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Alain Fischer

Veröffentlichungen von Alain Fischer zu Le Deist, Françoise ->
weitere Veröffentlichungen von Alain Fischer:
Long-term human T-helper lines producing specific helper factor reactive to influenza virus (1981)
A new peak in the ALPS (1999)
Cobalt(III) alkylperoxy complexes. Synthesis, x-ray structure, and role in the catalytic decomposition of alkyl hydroperoxides and in the hydroxylation of hydrocarbons (1985)
Independent mutations of the human CD3–ε gene resulting in a T cell receptor/CD3 complex immunodeficiency (1993)
A study of 25 patients with chronic granulomatous disease: A new classification by correlating respiratory burst, cytochrome b, and flavoprotein (1986)
Hyper-IgM immunodeficiency syndrome: Influence of lymphokines onin vitro maturation of peripheral B cells (1992)
Geochemical and isotopic evidence for seawater contamination of the hydrothermal system of Taal Volcano, Luzon, the Philippines (1998)
Clinical effects of mutations to CD95 (Fas): relevance to autoimmunity? (1998)
Clinical effects of mutations to CD95 (Fas): relevance to autoimmunity? (1998)
GENE THERAPY FOR SEVERE COMBINED IMMUNODEFICIENCY (2005)
Ferromagnetostrukturelle Beziehungen in den Verbindungen [Mn(OC6X3H2)2(bpy)]2, X = Cl, BrWir danken Prof. Dr. A. Herr und Ing. R. Poinsot für die Messungen mit dem SQUID-Magnetometer und J.-P. Lambour für die Messungen der Wärmekapazität. (1994)
Ferromagneto-Structural Correlations in [Mn(OC6X3H2)2(bipy)]2 Compounds, X = Cl, BrWe thank Prof. Dr. A. Herr and Ing. R. Poinsot for measurements on the SQUID magnetometer and Tech. J.-P. Lambour for the specific heat measurements, bpy = bipyridine. (1994)
Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene (1997)
Estimate of human gene number provided by genome-wide analysis using Tetraodon nigroviridis DNA sequence (2000)
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome (2000)
Veröffentlichungen zu Le Deist, Françoise
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1
Fischer, Alain, Rieux-Laucat, Frédéric, ... A new peak in the ALPS
in: Nature medicine . - New York, NY : Nature America Inc., ISSN 1546-170X, Vol. 5, No. 8 (1999), p. 876-877
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1999
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2
Soudais, Claire, de Villartay, Jean-Pierre, ... Independent mutations of the human CD3–ε gene resulting in a T cell receptor/CD3 complex immunodeficiency
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 3, No. 1 (1993), p. 77-81
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1993
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3
de Villartay, Jean-Pierre, Rieux-Laucat, Frédéric, ... Clinical effects of mutations to CD95 (Fas): relevance to autoimmunity?
in: Springer seminars in immunopathology , ISSN 1432-2196, Vol. 19 (3. 1998), p. 301-310
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1998
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4
Ménasché, Gaël, Pastural, Elodie, ... Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 25, No. 2 (2000), p. 173-176
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2000
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5
Rigaud, Stéphanie, Fondanèche, Marie-Claude, ... XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 444, No. 7115 (2006), p. 110-114
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2006
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6
Döffinger, Rainer, Smahi, Asma, ... X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 27, No. 3 (2001), p. 277-285
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2001