David Ginsburg US physician
Ginsburg, David.
Ginsburg, David, 19..-...., médecin
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
VIAF ID: 315719463 (Personal)
Permalink: http://viaf.org/viaf/315719463
Preferred Forms
4xx's: Alternate Name Forms (6)
Works
| Title | Sources |
|---|---|
| Absence of a red blood cell phenotype in mice with hematopoietic deficiency of SEC23B. |
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| The active conformation of plasminogen activator inhibitor 1, a target for drugs to control fibrinolysis and cell adhesion |
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| Analysis of MCFD2- and LMAN1-deficient mice demonstrates distinct functions in vivo |
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| The cargo receptor SURF4 promotes the efficient cellular secretion of PCSK9 |
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| Cargo selection in endoplasmic reticulum–to–Golgi transport and relevant diseases |
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| Characterization of large structural genetic mosaicism in human autosomes |
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| The COPII cargo adapter SEC24C is essential for neuronal homeostasis. |
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| The COPII pathway and hematologic disease |
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| A Critical Analysis of the Role of SNARE Protein SEC22B in Antigen Cross-Presentation. |
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| Detectable clonal mosaicism from birth to old age and its relationship to cancer |
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| Development of tag-free photoprobes for studies aimed at identifying the target of novel Group A Streptococcus antivirulence agents. |
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| A diagnosis of discernment: Identifying a novel ATRX mutation in myelodysplastic syndrome with acquired α-thalassemia |
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| Dimeric sorting code for concentrative cargo selection by the COPII coat. |
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| Disruption of the Sec24d gene results in early embryonic lethality in the mouse |
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| Exocyst function is regulated by effector phosphorylation. |
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| Functional display of platelet-binding VWF fragments on filamentous bacteriophage |
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| Functions of the COPII gene paralogs SEC23A and SEC23B are interchangeable in vivo |
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| Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels |
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| Genome-wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance. |
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| Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis |
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| High throughput protease profiling comprehensively defines active site specificity for thrombin and ADAMTS13. |
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| The in vivo endothelial cell translatome is highly heterogeneous across vascular beds |
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| Introduction of Francis S. Collins. |
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| Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association |
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| Mammalian COPII coat component SEC24C is required for embryonic development in mice |
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| Massively parallel enzyme kinetics reveals the substrate recognition landscape of the metalloprotease ADAMTS13. |
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| Mice deficient in LMAN1 exhibit FV and FVIII deficiencies and liver accumulation of α1-antitrypsin |
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| The molecular biology of von Willebrand disease |
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| Murine coagulation factor VIII is synthesized in endothelial cells. |
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| Nathan and Oski's hematology and oncology of infancy and childhood |
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| Pancreatic SEC23B deficiency is sufficient to explain the perinatal lethality of germline SEC23B deficiency in mice |
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| Principles of medical genetics |
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| Probing ADAMTS13 substrate specificity using phage display |
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| SEC23B is required for pancreatic acinar cell function in adult mice |
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| SEC24A deficiency lowers plasma cholesterol through reduced PCSK9 secretion |
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| Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci. |
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| Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice |
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| Spontaneous Irs1 passenger mutation linked to a gene-targeted SerpinB2 allele |
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| Training the next generation of biomedical investigators in glycosciences |
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| Visualization of an N-terminal fragment of von Willebrand factor in complex with factor VIII |
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| Von Willebrand Factor and ADAMTS13: Too Much or Too Little of a Good Thing? |
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| A von Willebrand factor fragment containing the D'D3 domains is sufficient to stabilize coagulation factor VIII in mice |
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| Whole exome sequencing of ENU-induced thrombosis modifier mutations in the mouse |
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