36 Publications

Mark all

[36]
2020 | Preprint | IST-REx-ID: 7800   OA
Morandell, J., Schwarz, L. A., Basilico, B., Tasciyan, S., Nicolas, A., Sommer, C. M., … Novarino, G. (n.d.). Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development. Cold Spring Harbor Laboratory.
View | Files available | Download (ext.)
 
[35]
2020 | Journal Article | IST-REx-ID: 7957   OA
Parenti, I., Garcia Rabaneda, L. E., Schön, H., & Novarino, G. (n.d.). Neurodevelopmental disorders: From genetics to functional pathways. Trends in Neurosciences. https://doi.org/10.1016/j.tins.2020.05.004
View | DOI | Download (ext.)
 
[34]
2020 | Journal Article | IST-REx-ID: 7586   OA
Weinert, S., Gimber, N., Deuschel, D., Stuhlmann, T., Puchkov, D., Farsi, Z., … Jentsch, T. J. (n.d.). Uncoupling endosomal CLC chloride/proton exchange causes severe neurodegeneration. EMBO Journal, e103358. https://doi.org/10.15252/embj.2019103358
View | Files available | DOI
 
[33]
2019 | Journal Article | IST-REx-ID: 105
Marsh, A., Novarino, G., Lockhart, P., & Leventer, R. (2019). CUGC for pontocerebellar hypoplasia type 9 and spastic paraplegia-63. European Journal of Human Genetics, 27, 161–166. https://doi.org/10.1038/s41431-018-0231-2
View | DOI
 
[32]
2019 | Journal Article | IST-REx-ID: 6896
Oliveira, B., Yahya, A. Ç., & Novarino, G. (2019). Modeling cell-cell interactions in the brain using cerebral organoids. Brain Research, 1724. https://doi.org/10.1016/j.brainres.2019.146458
View | DOI | PubMed | Europe PMC
 
[31]
2019 | Journal Article | IST-REx-ID: 7414
Knaus, L., Tarlungeanu, D.-C., & Novarino, G. (2019). S.16.03 A homozygous missense mutation in SLC7A5 leads to autism spectrum disorder and microcephaly. European Neuropsychopharmacology, 29(Supplement 6), S11. https://doi.org/10.1016/j.euroneuro.2019.09.039
View | DOI
 
[30]
2019 | Research Data | IST-REx-ID: 6074
Dotter, C., & Novarino, G. (2019). Supplementary data for the research paper “Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition.” IST Austria. https://doi.org/10.15479/AT:ISTA:6074
View | Files available | DOI
 
[29]
2019 | Journal Article | IST-REx-ID: 7415
Morandell, J., Nicolas, A., Schwarz, L. A., & Novarino, G. (2019). S.16.05 Illuminating the role of the e3 ubiquitin ligase cullin3 in brain development and autism. European Neuropsychopharmacology, 29(Supplement 6), S11–S12. https://doi.org/10.1016/j.euroneuro.2019.09.040
View | DOI
 
[28]
2019 | Journal Article | IST-REx-ID: 6088
Traxl, A., Mairinger, S., Filip, T., Sauberer, M., Stanek, J., Poschner, S., … Langer, O. (2019). Inhibition of ABCB1 and ABCG2 at the mouse blood-brain barrier with marketed drugs to improve brain delivery of the model ABCB1/ABCG2 substrate [11C]erlotinib. Molecular Pharmaceutics, 16(3), 1282–1293. https://doi.org/10.1021/acs.molpharmaceut.8b01217
View | DOI | PubMed | Europe PMC
 
[27]
2018 | Journal Article | IST-REx-ID: 456
Novarino, G. (2018). Zika-associated microcephaly: Reduce the stress and race for the treatment. Science Translational Medicine, 10(423). https://doi.org/10.1126/scitranslmed.aar7514
View | DOI
 
[26]
2018 | Journal Article | IST-REx-ID: 691   OA
Marin Valencia, I., Novarino, G., Johansen, A., Rosti, B., Issa, M., Musaev, D., … Gleeson, J. (2018). A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features. Journal of Medical Genetics, 55(1), 48–54. https://doi.org/10.1136/jmedgenet-2017-104627
View | DOI | Download (ext.) | PubMed | Europe PMC
 
[25]
2018 | Journal Article | IST-REx-ID: 546
Sacco, R., Cacci, E., & Novarino, G. (2018). Neural stem cells in neuropsychiatric disorders. Current Opinion in Neurobiology, 48(2), 131–138. https://doi.org/10.1016/j.conb.2017.12.005
View | DOI
 
