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1. Vuillaumier-Barrot, S; Le Bizec, C; Durand, G; Seta, N
   The T911C (F304S) substitution in the human ALG6 gene is a common polymorphism and not a causal mutation of CDG-Ic
   JOURNAL OF HUMAN GENETICS
   
   S. Vuillaumier-Barrot et al., "The T911C (F304S) substitution in the human ALG6 gene is a common polymorphism and not a causal mutation of CDG-Ic", J HUM GENET, 46(9), 2001, pp. 547-548
2. Kayano, T; Seta, N; Hotta, T; Fujiwara, K; Terao, S
   Component ASPs business of NTT Software Corporation
   NTT REVIEW
   
   T. Kayano et al., "Component ASPs business of NTT Software Corporation", NTT REVIEW, 13(4), 2001, pp. 37-41
3. Drouin-Garraud, V; Belgrand, M; Grunewald, S; Seta, N; Dacher, JN; Henocq, A; Matthijs, G; Cormier-Daire, V; Frebourg, T; Saugier-Veber, P
   Neurological presentation of a congenital disorder of glycosylation CDG-Ia: Implications for diagnosis and genetic counseling
   AMERICAN JOURNAL OF MEDICAL GENETICS
   
   V. Drouin-Garraud et al., "Neurological presentation of a congenital disorder of glycosylation CDG-Ia: Implications for diagnosis and genetic counseling", AM J MED G, 101(1), 2001, pp. 46-49
4. Arfi, C; Seta, N; Fraisse, D; Revel, A; Escande, JP; Momas, I
   Dioxins in adipose tissue of non-occupationally exposed persons in France:correlation with individual food exposure
   CHEMOSPHERE
   
   C. Arfi et al., "Dioxins in adipose tissue of non-occupationally exposed persons in France:correlation with individual food exposure", CHEMOSPHERE, 44(6), 2001, pp. 1347-1352
5. de Lonlay, P; Seta, N; Barrot, S; Chabrol, B; Drouin, V; Gabriel, BM; Journel, H; Kretz, M; Laurent, J; Le Merrer, M; Leroy, A; Pedespan, D; Sarda, P; Villeneuve, N; Schmitz, J; van Schaftingen, E; Matthijs, G; Jaeken, J; Korner, C; Munnich, A; Saudubray, JM; Cormier-Daire, V
   A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases
   JOURNAL OF MEDICAL GENETICS
   
   P. de Lonlay et al., "A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases", J MED GENET, 38(1), 2001, pp. 14-19
6. Dupre, T; Cuer, M; Barrot, S; Barnier, A; Cormier-Daire, V; Munnich, A; Durand, G; Seta, N
   Congenital disorder of glycosylation ia with deficient phosphomannomutase activity but normal plasma glycoprotein pattern
   CLINICAL CHEMISTRY
   
   T. Dupre et al., "Congenital disorder of glycosylation ia with deficient phosphomannomutase activity but normal plasma glycoprotein pattern", CLIN CHEM, 47(1), 2001, pp. 132-134
7. Seta, N; Granfors, K; Sahly, H; Kuipers, JG; Song, YW; Baeten, D; Veys, EM; Maksymowych, W; Marker-Hermann, E; Gu, JR; Huang, F; Kirveskari, J; Yu, DTY
   Expression of host defense scavenger receptors in spondylarthropathy
   ARTHRITIS AND RHEUMATISM
   
   N. Seta et al., "Expression of host defense scavenger receptors in spondylarthropathy", ARTH RHEUM, 44(4), 2001, pp. 931-939
8. Matthijs, G; Schollen, E; Bjursell, C; Erlandson, A; Freeze, H; Imtiaz, F; Kjaergaard, S; Martinsson, T; Schwartz, M; Seta, N; Vuillaumier-Barrot, S; Westphal, V; Winchester, B
   Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)
   HUMAN MUTATION
   
