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Increased efficiency of mRNA 3′ end formation: a new genetic mechanism contributing to hereditary thrombophilia
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/meth.1998.0705openalex-snapshot
Assaying the Polyadenylation State of mRNAs
inferredcites →https://doi.org/10.1016/0003-2697(90)90595-zopenalex-snapshot
Molecular cloning: A laboratory manual
inferredcites →https://doi.org/10.1016/s0022-2836(83)80101-6openalex-snapshot
Human beta and delta globin messenger RNAs turn over at different rates
inferredcites →https://doi.org/10.1016/s0049-3848(98)00136-4openalex-snapshot
The G20210A Mutation of the Prothrombin Gene in Patients with Previous First Episodes of Deep-Vein Thrombosis
inferredcites →https://doi.org/10.1017/s1355838299990829openalex-snapshot
Aberrant mRNAs with extended 3′ UTRs are substrates for rapid degradation by mRNA surveillance
inferredcites →https://doi.org/10.1055/s-0037-1614842openalex-snapshot
The VITA Project: Prothrombin G20210A Mutation and Venous Thromboembolism in the General Population
inferredcites →https://doi.org/10.1055/s-0038-1665427openalex-snapshot
Co-inheritance of the 20210A Allele of the Prothrombin Gene Increases the Risk of Thrombosis in Subjects with Familial Thrombophilia
inferredcites →https://doi.org/10.1093/emboj/17.12.3484openalex-snapshot
Binary specification of nonsense codons by splicing and cytoplasmic translation
inferredcites →https://doi.org/10.1093/emboj/20.3.532openalex-snapshot
Splicing and 3′ end formation in the definition of nonsense‐mediated decay‐competent human β‐globin mRNPs
inferredcites →https://doi.org/10.1093/nar/22.13.2525openalex-snapshot
Sequence and position requirements for uridylate-rich downstream elements of polyadenylation signals
inferredcites →https://doi.org/10.1093/nar/22.14.2811openalex-snapshot
Polyadenylation and transcription termination in gene constructs containing multiple tandem polyadenylation signals
inferredcites →https://doi.org/10.1093/nar/23.14.2614openalex-snapshot
Cleavage site determinants min the mammalian polydenylation signal
inferredcites →https://doi.org/10.1093/nar/23.3.413openalex-snapshot
Nuclear degradation of nonsense mutated β-globin mRNA: a post-transcriptional mechanism to protect heterozygotes from severe clinical manifestations of β-thalassemia?
inferredcites →https://doi.org/10.1101/gad.11.21.2755openalex-snapshot
Mechanism and regulation of mRNA polyadenylation
inferredcites →https://doi.org/10.1128/mcb.20.2.604-616.2000openalex-snapshot
A Nuclear 3′-5′ Exonuclease Involved in mRNA Degradation Interacts with Poly(A) Polymerase and the hnRNA Protein Npl3p
inferredcites →https://doi.org/10.1128/mmbr.63.2.405-445.1999openalex-snapshot
Formation of mRNA 3′ Ends in Eukaryotes: Mechanism, Regulation, and Interrelationships with Other Steps in mRNA Synthesis
inferredcites →https://doi.org/10.1182/blood.v88.10.3698.bloodjournal88103698openalex-snapshot
A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
inferredcites →https://doi.org/10.1182/blood.v95.5.1517.005k48_1517_1532openalex-snapshot
Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Independent 3'Untranslated Region Rna, A Novel Non-Coding Regulator Rna: What Do We Know Now?
