Publications by authors named "Kim D Falkenberg"

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Protocols for endothelial cell isolation from mouse tissues: kidney, spleen, and testis.
Sébastien J Dumas, Elda Meta, Nadine V Conchinha, Liliana Sokol, Rongyuan Chen, Kim D Falkenberg

STAR Protoc· September 2021

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Protocols for endothelial cell isolation from mouse tissues: brain, choroid, lung, and muscle.
Nadine V Conchinha, Liliana Sokol, Laure-Anne Teuwen, Koen Veys, Sébastien J Dumas, Kim D Falkenberg

STAR Protoc· September 2021

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Protocols for endothelial cell isolation from mouse tissues: small intestine, colon, heart, and liver.
Liliana Sokol, Vincent Geldhof, Melissa García-Caballero, Nadine V Conchinha, Sébastien J Dumas, Kim D Falkenberg

STAR Protoc· June 2021

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Autophagy Inhibitors Do Not Restore Peroxisomal Functions in Cells With the Most Common Peroxisome Biogenesis Defect.
Femke C C Klouwer, Kim D Falkenberg, Rob Ofman, Janet Koster, Démi van Gent

Front Cell Dev Biol· April 2021

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Single-Cell RNA Sequencing Maps Endothelial Metabolic Plasticity in Pathological Angiogenesis.
Katerina Rohlenova, Jermaine Goveia, Melissa García-Caballero, Abhishek Subramanian, Joanna Kalucka, Kim D Falkenberg

Cell Metab· April 2020

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Single-Cell Transcriptome Atlas of Murine Endothelial Cells.
Joanna Kalucka, Laura P M H de Rooij, Jermaine Goveia, Katerina Rohlenova, Sébastien J Dumas, Kim D Falkenberg

Cell· February 2020

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The metabolic engine of endothelial cells.
Kim D Falkenberg, Katerina Rohlenova, Yonglun Luo, Peter Carmeliet

Nat Metab· October 2019

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Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder.
Kim D Falkenberg, Nancy E Braverman, Ann B Moser, Steven J Steinberg, Femke C C Klouwer

Am J Hum Genet· December 2017

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Biochemical and genetic characterization of an unusual mild PEX3-related Zellweger spectrum disorder.
Kathrine Bjørgo, Roar Fjær, Hanne Håberg Mørk, Sacha Ferdinandusse, Kim D Falkenberg

Mol Genet Metab· August 2017

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Withaferin A, a natural compound with anti-tumor activity, is a potent inhibitor of transcription factor C/EBPβ.
Kim D Falkenberg, Anke Jakobs, Julian C Matern, Wolfgang Dörner, Sagar Uttarkar

Biochim Biophys Acta Mol Cell Res· July 2017

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ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism.
Sacha Ferdinandusse, Kim D Falkenberg, Janet Koster, Petra A Mooyer, Richard Jones

J Med Genet· May 2017

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Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6.
Ilham Ratbi, Kim D Falkenberg, Manou Sommen, Nada Al-Sheqaih, Soukaina Guaoua

Am J Hum Genet· October 2015

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