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SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Rubino, Elisa, Rainero, Innocenzo, Chiò, Adriano, Rogaeva, Ekaterina, Galimberti, Daniela, Fenoglio, Pierpaola, Grinberg, Yakov, Isaia, Giancarlo, Calvo, Andrea, Gentile, Salvatore, Bruni, Amalia Cecilia, St George-Hyslop, Peter Henry, Scarpini, Elio, Gallone, Salvatore, Pinessi, Lorenzo
Published in Neurology (09.10.2012)
Published in Neurology (09.10.2012)
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When autophagy meets cancer through p62/SQSTM1
Puissant, Alexandre, Fenouille, Nina, Auberger, Patrick
Published in American journal of cancer research (01.01.2012)
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Published in American journal of cancer research (01.01.2012)
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Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology
Teyssou, Elisa, Takeda, Takahiro, Lebon, Vincent, Boillée, Séverine, Doukouré, Brahima, Bataillon, Guillaume, Sazdovitch, Véronique, Cazeneuve, Cécile, Meininger, Vincent, LeGuern, Eric, Salachas, François, Seilhean, Danielle, Millecamps, Stéphanie
Published in Acta neuropathologica (01.04.2013)
Published in Acta neuropathologica (01.04.2013)
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Characteristics of Early Paget's Disease in SQSTM1 Mutation Carriers: Baseline Analysis of the ZiPP Study Cohort
Cronin, Owen, Subedi, Deepak, Forsyth, Laura, Goodman, Kirsteen, Lewis, Steff C, Keerie, Catriona, Walker, Allan, Porteous, Mary, Cetnarskyj, Roseanne, Ranganath, Lakshminarayan R, Selby, Peter L, Hampson, Geeta, Chandra, Rama, Ho, Shu, Tobias, Jon H, Young‐Min, Steven A, McKenna, Malachi J, Crowley, Rachel K, Fraser, William D, Tang, Jonathan, Gennari, Luigi, Nuti, Rannuccio, Brandi, Maria‐Luisa, Pino‐Montes, Javier, Devogelaer, Jean‐Pierre, Durnez, Anne, Isaia, Giovanni Carlo, Di Stefano, Marco, Rubio, Josep Blanch, Guanabens, Nuria, Seibel, Markus J, Walsh, John P, Kotowicz, Mark A, Nicholson, Geoffrey C, Duncan, Emma L, Major, Gabor, Horne, Anne, Gilchrist, Nigel L, Ralston, Stuart H
Published in Journal of bone and mineral research (01.07.2020)
Published in Journal of bone and mineral research (01.07.2020)
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Beyond dystonia and ataxia: Expanding the phenotype of SQSTM1 mutations
Zúñiga-Ramírez, Carlos, de Oliveira, Lais Machado, Kramis-Hollands, Mirelle, Algarni, Musleh, Soto-Escageda, Alberto, Sáenz-Farret, Michel, González-Usigli, Héctor Alberto, Fasano, Alfonso
Published in Parkinsonism & related disorders (01.05.2019)
Published in Parkinsonism & related disorders (01.05.2019)
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Recurrent Mutation of the Gene Encoding sequestosome 1 ( SQSTM1/p62) in Paget Disease of Bone
Laurin, Nancy, Brown, Jacques P., Morissette, Jean, Raymond, Vincent
Published in American journal of human genetics (01.06.2002)
Published in American journal of human genetics (01.06.2002)
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Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations
Luis, Elkin, Ortiz, Alexandra, Eudave, Luis, Ortega-Cubero, Sara, Borroni, Barbara, van der Zee, Julie, Gazzina, Stefano, Caroppo, Paola, Rubino, Elisa, D'Agata, Federico, Le Ber, Isabelle, Santana, Isabel, Cunha, Gil, Almeida, Maria R, Boutoleau-Bretonnière, Claire, Hannequin, Didier, Wallon, David, Rainero, Innocenzo, Galimberti, Daniela, Van Broeckhoven, Christine, Pastor, Maria A, Pastor, Pau
Published in Journal of Alzheimer's disease (22.06.2016)
Published in Journal of Alzheimer's disease (22.06.2016)
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Evolution of Paget's disease of bone in adults inheriting SQSTM1 mutations
Cundy, Tim, Rutland, Michael D., Naot, Dorit, Bolland, Mark
Published in Clinical endocrinology (Oxford) (01.09.2015)
Published in Clinical endocrinology (Oxford) (01.09.2015)
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The mRNA Expression of PTEN, LEF1, JAK3, LC3 and p62/SQSTM1 Genes in Patients with Chronic Myeloid Leukemia
Lak, Elahe Razmara, Tamaddon, Gholamhossein, Ramzi, Mani, Ranjbaran, Reza, Abedi, Elham, Sharifzadeh, Sedigheh
Published in Cardiovascular & hematological agents in medicinal chemistry (01.03.2023)
Published in Cardiovascular & hematological agents in medicinal chemistry (01.03.2023)
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Absence of Somatic SQSTM1 Mutations in Paget’s Disease of Bone
Matthews, Brya G., Naot, Dorit, Bava, Usha, Callon, Karen E., Pitto, Rocco P., McCowan, Stuart A., Wattie, Diana, Cundy, Tim, Cornish, Jill, Reid, Ian R.
