| A Novel Fibrinogen Mutation p.BbetaAla68Asp Causes an Inherited Dysfibrinogenemia. | A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia.
Jia K, Zeng M, Zheng X, Xie H, Yang L, Xie Y, Wang M. | 12/22/2023 |
| [Genetic analysis of a Chinese pedigree affected with Congenital dysfibrinogenemia due to variant of FGG gene]. | [Genetic analysis of a Chinese pedigree affected with Congenital dysfibrinogenemia due to variant of FGG gene].
Shao X, Ma J, Wang Z, Sun M, Huang Z, Jiang Z, Liu X, Li S, Liu Y. | 12/18/2023 |
| Pathogenic Role of Fibrinogen in the Neuropathology of Multiple Sclerosis: A Tale of Sorrows and Fears. | Pathogenic Role of Fibrinogen in the Neuropathology of Multiple Sclerosis: A Tale of Sorrows and Fears.
Alruwaili M, Al-Kuraishy HM, Alexiou A, Papadakis M, ALRashdi BM, Elhussieny O, Saad HM, Batiha GE., Free PMC Article | 09/25/2023 |
| Association between lipoprotein(a) and ischemic stroke: Fibrinogen as a mediator. | Association between lipoprotein(a) and ischemic stroke: Fibrinogen as a mediator.
Youyou Z, Ruirui J, Hui W, Zhaoyang L. | 09/13/2023 |
| The role of fibrinogen in traumatic brain injury: from molecular pathological mechanisms to clinical management. | The role of fibrinogen in traumatic brain injury: from molecular pathological mechanisms to clinical management.
Peng S, Lv K. | 08/28/2023 |
| Impact of Fibrinogen, Fibrin Thrombi, and Thrombin on Cancer Cell Extravasation Using In Vitro Microvascular Networks. | Impact of Fibrinogen, Fibrin Thrombi, and Thrombin on Cancer Cell Extravasation Using In Vitro Microvascular Networks.
Angelidakis E, Chen S, Zhang S, Wan Z, Kamm RD, Shelton SE., Free PMC Article | 07/31/2023 |
| Association between fibrinogen level and length of stay in patients with lower extremity atherosclerotic disease: a retrospective cohort study. | Association between fibrinogen level and length of stay in patients with lower extremity atherosclerotic disease: a retrospective cohort study.
Wang X, Yang Y, Yu L, Pang C, Sun W, Zang S, Li C., Free PMC Article | 07/27/2023 |
| Glycoprotein VI interplay with fibrin(ogen) in thrombosis. | Glycoprotein VI interplay with fibrin(ogen) in thrombosis.
Mangin PH, Gardiner EE, Ariëns RAS, Jandrot-Perrus M. | 06/23/2023 |
| Evaluating the Association Between Fibrinogen and Rotational Thromboelastometry and the Progression to Severe Obstetric Hemorrhage. | Evaluating the Association Between Fibrinogen and Rotational Thromboelastometry and the Progression to Severe Obstetric Hemorrhage.
Yurashevich M, Rosser M, Small M, Grotegut C, Kota N, Toffaletti J, Allen T., Free PMC Article | 05/24/2023 |
| Interaction Between Platelet and Fibrinogen on Clot Strength in Healthy Patients. | Interaction Between Platelet and Fibrinogen on Clot Strength in Healthy Patients.
Maslow A, Cheves T, Joyce MF, Apruzzese P, Sweeney J. | 05/8/2023 |
| miR-877-5p Inhibits Epithelial Mesenchymal Transformation of Breast Cancer Cells by Targeting FGB. | miR-877-5p Inhibits Epithelial Mesenchymal Transformation of Breast Cancer Cells by Targeting FGB.
Liu H, Xiang L, Mei Y., Free PMC Article | 12/10/2022 |
| [Analysis of two pedigrees affected with inherited dysfibrinogenemia due to a novel c.1115 T>A variant of the FGB gene]. | [Analysis of two pedigrees affected with inherited dysfibrinogenemia due to a novel c.1115 T>A variant of the FGB gene].
