Publikationen (Abteilung Neurogenetik)
2020
Eichel MA, Gargareta VI, D'Este E, Fledrich R, Kungl T, Buscham TJ, Lüders KA, Miracle C, Jung RB, Distler U, Kusch K, Möbius W, Hülsmann S, Tenzer S, Nave KA, Werner HB (2020).
CMTM6 expressed on the adaxonal Schwann cell surface restricts axonal diameters in peripheral nerves.
Nat Commun. 11, 4514-4514
Nave K, Deane G, Miller M, Clark A (2020).
Wilding the predictive brain.
Wiley Interdiscip Rev Cogn Sci. Epub ahead of print
Natsubori A, Tsunematsu T, Karashima A, Imamura H, Kabe N, Trevisiol A, Hirrlinger J, Kodama T, Sanagi T, Masamoto K, Takata N, Nave KA, Matsui K, Tanaka KF, Honda M (2020).
Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep-wake states.
Commun Biol. 3, 491-491
Prukop T, Wernick S, Boussicault L, Ewers D, Jäger K, Adam J, Winter L, Quintes S, Linhoff L, Barrantes-Freer A, Bartl M, Czesnik D, Zschüntzsch J, Schmidt J, Primas G, Laffaire J, Rinaudo P, Brureau A, Nabirotchkin S, Schwab MH, Nave KA, Hajj R, Cohen D, Sereda MW (2020).
Synergistic PXT3003 therapy uncouples neuromuscular function from dysmyelination in male Charcot-Marie-Tooth disease type 1A (CMT1A) rats.
J Neurosci Res. [Epub ahead of print]
Jean P, Anttonen T, Michanski S, de Diego AMG, Steyer AM, Neef A, Oestreicher D, Kroll J, Nardis C, Pangrši? T, Möbius W, Ashmore J, Wichmann C, Moser T (2020).
Macromolecular and electrical coupling between inner hair cells in the rodent cochlea.
Nat Commun. 11, 3208-3208
Stephan T, Brüser C, Deckers M, Steyer AM, Balzarotti F, Barbot M, Behr TS, Heim G, Hübner W, Ilgen P, Lange F, Pacheu-Grau D, Pape JK, Stoldt S, Huser T, Hell SW, Möbius W, Rehling P, Riedel D, Jakobs S (2020).
MICOS assembly controls mitochondrial inner membrane remodeling and crista junction redistribution to mediate cristae formation.
EMBO J. [Epub ahead of print]
Mukherjee C, Kling T, Russo B, Miebach K, Kess E, Schifferer M, Pedro LD, Weikert U, Fard MK, Kannaiyan N, Rossner M, Aicher ML, Goebbels S, Nave KA, Krämer-Albers EM, Schneider A, Simons M (2020).
Oligodendrocytes Provide Antioxidant Defense Function for Neurons by Secreting Ferritin Heavy Chain.
Cell Metab. [Epub ahead of print]
Gruenenfelder FI, McLaughlin M, Griffiths IR, Garbern J, Thomson G, Kuzman P, Barrie JA, McCulloch ML, Penderis J, Stassart R, Nave KA, Edgar JM (2020).
Neural stem cells restore myelin in a demyelinating model of Pelizaeus-Merzbacher disease.
Brain 143, 1383-1399
Marshall-Phelps KLH, Kegel L, Baraban M, Ruhwedel T, Almeida RG, Rubio-Brotons M, Klingseisen A, Benito-Kwiecinski SK, Early JJ, Bin JM, Suminaite D, Livesey MR, Möbius W, Poole RJ, Lyons DA (2020).
Neuronal activity disrupts myelinated axon integrity in the absence of NKCC1b.
J Cell Biol. 219, e201909022-e201909022
Tasche D, Weber M, Mrotzek J, Gerhard C, Wieneke S, Möbius W, Höfft O, Viöl W. (2020).
In Situ Investigation of the Formation Kinematics of Plasma-Generated Silver Nanoparticles.
Nanomaterials (Basel) 10, pii: E555-pii: E555
Steyer AM, Ruhwedel T, Nardis C, Werner HB, Nave KA, Möbius W (2020).
Pathology of myelinated axons in the PLP-deficient mouse model of spastic paraplegia type 2 revealed by volume imaging using focused ion beam-scanning electron microscopy.
J Struct Biol. [Epub ahead of print]
Wakhloo D, Scharkowski F, Curto Y, Javed Butt U, Bansal V, Steixner-Kumar AA, Wüstefeld L, Rajput A, Arinrad S, Zillmann MR, Seelbach A, Hassouna I, Schneider K, Qadir Ibrahim A, Werner HB, Martens H, Miskowiak K, Wojcik SM, Bonn S, Nacher J, Nave KA, Ehrenreich H (2020).
Functional hypoxia drives neuroplasticity and neurogenesis via brain erythropoietin.
Nat Commun. 11, 1313-1313
Siems SB, Jahn O, Eichel MA, Kannaiyan N, Wu LMN, Sherman DL, Kusch K, Hesse D, Jung RB, Fledrich R, Sereda MW, Rossner MJ, Brophy PJ, Werner HB (2020).
Proteome profile of peripheral myelin in healthy mice and in a neuropathy model.
Elife. PubMed - in process
Pan H, Steixner-Kumar AA, Seelbach A, Deutsch N, Ronnenberg A, Tapken D, von Ahsen N, Mitjans M, Worthmann H, Trippe R, Klein-Schmidt C, Schopf N, Rentzsch K, Begemann M, Wienands J, Stöcker W, Weissenborn K, Hollmann M, Nave KA, Lühder F, Ehrenreich H (2020).
