Publications

    Peer-reviewed scientific articles

    # Equal contribution / * shared corresponding author

    1. Ristori T, Sjöqvist M, Sahlgren CM. Ex vivo models to decipher the molecular mechanisms of genetic Notch cardiovascular disorders. Tissue Engineering: Part C. 2021. https://doi.org/10.1089/ten.TEC.2020.0327
    2. Prabhakar N, Belevich I, Peurla M, Heiligenstein X, Chang HC, Sahlgren  C, Jokitalo E, Rosenholm JM. Cell Volume (3D) Correlative Microscopy Facilitated by Intracellular Fluorescent Nanodiamonds as Multi-Modal Probes. 2020. Nanomaterials (Basel). https://doi.org/10.3390/nano11010014
    3. Stassen O, Ristori T, Sahlgren C. Notch in Mechanotransduction, from Molecular Mechanosensitivity to Tissue Mechanostasis. J Cell Sci. 2020. https://doi.org/10.1242/jcs.250738
    4. Sjöqvist M, Antfolk D, Suarez Rodriguez F, Sahlgren C. From structural resilience to cell specification – Intermediate filaments as regulators of cell fate. FASEB J. 2020. https://doi.org/10.1096/fj.202001627R
    5. Paramonov V, Sahlgren C, Rivero-Müller A, Pulliainen A. iGIST – a kinetic bioassay for pertussis toxin based on its effect on inhibitory GPCR signaling. ACS Sensors. 2020. https://doi.org/10.1021/acssensors.0c01340
    6. Paramonov VM#, Gerstenberg M#, Sahlgren C, Lindén M, Rivero-Müller A. In vitro targetability validation of peptide-functionalized mesoporous silica nanoparticles in the presence of serum proteins. Front Chem. 2020. https://doi.org/10.3389/fchem.2020.603616
    7. Driessen R#, Zhao F#, Hofmann S, Bouten C, Sahlgren C, Stassen O. Computational characterization of the dish-in-a-dish, a high yield culture platform for endothelial shear stress studies on the orbital shaker. Micromachines. 2020. https://doi.org/10.3390/mi11060552
    8. Özliseli E, Ṣen Karaman D, Soumyananda C, Slita A, Parikainen M, Sahlgren CM, Rosenholm JM. Rational evaluation of human serum albumin coated mesoporous silica nanoparticles for xenogenic-free stem cell therapies. Colloids Surf A Physicochem Eng Asp. 2020. https://doi.org/10.1016/j.colsurfa.2020.124945
    9. Tanaka N, Kanatani S, Kaczynska D, Fukumoto K, Louhivuori L, Mizutani T, Kopper O, Kronqvist P, Robertson S, Lindh C, Kis L, Pronk R, Niwa N, Matsumoto K, Oya M, Miyakawa A, Falk A, Hartman J, Sahlgren C, Clevers H, Uhlén P. Three-dimensional Single-Cell Imaging for the Analysis of RNA and Protein Expression in Intact Tumour Biopsies. Nat Biomed Eng. 2020. https://doi.org/1038/s41551-020-0576-z
    10. Ristori T, Stassen OMJA, Sahlgren CM, Loerakker S. Lateral Induction Limits the Impact of Cell Connectivity on Notch Signaling in Arterial Walls. Int J Numer Method Biomed Eng. 2020. https://doi.org/10.1002/cnm.3323
    11. Niemelä E, Desai D, Niemi R, Doroszko M, Özliseli E, Kemppainen K, Rahman NA, Sahlgren C, Törnquist K, Eriksson JE, Rosenholm JM. Nanoparticles Carrying Fingolimod and Methotrexate Enables Targeted Induction of Apoptosis and Immobilization of Invasive Thyroid Cancer. Eur J Pharm Biopharm. 2020. https://doi.org/10.1016/j.ejpb.2019.12.015