   G. Matthijs et al., "Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)", HUM MUTAT, 16(5), 2000, pp. 386-394
9. Aebi, M; Helenius, A; Schenk, B; Barone, R; Fiumara, A; Berger, EG; Hennet, T; Imbach, T; Stutz, A; Bjursell, C; Uller, A; Wahlstrom, JG; Briones, P; Cardo, E; Clayton, P; Winchester, B; Cormier-Daire, V; de Lonlay, P; Cuer, M; Dupre, T; Seta, N; de Koning, T; Dorland, L; de Loos, F; Kupers, L; Fabritz, L; Hasilik, M; Marquardt, T; Niehues, R; Freeze, H; Grunewald, S; Heykants, L; Jaeken, J; Matthijs, G; Schollen, E; Keir, G; Kjaergaard, S; Schwartz, M; Skovby, F; Klein, A; Roussel, P; Korner, C; Lubke, T; Thiel, C; von Figura, K; Koscielak, J; Krasnewich, D; Lehle, L; Peters, V; Raab, M; Saether, O; Schachter, H; Van Schaftingen, E; Verbert, A; Vilaseca, A; Wevers, R; Yamashita, K
   Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG
   GLYCOBIOLOGY
   
   M. Aebi et al., "Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG", GLYCOBIOLOG, 10(6), 2000, pp. III-V
10. Dupre, T; Barnier, A; de Lonlay, P; Cormier-Daire, V; Durand, G; Codogno, P; Seta, N
    Defect in N-glycosylation of proteins is tissue-dependent in congenital disorders of glycosylation Ia
    GLYCOBIOLOGY
    
    T. Dupre et al., "Defect in N-glycosylation of proteins is tissue-dependent in congenital disorders of glycosylation Ia", GLYCOBIOLOG, 10(12), 2000, pp. 1277-1281
11. de Lonlay, P; Cormier-Daire, V; Vuillaumier-Barrot, S; Cuer, M; Durand, G; Munnich, A; Saudubray, JM; Seta, N
    "Carbohydrate-deficient glycoprotein" syndrome.
    ARCHIVES DE PEDIATRIE
    
    P. de Lonlay et al., ""Carbohydrate-deficient glycoprotein" syndrome.", ARCH PED, 7(2), 2000, pp. 173-184
12. Seta, N; Arfi, C; Momas, I
    General population exposure to dioxins, human ubiquitous pollutants
    REVUE D EPIDEMIOLOGIE ET DE SANTE PUBLIQUE
    
    N. Seta et al., "General population exposure to dioxins, human ubiquitous pollutants", REV EPIDEM, 48(3), 2000, pp. 281-293
13. Vuillaumier-Barrot, S; Hetet, G; Barnier, A; Dupre, T; Cuer, M; de Lonlay, P; Cormier-Daire, V; Durand, G; Grandchamp, B; Seta, N
    Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients
    JOURNAL OF MEDICAL GENETICS
    
    S. Vuillaumier-Barrot et al., "Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients", J MED GENET, 37(8), 2000, pp. 579-580
14. Cormier-Daire, V; Amiel, J; Vuillaumier-Barrot, S; Tan, J; Durand, G; Munnich, A; Le Merrer, M; Seta, N
    Congenital disorders of glycosylation IIa cause growth retardation, mentalretardation, and facial dysmorphism
    JOURNAL OF MEDICAL GENETICS
    
    V. Cormier-Daire et al., "Congenital disorders of glycosylation IIa cause growth retardation, mentalretardation, and facial dysmorphism", J MED GENET, 37(11), 2000, pp. 875-877
15. Durand, G; Seta, N
    Protein glycosylation and diseases: Blood and urinary oligosaccharides as markers for diagnosis and therapeutic monitoring
    CLINICAL CHEMISTRY
    
    G. Durand e N. Seta, "Protein glycosylation and diseases: Blood and urinary oligosaccharides as markers for diagnosis and therapeutic monitoring", CLIN CHEM, 46(6), 2000, pp. 795-805
16. Cuer, M; Barnier, A; de la Salmoniere, P; Durand, G; Seta, N
    Fluorimetric measurement of plasma alpha-L-fucosidase activity with a centrifugal analyzer: Reference values in a healthy French adult population
    CLINICAL CHEMISTRY
    
    M. Cuer et al., "Fluorimetric measurement of plasma alpha-L-fucosidase activity with a centrifugal analyzer: Reference values in a healthy French adult population", CLIN CHEM, 46(4), 2000, pp. 562-564
17. Seta, N
    Carbohydrate-deficient glycoprotein syndrome and glycosylation of N-glycosyl proteins
    ARCHIVES DE PEDIATRIE
    