Multiple inducers and novel roles of autoantibodies against the obligatory NMDAR subunit NR1: a translational study from chronic life stress to brain injury.
Mol Psychiatry. [Epub ahead of print]
Stone S, Wu S, Nave KA, Lin W
The UPR preserves mature oligodendrocyte viability and function in adults by regulating autophagy of PLP.
2019
Cohen CCH, Popovic MA, Klooster J, Weil MT, Möbius W, Nave KA, Kole MHP (2019).
Saltatory Conduction along Myelinated Axons Involves a Periaxonal Nanocircuit.
Cell 180, 311-322
Fredrickx E, Colombo E, Canevazzi P, La Marca R, Pellegatta M, Dina G, Podini P, Nave KA, Quattrini A, Taveggia C (2019).
Ablation of neuronal ADAM17 impairs oligodendrocyte differentiation and myelination.
Glia [Epub ahead of print]
Rosiewicz KS, Crowley T, Saher G, Kerkering J, Alisch M, Siffrin V (2019).
Comparison of RNA isolation procedures for analysis of adult murine brain and spinal cord astrocytes.
J Neurosci Methods. [Epub ahead of print]
Fledrich R, Kungl T, Nave KA, Stassart RM (2019).
Axo-glial interdependence in peripheral nerve development.
Development 146, pii: dev151704-pii: dev151704
Kalinin S, Meares GP, Lin SX, Pietruczyk EA, Saher G, Spieth L, Nave KA, Boullerne AI, Lutz SE, Benveniste EN, Feinstein DL (2019).
Liver kinase B1 depletion from astrocytes worsens disease in a mouse model of multiple sclerosis.
Glia [Epub ahead of print]
Djannatian M, Timmler S, Arends M, Luckner M, Weil MT, Alexopoulos I, Snaidero N, Schmid B, Misgeld T, Möbius W, Schifferer M, Peles E, Simons M (2019).
Two adhesive systems cooperatively regulate axon ensheathment and myelin growth in the CNS.
Nat Commun. 10, 4794-4794
Jin W, Leitzen E, Goebbels S, Nave KA, Baumgärtner W, Hansmann F (2019).
Comparison of Theiler's Murine Encephalomyelitis Virus Induced Spinal Cord and Peripheral Nerve Lesions Following Intracerebral and Intraspinal Infection.
Int J Mol Sci. 20, pii:E5134-pii:E5134
Werner HB, Nave KA (2019).
Enhanced Actin Dynamics: A Therapeutic Strategy for Axonal Regeneration?
Neuron 103, 949-950
Stumpf SK, Berghoff SA, Trevisiol A, Spieth L, Düking T, Schneider LV, Schlaphoff L, Dreha-Kulaczewski S, Bley A, Burfeind D, Kusch K, Mitkovski M, Ruhwedel T, Guder P, Röhse H, Denecke J, Gärtner J, Möbius W, Nave KA, Saher G (2019).
Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus-Merzbacher disease.
Acta Neuropathol. [Epub ahead of print]
Buscham TJ, Eichel MA, Siems SB, Werner HB
Turning to myelin turnover.
Steyer AM, Schertel A, Nardis C, Möbius W (2019).
FIB-SEM of mouse nervous tissue: Fast and slow sample preparation.
Methods Cell Biol. 152, 1-21
So C, Seres KB, Steyer AM, Mönnich E, Clift D, Pejkovska A, Möbius W, Schuh M (2019).
A liquid-like spindle domain promotes acentrosomal spindle assembly in mammalian oocytes.
Science 364, pii: eaat9557-pii: eaat9557
Belin S, Ornaghi F, Shackleford G, Wang J, Scapin C, Lopez-Anido C, Silvestri N, Robertson N, Williamson C, Ishii A, Taveggia C, Svaren J, Bansal R, Schwab MH, Nave K, Fratta P, D'Antonio M, Poitelon Y, Feltri ML, Wrabetz L (2019).
Corrigendum: Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy.
Hum Mol Genet. 28, 2282-2282
Brahmer A, Neuberger E, Esch-Heisser L, Haller N, Jorgensen MM, Baek R, Möbius W, Simon P, Krämer-Albers EM (2019).
Platelets, endothelial cells and leukocytes contribute to the exercise-triggered release of extracellular vesicles into the circulation.
J Extracell Vesicles. 8, 1615820-1615820
Garcia-Agudo LF, Janova H, Sendler LE, Arinrad S, Steixner AA, Hassouna I, Balmuth E, Ronnenberg A, Schopf N, van der Flier FJ, Begemann M, Martens H, Weber MS, Boretius S, Nave KA, Ehrenreich H (2019).
Genetically induced brain inflammation by Cnp deletion transiently benefits from microglia depletion.
FASEB J. 33, 8634-8647
Joseph S, Vingill S, Jahn O, Fledrich R, Werner HB, Katona I, Möbius W, Mitkovski M, Huang Y, Weis J, Sereda MW, Schulz JB, Nave KA, Stegmüller J (2019).
Myelinating glia-specific deletion of Fbxo7 in mice triggers axonal degeneration in the central nervous system together with peripheral neuropathy.
J Neurosci. 39, 5606-5626
Steyer AM, Ruhwedel T, Möbius W (2019).