    12. Wilhelmsson U, Lebkuechner I, Leke R, Marasek P, Yang X, Antfolk D, Chen M, Mohseni P, Lasič E, Bobnar ST, Stenovec M, Zorec R, Nagy A, Sahlgren C, Pekna M, Pekny M. Nestin Regulates Neurogenesis in Mice Through Notch Signaling From Astrocytes to Neural Stem Cells. Cereb Cortex. 2019. https://doi.org/10.1093/cercor/bhy284
    13. van Engeland NCA#, Suarez Rodriguez F#, Rivero-Müller A, Ristori T, Duran CL, Stassen OMJA, Antfolk D, Driessen RCH, Ruohonen S, Ruohonen ST, Nuutinen S, Savontaus E, Loerakker S, Bayless KJ, Sjöqvist M, Bouten CVC, Eriksson JE, Sahlgren CM. Vimentin regulates Notch signaling strength and arterial remodeling in response to hemodynamic stress. Sci Rep. 2019. https://doi.org/10.1038/s41598-019-48218-w
    14. Putti M, de Jong SMJ, Stassen OMJA, Sahlgren CM, Dankers PYW. A Supramolecular Platform for the Introduction of Fc-Fusion Bioactive Proteins on Biomaterial Surfaces. ACS Appl Polym Mater. 2019. https://doi:10.1021/acsapm.9b00334
    15. Antfolk D, Antila C, Kemppainen K, Landor SK, Sahlgren C. Decoding the PTM-switchboard of Notch. Biochim Biophys Acta Mol Cell Res. 2019. https://doi.org/10.1016/j.bbamcr.2019.07.002
    16. Putti M, Stassen OMJA, Schotman MJG, Sahlgren CM, Dankers PYW. Influence of the Assembly State on the Functionality of a Supramolecular Jagged1-Mimicking Peptide Additive. ACS Omega. 2019. https://doi.org/10.1021/acsomega.9b00869
    17. Driessen RCH, Stassen OMJA, Sjöqvist M, Suarez Rodriguez F, Grolleman J, Bouten CVC, Sahlgren CM. Shear stress induces expression, intracellular reorganization and enhanced Notch activation potential of Jagged1. Integr Biol (Camb). 2018. https://doi.org/10.1039/c8ib00036k
    18. Mutvei AP, Landor SK, Fox R, Braune EB, Tsoi YL, Phoon YP, Sahlgren C, Hartman J, Bergh J, Jin S, Lendahl U. Notch signaling promotes a HIF2α-driven hypoxic response in multiple tumor cell types. Oncogene. 2018. https://doi.org/10.1038/s41388-018-0400-3
    19. Sleeboom JJF, Toonder JMJD, Sahlgren CM. MDA-MB-231 Breast Cancer Cells and Their CSC Population Migrate Towards Low Oxygen in a Microfluidic Gradient Device. Int J Mol Sci. 2018. https://doi.org/10.3390/ijms19103047
    20. Quirós-Solano WF, Gaio N, Stassen OMJA, Arik YB, Silvestri C, Van Engeland NCA, Van der Meer A, Passier R, Sahlgren CM, Bouten CVC, van den Berg A, Dekker R, Sarro PM. Microfabricated tuneable and transferable porous PDMS membranes for Organs-on-Chips. Sci Rep. 2018. https://doi.org/10.1038/s41598-018-31912-6
    21. Paramonov VM, Desai D, Kettiger H, Mamaeva V, Rosenholm JM, Sahlgren C, Rivero-Müller A. Targeting Somatostatin Receptors By Functionalized Mesoporous Silica Nanoparticles – Are We Striking Home? Nanotheranostics. 2018. https://doi.org/10.7150/ntno.23826
    22. van Engeland NCA, Pollet AMAO, den Toonder JMJ, Bouten CVC, Stassen OMJA, Sahlgren CM. A biomimetic microfluidic model to study signalling between endothelial and vascular smooth muscle cells under hemodynamic conditions. Lab Chip. 2018. https://doi.org/10.1039/c8lc00286j
    23. Tiemeijer LA, Frimat JP, Stassen OMJA, Bouten CVC, Sahlgren CM. Spatial patterning of the Notch ligand Dll4 controls endothelial sprouting in vitro. Sci Rep. 2018. https://doi.org/10.1038/s41598-018-24646-y.