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mRNA Formation: 3′‐End
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Molecular coagulation and thrombophilia
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Molecular coagulation and thrombophilia
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Molecular Coagulation and Thrombophilia
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Thrombophilia: Assays and Interpretation
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Matrix Proteases and the Degradome
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mRNA 3′end processing: A tale of the tail reaches the clinic
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A proteomic analysis of changes in prothrombin and plasma proteins associated with the G20210A mutation
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Connections between 3′ end processing and DNA damage response: Ten years later
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Two sides of the same medal: Noncoding mutations reveal new pathological mechanisms and insights into the regulation of gene expression
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Poly(A) tale: From A to A; RNA polyadenylation in prokaryotes and eukaryotes
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Angeborene und erworbene Thrombophilien
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Laboratory Evaluation of Thrombophilia
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Testing for Factor V Leiden (FVL) and Prothrombin G20210A Genetic Variants
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Principles of Molecular Pathology
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A systematic analysis of disease-associated variants in the 3′ regulatory regions of human protein-coding genes I: general principles and overview
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A distal auxiliary element facilitates cleavage and polyadenylation of Dux4 mRNA in the pathogenic haplotype of FSHD
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Association Between the G20210A Polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population
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Characterization and prediction of mRNA polyadenylation sites in human genes
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FV-Leiden- und Prothrombin-G20210A-Mutation
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The Prevalence of the Prothrombin (F2) 20210G>A Mutation in a Cohort of Sri Lankan Patients with Thromboembolic Disorders
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Hereditary thrombophilic risk factors for recurrent pregnancy loss
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Sequence variation in 3′UTR region of crtRB1 gene and its effect on β-carotene accumulation in maize kernel
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The effects of Factor II (rs1799963) polymorphism on recurrent pregnancy loss in Iranian Azeri women
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Human Gene Mutation in Inherited Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-383834-6.00060-4openalex-snapshot
Common Genetic Determinants of Coagulation and Fibrinolysis
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Hemophilias and Other Disorders of Hemostasis
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Molecular Diagnostics for Coagulopathies
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Hemophilias and Other Disorders of Hemostasis
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Disorders of Hemostasis and Thrombosis
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Human Genomic Variants and Inherited Disease
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Molecular diagnostics for coagulopathies
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Inherited Diseases
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10.1016/b978-1-4557-5414-4.00033-4
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Thrombophilia: Clinical and Laboratory Assessment and Management
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The Association of Prothrombin Gene G20210A Mutation with Recurrent Venous Thromboembolism: Evidence from a Meta-Analysis
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Mutations in cis that affect mRNA synthesis, processing and translation
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DNA-mounted self-assembly: New approaches for genomic analysis and SNP detection
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Identification and characterization of a novel 5 bp deletion in a putative insulin response element in the lipoprotein lipase gene
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Enzymatic activity of naturally occurring 1-acylglycerol-3-phosphate-O-acyltransferase 2 mutants associated with congenital generalized lipodystrophy
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A chemiluminescence-based reporter system to monitor nonsense-mediated mRNA decay
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Design of targeted, capture-based, next generation sequencing tests for precision cancer therapy
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Molecular analysis of homocystinuria in Brazilian patients
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Comprehensive Polyadenylation Site Maps in Yeast and Human Reveal Pervasive Alternative Polyadenylation
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A Deep Neural Network for Predicting and Engineering Alternative Polyadenylation
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Laboratory Evaluation of Hypercoagulability
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Molecular Diagnostics in Hemostatic Disorders
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Best Practices in Thrombophilia Testing
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Manipulating the epigenome for the treatment of disorders with thrombotic complications
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Double-homozygosity for Factor V Leiden and Prothrombin c.*97G > A Mutation in a Young Female with Recurrent Fetal Losses and no Venous Thromboembolism
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Poly(A) polymerase (PAP) diversity in gene expression – Star‐PAP vs canonical PAP
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The association of idiopathic recurrent pregnancy loss with polymorphisms in hemostasis-related genes
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High prevalence of factor V Leiden and prothrombin G20101A mutations in Kashmiri patients with venous thromboembolism
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A comprehensive analysis of core polyadenylation sequences and regulation by microRNAs in a set of cancer predisposition genes
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Venous thromboembolism laboratory testing (factor V Leiden and factor II c.∗97G>A), 2025 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG)
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Anti-inflammatory effects of Chrozophora plicata uncovered using network pharmacology and in-vivo carrageenan paw edema model
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Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis
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The prothrombin gene G20210A variant and puerperal cerebral venous and sinus thrombosis in South Indian women
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Four-color multiplex 5′ nuclease assay for the simultaneous detection of the factor V Leiden and the prothrombin G20210A mutations
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p38 MAPK Controls Prothrombin Expression by Regulated RNA 3′ End Processing
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Mechanisms and Consequences of Alternative Polyadenylation
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A novel insertion mutation in the FOXL2 gene is detected in a big Chinese family with blepharophimosis–ptosis–epicanthus inversus
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TNFR-associated factor-2 (TRAF-2) in Alzheimer's disease
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Screening, Testing, or Personalized Medicine: Where do Inherited Thrombophilias Fit Best?
