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Results: 1 to 20 of 122

1.

Molecular genetics of human antithrombin deficiency.

Perry DJ, Carrell RW.

Hum Mutat. 1996;7(1):7-22. Review.

PMID:
8664906
[PubMed - indexed for MEDLINE]
2.

Antithrombin and its inherited deficiencies.

Perry DJ.

Blood Rev. 1994 Mar;8(1):37-55. Review.

PMID:
8205009
[PubMed - indexed for MEDLINE]
3.

Molecular basis of inherited antithrombin deficiency in Portuguese families: identification of genetic alterations and screening for additional thrombotic risk factors.

David D, Ribeiro S, Ferrão L, Gago T, Crespo F.

Am J Hematol. 2004 Jun;76(2):163-71.

PMID:
15164384
[PubMed - indexed for MEDLINE]
4.

Genetic linkage studies in antithrombin-deficient kindreds using a highly polymorphic trinucleotide short tandem repeat (STR) within the human antithrombin gene.

Ni H, Waye JS, Sheffield WP, Eng B, Blajchman MA.

Am J Hematol. 1994 Jun;46(2):107-11.

PMID:
8172176
[PubMed - indexed for MEDLINE]
5.

Antithrombin and its deficiency states.

Lane DA, Olds RR, Thein SL.

Blood Coagul Fibrinolysis. 1992 Jun;3(3):315-41. Review.

PMID:
1643210
[PubMed - indexed for MEDLINE]
6.

Two novel antithrombin variants, Asn187Asp and Asn187Lys, indicate a functional role for asparagine 187.

Perry DJ, Marshall C, Borg JY, Tait RC, Daly ME, Walker ID, Carrell RW.

Blood Coagul Fibrinolysis. 1995 Feb;6(1):51-4.

PMID:
7795154
[PubMed - indexed for MEDLINE]
7.

The molecular basis of antithrombin deficiency in Belgian and Dutch families.

Jochmans K, Lissens W, Seneca S, Capel P, Chatelain B, Meeus P, Osselaer JC, Peerlinck K, Seghers J, Slacmeulder M, Stibbe J, van de Loo J, Vermylen J, Liebaers I, De Waele M.

Thromb Haemost. 1998 Sep;80(3):376-81.

PMID:
9759613
[PubMed - indexed for MEDLINE]
8.

Gene-gene and gene-environment interactions determine risk of thrombosis in families with inherited antithrombin deficiency.

van Boven HH, Vandenbroucke JP, Briët E, Rosendaal FR.

Blood. 1999 Oct 15;94(8):2590-4.

PMID:
10515862
[PubMed - indexed for MEDLINE]
Free Article
9.

Complete nucleotide sequence of the antithrombin gene: evidence for homologous recombination causing thrombophilia.

Olds RJ, Lane DA, Chowdhury V, De Stefano V, Leone G, Thein SL.

Biochemistry. 1993 Apr 27;32(16):4216-24.

PMID:
8476848
[PubMed - indexed for MEDLINE]
10.

Pleiotropic effects of antithrombin strand 1C substitution mutations.

Lane DA, Olds RJ, Conard J, Boisclair M, Bock SC, Hultin M, Abildgaard U, Ireland H, Thompson E, Sas G, et al.

J Clin Invest. 1992 Dec;90(6):2422-33.

PMID:
1469094
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Insertions/deletions in the antithrombin gene: 3 mutations associated with non-expression.

Daly M, Perry DJ, Harper PL, Daly HM, Roques AW, Carrell RW.

Thromb Haemost. 1992 May 4;67(5):521-5.

PMID:
1325679
[PubMed - indexed for MEDLINE]
12.

The molecular genetics of familial venous thrombosis.

Cooper DN.

Baillieres Clin Haematol. 1994 Sep;7(3):637-74. Review.

PMID:
7841604
[PubMed - indexed for MEDLINE]
13.

Antithrombin "Chicago": a functionally abnormal molecule with increased heparin affinity causing familial thrombophilia.

Bauer KA, Ashenhurst JB, Chediak J, Rosenberg RD.

Blood. 1983 Dec;62(6):1242-50.

PMID:
6640109
[PubMed - indexed for MEDLINE]
Free Article
14.

[Type I antithrombin deficiency due to 13389G deletion in antithrombin gene].

Fu Q, Xu X, Ding Q, Hu Y, Wang X, Wang H.

Zhonghua Xue Ye Xue Za Zhi. 2002 Nov;23(11):588-90. Chinese.

PMID:
12482344
[PubMed - indexed for MEDLINE]
15.

Molecular genetics of antithrombin deficiency.

Lane DA, Kunz G, Olds RJ, Thein SL.

Blood Rev. 1996 Jun;10(2):59-74. Review.

PMID:
8813337
[PubMed - indexed for MEDLINE]
16.

Screening for inherited thrombophilia: indications and therapeutic implications.

De Stefano V, Rossi E, Paciaroni K, Leone G.

Haematologica. 2002 Oct;87(10):1095-108. Review.

PMID:
12368166
[PubMed - indexed for MEDLINE]
Free Article
17.

Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis.

Millar DS, Wacey AI, Ribando J, Melissari E, Laursen B, Woods P, Kakkar VV, Cooper DN.

Hum Genet. 1994 Nov;94(5):509-12.

PMID:
7959685
[PubMed - indexed for MEDLINE]
18.

Characterization of antithrombins produced by active site mutagenesis of human alpha 1-antitrypsin expressed in yeast.

George PM, Pemberton P, Bathurst IC, Carrell RW, Gibson HL, Rosenberg S, Hallewell RA, Barr PJ.

Blood. 1989 Feb;73(2):490-6.

PMID:
2644977
[PubMed - indexed for MEDLINE]
Free Article
19.

Prevalence of antithrombin deficiency in the healthy population.

Tait RC, Walker ID, Perry DJ, Islam SI, Daly ME, McCall F, Conkie JA, Carrell RW.

Br J Haematol. 1994 May;87(1):106-12.

PMID:
7947234
[PubMed - indexed for MEDLINE]
20.

A novel 4 base pair deletion mutation inducing type I antithrombin deficiency.

Ozawa T, Niiya K, Inoue N, Kawahara N, Nakatsuka M, Tada K, Kudo T, Sakuragawa N.

Thromb Res. 1997 Mar 15;85(6):515-7. No abstract available.

PMID:
9101643
[PubMed - indexed for MEDLINE]
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