Literature DB >> 16689777

Molecular mechanism for hereditary protein C deficiency in two Chinese families with thrombosis.

R-F Zhou, X-H Cai, S Xie, X-F Wang, H-L Wang.   

Abstract

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Year:  2006        PMID: 16689777     DOI: 10.1111/j.1538-7836.2006.01913.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


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  6 in total

1.  The genetics of venous thromboembolism: a systematic review of thrombophilia families.

Authors:  Yu Zhang; Zhu Zhang; Shi Shu; Wenquan Niu; Wanmu Xie; Jun Wan; Zhenguo Zhai; Chen Wang
Journal:  J Thromb Thrombolysis       Date:  2021-02       Impact factor: 2.300

2.  Expression and functional characterisation of natural R147W and K150del variants of protein C in the Chinese population.

Authors:  Qiulan Ding; Likui Yang; Seyed Mahdi Hassanian; A R Rezaie
Journal:  Thromb Haemost       Date:  2013-02-07       Impact factor: 5.249

3.  Functional characterization of the protein C A267T mutation: evidence for impaired secretion due to defective intracellular transport.

Authors:  Lena Tjeldhorn; Nina Iversen; Kirsten Sandvig; Jonas Bergan; Per Morten Sandset; Grethe Skretting
Journal:  BMC Cell Biol       Date:  2010-09-06       Impact factor: 4.241

4.  Protein C mutation (A267T) results in ER retention and unfolded protein response activation.

Authors:  Lena Tjeldhorn; Nina Iversen; Kirsten Sandvig; Jonas Bergan; Per Morten Sandset; Grethe Skretting
Journal:  PLoS One       Date:  2011-08-25       Impact factor: 3.240

5.  [Clinical phenotype and gene mutation analysis of 12 patients with hereditary protein C deficiency in different families].

Authors:  Q Y Xu; L L Yang; H X Xie; Y H Jin; X L Li; X X Zhou; M N Liu; M S Wang
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2022-01-14

6.  Protein C deficiency resulting from two mutations in PROC presenting with recurrent venous thromboembolism.

Authors:  Weijia Xie; Zhenjie Liu; Bing Chen
Journal:  J Vasc Surg Cases Innov Tech       Date:  2017-12-18
  6 in total

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