Biological Sample Preparation by High-pressure Freezing, Microwave-assisted Contrast Enhancement, and Minimal Resin Embedding for Volume Imaging.
J Vis Exp. [PubMed - in process]
Fledrich R, Akkermann D, Schütza V, Abdelaal TA, Hermes D, Schäffner E, Soto-Bernardini MC, Götze T, Klink A, Kusch K, Krueger M, Kungl T, Frydrychowicz C, Möbius W, Brück W, Mueller WC, Bechmann I, Sereda MW, Schwab MH, Nave KA, Stassart RM (2019).
NRG1 type I dependent autoparacrine stimulation of Schwann cells in onion bulbs of peripheral neuropathies.
Nat Commun. 10, 1467-1467
Stumpf SK, Berghoff SA, Trevisiol A, Spieth L, Düking T, Schneider LV, Schlaphoff L, Dreha-Kulaczewski S, Bley A, Burfeind D, Kusch K, Mitkovski M, Ruhwedel T, Guder P, Röhse H, Denecke J, Gärtner J, Möbius W, Nave KA, Saher G (2019).
Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus-Merzbacher disease.
Acta Neuropathol. 138, 147-161
Leitzen E, Raddatz BB, Jin W, Goebbels S, Nave KA, Baumgärtner W, Hansmann F (2019).
Virus-triggered spinal cord demyelination is followed by a peripheral neuropathy resembling features of Guillain-Barré Syndrome.
4588 9, 4588-4588
Michanski S, Smaluch K, Steyer AM, Chakrabarti R, Setz C, Oestreicher D, Fischer C, Möbius W, Moser T, Vogl C, Wichmann C (2019).
Mapping developmental maturation of inner hair cell ribbon synapses in the apical mouse cochlea.
Proc Natl Acad Sci U S A. 116, 6415-6424
Weil MT, Ruhwedel T, Meschkat M, Sadowski B, Möbius W (2019).
Transmission Electron Microscopy of Oligodendrocytes and Myelin.
Methods Mol Biol. 1936, 343-375
Goebbels S, Nave KA (2019).
Conditional Mutagenesis in Oligodendrocyte Lineage Cells.
Methods Mol Biol. 1936, 249-274
Erwig MS, Hesse D, Jung RB, Uecker M, Kusch K, Tenzer S, Jahn O, Werner HB (2019).
Myelin: Methods for Purification and Proteome Analysis.
Methods Mol Biol. 1936, 37-63
Candelise N, Schmitz M, Llorens F, Villar-Piqué A, Cramm M, Thom T, da Silva Correia SM, Eriton Gomes da Cunha J, Möbius W, Outeiro TF, Álvarez VG, Banchelli M, D'Andrea C, de Angelis M, Zafar S, Rabano A, Matteini P, Zerr I (2019).
Seeding variability of different alpha synuclein strains in synucleinopathies.
Ann Neurol. 85, 691-703
Nave KA, Ehrenreich H (2019).
Time to revisit oligodendrocytes in multiple sclerosis.
Nat Med. 25, 364-366
Erwig MS, Patzig J, Steyer AM, Dibaj P, Heilmann M, Heilmann I, Jung RB, Kusch K, Möbius W, Jahn O, Nave KA, Werner HB (2019).
Anillin facilitates septin assembly to prevent pathological outfoldings of central nervous system myelin.
Elife. 8, pii: e43888-pii: e43888
Prukop T, Stenzel J, Wernick S, Kungl T, Mroczek M, Adam J, Ewers D, Nabirotchkin S, Nave KA, Hajj R, Cohen D, Sereda MW (2019).
Early short-term PXT3003 combinational therapy delays disease onset in a transgenic rat model of Charcot-Marie-Tooth disease 1A (CMT1A).
PLoS One. 14, e0209752-e0209752
Lüders KA, Nessler S, Kusch K, Patzig J, Jung RB, Möbius W, Nave KA, Werner HB (2019).
Maintenance of high proteolipid protein level in adult central nervous system myelin is required to preserve the integrity of myelin and axons.
Glia 67, 634-649
2018
Ramos-Gomes F, Möbius W, Bonacina L, Alves F, Markus MA (2018).
Bismuth Ferrite Second Harmonic Nanoparticles for Pulmonary Macrophage Tracking.
Small. 15, e1803776-e1803776
Belin S, Ornaghi F, Shackleford G, Wang J, Scapin C, Lopez-Anido C, Silvestri N, Robertson N, Williamson C, Ishii A, Taveggia C, Svaren J, Bansal R, Markus Schwab H, Nave K, Fratta P, D'Antonio M, Poitelon Y, Laura Feltri M, Wrabetz L (2018).
Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy.
Hum Mol Genet. 28, 2282-2282
Scapin C, Ferri C, Pettinato E, Zambroni D, Bianchi F, Del Carro U, Belin S, Caruso D, Mitro N, Pellegatta M, Taveggia C, Schwab MH, Nave KA, Laura Feltri M, Wrabetz L, D'Antonio M (2018).
Enhanced axonal Neuregulin-1 type-III signaling ameliorates neurophysiology and hypomyelination in a Charcot-Marie-Tooth type 1B mouse model.
Hum Mol Genet. 28, 992-1006
Wang J, Ho WY, Lim K, Feng J, Tucker-Kellogg G, Nave KA, Ling SC (2018).
Cell-autonomous requirement of TDP-43, an ALS/FTD signature protein, for oligodendrocyte survival and myelination.
