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Results:
1-16
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Results: 16
Authors:
Fischer, A
Hacein-Bey, S
Le Deist, F
de Saint Basile, G
Cavazzana-Calvo, M
Citation: A. Fischer et al., Gene therapy for human severe combined immunodeficiencies, IMMUNITY, 15(1), 2001, pp. 1-4
Authors:
de Saint Basile, G
Fischer, A
Citation: G. De Saint Basile et A. Fischer, The role of cytotoxicity in lymphocyte homeostasis, CURR OP IM, 13(5), 2001, pp. 549-554
Authors:
Weller, S
Faili, A
Garcia, C
Braun, MC
Le Deist, F
de Saint Basile, G
Hermine, O
Fischer, A
Reynaud, CA
Weill, JC
Citation: S. Weller et al., CD40-CD40L independent Ig gene hypermutation suggests a second B cell diversification pathway in humans, P NAS US, 98(3), 2001, pp. 1166-1170
Authors:
Ericson, KG
Fadeel, B
Nilsson-Ardnor, S
Soderhall, C
Samuelsson, A
Janka, G
Schneider, M
Gurgey, A
Yalman, N
Revesz, T
Egeler, RM
Jahnukainen, K
Storm-Mathiesen, I
Haraldsson, A
Poole, J
de Saint Basile, G
Nordenskjold, M
Henter, JI
Citation: Kg. Ericson et al., Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis, AM J HU GEN, 68(3), 2001, pp. 590-597
Authors:
Menasche, G
Pastural, E
Feldmann, J
Certain, S
Ersoy, F
Dupuis, S
Wulffraat, N
Bianchi, D
Fischer, A
Le Deist, F
de Saint Basile, G
Citation: G. Menasche et al., Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome, NAT GENET, 25(2), 2000, pp. 173-176
Authors:
Bachmeyer, C
Monge, M
Cazier, A
Le Deist, F
de Saint Basile, G
Durandy, A
Fischer, A
Mougeot-Martin, M
Citation: C. Bachmeyer et al., Gastric adenocarcinoma in a patient with X-linked agammaglobulinaemia, EUR J GASTR, 12(9), 2000, pp. 1033-1035
Authors:
de Saint Basile, G
Citation: G. De Saint Basile, Protein trafficking inherited disorders, M S-MED SCI, 16(6-7), 2000, pp. 745-750
Authors:
Sanal, O
Yel, L
Kucukali, T
Gilbert-Barnes, E
Tardieu, M
Tezcan, I
Ersoy, F
Metin, A
de Saint Basile, G
Citation: O. Sanal et al., An allelic variant of Griscelli disease: presentation with severe hypotonia, mental-motor retardation, and hypopigmentation consistent with Elejalde syndrome (neuroectodermal melanolysosomal disorder), J NEUROL, 247(7), 2000, pp. 570-572
Authors:
Stepp, SE
Mathew, PA
Bennett, M
de Saint Basile, G
Kumar, V
Citation: Se. Stepp et al., Perforin: more than just an effector molecule, IMMUNOL TOD, 21(6), 2000, pp. 254-256
Authors:
Bousso, P
Wahn, V
Douagi, I
Horneff, G
Pannetier, C
Le Deist, F
Zepp, F
Niehues, T
Kourilsky, P
Fischer, A
de Saint Basile, G
Citation: P. Bousso et al., Diversity, functionality, and stability of the T cell repertoire derived in vivo from a single human T cell precursor, P NAS US, 97(1), 2000, pp. 274-278
Authors:
Certain, S
Barrat, F
Pastural, E
Le Deist, F
Goyo-Rivas, J
Jabado, N
Benkerrou, M
Seger, R
Vilmer, E
Beullier, G
Schwarz, K
Fischer, A
de Saint Basile, G
Citation: S. Certain et al., Protein truncation test of LYST reveals heterogenous mutations in patientswith Chediak-Higashi syndrome, BLOOD, 95(3), 2000, pp. 979-983
Authors:
Fischer, A
Hacein-Bey, S
Le Deist, F
de Saint Basile, G
de Villartay, JP
Cavazzana-Calvo, M
Citation: A. Fischer et al., Gene therapy of immunodeficiency disorders, B ACA N MED, 184(7), 2000, pp. 1417-1430
Authors:
Dufourcq-Lagelouse, R
Lambert, N
Duval, M
Viot, G
Vilmer, E
Fischer, A
Prieur, M
de Saint Basile, G
Citation: R. Dufourcq-lagelouse et al., Chediak-Higashi syndrome associated with maternal uniparental isodisomy ofchromosome 1, EUR J HUM G, 7(6), 1999, pp. 633-637
Authors:
Dufourcq-Lagelouse, R
Pastural, E
Barrat, FJ
Le Deist, F
Fischer, A
de Saint Basile, G
Citation: R. Dufourcq-lagelouse et al., Genetic defects of T-lymphocyte activation control evolving into a lymphohistiocyte activation syndrome, ARCH PED, 6, 1999, pp. 417S-419S
Authors:
Barrat, FJ
Le Deist, F
Benkerrou, M
Bousso, P
Feldmann, J
Fischer, A
de Saint Basile, G
Citation: Fj. Barrat et al., Defective CTLA-4 cycling pathway in Chediak-Higashi syndrome: A possible mechanism for deregulation of T lymphocyte activation, P NAS US, 96(15), 1999, pp. 8645-8650
Authors:
de Saint Basile, G
Tabone, MD
Durandy, A
Phan, F
Fischer, A
Le Deist, F
Citation: G. De Saint Basile et al., CD40 ligand expression deficiency in a female carrier of the X-linked hyper-IgM syndrome as a result of X chromosome lyonization, EUR J IMMUN, 29(1), 1999, pp. 367-373
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