Titlebook: Human Tumour Xenografts in Anticancer Drug Development; Benjamin Winograd,Michael Peckham,Herbert Michael Conference proceedings 1988 Spr

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Human Tumour Xenografts in Anticancer Drug Development978-3-642-73252-2

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hen und wirtschaftlichen Verhältnissen besser gerecht werden kann. Richtlinien, die uns die Bestimmung der oberen und unteren Grenzen der Festigkeiten ermöglichen, werden vor jeder Schematisierung bewahren, die auf der Baustelle unter Umständen zu schlechten Erfahrungen führen kann. Der Verbraucher

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of the subjects discussed. It was decided to keep the layout very simple in order to keep costs to a minimum and make the monographs available in the shortest possible time, thus overcoming a com­ mon problem in medical literature: that of the material being outdated even before publication. Umberto Veronesi978-3-642-73254-6978-3-642-73252-2

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Biology of Human Ovarian Cancer Xenograftsgrowth rate. At present our human ovarian cancer model contains a series of lines which vary in histologic subtype and tumor doubling time, differences that may also be expected in a group of ovarian cancer patients.

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Screening of Analogs in Human Ovarian Cancer Xenografts the parent drug was reconfirmed in 5 other human ovarian cancer lines..The activity of trimelamol was similar to or higher than that of hexamethylmelamine in 8/9 lines studied. The human ovarian cancer model seems to have considerable value in the selection of analogs with potential activity in this malignancy.

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