Publication & Citation Trends
Publications
0 total
Impact of SERPINC1 mutation on thrombotic phenotype in children with congenital antithrombin deficiency - first analysis of the International Society on Thrombosis and Haemostasis (ISTH) Pediatric Antithrombin Deficiency Database and Biorepository. OA
Cited by 4
Semantic Scholar
Comparative Protein Structural Network Analysis Reveals C-Terminal Tail Phosphorylation Structural Communication Fingerprint in PTEN-Associated Mutations in Autism and Cancer OA
Cited by 5
Semantic Scholar
Shape shifting: The multiple conformational substates of the PTEN N‐terminal PIP2 ‐binding domain OA
Cited by 11
Semantic Scholar
Multisite Phosphorylation and Binding Alter Conformational Dynamics of the 4E-BP2 Protein OA
Cited by 10
Semantic Scholar
Non-cooperative 4E-BP2 folding with exchange between eIF4E-binding and binding-incompatible states tunes cap-dependent translation inhibition OA
Cited by 23
Semantic Scholar
Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibrinogenemia with a bleeding phenotype
Cited by 2
Semantic Scholar
Fibrinogen Columbus II: A novel c.1075G>T mutation in the FGG gene causing hypodysfibrinogenemia and thrombosis in an adolescent male
Cited by 2
Semantic Scholar
Research Topics
PI3K/AKT/mTOR signaling in cancer
(7)
Blood Coagulation and Thrombosis Mechanisms
(5)
Protein Kinase Regulation and GTPase Signaling
(4)
Cystic Fibrosis Research Advances
(4)
Venous Thromboembolism Diagnosis and Management
(3)
Affiliations
Kennedy Krieger Institute
St. Jude Children's Research Hospital
Cleveland Clinic
Louisiana State University Agricultural Center
University of Toronto