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Rare Diseases Volume 1, 2013 - Issue 1
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Addendum

Unfolded protein response, treatment and CMT1B

Yunhong Bai Department of Neurology; Carver College of Medicine; University of Iowa; Iowa City, IA USA
,
Agnes Patzko Department of Neurology; Carver College of Medicine; University of Iowa; Iowa City, IA USA
&
Michael E. Shy Department of Neurology; Carver College of Medicine; University of Iowa; Iowa City, IA USACorrespondence[email protected]
Article: e24049 | Received 11 Feb 2013, Accepted 19 Feb 2013, Published online: 20 Feb 2013

Citations (11)

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J Chad Hoyle, Michael C Isfort, Jennifer Roggenbuck & W David Arnold. (2015) The genetics of Charcot–Marie–Tooth disease: current trends and future implications for diagnosis and management. The Application of Clinical Genetics 8, pages 235-243.
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Articles from other publishers (10)

Marina Stavrou, Alexia Kagiava, Irene Sargiannidou, Elena Georgiou & Kleopas A. Kleopa. (2023) Charcot–Marie–Tooth neuropathies: Current gene therapy advances and the route toward translation . Journal of the Peripheral Nervous System 28:2, pages 150-168.
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Vera Fridman & Mario A. Saporta. (2021) Mechanisms and Treatments in Demyelinating CMT. Neurotherapeutics 18:4, pages 2236-2268.
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Marina Stavrou, Irene Sargiannidou, Elena Georgiou, Alexia Kagiava & Kleopas A. Kleopa. (2021) Emerging Therapies for Charcot-Marie-Tooth Inherited Neuropathies. International Journal of Molecular Sciences 22:11, pages 6048.
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Weronika Rzepnikowska, Joanna Kaminska, Dagmara Kabzińska, Katarzyna Binięda & Andrzej Kochański. (2020) A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: A Simple System for Complex, Heterogeneous Diseases. International Journal of Molecular Sciences 21:12, pages 4277.
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Jonathan Morena, Anirudh Gupta & J. Chad Hoyle. (2019) Charcot-Marie-Tooth: From Molecules to Therapy. International Journal of Molecular Sciences 20:14, pages 3419.
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Arne Raasakka, Salla Ruskamo, Robert Barker, Oda C. Krokengen, Guro H. Vatne, Cecilie K. Kristiansen, Erik I. Hallin, Maximilian W. A. Skoda, Ulrich Bergmann, Hanna Wacklin-Knecht, Nykola C. Jones, Søren V. Hoffmann & Petri Kursula. (2019) Neuropathy-related mutations alter the membrane binding properties of the human myelin protein P0 cytoplasmic tail. PLOS ONE 14:6, pages e0216833.
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Manisha Juneja, Joshua Burns, Mario A Saporta & Vincent Timmerman. (2019) Challenges in modelling the Charcot-Marie-Tooth neuropathies for therapy development. Journal of Neurology, Neurosurgery & Psychiatry 90:1, pages 58-67.
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Satish V. Khadilkar, Rakhil S. Yadav & Bhagyadhan A. PatelSatish V. Khadilkar, Rakhil S. Yadav & Bhagyadhan A. Patel. 2018. Neuromuscular Disorders. Neuromuscular Disorders 421 439 .
Alexander M. Rossor, Pedro J. Tomaselli & Mary M. Reilly. (2016) Recent advances in the genetic neuropathies. Current Opinion in Neurology 29:5, pages 537-548.
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Benjamin L.L. Clayton & Brian Popko. (2016) Endoplasmic reticulum stress and the unfolded protein response in disorders of myelinating glia. Brain Research 1648, pages 594-602.
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