Search Results - "Merciris, P"

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  1. 1

    Soil chemical and biological characteristics influence mineralization processes in different stands of a tropical wetland by Boulogne, I., Ozier-Lafontaine, H., Merciris, P., Vaillant, J., Labonte, L., Loranger-Merciris, G.

    Published in Soil use and management (01-09-2016)
    “…In the Caribbean, Pterocarpus officinalis swamp forest, a coastal freshwater wetland, has been locally transformed by human activities into Colocasia esculenta…”
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    Journal Article
  2. 2

    Regulation of K-Cl cotransport by Syk and Src protein tyrosine kinases in deoxygenated sickle cells by Merciris, P, Claussen, W J, Joiner, C H, Giraud, F

    Published in Pflügers Archiv (01-05-2003)
    “…Protein tyrosine kinases (PTK) of the Src family are thought to suppress K-Cl cotransport (KCC) activity via negative regulation of protein phosphatases…”
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    Journal Article
  3. 3

    Involvement of deoxygenation-induced increase in tyrosine kinase activity in sickle cell dehydration by Merciris, P, Hardy-Dessources, M D, Sauvage, M, Giraud, F

    Published in Pflügers Archiv (01-08-1998)
    “…Deoxygenation of sickle (SS) cells causes cationic alterations leading to cell dehydration by various mechanisms, including activation of Ca2+-sensitive K…”
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  4. 4
  5. 5

    Deoxygenation of sickle cells stimulates Syk tyrosine kinase and inhibits a membrane tyrosine phosphatase by Merciris, Patrick, Hardy-Dessources, Marie-Dominique, Giraud, Françoise

    Published in Blood (15-11-2001)
    “…Polymerization of hemoglobin S in sickle red cells, in deoxygenated conditions, is associated with K+ loss and cellular dehydration. It was previously reported…”
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    Journal Article
  6. 6

    Pathophysiology of a sickle cell trait mouse model: human alpha(beta)(S) transgenes with one mouse beta-globin allele by Noguchi, C T, Gladwin, M, Diwan, B, Merciris, P, Smith, R, Yu, X, Buzard, G, Fitzhugh, A, Keefer, L K, Schechter, A N, Mohandas, N

    Published in Blood cells, molecules, & diseases (01-11-2001)
    “…As a potential model for sickle cell trait (AS), we examined mice containing one normal mouse beta-globin allele in combination with a human hemoglobin S…”
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