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  1. 1
    Carolina Alquezar, Noemí Esteras, Ana de la Encarnación, Fermín Moreno, Adolfo López de Munain, Ángeles Martín-Requero, Increasing progranulin levels and blockade of the ERK1/2 pathway: Upstream and downstream strategies for the treatment of progranulin deficient frontotemporal dementia, European Neuropsychopharmacology, 2015,

    CrossRef

  2. 2
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  3. 3
    Joseph H. Lee, Amanda Kahn, Rong Cheng, Christiane Reitz, Badri Vardarajan, Rafael Lantigua, Martin Medrano, Ivonne Z. Jiménez-Velázquez, Jennifer Williamson, Peter Nagy, Richard Mayeux, Disease-related mutations among Caribbean Hispanics with familial dementia, Molecular Genetics & Genomic Medicine, 2014, 2, 5
  4. 4
    Bradley J. Hallam, Claudia Jacova, Ging-Yuek R. Hsiung, Dana Wittenberg, Pheth Sengdy, Phoenix Bouchard-Kerr, Penny Slack, Rosa Rademakers, Matthew Baker, Tiffany W. Chow, Brian Levine, Howard H. Feldman, Ian R. Mackenzie, Early Neuropsychological Characteristics of Progranulin Mutation Carriers, Journal of the International Neuropsychological Society, 2014, 20, 07, 694

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  5. 5
    Elena Milanesi, Andrea Pilotto, Microarray Gene and miRNA Expression Studies: Looking for New Therapeutic Targets for Frontotemporal Lobar Degeneration, Drug Development Research, 2014, 75, 6
  6. 6
    Joanna Siuda, Shinsuke Fujioka, Zbigniew K. Wszolek, Parkinsonian syndrome in familial frontotemporal dementia, Parkinsonism & Related Disorders, 2014, 20, 9, 957

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  7. 7
    Ana de la Encarnación, Carolina Alquézar, Noemí Esteras, Ángeles Martín-Requero, Progranulin Deficiency Reduces CDK4/6/pRb Activation and Survival of Human Neuroblastoma SH-SY5Y Cells, Molecular Neurobiology, 2014,

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  8. 8
    W. C. Lee, S. Almeida, M. Prudencio, T. R. Caulfield, Y.-J. Zhang, W. M. Tay, P. O. Bauer, J. Chew, H. Sasaguri, K. R. Jansen-West, T. F. Gendron, C. T. Stetler, N. Finch, I. R. Mackenzie, R. Rademakers, F.-B. Gao, L. Petrucelli, Targeted manipulation of the sortilin-progranulin axis rescues progranulin haploinsufficiency, Human Molecular Genetics, 2014, 23, 6, 1467

    CrossRef

  9. 9
    Xiao-dong Pan, Xiao-chun Chen, Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review, Translational Neurodegeneration, 2013, 2, 1, 8

    CrossRef

  10. 10
    Lubina Dillen, Tim Van Langenhove, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Stayko Sarafov, Ivailo Tournev, Celine Merlin, Patrick Cras, Rik Vandenberghe, Peter P. De Deyn, Albena Jordanova, Marc Cruts, Christine Van Broeckhoven, Julie van der Zee, Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients, Neurobiology of Aging, 2013, 34, 6, 1711.e1

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  11. 11
    Lingyan Shen, Eva Bagyinszky, Young Chul Youn, Seong Soo A. An, SangYun Kim, Genetic factors in frontotemporal dementia: A review, Toxicology and Environmental Health Sciences, 2013, 5, 3, 113

    CrossRef

  12. 12
    Gernot Kleinberger, Anja Capell, Christian Haass, Christine Van Broeckhoven, Mechanisms of Granulin Deficiency: Lessons from Cellular and Animal Models, Molecular Neurobiology, 2013, 47, 1, 337

