Pages that link to "Q74225887"

The following pages link to A database for human fibrinogen variants (Q74225887):

Displaying 33 items.

• Hereditary thrombophilia (Q21093254) (← links)
• The fibrinogen Aalpha R16C mutation results in fibrinolytic resistance (Q24297406) (← links)
• Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretion (Q24319923) (← links)
• Loss of fibrinogen in zebrafish results in symptoms consistent with human hypofibrinogenemia (Q27306700) (← links)
• The Internal Dynamics of Fibrinogen and Its Implications for Coagulation and Adsorption (Q27318502) (← links)
• Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations (Q28287771) (← links)
• Severe bleeding in a woman heterozygous for the fibrinogen gammaR275C mutation. (Q33959050) (← links)
• Natural history of patients with congenital dysfibrinogenemia. (Q34974082) (← links)
• MetAmyl: a METa-predictor for AMYLoid proteins (Q35048682) (← links)
• The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (A Cys36Gly, A Cys36Arg and A Cys45Tyr) confirms the role of N-terminal A disulfide bonds in protein assembly and secretion (Q35143518) (← links)
• The assembly of nonadhesive fibrinogen matrices depends on the αC regions of the fibrinogen molecule. (Q36451951) (← links)
• High prevalence of dysfibrinogenemia among patients with chronic thromboembolic pulmonary hypertension (Q37334638) (← links)
• A novel mutation in exon 2 of FGB caused by c.221G>T † substitution, predicting the replacement of the native Arginine at position 74 with a Leucine (p.Arg74Leu † ) in a proband from a Kurdish family with dysfibrinogenaemia and familial venous and a (Q37653966) (← links)
• Inherited bleeding disorders in pregnancy (Q37958611) (← links)
• Inherited risk factors for venous thromboembolism (Q38178063) (← links)
• What Is the Biological and Clinical Relevance of Fibrin? (Q38801282) (← links)
• Identification of respective lysine donor and glutamine acceptor sites involved in factor XIIIa-catalyzed fibrin α chain cross-linking (Q40042347) (← links)
• Fibrinogen Yecheon: congenital dysfibrinogenemia with gamma methionine-310 to threonine substitution (Q41780718) (← links)
• Use of purified fibrinogen concentrate for dysfibrinogenemia and importance of laboratory fibrinogen activity measurement (Q42555503) (← links)
• A Chinese family with congenital Dysfibrinogenemia carries a heterozygous missense mutation in FGA: Concerning the genetic abnormality and clinical treatment (Q42669524) (← links)
• Structural Basis of Interfacial Flexibility in Fibrin Oligomers. (Q43021082) (← links)
• Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains (Q46630483) (← links)
• Clinical Consequences and Molecular Bases of Low Fibrinogen Levels. (Q49495916) (← links)
• Dysregulated coagulation associated with hypofibrinogenaemia and plasma hypercoagulability: implications for identifying coagulopathic mechanisms in humans (Q51322573) (← links)
• Fibrinogen Šumperk II: Dysfibrinogenemia in an individual with two coding mutations (Q51353975) (← links)
• Total knee arthroplasty in a patient with hypofibrinogenemia. (Q53718851) (← links)
• Fibrinogen Hershey IV: a novel dysfibrinogen with a gammaV411I mutation in the integrin alpha(IIb)beta(3) binding site (Q57116809) (← links)
• Two novel fibrinogen variants found in patients with pulmonary embolism and their families (Q73690520) (← links)
• Bleeding tendency and prolonged wound healing in a patient with A alphaArg16His dysfibrinogenemia: fibrinogen Krakow IV (Q82954636) (← links)
• Two novel fibrinogen variants in the C-terminus of the Bβ-chain: fibrinogen Rokycany and fibrinogen Znojmo (Q84577545) (← links)
• Hypodysfibrinogenaemia due to production of mutant fibrinogen alpha-chains lacking fibrinopeptide A and polymerisation knob ‘A’ (Q84968512) (← links)
• Abnormal fibrinogen with an Aα 16Arg → Cys substitution is associated with multiple cerebral infarctions (Q88993173) (← links)
• [Surgical treatment of two patients with asymptomatic hereditary abnormal fibrinogen] (Q89762576) (← links)