
h-index: 0
机构: Univ Roma La Sapienza, Dipartimento Studi Farmaceut, Ist Pasteur Fdn Cenci Bolognetti, I-00185 Rome, Italy

论文数: 引用数:
h-index:
机构:

La Colla, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Roma La Sapienza, Dipartimento Studi Farmaceut, Ist Pasteur Fdn Cenci Bolognetti, I-00185 Rome, Italy
[9]
2-Sulfonyl-4-chloroanilino moiety: A potent pharmacophore for the anti-human immunodeficiency virus type 1 activity of pyrrolyl aryl sulfones
[J].
Artico, M
;
Silvestri, R
;
Massa, S
;
Loi, AG
;
Corrias, S
;
Piras, G
;
LaColla, P
.
JOURNAL OF MEDICINAL CHEMISTRY,
1996, 39 (02)
:522-530

Artico, M
论文数: 0 引用数: 0
h-index: 0
机构: UNIV SIENA, DIPARTIMENTO FARM CHIM TECNOL, I-53100 SIENA, ITALY

论文数: 引用数:
h-index:
机构:

论文数: 引用数:
h-index:
机构:

Loi, AG
论文数: 0 引用数: 0
h-index: 0
机构: UNIV SIENA, DIPARTIMENTO FARM CHIM TECNOL, I-53100 SIENA, ITALY

Corrias, S
论文数: 0 引用数: 0
h-index: 0
机构: UNIV SIENA, DIPARTIMENTO FARM CHIM TECNOL, I-53100 SIENA, ITALY

论文数: 引用数:
h-index:
机构:

LaColla, P
论文数: 0 引用数: 0
h-index: 0
机构: UNIV SIENA, DIPARTIMENTO FARM CHIM TECNOL, I-53100 SIENA, ITALY
[10]
Restoration of the immune system with anti-retroviral therapy
[J].
Autran, B
;
Carcelaint, G
;
Li, TS
;
Gorochov, G
;
Blanc, C
;
Renaud, M
;
Durali, M
;
Mathez, D
;
Calvez, V
;
Leibowitch, J
;
Katlama, C
;
Debré, P
.
IMMUNOLOGY LETTERS,
1999, 66 (1-3)
:207-211

Autran, B
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Carcelaint, G
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Li, TS
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Gorochov, G
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Blanc, C
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Renaud, M
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Durali, M
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Mathez, D
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Calvez, V
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Leibowitch, J
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Katlama, C
论文数: 0 引用数: 0
h-index: 0
机构: Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France

Debré, P
论文数: 0 引用数: 0
h-index: 0
机构:
Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France Hop La Pitie Salpetriere, Lab Immunol Cellulaire & Tissulaire, CNRS, UMR 7627, Paris, France