Published in The journal of clinical endocrinology and metabolism (01.02.2009)
Published in The journal of clinical endocrinology and metabolism (01.02.2009)
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Familial Paget Disease and SQSTM1 Mutations in New Zealand
Cundy, Tim, Naot, Dorit, Bava, Usha, Musson, David, Tong, Pak Cheung, Bolland, Mark
Published in Calcified tissue international (01.09.2011)
Published in Calcified tissue international (01.09.2011)
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The signalling domain of the multiadaptor protein p62/SQSTM1 links reactive oxygen species formation and obesity to increased TNFα-mediated joint damage
Korb, Adelheid, Hillmann, Anja, Heitzmann, Marianne, Bürgis, Susanne, Kollias, George, Hermann, Sven, Schäfers, Michael, Gessner, Andre, Pap, Thomas, Weide, Thomas, Pavenstädt, Hermann
Published in Annals of the rheumatic diseases (01.02.2012)
Published in Annals of the rheumatic diseases (01.02.2012)
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Two Novel Mutations at Exon 8 of the Sequestosome 1 (SQSTM1) Gene in an Italian Series of Patients Affected by Paget's Disease of Bone (PDB)
Falchetti, Alberto, Di Stefano, Marco, Marini, Francesca, Del Monte, Francesca, Mavilia, Carmelo, Strigoli, Debora, De Feo, Maria L, Isaia, Giovan, Masi, Laura, Amedei, Antonietta, Cioppi, Federica, Ghinoi, Valentina, Bongi, Susanna Maddali, Di Fede, Giuseppina, Sferrazza, Carmela, Rini, Giovan B, Melchiorre, Daniela, Matucci‐Cerinic, Marco, Brandi, Maria L
Published in Journal of bone and mineral research (01.06.2004)
Published in Journal of bone and mineral research (01.06.2004)
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Clinical and Cellular Phenotypes Associated With Sequestosome 1 (SQSTM1) Mutations
Leach, Robin J, Singer, Frederick R, Ench, Yasmin, Wisdom, Julie H, Pina, Diana S, Johnson‐Pais, Teresa L
Published in Journal of bone and mineral research (01.12.2006)
Published in Journal of bone and mineral research (01.12.2006)
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Familial Paget's disease of bone: Long-term follow-up of unaffected relatives with and without Sequestosome 1 mutations
Peeters, Joséphine J.M., De Ridder, Raphaël, Hamoen, Esther C., Eekhoff, E. Marelise W., Smit, Frits, Boudin, Eveline, Van Hul, Wim, Papapoulos, Socrates E., Appelman-Dijkstra, Natasha M.
Published in Bone (New York, N.Y.) (01.11.2019)
Published in Bone (New York, N.Y.) (01.11.2019)
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Harnessing the Noncanonical Keap1-Nrf2 Pathway for Human Cytomegalovirus Control
Ghosh, Ayan K., Su, Yu-Pin, Forman, Michael, Keyes, Robert F., Smith, Brian C., Hu, Xin, Ferrer, Marc, Arav-Boger, Ravit
Published in Journal of virology (27.04.2023)
Published in Journal of virology (27.04.2023)
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