Larsen JKR, Smerup MH
, Nørregaard R, Christensen JH, Sivesgaard K, Christensen SD, Christensen K, Sloth E, Torp P
, Gregersen N, et al. 2011.
Multiplex Analysis of Cardiac Hypertrophic Signaling: Reduced in vivoPhosphorylation of Glycogen Synthase Kinase-3β and Proline-Rich Akt Substrate (PRAS40).
Current Signal Transduction Therapy. 6(1):65-70.
Kristensen T
, Vang S, Laustsen PG, Hald S, Reinholdt H, Pugdahl K, Pedraza-Diaz S, Hardre R, Carrion AG, Rasmussen TE. 2001.
Insulin-regulated aminopeptidase (EC 3.4.11.3), a gluzincin aminopeptidase.
Excerpta Medica. 1218:275-282.
Koeberl DD, Young SP
, Gregersen N, Vockley J, Smith WE, Benjamin DK, Jr., An Y, Weavil SD, Chaing SH, et al. 2003.
Rare disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening.
Pediatr. Res. (54):219-223.
Joshi S
, Andersen RF, Jespersen B, Rasmussen M, Madsen LB, Hansen A, Nagaraj S
, Kjeldsen M, Olsen RKJ, Gregersen N, et al. 2015.
Genetic Variants in NPHS1, NPHS2 and INF2 in Patients with Primary Focal Segmental Glomerulosclerosis in Denmark. Poster session presented at 10th International Podocyte Conference, Freiburg, Germany.
Jensen TG, Andresen BS, Jensen HK, Jensen LG, Heath F, Pedersen S, Nielsen V
, Jensen UB, Lund TB, Gregersen N, et al. 1996.
Rapid characterization of disease-causing mutations in the low density lipoprotein receptor (LDL-R) gene by overexpression in COS cells.
Zeitschrift fuer Gastroenterologie. 34 Suppl 3:9-11.
Jensen TG, Bross P, Andresen BS
, Lund TB, Kristensen TJ
, Jensen UB, Jensen UB, Winther V, Kølvraa S
, Gregersen N, et al. 1995.
Comparison between medium-chain acyl-CoA dehydrogenase mutant proteins overexpressed in bacterial and mammalian cells.
Human Mutation. 6(3):226-31.
https://doi.org/10.1002/humu.1380060305
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
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
Hollensen AK, Thomsen HS, Lloret-Llinares M, Kamstrup AB, Jensen JM, Luckmann M
, Birkmose N, Palmfeldt J, Jensen TH, Hansen TB, et al. 2020.
circZNF827 nucleates a transcription inhibitory complex to balance neuronal differentiation.
eLife. 9:1-29.
https://doi.org/10.7554/eLife.58478
Ho G, Yonezawa A, Masuda S, Inui K, Sim KG, Carpenter K
, Olsen RK, Mitchell JJ, Rhead WJ, Peters G, et al. 2011.
Maternal riboflavin deficiency,resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by amicrodeletion in the riboflavin transporter gene GPR172B.
Human Mutation. 32/1.
Hansen JJ, Durr A, Cournu-Rebeix I, Georgopoulos C, Ang D, Nielsen MN, Davoine CS, Brice A, Fontaine B
, Gregersen N, et al. 2002.
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60.
Am. J. Hum. Genet. (70):1328-1332.