[24]
2018 | Journal Article | IST-REx-ID: 5888   OA
Tarlungeanu, D.-C., & Novarino, G. (2018). Genomics in neurodevelopmental disorders: an avenue to personalized medicine. Experimental & Molecular Medicine, 50(8). https://doi.org/10.1038/s12276-018-0129-7
View | Files available | DOI | PubMed | Europe PMC
 
[23]
2018 | Journal Article | IST-REx-ID: 3   OA
Deliu, E., Arecco, N., Morandell, J., Dotter, C., Contreras, X., Girardot, C., … Novarino, G. (2018). Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition. Nature Neuroscience, 21(12), 1717–1727. https://doi.org/10.1038/s41593-018-0266-2
View | Files available | DOI
 
[22]
2017 | Journal Article | IST-REx-ID: 667
Novarino, G. (2017). The antisocial side of antibiotics. Science Translational Medicine, 9(387). https://doi.org/10.1126/scitranslmed.aan2786
View | DOI
 
[21]
2017 | Journal Article | IST-REx-ID: 656
Novarino, G. (2017). Modeling Alzheimer’s disease in mice with human neurons. Science Translational Medicine, 9(381). https://doi.org/10.1126/scitranslmed.aam9867
View | DOI
 
[20]
2017 | Journal Article | IST-REx-ID: 702
Novarino, G. (2017). The riddle of CHD8 haploinsufficiency in autism spectrum disorder. Science Translational Medicine, 9(399), eaao0972. https://doi.org/10.1126/scitranslmed.aao0972
View | DOI
 
[19]
2017 | Journal Article | IST-REx-ID: 715
Novarino, G. (2017). More excitation for Rett syndrome. Science Translational Medicine, 9(405). https://doi.org/10.1126/scitranslmed.aao4218
View | DOI
 
[18]
2017 | Journal Article | IST-REx-ID: 689
Novarino, G. (2017). Rett syndrome modeling goes simian. Science Translational Medicine, 9(393). https://doi.org/10.1126/scitranslmed.aan8196
View | DOI
 
[17]
2017 | Book Chapter | IST-REx-ID: 634
Schroeder, J., Deliu, E., Novarino, G., & Schmeisser, M. (2017). Genetic and pharmacological reversibility of phenotypes in mouse models of autism spectrum disorder. In M. Schmeisser & T. Boekers (Eds.), Translational Anatomy and Cell Biology of Autism Spectrum Disorder (Vol. 224, pp. 189–211). Springer. https://doi.org/10.1007/978-3-319-52498-6_10
View | DOI
 
[16]
2017 | Journal Article | IST-REx-ID: 1228   OA
Sauerzopf, U., Sacco, R., Novarino, G., Niello, M., Weidenauer, A., Praschak Rieder, N., … Willeit, M. (2017). Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence. European Journal of Neuroscience, 45(1), 45–57. https://doi.org/10.1111/ejn.13418
View | Files available | DOI
 
[15]
2017 | Book Chapter | IST-REx-ID: 623
Hill Yardin, E., Mckeown, S., Novarino, G., & Grabrucker, A. (2017). Extracerebral dysfunction in animal models of autism spectrum disorder. In M. Schmeisser & T. Boekers (Eds.), Translational Anatomy and Cell Biology of Autism Spectrum Disorder (Vol. 224, pp. 159–187). Springer. https://doi.org/10.1007/978-3-319-52498-6_9
View | DOI
 
[14]
2017 | Journal Article | IST-REx-ID: 731
Novarino, G. (2017). The science of love in ASD and ADHD. Science Translational Medicine, 9(411). https://doi.org/10.1126/scitranslmed.aap8168
View | DOI
 
[13]
2016 | Journal Article | IST-REx-ID: 1183
Tarlungeanu, D.-C., Deliu, E., Dotter, C., Kara, M., Janiesch, P., Scalise, M., … Novarino, G. (2016). Impaired amino acid transport at the blood brain barrier is a cause of autism spectrum disorder. Cell, 167(6), 1481–1494. https://doi.org/10.1016/j.cell.2016.11.013
View | Files available | DOI
 
