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Items: 19

1.

Dominant factor XI deficiency caused by mutations in the factor XI catalytic domain.

Kravtsov DV, Wu W, Meijers JC, Sun MF, Blinder MA, Dang TP, Wang H, Gailani D.

Blood. 2004 Jul 1;104(1):128-34. Epub 2004 Mar 16.

2.

The mode of inheritance of PTA deficiency: evidence for the existence of major PTA deficiency and minor PTA deficiency.

RAPAPORT SI, PROCTOR RR, PATCH MJ, YETTRA M.

Blood. 1961 Aug;18:149-65. No abstract available.

3.

Plasma thromboplastin antecedent (PTA) deficiency.

CAMPBELL EW, MEDNICOFF IB, DAMESHEK W.

AMA Arch Intern Med. 1957 Aug;100(2):232-40. No abstract available.

PMID:
13443544
5.

Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion.

Duga S, Asselta R, Santagostino E, Zeinali S, Simonic T, Malcovati M, Mannucci PM, Tenchini ML.

Blood. 2000 Feb 15;95(4):1336-41.

6.

Heterozygous factor XI deficiency associated with three novel mutations.

Mitchell M, Cutler J, Thompson S, Moore G, Jenkins Ap Rees E, Smith M, Savidge G, Alhaq A.

Br J Haematol. 1999 Dec;107(4):763-5.

PMID:
10606881
7.
8.

Poor expression of MDR1 transgene in HeLa cells by bicistronic Moloney murine leukemia virus-based vector.

Zaboikin MM, Schuening FG.

Hum Gene Ther. 1998 Oct 10;9(15):2263-75.

PMID:
9794210
9.

The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European origin.

Peretz H, Mulai A, Usher S, Zivelin A, Segal A, Weisman Z, Mittelman M, Lupo H, Lanir N, Brenner B, Shpilberg O, Seligsohn U.

Blood. 1997 Oct 1;90(7):2654-9.

11.

Inheritance and bleeding in factor XI deficiency.

Bolton-Maggs PH, Young Wan-Yin B, McCraw AH, Slack J, Kernoff PB.

Br J Haematol. 1988 Aug;69(4):521-8.

PMID:
3408688
12.

Factor XI deficiency: genetic and clinical studies of a single kindred.

Litz CE, Swaim WR, Dalmasso AP.

Am J Hematol. 1988 May;28(1):8-12.

PMID:
3369441
13.
14.

Factor XI deficiency in Ashkenazi Jews in Israel.

Asakai R, Chung DW, Davie EW, Seligsohn U.

N Engl J Med. 1991 Jul 18;325(3):153-8.

15.

Location of the disulfide bonds in human coagulation factor XI: the presence of tandem apple domains.

McMullen BA, Fujikawa K, Davie EW.

Biochemistry. 1991 Feb 26;30(8):2056-60.

PMID:
1998667
16.

The coagulation cascade: initiation, maintenance, and regulation.

Davie EW, Fujikawa K, Kisiel W.

Biochemistry. 1991 Oct 29;30(43):10363-70. Review. No abstract available.

PMID:
1931959
17.

Apple four in human blood coagulation factor XI mediates dimer formation.

Meijers JC, Mulvihill ER, Davie EW, Chung DW.

Biochemistry. 1992 May 19;31(19):4680-4.

PMID:
1581318
18.
19.

Human blood coagulation factor XI. Purification, properties, and mechanism of activation by activated factor XII.

Bouma BN, Griffin JH.

J Biol Chem. 1977 Sep 25;252(18):6432-7. No abstract available.

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