143 related articles for article (PubMed ID: 33761690)
1. Pathogenic variants of PROC gene caused type II activity deficiency in a Chinese family: A case report.
Zhu H; Liu H; Liu J
Medicine (Baltimore); 2021 Mar; 100(12):e25160. PubMed ID: 33761690
[TBL] [Abstract][Full Text] [Related]
2. Genetic background analysis of protein C deficiency demonstrates a recurrent mutation associated with venous thrombosis in Chinese population.
Tang L; Guo T; Yang R; Mei H; Wang H; Lu X; Yu J; Wang Q; Hu Y
PLoS One; 2012; 7(4):e35773. PubMed ID: 22545135
[TBL] [Abstract][Full Text] [Related]
3. Compound heterozygous protein C deficiency in a family with venous thrombosis: Identification and in vitro study of p.Asp297His and p.Val420Leu mutations.
Liu H; Wang HF; Tang L; Yang Y; Wang QY; Zeng W; Wu YY; Cheng ZP; Hu B; Guo T; Hu Y
Gene; 2015 May; 563(1):35-40. PubMed ID: 25748729
[TBL] [Abstract][Full Text] [Related]
4. Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review.
Zhang Z; Yang Z; Chen M; Li Y
Medicine (Baltimore); 2022 Oct; 101(42):e31221. PubMed ID: 36281079
[TBL] [Abstract][Full Text] [Related]
5. [Analysis of PROC gene variant in a Chinese pedigree affected with hereditary protein C deficiency].
Chen Y; Shi J; Huang X; Sheng A; Lu C; Zhu M; Wang Q; Wang M; Wang D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Nov; 39(11):1233-1237. PubMed ID: 36317209
[TBL] [Abstract][Full Text] [Related]
6. Recurrent Cerebral Venous Thrombosis Treated with Direct Oral Anticoagulants in a Japanese Man with Hereditary Protein C Deficiency.
Saito K; Ishii K; Furuta K; Kobayashi M; Wada Y; Morishita E
J Stroke Cerebrovasc Dis; 2021 Jan; 30(1):105320. PubMed ID: 33131982
[TBL] [Abstract][Full Text] [Related]
7. Different impact of two mutations of a novel compound heterozygous protein C deficiency with late onset thrombosis.
Yang LH; Wang MS; Zheng FX; Li J; Chen Y; Jin YH; Xie HX; Yang XL; Chen BC
Genet Mol Res; 2014 Apr; 13(2):2969-77. PubMed ID: 24782131
[TBL] [Abstract][Full Text] [Related]
8. Analysis of four hereditary protein C deficiencies associated with vascular thromboembolism.
Chen X; Yuan C; Hu B; Lu C; Wang Y; Han Z; Zou M
Ann Hematol; 2024 Jun; 103(6):2145-2155. PubMed ID: 38433129
[TBL] [Abstract][Full Text] [Related]
9. [Analysis of an hereditary protein C deficiency pedigree with compound heterozygous gene mutations].
Yang LH; Zhu LQ; Yang XO; Wang MS; Li J; Chen BC; Jin YH; Zhang Z; Zheng FX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct; 29(5):515-8. PubMed ID: 23042384
[TBL] [Abstract][Full Text] [Related]
10. [Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene].
Liu S; Yu F; Luo S; Li X; Jin Y; Yang L; Zhou X; Zhang H; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1108-1112. PubMed ID: 32924112
[TBL] [Abstract][Full Text] [Related]
11. [A pedigree analysis of pulmonary embolism caused by compound heterozygous mutations of protein C].
Ye X; Liu X; Feng Y; Ding Q; Zhou X; Wang X
Nan Fang Yi Ke Da Xue Xue Bao; 2012 Jan; 32(1):109-12. PubMed ID: 22366017
[TBL] [Abstract][Full Text] [Related]
12. [Analysis of a hereditary protein C deficient consanguineous pedigree caused by Phe139Val homozygous mutation].
Yang LH; Zhu LQ; Wang YY; Xie HX; Xie YS; Jin YH; Wang MS; Chen BC; Yang XL
Zhonghua Xue Ye Xue Za Zhi; 2013 Sep; 34(9):767-70. PubMed ID: 24103874
[TBL] [Abstract][Full Text] [Related]
13. Pathogenic variants of PROC gene caused type I activity deficiency in a familial Chinese venous thrombosis.
Yue Y; Liu S; Han X; Xiao L; Huang Q; Li S; Zhuang K; Yang M; Zou C; Fu Y
J Cell Mol Med; 2019 Oct; 23(10):7099-7104. PubMed ID: 31338992
[TBL] [Abstract][Full Text] [Related]
14. [Analysis of phenotypes and genetic mutations in two pedigrees affected with hereditary protein C deficiency].
Yang L; Jin Y; Yang T; Chen X; Zhu L; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):10-14. PubMed ID: 28186585
[TBL] [Abstract][Full Text] [Related]
15. Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families.
Xu Q; Wang M; Jin Y; Liu S; Luo S; Yang L
Blood Coagul Fibrinolysis; 2021 Dec; 32(8):596-602. PubMed ID: 34261859
[TBL] [Abstract][Full Text] [Related]
16. Two novel compound heterozygous mutations associated with types I and II protein C deficiency with unusual phenotypes.
Deng MY; Liu ZX; Huang HF; Chen YH; Luo YJ; Sun NN; Cheng Z; Yan WZ; Zhang GS
Thromb Res; 2016 Sep; 145():93-9. PubMed ID: 27517348
[TBL] [Abstract][Full Text] [Related]
17. A Series of 14 Polish Patients with Thrombotic Events and PC Deficiency-Novel c.401-1G>A PROC Gene Splice Site Mutation in a Patient with Aneurysms.
Weronska A; Potaczek DP; Oto J; Medina P; Undas A; Wypasek E
Genes (Basel); 2022 Apr; 13(5):. PubMed ID: 35627118
[TBL] [Abstract][Full Text] [Related]
18. [A case of recurrent cerebral vein thrombosis with protein C gene mutation identified].
Sugahara Y; Ono N; Morishita E; Takashima H
Rinsho Shinkeigaku; 2018 Dec; 58(12):764-766. PubMed ID: 30487363
[TBL] [Abstract][Full Text] [Related]
19. Protein C deficiency (a novel mutation: ala291Thr) with systemic lupus erythematosus leads to the deep vein thrombosis.
Su K; Zhang H; Fang W; Zhang F; Yang L; Jin Y; Wang M
Blood Coagul Fibrinolysis; 2018 Dec; 29(8):714-719. PubMed ID: 30439769
[TBL] [Abstract][Full Text] [Related]
20. Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutation.
Yu T; Dai J; Liu H; Wang J; Ding Q; Wang H; Wang X; Fu Q
Pathology; 2012 Jun; 44(4):348-53. PubMed ID: 22531345
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]