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Items: 1 to 20 of 46

1.
The modular nature of apoptotic signaling proteins
K. Hofmann
Cell Mol Life Sci. 1999 Jul; 55(8-9): 1113–1128. doi: 10.1007/s000180050361
PMCID:
PMC11146888
AbstractArticlePDF–923K
2.
Ankyrin-R Links Kv3.3 to the Spectrin Cytoskeleton and Is Required for Purkinje Neuron Survival
Sharon R. Stevens, Meike E. van der Heijden, Yuki Ogawa, Tao Lin, Roy V. Sillitoe, Matthew N. Rasband
J Neurosci. 2022 Jan 5; 42(1): 2–15. doi: 10.1523/JNEUROSCI.1132-21.2021
PMCID:
PMC8741159
AbstractArticlePDF–7.0M
3.
Ankyrin-dependent Na+ channel clustering prevents neuromuscular synapse fatigue
Chuansheng Zhang, Abhijeet Joshi, Yanhong Liu, Ozlem Sert, Seth Haddix, Lindsay H. Teliska, Anne Rasband, George G. Rodney, Matthew N. Rasband
Curr Biol. Author manuscript; available in PMC 2022 Sep 13.
Published in final edited form as: Curr Biol. 2021 Sep 13; 31(17): 3810–3819.e4. Published online 2021 Jul 20. doi: 10.1016/j.cub.2021.06.052
PMCID:
PMC8440394
AbstractArticlePDF–1.9M
4.
Ankyrin-R regulates fast-spiking interneuron excitability through perineuronal nets and Kv3.1b K+ channels
Sharon R Stevens, Colleen M Longley, Yuki Ogawa, Lindsay H Teliska, Anithachristy S Arumanayagam, Supna Nair, Juan A Oses-Prieto, Alma L Burlingame, Matthew D Cykowski, Mingshan Xue, Matthew N Rasband
eLife. 2021; 10: e66491. Published online 2021 Jun 28. doi: 10.7554/eLife.66491
PMCID:
PMC8257253
AbstractArticlePDF–6.4M
5.
βIV Spectrinopathies Cause Profound Intellectual Disability, Congenital Hypotonia, and Motor Axonal Neuropathy
Chih-Chuan Wang, Xilma R. Ortiz-González, Sabrina W. Yum, Sara M. Gill, Amy White, Erin Kelter, Laurie H. Seaver, Sansan Lee, Graham Wiley, Patrick M. Gaffney, Klaas J. Wierenga, Matthew N. Rasband
Am J Hum Genet. 2018 Jun 7; 102(6): 1158–1168. Published online 2018 May 31. doi: 10.1016/j.ajhg.2018.04.012
PMCID:
PMC5992132
AbstractArticlePDF–1.9M
6.
Gene expression profiling in the developing secondary palate in the absence of Tbx1 function
Maria Zoupa, Guilherme Machado Xavier, Stephanie Bryan, Ioannis Theologidis, Matthew Arno, Martyn T. Cobourne
BMC Genomics. 2018; 19: 429. Published online 2018 Jun 4. doi: 10.1186/s12864-018-4782-y
PMCID:
PMC5987606
AbstractArticlePDF–2.6M
7.
Ankyrin-1 Gene Exhibits Allelic Heterogeneity in Conferring Protection Against Malaria
Hong Ming Huang, Denis C. Bauer, Patrick M. Lelliott, Matthew W. A. Dixon, Leann Tilley, Brendan J. McMorran, Simon J. Foote, Gaetan Burgio
G3 (Bethesda) 2017 Sep; 7(9): 3133–3144. Published online 2017 Jul 26. doi: 10.1534/g3.117.300079
PMCID:
PMC5592938
AbstractArticlePDF–1.3M
8.
