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Items: 18

1.
Cross-Linking Mass Spectrometry Uncovers Interactions Between High-Density Lipoproteins and the SARS-CoV-2 Spike Glycoprotein
Sean A. Burnap, Ana Maria Ortega-Prieto, Jose M. Jimenez-Guardeño, Hashim Ali, Kaloyan Takov, Matthew Fish, Manu Shankar-Hari, Mauro Giacca, Michael H. Malim, Manuel Mayr
Mol Cell Proteomics. 2023 Aug; 22(8): 100600. Published online 2023 Jun 19. doi: 10.1016/j.mcpro.2023.100600
PMCID:
PMC10279469
AbstractArticlePDF–3.2M
2.
ZZW-115–dependent inhibition of NUPR1 nuclear translocation sensitizes cancer cells to genotoxic agents
Wenjun Lan, Patricia Santofimia-Castaño, Mirna Swayden, Yi Xia, Zhengwei Zhou, Stephane Audebert, Luc Camoin, Can Huang, Ling Peng, Ana Jiménez-Alesanco, Adrián Velázquez-Campoy, Olga Abián, Gwen Lomberk, Raul Urrutia, Bruno Rizzuti, Vincent Geli, Philippe Soubeyran, José L. Neira, Juan Iovanna
JCI Insight. 2020 Sep 17; 5(18): e138117. Published online 2020 Sep 17. doi: 10.1172/jci.insight.138117
PMCID:
PMC7526551
AbstractArticlePDF–9.1M
3.
Inhibition of calpain 1 restores plasma membrane stability to pharmacologically rescued Phe508del-CFTR variant
Ana M. Matos, Francisco R. Pinto, Patrícia Barros, Margarida D. Amaral, Rainer Pepperkok, Paulo Matos
J Biol Chem. 2019 Sep 6; 294(36): 13396–13410. Published online 2019 Jul 19. doi: 10.1074/jbc.RA119.008738
PMCID:
PMC6737230
AbstractArticlePDF–2.6M
4.
Interaction of Tumor Necrosis Factor Receptor-associated Factor 6 (TRAF6) and Vav3 in the Receptor Activator of Nuclear Factor κB (RANK) Signaling Complex Enhances Osteoclastogenesis
Jiyeon Yu, Hyeongseok Yun, Bongjin Shin, Yongjin Kim, Eui-Soon Park, Seunga Choi, Jungeun Yu, Dulshara Sachini Amarasekara, Sumi Kim, Jun-ichiro Inoue, Matthew C. Walsh, Yongwon Choi, Masamichi Takami, Jaerang Rho
J Biol Chem. 2016 Sep 23; 291(39): 20643–20660. Published online 2016 Aug 9. doi: 10.1074/jbc.M116.728303
PMCID:
PMC5034056
AbstractArticlePDF–5.7M
5.
SPATA2 Links CYLD to LUBAC, Activates CYLD, and Controls LUBAC Signaling
Paul R. Elliott, Derek Leske, Matous Hrdinka, Katrin Bagola, Berthe K. Fiil, Stephen H. McLaughlin, Jane Wagstaff, Norbert Volkmar, John C. Christianson, Benedikt M. Kessler, Stefan M.V. Freund, David Komander, Mads Gyrd-Hansen
Mol Cell. 2016 Sep 15; 63(6): 990–1005. doi: 10.1016/j.molcel.2016.08.001
PMCID:
PMC5031558
AbstractArticlePDF–5.9M
6.
Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy
Edwin H.A. Allen, David G. Courtney, Sarah D. Atkinson, Johnny E. Moore, Laura Mairs, Ebbe Toftgaard Poulsen, Davide Schiroli, Eleonora Maurizi, Christian Cole, Robyn P. Hickerson, John James, Helen Murgatroyd, Frances J.D. Smith, Carrie MacEwen, Jan J. Enghild, M. Andrew Nesbit, Deena M. Leslie Pedrioli, W.H. Irwin McLean, C.B. Tara Moore
Hum Mol Genet. 2016 Mar 15; 25(6): 1176–1191. Published online 2016 Jan 11. doi: 10.1093/hmg/ddw001
PMCID:
PMC4764196
AbstractArticlePDF–1.1M
7.
PAX6 Isoforms, along with Reprogramming Factors, Differentially Regulate the Induction of Cornea-specific Genes
Yuzuru Sasamoto, Ryuhei Hayashi, Sung-Joon Park, Mihoko Saito-Adachi, Yutaka Suzuki, Satoshi Kawasaki, Andrew J. Quantock, Kenta Nakai, Motokazu Tsujikawa, Kohji Nishida
Sci Rep. 2016; 6: 20807. Published online 2016 Feb 22. doi: 10.1038/srep20807
PMCID:
PMC4761963
AbstractArticlePDF–2.7M
8.
