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Oktober 2021 / J Cell Sci ApoE4 disrupts interaction of sortilin with fatty acid-binding protein 7 essential to promote lipid signaling A. Asaro R. Sinha M. Bakun O. Kalnytska A.S. Carlo-Spiewok T. Rubel A. Rozeboom M. Dadlez B. Kaminska E. Aronica A.R. Malik T.E. Willnow 01. November 2020 / Trends Neurosci VPS10P domain receptors: sorting out brain health and disease A.R. Malik T.E. Willnow 01. September 2020 / Alzheimers Dement Apolipoprotein E4 disrupts the neuroprotective action of sortilin in neuronal lipid metabolism and endocannabinoid signaling A. Asaro A.S. Carlo-Spiewok A.R. Malik M. Rothe C.G. Schipke O. Peters J. Heeren T.E. Willnow 12. November 2019 / Int J Mol Sci Excitatory amino acid transporters in physiology and disorders of the central nervous system A.R. Malik T.E. Willnow 01. Juni 2020 / Glia SorCS2 facilitates release of endostatin from astrocytes and controls post-stroke angiogenesis A.R. Malik Janet Lips M. Gorniak-Walas D.W.M. Broekaart A. Asaro M.T.C. Kuffner C.J. Hoffmann M. Kikhia M. Dopatka P. Boehm-Sturm S. Mueller U. Dirnagl E. Aronica C. Harms T.E. Willnow 05. März 2019 / Cell Rep SorCS2 controls functional expression of amino acid transporter EAAT3 and protects neurons from oxidative stress and epilepsy-induced pathology A.R. Malik K. Szydlowska K. Nizinska A. Asaro E.A. van Vliet O. Popp G. Dittmar R. Fritsche-Guenther J.A. Kirwan A. Nykjaer K. Lukasiuk E. Aronica T.E. Willnow 20. September 2018 / Cell Mutations in disordered regions can cause disease by creating dileucine motifs K. Meyer M. Kirchner B. Uyar J.Y. Cheng G. Russo L.R. Hernandez-Miranda A. Szymborska H. Zauber I.M. Rudolph T.E. Willnow A. Akalin V. Haucke H. Gerhardt C. Birchmeier R. Kühn M. Krauss S. Diecke J.M. Pascual M. Selbach 01. Januar 2005 / Development A splice variant of the Wilms' tumour suppressor Wt1 is required for normal development of the olfactory system N. Wagner K.D. Wagner A. Hammes K.M. Kirschner V.R. Vidal A. Schedl H. Scholz 01. September 2004 / Am J Physiol Regul Integr Comp Physiol α-tropomyosin mutations Asp175Asn and Glu180Gly affect cardiac function in transgenic rats in different ways D. Wernicke C. Thiel C.M. Duja-Isac K.V. Essine M. Spindler D.J.R. Nunez R. Plehm N. Wessel A. Hammes R.J. Edwards A. Lippoldt U. Zacharias H. Stroemer S. Neubauer M.J. Davies I. Morano L. Thierfelder 01. Juni 2011 / Dev Dyn Loss of Lrp2 in zebrafish disrupts pronephric tubular clearance but not forebrain development E. Kur A. Christa K.N. Veth C.R. Gajera M.A. Andrade-Navarro J. Zhang J.R. Willer R.G. Gregg S. Abdelilah-Seyfried S. Bachmann B.A. Link A. Hammes T.E. Willnow Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Nächste Seite Next › Letzte Seite Last »
15. Oktober 2021 / J Cell Sci ApoE4 disrupts interaction of sortilin with fatty acid-binding protein 7 essential to promote lipid signaling A. Asaro R. Sinha M. Bakun O. Kalnytska A.S. Carlo-Spiewok T. Rubel A. Rozeboom M. Dadlez B. Kaminska E. Aronica A.R. Malik T.E. Willnow
01. November 2020 / Trends Neurosci VPS10P domain receptors: sorting out brain health and disease A.R. Malik T.E. Willnow
01. September 2020 / Alzheimers Dement Apolipoprotein E4 disrupts the neuroprotective action of sortilin in neuronal lipid metabolism and endocannabinoid signaling A. Asaro A.S. Carlo-Spiewok A.R. Malik M. Rothe C.G. Schipke O. Peters J. Heeren T.E. Willnow
12. November 2019 / Int J Mol Sci Excitatory amino acid transporters in physiology and disorders of the central nervous system A.R. Malik T.E. Willnow
01. Juni 2020 / Glia SorCS2 facilitates release of endostatin from astrocytes and controls post-stroke angiogenesis A.R. Malik Janet Lips M. Gorniak-Walas D.W.M. Broekaart A. Asaro M.T.C. Kuffner C.J. Hoffmann M. Kikhia M. Dopatka P. Boehm-Sturm S. Mueller U. Dirnagl E. Aronica C. Harms T.E. Willnow
05. März 2019 / Cell Rep SorCS2 controls functional expression of amino acid transporter EAAT3 and protects neurons from oxidative stress and epilepsy-induced pathology A.R. Malik K. Szydlowska K. Nizinska A. Asaro E.A. van Vliet O. Popp G. Dittmar R. Fritsche-Guenther J.A. Kirwan A. Nykjaer K. Lukasiuk E. Aronica T.E. Willnow
20. September 2018 / Cell Mutations in disordered regions can cause disease by creating dileucine motifs K. Meyer M. Kirchner B. Uyar J.Y. Cheng G. Russo L.R. Hernandez-Miranda A. Szymborska H. Zauber I.M. Rudolph T.E. Willnow A. Akalin V. Haucke H. Gerhardt C. Birchmeier R. Kühn M. Krauss S. Diecke J.M. Pascual M. Selbach
01. Januar 2005 / Development A splice variant of the Wilms' tumour suppressor Wt1 is required for normal development of the olfactory system N. Wagner K.D. Wagner A. Hammes K.M. Kirschner V.R. Vidal A. Schedl H. Scholz
01. September 2004 / Am J Physiol Regul Integr Comp Physiol α-tropomyosin mutations Asp175Asn and Glu180Gly affect cardiac function in transgenic rats in different ways D. Wernicke C. Thiel C.M. Duja-Isac K.V. Essine M. Spindler D.J.R. Nunez R. Plehm N. Wessel A. Hammes R.J. Edwards A. Lippoldt U. Zacharias H. Stroemer S. Neubauer M.J. Davies I. Morano L. Thierfelder
01. Juni 2011 / Dev Dyn Loss of Lrp2 in zebrafish disrupts pronephric tubular clearance but not forebrain development E. Kur A. Christa K.N. Veth C.R. Gajera M.A. Andrade-Navarro J. Zhang J.R. Willer R.G. Gregg S. Abdelilah-Seyfried S. Bachmann B.A. Link A. Hammes T.E. Willnow