69 related articles for article (PubMed ID: 1325679)
1. Insertions/deletions in the antithrombin gene: 3 mutations associated with non-expression.
Daly M; Perry DJ; Harper PL; Daly HM; Roques AW; Carrell RW
Thromb Haemost; 1992 May; 67(5):521-5. PubMed ID: 1325679
[TBL] [Abstract][Full Text] [Related]
2. [Type I antithrombin deficiency due to 13389G deletion in antithrombin gene].
Fu Q; Xu X; Ding Q; Hu Y; Wang X; Wang H
Zhonghua Xue Ye Xue Za Zhi; 2002 Nov; 23(11):588-90. PubMed ID: 12482344
[TBL] [Abstract][Full Text] [Related]
3. The molecular basis of antithrombin deficiency in Belgian and Dutch families.
Jochmans K; Lissens W; Seneca S; Capel P; Chatelain B; Meeus P; Osselaer JC; Peerlinck K; Seghers J; Slacmeulder M; Stibbe J; van de Loo J; Vermylen J; Liebaers I; De Waele M
Thromb Haemost; 1998 Sep; 80(3):376-81. PubMed ID: 9759613
[TBL] [Abstract][Full Text] [Related]
4. [A novel mutation in antithrombin gene results in hereditary antithrombin deficiency].
Zhang FH; Ding QL; Wu JS; Zhou RF; Wang XF; Xu XC
Zhonghua Xue Ye Xue Za Zhi; 2006 Sep; 27(9):598-601. PubMed ID: 17278425
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Characterization of two novel mutations of the antithrombin gene observed in Japanese thrombophilic patients.
Kurihara M; Watanabe K; Inoue S; Wada Y; Ono M; Wakiyama M; Iida H; Kinoshita S; Hamasaki N
Thromb Res; 2005; 115(5):351-8. PubMed ID: 15733967
[TBL] [Abstract][Full Text] [Related]
7. CpG dinucleotides are "hotspots" for mutation in the antithrombin III gene. Twelve variants identified using the polymerase chain reaction.
Perry DJ; Carrell RW
Mol Biol Med; 1989 Jun; 6(3):239-43. PubMed ID: 2615648
[TBL] [Abstract][Full Text] [Related]
8. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
9. Genetic bases of human complement C7 deficiency.
Nishizaka H; Horiuchi T; Zhu ZB; Fukumori Y; Volanakis JE
J Immunol; 1996 Nov; 157(9):4239-43. PubMed ID: 8892662
[TBL] [Abstract][Full Text] [Related]
10. Alterations of the p53 tumor suppressor gene and its association with activation of the c-K-ras-2 protooncogene in premalignant and malignant lesions of the human uterine endometrium.
Enomoto T; Fujita M; Inoue M; Rice JM; Nakajima R; Tanizawa O; Nomura T
Cancer Res; 1993 Apr; 53(8):1883-8. PubMed ID: 8385572
[TBL] [Abstract][Full Text] [Related]
11. Biochemical activity and gene analysis of inherited protein C and antithrombin deficiency in two Chinese pedigrees.
Zhou RF; Fu QH; Wang WB; Xie S; Hu YQ; Wang XF; Wang ZY; Wang HL
Chin Med J (Engl); 2004 Jun; 117(6):813-7. PubMed ID: 15198878
[TBL] [Abstract][Full Text] [Related]
12. Molecular basis of antithrombin type I deficiency: the first large in-frame deletion and two novel mutations in exon 6.
Emmerich J; Chadeuf G; Alhenc-Gelas M; Gouault-Heilman M; Toulon P; Fiessinger JN; Aiach M
Thromb Haemost; 1994 Oct; 72(4):534-9. PubMed ID: 7878627
[TBL] [Abstract][Full Text] [Related]
13. Molecular basis of inherited antithrombin deficiency in Portuguese families: identification of genetic alterations and screening for additional thrombotic risk factors.
David D; Ribeiro S; Ferrão L; Gago T; Crespo F
Am J Hematol; 2004 Jun; 76(2):163-71. PubMed ID: 15164384
[TBL] [Abstract][Full Text] [Related]
14. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
15. Identification of eight point mutations in protein S deficiency type I--analysis of 15 pedigrees.
Gómez E; Poort SR; Bertina RM; Reitsma PH
Thromb Haemost; 1995 May; 73(5):750-5. PubMed ID: 7482398
[TBL] [Abstract][Full Text] [Related]
16. Type I antithrombin deficiency: five novel mutations associated with thrombosis.
Daly M; Perry DJ; Bruce DB; Harper PL; Tait RC; Walker ID; Mayne EE; Daly HM; Brown K; Carrell RW
Blood Coagul Fibrinolysis; 1996 Mar; 7(2):139-43. PubMed ID: 8735803
[TBL] [Abstract][Full Text] [Related]
17. Three missense mutations in the protein C heavy chain causing type I and type II protein C deficiency.
Miyata T; Zheng YZ; Sakata T; Tsushima N; Kato H
Thromb Haemost; 1994 Jan; 71(1):32-7. PubMed ID: 8165644
[TBL] [Abstract][Full Text] [Related]
18. Antithrombin III Kumamoto: identification of a point mutation and genotype analysis of the family.
Ueyama H; Murakami T; Nishiguchi S; Maeda S; Hashimoto Y; Okajima K; Shimada K; Araki S
Thromb Haemost; 1990 Apr; 63(2):231-4. PubMed ID: 2194315
[TBL] [Abstract][Full Text] [Related]
19. Dominantly Inherited beta-Thalassemia.
Efremov GD
Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
[TBL] [Abstract][Full Text] [Related]
20. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
Jensen HK
Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]