[12]
2015 | Journal Article | IST-REx-ID: 1789   OA
Kuechler, A., Zink, A., Wieland, T., Lüdecke, H., Cremer, K., Salviati, L., … Engels, H. (2015). Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome. European Journal of Human Genetics, 23(6), 753–760. https://doi.org/10.1038/ejhg.2014.165
View | DOI | Download (ext.) | PubMed | Europe PMC
 
[11]
2014 | Journal Article | IST-REx-ID: 1916   OA
Novarino, G., Fenstermaker, A., Zaki, M., Hofree, M., Silhavy, J., Heiberg, A., … Gleeson, J. (2014). Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. Science, 343(6170), 506–511. https://doi.org/10.1126/science.1247363
View | DOI | Download (ext.) | PubMed | Europe PMC
 
[10]
2014 | Journal Article | IST-REx-ID: 1791
Baek, S., Kerjan, G., Bielas, S., Lee, J., Fenstermaker, A., Novarino, G., & Gleeson, J. (2014). Off-target effect of doublecortin family shRNA on neuronal migration associated with endogenous MicroRNA dysregulation. Neuron, 82(6), 1255–1262. https://doi.org/10.1016/j.neuron.2014.04.036
View | DOI
 
[9]
2013 | Journal Article | IST-REx-ID: 1790
Novarino, G., Baek, S., & Gleeson, J. (2013). The sacred disease: The puzzling genetics of epileptic disorders. Neuron, 80(1), 9–11. https://doi.org/10.1016/j.neuron.2013.09.019
View | DOI
 
[8]
2012 | Journal Article | IST-REx-ID: 2313
Dixon Salazar, T., Silhavy, J., Udpa, N., Schroth, J., Bielas, S., Schaffer, A., … Gleeson, J. (2012). Exome sequencing can improve diagnosis and alter patient management. Science Translational Medicine, 4(138). https://doi.org/10.1126/scitranslmed.3003544
View | DOI
 
[7]
2012 | Journal Article | IST-REx-ID: 2314
Novarino, G., El Fishawy, P., Kayserili, H., Meguid, N., Scott, E., Schroth, J., … Gleeson, J. (2012). Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy. Science, 338(6105), 394–397. https://doi.org/10.1126/science.1224631
View | DOI
 
[6]
2011 | Book Review | IST-REx-ID: 2312
Novarino, G., Akizu, N., & Gleeson, J. (2011). Modeling human disease in humans: The ciliopathies. Cell. Cell Press. https://doi.org/10.1016/j.cell.2011.09.014
View | DOI
 
[5]
2010 | Book Chapter | IST-REx-ID: 2309
Stauber, T., Novarino, G., & Jentsch, T. (2010). The CLC family of chloride channels and transporters. In Physiology and Pathology of chloride transporters and channels in the nervous system (pp. 209–231). Elsevier. https://doi.org/10.1016/B978-0-12-374373-2.00012-1
View | DOI
 
[4]
2010 | Journal Article | IST-REx-ID: 2311
Rickheit, G., Wartosch, L., Schaffer, S., Stobrawa, S., Novarino, G., Weinert, S., & Jentsch, T. (2010). Role of ClC-5 in renal endocytosis is unique among ClC exchangers and does not require PY-motif-dependent ubiquitylation. Journal of Biological Chemistry, 285(23), 17595–17603. https://doi.org/10.1074/jbc.M110.115600
View | DOI
 
[3]
2010 | Journal Article | IST-REx-ID: 2310
Novarino, G., Weinert, S., Rickheit, G., & Jentsch, T. (2010). Endosomal chloride-proton exchange rather than chloride conductance is crucial for renal endocytosis. Science, 328(5984), 1398–1401. https://doi.org/10.1126/science.1188070
View | DOI
 
[2]
2005 | Journal Article | IST-REx-ID: 2307
Schwartz, J., Novarino, G., Piston, D., & Defelice, L. (2005). Substrate binding stoichiometry and kinetics of the norepinephrine transporter. Journal of Biological Chemistry, 280(19), 19177–19184. https://doi.org/10.1074/jbc.M412923200
View | DOI
 
[1]
2004 | Journal Article | IST-REx-ID: 2308
Novarino, G., Fabrizi, C., Tonini, R., Denti, M., Malchiodi, A., Lauro, G., … Mazzanti, M. (2004). Involvement of the intracellular ion channel CLIC1 in microglia-mediated β-amyloid-induced neurotoxicity. Journal of Neuroscience, 24(23), 5322–5330. https://doi.org/10.1523/JNEUROSCI.1170-04.2004
View | DOI
 

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36 Publications

Mark all

[36]
2020 | Preprint | IST-REx-ID: 7800   OA
Morandell, J., Schwarz, L. A., Basilico, B., Tasciyan, S., Nicolas, A., Sommer, C. M., … Novarino, G. (n.d.). Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development. Cold Spring Harbor Laboratory.
View | Files available | Download (ext.)
 