    24. Loerakker S*, Stassen OMJA, Ter Huurne FM, Boareto M, Bouten CVC, Sahlgren CM*. Mechanosensitivity of Jagged-Notch signaling can induce a switch-type behavior in vascular homeostasis. Proc Natl Acad Sci U S A. 2018. https://doi.org/10.1073/pnas.1715277115
    25. Tanaka N, Kaczynska D, Kanatani S, Sahlgren C, Mitura P, Stepulak A, Miyakawa A, Wiklund P, Uhlén P. Mapping of the three-dimensional lymphatic microvasculature in bladder tumours using light-sheet microscopy. Br J Cancer. 2018. https://doi.org/10.1038/s41416-018-0016-y
    26. Sleeboom JJF, Eslami Amirabadi H, Nair P, Sahlgren CM, den Toonder JMJ. Metastasis in context: modeling the tumor microenvironment with cancer-on-a-chip approaches. Dis Model Mech. 2018. https://doi.org/10.1242/dmm.033100
    27. Antila CJM, Rraklli V, Blomster HA, Dahlström KM, Salminen TA, Holmberg J, Sistonen L, Sahlgren C. Sumoylation of Notch1 represses its target gene expression during cell stress. Cell Death Differ. 2018. https://doi.org/10.1038/s41418-017-0002-6
    28. Sahlgren C, Meinander A, Zhang H, Cheng F, Preis M, Xu C, Salminen TA, Toivola D, Abankwa D, Rosling A, Karaman DŞ, Salo-Ahen OMH, Österbacka R, Eriksson JE, Willför S, Petre I, Peltonen J, Leino R, Johnson M, Rosenholm J, Sandler N. Tailored Approaches in Drug Development and Diagnostics: From Molecular Design to Biological Model Systems. Adv Healthc Mater. 2017. https://doi.org/10.1002/adhm.201700258
    29. Tanaka N, Kanatani S, Tomer R, Sahlgren C, Kronqvist P, Kaczynska D, Louhivuori L, Kis L, Lindh C, Mitura P, Stepulak A, Corvigno S, Hartman J, Micke P, Mezheyeuski A, Strell C, Carlson JW, Fernández Moro C, Dahlstrand H, Östman A, Matsumoto K, Wiklund P, Oya M, Miyakawa A, Deisseroth K, Uhlén P. Whole-tissue biopsy phenotyping of three-dimensional tumours reveals patterns of cancer heterogeneity. Nat Biomed Eng. 2017. https://doi.org/10.1038/s41551-017-0139-0
    30. Mauretti A, Rossi F, Bax NAM, Miano C, Miraldi F, Goumans MJ, Messina E, Giacomello A, Bouten CVC, Sahlgren C. Spheroid three-dimensional culture enhances Notch signaling in cardiac progenitor cells. MRS Commun. 2017. https://doi.org/10.1557/mrc.2017.82
    31. Paatero I, Casals E, Niemi R, Özliseli E, Rosenholm JM, Sahlgren C. Analyses in zebrafish embryos reveal that nanotoxicity profiles are dependent on surface-functionalization controlled penetrance of biological membranes. Sci Rep. 2017. https://doi.org/10.1038/s41598-017-09312-z
    32. Antfolk D, Sjöqvist M, Cheng F, Isoniemi K, Duran CL, Rivero-Muller A, Antila C, Niemi R, Landor S, Bouten CVC, Bayless KJ, Eriksson JE, Sahlgren CM. Selective regulation of Notch ligands during angiogenesis is mediated by vimentin. Proc Natl Acad Sci U S A. 2017. https://doi.org/10.1073/pnas.1703057114
    33. Lähdeniemi IAK, Misiorek JO, Antila CJM, Landor SK, Stenvall CA, Fortelius LE, Bergström LK, Sahlgren C*, Toivola DM*. Keratins regulate colonic epithelial cell differentiation through the Notch1 signalling pathway. Cell Death Differ. 2017. https://doi.org/10.1038/cdd.2017.28
