175 related articles for article (PubMed ID: 27846449)
1. A novel PROS1 mutation, c.74dupA, was identified in a protein S deficiency family.
Zhang Y; Yang H; Chen Q; Yu J; Chen X; Liu S; Gao G; Song Y; Zhou Z
Thromb Res; 2016 Dec; 148():125-127. PubMed ID: 27846449
[TBL] [Abstract][Full Text] [Related]
2. Severe arterial thrombosis in a family with type III protein S deficiency caused by a frameshift mutation in the PROS1 gene.
Larsen TB; Brusgaard K; Nybo M
Thromb Res; 2010 Aug; 126(2):e159-61. PubMed ID: 20398916
[No Abstract] [Full Text] [Related]
3. A novel nonsense mutation Tyr301* of PROS1 causing protein S deficiency.
Jang MA; Kim SH; Kim DK; Kim HJ
Blood Coagul Fibrinolysis; 2015 Mar; 26(2):223-4. PubMed ID: 25255242
[TBL] [Abstract][Full Text] [Related]
4. PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations.
Ten Kate MK; Platteel M; Mulder R; Terpstra P; Nicolaes GA; Reitsma PH; van der Steege G; van der Meer J
Hum Mutat; 2008 Jul; 29(7):939-47. PubMed ID: 18435454
[TBL] [Abstract][Full Text] [Related]
5. Hereditary protein S deficiency leads to ischemic stroke.
Wang ZH; Zhao ZJ; Xu K; Sun GB; Song L; Yin HX; Chen XQ
Mol Med Rep; 2015 Sep; 12(3):3279-3284. PubMed ID: 25997409
[TBL] [Abstract][Full Text] [Related]
6. Compound heterozygous mutations identified in severe type I protein S deficiency impaired the secretion of protein S.
Zhou J; Shen W; Gu Y; Li M; Shen W
J Clin Pathol; 2020 Jan; 73(1):7-13. PubMed ID: 31422373
[TBL] [Abstract][Full Text] [Related]
7. Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review.
Wypasek E; Karpinski M; Alhenc-Gelas M; Undas A
J Genet; 2017 Dec; 96(6):1047-1051. PubMed ID: 29321366
[TBL] [Abstract][Full Text] [Related]
8. Recurrent pulmonary embolism associated with deep venous thrombosis diagnosed as protein s deficiency owing to a novel mutation in PROS1: A case report.
Huang X; Xu F; Assa CR; Shen L; Chen B; Liu Z
Medicine (Baltimore); 2018 May; 97(19):e0714. PubMed ID: 29742732
[TBL] [Abstract][Full Text] [Related]
9. A novel mutation Gly222Arg in PROS1 causing protein S deficiency in a patient with pulmonary embolism.
Xu J; Peng G; Ouyang Y
J Clin Lab Anal; 2020 Apr; 34(4):e23111. PubMed ID: 31743498
[TBL] [Abstract][Full Text] [Related]
10. PROS1 variant c.1574C>T p.Ala525Val causes portal vein thrombosis with protein S deficiency.
Ye X; Mi X; Sun J; ShenTu Y; Fei Y; Tang D; Ye X; Ma X; Shi J; Chen G; Gong L
Clin Res Hepatol Gastroenterol; 2023 May; 47(6):102141. PubMed ID: 37207893
[TBL] [Abstract][Full Text] [Related]
11. [A family of hereditary protein S deficiency with the onset of pulmonary embolism and literature review].
Wei CJ; Guo CY; Li QR; Ye LP
Zhonghua Er Ke Za Zhi; 2022 Feb; 60(2):134-138. PubMed ID: 35090231
[No Abstract] [Full Text] [Related]
12. One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.
Mizukami K; Nakabayashi T; Naitoh S; Takeda M; Tarumi T; Mizoguchi I; Ieko M; Koike T
Am J Hematol; 2006 Oct; 81(10):787-97. PubMed ID: 16868938
[TBL] [Abstract][Full Text] [Related]
13. Clinical Manifestation and Mutation Spectrum of 53 Unrelated Pedigrees with Protein S Deficiency in China.
Li L; Wu X; Wu W; Ding Q; Cai X; Wang X
Thromb Haemost; 2019 Mar; 119(3):449-460. PubMed ID: 30669159
[TBL] [Abstract][Full Text] [Related]
14. Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency.
Xu F; Zhou X; Jin Y; Yang L; Pan J; Wang M; Chen X
Ann Hematol; 2024 Feb; 103(2):653-662. PubMed ID: 38175252
[TBL] [Abstract][Full Text] [Related]
15. Genotype and laboratory and clinical phenotypes of protein s deficiency.
Duebgen S; Kauke T; Marschall C; Giebl A; Lison S; Hart C; Dick A; Spannagl M
Am J Clin Pathol; 2012 Feb; 137(2):178-84. PubMed ID: 22261441
[TBL] [Abstract][Full Text] [Related]
16. [A homozygous variant in a consanguineous pedigree with inherited protein S deficiency].
Xie HX; Jin YH; Yang LL; Xie YY; Liu SQ; Luo SS; Wang MS
Zhonghua Jie He He Hu Xi Za Zhi; 2021 Apr; 44(4):360-364. PubMed ID: 33832024
[No Abstract] [Full Text] [Related]
17. Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.
Pintao MC; Garcia AA; Borgel D; Alhenc-Gelas M; Spek CA; de Visser MC; Gandrille S; Reitsma PH
Hum Genet; 2009 Sep; 126(3):449-56. PubMed ID: 19466456
[TBL] [Abstract][Full Text] [Related]
18. Compound heterozygous mutations in the PROS1 gene responsible for quantitative and qualitative protein S deficiency.
Yamanouchi J; Hato T; Tamura T; Fujiwara H; Yakushijin Y; Yasukawa M
Int J Hematol; 2009 Nov; 90(4):537-539. PubMed ID: 19826897
[No Abstract] [Full Text] [Related]
19. [Portal-splenic-mesenteric venous thrombosis in a patients with protein S deficiency due to novel PROS1 gene mutation].
Hwang ET; Kang WS; Park JW; Lee JH; Han HJ; Shin SY; Kim HJ; Choi JS
Korean J Gastroenterol; 2014 Aug; 64(2):110-4. PubMed ID: 25168054
[TBL] [Abstract][Full Text] [Related]
20. Identification of a novel PROS1 c.1113T-->GG frameshift mutation in a family with mixed type I/type III protein S deficiency.
ten Kate MK; Mulder R; Platteel M; Brouwer JL; van der Steege G; van der Meer J
Haematologica; 2006 Aug; 91(8):1151-2. PubMed ID: 16885060
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]