[35]
2020 | Journal Article | IST-REx-ID: 7957   OA
Parenti, I., Garcia Rabaneda, L. E., Schön, H., & Novarino, G. (n.d.). Neurodevelopmental disorders: From genetics to functional pathways. Trends in Neurosciences. https://doi.org/10.1016/j.tins.2020.05.004
View | DOI | Download (ext.)
 
[34]
2020 | Journal Article | IST-REx-ID: 7586   OA
Weinert, S., Gimber, N., Deuschel, D., Stuhlmann, T., Puchkov, D., Farsi, Z., … Jentsch, T. J. (n.d.). Uncoupling endosomal CLC chloride/proton exchange causes severe neurodegeneration. EMBO Journal, e103358. https://doi.org/10.15252/embj.2019103358
View | Files available | DOI
 
[33]
2019 | Journal Article | IST-REx-ID: 105
Marsh, A., Novarino, G., Lockhart, P., & Leventer, R. (2019). CUGC for pontocerebellar hypoplasia type 9 and spastic paraplegia-63. European Journal of Human Genetics, 27, 161–166. https://doi.org/10.1038/s41431-018-0231-2
View | DOI
 
[32]
2019 | Journal Article | IST-REx-ID: 6896
Oliveira, B., Yahya, A. Ç., & Novarino, G. (2019). Modeling cell-cell interactions in the brain using cerebral organoids. Brain Research, 1724. https://doi.org/10.1016/j.brainres.2019.146458
View | DOI | PubMed | Europe PMC
 
[31]
2019 | Journal Article | IST-REx-ID: 7414
Knaus, L., Tarlungeanu, D.-C., & Novarino, G. (2019). S.16.03 A homozygous missense mutation in SLC7A5 leads to autism spectrum disorder and microcephaly. European Neuropsychopharmacology, 29(Supplement 6), S11. https://doi.org/10.1016/j.euroneuro.2019.09.039
View | DOI
 
[30]
2019 | Research Data | IST-REx-ID: 6074
Dotter, C., & Novarino, G. (2019). Supplementary data for the research paper “Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition.” IST Austria. https://doi.org/10.15479/AT:ISTA:6074
View | Files available | DOI
 
[29]
2019 | Journal Article | IST-REx-ID: 7415
Morandell, J., Nicolas, A., Schwarz, L. A., & Novarino, G. (2019). S.16.05 Illuminating the role of the e3 ubiquitin ligase cullin3 in brain development and autism. European Neuropsychopharmacology, 29(Supplement 6), S11–S12. https://doi.org/10.1016/j.euroneuro.2019.09.040
View | DOI
 
[28]
2019 | Journal Article | IST-REx-ID: 6088
Traxl, A., Mairinger, S., Filip, T., Sauberer, M., Stanek, J., Poschner, S., … Langer, O. (2019). Inhibition of ABCB1 and ABCG2 at the mouse blood-brain barrier with marketed drugs to improve brain delivery of the model ABCB1/ABCG2 substrate [11C]erlotinib. Molecular Pharmaceutics, 16(3), 1282–1293. https://doi.org/10.1021/acs.molpharmaceut.8b01217
View | DOI | PubMed | Europe PMC
 
[27]
2018 | Journal Article | IST-REx-ID: 456
Novarino, G. (2018). Zika-associated microcephaly: Reduce the stress and race for the treatment. Science Translational Medicine, 10(423). https://doi.org/10.1126/scitranslmed.aar7514
View | DOI
 
[26]
2018 | Journal Article | IST-REx-ID: 691   OA
Marin Valencia, I., Novarino, G., Johansen, A., Rosti, B., Issa, M., Musaev, D., … Gleeson, J. (2018). A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features. Journal of Medical Genetics, 55(1), 48–54. https://doi.org/10.1136/jmedgenet-2017-104627
View | DOI | Download (ext.) | PubMed | Europe PMC
 
[25]
2018 | Journal Article | IST-REx-ID: 546
Sacco, R., Cacci, E., & Novarino, G. (2018). Neural stem cells in neuropsychiatric disorders. Current Opinion in Neurobiology, 48(2), 131–138. https://doi.org/10.1016/j.conb.2017.12.005
View | DOI
 
