Abstract
María C. M. Aboy-Pardal, Daniel Jiménez‐Carretero, Sara Terrés-Domínguez, Dácil María Pavón, Laura Sotodosos-Alonso, Víctor Jiménez-Jiménez, Fátima Sánchez‐Cabo, Miguel Á. del Pozo
Abstract
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Junctional complexes in various epithelia
10.1083/jcb.17.2.375 · 1963
Some Aspects of the Fine Structure of the Gall Bladder Epithelium of the Mouse
10.2535/ofaj1936.45.1_11 · 1968
10.1083/jcb.201504042
10.1083/jcb.201504042
Dystrophy-associated caveolin-3 mutations reveal that caveolae couple IL6/STAT3 signaling with mechanosensing in human muscle cells
2019
10.1016/j.cub.2017.05.035
10.1016/j.cub.2017.05.035
10.1016/j.cub.2017.05.067
10.1016/j.cub.2017.05.067
10.1083/jcb.201501046
10.1083/jcb.201501046
10.1016/j.cell.2010.12.031
10.1016/j.cell.2010.12.031
Heterozygous CAV1 frameshift mutations (MIM 601047) in patients with atypical partial lipodystrophy and hypertriglyceridemia
10.1186/1476-511x-7-3 · 2008
10.1002/ajmg.a.37115
10.1002/ajmg.a.37115
10.1210/jc.2007-1328
10.1210/jc.2007-1328
Berardinelli-Seip syndrome and achalasia: a shared pathomechanism?
10.1007/s00431-015-2556-y · 2015
A frame-shift mutation in CAV1 is associated with a severe neonatal progeroid and lipodystrophy syndrome
2015
Caveolin-1 mutations (P132L and null) and the pathogenesis of breast cancer: Caveolin-1 (P132L) behaves in a dominant-negative manner and caveolin-1 (-/-) null mice show mammary epithelial cell hyperplasia
10.1016/s0002-9440(10)64412-4 · 2002
Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy
10.1186/1471-2350-14-89 · 2013
10.1172/jci38660
10.1172/jci38660
Congenital generalized lipodystrophy type 4 with muscular dystrophy: Clinical and pathological manifestations in early childhood
10.1016/j.nmd.2013.02.005 · 2013
Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutations
10.1371/journal.pgen.1000874 · 2010
Congenital generalized lipodystrophy, type 4 (CGL4) associated with myopathy due to novel PTRF mutations
10.1002/ajmg.a.33578 · 2010
10.1016/j.ejmg.2015.02.002
10.1016/j.ejmg.2015.02.002
Spectrum of clinical manifestations in two young Turkish patients with congenital generalized lipodystrophy type 4
10.1016/j.ejmg.2016.05.001 · 2016
Congenital generalized lipodystrophy: The evaluation of clinical follow-up findings in a series of five patients with type 1 and two patients with type 4
2019
Postmortem Findings in a Young Man With Congenital Generalized Lipodystrophy, Type 4 Due to CAVIN1 Mutations
10.1210/jc.2018-01331 · 2019
10.1038/s41598-021-86770-6
10.1038/s41598-021-86770-6
10.1038/s41598-019-46174-z
10.1038/s41598-019-46174-z
10.1038/s41598-018-27216-4
10.1038/s41598-018-27216-4
10.1074/jbc.m116.768499
10.1074/jbc.m116.768499
10.1371/journal.pone.0068759
10.1371/journal.pone.0068759
Caveolae - mechanosensitive membrane invaginations linked to actin filaments
2015
Caveolar domain organization and trafficking is regulated by Abl kinases and mDia1
10.1242/jcs.120816 · 2012
An Abl-FBP17 mechanosensing system couples local plasma membrane curvature and stress fiber remodeling during mechanoadaptation
2019
Membrane Curvature and Tension Control the Formation and Collapse of Caveolar Superstructures
10.1016/j.devcel.2018.12.005 · 2019
10.1038/ncb1293
10.1038/ncb1293
10.1038/nmeth.2019
10.1038/nmeth.2019
Unresolved referenced work
Kept as external metadata until matched
10.1007/s11263-019-01228-7
10.1007/s11263-019-01228-7
10.1016/0026-2862(83)90025-0
10.1016/0026-2862(83)90025-0
Endothelial plasmalemmal vesicles as elements in a system of branching invaginations from the cell surface
10.1073/pnas.76.12.6439 · 1979
No additional external references are available.