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Items: 1 to 20 of 25

1.
VEGFR2 Trafficking by KIF13B Is a Novel Therapeutic Target for Wet Age-Related Macular Degeneration
Stephen B. Waters, Christopher Zhou, Tara Nguyen, Ruth Zelkha, Hyun Lee, Andrius Kazlauskas, Mark I. Rosenblatt, Asrar B. Malik, Kaori H. Yamada
Invest Ophthalmol Vis Sci. 2021 Feb; 62(2): 5. Published online 2021 Feb 3. doi: 10.1167/iovs.62.2.5
PMCID:
PMC7862734
ArticlePDF–4.4M
2.
KIF13B-mediated VEGFR2 trafficking is essential for vascular leakage and metastasis in vivo
Stephen B Waters, Joseph R Dominguez, Hyun-Dong Cho, Nicolene A Sarich, Asrar B Malik, Kaori H Yamada
Life Sci Alliance. 2022 Jan; 5(1): e202101170. Published online 2021 Oct 20. doi: 10.26508/lsa.202101170
PMCID:
PMC8548263
ArticlePDF–2.9M
3.
KIF13B enhances the endocytosis of LRP1 by recruiting LRP1 to caveolae
Yoshimitsu Kanai, Daliang Wang, Nobutaka Hirokawa
J Cell Biol. 2014 Feb 3; 204(3): 395–408. doi: 10.1083/jcb.201309066
PMCID:
PMC3912526
ArticlePDF–4.1M
4.
Myosin X Interaction with KIF13B, a Crucial Pathway for Netrin-1-Induced Axonal Development
Hua-Li Yu, Yun Peng, Yang Zhao, Yong-Sheng Lan, Bo Wang, Lu Zhao, Dong Sun, Jin-Xiu Pan, Zhao-Qi Dong, Lin Mei, Yu-Qiang Ding, Xiao-Juan Zhu, Wen-Cheng Xiong
J Neurosci. 2020 Nov 25; 40(48): 9169–9185. doi: 10.1523/JNEUROSCI.0929-20.2020
PMCID:
PMC7687062
ArticlePDF–9.0M
5.
KIF13B regulates angiogenesis through Golgi to plasma membrane trafficking of VEGFR2
Kaori H. Yamada, Yuki Nakajima, Melissa Geyer, Kishore K. Wary, Masuko Ushio-Fukai, Yulia Komarova, Asrar B. Malik
J Cell Sci. 2014 Oct 15; 127(20): 4518–4530. doi: 10.1242/jcs.156109
PMCID:
PMC4197089
Article
6.
A two-kinesin mechanism controls neurogenesis in the developing brain
Paige Helmer, Richard B. Vallee
Commun Biol. 2023; 6: 1219. Published online 2023 Dec 1. doi: 10.1038/s42003-023-05604-5
PMCID:
PMC10692124
ArticlePDF–6.1M
7.
Kif13b Regulates PNS and CNS Myelination through the Dlg1 Scaffold
Roberta Noseda, Marta Guerrero-Valero, Valeria Alberizzi, Stefano C. Previtali, Diane L. Sherman, Marilena Palmisano, Richard L. Huganir, Klaus-Armin Nave, Ana Cuenda, Maria Laura Feltri, Peter J. Brophy, Alessandra Bolino
PLoS Biol. 2016 Apr; 14(4): e1002440. Published online 2016 Apr 12. doi: 10.1371/journal.pbio.1002440
PMCID:
PMC4829179
ArticlePDF–7.9M
8.
LDL receptor related protein 1 requires the I3 domain of Discs-large homolog 1/DLG1 for interaction with the kinesin motor protein KIF13B
Joslyn Mills, Toshihiko Hanada, Yoichi Hase, Laura Liscum, Athar H. Chishti
Biochim Biophys Acta Mol Cell Res. Author manuscript; available in PMC 2020 Dec 1.
Published in final edited form as: Biochim Biophys Acta Mol Cell Res. 2019 Dec; 1866(12): 118552. Published online 2019 Sep 2. doi: 10.1016/j.bbamcr.2019.118552
PMCID:
PMC6851494
ArticlePDF–2.0M
9.
Reduction of endoplasmic reticulum stress attenuates the defects caused by Drosophila mitofusin depletion
Valentina Debattisti, Diana Pendin, Elena Ziviani, Andrea Daga, Luca Scorrano
J Cell Biol. 2014 Feb 3; 204(3): 303–312. doi: 10.1083/jcb.201306121
PMCID:
PMC3912536
ArticlePDF–3.8M
10.
Identification and classification of 16 new kinesin superfamily (KIF) proteins in mouse genome
Terunaga Nakagawa, Yosuke Tanaka, Eiji Matsuoka, Satoru Kondo, Yasushi Okada, Yasuko Noda, Yoshimitsu Kanai, Nobutaka Hirokawa
Proc Natl Acad Sci U S A. 1997 Sep 2; 94(18): 9654–9659. doi: 10.1073/pnas.94.18.9654
Correction in:
Proc Natl Acad Sci U S A. 1999 Mar 30; 96(7): 4214.
PMCID:
PMC23244
ArticlePDF–428K
11.