Proc Natl Acad Sci U S A. [Epub ahead of print]
Deakin IH, Godlewska BR, Walker MA, Huang GJ, Schwab MH, Nave KA, Law AJ, Harrison PJ (2018).
Altered hippocampal gene expression and structure in transgenic mice overexpressing neuregulin 1 (Nrg1) type I.
Transl Psychiatry. 8, 229-229
Myllykoski M, Eichel MA, Jung RB, Kelm S, Werner HB, Kursula P (2018).
High-affinity heterotetramer formation between the large myelin-associated glycoprotein and the dynein light chain DYNLL1.
J Neurochem. 147, 764-783
Schirmer L, Möbius W, Zhao C, Cruz-Herranz A, Ben Haim L, Cordano C, Shiow LR, Kelley KW, Sadowski B, Timmons G, Pröbstel AK, Wright JN, Sin JH, Devereux M, Morrison DE, Chang SM, Sabeur K, Green A, Nave KA, Franklin RJ, Rowitch DH (2018).
Oligodendrocyte-encoded Kir4.1 function is required for axonal integrity.
Elife 7, pii: e36428-pii: e36428
Möbius W, Posthuma G (2018).
Sugar and ice: Immunoelectron microscopy using cryosections according to the Tokuyasu method.
Tissue Cell 57, 90-102
Fledrich R, Abdelaal T, Rasch L, Bansal V, Schütza V, Brügger B, Lüchtenborg C, Prukop T, Stenzel J, Rahman RU, Hermes D, Ewers D, Möbius W, Ruhwedel T, Katona I, Weis J, Klein D, Martini R, Brück W, Müller WC, Bonn S, Bechmann I, Nave KA, Stassart RM, Sereda MW (2018).
Targeting myelin lipid metabolism as a potential therapeutic strategy in a model of CMT1A neuropathy.
Nat Commun. 9, 3025-3025
Stassart RM, Möbius W, Nave KA, Edgar JM (2018).
The Axon-Myelin Unit in Development and Degenerative Disease.
Front Neurosci. 12, 467-467
Weil MT, Heibeck S, Töpperwien M, Tom Dieck S, Ruhwedel T, Salditt T, Rodicio MC, Morgan JR, Nave KA, Möbius W, Werner HB (2018).
Axonal ensheathment in the nervous system of lamprey: Implications for the evolution of myelinating glia.
J Neurosci. 38, 6586-6596
Cathomas F, Azzinnari D, Bergamini G, Sigrist H, Buerge M, Hoop V, Wicki B, Goetze L, Soares S, Kukelova D, Seifritz E, Goebbels S, Nave KA, Said Ghandour M, Seoighe C, Hildebrandt T, Leparc G, Klein H, Stupka E, Hengerer B, Pryce CR (2018).
Oligodendrocyte gene expression is reduced by and influences effects of chronic social stress in mice.
Genes Brain Behav. 18, e12475-e12475
He X, Zhang L, Queme LF, Liu X, Lu A, Waclaw RR, Dong X, Zhou W, Kidd G, Yoon SO, Buonanno A, Rubin JB, Xin M, Nave KA, Trapp BD, Jankowski MP, Lu QR (2018).
A histone deacetylase 3-dependent pathway delimits peripheral myelin growth and functional regeneration.
Nat Med. 24, 338-351
Pan H, Oliveira B, Saher G, Dere E, Tapken D, Mitjans M, Seidel J, Wesolowski J, Wakhloo D, Klein-Schmidt C, Ronnenberg A, Schwabe K, Trippe R, Mätz-Rensing K, Berghoff S, Al-Krinawe Y, Martens H, Begemann M, Stöcker W, Kaup FJ, Mischke R, Boretius S, Nave KA, Krauss JK, Hollmann M, Lühder F, Ehrenreich H (2018).
Uncoupling the widespread occurrence of anti-NMDAR1 autoantibodies from neuropsychiatric disease in a novel autoimmune model.
Mol Psychiatry. 24, 1489-1501
Duchesne M, Danigo A, Richard L, Vallat JM, Attarian S, Gonnaud PM, Lacour A, Péréon Y, Stojkovic T, Nave KA, Bertrand V, Nabirotchkin S, Cohen D, Demiot C, Magy L (2018).
Skin Biopsy Findings in Patients With CMT1A: Baseline Data From the CLN-PXT3003-01 Study Provide New Insights Into the Pathophysiology of the Disorder.
J Neuropathol Exp Neurol. 77, 274-281
Cantuti-Castelvetri L, Fitzner D, Bosch-Queralt M, Weil MT, Su M, Sen P, Ruhwedel T, Mitkovski M, Trendelenburg G, Lütjohann D, Möbius W, Simons M (2018).
Defective cholesterol clearance limits remyelination in the aged central nervous system.
Science 359, 684-688
Nave KA, Ehrenreich H (2018).
A bloody brake on myelin repair.
Nature 553, 31-32
Micu I, Plemel JR, Caprariello AV, Nave KA, Stys PK (2018).
Axo-myelinic neurotransmission: a novel mode of cell signalling in the central nervous system.
Nat Rev Neurosci. 19, 49-58
2017
Bang ML, Vainshtein A, Yang HJ, Eshed-Eisenbach Y, Devaux J, Werner HB, Peles E (2017).
Glial M6B stabilizes the axonal membrane at peripheral nodes of Ranvier.
