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Items: 1 to 20 of 25

1.
Tricellulin secures the epithelial barrier at tricellular junctions by interacting with actomyosin
Yuma Cho, Daichi Haraguchi, Kenta Shigetomi, Kenji Matsuzawa, Seiichi Uchida, Junichi Ikenouchi
J Cell Biol. 2022 Apr 4; 221(4): e202009037. Published online 2022 Feb 11. doi: 10.1083/jcb.202009037
PMCID:
PMC8847807
ArticlePDF–10M
2.
Tricellulin Expression and its Deletion Effects in the Endolymphatic Sac
Ai Matsubara, Takenori Miyashita, Ryuhei Inamoto, Hirofumi Sakaguchi, Toru Kamitani, Nozomu Mori, Hiroshi Hoshikawa
J Int Adv Otol. 2018 Aug; 14(2): 312–316. Published online 2018 Aug 3. doi: 10.5152/iao.2018.5473
PMCID:
PMC6354451
ArticlePDF–2.5M
3.
Deletion of Tricellulin Causes Progressive Hearing Loss Associated with Degeneration of Cochlear Hair Cells
Toru Kamitani, Hirofumi Sakaguchi, Atsushi Tamura, Takenori Miyashita, Yuji Yamazaki, Reitaro Tokumasu, Ryuhei Inamoto, Ai Matsubara, Nozomu Mori, Yasuo Hisa, Sachiko Tsukita
Sci Rep. 2015; 5: 18402. Published online 2015 Dec 18. doi: 10.1038/srep18402
PMCID:
PMC4683410
ArticlePDF–2.4M
4.
Histone deacetylase inhibition prevents cell death induced by loss of tricellular tight junction proteins in temperature-sensitive mouse cochlear cells
Kenichi Takano, Takuya Kakuki, Yakuto Kaneko, Takayuki Kohno, Shin Kikuchi, Tetsuo Himi, Takashi Kojima
PLoS One. 2017; 12(8): e0182291. Published online 2017 Aug 2. doi: 10.1371/journal.pone.0182291
PMCID:
PMC5540400
ArticlePDF–11M
5.
ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells
Eva L. Morozko, Ayako Nishio, Neil J. Ingham, Rashmi Chandra, Tracy Fitzgerald, Elisa Martelletti, Guntram Borck, Elizabeth Wilson, Gavin P. Riordan, Philine Wangemann, Andrew Forge, Karen P. Steel, Rodger A. Liddle, Thomas B. Friedman, Inna A. Belyantseva
Hum Mol Genet. 2015 Feb 1; 24(3): 609–624. Published online 2014 Sep 12. doi: 10.1093/hmg/ddu474
PMCID:
PMC4291242
ArticlePDF–1.8M
6.
Loss of Occludin Affects Tricellular Localization of Tricellulin
Junichi Ikenouchi, Hiroyuki Sasaki, Sachiko Tsukita, Mikio Furuse, Shoichiro Tsukita
Mol Biol Cell. 2008 Nov; 19(11): 4687–4693. doi: 10.1091/mbc.E08-05-0530
PMCID:
PMC2575184
ArticlePDF–1.4M
7.
Tricellulin Is a Tight-Junction Protein Necessary for Hearing
Saima  Riazuddin, Zubair M.  Ahmed, Alan S.  Fanning, Ayala  Lagziel, Shin-ichiro  Kitajiri, Khushnooda  Ramzan, Shaheen N.  Khan, Parna  Chattaraj, Penelope L.  Friedman, James M.  Anderson, Inna A.  Belyantseva, Andrew  Forge, Sheikh  Riazuddin, Thomas B.  Friedman
Am J Hum Genet. 2006 Dec; 79(6): 1040–1051. Published online 2006 Oct 31. doi: 10.1086/510022
PMCID:
PMC1698716
ArticlePDF–7.4M
8.