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Propagation of genetic variation in gene regulatory networks
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Cleavage site heterogeneity at the pre-mRNA 3′-untranslated region regulates gene expression in oxidative stress response
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Duplication of the prothrombin gene is associated with a significant increase in thrombin generation
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Prothombin gene G20210A mutation is not a risk factor for ischemic stroke in a South Indian Hyderabadi Population
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A potential regulatory role for mRNA secondary structures within the prothrombin 3'UTR
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Prothrombin time, activated partial thromboplastin time and dilute Russell's Viper Venom times are not shorter in patients with the prothrombin G20210A mutation, and dilute Russell's Viper Venom time may be longer
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Haplotypes of TAFI gene and the risk of cerebral venous thrombosis - a case-control study
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Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes
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Heterogeneity in mammalian RNA 3′ end formation
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Polymorphisms in coagulation factor genes and their impact on arterial and venous thrombosis
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Regulation of Protease and Protease Inhibitor Gene Expression: The Role of the 3′‐UTR and Lessons from the Plasminogen Activating System
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When the Message Goes Awry
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Translational control by the 3′-UTR: the ends specify the means
inferred← citeshttps://doi.org/10.1016/s1097-2765(03)00142-4openalex-snapshot
Y14 and hUpf3b Form an NMD-Activating Complex
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Anomalies constitutionnelles de la coagulation prédisposant à la thrombose
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Prothrombin Gene Variants in Non-Caucasians with Fetal Loss and Intrauterine Growth Retardation
inferred← citeshttps://doi.org/10.1021/acs.jafc.6c01228openalex-snapshot
Chicken PPARγ Undergoes Alternative Polyadenylation to Produce Five 3′UTR Isoforms with Distinct Regulatory Functions
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Acute pyelonephritis and renal scarring are caused by dysfunctional innate immunity in mCxcr2 heterozygous mice
inferred← citeshttps://doi.org/10.1038/npg.els.0005471openalex-snapshot
Mutations in Human Genetic Disease
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Human and mouse proteases: a comparative genomic approach
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The role of untranslated region variants in Mendelian disease: a review
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Venous thromboembolism laboratory testing (factor V Leiden andfactor II c.*97G>A), 2018 update: a technical standard of the American College of Medical Genetics and Genomics (ACMG)
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Enhancers regulate 3′ end processing activity to control expression of alternative 3′UTR isoforms
inferred← citeshttps://doi.org/10.1038/s41576-019-0145-zopenalex-snapshot
Alternative cleavage and polyadenylation in health and disease
inferred← citeshttps://doi.org/10.1038/s41576-025-00928-wopenalex-snapshot
Regulation of gene expression by alternative polyadenylation in health and disease
inferred← citeshttps://doi.org/10.1038/s41580-022-00507-5openalex-snapshot
Context-specific regulation and function of mRNA alternative polyadenylation