Glia 66, 801-812
Janova H, Arinrad S, Balmuth E, Mitjans M, Hertel J, Habes M, Bittner RA, Pan H, Goebbels S, Begemann M, Gerwig UC, Langner S, Werner HB, Kittel-Schneider S, Homuth G, Davatzikos C, Völzke H, West BL, Reif A, Grabe HJ, Boretius S, Ehrenreich H, Nave KA (2017).
Microglia ablation alleviates myelin-associated catatonic signs in mice.
J Clin Invest. 128, 734-745
Berghoff SA, Düking T, Spieth L, Winchenbach J, Stumpf SK, Gerndt N, Kusch K, Ruhwedel T, Möbius W, Saher G (2017).
Blood-brain barrier hyperpermeability precedes demyelination in the cuprizone model.
Acta Neuropathol Commun. 5, 94-94
Wang L, Winnewisser J, Federle C, Jessberger G, Nave KA, Werner HB, Kyewski B, Klein L, Hinterberger M (2017).
Epitope-Specific Tolerance Modes Differentially Specify Susceptibility to Proteolipid Protein-Induced Experimental Autoimmune Encephalomyelitis.
Front Immunol. 8, 1511-1511
Lissek T, Adams M, Adelman J, Ahissar E, Akaaboune M, Akil H, al'Absi M, Arain F, Arango-Lasprilla JC, Atasoy D, Avila J, Badawi A, Bading H, Baig AM, Baleriola J, Belmonte C, Bertocchi I, Betz H, Blakemore C, Blanke O, Boehm-Sturm P, Bonhoeffer T, Bonifazi P, Brose N, Campolongo P, Celikel T, Chang CC, Chang TY, Citri A, Cline HT, Cortes JM, Cullen K, Dean K, Delgado-Garcia JM, Desroches M, Disterhoft JF, Dowling JE, Draguhn A, El-Khamisy SF, El Manira A, Enam SA, Encinas JM, Erramuzpe A, Esteban JA, Fariñas I, Fischer E, Fukunaga I, Gabilondo I, Ganten D, Gidon A, Gomez-Esteban JC, Greengard P, Grinevich V, Gruart A, Guillemin R, Hariri AR, Hassan B, Häusser M, Hayashi Y, Hussain NK, Jabbar AA, Jaber M, Jahn R, Janahi EM, Kabbaj M, Kettenmann H, Kindt M, Knafo S, Köhr G, Komai S, Krugers H, Kuhn B, Ghazal NL, Larkum ME, London M, Lutz B, Matute C, Martinez-Millan L, Maroun M, McGaugh J, Moustafa AA, Nasim A, Nave KA, Neher E, Nikolich K, Outeiro T, Palmer LM, Penagarikano O, Perez-Otano I, Pfaff DW, Poucet B, Rahman AU, Ramos-Cabrer P, Rashidy-Pour A, Roberts RJ, Rodrigues S, Sanes JR, Schaefer AT, Segal M, Segev I, Shafqat S, Siddiqui NA, Soreq H, Soriano-García E, Spanagel R, Sprengel R, Stuart G, Südhof TC, Tønnesen J, Treviño M, Uthman BM, Venter JC, Verkhratsky A, Weiss C, Wiesel TN, Yaksi E, Yizhar O, Young LJ, Young P, Zawia NH, Zugaza JL, Hasan MT (2017).
Building Bridges through Science.
Neuron 96, 730-735
Nave KA, Tzvetanova ID, Schirmeier S (2017).
Glial Cell Evolution: The Origins of a Lipid Store.
Cell Metab. 26, 701-702
Saab AS, Nave KA (2017).
Myelin dynamics: protecting and shaping neuronal functions.
Curr Opin Neurobiol. 47, 104-112
Fledrich R, Mannil M, Leha A, Ehbrecht C, Solari A, Pelayo-Negro AL, Berciano J, Schlotter-Weigel B, Schnizer TJ, Prukop T, Garcia-Angarita N, Czesnik D, Haberlová J, Mazanec R, Paulus W, Beissbarth T, Walter MC, Triaal C, Hogrel JY, Dubourg O, Schenone A, Baets J, De Jonghe P, Shy ME, Horvath R, Pareyson D, Seeman P, Young P, Sereda MW (2017).
Biomarkers predict outcome in Charcot- Marie-Tooth disease 1A.
J Neurol Neurosurg Psychiatry. 88, 941-952
Lüders KA, Patzig J, Simons M, Nave KA, Werner HB (2017).
Genetic dissection of oligodendroglial and neuronal Plp1 function in a novel mouse model of spastic paraplegia type 2.
Glia 65, 1762-1776
Wehr MC, Hinrichs W, Brzózka MM, Unterbarnscheidt T, Herholt A, Wintgens JP, Papiol S, Soto-Bernardini MC, Kravchenko M, Zhang M, Nave KA, Wichert SP, Falkai P, Zhang W, Schwab MH, Rossner MJ (2017).
Spironolactone is an antagonist of NRG1-ERBB4 signaling and schizophrenia-relevant endophenotypes in mice.
EMBO Mol Med. 9, 1448-1462
Ghidinelli M, Poitelon Y, Shin YK, Ameroso D, Williamson C, Ferri C, Pellegatta M, Espino K, Mogha A, Monk K, Podini P, Taveggia C, Nave KA, Wrabetz L, Park HT, Feltri ML (2017).
Laminin 211 inhibits protein kinase A in Schwann cells to modulate neuregulin 1 type III-driven myelination.
