These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 3853270)

  • 1. Evaluation of the clotting defect in a factor XII-deficient kindred.
    Chistolini A; Mazzucconi MG; Motta M; Solinas S; Tirindelli MC; Mariani G
    Ric Clin Lab; 1985; 15(3):241-5. PubMed ID: 3853270
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Factor XII Osaka: abnormal factor XII with partially defective prekallikrein cleavage activity.
    Iijima K; Arakawa Y; Sugahara Y; Matsushita M; Moriguchi Y; Shimohiro H; Nakagawa M
    Thromb Haemost; 2011 Mar; 105(3):473-8. PubMed ID: 21264442
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comparable levels of activity and antigen in factor XII deficiency: a study of 21 homozygotes and 58 heterozygotes.
    Girolami A; Gavasso S; Pacquola E; Cabrio L; Lombardi AM; Girolami B
    Clin Appl Thromb Hemost; 2005 Jul; 11(3):335-8. PubMed ID: 16015420
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel homozygous missense mutation (Met527Ile) in a consanguineous marriage family with inherited factor XII deficiency.
    Liu M; Wang H; Lin M; Jin Y; Yang L; Wang M
    Hematology; 2020 Dec; 25(1):502-506. PubMed ID: 33317433
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Use of chromogenic substrates in the clarification of disorders in the early stages of blood coagulation].
    Vogel G; Stürzebecher J; Klessen C; Lauten G
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1982; 109(1):115-20. PubMed ID: 6177592
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Analysis of a consanguineous pedigree affected with hereditary coagulation factor XII deficiency caused by homozygous Gly341Arg mutation].
    Yang L; Jin S; Ji W; Cheng X; Li X; Jin Y; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):69-73. PubMed ID: 29419864
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic analysis of a pedigree with hereditary coagulation factor XII deficiency.
    Zhang H; Pan D; Shen W
    Blood Coagul Fibrinolysis; 2021 Sep; 32(6):406-410. PubMed ID: 33973893
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Functional characterization of a variant factor XII (F XII Locarno) in a cross reacting material positive F XII deficient plasma.
    Wuillemin WA; Furlan M; Stricker H; Lämmle B
    Thromb Haemost; 1992 Feb; 67(2):219-25. PubMed ID: 1621242
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic analysis of a hereditary factor XII deficiency pedigree of a consanguineous marriage due to a homozygous F12 gene mutation: Gly341Arg.
    Cheng X; Yang L; Huang G; Jin Y; Hao X; Wang M
    Hematology; 2017 Jun; 22(5):310-315. PubMed ID: 28007010
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Plasma levels of bradykinin are suppressed in factor XII-deficient mice.
    Iwaki T; Castellino FJ
    Thromb Haemost; 2006 Jun; 95(6):1003-10. PubMed ID: 16732380
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A comparison of the effects of factor XII deficiency and prekallikrein deficiency on thrombus formation.
    Kokoye Y; Ivanov I; Cheng Q; Matafonov A; Dickeson SK; Mason S; Sexton DJ; Renné T; McCrae K; Feener EP; Gailani D
    Thromb Res; 2016 Apr; 140():118-124. PubMed ID: 26950760
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Functional characterization of an abnormal factor XII molecule (F XII Bern).
    Wuillemin WA; Huber I; Furlan M; Lämmle B
    Blood; 1991 Aug; 78(4):997-1004. PubMed ID: 1868256
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Kallikrein and prekallikrein levels in a large number of congenital clotting deficiencies and abnormalities.
    Patrassi GM; Martinelli S; Vianello C; Girolami A
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1982; 109(4):644-54. PubMed ID: 6184289
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Pedigree Analysis of Hereditary Coagulation Factor XII Deficiency Caused by Compound Heterozygous Mutation p.Gly175Cys and p.Gly542Ser of
    Cheng XL; Yang T; Yang L; Xin YJ; He M; Zhu L; Liu JY
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2024 Jun; 32(3):862-867. PubMed ID: 38926981
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification and characterization of two novel mutations (Q421 K and R123P) in congenital factor XII deficiency.
    Kanaji T; Kanaji S; Osaki K; Kuroiwa M; Sakaguchi M; Mihara K; Niho Y; Okamura T
    Thromb Haemost; 2001 Dec; 86(6):1409-15. PubMed ID: 11776307
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Improved methods to assay contact activation.
    Soulier JP; Gozin D
    Adv Biosci; 1978 Jul; 17():271-80. PubMed ID: 755703
    [No Abstract]   [Full Text] [Related]  

  • 17. Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotes.
    Lombardi AM; Bortoletto E; Scarparo P; Scapin M; Santarossa L; Girolami A
    Blood Coagul Fibrinolysis; 2008 Oct; 19(7):639-43. PubMed ID: 18832903
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Phenotypic and genetic analysis of two pedigrees affected with hereditary coagulation FXII deficiency].
    Li S; Shen C; Shu K; Liu J; Wang X; Li F; Yang X; Zhang Z; Chen B; Jiang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec; 35(6):800-803. PubMed ID: 30512149
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Identification of a novel heterozygous mutation in a pedigree with hereditary coagulation factor XII deficiency].
    Yang L; Hao X; Wang Y; Xie H; Jin Y; Zhu L; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):343-7. PubMed ID: 26037346
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Report 2 cases of congenital factor XII deficiency: a rare coagulation disorder.
    Kanjanapongkul S
    J Med Assoc Thai; 2011 Aug; 94 Suppl 3():S231-2. PubMed ID: 22043782
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.