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Items: 1 to 20 of 32

1.
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
AbstractArticlePDF–4.8M
2.
Inter-axonal molecular crosstalk via Lumican proteoglycan sculpts murine cervical corticospinal innervation by distinct subpopulations
Yasuhiro Itoh, Vibhu Sahni, Sara J. Shnider, Holly McKee, Jeffrey D. Macklis
Cell Rep. Author manuscript; available in PMC 2023 May 9.
Published in final edited form as: Cell Rep. 2023 Mar 28; 42(3): 112182. Published online 2023 Mar 17. doi: 10.1016/j.celrep.2023.112182
PMCID:
PMC10167627
AbstractArticlePDF–3.5M
3.
Cbln1 Directs Axon Targeting by Corticospinal Neurons Specifically toward Thoraco-Lumbar Spinal Cord
Janet H.T. Song, Carolin Ruven, Payal Patel, Frances Ding, Jeffrey D. Macklis, Vibhu Sahni
J Neurosci. 2023 Mar 15; 43(11): 1871–1887. doi: 10.1523/JNEUROSCI.0710-22.2023
PMCID:
PMC10027075
AbstractArticlePDF–8.4M
4.
A functional cellular framework for sex and estrous cycle-dependent gene expression and behavior
Joseph R. Knoedler, Sayaka Inoue, Daniel W. Bayless, Taehong Yang, Adarsh Tantry, Chung-ha Davis, Nicole Y. Leung, Srinivas Parthasarathy, Grace Wang, Maricruz Alvarado, Abbas H. Rizvi, Lief E. Fenno, Charu Ramakrishnan, Karl Deisseroth, Nirao M. Shah
Cell. Author manuscript; available in PMC 2023 Feb 17.
Published in final edited form as: Cell. 2022 Feb 17; 185(4): 654–671.e22. Published online 2022 Jan 21. doi: 10.1016/j.cell.2021.12.031
Correction in:
Cell. 2024 Jul 11; 187(14): 3781.
PMCID:
PMC8956134
AbstractArticlePDF–4.6M
5.
Crim1 and Kelch-like 14 exert complementary dual-directional developmental control over segmentally specific corticospinal axon projection targeting
Vibhu Sahni, Yasuhiro Itoh, Sara J. Shnider, Jeffrey D. Macklis
Cell Rep. Author manuscript; available in PMC 2021 Dec 23.
Published in final edited form as: Cell Rep. 2021 Oct 19; 37(3): 109842. doi: 10.1016/j.celrep.2021.109842
PMCID:
PMC8697027
AbstractArticlePDF–2.7M
6.
Corticospinal neuron subpopulation-specific developmental genes prospectively indicate mature segmentally specific axon projection targeting
Vibhu Sahni, Sara J. Shnider, Denis Jabaudon, Janet H.T. Song, Yasuhiro Itoh, Luciano C. Greig, Jeffrey D. Macklis
Cell Rep. Author manuscript; available in PMC 2021 Dec 8.
Published in final edited form as: Cell Rep. 2021 Oct 19; 37(3): 109843. doi: 10.1016/j.celrep.2021.109843
PMCID:
PMC8653526
AbstractArticlePDF–3.3M
7.
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
AbstractArticlePDF–1.6M
8.
Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease
Scott E. Youlten, John P. Kemp, John G. Logan, Elena J. Ghirardello, Claudio M. Sergio, Michael R. G. Dack, Siobhan E. Guilfoyle, Victoria D. Leitch, Natalie C. Butterfield, Davide Komla-Ebri, Ryan C. Chai, Alexander P. Corr, James T. Smith, Sindhu T. Mohanty, John A. Morris, Michelle M. McDonald, Julian M. W. Quinn, Amelia R. McGlade, Nenad Bartonicek, Matt Jansson, Konstantinos Hatzikotoulas, Melita D. Irving, Ana Beleza-Meireles, Fernando Rivadeneira, Emma Duncan, J. Brent Richards, David J. Adams, Christopher J. Lelliott, Robert Brink, Tri Giang Phan, John A. Eisman, David M. Evans, Eleftheria Zeggini, Paul A. Baldock, J. H. Duncan Bassett, Graham R. Williams, Peter I. Croucher
Nat Commun. 2021; 12: 2444. Published online 2021 May 5. doi: 10.1038/s41467-021-22517-1
PMCID:
PMC8100170
AbstractArticlePDF–11M
9.
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
AbstractArticlePDF–5.1M
10.
Placentation defects are highly prevalent in embryonic lethal mouse mutants
Vicente Perez-Garcia, Elena Fineberg, Robert Wilson, Alexander Murray, Cecilia Icoresi Mazzeo, Catherine Tudor, Arnold Sienerth, Jacqueline K. White, Elizabeth Tuck, Edward J. Ryder, Diane Gleeson, Emma Siragher, Hannah Wardle-Jones, Nicole Staudt, Neha Wali, John Collins, Stefan Geyer, Elisabeth M. Busch-Nentwich, Antonella Galli, James C. Smith, Elizabeth Robertson, David J. Adams, Wolfgang J. Weninger, Timothy Mohun, Myriam Hemberger
Nature. Author manuscript; available in PMC 2018 Sep 14.