    CrossRef

  13. 13
    E. Gómez-Tortosa, R. Guerrero-López, E. Gil-Neciga, E. Franco, T. del Ser, A. Jiménez Escrig, J. Pérez-Pérez, M. J. Sainz, Plasma progranulin levels in cortical dementia phenotypes with asymmetric perisylvian atrophy, European Journal of Neurology, 2013, 20, 9
  14. 14
    Julia Banzhaf-Strathmann, Rainer Claus, Oliver Mücke, Kristin Rentzsch, Julie van der Zee, Sebastiaan Engelborghs, Peter P De Deyn, Marc Cruts, Christine van Broeckhoven, Christoph Plass, Dieter Edbauer, Promoter DNA methylation regulates progranulin expression and is altered in FTLD, Acta Neuropathologica Communications, 2013, 1, 1, 16

    CrossRef

  15. 15
    Cinzia Coppola, Giacomina Rossi, Anna Maria Barbarulo, Giuseppe Di Fede, Carolina Foglia, Elena Piccoli, Giuseppe Piscosquito, Dario Saracino, Fabrizio Tagliavini, Roberto Cotrufo, A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration, Neurological Sciences, 2012, 33, 1, 93

    CrossRef

  16. 16
    Rosa Rademakers, Manuela Neumann, Ian R. Mackenzie, Advances in understanding the molecular basis of frontotemporal dementia, Nature Reviews Neurology, 2012,

    CrossRef

  17. 17
    Carolina Alquezar, Noemí Esteras, Fernando Bartolomé, José J. Merino, Ainhoa Alzualde, Adolfo López de Munain, Ángeles Martín-Requero, Alteration in cell cycle-related proteins in lymphoblasts from carriers of the c.709-1G>A PGRN mutation associated with FTLD-TDP dementia, Neurobiology of Aging, 2012, 33, 2, 429.e7

    CrossRef

  18. 18
    James Dominic Mills, Michal Janitz, Alternative splicing of mRNA in the molecular pathology of neurodegenerative diseases, Neurobiology of Aging, 2012, 33, 5, 1012.e11

