[HTML][HTML] Cellular functions of actin-and microtubule-associated septins
ET Spiliotis, K Nakos - Current Biology, 2021 - cell.com
Septins are an integral component of the cytoskeleton, assembling into higher-order
oligomers and filamentous polymers that associate with actin filaments, microtubules and …
oligomers and filamentous polymers that associate with actin filaments, microtubules and …
Neuralgic amyotrophy: an update on diagnosis, pathophysiology, and treatment
JJJ Van Eijk, JT Groothuis, N Van Alfen - Muscle & nerve, 2016 - Wiley Online Library
In this review we provide a current overview of the clinical features, pathophysiology,
epidemiology, and diagnostic and therapeutic strategies in neuralgic amyotrophy (NA). The …
epidemiology, and diagnostic and therapeutic strategies in neuralgic amyotrophy (NA). The …
Pain genetics: past, present and future
JS Mogil - Trends in Genetics, 2012 - cell.com
Chronic pain is a classic example of gene× environment interaction: inflammatory and/or
nerve injuries are known or suspected to be the etiology of most chronic pain syndromes …
nerve injuries are known or suspected to be the etiology of most chronic pain syndromes …
The clinical spectrum of neuralgic amyotrophy in 246 cases
N Van Alfen, BGM Van Engelen - Brain, 2006 - academic.oup.com
We investigated the symptoms, course and prognosis of neuralgic amyotrophy (NA) in a
large group of patients with idiopathic neuralgic amyotrophy (INA, n= 199) and hereditary …
large group of patients with idiopathic neuralgic amyotrophy (INA, n= 199) and hereditary …
[HTML][HTML] Genetics of Charcot-Marie-Tooth (CMT) disease within the frame of the human genome project success
V Timmerman, AV Strickland, S Züchner - Genes, 2014 - mdpi.com
Charcot-Marie-Tooth (CMT) neuropathies comprise a group of monogenic disorders
affecting the peripheral nervous system. CMT is characterized by a clinically and genetically …
affecting the peripheral nervous system. CMT is characterized by a clinically and genetically …
Neuralgic amyotrophy: a paradigm shift in diagnosis and treatment
C Gstoettner, JA Mayer, S Rassam, LA Hruby… - Journal of Neurology …, 2020 - jnnp.bmj.com
Neuralgic amyotrophy (NA), also known as Parsonage-Turner syndrome, is characterised by
sudden pain attacks, followed by patchy muscle paresis in the upper extremity. Recent …
sudden pain attacks, followed by patchy muscle paresis in the upper extremity. Recent …
Structural insight into filament formation by mammalian septins
M Sirajuddin, M Farkasovsky, F Hauer, D Kühlmann… - Nature, 2007 - nature.com
Septins are GTP-binding proteins that assemble into homo-and hetero-oligomers and
filaments. Although they have key roles in various cellular processes, little is known …
filaments. Although they have key roles in various cellular processes, little is known …
The septin family of GTPases: architecture and dynamics
CS Weirich, JP Erzberger, Y Barral - Nature reviews Molecular cell …, 2008 - nature.com
Septins comprise a conserved family of proteins that are found primarily in fungi and
animals. These GTP-binding proteins have several roles during cell division, cytoskeletal …
animals. These GTP-binding proteins have several roles during cell division, cytoskeletal …
[HTML][HTML] Entrapment of intracytosolic bacteria by septin cage-like structures
Actin-based motility is used by various pathogens for dissemination within and between
cells. Yet host factors restricting this process have not been identified. Septins are GTP …
cells. Yet host factors restricting this process have not been identified. Septins are GTP …
[HTML][HTML] PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies
BW van Paassen, AJ van der Kooi… - Orphanet journal of rare …, 2014 - Springer
Abstract PMP22 related neuropathies comprise (1) PMP22 duplications leading to Charcot-
Marie-Tooth disease type 1A (CMT1A),(2) PMP22 deletions, leading to Hereditary …
Marie-Tooth disease type 1A (CMT1A),(2) PMP22 deletions, leading to Hereditary …