Tricellulin, α-Catenin and Microfibrillar-Associated Protein 5 Exhibit Concomitantly Altered Immunosignals along with Vascular, Extracellular and Cytoskeletal Elements after Experimental Focal Cerebral Ischemia
Corinna Höfling, Steffen Roßner, Bianca Flachmeyer, Martin Krueger, Wolfgang Härtig, Dominik Michalski
Int J Mol Sci. 2023 Aug; 24(15): 11893. Published online 2023 Jul 25. doi: 10.3390/ijms241511893
PMCID:
PMC10418498
ArticlePDF–5.9M
9.
Tricellulin Is Expressed in Autotypic Tight Junctions of Peripheral Myelinating Schwann Cells
Shin Kikuchi, Takafumi Ninomiya, Haruyuki Tatsumi, Norimasa Sawada, Takashi Kojima
J Histochem Cytochem. 2010 Dec; 58(12): 1067–1073. doi: 10.1369/jhc.2010.956326
PMCID:
PMC2989243
ArticlePDF–1.1M
10.
Tricellulin constitutes a novel barrier at tricellular contacts of epithelial cells
Junichi Ikenouchi, Mikio Furuse, Kyoko Furuse, Hiroyuki Sasaki, Sachiko Tsukita, Shoichiro Tsukita
J Cell Biol. 2005 Dec 19; 171(6): 939–945. doi: 10.1083/jcb.200510043
PMCID:
PMC2171318
ArticlePDF–1.2M
11.
Tricellulin deficiency affects tight junction architecture and cochlear hair cells
Gowri Nayak, Sue I. Lee, Rizwan Yousaf, Stephanie E. Edelmann, Claire Trincot, Christina M. Van Itallie, Ghanshyam P. Sinha, Maria Rafeeq, Sherri M. Jones, Inna A. Belyantseva, James M. Anderson, Andrew Forge, Gregory I. Frolenkov, Saima Riazuddin
J Clin Invest. 2013 Sep 3; 123(9): 4036–4049. Published online 2013 Aug 27. doi: 10.1172/JCI69031
PMCID:
PMC3754262
ArticlePDF–6.2M
12.
Tight Junction–associated MARVEL Proteins MarvelD3, Tricellulin, and Occludin Have Distinct but Overlapping Functions
David R. Raleigh, Amanda M. Marchiando, Yong Zhang, Le Shen, Hiroyuki Sasaki, Yingmin Wang, Manyuan Long, Jerrold R. Turner
Mol Biol Cell. 2010 Apr 1; 21(7): 1200–1213. doi: 10.1091/mbc.E09-08-0734
PMCID:
PMC2847524
ArticlePDF–3.9M
13.
Spatio-temporal expression pattern and role of the tight junction protein MarvelD3 in pancreas development and function
Charlotte Heymans, Ophélie Delcorte, Catherine Spourquet, Mylah Villacorte-Tabelin, Sébastien Dupasquier, Younes Achouri, Siam Mahibullah, Pascale Lemoine, Maria S. Balda, Karl Matter, Christophe E. Pierreux
Sci Rep. 2021; 11: 14519. Published online 2021 Jul 15. doi: 10.1038/s41598-021-93654-2
PMCID:
PMC8282860
ArticlePDF–6.6M
14.
Claudin-9 constitutes tight junctions of folliculo-stellate cells in the anterior pituitary gland
Atsuko Y. Higashi, Tomohito Higashi, Kyoko Furuse, Kana Ozeki, Mikio Furuse, Hideki Chiba
Sci Rep. 2021; 11: 21642. Published online 2021 Nov 4. doi: 10.1038/s41598-021-01004-z
PMCID:
PMC8568902
ArticlePDF–7.0M
15.
Understanding the development of oral epithelial organs through single cell transcriptomic analysis
Qianlin Ye, Arshia Bhojwani, Jimmy K. Hu
Development. 2022 Aug 15; 149(16): dev200539. Published online 2022 Aug 17. doi: 10.1242/dev.200539
PMCID:
PMC9481975
Article
16.