    CrossRef

  19. 19
    H Rob Taal, Beate St Pourcain, Elisabeth Thiering, Shikta Das, Dennis O Mook-Kanamori, Nicole M Warrington, Marika Kaakinen, Eskil Kreiner-Møller, Jonathan P Bradfield, Rachel M Freathy, Frank Geller, Mònica Guxens, Diana L Cousminer, Marjan Kerkhof, Nicholas J Timpson, M Arfan Ikram, Lawrence J Beilin, Klaus Bønnelykke, Jessica L Buxton, Pimphen Charoen, Bo Lund Krogsgaard Chawes, Johan Eriksson, David M Evans, Albert Hofman, John P Kemp, Cecilia E Kim, Norman Klopp, Jari Lahti, Stephen J Lye, George McMahon, Frank D Mentch, Martina Müller-Nurasyid, Paul F O'Reilly, Inga Prokopenko, Fernando Rivadeneira, Eric A P Steegers, Jordi Sunyer, Carla Tiesler, Hanieh Yaghootkar, M Arfan Ikram, Myriam Fornage, Albert V Smith, Sudha Seshadri, Reinhold Schmidt, Stéphanie Debette, Henri A Vrooman, Sigurdur Sigurdsson, Stefan Ropele, Laura H Coker, W T Longstreth, Wiro J Niessen, Anita L DeStefano, Alexa Beiser, Alex P Zijdenbos, Maksim Struchalin, Clifford R Jack, Mike A Nalls, Rhoda Au, Albert Hofman, Haukur Gudnason, Aad van der Lugt, Tamara B Harris, William M Meeks, Meike W Vernooij, Mark A van Buchem, Diane Catellier, Vilmundur Gudnason, B Gwen Windham, Philip A Wolf, Cornelia M van Duijn, Thomas H Mosley, Helena Schmidt, Lenore J Launer, Monique M B Breteler, Charles DeCarli, Monique M B Breteler, Stéphanie Debette, Myriam Fornage, Vilmundur Gudnason, Lenore J Launer, Aad van der Lugt, Thomas H Mosley, Sudha Seshadri, Albert V Smith, Meike W Vernooij, Wei Ang, Toos van Beijsterveldt, Nienke Bergen, Kelly Benke, Diane Berry, Jonathan P Bradfield, Pimphen Charoen, Lachlan Coin, Diana L Cousminer, Shikta Das, Paul Elliott, David M Evans, Tim Frayling, Rachel M Freathy, Romy Gaillard, Maria Groen-Blokhuis, Mònica Guxens, Dexter Hadley, Jouke Jan Hottenga, Ville Huikari, Elina Hypponen, Marika Kaakinen, Matthew Kowgier, Debbie A Lawlor, Alex Lewin, Cecilia Lindgren, Julie Marsh, Christel Middeldorp, Iona Millwood, Dennis O Mook-Kanamori, Michel Nivard, Paul F O'Reilly, Lyle J Palmer, Inga Prokopenko, Alina Rodriguez, Sylvain Sebert, Ulla Sovio, Beate St Pourcain, Marie Standl, David P Strachan, Jordi Sunyer, H Rob Taal, Elisabeth Thiering, Carla Tiesler, Andre G Uitterlinden, Beatriz Valcárcel, Nicole M Warrington, Scott White, Gonneke Willemsen, Hanieh Yaghootkar, Dorret I Boomsma, Xavier Estivill, Struan F A Grant, Hakon Hakonarson, Andrew T Hattersley, Joachim Heinrich, Vincent W V Jaddoe, Marjo-Riitta Jarvelin, Mark I McCarthy, Craig E Pennell, Chris Power, Nicholas J Timpson, Elisabeth Widen, Alexandra I F Blakemore, Rosetta M Chiavacci, Bjarke Feenstra, Julio Fernandez-Banet, Struan F A Grant, Anna-Liisa Hartikainen, Albert J van der Heijden, Carmen Iñiguez, Mark Lathrop, Wendy L McArdle, Anne Mølgaard, John P Newnham, Lyle J Palmer, Aarno Palotie, Annneli Pouta, Susan M Ring, Ulla Sovio, Marie Standl, Andre G Uitterlinden, H-Erich Wichmann, Nadja Hawwa Vissing, Charles DeCarli, Cornelia M van Duijn, Mark I McCarthy, Gerard H Koppelman, Xavier Estivill, Andrew T Hattersley, Mads Melbye, Hans Bisgaard, Craig E Pennell, Elisabeth Widen, Hakon Hakonarson, George Davey Smith, Joachim Heinrich, Marjo-Riitta Jarvelin, Vincent W V Jaddoe, Linda S Adair, Wei Ang, Mustafa Atalay, Toos van Beijsterveldt, Nienke Bergen, Kelly Benke, Diane Berry, Jonathan P Bradfield, Pimphen Charoen, Lachlan Coin, Diana L Cousminer, Shikta Das, Oliver S P Davis, Paul Elliott, David M Evans, Bjarke Feenstra, Claudia Flexeder, Tim Frayling, Rachel M Freathy, Romy Gaillard, Frank Geller, Maria Groen-Blokhuis, Liang-Kee Goh, Mònica Guxens, Claire M A Haworth, Dexter Hadley, Johannes Hedebrand, Anke Hinney, Joel N Hirschhorn, John W Holloway, Claus Holst, Jouke Jan Hottenga, Momoko Horikoshi, Ville Huikari, Elina Hypponen, Carmen Iñiguez, Marika Kaakinen, Tuomas O Kilpeläinen, Mirna Kirin, Matthew Kowgier, Hanna-Maaria Lakka, Leslie A Lange, Debbie A Lawlor, Terho Lehtimäki, Alex Lewin, Cecilia Lindgren, Virpi Lindi, Reedik Maggi, Julie Marsh, Christel Middeldorp, Iona Millwood, Dennis O Mook-Kanamori, Jeffrey C Murray, Michel Nivard, Ellen Aagaard Nohr, Ioanna Ntalla, Emily Oken, Paul F O'Reilly, Lyle J Palmer, Kalliope Panoutsopoulou, Jennifer Pararajasingham, Inga Prokopenko, Alina Rodriguez, Rany M Salem, Sylvain Sebert, Niina Siitonen, Ulla Sovio, Beate St Pourcain, David P Strachan, Jordi Sunyer, H Rob Taal, Yik-Ying Teo, Elisabeth Thiering, Carla Tiesler, Andre G Uitterlinden, Beatriz Valcárcel, Nicole M Warrington, Scott White, Gonneke Willemsen, Hanieh Yaghootkar, Eleftheria Zeggini, Dorret I Boomsma, Cyrus Cooper, Xavier Estivill, Matthew Gillman, Struan F A Grant, Hakon Hakonarson, Andrew T Hattersley, Joachim Heinrich, Berthold Hocher, Vincent W V Jaddoe, Marjo-Riitta Jarvelin, Timo A Lakka, Mark I McCarthy, Mads Melbye, Karen L Mohlke, George V Dedoussis, Ken K Ong, Ewan R Pearson, Craig E Pennell, Thomas S Price, Chris Power, Olli T Raitakari, Seang-Mei Saw, Andre Scherag, Olli Simell, Thorkild I A Sørensen, Nicholas J Timpson, Elisabeth Widen, James F Wilson, Common variants at 12q15 and 12q24 are associated with infant head circumference, Nature Genetics, 2012, 44, 5, 532

