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.
2. A novel frameshift mutation in exon 4 causing a deficiency of high-molecular-weight kininogen in a patient with splenic infarction. Fukushima N; Itamura H; Wada H; Ikejiri M; Igarashi Y; Masaki H; Sano M; Komiyama Y; Ichinohe T; Kimura S Intern Med; 2014; 53(3):253-7. PubMed ID: 24492696 [TBL] [Abstract][Full Text] [Related]
3. Characterization of molecular defects of Fitzgerald trait and another novel high-molecular-weight kininogen-deficient patient: insights into structural requirements for kininogen expression. Krijanovski Y; Proulle V; Mahdi F; Dreyfus M; Müller-Esterl W; Schmaier AH Blood; 2003 Jun; 101(11):4430-6. PubMed ID: 12576314 [TBL] [Abstract][Full Text] [Related]
4. Severe high-molecular-weight kininogen deficiency due to a homozygous c.1456C > T nonsense variant in a large Chinese family. Yang J; Fan L; Qiao Y; Zhao Y; Zhu T J Thromb Thrombolysis; 2020 Nov; 50(4):989-994. PubMed ID: 32185598 [TBL] [Abstract][Full Text] [Related]
5. The First Korean Case of High-Molecular-Weight Kininogen Deficiency, With a Novel Variant, c.488delG, in the Jeong D; Goo JY; Kim HK; Chong SY; Kang MS Ann Lab Med; 2020 May; 40(3):264-266. PubMed ID: 31858768 [No Abstract] [Full Text] [Related]
7. Strain-specific deletions in exon 10 of rat K-kininogen and T1-kininogen genes allow mapping of both genes to rat chromosome 11. Harris EL; Grigor MR; Innes BA; Harrap SB; Koike G; Jacob HJ Mamm Genome; 1997 Oct; 8(10):791-2. PubMed ID: 9321484 [No Abstract] [Full Text] [Related]
8. Identification of one base deletion in exon IX of the protein C gene that causes a type I deficiency. Tokunaga F; Wakabayashi S; Sato H; Arakawa M; Tawaraya H; Koide T Thromb Res; 1992 Dec; 68(4-5):417-23. PubMed ID: 1290170 [No Abstract] [Full Text] [Related]
9. Evidence for the presence of a kininogen-like species in a case of total deficiency of low and high molecular weight kininogens. Veloso D Braz J Med Biol Res; 1998 Jul; 31(7):901-10. PubMed ID: 9698753 [TBL] [Abstract][Full Text] [Related]
15. Structure and expression of two kininogen genes in mice. Cardoso CC; Garrett T; Cayla C; Meneton P; Pesquero JB; Bader M Biol Chem; 2004; 385(3-4):295-301. PubMed ID: 15134344 [TBL] [Abstract][Full Text] [Related]
16. Two mutations in exon XII of the protein S alpha gene in four thrombophilic families resulting in premature stop codons and depressed levels of mutated mRNA. Andersen BD; Lind B; Philips M; Hansen AB; Ingerslev J; Thorsen S Thromb Haemost; 1996 Aug; 76(2):143-50. PubMed ID: 8865520 [TBL] [Abstract][Full Text] [Related]
17. Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis. Chi J; Nicolaou KA; Nicolaidou V; Koumas L; Mitsidou A; Pierides C; Manoloukos M; Barbouti K; Melanthiou F; Prokopiou C; Vassiliou GS; Costeas P Leukemia; 2014 May; 28(5):1152-4. PubMed ID: 24365789 [No Abstract] [Full Text] [Related]
18. Influence of contact system deficiencies during cardiopulmonary bypass. Agostoni A; Cugno M Thromb Haemost; 2001 Feb; 85(2):191-2. PubMed ID: 11246529 [No Abstract] [Full Text] [Related]
19. Combined high molecular weight Kininogen and factor XI deficiency. Ahmadinejad M; Alavi S; Ebadi M; Rashidi A; Tabatabaei M; Rezvani A Haemophilia; 2016 Jan; 22(1):e60-1. PubMed ID: 26572243 [No Abstract] [Full Text] [Related]
20. Kininogen deficiency in Fitzgerald trait: role of high molecular weight kininogen in clotting and fibrinolysis. Donaldson VH; Glueck HI; Miller MA; Movat HZ; Habal F J Lab Clin Med; 1976 Feb; 87(2):327-37. PubMed ID: 1245795 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]