Sol Schulman, Ph.D.
Affiliations: | 2010 | Harvard University, Cambridge, MA, United States |
Area:
Endoplasmic Reticulum, SecretionGoogle:
"Sol Schulman"Parents
Sign in to add mentor| Tom A. Rapoport | grad student | 2010 | Harvard | |
| (Secretory Protein Biogenesis: From Membrane Translocation to Vitamin K-Dependent Disulfide Bridge Formation.) | ||||
| Bruce Furie | post-doc | 2014-2019 | Harvard - BIDMC (Chemistry Tree) | |
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Publications
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| Asquith NL, Becker IC, Scimone MT, et al. (2024) Targeting cargo to an unconventional secretory system within megakaryocytes allows the release of transgenic proteins from platelets. Journal of Thrombosis and Haemostasis : Jth |
| Muse O, Patell R, Peters CG, et al. (2023) The unfolded protein response links ER stress to cancer-associated thrombosis. Jci Insight |
| Schmaier AA, Anderson PF, Chen SM, et al. (2023) TMEM16E regulates endothelial cell procoagulant activity and thrombosis. The Journal of Clinical Investigation |
| Schulman S, El-Darzi E, Florido MH, et al. (2020) A coagulation defect arising from heterozygous premature termination of tissue factor. The Journal of Clinical Investigation |
| Muse O, Patell R, Peters C, et al. (2019) The Unfolded Protein Response Causes Prothrombotic Transformation of Pancreatic Cancer Linking Tumor Progression with Cancer-Associated Thrombosis Blood. 134: 632-632 |
| Higgins SJ, Ceunynck K, Kellum J, et al. (2018) Tie2 protects the vasculature against thrombus formation in systemic inflammation. The Journal of Clinical Investigation |
| Simeoni I, Stephens JC, Hu F, et al. (2016) A comprehensive high-throughput sequencing test for the diagnosis of inherited bleeding, thrombotic and platelet disorders. Blood |
| Stritt S, Nurden P, Turro E, et al. (2016) A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss. Blood |
| Schulman S, Bendapudi P, Sharda A, et al. (2015) EXTRACELLULAR THIOL ISOMERASES AND THEIR ROLE IN THROMBUS FORMATION. Antioxidants & Redox Signaling |
| Westbury SK, Turro E, Greene D, et al. (2015) Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders. Genome Medicine. 7: 36 |