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Improvement of the transient expression system for production of recombinant proteins in plants
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Genome-wide atlas of alternative polyadenylation in the forage legume red clover
inferred← citeshttps://doi.org/10.1038/sj.emboj.7601699openalex-snapshot
Splicing factors stimulate polyadenylation via USEs at non‐canonical 3′ end formation signals
inferred← citeshttps://doi.org/10.1038/sj.emboj.7601932openalex-snapshot
3′ end mRNA processing: molecular mechanisms and implications for health and disease
inferred← citeshttps://doi.org/10.1038/sj.ki.5001551openalex-snapshot
Renal vascular sclerosis is associated with inherited thrombophilias
inferred← citeshttps://doi.org/10.1038/srep39255openalex-snapshot
The Unravelling of the Genetic Architecture of Plasminogen Deficiency and its Relation to Thrombotic Disease
inferred← citeshttps://doi.org/10.1046/j.1365-2230.2002.01090.xopenalex-snapshot
Cardiac complications in Behçet's disease
inferred← citeshttps://doi.org/10.1046/j.1538-7836.2003.00393.xopenalex-snapshot
Functional characterization of transcription factor binding sites for HNF1-alpha, HNF3-beta (FOXA2), HNF4-alpha, Sp1 and Sp3 in the human prothrombin gene enhancer
inferred← citeshttps://doi.org/10.1053/j.seminhematol.2007.01.006openalex-snapshot
Plasma Coagulation Factor Levels in Venous Thrombosis
inferred← citeshttps://doi.org/10.1053/scds.2002.32657openalex-snapshot
Cerebral venous thrombosis: Incidence in prothrombotic states
inferred← citeshttps://doi.org/10.1055/s-0037-1613095openalex-snapshot
Prothrombin G20210A is a Bifunctional Gene Polymorphism
inferred← citeshttps://doi.org/10.1055/s-0040-1716541openalex-snapshot
Coagulation Characterization of Prothrombin 20209C > T Variant: About 27 New Cases
inferred← citeshttps://doi.org/10.1073/pnas.0607620104openalex-snapshot
Identification of Abcc6 as the major causal gene for dystrophic cardiac calcification in mice through integrative genomics
inferred← citeshttps://doi.org/10.1073/pnas.0706217104openalex-snapshot
A miR-24 microRNA binding-site polymorphism in dihydrofolate reductase gene leads to methotrexate resistance
inferred← citeshttps://doi.org/10.1074/mcp.m115.054056openalex-snapshot
Proteomic Analysis Reveals Branch-specific Regulation of the Unfolded Protein Response by Nonsense-mediated mRNA Decay
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Correlation of single nucleotide polymorphisms in the promoter region of the ANXA5 (annexin A5) gene with recurrent miscarriages in women of Greek origin
inferred← citeshttps://doi.org/10.1080/15476286.2017.1306171openalex-snapshot
Cleavage and polyadenylation: Ending the message expands gene regulation
inferred← citeshttps://doi.org/10.1089/104454902320908450openalex-snapshot
Defects in Pre-mRNA Processing as Causes of and Predisposition to Diseases
inferred← citeshttps://doi.org/10.1089/dna.2011.1391openalex-snapshot
Characterization of the Human Ornithine Transcarbamylase 3′ Untranslated Regulatory Region
inferred← citeshttps://doi.org/10.1093/aje/kwj092openalex-snapshot
Common Genetic Variation in the Prothrombin Gene, Hormone Therapy, and Incident Nonfatal Myocardial Infarction in Postmenopausal Women
inferred← citeshttps://doi.org/10.1093/annonc/mdq542openalex-snapshot
Allele polymorphisms of tumor integrins correlate with peritoneal carcinosis capability of gastric cancer cells in radically resected patients
inferred← citeshttps://doi.org/10.1093/bioinformatics/btl394openalex-snapshot
Prediction of mRNA polyadenylation sites by support vector machine
inferred← citeshttps://doi.org/10.1093/carcin/bgr273openalex-snapshot
Functional analysis of arylamine N-acetyltransferase 1 (NAT1) NAT1*10 haplotypes in a complete NATb mRNA construct
inferred← citeshttps://doi.org/10.1093/carcin/bgs224openalex-snapshot