Published in final edited form as: Nature. 2018 Mar 22; 555(7697): 463–468. Published online 2018 Mar 14. doi: 10.1038/nature26002
PMCID:
PMC5866719
AbstractArticlePDF–7.4M
11.
Gene expression analysis of the embryonic subplate
Franziska M. Oeschger, Wei-Zhi Wang, Sheena Lee, Fernando García-Moreno, André M. Goffinet, Mariona Arbones, Sonia Rakic, Zoltán Molnár
Cereb Cortex. Author manuscript; available in PMC 2016 Aug 3.
Published in final edited form as: Cereb Cortex. 2012 Jun; 22(6): 1343–1359. Published online 2011 Aug 22. doi: 10.1093/cercor/bhr197
PMCID:
PMC4972418
AbstractArticlePDF–7.1M
12.
Ctip1 controls acquisition of sensory area identity and establishment of sensory input fields in the developing neocortex
Luciano C. Greig, Mollie B. Woodworth, Chloé Greppi, Jeffrey D. Macklis
Neuron. Author manuscript; available in PMC 2017 Apr 20.
Published in final edited form as: Neuron. 2016 Apr 20; 90(2): 261–277. doi: 10.1016/j.neuron.2016.03.008
PMCID:
PMC4873772
AbstractArticlePDF–2.0M
13.
Crim1 has cell-autonomous and paracrine roles during embryonic heart development
Swati Iyer, Fang Yu Chou, Richard Wang, Han Sheng Chiu, Vinay K. Sundar Raju, Melissa H. Little, Walter G. Thomas, Michael Piper, David J. Pennisi
Sci Rep. 2016; 6: 19832. Published online 2016 Jan 29. doi: 10.1038/srep19832
PMCID:
PMC4731764
AbstractArticlePDF–3.0M
14.
Crim1 regulates integrin signaling in murine lens development
Ying Zhang, Jieqing Fan, Joshua W. K. Ho, Tommy Hu, Stephen C. Kneeland, Xueping Fan, Qiongchao Xi, Michael A. Sellarole, Wilhelmine N. de Vries, Weining Lu, Salil A. Lachke, Richard A. Lang, Simon W. M. John, Richard L. Maas
Development. 2016 Jan 15; 143(2): 356–366. doi: 10.1242/dev.125591
PMCID:
PMC4725338
AbstractArticle
15.
CRIM1 haploinsufficiency causes defects in eye development in human and mouse
Filippo Beleggia, Yun Li, Jieqing Fan, Nursel H. Elciog˘lu, Ebru Toker, Thomas Wieland, Irene H. Maumenee, Nurten A. Akarsu, Thomas Meitinger, Tim M. Strom, Richard Lang, Bernd Wollnik
Hum Mol Genet. 2015 Apr 15; 24(8): 2267–2273. Published online 2015 Jan 5. doi: 10.1093/hmg/ddu744
PMCID:
PMC4380072
AbstractArticlePDF–632K
16.
Crim1 maintains retinal vascular stability during development by regulating endothelial cell Vegfa autocrine signaling
Jieqing Fan, Virgilio G. Ponferrada, Tomohito Sato, Shruti Vemaraju, Marcus Fruttiger, Holger Gerhardt, Napoleone Ferrara, Richard A. Lang
Development. 2014 Jan 15; 141(2): 448–459. doi: 10.1242/dev.097949
PMCID:
PMC3879820
AbstractArticle
17.
Inactivation of the microRNA-183/96/182 cluster results in syndromic retinal degeneration
Stephen Lumayag, Caroline E. Haldin, Nicola J. Corbett, Karl J. Wahlin, Colleen Cowan, Sanja Turturro, Peter E. Larsen, Beatrix Kovacs, P. Dane Witmer, David Valle, Donald J. Zack, Daniel A. Nicholson, Shunbin Xu
Proc Natl Acad Sci U S A. 2013 Feb 5; 110(6): E507–E516. Published online 2013 Jan 22. doi: 10.1073/pnas.1212655110
PMCID:
PMC3568372
AbstractArticlePDF–2.1M
18.
KIF14 negatively regulates Rap1a–Radil signaling during breast cancer progression
Syed M. Ahmed, Brigitte L. Thériault, Maruti Uppalapati, Catherine W.N. Chiu, Brenda L. Gallie, Sachdev S. Sidhu, Stéphane Angers
J Cell Biol. 2012 Dec 10; 199(6): 951–967. doi: 10.1083/jcb.201206051
PMCID:
PMC3518219
AbstractArticlePDF–3.7M
19.
Production of a Mouse Line with a Conditional Crim1 Mutant Allele
Han Sheng Chiu, J. Philippe York, Lorine Wilkinson, Pumin Zhang, Melissa H. Little, David J. Pennisi
Genesis. Author manuscript; available in PMC 2013 Sep 1.
Published in final edited form as: Genesis. 2012 Sep; 50(9): 711–716. Published online 2012 May 19. doi: 10.1002/dvg.22032
PMCID:
PMC3429722
AbstractArticlePDF–2.1M
20.
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

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