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Results: 1 to 20 of 163

Similar articles for PubMed (Select 3663935)

1.
2.

Hereditary thrombosis in a Utah kindred is caused by a dysfunctional antithrombin III gene.

Bock SC, Harris JF, Schwartz CE, Ward JH, Hershgold EJ, Skolnick MH.

Am J Hum Genet. 1985 Jan;37(1):32-41.

3.

Molecular genetics of inherited antithrombin III deficiencies.

Prochownik EV.

Am J Med. 1989 Sep 11;87(3B):15S-18S. Review.

PMID:
2572168
5.

Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindreds.

Sacks SH, Old JM, Reeders ST, Weatherall DJ, Douglas AS, Winter JH, Rizza CR.

J Med Genet. 1988 Jan;25(1):20-4.

6.

Recurrent deletion in the human antithrombin III gene.

Grundy CB, Thomas F, Millar DS, Krawczak M, Melissari E, Lindo V, Moffat E, Kakkar VV, Cooper DN.

Blood. 1991 Aug 15;78(4):1027-32.

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Cloning and expression of the cDNA for human antithrombin III.

Bock SC, Wion KL, Vehar GA, Lawn RM.

Nucleic Acids Res. 1982 Dec 20;10(24):8113-25.

10.

Hereditary antithrombin deficiency: heterogeneity of the molecular basis and mortality in Dutch families.

van Boven HH, Olds RJ, Thein SL, Reitsma PH, Lane DA, Briët E, Vandenbroucke JP, Rosendaal FR.

Blood. 1994 Dec 15;84(12):4209-13.

11.

Antithrombin III deficiency: a report of 14 cases belonging to three different kindreds.

Girolami A, Cappellato MG, Vicarioto M, Marafiotti F, Traverso R, Vergolani A, Boeri G.

Folia Haematol Int Mag Klin Morphol Blutforsch. 1985;112(4):594-606.

PMID:
2414189
12.

Isolation of a cDNA clone for human antithrombin III.

Prochownik EV, Markham AF, Orkin SH.

J Biol Chem. 1983 Jul 10;258(13):8389-94.

13.

[Hereditary deficiency of antithrombin III, protein C and protein S. A study of 31 patients from 8 unrelated families].

Lefrançois C, Derlon A, Le Querrec A, Lochu T, Sillard B, Deshayes JP, Delassus P, Bricard H.

Ann Fr Anesth Reanim. 1990;9(6):485-94. Review. French.

PMID:
2177589
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15.

A frameshift mutation leading to type 1 antithrombin deficiency and thrombosis.

Olds RJ, Lane DA, Finazzi G, Barbui T, Thein SL.

Blood. 1990 Dec 1;76(11):2182-6.

16.

Antithrombin III Utah: proline-407 to leucine mutation in a highly conserved region near the inhibitor reactive site.

Bock SC, Marrinan JA, Radziejewska E.

Biochemistry. 1988 Aug 9;27(16):6171-8. Erratum in: Biochemistry 1989 Apr 18;28(8):3628.

PMID:
3191114
17.

Quantitative and qualitative congenital deficiency of antithrombin III: a new molecular variant called ATIII-Barcelona 2.

Fontcuberta J, Grau E, Rubio N, Félez J, Rutllant ML.

Thromb Res. 1988 Jul 1;51(1):75-81.

PMID:
3413737
18.

[Antithrombin deficiency due to heterozygous antithrombin gene mutation and a pedigree study].

Ye X, Feng Y, Jin PP, Zhou XH, Ding QL, Wang XF.

Zhonghua Xue Ye Xue Za Zhi. 2007 Sep;28(9):587-9. Chinese.

PMID:
18246812
19.

[Sinus thrombosis caused by hereditary coagulation defects].

Kristensen B.

Lakartidningen. 1991 May 1;88(18):1691-4. Swedish. No abstract available.

PMID:
2041417
20.

A study of polymorphism of antithrombin III at the level of both protein and DNA in a Chinese population.

Gou Q, Hou Y, Zhang Y, Wu M.

Exp Clin Immunogenet. 1996;13(2):112-6.

PMID:
9063703
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