    CrossRef

  20. 20
    M Arfan Ikram, Myriam Fornage, Albert V Smith, Sudha Seshadri, Reinhold Schmidt, Stéphanie Debette, Henri A Vrooman, Sigurdur Sigurdsson, Stefan Ropele, H Rob Taal, Dennis O Mook-Kanamori, Laura H Coker, W T Longstreth, Wiro J Niessen, Anita L DeStefano, Alexa Beiser, Alex P Zijdenbos, Maksim Struchalin, Clifford R Jack, Fernando Rivadeneira, Andre G Uitterlinden, David S Knopman, Anna-Liisa Hartikainen, Craig E Pennell, Elisabeth Thiering, Eric A P Steegers, Hakon Hakonarson, Joachim Heinrich, Lyle J Palmer, Marjo-Riitta Jarvelin, Mark I McCarthy, Struan F A Grant, Beate St Pourcain, Nicholas J Timpson, George Davey Smith, Ulla Sovio, Mike A Nalls, Rhoda Au, Albert Hofman, Haukur Gudnason, Aad van der Lugt, Tamara B Harris, William M Meeks, Meike W Vernooij, Mark A van Buchem, Diane Catellier, Vincent W V Jaddoe, Vilmundur Gudnason, B Gwen Windham, Philip A Wolf, Cornelia M van Duijn, Thomas H Mosley, Helena Schmidt, Lenore J Launer, Monique M B Breteler, Charles DeCarli, Linda S Adair, Wei Ang, Mustafa Atalay, Toos van Beijsterveldt, Nienke Bergen, Kelly Benke, Diane Berry, Lachlan Coin, Oliver S P Davis, Paul Elliott, Claudia Flexeder, Tim Frayling, Romy Gaillard, Maria Groen-Blokhuis, Liang-Kee Goh, Claire M A Haworth, Dexter Hadley, Johannes Hedebrand, Anke Hinney, Joel N Hirschhorn, John W Holloway, Claus Holst, Jouke Jan Hottenga, Momoko Horikoshi, Ville Huikari, Elina Hypponen, Tuomas O Kilpeläinen, Mirna Kirin, Matthew Kowgier, Hanna-Maaria Lakka, Leslie A Lange, Debbie A Lawlor, Terho Lehtimäki, Alex Lewin, Cecilia Lindgren, Virpi Lindi, Reedik Maggi, Julie Marsh, Christel Middeldorp, Iona Millwood, Jeffrey C Murray, Michel Nivard, Ellen Aagaard Nohr, Ioanna Ntalla, Emily Oken, Kalliope Panoutsopoulou, Jennifer Pararajasingham, Alina Rodriguez, Rany M Salem, Sylvain Sebert, Niina Siitonen, David P Strachan, Yik-Ying Teo, Beatriz Valcárcel, Gonneke Willemsen, Eleftheria Zeggini, Dorret I Boomsma, Cyrus Cooper, Matthew Gillman, Berthold Hocher, Timo A Lakka, Karen L Mohlke, George V Dedoussis, Ken K Ong, Ewan R Pearson, Thomas S Price, Chris Power, Olli T Raitakari, Seang-Mei Saw, Andre Scherag, Olli Simell, Thorkild I A Sørensen, James F Wilson, Common variants at 6q22 and 17q21 are associated with intracranial volume, Nature Genetics, 2012, 44, 5, 539