Functional analysis of arylamine N-acetyltransferase 1 (NAT1) NAT1*10 haplotypes in a complete NATb mRNA construct
inferred← citeshttps://doi.org/10.1093/clinchem/hvz015openalex-snapshot
The Silence Speaks, but We Do Not Listen: Synonymous c.1824C>T Gene Variant in the Last Exon of the Prothrombin Gene as a New Prothrombotic Risk Factor
inferred← citeshttps://doi.org/10.1093/cvr/cvad046openalex-snapshot
Post-transcriptional control of haemostatic genes: mechanisms and emerging therapeutic concepts in thrombo-inflammatory disorders
inferred← citeshttps://doi.org/10.1093/embo-reports/kve207openalex-snapshot
Genetic dangers in poly(A) signals
inferred← citeshttps://doi.org/10.1093/hmg/ddm017openalex-snapshot
A common haplotype of the annexin A5 (ANXA5) gene promoter is associated with recurrent pregnancy loss
inferred← citeshttps://doi.org/10.1093/nar/gki055openalex-snapshot
PolyA_DB: a database for mammalian mRNA polyadenylation
inferred← citeshttps://doi.org/10.1093/nar/gki245openalex-snapshot
The relationship between the prothrombin upstream sequence element and the G20210A polymorphism: the influence of a competitive environment for mRNA 3'-end formation
inferred← citeshttps://doi.org/10.1097/00019606-200209000-00005openalex-snapshot
Detection of a Novel Point Mutation of the Prothrombin Gene at Position 20209
inferred← citeshttps://doi.org/10.1097/01.gim.0000067987.77803.d0openalex-snapshot
Role of the geneticist in testing and counseling for inherited thrombophilia
inferred← citeshttps://doi.org/10.1097/01.gim.0000172641.57755.3aopenalex-snapshot
Technical standards and guidelines: Venous thromboembolism (Factor V Leiden and prothrombin 20210G>A testing): A disease-specific supplement to the standards and guidelines for clinical genetics laboratories
inferred← citeshttps://doi.org/10.1097/01.mbc.0000245303.95138.01openalex-snapshot
Abnormal melt curve profile during prothrombin 20210G → A analysis due to the 20209C → T variant
inferred← citeshttps://doi.org/10.1097/01.tp.0000107185.50838.eeopenalex-snapshot
THROMBOPHILIA AND THROMBOTIC PROBLEMS IN RENAL TRANSPLANT PATIENTS
inferred← citeshttps://doi.org/10.1097/mbc.0b013e32832545f3openalex-snapshot
Association of inherited thrombophilia with embryonic and postembryonic recurrent pregnancy loss
inferred← citeshttps://doi.org/10.1097/mbc.0b013e32832f5d7aopenalex-snapshot
Prevalence of factor V Leiden and prothrombin G20210A mutation in a large French population selected for nonthrombotic history: geographical and age distribution
inferred← citeshttps://doi.org/10.1101/gad.17268411openalex-snapshot
Ending the message: poly(A) signals then and now
inferred← citeshttps://doi.org/10.1109/icsmc.2011.6083769openalex-snapshot
Identification of plant messenger RNA polyadenylation sites using length-variable second order Markov model
inferred← citeshttps://doi.org/10.1111/bjh.15004openalex-snapshot
What is currently known about the genetics of venous thromboembolism at the dawn of next generation sequencing technologies
inferred← citeshttps://doi.org/10.1111/ijlh.12672openalex-snapshot
Optimal utilization of thrombophilia testing
inferred← citeshttps://doi.org/10.1111/j.1365-2141.2004.05041.xopenalex-snapshot
Hormones and pregnancy: thromboembolic risks for women
inferred← citeshttps://doi.org/10.1111/j.1365-2257.2005.00720.xopenalex-snapshot
Mutation screening for the prothrombin variant G20210A by melting point analysis with the Light Cycler system: atypical results, detection of the variant C20209T and possible clinical implications
inferred← citeshttps://doi.org/10.1111/j.1365-2265.2006.02670.xopenalex-snapshot
Mutational analysis of the PTH 3′‐untranslated region in parathyroid disorders
inferred← citeshttps://doi.org/10.1111/j.1399-0012.2006.00574.xopenalex-snapshot
Do inherited hypercoagulable states play a role in thrombotic events affecting kidney/pancreas transplant recipients?
