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Items: 1 to 20 of 32

1.
Syntaxin-3 is dispensable for basal neurotransmission and synaptic plasticity in postsynaptic hippocampal CA1 neurons
Shan Shi, Ke Ma, Na-Ryum Bin, Hidekiyo Harada, Xiaoyu Xie, Mengjia Huang, Haiyu Liu, Soomin Lee, Xue Fan Wang, Roberto Adachi, Philippe P. Monnier, Liang Zhang, Shuzo Sugita
Sci Rep. 2020; 10: 709. Published online 2020 Jan 20. doi: 10.1038/s41598-019-57388-6
PMCID:
PMC6971263
AbstractArticlePDF–1.7M
2.
The dendritic SNARE fusion machinery involved in AMPARs insertion during long-term potentiation
Sandra Jurado
Front Cell Neurosci. 2014; 8: 407. Prepublished online 2014 Oct 22. Published online 2014 Dec 22. doi: 10.3389/fncel.2014.00407
PMCID:
PMC4273633
AbstractArticlePDF–710K
3.
Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects
Andreas R. Janecke, Xiaoqin Liu, Rüdiger Adam, Sumanth Punuru, Arne Viestenz, Valeria Strauß, Martin Laass, Elizabeth Sanchez, Roberto Adachi, Martha P. Schatz, Ujwala S. Saboo, Naveen Mittal, Klaus Rohrschneider, Johanna Escher, Anuradha Ganesh, Sana Al Zuhaibi, Fathiya Al Murshedi, Badr AlSaleem, Majid Alfadhel, Siham Al Sinani, Fowzan S. Alkuraya, Lukas A. Huber, Thomas Müller, Ruth Heidelberger, Roger Janz
Hum Genet. 2021; 140(8): 1143–1156. Published online 2021 May 11. doi: 10.1007/s00439-021-02284-1
PMCID:
PMC8263458
AbstractArticlePDF–3.5M
4.
SYNTAXIN 3B IS A T-SNARE SPECIFIC FOR RIBBON SYNAPSES OF THE RETINA
LEIGH B. CURTIS, BLAIR DONESKE, XIAOQIN LIU, CHRISTINA THALLER, JAMES A. MCNEW, ROGER JANZ
J Comp Neurol. Author manuscript; available in PMC 2010 Jun 28.
Published in final edited form as: J Comp Neurol. 2008 Oct 10; 510(5): 550–559. doi: 10.1002/cne.21806
PMCID:
PMC2893228
AbstractArticlePDF–507K
5.
Syntaxin 3 is essential for photoreceptor outer segment protein trafficking and survival
Mashal Kakakhel, Lars Tebbe, Mustafa S. Makia, Shannon M. Conley, David M. Sherry, Muayyad R. Al-Ubaidi, Muna I. Naash
Proc Natl Acad Sci U S A. 2020 Aug 25; 117(34): 20615–20624. Published online 2020 Aug 10. doi: 10.1073/pnas.2010751117
PMCID:
PMC7456102
AbstractArticlePDF–3.6M
6.
Syntaxin 3, but not syntaxin 4, is required for mast cell–regulated exocytosis, where it plays a primary role mediating compound exocytosis
Elizabeth Sanchez, Erika A. Gonzalez, David S. Moreno, Rodolfo A. Cardenas, Marco A. Ramos, Alfredo J. Davalos, John Manllo, Alejandro I. Rodarte, Youlia Petrova, Daniel C. Moreira, Miguel A. Chavez, Alejandro Tortoriello, Adolfo Lara, Berenice A. Gutierrez, Alan R. Burns, Ruth Heidelberger, Roberto Adachi
J Biol Chem. 2019 Mar 1; 294(9): 3012–3023. Published online 2018 Dec 18. doi: 10.1074/jbc.RA118.005532
PMCID:
PMC6398129
AbstractArticlePDF–2.4M
7.
Phosphorylation of Syntaxin 3B by CaMKII regulates the formation of t-SNARE complexes
XIAOQIN LIU, RUTH HEIDELBERGER, ROGER JANZ
Mol Cell Neurosci. Author manuscript; available in PMC 2015 May 1.
Published in final edited form as: Mol Cell Neurosci. 2014 May; 60: 53–62. Published online 2014 Mar 27. doi: 10.1016/j.mcn.2014.03.002
PMCID:
PMC4066811
AbstractArticlePDF–3.4M
8.
Rab11a regulates syntaxin 3 localization and microvillus assembly in enterocytes
Byron C. Knowles, Victoria G. Weis, Shiyan Yu, Joseph T. Roland, Janice A. Williams, Gabriela S. Alvarado, Lynne A. Lapierre, Mitchell D. Shub, Nan Gao, James R. Goldenring
J Cell Sci. 2015 Apr 15; 128(8): 1617–1626. doi: 10.1242/jcs.163303
PMCID:
PMC4518445
AbstractArticle
9.
SNAREs and SNARE regulators in membrane fusion and exocytosis
J. E. Gerst
Cell Mol Life Sci. 1999 May; 55(5): 707–734. Published online 2014 Jan 30. doi: 10.1007/s000180050328
PMCID:
PMC11146948
AbstractArticlePDF–433K
10.