    N. Seta, "Carbohydrate-deficient glycoprotein syndrome and glycosylation of N-glycosyl proteins", ARCH PED, 6, 1999, pp. 206S-208S
18. Dupre, T; Ogier-Denis, E; Moore, SEH; Cormier-Daire, V; Dehoux, M; Durand, G; Seta, N; Codogno, P
    Alteration of mannose transport in fibroblasts from type I carbohydrate deficient glycoprotein syndrome patients
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    
    T. Dupre et al., "Alteration of mannose transport in fibroblasts from type I carbohydrate deficient glycoprotein syndrome patients", BBA-MOL BAS, 1453(3), 1999, pp. 369-377
19. Seta, N; Dupre, T; Cormier-Daire, V; de Lonlay, P; Moore, S; Durand, G; Codogno, P
    Mannose metabolism and carbohydrate deficient glycoprotein syndrome type I
    M S-MEDECINE SCIENCES
    
    N. Seta et al., "Mannose metabolism and carbohydrate deficient glycoprotein syndrome type I", M S-MED SCI, 15(11), 1999, pp. 1202-1210
20. de Lonlay, P; Cuer, M; Vuillaumier-Barrot, S; Beaune, G; Castelnau, P; Kretz, M; Durand, G; Saudubray, JM; Seta, N
    Hypersulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: A new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose
    JOURNAL OF PEDIATRICS
    
    P. de Lonlay et al., "Hypersulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: A new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose", J PEDIAT, 135(3), 1999, pp. 379-383
21. BOUTTEN A; VENEMBRE P; SETA N; HAMELIN J; AUBIER M; DURAND G; DEHOUX MS
    ONCOSTATIN-M IS A POTENT STIMULATOR OF ALPHA(1)-ANTITRYPSIN SECRETIONIN LUNG EPITHELIAL-CELLS - MODULATION BY TRANSFORMING-GROWTH-FACTOR-BETA AND INTERFERON-GAMMA
    American journal of respiratory cell and molecular biology
    
    A. Boutten et al., "ONCOSTATIN-M IS A POTENT STIMULATOR OF ALPHA(1)-ANTITRYPSIN SECRETIONIN LUNG EPITHELIAL-CELLS - MODULATION BY TRANSFORMING-GROWTH-FACTOR-BETA AND INTERFERON-GAMMA", American journal of respiratory cell and molecular biology, 18(4), 1998, pp. 511-520
22. IKAWA T; IKEDA M; YAMAGUCHI A; TSAI WC; TAMURA N; SETA N; TRUCKSESS M; RAYBOURNE RB; YU DTY
    EXPRESSION OF ARTHRITIS-CAUSING HLA-B27 ON HELA-CELLS PROMOTES INDUCTION OF C-FOS IN RESPONSE TO IN-VITRO INVASION BY SALMONELLA-TYPHIMURIUM
    The Journal of clinical investigation
    
    T. Ikawa et al., "EXPRESSION OF ARTHRITIS-CAUSING HLA-B27 ON HELA-CELLS PROMOTES INDUCTION OF C-FOS IN RESPONSE TO IN-VITRO INVASION BY SALMONELLA-TYPHIMURIUM", The Journal of clinical investigation, 101(1), 1998, pp. 263-272
23. SEKI M; USHIYAMA C; ABE K; SETA N; FUKAZAWA T; ASAKAWA J; TAKASAKI Y; HASHIMOTO H
    IN-VITRO CELLULAR-DRUG RESISTANCE AND INCREASED EXPRESSION OF BCL-2 IN LYMPHOCYTES FROM PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS
    Arthritis and rheumatism
    
    M. Seki et al., "IN-VITRO CELLULAR-DRUG RESISTANCE AND INCREASED EXPRESSION OF BCL-2 IN LYMPHOCYTES FROM PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS", Arthritis and rheumatism, 41(9), 1998, pp. 1790-1790
24. SEKI M; USHIYAMA C; SETA N; ABE K; FUKAZAWA T; ASAKAWA J; TAKASAKI Y; HASHIMOTO H
    APOPTOSIS OF LYMPHOCYTES INDUCED BY GLUCOCORTICOIDS AND RELATIONSHIP TO THERAPEUTIC EFFICACY IN PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS
    Arthritis and rheumatism
    
    M. Seki et al., "APOPTOSIS OF LYMPHOCYTES INDUCED BY GLUCOCORTICOIDS AND RELATIONSHIP TO THERAPEUTIC EFFICACY IN PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS", Arthritis and rheumatism, 41(5), 1998, pp. 823-830
25. ODOUX C; CRESTANI B; LEBRUN G; ROLLAND C; AUBIN P; SETA N; KAHN MF; FIET J; AUBIER M
    ENDOTHELIN-1 SECRETION BY ALVEOLAR MACROPHAGES IN SYSTEMIC-SCLEROSIS
    American journal of respiratory and critical care medicine
    