    CrossRef

  21. You have free access to this content21
    Christina M. Lill, Lars Bertram, Developing the “next generation” of genetic association databases for complex diseases, Human Mutation, 2012, 33, 9
  22. 22
    Marc Cruts, Jessie Theuns, Christine Van Broeckhoven, Locus-specific mutation databases for neurodegenerative brain diseases, Human Mutation, 2012, 33, 9
  23. 23
    Roberta Ghidoni, Anna Paterlini, Valentina Albertini, Giuliano Binetti, Luisa Benussi, Losing protein in the brain: The case of progranulin, Brain Research, 2012, 1476, 172

    CrossRef

  24. 24
    Roberta Ghidoni, Elena Stoppani, Giacomina Rossi, Elena Piccoli, Valentina Albertini, Anna Paterlini, Michela Glionna, Eleonora Pegoiani, Luigi F. Agnati, Chiara Fenoglio, Elio Scarpini, Daniela Galimberti, Michela Morbin, Fabrizio Tagliavini, Giuliano Binetti, Luisa Benussi, Optimal Plasma Progranulin Cutoff Value for Predicting Null Progranulin Mutations in Neurodegenerative Diseases: A Multicenter Italian Study, Neurodegenerative Diseases, 2012, 9, 3, 121

    CrossRef

  25. 25
    Alexandra M Nicholson, Jennifer Gass, Leonard Petrucelli, Rosa Rademakers, Progranulin axis and recent developments in frontotemporal lobar degeneration, Alzheimer's Research & Therapy, 2012, 4, 1, 4

    CrossRef

  26. 26
    Biruta Kierdaszuk, Mariusz Berdyński, Cezary Żekanowski, Anna Kamińska, Proteinopatie TDP-43 – od zwyrodnienia czołowo-skroniowego do wtrętowego zapalenia mięśni, Neurologia i Neurochirurgia Polska, 2012, 46, 4, 384

    CrossRef

  27. 27
    Guido M. Cavallera, Simonettta Giudici, Luca Tommasi, Shadows and darkness in the brain of a genius: Aspects of the neuropsychological literature about the final illness of Maurice Ravel (1875–1937), Medical Science Monitor, 2012, 18, 10, MH1

    CrossRef

  28. 28
    Anne Sieben, Tim Van Langenhove, Sebastiaan Engelborghs, Jean-Jacques Martin, Paul Boon, Patrick Cras, Peter-Paul De Deyn, Patrick Santens, Christine Van Broeckhoven, Marc Cruts, The genetics and neuropathology of frontotemporal lobar degeneration, Acta Neuropathologica, 2012, 124, 3, 353

    CrossRef

  29. 29
    Jeffrey L. Cummings, Alzheimer’s Disease Clinical Trials: Changing the Paradigm, Current Psychiatry Reports, 2011, 13, 6, 437

