Ldlr⁻ ^/ ⁻ and ApoE⁻ ^/ ⁻ mice better mimic the human metabolite signature of increased carotid intima media thickness compared to other animal models of cardiovascular disease

Jean Sébastien Saulnier-Blache, Rory Wilson, Kristaps Klavins, Delyth Graham, Ioana Alesutan, Gabi Kastenmüller, Rui Wang-Sattler, Jerzy Adamski, Michael Roden, Wolfgang Rathmann, Jochen Seissler, Christine Meisinger, Wolfgang Koenig, Joachim Thiery, Karsten Suhre, Annette Peters, Makuto Kuro-O, Florian Lang, Guido Dallmann, Christian DellesJakob Voelkl, Melanie Waldenberger, Jean Loup Bascands, Julie Klein, Joost P. Schanstra

Pathology
Pathology

Research output: Contribution to journal › Article › peer-review

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Ldlr⁻ ^/ ⁻ and ApoE⁻ ^/ ⁻ mice better mimic the human metabolite signature of increased carotid intima media thickness compared to other animal models of cardiovascular disease

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Medicine & Life Sciences

Ldlr− / − and ApoE− / − mice better mimic the human metabolite signature of increased carotid intima media thickness compared to other animal models of cardiovascular disease

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Medicine & Life Sciences

Ldlr⁻ ^/ ⁻ and ApoE⁻ ^/ ⁻ mice better mimic the human metabolite signature of increased carotid intima media thickness compared to other animal models of cardiovascular disease