High-throughput discovery of novel developmental phenotypes
Mary E. Dickinson, Ann M. Flenniken, Xiao Ji, Lydia Teboul, Michael D. Wong, Jacqueline K. White, Terrence F. Meehan, Wolfgang J. Weninger, Henrik Westerberg, Hibret Adissu, Candice N. Baker, Lynette Bower, James M. Brown, L. Brianna Caddle, Francesco Chiani, Dave Clary, James Cleak, Mark J. Daly, James M. Denegre, Brendan Doe, Mary E. Dolan, Sarah M. Edie, Helmut Fuchs, Valerie Gailus-Durner, Antonella Galli, Alessia Gambadoro, Juan Gallegos, Shiying Guo, Neil R. Horner, Chih-wei Hsu, Sara J. Johnson, Sowmya Kalaga, Lance C. Keith, Louise Lanoue, Thomas N. Lawson, Monkol Lek, Manuel Mark, Susan Marschall, Jeremy Mason, Melissa L. McElwee, Susan Newbigging, Lauryl M.J. Nutter, Kevin A. Peterson, Ramiro Ramirez-Solis, Douglas J. Rowland, Edward Ryder, Kaitlin E. Samocha, John R. Seavitt, Mohammed Selloum, Zsombor Szoke-Kovacs, Masaru Tamura, Amanda G Trainor, Ilinca Tudose, Shigeharu Wakana, Jonathan Warren, Olivia Wendling, David B. West, Leeyean Wong, Atsushi Yoshiki, The International Mouse Phenotyping Consortium, Daniel G. MacArthur, Glauco P. Tocchini-Valentini, Xiang Gao, Paul Flicek, Allan Bradley, William C. Skarnes, Monica J. Justice, Helen E. Parkinson, Mark Moore, Sara Wells, Robert E. Braun, Karen L. Svenson, Martin Hrabe de Angelis, Yann Herault, Tim Mohun, Ann-Marie Mallon, R. Mark Henkelman, Steve D.M. Brown, David J. Adams, K.C. Kent Lloyd, Colin McKerlie, Arthur L. Beaudet, Maja Bucan, Stephen A. Murray
Nature. Author manuscript; available in PMC 2017 Mar 14.
Published in final edited form as: Nature. 2016 Sep 22; 537(7621): 508–514. Published online 2016 Sep 14. doi: 10.1038/nature19356
Correction in:
Nature. 2017 Nov 16; 551(7680): 398.
PMCID:
PMC5295821
ArticlePDF–3.0M
17.
The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data
Gautier Koscielny, Gagarine Yaikhom, Vivek Iyer, Terrence F. Meehan, Hugh Morgan, Julian Atienza-Herrero, Andrew Blake, Chao-Kung Chen, Richard Easty, Armida Di Fenza, Tanja Fiegel, Mark Grifiths, Alan Horne, Natasha A. Karp, Natalja Kurbatova, Jeremy C. Mason, Peter Matthews, Darren J. Oakley, Asfand Qazi, Jack Regnart, Ahmad Retha, Luis A. Santos, Duncan J. Sneddon, Jonathan Warren, Henrik Westerberg, Robert J. Wilson, David G. Melvin, Damian Smedley, Steve D. M. Brown, Paul Flicek, William C. Skarnes, Ann-Marie Mallon, Helen Parkinson
Nucleic Acids Res. 2014 Jan 1; 42(Database issue): D802–D809. Published online 2013 Nov 3. doi: 10.1093/nar/gkt977
PMCID:
PMC3964955
ArticlePDF–5.7M
18.
