Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 194

1.

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. doi: 10.1371/journal.pone.0035773. Epub 2012 Apr 24.

2.

PROC c.574_576del polymorphism: a common genetic risk factor for venous thrombosis in the Chinese population.

Tang L, Lu X, Yu JM, Wang QY, Yang R, Guo T, Mei H, Hu Y.

J Thromb Haemost. 2012 Oct;10(10):2019-26. doi: 10.1111/j.1538-7836.2012.04862.x.

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 25;563(1):35-40. doi: 10.1016/j.gene.2015.03.002. Epub 2015 Mar 4.

PMID:
25748729
4.

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. doi: 10.1097/PAT.0b013e328353a218.

PMID:
22531345
5.
6.

Clinical and genetic features of protein C deficiency in 23 unrelated Chinese patients.

Ding Q, Shen W, Ye X, Wu Y, Wang X, Wang H.

Blood Cells Mol Dis. 2013 Jan;50(1):53-8. doi: 10.1016/j.bcmd.2012.08.004. Epub 2012 Aug 27.

PMID:
22951146
7.

Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study.

Fidalgo T, Martinho P, Salvado R, Manco L, Oliveira AC, Pinto CS, Gonçalves E, Marques D, Sevivas T, Martins N, Ribeiro ML.

Eur J Haematol. 2015 Oct;95(4):294-307. doi: 10.1111/ejh.12488. Epub 2015 Mar 13.

PMID:
25533856
8.

Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis.

Tjeldhorn L, Sandset PM, Haugbro K, Skretting G.

Thromb Res. 2010 Mar;125(3):230-4. doi: 10.1016/j.thromres.2009.05.013. Epub 2009 Jun 17.

PMID:
19535131
9.

Hereditary protein C deficiency in Indian patients with venous thrombosis.

Pai N, Ghosh K, Shetty S.

Ann Hematol. 2012 Sep;91(9):1471-6. doi: 10.1007/s00277-012-1483-5. Epub 2012 May 11.

PMID:
22576310
10.

Acroangiodermatitis of Mali in protein C deficiency due to a novel PROC gene mutation.

Wei-Min Tan A, Lee JS, Pramono ZA, Chong WS.

Am J Dermatopathol. 2012 Apr;34(2):e19-21. doi: 10.1097/DAD.0b013e3182169528.

PMID:
22441373
11.
12.

Protein C deficiency in a controlled series of unselected outpatients: an infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study)

Koster T, Rosendaal FR, Briët E, van der Meer FJ, Colly LP, Trienekens PH, Poort SR, Reitsma PH, Vandenbroucke JP.

Blood. 1995 May 15;85(10):2756-61.

13.

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.

PMID:
15198878
14.

Hereditary basis of protein C deficiency (PCD) in thrombosis patients: first report from India.

Pai N, Shetty S, Idicula-Thomas S, Kulkarni B, Ghosh K.

Thromb Haemost. 2009 Apr;101(4):785-7. No abstract available.

PMID:
19350130
15.

[Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis].

Miljić P, Rolović Z, Elezović I, Antunović P, Stanojević M, Colović M.

Srp Arh Celok Lek. 1999 Jan-Feb;127(1-2):21-7. Serbian.

PMID:
10377836
16.

Molecular basis and thrombotic manifestations of antithrombin deficiency in 15 unrelated Chinese patients.

Ding Q, Wang M, Xu G, Ye X, Xi X, Yu T, Wang X, Wang H.

Thromb Res. 2013 Sep;132(3):367-73. doi: 10.1016/j.thromres.2013.07.013. Epub 2013 Aug 8.

PMID:
23932013
18.

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 16;13(2):2969-77. doi: 10.4238/2014.April.16.5.

19.

[Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency].

Xia Y, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Wang XF, Xi XD, Wang HL.

Zhonghua Xue Ye Xue Za Zhi. 2011 Dec;32(12):848-53. Chinese.

PMID:
22339960
20.

Supplemental Content

Support Center