Suppr超能文献

相似文献

1
The nucleotide sequence of the gene for human protein C.
Proc Natl Acad Sci U S A. 1985 Jul;82(14):4673-7. doi: 10.1073/pnas.82.14.4673.
2
Nucleotide sequence of the gene for human factor IX (antihemophilic factor B).
Biochemistry. 1985 Jul 2;24(14):3736-50. doi: 10.1021/bi00335a049.
3
Cloning and sequencing of liver cDNA coding for bovine protein C.
Proc Natl Acad Sci U S A. 1984 Sep;81(18):5653-6. doi: 10.1073/pnas.81.18.5653.
4
Characterization of a cDNA coding for human protein C.
Proc Natl Acad Sci U S A. 1984 Aug;81(15):4766-70. doi: 10.1073/pnas.81.15.4766.
5
Nucleotide sequence of the gene for the b subunit of human factor XIII.
Biochemistry. 1990 Dec 25;29(51):11195-209. doi: 10.1021/bi00503a007.
7
Isolation and characterization of a cDNA coding for human factor IX.
Proc Natl Acad Sci U S A. 1982 Nov;79(21):6461-4. doi: 10.1073/pnas.79.21.6461.
9
Nucleotide sequence of the gene for human prothrombin.
Biochemistry. 1987 Sep 22;26(19):6165-77. doi: 10.1021/bi00393a033.
10
Organization of the gene for human factor XI.
Biochemistry. 1987 Nov 17;26(23):7221-8. doi: 10.1021/bi00397a004.

引用本文的文献

1
The novel protein C variant p.C101F results in early intracellular degradation that drives type I protein C deficiency.
Int J Hematol. 2025 Jun;121(6):774-781. doi: 10.1007/s12185-025-03943-z. Epub 2025 Feb 10.
3
Molecular basis of inherited protein C deficiency results from genetic variations in the signal peptide and propeptide regions.
J Thromb Haemost. 2023 Nov;21(11):3124-3137. doi: 10.1016/j.jtha.2023.06.021. Epub 2023 Jun 29.
4
A case of venous thromboembolism caused by protein C deficiency due to a novel gene mutation.
J Cardiol Cases. 2022 Aug 12;26(5):360-363. doi: 10.1016/j.jccase.2022.07.012. eCollection 2022 Nov.
6
Supplementary research on K150del variant of activated protein C.
Aging (Albany NY). 2021 Apr 25;13(9):12466-12478. doi: 10.18632/aging.202904.
8
Laboratory Limitations of Excluding Hereditary Protein C Deficiency by Chromogenic Assay: Discrepancies of Phenotype and Genotype.
Clin Appl Thromb Hemost. 2020 Jan-Dec;26:1076029620912028. doi: 10.1177/1076029620912028.
9
R147W in PROC Gene Is a Risk Factor of Thromboembolism in Thai Children.
Clin Appl Thromb Hemost. 2018 Mar;24(2):263-267. doi: 10.1177/1076029617709085. Epub 2017 May 17.
10
The Importance of Exosite Interactions for Substrate Cleavage by Human Thrombin.
PLoS One. 2015 Jun 25;10(6):e0129511. doi: 10.1371/journal.pone.0129511. eCollection 2015.

本文引用的文献

1
Preparation and properties of bovine factor VIII (antihemophilic factor).
Biochemistry. 1980 Feb 5;19(3):401-10. doi: 10.1021/bi00544a001.
2
A catalogue of splice junction sequences.
Nucleic Acids Res. 1982 Jan 22;10(2):459-72. doi: 10.1093/nar/10.2.459.
3
Identification of an endothelial cell cofactor for thrombin-catalyzed activation of protein C.
Proc Natl Acad Sci U S A. 1981 Apr;78(4):2249-52. doi: 10.1073/pnas.78.4.2249.
5
Deficiency of protein C in congenital thrombotic disease.
J Clin Invest. 1981 Nov;68(5):1370-3. doi: 10.1172/jci110385.
8
Organization and expression of eucaryotic split genes coding for proteins.
Annu Rev Biochem. 1981;50:349-83. doi: 10.1146/annurev.bi.50.070181.002025.
10
Characterization of a cDNA coding for human protein C.
Proc Natl Acad Sci U S A. 1984 Aug;81(15):4766-70. doi: 10.1073/pnas.81.15.4766.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验