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Zoology and wildlife conservation

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Abstracts » Zoology and wildlife conservation

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

Article Abstract:

Almost half of the homozygous mice embryos lacking coagulation factor V die on the ninth or tenth embryonic day due to an abnormality in the yolk-sac vasculature. The other 50% of the homozygous mice die within two hours of birth due to massive haemorrhage. Coagulation factor V is important for the stimulation of prothrombin to thrombin, and the study reveals the vital homeostatic function of thrombin besides fibrin clot formation. The genetic deficiency of coagulation factor V causes the congenital bleeding disorder called parahaemophilia.

Author: Ginsburg, David, Saunders, Thomas L., O'Shea, K. Sue, Cui, Jisong, Purkayastha, Anjali
Publisher: Macmillan Publishing Ltd.
Publication Name: Nature
Subject: Zoology and wildlife conservation
ISSN: 0028-0836
Year: 1996
Observations, Blood coagulation factors, Embryology, Animal embryology, Mice as laboratory animals, House mouse

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Early peak in Antarctic oscillation index

Article Abstract:

The principal extratropical atmospheric circulation mode in the Southern Hemisphere, the Antarctic oscillation, shows a trend towards a positive index in austral summer, which is linked to stratospheric ozone depletion and to increased atmospheric greenhouse-gas concentrations. This positive Antarctic oscillation index, together with the later negative trend after 1960, indicate that natural forcing factors must strongly influence the state of the Antarctic oscillation.

Author: Jones, Julie M., Widmann, Martin
Publisher: Macmillan Publishing Ltd.
Publication Name: Nature
Subject: Zoology and wildlife conservation
ISSN: 0028-0836
Year: 2004
Science & research, Antarctica, Research, Environmental aspects, Greenhouse gases, Ozone layer depletion

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Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice

Article Abstract:

Results show that the nuclear-encoded mitochondrial serine protese Omi is reduced in the motor neuron degeneration 2, mnd2, mutant mice. Data indicate that deletion of the PDZ domain partially restores protease activity to the inactive recombinant Omni protein. Furthermore, loss of Omi protease activity enhances the susceptibility of mitochondria to permeability disorders.

Author: Datta, Pinaki, Fernandes-Alnemri, Teresa, Jones, Julie M., Srinivasula, Srinivas M., Ji, Weizhen, Gupta, Sanjeev, Zhang, ZhiJia, Davies, Erika, Hajnoczky, Gyorgy, Saunders, Thomas L., Van Keuren, Margaret L., Meisler, Miriam, alnemri. Emad S.
Publisher: Macmillan Publishing Ltd.
Publication Name: Nature
Subject: Zoology and wildlife conservation
ISSN: 0028-0836
Year: 2003
Analysis, Proteases, Motor neurons, Mitochondria, Structure-activity relationships (Biochemistry), Animal mutation

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Subjects list: Physiological aspects, United States
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