    34. Mauretti A, Spaans S, Bax NAM, Sahlgren C, Bouten CVC. Cardiac Progenitor Cells and the Interplay with Their Microenvironment. Stem Cells Int. 2017. https://doi.org/10.1155/2017/7471582
    35. Mauretti A, Bax NA, van Marion MH, Goumans MJ, Sahlgren C, Bouten CV. Cardiomyocyte progenitor cell mechanoresponse unrevealed: strain avoidance and mechanosome development. Integr Biol (Camb). 2016. https://doi.org/10.1039/c6ib00117c
    36. Baghirov H, Karaman D, Viitala T, Duchanoy A, Lou YR, Mamaeva V, Pryazhnikov E, Khiroug L, de Lange Davies C, Sahlgren C*, Rosenholm JM*. Feasibility Study of the Permeability and Uptake of Mesoporous Silica Nanoparticles across the Blood-Brain Barrier. PLoS One. 2016. https://doi.org/10.1371/journal.pone.0160705
    37. Santio NM, Landor SK, Vahtera L, Ylä-Pelto J, Paloniemi E, Imanishi SY, Corthals G, Varjosalo M, Manoharan GB, Uri A, Lendahl U, Sahlgren C*, Koskinen PJ*. Phosphorylation of Notch1 by Pim kinases promotes oncogenic signaling in breast and prostate cancer cells. Oncotarget. 2016. https://doi.org/10.18632/oncotarget.9215
    38. Braune EB, Tsoi YL, Phoon YP, Landor S, Silva Cascales H, Ramsköld D, Deng Q, Lindqvist A, Lian X, Sahlgren C, Jin SB, Lendahl U. Loss of CSL Unlocks a Hypoxic Response and Enhanced Tumor Growth Potential in Breast Cancer Cells. Stem Cell Reports. 2016. https://doi.org/10.1016/j.stemcr.2016.03.004
    39. Mamaeva V, Niemi R, Beck M, Özliseli E, Desai D, Landor S, Gronroos T, Kronqvist P, Pettersen IK, McCormack E, Rosenholm JM, Linden M, Sahlgren C. Inhibiting Notch Activity in Breast Cancer Stem Cells by Glucose Functionalized Nanoparticles Carrying γ-secretase Inhibitors. Mol Ther. 2016. https://doi.org/10.1038/mt.2016.42
    40. Rosenholm JM, Gulin-Sarfraz T, Mamaeva V, Niemi R, Özliseli E, Desai D, Antfolk D, von Haartman E, Lindberg D, Prabhakar N, Näreoja T, Sahlgren C. Prolonged Dye Release from Mesoporous Silica-Based Imaging Probes Facilitates Long-Term Optical Tracking of Cell Populations In Vivo. Small. 2016. https://doi.org/10.1002/smll.201503392
    41. Rosenholm JM, Zhang J, Linden M, Sahlgren C. Mesoporous silica nanoparticles in tissue engineering – Nanomedicine (Lond). 2016. https://doi.org/10.2217/nnm.15.212
    42. Desai D, Prabhakar N, Mamaeva V, Karaman DŞ, Lähdeniemi IA, Sahlgren C*, Rosenholm JM*, Toivola DM*. Targeted modulation of cell differentiation in distinct regions of the gastrointestinal tract via oral administration of differently PEG-PEI functionalized mesoporous silica nanoparticles. Int J Nanomedicine. 2016. https://doi.org/10.2147/IJN.S94013
    43. Paramonov VM, Mamaeva V, Sahlgren C, Rivero-Müller A. Genetically-encoded tools for cAMP probing and modulation in living systems. Front Pharmacol. 2015. https://doi.org/10.3389/fphar.2015.00196.