All kinesin superfamily protein, KIF, genes in mouse and human
Harukata Miki, Mitsutoshi Setou, Kiyofumi Kaneshiro, Nobutaka Hirokawa
Proc Natl Acad Sci U S A. 2001 Jun 19; 98(13): 7004–7011. doi: 10.1073/pnas.111145398
PMCID:
PMC34614
ArticlePDF–911K
12.
Spatio-temporal profile of postynaptic interactomes integrates components of complex brain disorders
Jing Li, Wangshu Zhang, Hui Yang, Daniel P. Howrigan, Brent Wilkinson, Tade Souaiaia, Oleg V. Evgrafov, Giulio Genovese, Veronica A. Clementel, Jennifer C. Tudor, Ted Abel, James A. Knowles, Benjamin M. Neale, Kai Wang, Fengzhu Sun, Marcelo P. Coba
Nat Neurosci. Author manuscript; available in PMC 2018 Aug 1.
Published in final edited form as: Nat Neurosci. 2017 Aug; 20(8): 1150–1161. Published online 2017 Jun 26. doi: 10.1038/nn.4594
PMCID:
PMC5645082
ArticlePDF–2.3M
13.
Construction of Long-Transcript Enriched cDNA Libraries from Submicrogram Amounts of Total RNAs by a Universal PCR Amplification Method
Yulan Piao, Naomi T. Ko, Meng K. Lim, Minoru S.H. Ko
Genome Res. 2001 Sep; 11(9): 1553–1558. doi: 10.1101/gr.185501
PMCID:
PMC311119
ArticlePDF–743K
14.
Mouse screen reveals multiple new genes underlying mouse and human hearing loss
Neil J. Ingham, Selina A. Pearson, Valerie E. Vancollie, Victoria Rook, Morag A. Lewis, Jing Chen, Annalisa Buniello, Elisa Martelletti, Lorenzo Preite, Chi Chung Lam, Felix D. Weiss, Zӧe Powis, Pim Suwannarat, Christopher J. Lelliott, Sally J. Dawson, Jacqueline K. White, Karen P. Steel
PLoS Biol. 2019 Apr; 17(4): e3000194. Published online 2019 Apr 11. doi: 10.1371/journal.pbio.3000194
PMCID:
PMC6459510
ArticlePDF–5.1M
15.
Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development
Francesco Bedogni, Robert F. Hevner
Front Mol Neurosci. 2021; 14: 686034. Published online 2021 Jul 12. doi: 10.3389/fnmol.2021.686034
PMCID:
PMC8313239
ArticlePDF–1.6M
16.
A large-scale, gene-driven mutagenesis approach for the functional analysis of the mouse genome
Jens Hansen, Thomas Floss, Petra Van Sloun, Ernst-Martin Füchtbauer, Franz Vauti, Hans-Hennig Arnold, Frank Schnütgen, Wolfgang Wurst, Harald von Melchner, Patricia Ruiz
Proc Natl Acad Sci U S A. 2003 Aug 19; 100(17): 9918–9922. Published online 2003 Aug 6. doi: 10.1073/pnas.1633296100
PMCID:
PMC187885
ArticlePDF–287K
17.
BayGenomics: a resource of insertional mutations in mouse embryonic stem cells
Doug Stryke, Michiko Kawamoto, Conrad C. Huang, Susan J. Johns, Leslie A. King, Courtney A. Harper, Elaine C. Meng, Roy E. Lee, Alice Yee, Larry L'Italien, Pao-Tien Chuang, Stephen G. Young, William C. Skarnes, Patricia C. Babbitt, Thomas E. Ferrin
Nucleic Acids Res. 2003 Jan 1; 31(1): 278–281. doi: 10.1093/nar/gkg064
PMCID:
PMC165511
ArticlePDF–217K
18.
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells
Gwenn M. Hansen, Diane C. Markesich, Michael B. Burnett, Qichao Zhu, Karen M. Dionne, Lizabeth J. Richter, Richard H. Finnell, Arthur T. Sands, Brian P. Zambrowicz, Alejandro Abuin
Genome Res. 2008 Oct; 18(10): 1670–1679. doi: 10.1101/gr.078352.108
PMCID:
PMC2556270
ArticlePDF–493K
19.
Genetic determinants of micronucleus formation in vivo
D. J. Adams, B. Barlas, R. E. McIntyre, I. Salguero, L. van der Weyden, A. Barros, J. R. Vicente, N. Karimpour, A. Haider, M. Ranzani, G. Turner, N. A. Thompson, V. Harle, R. Olvera-León, C. D. Robles-Espinoza, A. O. Speak, N. Geisler, W. J. Weninger, S. H. Geyer, J. Hewinson, N. A. Karp, The Sanger Mouse Genetics Project, B. Fu, F. Yang, Z. Kozik, J. Choudhary, L. Yu, M. S. van Ruiten, B. D. Rowland, C. J. Lelliott, M. del Castillo Velasco-Herrera, R. Verstraten, L. Bruckner, A. G. Henssen, M. A. Rooimans, J. de Lange, T. J. Mohun, M. J. Arends, K. A. Kentistou, P. A. Coelho, Y. Zhao, H. Zecchini, J. R. B. Perry, S. P. Jackson, G. Balmus
Nature. 2024; 627(8002): 130–136. Published online 2024 Feb 14. doi: 10.1038/s41586-023-07009-0
PMCID:
PMC10917660
ArticlePDF–4.8M
20.
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

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