BraInMap elucidates the macromolecular connectivity landscape of mammalian brain
Reza Pourhaghighi, Peter E. A. Ash, Sadhna Phanse, Florian Goebels, Lucas Z. M. Hu, Siwei Chen, Yingying Zhang, Shayne D. Wierbowski, Samantha Boudeau, Mohamed T. Moutaoufik, Ramy H. Malty, Edyta Malolepsza, Kalliopi Tsafou, Aparna Nathan, Graham Cromar, Hongbo Guo, Ali Al Abdullatif, Daniel J. Apicco, Lindsay A. Becker, Aaron D. Gitler, Stefan M. Pulst, Ahmed Youssef, Ryan Hekman, Pierre C. Havugimana, Carl A. White, Benjamin C. Blum, Antonia Ratti, Camron D. Bryant, John Parkinson, Kasper Lage, Mohan Babu, Haiyuan Yu, Gary D. Bader, Benjamin Wolozin, Andrew Emili
Cell Syst. Author manuscript; available in PMC 2021 Apr 22.
Published in final edited form as: Cell Syst. 2020 Apr 22; 10(4): 333–350.e14. doi: 10.1016/j.cels.2020.03.003
Correction in:
Cell Syst. 2020 Aug 26; 11(2): 208.
PMCID:
PMC7938770
ArticlePDF–2.0M
19.
A conditional knockout resource for the genome–wide study of mouse gene function
William C. Skarnes, Barry Rosen, Anthony P. West, Manousos Koutsourakis, Wendy Bushell, Vivek Iyer, Alejandro O. Mujica, Mark Thomas, Jennifer Harrow, Tony Cox, David Jackson, Jessica Severin, Patrick Biggs, Jun Fu, Michael Nefedov, Pieter J. de Jong, A. Francis Stewart, Allan Bradley
Nature. Author manuscript; available in PMC 2013 Feb 14.
Published in final edited form as: Nature. 2011 Jun 15; 474(7351): 337–342. Published online 2011 Jun 15. doi: 10.1038/nature10163
PMCID:
PMC3572410
ArticlePDF–1.1M
20.
A High-Resolution Anatomical Atlas of the Transcriptome in the Mouse Embryo
Graciana Diez-Roux, Sandro Banfi, Marc Sultan, Lars Geffers, Santosh Anand, David Rozado, Alon Magen, Elena Canidio, Massimiliano Pagani, Ivana Peluso, Nathalie Lin-Marq, Muriel Koch, Marchesa Bilio, Immacolata Cantiello, Roberta Verde, Cristian De Masi, Salvatore A. Bianchi, Juliette Cicchini, Elodie Perroud, Shprese Mehmeti, Emilie Dagand, Sabine Schrinner, Asja Nürnberger, Katja Schmidt, Katja Metz, Christina Zwingmann, Norbert Brieske, Cindy Springer, Ana Martinez Hernandez, Sarah Herzog, Frauke Grabbe, Cornelia Sieverding, Barbara Fischer, Kathrin Schrader, Maren Brockmeyer, Sarah Dettmer, Christin Helbig, Violaine Alunni, Marie-Annick Battaini, Carole Mura, Charlotte N. Henrichsen, Raquel Garcia-Lopez, Diego Echevarria, Eduardo Puelles, Elena Garcia-Calero, Stefan Kruse, Markus Uhr, Christine Kauck, Guangjie Feng, Nestor Milyaev, Chuang Kee Ong, Lalit Kumar, MeiSze Lam, Colin A. Semple, Attila Gyenesei, Stefan Mundlos, Uwe Radelof, Hans Lehrach, Paolo Sarmientos, Alexandre Reymond, Duncan R. Davidson, Pascal Dollé, Stylianos E. Antonarakis, Marie-Laure Yaspo, Salvador Martinez, Richard A. Baldock, Gregor Eichele, Andrea Ballabio
PLoS Biol. 2011 Jan; 9(1): e1000582. Published online 2011 Jan 18. doi: 10.1371/journal.pbio.1000582
PMCID:
PMC3022534
ArticlePDF–3.8M

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