    44. Shokry H, Vanamo U, Wiltschka O, Niinimäki J, Lerche M, Levon K, Linden M, Sahlgren C. Mesoporous silica particle-PLA-PANI hybrid scaffolds for cell-directed intracellular drug delivery and tissue vascularization. Nanoscale. 2015. https://doi.org/10.1039/c5nr03983e
    45. Chivukula IV, Ramsköld D, Storvall H, Anderberg C, Jin S, Mamaeva V, Sahlgren C, Pietras K, Sandberg R, Lendahl U. Decoding breast cancer tissue-stroma interactions using species-specific sequencing. Breast Cancer Res. 2015. https://doi.org/10.1186/s13058-015-0616-x
    46. Rosenholm JM, Korpi RM, Lammentausta E, Lehtonen S, Lehenkari P, Niemi R, Xiao W, Zhang J, Råtts N, Gu H, Sahlgren C*, Sequeiros RB*. Novel, Fast-Processed Crystalline and Amorphous Manganese Oxide Nanoparticles for Stem Cell Labeling. Inorg Chem Front. 2015. https://doi.org/10.1039/C5QI00033E
    47. Wittig R*, Rosenholm JM, von Haartman E, Hemming J, Genze F, Bergman L, Simmet T, Lindén M, Sahlgren C*. Active targeting of mesoporous silica drug carriers enhances γ-secretase inhibitor efficacy in an in vivo model for breast cancer. Nanomedicine (Lond). 2014. https://doi.org/10.2217/nnm.13.62
    48. Sjöqvist M, Antfolk D, Ferraris S, Rraklli V, Haga C, Antila C, Mutvei A, Imanishi SY, Holmberg J, Jin S, Eriksson JE, Lendahl U, Sahlgren C. PKCζ regulates Notch receptor routing and activity in a Notch signaling-dependent manner. Cell Res. 2014. https://doi.org/10.1038/cr.2014.34
    49. Wiltschka O, Böcking D, Brenner R, Sahlgren C, Lindén M. Preparation, characterization, and preliminary biocompatibility evaluation of particulate spin-coated mesoporous silica films. Microporous Mesoporous Mater. 2014. https://doi.org/10.1016/j.micromeso.2014.01.006
    50. Böcking D, Wiltschka O, Niinimäki J, Shokry H, Brenner R, Lindén M, Sahlgren C. Mesoporous silica nanoparticle-based substrates for cell directed delivery of Notch signalling modulators to control myoblast differentiation. Nanoscale. 2014. https://doi.org/10.1039/c3nr04022d
    51. Gulin-Sarfraz TJ, Zhang J, Desai D, Teuho J, Sarfraz J, Jiang H, Zhang C, Sahlgren C, Lindén M, Gu H, Rosenholm JM. Combination of magnetic field and surface functionalization for reaching synergistic effects in cellular labeling by magnetic core-shell nanospheres. Biomater Sci. 2014. https://doi.org/10.1039/C4BM00221K
    52. Jin S, Mutvei AP, Chivukula IV, Andersson ER, Ramsköld D, Sandberg R, Lee KL, Kronqvist P, Mamaeva V, Ostling P, Mpindi JP, Kallioniemi O, Screpanti I, Poellinger L, Sahlgren C, Lendahl U. Non-canonical Notch signaling activates IL-6/JAK/STAT signaling in breast tumor cells and is controlled by p53 and IKKα/IKKβ. Oncogene. 2013. https://doi.org/10.1038/onc.2012.517
    53. Prabhakar N, Näreoja T, von Haartman E, Karaman DŞ, Jiang H, Koho S, Dolenko TA, Hänninen PE, Vlasov DI, Ralchenko VG, Hosomi S, Vlasov II, Sahlgren C, Rosenholm JM. Core-shell designs of photoluminescent nanodiamonds with porous silica coatings for bioimaging and drug delivery II: application. Nanoscale. 2013. https://doi.org/10.1039/c3nr33926b
    54. Mamaeva V, Sahlgren C*, Lindén M*. Mesoporous silica nanoparticles in medicine – recent advances. Adv Drug Deliv Rev. 2013. https://doi.org/10.1016/j.addr.2012.07.018