    CrossRef

  30. 30
    Jindong Xu, Maria Xilouri, Julien Bruban, Junichi Shioi, Zhiping Shao, Ioannis Papazoglou, Kostas Vekrellis, Nikolaos K. Robakis, Extracellular progranulin protects cortical neurons from toxic insults by activating survival signaling, Neurobiology of Aging, 2011, 32, 12, 2326.e5

    CrossRef

  31. 31
    Raffaele Ferrari, John Hardy, Parastoo Momeni, Frontotemporal Dementia: From Mendelian Genetics Towards Genome Wide Association Studies, Journal of Molecular Neuroscience, 2011, 45, 3, 500

    CrossRef

  32. 32
    J. van der Zee, T. Van Langenhove, G. Kleinberger, K. Sleegers, S. Engelborghs, R. Vandenberghe, P. Santens, M. Van den Broeck, G. Joris, J. Brys, M. Mattheijssens, K. Peeters, P. Cras, P. P. De Deyn, M. Cruts, C. Van Broeckhoven, TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort, Brain, 2011, 134, 3, 808

    CrossRef

  33. 33
    Vivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, Alice Chen-Plotkin, Li-San Wang, Neill R Graff-Radford, Dennis W Dickson, Rosa Rademakers, Bradley F Boeve, Murray Grossman, Steven E Arnold, David M A Mann, Stuart M Pickering-Brown, Harro Seelaar, Peter Heutink, John C van Swieten, Jill R Murrell, Bernardino Ghetti, Salvatore Spina, Jordan Grafman, John Hodges, Maria Grazia Spillantini, Sid Gilman, Andrew P Lieberman, Jeffrey A Kaye, Randall L Woltjer, Eileen H Bigio, Marsel Mesulam, Safa al-Sarraj, Claire Troakes, Roger N Rosenberg, Charles L White, Isidro Ferrer, Albert Lladó, Manuela Neumann, Hans A Kretzschmar, Christine Marie Hulette, Kathleen A Welsh-Bohmer, Bruce L Miller, Ainhoa Alzualde, Adolfo Lopez de Munain, Ann C McKee, Marla Gearing, Allan I Levey, James J Lah, John Hardy, Jonathan D Rohrer, Tammaryn Lashley, Ian R A Mackenzie, Howard H Feldman, Ronald L Hamilton, Steven T Dekosky, Julie van der Zee, Samir Kumar-Singh, Christine Van Broeckhoven, Richard Mayeux, Jean Paul G Vonsattel, Juan C Troncoso, Jillian J Kril, John B J Kwok, Glenda M Halliday, Thomas D Bird, Paul G Ince, Pamela J Shaw, Nigel J Cairns, John C Morris, Catriona Ann McLean, Charles DeCarli, William G Ellis, Stefanie H Freeman, Matthew P Frosch, John H Growdon, Daniel P Perl, Mary Sano, David A Bennett, Julie A Schneider, Thomas G Beach, Eric M Reiman, Bryan K Woodruff, Jeffrey Cummings, Harry V Vinters, Carol A Miller, Helena C Chui, Irina Alafuzoff, Päivi Hartikainen, Danielle Seilhean, Douglas Galasko, Eliezer Masliah, Carl W Cotman, M Teresa Tuñón, M Cristina Caballero Martínez, David G Munoz, Steven L Carroll, Daniel Marson, Peter F Riederer, Nenad Bogdanovic, Gerard D Schellenberg, Hakon Hakonarson, John Q Trojanowski, Virginia M-Y Lee, Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions, Nature Genetics, 2010, 42, 3, 234

