Cicardi M - Search Results

1

A dysfunctional C1 inhibitor protein with a new reactive center mutation (Arg-444-->Leu).

Frangi D, Aulak KS, Cicardi M, Harrison RA, Davis AE 3rd. Frangi D, et al. Among authors: cicardi m. FEBS Lett. 1992 Apr 13;301(1):34-6. doi: 10.1016/0014-5793(92)80204-t. FEBS Lett. 1992. PMID: 1451784 Free article.

2

Plasma levels of C1- inhibitor complexes and cleaved C1- inhibitor in patients with hereditary angioneurotic edema.

Cugno M, Nuijens J, Hack E, Eerenberg A, Frangi D, Agostoni A, Cicardi M. Cugno M, et al. Among authors: cicardi m. J Clin Invest. 1990 Apr;85(4):1215-20. doi: 10.1172/JCI114555. J Clin Invest. 1990. PMID: 2318974 Free PMC article.

3

Identification of a new P1 residue mutation (444Arg----Ser) in a dysfunctional C1 inhibitor protein contained in a type II hereditary angioedema plasma.

Aulak KS, Cicardi M, Harrison RA. Aulak KS, et al. Among authors: cicardi m. FEBS Lett. 1990 Jun 18;266(1-2):13-6. doi: 10.1016/0014-5793(90)81494-9. FEBS Lett. 1990. PMID: 2365061 Free article.

4

Restriction fragment length polymorphism of the C1 inhibitor gene in hereditary angioneurotic edema.

Cicardi M, Igarashi T, Kim MS, Frangi D, Agostoni A, Davis AE 3rd. Cicardi M, et al. J Clin Invest. 1987 Dec;80(6):1640-3. doi: 10.1172/JCI113252. J Clin Invest. 1987. PMID: 2890659 Free PMC article.

5

Nonsense mutations affect C1 inhibitor messenger RNA levels in patients with type I hereditary angioneurotic edema.

Frangi D, Cicardi M, Sica A, Colotta F, Agostoni A, Davis AE 3rd. Frangi D, et al. Among authors: cicardi m. J Clin Invest. 1991 Sep;88(3):755-9. doi: 10.1172/JCI115373. J Clin Invest. 1991. PMID: 1885769 Free PMC article.

6

Type II hereditary angioneurotic edema that may result from a single nucleotide change in the codon for alanine-436 in the C1 inhibitor gene.

Levy NJ, Ramesh N, Cicardi M, Harrison RA, Davis AE 3rd. Levy NJ, et al. Among authors: cicardi m. Proc Natl Acad Sci U S A. 1990 Jan;87(1):265-8. doi: 10.1073/pnas.87.1.265. Proc Natl Acad Sci U S A. 1990. PMID: 2296585 Free PMC article.

7

Mutations in the C1 inhibitor gene that result in hereditary angioneurotic edema.

Davis AE 3rd, Bissler JJ, Cicardi M. Davis AE 3rd, et al. Among authors: cicardi m. Behring Inst Mitt. 1993 Dec;(93):313-20. Behring Inst Mitt. 1993. PMID: 8172583 Review.

8

A hinge region mutation in C1-inhibitor (Ala436-->Thr) results in nonsubstrate-like behavior and in polymerization of the molecule.

Aulak KS, Eldering E, Hack CE, Lubbers YP, Harrison RA, Mast A, Cicardi M, Davis AE 3rd. Aulak KS, et al. Among authors: cicardi m. J Biol Chem. 1993 Aug 25;268(24):18088-94. J Biol Chem. 1993. PMID: 8349686 Free article.

9

Molecular defects in hereditary angioneurotic edema.

Bissler JJ, Aulak KS, Donaldson VH, Rosen FS, Cicardi M, Harrison RA, Davis AE 3rd. Bissler JJ, et al. Among authors: cicardi m. Proc Assoc Am Physicians. 1997 Mar;109(2):164-73. Proc Assoc Am Physicians. 1997. PMID: 9069585

10

Human inhibitor of the first component of complement, C1: characterization of cDNA clones and localization of the gene to chromosome 11.

Davis AE 3rd, Whitehead AS, Harrison RA, Dauphinais A, Bruns GA, Cicardi M, Rosen FS. Davis AE 3rd, et al. Among authors: cicardi m. Proc Natl Acad Sci U S A. 1986 May;83(10):3161-5. doi: 10.1073/pnas.83.10.3161. Proc Natl Acad Sci U S A. 1986. PMID: 3458172 Free PMC article.

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