AQP2 exocytosis in the renal collecting duct – involvement of SNARE isoforms and the regulatory role of Munc18b
Giuseppe Procino, Claudia Barbieri, Grazia Tamma, Leonarda De Benedictis, Jeffrey E. Pessin, Maria Svelto, Giovanna Valenti
J Cell Sci. Author manuscript; available in PMC 2015 Feb 14.
Published in final edited form as: J Cell Sci. 2008 Jun 15; 121(0 12): 2097–2106. Published online 2008 May 27. doi: 10.1242/jcs.022210
PMCID:
PMC4327994
AbstractArticlePDF–592K
11.
Loss of MYO5B in Mice Recapitulates Microvillus Inclusion Disease and Reveals an Apical Trafficking Pathway Distinct to Neonatal Duodenum
Victoria G. Weis, Byron C. Knowles, Eunyoung Choi, Anna E. Goldstein, Janice A. Williams, Elizabeth H. Manning, Joseph T. Roland, Lynne A. Lapierre, James R. Goldenring
Cell Mol Gastroenterol Hepatol. 2016 Mar; 2(2): 131–157. Published online 2015 Dec 12. doi: 10.1016/j.jcmgh.2015.11.009
PMCID:
PMC4806369
AbstractArticlePDF–12M
12.
LTP Requires a Unique Postsynaptic SNARE Fusion Machinery
Sandra Jurado, Debanjan Goswami, Yingsha Zhang, Alfredo J. Miñano Molina, Thomas C. Südhof, Robert C. Malenka
Neuron. Author manuscript; available in PMC 2014 Feb 6.
Published in final edited form as: Neuron. 2013 Feb 6; 77(3): 542–558. doi: 10.1016/j.neuron.2012.11.029
PMCID:
PMC3569727
AbstractArticlePDF–6.2M
13.
VAMP8 is the v-SNARE that mediates basolateral exocytosis in a mouse model of alcoholic pancreatitis
Laura I. Cosen-Binker, Marcelo G. Binker, Cheng-Chun Wang, Wanjin Hong, Herbert Y. Gaisano
J Clin Invest. 2008 Jul 1; 118(7): 2535–2551. Published online 2008 Jun 5. doi: 10.1172/JCI34672
PMCID:
PMC2413188
AbstractArticlePDF–2.0M
14.
Sdmg1 is a conserved transmembrane protein associated with germ cell sex determination and germline-soma interactions in mice
Diana Best, Daniela A. Sahlender, Norbert Walther, Andrew A. Peden, Ian R. Adams
Development. Author manuscript; available in PMC 2008 Nov 18.
Published in final edited form as: Development. 2008 Apr; 135(8): 1415–1425. Published online 2008 Mar 5. doi: 10.1242/dev.019497
PMCID:
PMC2584365
AbstractArticlePDF–3.5M
15.
Global Analysis of Gene Expression in the Developing Brain of Gtf2ird1 Knockout Mice
Jennifer O'Leary, Lucy R. Osborne
PLoS One. 2011; 6(8): e23868. Published online 2011 Aug 31. doi: 10.1371/journal.pone.0023868
PMCID:
PMC3166129
AbstractArticlePDF–436K
16.
The splicing regulator Rbfox2 is required for both cerebellar development and mature motor function
Lauren T. Gehman, Pratap Meera, Peter Stoilov, Lily Shiue, Janelle E. O'Brien, Miriam H. Meisler, Manuel Ares, Jr., Thomas S. Otis, Douglas L. Black
Genes Dev. 2012 Mar 1; 26(5): 445–460. doi: 10.1101/gad.182477.111
PMCID:
PMC3305983
AbstractArticlePDF–2.2M
17.
A Mutation in the Srrm4 Gene Causes Alternative Splicing Defects and Deafness in the Bronx Waltzer Mouse
Yoko Nakano, Israt Jahan, Gregory Bonde, Xingshen Sun, Michael S. Hildebrand, John F. Engelhardt, Richard J. H. Smith, Robert A. Cornell, Bernd Fritzsch, Botond Bánfi
PLoS Genet. 2012 Oct; 8(10): e1002966. Published online 2012 Oct 4. doi: 10.1371/journal.pgen.1002966
PMCID:
PMC3464207
AbstractArticlePDF–4.1M
18.
The Deubiquitinating Enzyme USP48 Interacts with the Retinal Degeneration-Associated Proteins UNC119a and ARL3
Laura Sánchez-Bellver, Andrea Férriz-Gordillo, Marc Carrillo-Pz, Laura Rabanal, Francesc R. Garcia-Gonzalo, Gemma Marfany
Int J Mol Sci. 2022 Oct; 23(20): 12527. Published online 2022 Oct 19. doi: 10.3390/ijms232012527
PMCID:
PMC9603860
AbstractArticlePDF–3.4M
19.
Genomic Analysis of Mouse Retinal Development
Seth Blackshaw, Sanjiv Harpavat, Jeff Trimarchi, Li Cai, Haiyan Huang, Winston P Kuo, Griffin Weber, Kyungjoon Lee, Rebecca E Fraioli, Seo-Hee Cho, Rachel Yung, Elizabeth Asch, Lucila Ohno-Machado, Wing H Wong, Constance L Cepko
PLoS Biol. 2004 Sep; 2(9): e247. Published online 2004 Jun 29. doi: 10.1371/journal.pbio.0020247
PMCID:
PMC439783
AbstractArticlePDF–975K
20.
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
AbstractArticlePDF–3.0M

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