Pernille Bøttger

发表

Mapping of the minimal inorganic phosphate transporting unit of human PiT2 suggests a structure universal to PiT-related proteins from all kingdoms of life

L. Pedersen, Pernille Bøttger, 2011, BMC Biochemistry.

Evolutionary and experimental analyses of inorganic phosphate transporter PiT family reveals two related signature sequences harboring highly conserved aspartic acids critical for sodium‐dependent phosphate transport function of human PiT2

L. Pedersen, Pernille Bøttger, 2005, The FEBS journal.

Glutamate-system defects behind psychiatric manifestations in a familial hemiplegic migraine type 2 disease-mutation mouse model

M. Lauritzen, E. Füchtbauer, P. Nissen, 2016, Scientific Reports.

Migraine- and dystonia-related disease-mutations of Na+/K+-ATPases: Relevance of behavioral studies in mice to disease symptoms and neurological manifestations in humans

Pernille Bøttger, K. Lykke-Hartmann, C. Doğanlı, 2012, Neuroscience & Biobehavioral Reviews.

Distribution of Na/K‐ATPase alpha 3 isoform, a sodium‐potassium P‐type pump associated with rapid‐onset of dystonia parkinsonism (RDP) in the adult mouse brain

P. Nissen, M. Romero-Ramos, Pernille Bøttger, 2011, The Journal of comparative neurology.

Two Highly Conserved Glutamate Residues Critical for Type III Sodium-dependent Phosphate Transport Revealed by Uncoupling Transport Function from Retroviral Receptor Function* 210

L. Pedersen, Pernille Bøttger, 2002, The Journal of Biological Chemistry.

The Central Half of Pit2 Is Not Required for Its Function as a Retroviral Receptor

L. Pedersen, Pernille Bøttger, 2004, Journal of Virology.

Characterization of transport mechanisms and determinants critical for Na+-dependent Pi symport of the PiT family paralogs human PiT1 and PiT2.

L. Pedersen, M. Grunnet, D. Klaerke, 2006, American journal of physiology. Cell physiology.

Pazopanib-Induced Liver Toxicity in Patients With Metastatic Renal Cell Carcinoma: Effect of UGT1A1 Polymorphism on Pazopanib Dose Reduction, Safety, and Patient Outcomes.

S. Hamilton-Dutoit, F. Donskov, P. Nissen, 2020, Clinical genitourinary cancer.

Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO.

T. Ørntoft, T. Mogensen, C. Larsen, 2016, The Journal of allergy and clinical immunology.

Cognitive deficits caused by a disease-mutation in the α3 Na+/K+-ATPase isoform

J. Nyengaard, E. Füchtbauer, P. Nissen, 2016, Scientific Reports.

A prospective evaluation of the diagnostic potential of EBV-DNA in plasma and whole blood.

B. Bibby, S. Hamilton-Dutoit, F. d'Amore, 2023, Journal of Clinical Virology.