Wang X, Yao Y, Lin S, Wang J, Shu K, Ai X, Jiang M. | 07/16/2022 |
| miR-139-5p Suppresses Proliferation and Angiogenesis of Intracranial Aneurysm via FGB. | miR-139-5p Suppresses Proliferation and Angiogenesis of Intracranial Aneurysm via FGB.
Jin T, Chen G, An Q, Qin X, Hu Y, Yan Y, Hu J, Zhou B, Leng B., Free PMC Article | 04/30/2022 |
| Fibrinogen beta chain and FXIII polymorphisms affect fibrin clot properties in acute pulmonary embolism. | Fibrinogen β chain and FXIII polymorphisms affect fibrin clot properties in acute pulmonary embolism.
Klajmon A, Chmiel J, Ząbczyk M, Pociask E, Wypasek E, Malinowski KP, Undas A, Natorska J. | 03/19/2022 |
| Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder. | Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder.
Ceznerová E, Kaufmanová J, Sovová Ž, Štikarová J, Loužil J, Kotlín R, Suttnar J., Free PMC Article | 02/12/2022 |
| The Correlation Between FGB Promoter Polymorphism and Clotting Function in Patients With Idiopathic Lower Extremity Deep Venous Thrombosis. | The Correlation Between FGB Promoter Polymorphism and Clotting Function in Patients With Idiopathic Lower Extremity Deep Venous Thrombosis.
Han S, Yang B, Feng Y, Zhao L, Feng Q, Guan H, Song D, Yin F, Zhuang L., Free PMC Article | 02/5/2022 |
| An association between fibrinogen gene polymorphisms and diabetic peripheral neuropathy in young patients with type 1 diabetes. | An association between fibrinogen gene polymorphisms and diabetic peripheral neuropathy in young patients with type 1 diabetes.
Vojtková J, Kolková Z, Motyková K, Kostková M, Suroviaková S, Grendár M, Bánovčin P. | 01/1/2022 |
| Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population. | Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population.
Shen MC, Wang JD, Tsai W, Lin CY, Lin JS, Kuo SF, Lin PT, Huang YC, Hung MH. | 12/4/2021 |
| A pilot proteomic study with a prospective cohort suspected to develop preeclampsia. | A pilot proteomic study with a prospective cohort suspected to develop preeclampsia.
Liu J, Liu X, Zhao S, Zheng Y, Chen L, Wang J, Zhan S, Hu S, Dong Y, Tang G, Lu Y, Zhai Y, Cao Z. | 10/16/2021 |
| Identification of a novel mutation in congenital afibrinogenemia in Iranian patients. | Identification of a novel mutation in congenital afibrinogenemia in Iranian patients.
Nojehdeh ST, Mojbafan M, Masoodifard M, Amini M, Zeinali S. | 07/17/2021 |
| Identification and characterization of novel mutations in Chinese patients with congenital fibrinogen disorders. | Identification and characterization of novel mutations in Chinese patients with congenital fibrinogen disorders.
Zhou P, Yu M, Peng Y, Ma P, Wan L. | 07/3/2021 |
| Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype. | Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
Simurda T, Brunclikova M, Asselta R, Caccia S, Zolkova J, Kolkova Z, Loderer D, Skornova I, Hudecek J, Lasabova Z, Stasko J, Kubisz P., Free PMC Article | 04/17/2021 |
| A Novel Amino Acid Substitution, Fibrinogen Bbetap.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion. | A Novel Amino Acid Substitution, Fibrinogen Bβp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion.
Kaido T, Yoda M, Kamijo T, Arai S, Taira C, Higuchi Y, Okumura N., Free PMC Article | 03/6/2021 |
| Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the Turkish Population. | Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the Turkish Population.
Özkan DT, Sarper N, Akar N. | 01/16/2021 |
| Evaluation of lipoprotein-associated phospholipase A2, serum amyloid A, and fibrinogen as diagnostic biomarkers for patients with acute cerebral infarction. | Evaluation of lipoprotein-associated phospholipase A2, serum amyloid A, and fibrinogen as diagnostic biomarkers for patients with acute cerebral infarction.
Tao L, ShiChuan W, DeTai Z, Lihua H., Free PMC Article | 12/19/2020 |