PLoS Biol. 15, e2001408-e2001408
Camargo N, Goudriaan A, van Deijk AF, Otte WM, Brouwers JF, Lodder H, Gutmann DH, Nave KA, Dijkhuizen RM, Mansvelder HD, Chrast R, Smit AB, Verheijen MHG (2017).
Oligodendroglial myelination requires astrocyte-derived lipids.
PLoS Biol. 15, e1002605-e1002605
Kleinecke S, Richert S, de Hoz L, Brügger B, Kungl T, Asadollahi E, Quintes S, Blanz J, McGonigal R, Naseri K, Sereda MW, Sachsenheimer T, Lüchtenborg C, Möbius W, Willison H, Baes M, Nave KA, Kassmann CM (2017).
Peroxisomal dysfunctions cause lysosomal storage and axonal Kv1 channel redistribution in peripheral neuropathy.
Elife 6, e23332-e23332
Karamita M, Barnum C, Möbius W, Tansey MG, Szymkowski DE, Lassmann H, Probert L (2017).
Therapeutic inhibition of soluble brain TNF promotes remyelination by increasing myelin phagocytosis by microglia.
JCI Insight [Epub ahead of print]
Trevisiol A, Saab AS, Winkler U, Marx G, Imamura H, Möbius W, Kusch K, Nave KA, Hirrlinger J (2017).
Monitoring ATP dynamics in electrically active white matter tracts.
Elife 6, e24241-e24241
Vogelgesang S, Niebert S, Renner U, Möbius W, Hülsmann S, Manzke T, Niebert M (2017).
Analysis of the Serotonergic System in a Mouse Model of Rett Syndrome Reveals Unusual Upregulation of Serotonin Receptor 5b.
Front Mol Neurosci. [PubMed - in process]
Feldman EL, Nave KA, Jensen TS, Bennett DL (2017).
New Horizons in Diabetic Neuropathy: Mechanisms, Bioenergetics, and Pain
Neuron 93, 1296-1313
Supplie LM, Düking T, Campbell G, Diaz F, Moraes CT, Götz M, Hamprecht B, Boretius S, Mahad D, Nave KA (2017).
Respiration-deficient astrocytes survive as glycolytic cells in vivo.
J Neurosci. 37, 4231-4242
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Ruprecht-Karl Universität Heidelberg (2002)
Lappe-Siefke, C.
Inaktivierung des CNP-Gens in der Maus und Expression der Cre-Rekombinase in myelinisierenden Gliazellen
Ruprecht-Karl Universität Heidelberg (2002)
Göbbels, S.
Zelltyp-spezifische Expression der Rekombinase Cre im Nervensystem der Maus
Ruprecht-Karl Universität Heidelberg (2002)
Sereda MW, Schöls L and Nave KA
Molekulargenetische Grundlagen der Charcot-Marie-Tooth Neuropathie (CMT/HMSN).
In: Schöls L, Riess O Neurogenetik, Kohlhammer. (2002) pp.
2001
Cerghet M, Bessert DA, Nave KA, Skoff RP (2001).
Differential expression of apoptotic markers in jimpy and in Plp overexpressors: evidence for different apoptotic pathways.
J. Neurocytol. 30, 841-55
Werner H, Dimou L, Klugmann M, Pfeiffer S, Nave KA (2001).
Multiple splice isoforms of proteolipid M6B in neurons and oligodendrocytes.
Mol. Cell. Neurosci. 18, 593-605
Yamada M, Jung M, Tetsushi K, Ivanova A, Nave KA, Ikenaka K (2001).
Mutant Plp/DM20 cannot be processed to secrete PLP-related oligodendrocyte differentiation/survival factor.
Neurochem. Res. 26, 639-45
Nobbio L, Mancardi G, Grandis M, Levi G, Suter U, Nave KA, Windebank AJ, Abbruzzese M, Schenone A (2001).
PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A.
Ann. Neurol. 50, 47-55
Krämer EM, Schardt A, Nave KA (2001).
Membrane traffic in myelinating oligodendrocytes.
Microsc. Res. Tech. 52, 656-71
Yool DA, Klugmann M, McLaughlin M, Vouyiouklis DA, Dimou L, Barrie JA, McCulloch MC, Nave KA, Griffiths IR (2001).
Myelin proteolipid proteins promote the interaction of oligodendrocytes and axons.
J. Neurosci. Res. 63, 151-64
Schneider S, Bosse F, D'Urso D, Muller H, Sereda MW, Nave K, Niehaus A, Kempf T, Schnolzer M, Trotter J (2001).
The AN2 protein is a novel marker for the Schwann cell lineage expressed by immature and nonmyelinating Schwann cells.
J. Neurosci. 21, 920-933
Britsch S, Goerich DE, Riethmacher D, Peirano RI, Rossner M, Nave KA, Birchmeier C, Wegner M (2001).
The transcription factor Sox10 is a key regulator of peripheral glial development.
Genes Dev. 15, 66-78
2000
Niemann S, Sereda MW, Suter U, Griffiths IR, Nave KA (2000).
Uncoupling of myelin assembly and schwann cell differentiation by transgenic overexpression of peripheral myelin protein 22.
J. Neurosci. 20, 4120-8
Schwab MH, Bartholomae A, Heimrich B, Feldmeyer D, Druffel-Augustin S, Goebbels S, Naya FJ, Zhao S, Frotscher M, Tsai MJ, Nave KA (2000).