[24]
2018 | Journal Article | IST-REx-ID: 5888   OA
Tarlungeanu, D.-C., & Novarino, G. (2018). Genomics in neurodevelopmental disorders: an avenue to personalized medicine. Experimental & Molecular Medicine, 50(8). https://doi.org/10.1038/s12276-018-0129-7
View | Files available | DOI | PubMed | Europe PMC
 
[23]
2018 | Journal Article | IST-REx-ID: 3   OA
Deliu, E., Arecco, N., Morandell, J., Dotter, C., Contreras, X., Girardot, C., … Novarino, G. (2018). Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition. Nature Neuroscience, 21(12), 1717–1727. https://doi.org/10.1038/s41593-018-0266-2
View | Files available | DOI
 
[22]
2017 | Journal Article | IST-REx-ID: 667
Novarino, G. (2017). The antisocial side of antibiotics. Science Translational Medicine, 9(387). https://doi.org/10.1126/scitranslmed.aan2786
View | DOI
 
[21]
2017 | Journal Article | IST-REx-ID: 656
Novarino, G. (2017). Modeling Alzheimer’s disease in mice with human neurons. Science Translational Medicine, 9(381). https://doi.org/10.1126/scitranslmed.aam9867
View | DOI
 
[20]
2017 | Journal Article | IST-REx-ID: 702
Novarino, G. (2017). The riddle of CHD8 haploinsufficiency in autism spectrum disorder. Science Translational Medicine, 9(399), eaao0972. https://doi.org/10.1126/scitranslmed.aao0972
View | DOI
 
[19]
2017 | Journal Article | IST-REx-ID: 715
Novarino, G. (2017). More excitation for Rett syndrome. Science Translational Medicine, 9(405). https://doi.org/10.1126/scitranslmed.aao4218
View | DOI
 
[18]
2017 | Journal Article | IST-REx-ID: 689
Novarino, G. (2017). Rett syndrome modeling goes simian. Science Translational Medicine, 9(393). https://doi.org/10.1126/scitranslmed.aan8196
View | DOI
 
[17]
2017 | Book Chapter | IST-REx-ID: 634
Schroeder, J., Deliu, E., Novarino, G., & Schmeisser, M. (2017). Genetic and pharmacological reversibility of phenotypes in mouse models of autism spectrum disorder. In M. Schmeisser & T. Boekers (Eds.), Translational Anatomy and Cell Biology of Autism Spectrum Disorder (Vol. 224, pp. 189–211). Springer. https://doi.org/10.1007/978-3-319-52498-6_10
View | DOI
 
[16]
2017 | Journal Article | IST-REx-ID: 1228   OA
Sauerzopf, U., Sacco, R., Novarino, G., Niello, M., Weidenauer, A., Praschak Rieder, N., … Willeit, M. (2017). Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence. European Journal of Neuroscience, 45(1), 45–57. https://doi.org/10.1111/ejn.13418
View | Files available | DOI
 
[15]
2017 | Book Chapter | IST-REx-ID: 623
Hill Yardin, E., Mckeown, S., Novarino, G., & Grabrucker, A. (2017). Extracerebral dysfunction in animal models of autism spectrum disorder. In M. Schmeisser & T. Boekers (Eds.), Translational Anatomy and Cell Biology of Autism Spectrum Disorder (Vol. 224, pp. 159–187). Springer. https://doi.org/10.1007/978-3-319-52498-6_9
View | DOI
 
[14]
2017 | Journal Article | IST-REx-ID: 731
Novarino, G. (2017). The science of love in ASD and ADHD. Science Translational Medicine, 9(411). https://doi.org/10.1126/scitranslmed.aap8168
View | DOI
 
[13]
2016 | Journal Article | IST-REx-ID: 1183
Tarlungeanu, D.-C., Deliu, E., Dotter, C., Kara, M., Janiesch, P., Scalise, M., … Novarino, G. (2016). Impaired amino acid transport at the blood brain barrier is a cause of autism spectrum disorder. Cell, 167(6), 1481–1494. https://doi.org/10.1016/j.cell.2016.11.013
View | Files available | DOI
 