    CrossRef

  34. 34
    Minerva M. Carrasquillo, Alexandra M. Nicholson, NiCole Finch, J. Raphael Gibbs, Matt Baker, Nicola J. Rutherford, Talisha A. Hunter, Mariely DeJesus-Hernandez, Gina D. Bisceglio, Ian R. Mackenzie, Andrew Singleton, Mark R. Cookson, Julia E. Crook, Allissa Dillman, Dena Hernandez, Ronald C. Petersen, Neill R. Graff-Radford, Steven G. Younkin, Rosa Rademakers, Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human Plasma, The American Journal of Human Genetics, 2010, 87, 6, 890

    CrossRef

  35. 35
    Kristel Sleegers, Marc Cruts, Christine Van Broeckhoven, Molecular Pathways of Frontotemporal Lobar Degeneration, Annual Review of Neuroscience, 2010, 33, 1, 71

    CrossRef

  36. 36
    Luisa Benussi, Roberta Ghidoni, Giuliano Binetti, Progranulin Mutations are a Common Cause of FTLD in Northern Italy, Alzheimer Disease & Associated Disorders, 2010, 24, 3, 308

    CrossRef

  37. 37
    Xue Gao, Alvin P. Joselin, Lei Wang, Amar Kar, Payal Ray, Andrew Bateman, Alison M. Goate, Jane Y. Wu, Progranulin promotes neurite outgrowth and neuronal differentiation by regulating GSK-3β, Protein & Cell, 2010, 1, 6, 552

    CrossRef

  38. 38
    Kristel Sleegers, Nathalie Brouwers, Christine Van Broeckhoven, Role of progranulin as a biomarker for Alzheimer’s disease, Biomarkers in Medicine, 2010, 4, 1, 37

    CrossRef

  39. 39
    Katie Moisse, Jennifer Mepham, Kathryn Volkening, Ian Welch, Tracy Hill, Michael J. Strong, Cytosolic TDP-43 expression following axotomy is associated with caspase 3 activation in NFL−/− mice: Support for a role for TDP-43 in the physiological response to neuronal injury, Brain Research, 2009, 1296, 176

    CrossRef

  40. 40
    Lucio Tremolizzo, Giorgio Gelosa, Alessio Galbussera, Valeria Isella, Cristina Arosio, Francesca Bertola, Giorgio Casati, Alberto Piperno, Carlo Ferrarese, Ildebrando Appollonio, Higher Than Expected Progranulin Mutation Rate in a Case Series of Italian FTLD Patients, Alzheimer Disease & Associated Disorders, 2009, 23, 3, 301

    CrossRef

  41. 41
    N. Finch, M. Baker, R. Crook, K. Swanson, K. Kuntz, R. Surtees, G. Bisceglio, A. Rovelet-Lecrux, B. Boeve, R. C. Petersen, D. W. Dickson, S. G. Younkin, V. Deramecourt, J. Crook, N. R. Graff-Radford, R. Rademakers, Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members, Brain, 2009, 132, 3, 583

    CrossRef

  42. 42
    T. D. Bird, Progranulin plasma levels in the diagnosis of frontotemporal dementia, Brain, 2009, 132, 3, 568

    CrossRef

  43. 43
    Dorothee Dormann, Anja Capell, Aaron M. Carlson, Sunita S. Shankaran, Ramona Rodde, Manuela Neumann, Elisabeth Kremmer, Takashi Matsuwaki, Keitaro Yamanouchi, Masugi Nishihara, Christian Haass, Proteolytic processing of TAR DNA binding protein-43 by caspases produces C-terminal fragments with disease defining properties independent of progranulin, Journal of Neurochemistry, 2009, 110, 3
  44. 44
    Rosa Rademakers, Anne Rovelet-Lecrux, Recent insights into the molecular genetics of dementia, Trends in Neurosciences, 2009, 32, 8, 451

    CrossRef

  45. You have free access to this content45
    Andrew Bateman, Hugh P. J. Bennett, The granulin gene family: from cancer to dementia, BioEssays, 2009, 31, 11
  46. 46
    Raffaele Ferrari, Avinash Thumma, Parastoo Momeni, Molecular Genetics of Frontotemporal Dementia, eLS,