247 related articles for article (PubMed ID: 31022435)
1. Factor XII deficiency is common in domestic cats and associated with two high frequency F12 mutations.
Maruyama H; Brooks MB; Stablein A; Frye A
Gene; 2019 Jul; 706():6-12. PubMed ID: 31022435
[TBL] [Abstract][Full Text] [Related]
2. Molecular characterization of cat factor XII gene and identification of a mutation causing factor XII deficiency in a domestic shorthair cat colony.
Bender DE; Kloos MT; Pontius JU; Hinsdale ME; Bellinger DA
Vet Pathol; 2015 Mar; 52(2):312-20. PubMed ID: 24793828
[TBL] [Abstract][Full Text] [Related]
3. A novel missense mutation in the factor XII gene in a litter of cats with factor XII deficiency.
Maruyama H; Hosoe H; Nagamatsu K; Kano R; Kamata H
J Vet Med Sci; 2017 May; 79(5):822-826. PubMed ID: 28392508
[TBL] [Abstract][Full Text] [Related]
4. Novel deleterious mutation in the F12 gene in a Korean family with severe coagulation factor XII deficiency.
Kim HJ; Kim HJ; Kwon EH; Lee KO; Park IA; Kim SH
Blood Coagul Fibrinolysis; 2010 Oct; 21(7):683-6. PubMed ID: 20729721
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. [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]
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. Homozygous missense variant F12 (Gly506Asp) associated with severe factor XII deficiency: a case report.
Aljabry M; Algazlan A; Alsubaie N; Dher SB; Aljabri HS; Alotaibi GS
J Med Case Rep; 2023 Dec; 17(1):504. PubMed ID: 38057855
[TBL] [Abstract][Full Text] [Related]
9. Compound heterozygous mutations Glu502Lys and Met527Thr of the FXII gene in a patient with factor XII deficiency.
Zhang H; Liu S; Lin C; Luo S; Yang L; Jin Y; Zhu L; Wang M
Hematology; 2019 Dec; 24(1):420-425. PubMed ID: 30929639
[TBL] [Abstract][Full Text] [Related]
10. Factor XII deficiency: a clinical and molecular genetic study.
Demidova E; Salomashkina V; Pshenichnikova O; Selivanova D; Yakovleva E; Zozulya N; Gorgidze L; Surin V
Int J Hematol; 2023 May; 117(5):678-683. PubMed ID: 36627437
[TBL] [Abstract][Full Text] [Related]
11. Combined cis-regulator elements as important mechanism affecting FXII plasma levels.
Sabater-Lleal M; Chillón M; Mordillo C; Martínez A; Gil E; Mateo J; Blangero J; Almasy L; Fontcuberta J; Soria JM
Thromb Res; 2010 Feb; 125(2):e55-60. PubMed ID: 19786295
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Molecular genetic analysis of Korean patients with coagulation factor XII deficiency.
Kwon MJ; Kim HJ; Lee KO; Jung CW; Kim SH
Blood Coagul Fibrinolysis; 2010 Jun; 21(4):308-12. PubMed ID: 20386432
[TBL] [Abstract][Full Text] [Related]
14. [Identification of compound heterozygous variants of F12 gene in a pedigree affected with inherited coagulation factor XII deficiency].
Xie H; Zhang H; Xu M; Zou A; Jin Y; Yang L; Pan J; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 May; 37(5):519-522. PubMed ID: 32335876
[TBL] [Abstract][Full Text] [Related]
15. The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosis.
Wu X; Ding Q; Wang X; Dai J; Wu W
BMC Med Genet; 2018 Mar; 19(1):50. PubMed ID: 29587641
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. 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]
18. [Genetic analysis of a Chinese pedigree affected with Congenital coagulation factor XII deficiency due to a c.1A>G start codon variant of F12 gene].
Ji W; Lin S; Chen J; Jin C; Lin X; Ye Z; Qiu L; Qian D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 May; 40(5):547-551. PubMed ID: 37102287
[TBL] [Abstract][Full Text] [Related]
19. A novel factor XII mutation, FXII R84P, causing factor XII deficiency in a patient with hereditary spastic paraplegia.
Matsuki E; Miyakawa Y; Okamoto S
Blood Coagul Fibrinolysis; 2011 Apr; 22(3):227-30. PubMed ID: 21297451
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