[12]
2015 | Journal Article | IST-REx-ID: 1789   OA
Kuechler, A., Zink, A., Wieland, T., Lüdecke, H., Cremer, K., Salviati, L., … Engels, H. (2015). Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome. European Journal of Human Genetics, 23(6), 753–760. https://doi.org/10.1038/ejhg.2014.165
View | DOI | Download (ext.) | PubMed | Europe PMC
 
[11]
2014 | Journal Article | IST-REx-ID: 1916   OA
Novarino, G., Fenstermaker, A., Zaki, M., Hofree, M., Silhavy, J., Heiberg, A., … Gleeson, J. (2014). Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. Science, 343(6170), 506–511. https://doi.org/10.1126/science.1247363
View | DOI | Download (ext.) | PubMed | Europe PMC
 
[10]
2014 | Journal Article | IST-REx-ID: 1791
Baek, S., Kerjan, G., Bielas, S., Lee, J., Fenstermaker, A., Novarino, G., & Gleeson, J. (2014). Off-target effect of doublecortin family shRNA on neuronal migration associated with endogenous MicroRNA dysregulation. Neuron, 82(6), 1255–1262. https://doi.org/10.1016/j.neuron.2014.04.036
View | DOI
 
[9]
2013 | Journal Article | IST-REx-ID: 1790
Novarino, G., Baek, S., & Gleeson, J. (2013). The sacred disease: The puzzling genetics of epileptic disorders. Neuron, 80(1), 9–11. https://doi.org/10.1016/j.neuron.2013.09.019
View | DOI
 
[8]
2012 | Journal Article | IST-REx-ID: 2313
Dixon Salazar, T., Silhavy, J., Udpa, N., Schroth, J., Bielas, S., Schaffer, A., … Gleeson, J. (2012). Exome sequencing can improve diagnosis and alter patient management. Science Translational Medicine, 4(138). https://doi.org/10.1126/scitranslmed.3003544
View | DOI
 
[7]
2012 | Journal Article | IST-REx-ID: 2314
Novarino, G., El Fishawy, P., Kayserili, H., Meguid, N., Scott, E., Schroth, J., … Gleeson, J. (2012). Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy. Science, 338(6105), 394–397. https://doi.org/10.1126/science.1224631
View | DOI
 
[6]
2011 | Book Review | IST-REx-ID: 2312
Novarino, G., Akizu, N., & Gleeson, J. (2011). Modeling human disease in humans: The ciliopathies. Cell. Cell Press. https://doi.org/10.1016/j.cell.2011.09.014
View | DOI
 
[5]
2010 | Book Chapter | IST-REx-ID: 2309
Stauber, T., Novarino, G., & Jentsch, T. (2010). The CLC family of chloride channels and transporters. In Physiology and Pathology of chloride transporters and channels in the nervous system (pp. 209–231). Elsevier. https://doi.org/10.1016/B978-0-12-374373-2.00012-1
View | DOI
 
[4]
2010 | Journal Article | IST-REx-ID: 2311
Rickheit, G., Wartosch, L., Schaffer, S., Stobrawa, S., Novarino, G., Weinert, S., & Jentsch, T. (2010). Role of ClC-5 in renal endocytosis is unique among ClC exchangers and does not require PY-motif-dependent ubiquitylation. Journal of Biological Chemistry, 285(23), 17595–17603. https://doi.org/10.1074/jbc.M110.115600
View | DOI
 
[3]
2010 | Journal Article | IST-REx-ID: 2310
Novarino, G., Weinert, S., Rickheit, G., & Jentsch, T. (2010). Endosomal chloride-proton exchange rather than chloride conductance is crucial for renal endocytosis. Science, 328(5984), 1398–1401. https://doi.org/10.1126/science.1188070
View | DOI
 
[2]
2005 | Journal Article | IST-REx-ID: 2307
Schwartz, J., Novarino, G., Piston, D., & Defelice, L. (2005). Substrate binding stoichiometry and kinetics of the norepinephrine transporter. Journal of Biological Chemistry, 280(19), 19177–19184. https://doi.org/10.1074/jbc.M412923200
View | DOI
 
[1]
2004 | Journal Article | IST-REx-ID: 2308
Novarino, G., Fabrizi, C., Tonini, R., Denti, M., Malchiodi, A., Lauro, G., … Mazzanti, M. (2004). Involvement of the intracellular ion channel CLIC1 in microglia-mediated β-amyloid-induced neurotoxicity. Journal of Neuroscience, 24(23), 5322–5330. https://doi.org/10.1523/JNEUROSCI.1170-04.2004
View | DOI
 

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