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Cited by 279

The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.

Targeted disruption of the murine tissue factor gene results in embryonic lethality

Open access
Toomey, JR, Kratzer, KE, Lasky, NM, Stanton, JJ, Broze, GJ Jr·1996·Blood

Abstract

Tissue factor (TF) is an integral membrane glycoprotein that is believed to be the physiologic initiator of the blood coagulation cascade. Disruption of the mouse tissue factor gene leads to embryonic lethality between days E9.5-E11.5 of gestation. On E9.5, TF(-/-) embryos appear indistinguishable from their TF(+/+) and TF(+/-) littermates. By E10.5, TF(-/-) embryos are severely growth retarded, appear nearly bloodless, and are in most cases dead. Initial observations suggest that TF(-/-) embryos are dying of circulatory failure. Approximately 15% of the TF(-/-) embryos survive beyond E10.5, but none complete gestation. Heterozygotes appear normal and free of bleeding complications.

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Crossref · 10.1182/blood.v88.5.1583.1583

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Metadata

Authors
Toomey, Jr., Kratzer, K., Lasky, N., Stanton, J., & Broze, G. J.
Venue
Blood
Published
1996-09-01
Volume
88
Issue
5
Pages
1583-1587
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W9494736
Cited by
279
References
25
FWCI
8.61
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Targeted disruption of the murine tissue factor gene results in embryonic lethality. https://app.cochat.ai/papers/10.1182/blood.v88.5.1583.1583
The paper
Toomey, Jr., Kratzer, K., Lasky, N., Stanton, J., & Broze, G. J. (1996). Targeted disruption of the murine tissue factor gene results in embryonic lethality. Blood. https://doi.org/10.1182/blood.v88.5.1583.1583

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.