210 related articles for article (PubMed ID: 29321366)
1. 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]
2. Novel Splice Site Mutation in the
Mrożek M; Wypasek E; Alhenc-Gelas M; Potaczek DP; Undas A
Medicina (Kaunas); 2020 Sep; 56(9):. PubMed ID: 32971918
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [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]
5. 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]
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. 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]
8. 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]
9. A novel rare c.-39C>T mutation in the PROS1 5'UTR causing PS deficiency by creating a new upstream translation initiation codon.
Labrouche-Colomer S; Soukarieh O; Proust C; Mouton C; Huguenin Y; Roux M; Besse C; Boland A; Olaso R; Constans J; Deleuze JF; Morange PE; Jaspard-Vinassa B; Trégouët DA;
Clin Sci (Lond); 2020 May; 134(10):1181-1190. PubMed ID: 32426810
[TBL] [Abstract][Full Text] [Related]
10. Two Novel Variants in the Protein S Gene PROS1 Are Associated with Protein S Deficiency and Thrombophilia.
Juhl D; Kuta P; Shneyder M; Wünsche F; Nowak-Göttl U
Acta Haematol; 2021; 144(2):222-226. PubMed ID: 32653888
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A rare splicing mutation in the PROS1 gene of a Korean patient with type I hereditary protein S deficiency.
Choi J; Kim HJ; Chang MH; Choi JR; Yoo JH
Ann Clin Lab Sci; 2011; 41(4):397-400. PubMed ID: 22166512
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. A Case of a Pediatric Patient With Protein S Heerlen Polymorphism and Deep Venous Thrombosis.
Kacar M; Bhatt M
J Pediatr Hematol Oncol; 2022 Mar; 44(2):e442-e443. PubMed ID: 34486549
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. PROS1 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency.
Alhenc-Gelas M; Plu-Bureau G; Horellou MH; Rauch A; Suchon P;
Thromb Haemost; 2016 Mar; 115(3):570-9. PubMed ID: 26466767
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Genetic characterization of antithrombin, protein C, and protein S deficiencies in Polish patients.
Wypasek E; Corral J; Alhenc-Gelas M; Sydor W; Iwaniec T; Celińska-Lowenhoff M; Potaczek DP; Blecharczyk A; Zawilska K; Musiał J; Undas A
Pol Arch Intern Med; 2017 Aug; 127(7-8):512-523. PubMed ID: 28607330
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