Neuronal basic helix-loop-helix proteins (NEX and BETA2/Neuro D) regulate terminal granule cell differentiation in the hippocampus.
J. Neurosci. 20, 3714-24
Dimou L, Klugmann M, Werner H, Jung M, Griffiths IR, Nave KA (2000).
Dysmyelination in mice and the proteolipid protein gene family.
Adv. Exp. Med. Biol. 468, 261-71
Nave KA, Trapp B (2000).
Foreword
Glia 29, 103-
Klein L, Klugmann M, Nave KA, Tuohy VK, Kyewski B (2000).
Shaping of the autoreactive T-cell repertoire by a splice variant of self protein expressed in thymic epithelial cells.
Nat. Med. 6, 56-61
Bradl M, Bauer J, Inomata T, Zielasek J, Nave KA, Toyka K, Lassmann H, Wekerle H (2000).
Transgenic Lewis rats overexpressing the proteolipid protein gene: myelin degeneration and its effect on T cell-mediated experimental autoimmune encephalomyelitis.
Acta Neuropathol. 97, 595-606
1999
Werner H, Jung M, Klugmann M, Sereda M, Griffiths IR, Nave KA (1999).
Mouse models of myelin diseases.
Brain Pathol. 8, 771-93
Sereda MW (1999).
Altered protein synthesis in sciatic nerve by transgenic overexpression of PMP22 in the CMT rat.
Ann. N. Y. Acad. Sci. 883, 530-532
Niemann S, Sereda MW, Rossner M, Stewart H, Suter U, Meinck HM, Griffiths IR, Nave KA (1999).
The "CMT rat": peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22.
Ann. N. Y. Acad. Sci. 883, 254-61
Suter U, Nave KA (1999).
Transgenic mouse models of CMT1A and HNPP.
Ann. N. Y. Acad. Sci. 883, 247-53
Anderson TJ, Klugmann M, Thomson CE, Schneider A, Readhead C, Nave KA, Griffiths IR (1999).
Distinct phenotypes associated with increasing dosage of the PLP gene: implications for CMT1A due to PMP22 gene duplication.
Ann. N. Y. Acad. Sci. 883, 234-46
Coetzee T, Suzuki K, Nave KA, Popko B (1999).
Myelination in the absence of galactolipids and proteolipid proteins.
Mol. Cell. Neurosci. 14, 41-51
1998
Niemann S, Sidman RL, Nave KA (1998).
Evidence against altered forms of MAG in the dysmyelinated mouse mutant claw paw.
Mamm. Genome 9, 903-4
Griffiths I, Klugmann M, Anderson T, Thomson C, Vouyiouklis D, Nave KA (1998).
Current concepts of PLP and its role in the nervous system.
Microsc. Res. Tech. 41, 344-58
Vouyiouklis DA, Werner H, Griffiths IR, Stewart GJ, Armin-Nave K, Thomson CE (1998).
Molecular cloning and transfection studies of M6b-2, a novel splice variant of a member of the PLP-DM20/M6 gene family.
J Neurosci Res. 52, 633-640
Griffiths I, Klugmann M, Anderson T, Yool D, Thomson C, Schwab MH, Schneider A, Zimmermann F, McCulloch M, Nadon N, Nave KA (1998).
Axonal swellings and degeneration in mice lacking the major proteolipid of myelin.
Science 280, 1610-3
Anderson TJ, Schneider A, Barrie JA, Klugmann M, McCulloch MC, Kirkham D, Kyriakides E, Nave KA, Griffiths IR (1998).
Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene.
J. Comp. Neurol. 394, 506-19
Rossner MJ, Dörr J, Gass P, Schwab MH, Nave KA (1998).
SHARPs: mammalian enhancer-of-split- and hairy-related proteins coupled to neuronal stimulation.
Mol. Cell. Neurosci. 10, 460-75
Schwab MH, Druffel-Augustin S, Gass P, Jung M, Klugmann M, Bartholomae A, Rossner MJ, Nave KA (1998).
Neuronal basic helix-loop-helix proteins (NEX, neuroD, NDRF): spatiotemporal expression and targeted disruption of the NEX gene in transgenic mice.
J. Neurosci. 18, 1408-18
Forss-Petter S, Werner H, Berger J, Lassmann H, Molzer B, Schwab MH, Bernheimer H, Zimmermann F, Nave KA (1998).
Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice.
J. Neurosci. Res. 50, 829-43
Stewart HJ, Zoidl G, Rossner M, Brennan A, Zoidl C, Nave KA, Mirsky R, Jessen KR (1998).
Helix-loop-helix proteins in Schwann cells: a study of regulation and subcellular localization of Ids, REB, and E12/47 during embryonic and postnatal development.
J. Neurosci. Res. 50, 684-701
Rossner MJ, Dörr J, Gass P, Schwab MH, Nave KA (1998).
SHARPs: mammalian enhancer-of-split- and hairy-related proteins coupled to neuronal stimulation.
Mol. Cell. Neurosci. 9, 460-75
1997
Anderson TJ, Montague P, Nadon N, Nave KA, Griffiths IR (1997).
Modification of Schwann cell phenotype with Plp transgenes: evidence that the PLP and DM20 isoproteins are targeted to different cellular domains.
J. Neurosci. Res. 50, 13-22
Thomson CE, Montague P, Jung M, Nave KA, Griffiths IR (1997).