    55. Wilhelmsson U, Faiz M, de Pablo Y, Sjöqvist M, Andersson D, Widestrand A, Potokar M, Stenovec M, Smith PL, Shinjyo N, Pekny T, Zorec R, Ståhlberg A, Pekna M, Sahlgren C, Pekny M. Astrocytes negatively regulate neurogenesis through the Jagged1-mediated Notch pathway. Stem Cells. 2012. https://doi.org/10.1002/stem.1196
    56. Karaman DS, Desai D, Senthilkumar R, Johansson EM, Råtts N, Odén M, Eriksson JE, Sahlgren C, Toivola DM, Rosenholm JM. Shape engineering vs organic modification of inorganic nanoparticles as a tool for enhancing cellular internalization. Nanoscale Res Lett. 2012. https://doi.org/10.1186/1556-276X-7-358
    57. Rosenholm JM, Mamaeva V, Sahlgren C*, Lindén M*. Nanoparticles in targeted cancer therapy: mesoporous silica nanoparticles entering preclinical development stage. Nanomedicine (Lond). 2012. https://doi.org/10.2217/nnm.11.166
    58. Landor SK, Mutvei AP, Mamaeva V, Jin S, Busk M, Borra R, Grönroos TJ, Kronqvist P, Lendahl U, Sahlgren CM. Hypo- and hyperactivated Notch signaling induce a glycolytic switch through distinct mechanisms. Proc Natl Acad Sci U S A. 2011. https://doi.org/10.1073/pnas.1104943108
    59. Mamaeva V, Rosenholm JM, Bate-Eya LT, Bergman L, Peuhu E, Duchanoy A, Fortelius LE, Landor S, Toivola DM, Lindén M, Sahlgren C. Mesoporous silica nanoparticles as drug delivery systems for targeted inhibition of Notch signaling in cancer. Mol Ther. 2011. https://doi.org/10.1038/mt.2011.105
    60. Rosenholm JM, Sahlgren C*, Lindén M*. Multifunctional mesoporous silica nanoparticles for combined therapeutic, diagnostic and targeted action in cancer treatment. Curr Drug Targets. 2011. https://doi.org/10.2174/138945011795906624
    61. Pallari HM, Lindqvist J, Torvaldson E, Ferraris SE, He T, Sahlgren C, Eriksson JE. Nestin as a regulator of Cdk5 in differentiating myoblasts. Mol Biol Cell. 2011. https://doi.org/10.1091/mbc.E10-07-0568
    62. Das D, Lanner F, Main H, Andersson ER, Bergmann O, Sahlgren C, Heldring N, Hermanson O, Hansson EM, Lendahl U. Notch induces cyclin-D1-dependent proliferation during a specific temporal window of neural differentiation in ES cells. Dev Biol. 2010. https://doi.org/10.1016/j.ydbio.2010.09.018
    63. Rosenholm JM, Sahlgren C*, Lindén M*. Towards multifunctional, targeted drug delivery systems using mesoporous silica nanoparticles–opportunities & challenges. Nanoscale. 2010. https://doi.org/10.1039/c0nr00156b
    64. Rosenholm JM, Peuhu E, Bate-Eya LT, Eriksson JE, Sahlgren C*, Lindén M*. Cancer-cell-specific induction of apoptosis using mesoporous silica nanoparticles as drug-delivery vectors. Small. 2010. https://doi.org/10.1002/smll.200902355
    65. Main H, Lee KL, Yang H, Haapa-Paananen S, Edgren H, Jin S, Sahlgren C, Kallioniemi O, Poellinger L, Lim B, Lendahl U. Interactions between Notch- and hypoxia-induced transcriptomes in embryonic stem cells. Exp Cell Res. 2010. https://doi.org/10.1016/j.yexcr.2009.12.012
    66. de Thonel A, Ferraris SE, Pallari HM, Imanishi SY, Kochin V, Hosokawa T, Hisanaga S, Sahlgren C, Eriksson JE. Protein kinase Czeta regulates Cdk5/p25 signaling during myogenesis. Mol Biol Cell. 2010. https://doi.org/10.1091/mbc.E09-10-0847
    67. Rosenholm JM, Sahlgren C*, Linden M*. Cancer-cell targeting and cell-specific delivery by mesoporous silica nanoparticles. Journal of Material Chemistry.2010. https://doi.org/10.1039/B920076B
