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CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome.
Notarangelo LD, Peitsch MC, Abrahamsen TG, Bachelot C, Bordigoni P, Cant AJ, Chapel H, Clementi M, Deacock S, de Saint Basile G, Duse M, Espanol T, Etzioni A, Fasth A, Fischer A, Giliani S, Gomez L, Hammarstorm L, Jones A, Kanariou M, Kinnon C, Klemola T, Kroczek RA, Levy J, Matamoros N, Monafo V, Paolucci P, Reznick I, Sanal O, Smith CI, Thompson RA, Tovo P, Villa A, Vihinen M, Vossen J, Zegers BJ. Notarangelo LD, et al. Among authors: smith ci. Immunol Today. 1996 Nov;17(11):511-6. doi: 10.1016/0167-5699(96)30059-5. Immunol Today. 1996. PMID: 8961627
BTKbase, mutation database for X-linked agammaglobulinemia (XLA).
Vihinen M, Iwata T, Kinnon C, Kwan SP, Ochs HD, Vorechovský I, Smith CI. Vihinen M, et al. Among authors: smith ci. Nucleic Acids Res. 1996 Jan 1;24(1):160-5. doi: 10.1093/nar/24.1.160. Nucleic Acids Res. 1996. PMID: 8594569 Free PMC article.
Molecular basis for X-linked immunodeficiencies.
Smith CI, Notarangelo LD. Smith CI, et al. Adv Genet. 1997;35:57-115. doi: 10.1016/s0065-2660(08)60448-4. Adv Genet. 1997. PMID: 9348646 No abstract available.
Structural aspects of signal transduction in B-cells.
Vihinen M, Smith CI. Vihinen M, et al. Among authors: smith ci. Crit Rev Immunol. 1996;16(3):251-75. doi: 10.1615/critrevimmunol.v16.i3.20. Crit Rev Immunol. 1996. PMID: 8922899 Review.
Primary immunodeficiency mutation databases.
Vihinen M, Arredondo-Vega FX, Casanova JL, Etzioni A, Giliani S, Hammarström L, Hershfield MS, Heyworth PG, Hsu AP, Lähdesmäki A, Lappalainen I, Notarangelo LD, Puck JM, Reith W, Roos D, Schumacher RF, Schwarz K, Vezzoni P, Villa A, Väliaho J, Smith CI. Vihinen M, et al. Among authors: smith ci. Adv Genet. 2001;43:103-88. doi: 10.1016/s0065-2660(01)43005-7. Adv Genet. 2001. PMID: 11037300 Review.
626 results