Allele-specific siRNA silencing for the common Keratin 12 founder mutation in Meesmann epithelial corneal dystrophy
Edwin H. A. Allen, Sarah D. Atkinson, Haihui Liao, Jonathan E. Moore, Deena M. Leslie Pedrioli, Frances J. D. Smith, W. H. Irwin McLean, C. B. Tara Moore
Invest Ophthalmol Vis Sci. Author manuscript; available in PMC 2013 Dec 21.
Published in final edited form as: Invest Ophthalmol Vis Sci. 2013 Jan 17; 54(1): 10.1167/iovs.12-10528. Published online 2013 Jan 17. doi: 10.1167/iovs.12-10528
PMCID:
PMC3869971
AbstractArticlePDF–2.1M
9.
Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12
H Hassan, C Thaung, N D Ebenezer, G Larkin, A J Hardcastle, S J Tuft
Eye (Lond) 2013 Mar; 27(3): 367–373. Published online 2012 Dec 7. doi: 10.1038/eye.2012.261
PMCID:
PMC3597869
AbstractArticlePDF–1.0M
10.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M
11.
Identification of a novel mutation in the cornea specific keratin 12 gene causing Meesmann`s corneal dystrophy in a German family
Ina Clausen, Gernot I.W. Duncker, Claudia Grünauer-Kloevekorn
Mol Vis. 2010; 16: 954–960. Published online 2010 May 29.
PMCID:
PMC2890559
AbstractArticlePDF–2.1M
12.
A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy
Lori S. Sullivan, Eric B. Baylin, Ramon Font, Stephen P. Daiger, Jay S. Pepose, Thomas E. Clinch, Hisashi Nakamura, Xinping C. Zhao, Richard W. Yee
Mol Vis. 2007; 13: 975–980. Published online 2007 Jun 21.
PMCID:
PMC2774455
AbstractArticlePDF–463K
13.
Proteomic Analysis of Human Parotid Gland Exosomes by Multidimensional Protein Identification Technology (MudPIT)
Mireya Gonzalez-Begne, Bingwen Lu, Xuemei Han, Fred K. Hagen, Arthur R. Hand, James E. Melvin, John R. Yates, III
J Proteome Res. Author manuscript; available in PMC 2010 Mar 6.
Published in final edited form as: J Proteome Res. 2009 Mar 6; 8(3): 1304–1314. doi: 10.1021/pr800658c
PMCID:
PMC2693447
AbstractArticlePDF–1.5M
14.
Charting the molecular network of the drug target Bcr-Abl
Marc Brehme, Oliver Hantschel, Jacques Colinge, Ines Kaupe, Melanie Planyavsky, Thomas Köcher, Karl Mechtler, Keiryn L. Bennett, Giulio Superti-Furga
Proc Natl Acad Sci U S A. 2009 May 5; 106(18): 7414–7419. Published online 2009 Apr 20. doi: 10.1073/pnas.0900653106
PMCID:
PMC2670881
AbstractArticlePDF–813K
15.
New consensus nomenclature for mammalian keratins
Jürgen Schweizer, Paul E. Bowden, Pierre A. Coulombe, Lutz Langbein, E. Birgitte Lane, Thomas M. Magin, Lois Maltais, M. Bishr Omary, David A.D. Parry, Michael A. Rogers, Mathew W. Wright
J Cell Biol. 2006 Jul 17; 174(2): 169–174. doi: 10.1083/jcb.200603161
PMCID:
PMC2064177
AbstractArticlePDF–829K
16.
A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann’s corneal dystrophy
M K Yoon, J F Warren, D S Holsclaw, D C Gritz, T P Margolis
Br J Ophthalmol. 2004 Jun; 88(6): 752–756. doi: 10.1136/bjo.2003.032870
PMCID:
PMC1772161
AbstractArticlePDF–646K
17.
A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy
L Corden, O Swensson, B Swensson, R Rochels, B Wannke, H Thiel, W McLean
Br J Ophthalmol. 2000 May; 84(5): 527–530. doi: 10.1136/bjo.84.5.527
PMCID:
PMC1723457
SummaryPDF–224K
18.
Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy.
K Nishida, Y Honma, A Dota, S Kawasaki, W Adachi, T Nakamura, A J Quantock, H Hosotani, S Yamamoto, M Okada, Y Shimomura, S Kinoshita
Am J Hum Genet. 1997 Dec; 61(6): 1268–1275. doi: 10.1086/301650
PMCID:
PMC1716060
SummaryPage BrowsePDF–1.8M

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