Circulating primitive erythroblasts establish a functional, protein 4.1R-dependent cytoskeletal network prior to enucleating
Yu-Shan Huang, Luis F. Delgadillo, Kathryn H. Cyr, Paul D. Kingsley, Xiuli An, Kathleen E. McGrath, Narla Mohandas, John G. Conboy, Richard E. Waugh, Jiandi Wan, James Palis
Sci Rep. 2017; 7: 5164. Published online 2017 Jul 12. doi: 10.1038/s41598-017-05498-4
PMCID:
PMC5507979
AbstractArticlePDF–2.1M
9.
A novel ENU-induced ankyrin-1 mutation impairs parasite invasion and increases erythrocyte clearance during malaria infection in mice
Hong Ming Huang, Denis C. Bauer, Patrick M. Lelliott, Andreas Greth, Brendan J. McMorran, Simon J. Foote, Gaetan Burgio
Sci Rep. 2016; 6: 37197. Published online 2016 Nov 16. doi: 10.1038/srep37197
PMCID:
PMC5111128
AbstractArticlePDF–1.3M
10.
Transgenically-expressed secretoglobin 3A2 accelerates resolution of bleomycin-induced pulmonary fibrosis in mice
Yan Cai, Mitsuhiro Yoneda, Takeshi Tomita, Reiko Kurotani, Minoru Okamoto, Taketomo Kido, Hiroyuki Abe, Wayne Mitzner, Arjun Guha, Shioko Kimura
BMC Pulm Med. 2015; 15: 72. Published online 2015 Jul 16. doi: 10.1186/s12890-015-0065-4
PMCID:
PMC4504078
AbstractArticlePDF–2.0M
11.
Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders
Heather Fairfield, Anuj Srivastava, Guruprasad Ananda, Rangjiao Liu, Martin Kircher, Anuradha Lakshminarayana, Belinda S. Harris, Son Yong Karst, Louise A. Dionne, Coleen C. Kane, Michelle Curtain, Melissa L. Berry, Patricia F. Ward-Bailey, Ian Greenstein, Candice Byers, Anne Czechanski, Jocelyn Sharp, Kristina Palmer, Polyxeni Gudis, Whitney Martin, Abby Tadenev, Laurent Bogdanik, C. Herbert Pratt, Bo Chang, David G. Schroeder, Gregory A. Cox, Paul Cliften, Jeffrey Milbrandt, Stephen Murray, Robert Burgess, David E. Bergstrom, Leah Rae Donahue, Hanan Hamamy, Amira Masri, Federico A. Santoni, Periklis Makrythanasis, Stylianos E. Antonarakis, Jay Shendure, Laura G. Reinholdt
Genome Res. 2015 Jul; 25(7): 948–957. doi: 10.1101/gr.186882.114
PMCID:
PMC4484392
AbstractArticlePDF–604K
12.
A HIERARCHY OF ANKYRIN/SPECTRIN COMPLEXES CLUSTERS SODIUM CHANNELS AT NODES OF RANVIER
Tammy Szu-Yu Ho, Daniel R. Zollinger, Kae-Jiun Chang, Mingxuan Xu, Edward C. Cooper, Michael C. Stankewich, Vann Bennett, Matthew N. Rasband
Nat Neurosci. Author manuscript; available in PMC 2015 Jun 1.
Published in final edited form as: Nat Neurosci. 2014 Dec; 17(12): 1664–1672. Published online 2014 Nov 2. doi: 10.1038/nn.3859
PMCID:
PMC4271271
AbstractArticlePDF–2.4M
13.
β-III spectrin underpins ankyrin R function in Purkinje cell dendritic trees: protein complex critical for sodium channel activity is impaired by SCA5-associated mutations
Yvonne L. Clarkson, Emma M. Perkins, Callum J. Cairncross, Alastair R. Lyndon, Paul A. Skehel, Mandy Jackson
Hum Mol Genet. 2014 Jul 15; 23(14): 3875–3882. Published online 2014 Mar 6. doi: 10.1093/hmg/ddu103
PMCID:
PMC4065159
AbstractArticlePDF–617K
14.