Phenotypic severity of murine Plp mutants reflects in vivo and in vitro variations in transport of PLP isoproteins.
Glia 20, 322-32
Klugmann M, Schwab MH, Pühlhofer A, Schneider A, Zimmermann F, Griffiths IR, Nave KA (1997).
Assembly of CNS myelin in the absence of proteolipid protein.
Neuron 18, 59-70
Jung M, Sommer I, Schachner M, Nave KA (1997).
Monoclonal antibody O10 defines a conformationally sensitive cell-surface epitope of proteolipid protein (PLP): evidence that PLP misfolding underlies dysmyelination in mutant mice.
J. Neurosci. 16, 7920-9
1996
Sereda M, Griffiths I, Pühlhofer A, Stewart H, Rossner MJ, Zimmerman F, Magyar JP, Schneider A, Hund E, Meinck HM, Suter U, Nave KA (1996).
A transgenic rat model of Charcot-Marie-Tooth disease.
Neuron 16, 1049-60
Griffiths IR, Schneider A, Anderson J, Nave KA (1996).
Transgenic and natural mouse models of proteolipid protein (PLP)-related dysmyelination and demyelination.
Brain Pathol. 5, 275-81
Nave KA (1996).
Myelin genetics: new insight into old diseases.
Brain Pathol. 5, 231-2
1995
Nave KA (1995).
Neurological mouse mutants and the genes of myelin.
J. Neurosci. Res. 38, 607-12
Bartholomä A, Nave KA (1995).
NEX-1: a novel brain-specific helix-loop-helix protein with autoregulation and sustained expression in mature cortical neurons.
Mech. Dev. 48, 217-28
Schneider AM, Griffiths IR, Readhead C, Nave KA (1995).
Dominant-negative action of the jimpy mutation in mice complemented with an autosomal transgene for myelin proteolipid protein.
Proc. Natl. Acad. Sci. U.S.A. 92, 4447-51
Vellutini C, Horschowski N, Philippon V, Gambarelli D, Nave KA, Filippi P (1995).
Development of lymphoid hyperplasia in transgenic mice expressing the HIV tat gene.
AIDS Res. Hum. Retroviruses 11, 21-9
1994
Vellutini C, Philippon V, Gambarelli D, Horschowski N, Nave KA, Navarro JM, Auphan M, Courcoul MA, Filippi P (1994).
The maedi-visna virus Tat protein induces multiorgan lymphoid hyperplasia in transgenic mice.
J. Virol. 68, 4955-62
Montag D, Giese KP, Bartsch U, Martini R, Lang Y, Blüthmann H, Karthigasan J, Kirschner DA, Wintergerst ES, Nave KA et al. (1994).
Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin.
Neuron 13, 229-46
Readhead C, Schneider A, Griffiths I, Nave KA (1994).
Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage.
Neuron 12, 583-95
1993
Fanarraga ML, Sommer IU, Griffiths IR, Montague P, Groome NP, Nave KA, Schneider A, Brophy PJ, Kennedy PG (1993).
Oligodendrocyte development and differentiation in the rumpshaker mutation.
Glia 9, 146-56
1992
Schneider A, Montague P, Griffiths I, Fanarraga M, Kennedy P, Brophy P, Nave KA (1992).
Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene.
Nature 358, 758-61
1991
Nave KA, Lemke G (1991).
Induction of the myelin proteolipid protein (PLP) gene in C6 glioblastoma cells: functional analysis of the PLP promotor.
J. Neurosci. 11, 3060-9
Milner RJ, Lai C, Nave KA, Montag D, Farber L, Sutcliffe JG (1991).
Organization of myelin protein genes: myelin-associated glycoprotein.
Ann. N. Y. Acad. Sci. 605, 254-61
1989
Nave KA, Milner RJ (1989).
Proteolipid proteins: structure and genetic expression in normal and myelin-deficient mutant mice.
Crit Rev Neurobiol. 5, 65-91
1987
Nave KA, Bloom FE, Milner RJ (1987).
A single nucleotide difference in the gene for myelin proteolipid protein defines the jimpy mutation in mouse.
J. Neurochem. 49, 1873-7
Nave KA, Lai C, Bloom FE, Milner RJ (1987).
Splice site selection in the proteolipid protein (PLP) gene transcript and primary structure of the DM-20 protein of central nervous system myelin.
Proc. Natl. Acad. Sci. U.S.A. 84, 5665-9
Lai C, Brow MA, Nave KA, Noronha AB, Quarles RH, Bloom FE, Milner RJ, Sutcliffe JG (1987).
Two forms of 1B236/myelin-associated glycoprotein, a cell adhesion molecule for postnatal neural development, are produced by alternative splicing.
Proc. Natl. Acad. Sci. U.S.A. 84, 4337-41
1986
Nave KA, Lai C, Bloom FE, Milner RJ (1986).
Jimpy mutant mouse: a 74-base deletion in the mRNA for myelin proteolipid protein and evidence for a primary defect in RNA splicing.
Proc. Natl. Acad. Sci. U.S.A. 83, 9264-8
1985
Nave KA, Probstmeier R, Schachner M (1985).
Epidermal growth factor does not cross the blood-brain barrier.
Cell Tissue Res. 241, 453-7
Milner RJ, Lai C, Nave KA, Lenoir D, Ogata J, Sutcliffe JG (1985).
Nucleotide sequences of two mRNAs for rat brain myelin proteolipid protein.
Cell 42, 931-9