Sabaratnam R, Skov V
, Paulsen SK, Juhl S, Kruse R, Hansen T, Halkier C, Kristensen JM, Vind BF
, Richelsen B, et al. 2022.
A Signature of Exaggerated Adipose Tissue Dysfunction in Type 2 Diabetes Is Linked to Low Plasma Adiponectin and Increased Transcriptional Activation of Proteasomal Degradation in Muscle.
Cells. 11(13):Article 2005.
https://doi.org/10.3390/cells11132005
Ghavami M
, Pedersen JG, Kjeldsen RB
, Alstrup AKO, Zhang Z, Koulianou V
, Palmfeldt J, Vorup-Jensen T, Thamdrup LHE, Boisen A. 2023.
A self-unfolding proximity enabling device for oral delivery of macromolecules.
Journal of Controlled Release. 361:40-52.
https://doi.org/10.1016/j.jconrel.2023.07.041,
https://doi.org/10.1016/j.jconrel.2023.07.041
Andresen BS, Bross P, Jensen TG, Winter V
, Knudsen I, Kølvraa S, Jensen UB, Bolund L, Duran M, Kim JJ. 1993.
A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD).
American Journal of Human Genetics. 53(3):730-9.
Jacobsen KM, Villadsen NL, Tørring T, Nielsen CB, Salomón T, Nielsen MM, Tsakos M, Sibbersen C, Scavenius C, Nielsen R, et al. 2018.
APD-Containing Cyclolipodepsipeptides Target Mitochondrial Function in Hypoxic Cancer Cells.
Cell Chemical Biology. 25(11):1337-1349.e12.
https://doi.org/10.1016/j.chembiol.2018.07.010
Pedersen CB, Zolkipli Z
, Vang S, Palmfeldt J, Kjeldsen M, Stenbroen V, Schmidt S, Wanders RJA, Ruiter JPN, Wibrand F, et al. 2010.
Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduria.
Journal of Inherited Metabolic Disease. 33(3):211-22.
https://doi.org/10.1007/s10545-010-9086-6
Fahlquist-Hagert C, Wittenborn TR, Terczyńska-Dyla E, Kastberg KS, Yang E, Rallistan AN, Markett QR
, Winther G, Fonager S, Voss LF, et al. 2023.
Antigen presentation by B cells enables epitope spreading across an MHC barrier.
Nature Communications. 14(1):Article 6941.
https://doi.org/10.1038/s41467-023-42541-7
Ryder B, Tolomeo M, Colella M, Barile M
, Olsen RK, Inbar-Feigenberg M
, Nochi Z. 2019.
A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy. Morava E, Baumgartner M, Patterson M, Rahman S, Zschocke J, Peters V, editors. In JIMD Reports. Springer. pp. 37-44. (JIMD Reports , Vol. 45).
https://doi.org/10.1007/8904_2018_139
Dessein A-F, Fontaine M
, Andresen BS, Gregersen N, Brivet M, Rabier D, Napuri-Gouel S, Dobbelaere D, Mention-Mulliez K, Martin-Ponthieu A, et al. 2010.
A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report.
Orphanet Journal of Rare Diseases. 5:26.
https://doi.org/10.1186/1750-1172-5-26
Dinesen A, Winther A, Wall A
, Märcher A, Palmfeldt J, Chudasama V, Wengel J
, Gothelf KV, Baker JR
, Howard K. 2022.
An Albumin Biomolecular Drug Design Stabilized through Improved Thiol Conjugation and a Modular Locked Nucleic Acid Assembly. Poster session presented at Controlled Release Society 2022 Annual Meeting, Montreal, Quebec, Canada.
Fentz J, Kjøbsted R, Birk JB, Jordy AB, Jeppesen J
, Thorsen K, Schjerling P, Kiens B
, Jessen N, Viollet B, et al. 2015.
AMPKα is critical for enhancing skeletal muscle fatty acid utilization during in vivo exercise in mice.
F A S E B Journal. 29(5):1725-1738.
https://doi.org/10.1096/fj.14-266650
Ipsen MB, Sørensen EMG, Thomsen EA, Weiss S, Haldrup J, Dalby A, Palmfeldt J, Bross P, Rasmussen M, Fredsøe J, et al. 2022.
A genome-wide CRISPR-Cas9 knockout screen identifies novel PARP inhibitor resistance genes in prostate cancer.
Oncogene. 41(37):4271-4281.
https://doi.org/10.1038/s41388-022-02427-2