Fatal haemorrhage and incomplete block to embryogenesis in mice lacking coagulation factor V (Q28591072)

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English	Fatal haemorrhage and incomplete block to embryogenesis in mice lacking coagulation factor V	scientific journal article

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scholarly article

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31 January 2017

Fatal haemorrhage and incomplete block to embryogenesis in mice lacking coagulation factor V (English)

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31 January 2017

internal bleeding

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Coagulation factor V

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GOA release 2020-03-11

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based on heuristic

inferred from title

author name string

J. Cui

1

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31 January 2017

K. S. O'Shea

2

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31 January 2017

A. Purkayastha

3

1 reference

31 January 2017

T. L. Saunders

4

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31 January 2017

D. Ginsburg

5

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31 January 2017

language of work or name

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publication date

7 November 1996

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31 January 2017

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31 January 2017

384

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31 January 2017

6604

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31 January 2017

66–68

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31 January 2017

Molecular and cellular biology of blood coagulation

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https://api.crossref.org/works/10.1038%2F384066A0

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based on heuristic

inferred from DOI database lookup

The coagulation cascade: initiation, maintenance, and regulation

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Abnormal formation of the prothrombinase complex: factor V deficiency and related disorders

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https://api.crossref.org/works/10.1038%2F384066A0

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based on heuristic

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Mutation in blood coagulation factor V associated with resistance to activated protein C.

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Resistance to activated protein C as a basis for venous thrombosis.

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Targeted disruption of the mouse factor VIII gene produces a model of haemophilia A.

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Resolution of spontaneous bleeding events but failure of pregnancy in fibrinogen-deficient mice

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Molecular cloning of a functional thrombin receptor reveals a novel proteolytic mechanism of receptor activation

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Interruption of acute platelet-dependent thrombosis by the synthetic antithrombin D-phenylalanyl-L-prolyl-L-arginyl chloromethyl ketone

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Fatal embryonic bleeding events in mice lacking tissue factor, the cell-associated initiator of blood coagulation

1 reference

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Role of tissue factor in embryonic blood vessel development.

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Role of the thrombin receptor in development and evidence for a second receptor.

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Oral anticoagulant drugs

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A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy

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Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20.

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Vitronectin is not essential for normal mammalian development and fertility.

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Identifiers

10.1038/384066A0

1 reference

31 January 2017

Dimensions Publication ID

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31 January 2017

ResearchGate publication ID

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Springer Nature article ID

10.1038/384066a0

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