inferred← citeshttps://doi.org/10.1111/j.1478-3231.2008.01843.xopenalex-snapshot
Integrin alpha V polymorphisms and haplotypes in a Korean population are associated with susceptibility to chronic hepatitis and hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2003.00493.xopenalex-snapshot
G20210A is a functional mutation in the prothrombin gene; effect on protein levels and 3′‐end formation
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2003.0543e.xopenalex-snapshot
Rapid detection of the prothrombin C20209T variant by differential sensitivity to restriction endonuclease digestion
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2006.01885.xopenalex-snapshot
The prothrombin 20209 C→T mutation in Jewish‐Moroccan Caucasians: molecular analysis of gain‐of‐function of 3′ end processing
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2006.02102.xopenalex-snapshot
Functional analysis of two prothrombin 3′‐untranslated region variants: the C20209T variant, mainly found among African‐Americans, and the C20209A variant
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2006.02126.xopenalex-snapshot
More on: functional analysis of two prothrombin 3′‐UTR variants: the C20209T variant, mainly found among African‐Americans, and the C20209A variant
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2006.02216.xopenalex-snapshot
Prothrombin A19911G polymorphism and the risk of venous thromboembolism
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2007.02448.xopenalex-snapshot
Differential effects of high prothrombin levels on thrombin generation depending on the cause of the hyperprothrombinemia
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2007.02566.xopenalex-snapshot
Polymorphism 10034C>T is located in a region regulating polyadenylation of FGG transcripts and influences the fibrinogen γ′/γA mRNA ratio
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2007.02630.xopenalex-snapshot
The genetic interaction between VKORC1 c1173t and calumenin a29809g modulates the anticoagulant response of acenocoumarol
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2010.04026.xopenalex-snapshot
Cytoplasmic stabilities of 3′UTR‐polymorphic prothrombin mRNAs
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2011.04311.xopenalex-snapshot
Lessons from genome‐wide association studies in venous thrombosis
inferred← citeshttps://doi.org/10.1111/j.1600-0625.2011.01381.xopenalex-snapshot
Analysis of the 3′UTR of the prostaglandin synthetase-2 (PTGS-2 / COX-2) gene in non-melanoma skin cancer after organ transplantation
inferred← citeshttps://doi.org/10.1126/science.1101659openalex-snapshot
Cis-Acting Regulatory Variation in the Human Genome
inferred← citeshttps://doi.org/10.1128/mcb.24.10.4174-4183.2004openalex-snapshot
Polypyrimidine Tract Binding Protein Modulates Efficiency of Polyadenylation
inferred← citeshttps://doi.org/10.1134/s0022093023050216openalex-snapshot
Thrombin in the Crossroad Hemostasis and Inflammation
inferred← citeshttps://doi.org/10.1134/s1022795411100048openalex-snapshot
Analysis of acute ischemic stroke DNA markers in Russian and Moldavian populations
inferred← citeshttps://doi.org/10.1137/120887266openalex-snapshot
Mathematical Modeling of Alternative Polyadenylation in the Human Gene, CSTF 3
inferred← citeshttps://doi.org/10.1152/ajplung.00375.2002openalex-snapshot
Human SP-A 3′-UTR variants mediate differential gene expression in basal levels and in response to dexamethasone
inferred← citeshttps://doi.org/10.1155/2013/792941openalex-snapshot
