Human stem cell models of disease and the prognosis of academic medicine von Patani, Rickie

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The microglial component of amyotrophic lateral sclerosis von Clarke, Benjamin E, Patani, Rickie

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Cellular infiltration in traumatic brain injury von Alam, Aftab, Thelin, Eric P, Tajsic, Tamara, Khan, Danyal Z, Khellaf, Abdelhakim, Patani, Rickie, Helmy, Adel

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Intron retention and nuclear loss of SFPQ are molecular hallmarks of ALS von Luisier, Raphaelle, Tyzack, Giulia E., Hall, Claire E., Mitchell, Jamie S., Devine, Helen, Taha, Doaa M., Malik, Bilal, Meyer, Ione, Greensmith, Linda, Newcombe, Jia, Ule, Jernej, Luscombe, Nicholas M., Patani, Rickie

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A Liquid to Solid Phase Transition Underlying Pathological Huntingtin Exon1 Aggregation von Peskett, Thomas R., Rau, Frédérique, O’Driscoll, Jonathan, Patani, Rickie, Lowe, Alan R., Saibil, Helen R.

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Generating Diverse Spinal Motor Neuron Subtypes from Human Pluripotent Stem Cells von Patani, Rickie

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Autologous mesenchymal stem cells for the treatment of secondary progressive multiple sclerosis: an open-label phase 2a proof-of-concept study von Connick, Peter, MRCP, Kolappan, Madhan, MRCP, Crawley, Charles, FRCP, Webber, Daniel J, PhD, Patani, Rickie, MRCP, Michell, Andrew W, PhD, Du, Ming-Qing, Prof, Luan, Shi-Lu, PhD, Altmann, Daniel R, PhD, Thompson, Alan J, Prof, Compston, Alastair, Prof, Scott, Michael A, PhD, Miller, David H, Prof, Chandran, Siddharthan, Prof

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Major Shifts in Glial Regional Identity Are a Transcriptional Hallmark of Human Brain Aging von Soreq, Lilach, Rose, Jamie, Soreq, Eyal, Hardy, John, Trabzuni, Daniah, Cookson, Mark R., Smith, Colin, Ryten, Mina, Patani, Rickie, Ule, Jernej

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TDP-43 condensation properties specify its RNA-binding and regulatory repertoire von Hallegger, Martina, Chakrabarti, Anob M., Lee, Flora C.Y., Lee, Bo Lim, Amalietti, Aram G., Odeh, Hana M., Copley, Katie E., Rubien, Jack D., Portz, Bede, Kuret, Klara, Huppertz, Ina, Rau, Frédérique, Patani, Rickie, Fawzi, Nicolas L., Shorter, James, Luscombe, Nicholas M., Ule, Jernej

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Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosis von Tyzack, Giulia E, Luisier, Raphaelle, Taha, Doaa M, Neeves, Jacob, Modic, Miha, Mitchell, Jamie S, Meyer, Ione, Greensmith, Linda, Newcombe, Jia, Ule, Jernej, Luscombe, Nicholas M, Patani, Rickie

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Distinct responses of neurons and astrocytes to TDP-43 proteinopathy in amyotrophic lateral sclerosis von Smethurst, Phillip, Risse, Emmanuel, Tyzack, Giulia E, Mitchell, Jamie S, Taha, Doaa M, Chen, Yun-Ru, Newcombe, Jia, Collinge, John, Sidle, Katie, Patani, Rickie

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In vitro prion-like behaviour of TDP-43 in ALS von Smethurst, Phillip, Newcombe, Jia, Troakes, Claire, Simone, Roberto, Chen, Yun-Ru, Patani, Rickie, Sidle, Katie

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Therapeutic potential of APP antisense oligonucleotides for Alzheimer's disease and down syndrome-related Alzheimer's disease von Thirumalai, Srishruthi, Patani, Rickie, Hung, Christy

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Regionally encoded functional heterogeneity of astrocytes in health and disease: A perspective von Clarke, Benjamin E., Taha, Doaa M., Tyzack, Giulia E., Patani, Rickie

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Harnessing cellular aging in human stem cell models of amyotrophic lateral sclerosis von Ziff, Oliver J., Patani, Rickie

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Characterizing the RNA targets and position-dependent splicing regulation by TDP-43 von Tollervey, James R, Curk, Tomaž, Rogelj, Boris, Briese, Michael, Cereda, Matteo, Kayikci, Melis, König, Julian, Hortobágyi, Tibor, Nishimura, Agnes L, Župunski, Vera, Patani, Rickie, Chandran, Siddharthan, Rot, Gregor, Zupan, Blaž, Shaw, Christopher E, Ule, Jernej

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Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering von Maffioletti, Sara Martina, Sarcar, Shilpita, Henderson, Alexander B.H., Mannhardt, Ingra, Pinton, Luca, Moyle, Louise Anne, Steele-Stallard, Heather, Cappellari, Ornella, Wells, Kim E., Ferrari, Giulia, Mitchell, Jamie S., Tyzack, Giulia E., Kotiadis, Vassilios N., Khedr, Moustafa, Ragazzi, Martina, Wang, Weixin, Duchen, Michael R., Patani, Rickie, Zammit, Peter S., Wells, Dominic J., Eschenhagen, Thomas, Tedesco, Francesco Saverio

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Gene expression analysis reveals early dysregulation of disease pathways and links Chmp7 to pathogenesis of spinal and bulbar muscular atrophy von Malik, Bilal, Devine, Helen, Patani, Rickie, La Spada, Albert R., Hanna, Michael G., Greensmith, Linda

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Integrated transcriptome landscape of ALS identifies genome instability linked to TDP-43 pathology von Ziff, Oliver J., Neeves, Jacob, Mitchell, Jamie, Tyzack, Giulia, Martinez-Ruiz, Carlos, Luisier, Raphaelle, Chakrabarti, Anob M., McGranahan, Nicholas, Litchfield, Kevin, Boulton, Simon J., Al-Chalabi, Ammar, Kelly, Gavin, Humphrey, Jack, Patani, Rickie

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A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models von Tyzack, Giulia E., Hall, Claire E., Sibley, Christopher R., Cymes, Tomasz, Forostyak, Serhiy, Carlino, Giulia, Meyer, Ione F., Schiavo, Giampietro, Zhang, Su-Chun, Gibbons, George M., Newcombe, Jia, Patani, Rickie, Lakatos, András

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