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Michael Detmar

Researcher at École Polytechnique Fédérale de Lausanne

Publications -  351
Citations -  43193

Michael Detmar is an academic researcher from École Polytechnique Fédérale de Lausanne. The author has contributed to research in topics: Lymphatic system & Lymphangiogenesis. The author has an hindex of 94, co-authored 334 publications receiving 39086 citations. Previous affiliations of Michael Detmar include Harvard University & Beth Israel Deaconess Medical Center.

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Journal ArticleDOI

High-Fat Diet in the Absence of Obesity Does Not Aggravate Surgically Induced Lymphoedema in Mice.

TL;DR: Increased adiposity rather than dietary influences determines predisposition to or severity of lymphedema, as indicated by results of a mouse tail lymphoedema model.
Book ChapterDOI

Molecular Mechanisms of Lymph Node Metastasis

TL;DR: Results indicate that tumors can also induce lymphatic vessel growth in sentinel lymph nodes, even before the onset of metastasis, and that lymph node lymphangiogenesis further promotes cancer spread to distant lymph nodes and to distant organs.
Journal ArticleDOI

Growth characteristics and differentiation of basal cell carcinoma in vitro--immunohistochemical, gel electrophoretic, and ultrastructural analysis.

TL;DR: It is indicated that cultured BCC cells may preserve in vitro some in vivo characteristics and maintain a growth and differentiation pattern that differs from cultured nKC.
Journal ArticleDOI

Mutation of Threonine 34 in Mouse Podoplanin-Fc Reduces CLEC-2 Binding and Toxicity in Vivo While Retaining Anti-lymphangiogenic Activity

TL;DR: The data suggest that the function of PdPN in lymphangiogenesis does not depend on threonine 34 in the CLEC-2 binding domain and that PdpnT34A-Fc might be an improved inhibitor of lymphang iogenesis with fewer toxic side effects.
Book ChapterDOI

In vivo imaging of lymph node lymphangiogenesis by immuno-positron emission tomography.

TL;DR: A noninvasive methodology is presented to image lymphangiogenesis in vivo in mice based on the intravenous injection of a radioactively labeled antibody against the lymphatic vessel endothelial hyaluronan receptor-1 (LYVE-1), which is almost exclusively expressed on lymphatic vessels.