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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)
Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
Conference Proceeding
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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Journal Article
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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Journal Article
Autophagy-independent increase of ATG5 expression in T cells of multiple sclerosis patients
Paunovic, Verica, Petrovic, Irena Vukovic, Milenkovic, Marina, Janjetovic, Kristina, Pravica, Vera, Dujmovic, Irena, Milosevic, Emina, Martinovic, Vanja, Mesaros, Sarlota, Drulovic, Jelena, Trajkovic, Vladimir
Published in Journal of neuroimmunology (15.06.2018)
Published in Journal of neuroimmunology (15.06.2018)
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Journal Article
Distinct cell death markers identified in critical care patient survivors diagnosed with sepsis
Mallarpu, Chandra Shekar, Ponnana, Meenakshi, Prasad, Sudhir, Singarapu, Maneendra, Kim, Jean, Haririparsa, Neda, Bratic, Nemanja, Brar, Harvinder, Chelluri, Lakshmi Kiran, Madiraju, Charitha
Published in Immunology letters (01.03.2021)
Published in Immunology letters (01.03.2021)
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Journal Article