Pedersen, Lotte Bang

Cellular signalling by primary cilia in development, organ function and disease

Anvarian, Z., Mykytyn, K., Mukhopadhyay, S., Pedersen, L. B., & Christensen, S. T. (2019) · Nature Reviews Nephrology

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 845

Chapter Two Intraflagellar Transport (IFT)

Pedersen, L. B., & Rosenbaum, J. L. (2008) · Current Topics in Developmental Biology

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 521

Primary cilia as dynamic and diverse signalling hubs in development and disease

Mill, P., Christensen, S. T., & Pedersen, L. B. (2023) · Nature Reviews Genetics

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 417

Ins and outs of GPCR signaling in primary cilia

Schou, K. B., Pedersen, L. B., & Christensen, S. T. (2015) · The EMBO Reports

Genetic and Kidney Cyst DiseasesReceptor Mechanisms and Signaling

Cited by 221

A Proteome-wide Screen for Mammalian SxIP Motif-Containing Microtubule Plus-End Tracking Proteins

Jiang, K., Toedt, G., Montenegro Gouveia, S., Davey, N. E., Hua, S., van der Vaart, B., Grigoriev, I., Larsen, J., Pedersen, L. B., Bezstarosti, K., et al. (2012) · Current Biology

Microtubule and mitosis dynamicsGenetic and Kidney Cyst Diseases

Cited by 209

Primary cilia and coordination of receptor tyrosine kinase (RTK) signalling

Christensen, S. T., Clement, C. A., Satir, P., & Pedersen, L. B. (2012) · The Journal of Pathology

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 181

Chlamydomonas IFT172 Is Encoded by FLA11, Interacts with CrEB1, and Regulates IFT at the Flagellar Tip

Pedersen, L. B., Miller, M. S., Geimer, S., Leitch, J. M., Rosenbaum, J. L., & Cole, D. G. (2005) · Current Biology

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 164

Primary Cilia and Coordination of Receptor Tyrosine Kinase (RTK) and Transforming Growth Factor β (TGF-β) Signaling

Christensen, S. T., Morthorst, S. K., Mogensen, J. B., & Pedersen, L. B. (2017) · Cold Spring Harbor Perspectives in Biology

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 125

The Na+/H+ exchanger NHE1 is required for directional migration stimulated via PDGFR-α in the primary cilium

Schneider, L., Stock, C.-M., Dieterich, P., Jensen, B. H., Pedersen, L. B., Satir, P., Schwab, A., Christensen, S. T., & Pedersen, S. F. (2009) · Journal of Cell Biology

Genetic and Kidney Cyst DiseasesIon Transport and Channel Regulation

Cited by 94

Concerted action of kinesins KIF5B and KIF13B promotes efficient secretory vesicle transport to microtubule plus ends

Serra-Marques, A., Martin, M., Katrukha, E. A., Grigoriev, I., Peeters, C. A., Liu, Q., Hooikaas, P. J., Yao, Y., Solianova, V., Smal, I., et al. (2020) · eLife

Microtubule and mitosis dynamicsCellular transport and secretion

Cited by 93

Cilia and coordination of signaling networks during heart development

Koefoed, K., Veland, I. R., Pedersen, L. B., Larsen, L. A., & Christensen, S. T. (2014) · Organogenesis

Genetic and Kidney Cyst DiseasesCongenital heart defects research

Cited by 84

KIF13B establishes a CAV1-enriched microdomain at the ciliary transition zone to promote Sonic hedgehog signalling

Schou, K. B., Mogensen, J. B., Morthorst, S. K., Nielsen, B. S., Aleliunaite, A., Serra-Marques, A., Fürstenberg, N., Saunier, S., Bizet, A. A., Veland, I. R., et al. (2017) · Nature Communications

Genetic and Kidney Cyst DiseasesHedgehog Signaling Pathway Studies

Cited by 72

Inversin/Nephrocystin-2 Is Required for Fibroblast Polarity and Directional Cell Migration

Veland, I. R., Montjean, R., Eley, L., Pedersen, L. B., Schwab, A., Goodship, J., Kristiansen, K., Pedersen, S. F., Saunier, S., & Christensen, S. T. (2013) · PLoS ONE

Genetic and Kidney Cyst DiseasesCellular Mechanics and Interactions

Cited by 67

Regulation of ciliary membrane protein trafficking and signalling by kinesin motor proteins

Morthorst, S. K., Christensen, S. T., & Pedersen, L. B. (2018) · The FEBS Journal

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 49

TSC1 and TSC2 regulate cilia length and canonical Hedgehog signaling via different mechanisms

Rosengren, T., Larsen, L. J., Pedersen, L. B., Christensen, S. T., & Møller, L. B. (2018) · Cellular and Molecular Life Sciences

Genetic and Kidney Cyst DiseasesTuberous Sclerosis Complex Research

Cited by 45

PDGFRβ and oncogenic, mutant PDGFRα D842V promote disassembly of primary cilia by a PLCγ and AURKA dependent mechanism

Nielsen, B. S., Malinda, R. R., Schmid, F. M., Pedersen, S. F., Christensen, S. T., & Pedersen, L. B. (2015) · Journal of Cell Science

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 36

DLG1 functions upstream of SDCCAG3 and IFT20 to control ciliary targeting of polycystin-2

Rezi, C. K., Aslanyan, M. G., Diwan, G. D., Cheng, T., Chamlali, M., Junger, K., Anvarian, Z., Lorentzen, E., Pauly, K. B., Afshar-Bahadori, Y., et al. (2024) · EMBO Reports

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 13