Involvement of Fibroblast Growth Factor Receptor Genes in Benign Prostate Hyperplasia in a Korean Population
inferred← citeshttps://doi.org/10.1159/000083835openalex-snapshot
Elevated Clotting Factor Levels and Venous Thrombosis
inferred← citeshttps://doi.org/10.1159/000090934openalex-snapshot
3′ End Processing of the Prothrombin mRNA in Thrombophilia
inferred← citeshttps://doi.org/10.1160/th03-02-0096openalex-snapshot
Homozygous and double heterozygous Factor V Leiden and Factor II G20210A genotypes predispose infants to thromboembolism but are not associated with an increase of foetal loss
inferred← citeshttps://doi.org/10.1160/th05-11-0777openalex-snapshot
Epistatic and pleiotropic effects of polymorphisms in the fibrinogen and coagulation factor XIII genes on plasma fibrinogen concentration, fibrin gel structure and risk of myocardial infarction
inferred← citeshttps://doi.org/10.11606/d.5.2007.tde-22042007-204736openalex-snapshot
Rastreamento de mutações nos genes VHL, SDHB e SDHD em pacientes portadores de feocromocitoma ou também, paraganglioma esporádico
inferred← citeshttps://doi.org/10.1161/01.atv.0000084640.21712.9copenalex-snapshot
Human CRP Gene Polymorphism Influences CRP Levels
inferred← citeshttps://doi.org/10.1161/circulationaha.110.976134openalex-snapshot
Ethnic Differences in Out-of-Hospital Fatal Pulmonary Embolism
inferred← citeshttps://doi.org/10.1177/108925320300700407openalex-snapshot
Genetically Determined Procoagulant States and Heparin Use
inferred← citeshttps://doi.org/10.1177/2374289521990788openalex-snapshot
Education Case: Hereditary Thrombophilia With Double Heterozygous Factor V Leiden and Factor II c.*97G>A Mutations
inferred← citeshttps://doi.org/10.1182/blood-2002-02-0412openalex-snapshot
The G20210A mutation does not affect the stability of prothrombin mRNA in vivo
inferred← citeshttps://doi.org/10.1182/blood-2003-02-0419openalex-snapshot
The intronic prothrombin 19911A>G polymorphism influences splicing efficiency and modulates effects of the 20210G>A polymorphism on mRNA amount and expression in a stable reporter gene assay system
inferred← citeshttps://doi.org/10.1182/blood-2003-07-2520openalex-snapshot
A haplotype of the EPCR gene is associated with increased plasma levels of sEPCR and is a candidate risk factor for thrombosis
inferred← citeshttps://doi.org/10.1182/blood-2003-08-2894openalex-snapshot
The prothrombin 3′end formation signal reveals a unique architecture that is sensitive to thrombophilic gain-of-function mutations
inferred← citeshttps://doi.org/10.1182/blood-2005-12-5158openalex-snapshot
Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24 000 years ago
inferred← citeshttps://doi.org/10.1182/blood-2007-03-078543openalex-snapshot
Effect of single nucleotide polymorphisms on expression of the gene encoding thrombin-activatable fibrinolysis inhibitor: a functional analysis
inferred← citeshttps://doi.org/10.1182/blood-2008-07-169003openalex-snapshot
Genetic elimination of prothrombin in adult mice is not compatible with survival and results in spontaneous hemorrhagic events in both heart and brain
inferred← citeshttps://doi.org/10.1182/blood-2011-08-373928openalex-snapshot
Prothrombin 20210G>A genotype and C-reactive protein level
inferred← citeshttps://doi.org/10.1182/blood-2013-10-529628openalex-snapshot
A meta-analysis of genome-wide association studies identifies ORM1 as a novel gene controlling thrombin generation potential
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