| 1 | F11, LRP8
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| Identification of coagulation factor XI as a ligand for platelet apolipoprotein E receptor 2 (ApoER2).
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| White-Adams TC, Berny MA, Tucker EI, Gertz JM, Gailani D, Urbanus RT, de Groot PG, Gruber A, McCarty OJ.
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| Arterioscler Thromb Vasc Biol 29(10):1602-7. Epub 2009 Aug 6.PMID: 19661487 2009
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| 2 | F11
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| Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiency.
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| Saunders RE, Shiltagh N, Gomez K, Mellars G, Cooper C, Perry DJ, Tuddenham EG, Perkins SJ.
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| Thromb Haemost 102(2):287-301.PMID: 19652879 2009
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| 3 | F11
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| Factor XI protein in human pancreas and kidney.
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| Cheng Q, Kantz J, Poffenberger G, Powers AC, Gailani D.
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| Thromb Haemost 100(1):158-60. No abstract available. PMID: 18612554 2008
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| 4 | F11, F12
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| Factor XI homodimer structure is essential for normal proteolytic activation by factor XIIa, thrombin, and factor XIa.
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| Wu W, Sinha D, Shikov S, Yip CK, Walz T, Billings PC, Lear JD, Walsh PN.
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| J Biol Chem 283(27):18655-64. Epub 2008 Apr 25.PMID: 18441012 2008
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| 5 | F11
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| Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defect.
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| Guella I, Soldą G, Spena S, Asselta R, Ghiotto R, Tenchini ML, Castaman G, Duga S.
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| Thromb Haemost 99(3):523-30.PMID: 18327400 2008
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| 6 | F11
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| Characterization of seven novel mutations causing factor XI deficiency.
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| Zucker M, Zivelin A, Landau M, Salomon O, Kenet G, Bauduer F, Samama M, Conard J, Denninger MH, Hani AS, Berruyer M, Feinstein D, Seligsohn U.
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| Haematologica 92(10):1375-80.PMID: 18024374 2007
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| 7 | F11
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| Characterization of seven novel mutations causing factor XI deficiency.
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| Zucker M, Zivelin A, Landau M, Salomon O, Kenet G, Bauduer F, Samama M, Conard J, Denninger MH, Hani AS, Berruyer M, Feinstein D, Seligsohn U.
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| Haematologica 92(10):1375-80.PMID: 18024374 2007
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| 8 | F11
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| A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency.
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| Soldą G, Asselta R, Ghiotto R, Tenchini ML, Castaman G, Duga S.
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| Haematologica 90(12):1716-8.PMID: 16330457 2005
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| 9 | F11
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| Cloning and characterization of the human factor XI gene promoter: transcription factor hepatocyte nuclear factor 4alpha (HNF-4alpha ) is required for hepatocyte-specific expression of factor XI.
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| Tarumi T, Kravtsov DV, Zhao M, Williams SM, Gailani D.
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| J Biol Chem 277(21):18510-6. Epub 2002 Mar 12. 2002
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| 10 | F11
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| High levels of coagulation factor XI as a risk factor for venous thrombosis.
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| Meijers JC, Tekelenburg WL, Bouma BN, Bertina RM, Rosendaal FR.
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| N Engl J Med 342(10):696-701. 2000
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| 11 | F11
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| Heterozygous factor XI deficiency associated with three novel mutations.
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| Mitchell M, Cutler J, Thompson S, Moore G, Jenkins Ap Rees E, Smith M, Savidge G, Alhaq A.
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| Br J Haematol 107(4):763-5. 1999
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| 12 | F11
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| Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11.
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| Wistinghausen B, Reischer A, Oddoux C, Ostrer H, Nardi M, Karpatkin M.
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| Br J Haematol 99(3):575-7. 1997
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| 13 | F11
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| A 14-bp deletion (codon 554 del AAGgtaacagagtg) at exon 14/intron N junction of the coagulation factor XI gene disrupts splicing and causes severe factor XI deficiency.
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| Peretz H, et al.
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| Hum Mutat 8 : 77-78. 1996
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| 14 | F11
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| Identification of two novel mutations in non-Jewish factor XI deficiency.
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| Imanaka Y, et al.
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| Br J Haematol 90 : 916-920. 1995
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| 15 | F11
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| One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews.
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| Shpilberg O, et al.
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| Blood 85 : 429-432. 1995
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| 16 | F11
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| Six point mutations that cause factor XI deficiency.
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| Pugh RE, et al.
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| Blood 85 : 1509-1516. 1995
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| 17 | F11
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| Expression of human blood coagulation factor XI: Characterization of the defect in factor XI type III deficiency.
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| Meijers JCM, et al.
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| Blood 79 : 1435-1440. 1992
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| 18 | F11
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| A molecular genetic study of factor XI deficiency.
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| Hancock JF, et al.
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| Blood 77 : 1942-1948. 1991
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| 19 | F11
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| Factor XI deficiency in Ashkenazi Jews in Israel.
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| Asakai R, et al.
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| N Engl J Med 325 : 153-158. 1991
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| 20 | F11
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| Dinucleotide repeat polymorphism in the human coagulation factor XI gene, intron B (F11), detected using the polymerase chain reaction.
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| Bodfish P, et al.
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| Nucleic Acids Res 19 : 6979. 1991
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| 21 | F11
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| RFLP for intron E of factor XI gene.
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| Butler MG, et al.
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| Nucleic Acids Res 18 : 5327. 1990
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| 22 | F11
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| Factor XI (F11) is located on the distal end of the long arm of chromosome 4.
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| Kato A, et al.
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| Cytogenet Cell Genet 52 : 77-78. 1989
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| 23 | F11
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| Organization of the gene for human factor XI.
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| Asakai R, et al.
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| Biochemistry 26 : 7221-7228. 1987
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| 24 | F2, F5TPH, F7, VWF, F10, F11, F12, F13A1, F13B, FG@
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| The genetics of blood coagulation.
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| Graham JB, et al.
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| Adv Hum Genet 13 : 1-65. 1983
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