Characterization of ENU-induced Mutations in Red Blood Cell Structural Proteins
Katrina Kildey, Robert L. Flower, Thu V. Tran, Robert Tunningley, Jonathan Harris, Melinda M. Dean
Comput Struct Biotechnol J. 2013; 6: e201303012. Published online 2013 Sep 23. doi: 10.5936/csbj.201303012
PMCID:
PMC3962129
AbstractArticlePDF–2.4M
15.
Conserved molecular signatures of neurogenesis in the hippocampal subgranular zone of rodents and primates
Jeremy A. Miller, Jason Nathanson, Daniel Franjic, Sungbo Shim, Rachel A. Dalley, Sheila Shapouri, Kimberly A. Smith, Susan M. Sunkin, Amy Bernard, Jeffrey L. Bennett, Chang-Kyu Lee, Michael J. Hawrylycz, Allan R. Jones, David G. Amaral, Nenad Sestan, Fred H. Gage, Ed S. Lein
Development. 2013 Nov 15; 140(22): 4633–4644. doi: 10.1242/dev.097212
PMCID:
PMC3817946
AbstractArticle
16.
A Deep Intronic Mutation in the Ankyrin-1 Gene Causes Diminished Protein Expression Resulting in Hemolytic Anemia in Mice
Hua Huang, PengXiang Zhao, Kei Arimatsu, Koichi Tabeta, Kazuhisa Yamazaki, Lara Krieg, Emily Fu, Tian Zhang, Xin Du
G3 (Bethesda) 2013 Oct; 3(10): 1687–1695. Published online 2013 Oct 1. doi: 10.1534/g3.113.007013
PMCID:
PMC3789793
AbstractArticlePDF–1.5M
17.
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
AbstractArticlePDF–1.1M
18.
Suppression of Hepcidin Expression and Iron Overload Mediate Salmonella Susceptibility in Ankyrin 1 ENU-Induced Mutant
Kyoko E. Yuki, Megan M. Eva, Etienne Richer, Dudley Chung, Marilène Paquet, Mathieu Cellier, François Canonne-Hergaux, Sophie Vaulont, Silvia M. Vidal, Danielle Malo
PLoS One. 2013; 8(2): e55331. Published online 2013 Feb 4. doi: 10.1371/journal.pone.0055331
PMCID:
PMC3563626
AbstractArticlePDF–956K
19.
Network Organization of the Huntingtin Proteomic Interactome in Mammalian Brain
Dyna I. Shirasaki, Erin R. Greiner, Ismael Al-Ramahi, Michelle Gray, Pinmanee Boontheung, Daniel H. Geschwind, Juan Botas, Giovanni Coppola, Steve Horvath, Joseph A. Loo, X. William Yang
Neuron. Author manuscript; available in PMC 2013 Jul 12.
Published in final edited form as: Neuron. 2012 Jul 12; 75(1): 41–57. doi: 10.1016/j.neuron.2012.05.024
PMCID:
PMC3432264
AbstractArticlePDF–4.9M
20.
A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis
Michael R. Hughes, Nicole Anderson, Steven Maltby, Justin Wong, Zorana Berberovic, Connie S. Birkenmeier, D. James Haddon, Kamal Garcha, Ann Flenniken, Lucy R. Osborne, S. Lee Adamson, Janet Rossant, Luanne L. Peters, Mark D. Minden, Robert F. Paulson, Chen Wang, Dwayne L. Barber, Kelly M. McNagny, William L. Stanford
Exp Hematol. Author manuscript; available in PMC 2012 Jul 25.
Published in final edited form as: Exp Hematol. 2011 Mar; 39(3): 305–320.e2. Published online 2010 Dec 28. doi: 10.1016/j.exphem.2010.12.009
Correction in:
on page 601
PMCID:
PMC3404605
AbstractArticlePDF–2.9M

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