Rouleau guy (12 résultats)

Paperback. Etat : New.

Etat : New. In English.

Etat : Good. Volume 63. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. In good all round condition. No dust jacket. Library sticker on front cover. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,500grams, ISBN:9780123745279.…

Etat : New.

Etat : Sehr gut. Zustand: Sehr gut | Sprache: Englisch | Produktart: Bücher | Keine Beschreibung verfügbar.

Paperback. Etat : Brand New. 168 pages. 9.00x6.00x0.38 inches. In Stock.

Paperback. Etat : Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

PAP. Etat : New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Etat : New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - La neuropathie sensitive et motrice héréditaire avec agénésie du corps calleux (NSMH/ACC) est une maladie fatale qui se traduit par une atteinte neurodégénérative sévère dès l'adolescence, des anomalies développementales du système nerveux central et du retard mental. Bien que rare dans le monde, ce désordre autosomique récessif est particulièrement fréquent dans la population Québécoise du Canada Français du fait d un effet fondateur. La mutation la plus fréquente au Québec cible le gène qui code pour le co-transporteur de potassium-chlore 3 (KCC3) et conduit a la perte de fonction de la protéine KCC3. Nous montrons ici qu'il en est de même pour l'ensemble des cas retrouvés en Afrique du Sud, Algérie, Allemagne, Hollande, Italie, Soudan et Turquie, et que la perte d interaction entre le co-transporteur KCC3 et la créatine kinase CK-B ainsi que les défauts de transit intracellulaire de la protéine KCC3 sont des mécanismes pathologiques majeurs à l'origine de cette maladie dévastatrice.…

Buch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Ion channel dysfunction in humans leads to impairment of the excitable processes necessary for the normal function of several tissues, such as muscle and brain. It follows that an increasing number of human diseases have been associated with malfunctioning ion channels, many of which have a genetic component. This volume of Advances in Genetics presents a broad and comprehensive overview of the inherited channelopathies in humans, including clinical, genetic and molecular aspects of these conditions. Keeping true to the scope of the serial, novel genomic and modeling research approaches and a review of potential therapeutic approaches for each of these conditions are also incorporated. Englisch.…

Buch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Ion channel dysfunction in humans leads to impairment of the excitable processes necessary for the normal function of several tissues, such as muscle and brain. It follows that an increasing number of human diseases have been associated with malfunctioning ion channels, many of which have a genetic component. This volume of Advances in Genetics presents a broad and comprehensive overview of the inherited channelopathies in humans, including clinical, genetic and molecular aspects of these conditions. Keeping true to the scope of the serial, novel genomic and modeling research approaches and a review of potential therapeutic approaches for each of these conditions are also incorporated.…