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26. SETA N; GAYNO S; JEZEQUELCUER M; TOUEG ML; ERLINGER S; DURAND G
    SEQUENTIAL STUDY OF SERUM GLYCOPROTEIN FUCOSYLATION IN ACUTE HEPATITIS
    Journal of hepatology
    
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27. BOUTTEN A; DEHOUX MS; SETA N; OSTINELLI J; VENEMBRE P; CRESTANI B; DOMBRET MC; DURAND G; AUBIER M
    COMPARTMENTALIZED IL-8 AND ELASTASE RELEASE WITHIN THE HUMAN LUNG IN UNILATERAL PNEUMONIA
    American journal of respiratory and critical care medicine
    
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28. CHEMLAL K; SAINTJULIEN L; JOLY V; FARINOTTI R; SETA N; YENI P; CARBON C
    COMPARISON OF FLUCONAZOLE AND AMPHOTERICIN-B FOR TREATMENT OF EXPERIMENTAL CANDIDA-ALBICANS ENDOCARDITIS IN RABBITS
    Antimicrobial agents and chemotherapy
    
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29. SETA N; BARNIER A; HOCHEDEZ F; BESNARD MA; DURAND G
    DIAGNOSTIC-VALUE OF WESTERN BLOTTING IN CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME
    Clinica chimica acta
    
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30. CRESTANI B; SETA N; PALAZZO E; ROLLAND C; VENEMBRE P; DEHOUX M; BOUTTEN A; SOLER P; DOMBRET MC; KAHN MF; AUBIER M
    INTERLEUKIN-8 AND NEUTROPHILS IN SYSTEMIC-SCLEROSIS WITH LUNG INVOLVEMENT
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31. DEHOUX MS; BOUTTEN A; OSTINELLI J; SETA N; DOMBRET MC; CRESTANI B; DESCHENES M; TROUILLET JL; AUBIER M
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    American journal of respiratory and critical care medicine
    
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32. LEBOURDELLES G; VIIRES N; BOCZKOWSKI J; SETA N; PAVLOVIC D; AUBIER M
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    American journal of respiratory and critical care medicine
    
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33. CRESTANI B; SETA N; DEBANDT M; SOLER P; ROLLAND C; DEHOUX M; BOUTTEN A; DOMBRET MC; PALAZZO E; KAHN MF; AUBIER M
    INTERLEUKIN-6 SECRETION BY MONOCYTES AND ALVEOLAR MACROPHAGES IN SYSTEMIC-SCLEROSIS WITH LUNG INVOLVEMENT
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34. HANSLIK T; BLANCHET F; NOCHY D; PIROTZKY E; GUILMARD C; SETA N; CARBON C
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    Toxicology and applied pharmacology
    
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35. VENEMBRE P; BOUTTEN A; SETA N; DEHOUX MS; CRESTANI B; AUBIER M; DURAND G
    SECRETION OF ALPHA-1-ANTITRYPSIN BY ALVEOLAR EPITHELIAL-CELLS
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36. VENEMBRE P; SETA N; BOUTTEN A; DEHOUX M; AUBIER M; DURAND G
    COMPARISON OF ENHANCED CHEMILUMINESCENCE AND COLORIMETRIC TECHNIQUES FOR THE IMMUNO-DETECTION OF ALPHA(1)-ANTITRYPSIN
    Clinica chimica acta
    
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37. CRESTANI B; DEHOUX M; SETA N; CUER M; AUBIER M
    CELL-SURFACE CARBOHYDRATES OF RAT ALVEOLAR TYPE-II CELLS IN PRIMARY CULTURE
    American journal of respiratory cell and molecular biology
    
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38. LORTHOLARY O; BLANCHET F; NOCHY D; HEUDES D; SETA N; AMIRAULT P; CARBON C
    EFFECTS OF DILTIAZEM ON NETILMICIN-INDUCED NEPHROTOXICITY IN RABBITS
    Antimicrobial agents and chemotherapy
    
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39. VENEMBRE P; SETA N; BOUTTEN A; DEHOUX M; AUBIER M; DURAND G
    PRODUCTION OF ALPHA-1-ANTITRYPSIN BY THP-1 CELLS
    The American review of respiratory disease
    
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