    68. Rosenholm JM, Peuhu E, Eriksson JE, Sahlgren C*, Lindén M*. Targeted intracellular delivery of hydrophobic agents using mesoporous hybrid silica nanoparticles as carrier systems. Nano Lett. 2009. https://doi.org/10.1021/nl901589y
    69. Rosenholm JM, Meinander A, Peuhu E, Niemi R, Eriksson JE, Sahlgren C*, Lindén M*. Targeting of porous hybrid silica nanoparticles to cancer cells. ACS Nano. 2009. https://doi.org/10.1021/nn800781r
    70. Jin S, Hansson EM, Tikka S, Lanner F, Sahlgren C, Farnebo F, Baumann M, Kalimo H, Lendahl U. Notch signaling regulates platelet-derived growth factor receptor-beta expression in vascular smooth muscle cells. Circ Res. 2008. https://doi.org/10.1161/CIRCRESAHA.107.167965
    71. Sahlgren C, Gustafsson MV, Jin S, Poellinger L, Lendahl U. Notch signaling mediates hypoxia-induced tumor cell migration and invasion. Proc Natl Acad Sci U S A. 2008. https://doi.org/10.1073/pnas.0802047105
    72. Chapman G, Liu L, Sahlgren C, Dahlqvist C, Lendahl U. High levels of Notch signaling down-regulate Numb and Numblike. J Cell Biol. 2006. https://doi.org/10.1083/jcb.200602009.
    73. Sahlgren CM, Pallari HM, He T, Chou YH, Goldman RD, Eriksson JE. A nestin scaffold links Cdk5/p35 signaling to oxidant-induced cell death. EMBO J. 2006. https://doi.org/10.1038/sj.emboj.7601366
    74. Sahlgren C, Lendahl U. Notch signaling and its integration with other signaling mechanisms. Regen Med. 2006. https://doi.org/10.2217/17460751.1.2.195
    75. Sahlgren CM, Mikhailov A, Vaittinen S, Pallari HM, Kalimo H, Pant HC, Eriksson JE. Cdk5 regulates the organization of Nestin and its association with p35. Mol Cell Biol. 2003. https://doi.org/10.1128/mcb.23.14.5090-5106.2003
    76. Vaittinen S, Lukka R, Sahlgren C, Hurme T, Rantanen J, Lendahl U, Eriksson JE, Kalimo H. The expression of intermediate filament protein nestin as related to vimentin and desmin in regenerating skeletal muscle. J Neuropathol Exp Neurol. 2001. https://doi.org/10.1093/jnen/60.6.588
    77. Sahlgren CM, Mikhailov A, Hellman J, Chou YH, Lendahl U, Goldman RD, Eriksson JE. Mitotic reorganization of the intermediate filament protein nestin involves phosphorylation by cdc2 kinase. J Biol Chem. 2001. https://doi.org/10.1074/jbc.M009669200
    78. Eliasson C, Sahlgren C, Berthold CH, Stakeberg J, Celis JE, Betsholtz C, Eriksson JE, Pekny M. Intermediate filament protein partnership in astrocytes. J Biol Chem. 1999. https://doi.org/10.1074/jbc.274.34.23996
    79. Vaittinen S, Lukka R, Sahlgren C, Rantanen J, Hurme T, Lendahl U, Eriksson JE, Kalimo H. Specific and innervation-regulated expression of the intermediate filament protein nestin at neuromuscular and myotendinous junctions in skeletal muscle. Am J Pathol. 1999. https://doi.org/10.1016/S0002-9440(10)65304-7
    80. Eriksson JE, Toivola DM, Sahlgren C, Mikhailov A, Härmälä-Braskén AS. Strategies to assess phosphoprotein phosphatase and protein kinase-mediated regulation of the cytoskeleton. Methods Enzymol. 1998. https://doi.org/10.1016/s0076-6879(98)98044-2
    81. Reuter M, Gustafsson MK, Sahlgren C, Halton DW, Maule AG, Shaw C. The nervous system of Tricladida. I. Neuroanatomy of Procerodes littoralis (Maricola, Procerodidae): an immunocytochemical study. Invert Neurosci. 1995;1(2):113-22