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Items: 1 to 20 of 24

1.
The Wnt Inhibitor Apcdd1 Coordinates Vascular Remodeling and Barrier Maturation of Retinal Blood Vessels
Jenna Mazzoni, Julian R. Smith, Sanjid Shahriar, Tyler Cutforth, Bernardo Ceja, Dritan Agalliu
Neuron. Author manuscript; available in PMC 2018 Dec 6.
Published in final edited form as: Neuron. 2017 Dec 6; 96(5): 1055–1069.e6. Published online 2017 Nov 16. doi: 10.1016/j.neuron.2017.10.025
PMCID:
PMC5728434
AbstractArticlePDF–1.8M
2.
Mural Wnt/β-catenin signaling regulates Lama2 expression to promote neurovascular unit maturation
Saptarshi Biswas, Sanjid Shahriar, Nicholas P. Giangreco, Panos Arvanitis, Markus Winkler, Nicholas P. Tatonetti, William J. Brunken, Tyler Cutforth, Dritan Agalliu
Development. 2022 Sep 1; 149(17): dev200610. Published online 2022 Sep 13. doi: 10.1242/dev.200610
PMCID:
PMC9578690
AbstractArticle
3.
A novel role for the Wnt inhibitor APCDD1 in adipocyte differentiation: Implications for diet-induced obesity
Nicole K. H. Yiew, Tapan K. Chatterjee, Yao Liang Tang, Rod Pellenberg, Brian K. Stansfield, Zsolt Bagi, David J. Fulton, David W. Stepp, Weiqin Chen, Vijay Patel, Vinayak M. Kamath, Sheldon E. Litwin, David Y. Hui, Steven M. Rudich, Ha Won Kim, Neal L. Weintraub
J Biol Chem. 2017 Apr 14; 292(15): 6312–6324. Published online 2017 Feb 27. doi: 10.1074/jbc.M116.758078
PMCID:
PMC5391760
AbstractArticlePDF–3.5M
4.
Transposition-Based Method for the Rapid Generation of Gene-Targeting Vectors to Produce Cre/Flp-Modifiable Conditional Knock-Out Mice
Hilkka Turakainen, Jonna Saarimäki-Vire, Natalia Sinjushina, Juha Partanen, Harri Savilahti
PLoS One. 2009; 4(2): e4341. Published online 2009 Feb 5. doi: 10.1371/journal.pone.0004341
PMCID:
PMC2632748
AbstractArticlePDF–606K
5.
Vascular-derived SPARC and SerpinE1 regulate interneuron tangential migration and accelerate functional maturation of human stem cell-derived interneurons
Matthieu Genestine, Daisy Ambriz, Gregg W Crabtree, Patrick Dummer, Anna Molotkova, Michael Quintero, Angeliki Mela, Saptarshi Biswas, Huijuan Feng, Chaolin Zhang, Peter Canoll, Gunnar Hargus, Dritan Agalliu, Joseph A Gogos, Edmund Au
eLife. 2021; 10: e56063. Published online 2021 Apr 27. doi: 10.7554/eLife.56063
PMCID:
PMC8099424
AbstractArticlePDF–3.9M
6.
Apcdd1 stimulates oligodendrocyte differentiation after white matter injury
Hyun Kyoung Lee, Dylan Laug, Wenyi Zhu, Jay M Patel, Kevin Ung, Benjamin R Arenkiel, Stephen PJ Fancy, Carrie Mohila, Benjamin Deneen
Glia. Author manuscript; available in PMC 2016 Oct 1.
Published in final edited form as: Glia. 2015 Oct; 63(10): 1840–1849. Published online 2015 May 6. doi: 10.1002/glia.22848
PMCID:
PMC4534334
AbstractArticlePDF–1.2M
7.
Trps1 activates a network of secreted Wnt inhibitors and transcription factors crucial to vibrissa follicle morphogenesis
Katherine A. Fantauzzo, Angela M. Christiano
Development. 2012 Jan 1; 139(1): 203–214. doi: 10.1242/dev.069971
PMCID:
PMC3231778
AbstractArticle
8.
Sox9 and NFIA Coordinate a Transcriptional Regulatory Cascade during the Initiation of Gliogenesis
Peng Kang, Hyun Kyoung Lee, Stacey M. Glasgow, Meggie Finley, Tataka Donti, Zachary B. Gaber, Brett H. Graham, Aaron E. Foster, Bennett G. Novitch, Richard M. Gronostajski, Benjamin Deneen
Neuron. Author manuscript; available in PMC 2013 Apr 12.
Published in final edited form as: Neuron. 2012 Apr 12; 74(1): 79–94. doi: 10.1016/j.neuron.2012.01.024
PMCID:
PMC3543821
AbstractArticlePDF–2.9M
9.
Hemodynamic forces sculpt developing heart valves through a KLF2-WNT9B paracrine signaling axis
Lauren M. Goddard, Anne-Laure Duchemin, Harini Ramalingan, Bingruo Wu, Mei Chen, Sharika Bamezai, Jisheng Yang, Li Li, Michael Morley, Tao Wang, Marielle Scherrer-Crosbie, Dave B. Frank, Kurt A. Engleka, Stephen C. Jameson, Edward E. Morrisey, Thomas J. Carroll, Bin Zhou, Julien Vermot, Mark L. Kahn
Dev Cell. Author manuscript; available in PMC 2018 Nov 6.
Published in final edited form as: Dev Cell. 2017 Nov 6; 43(3): 274–289.e5. Published online 2017 Oct 19. doi: 10.1016/j.devcel.2017.09.023
PMCID:
PMC5760194
AbstractArticlePDF–2.0M
10.
beta-Catenin Regulates Intercellular Signalling Networks and Cell-Type Specific Transcription in the Developing Mouse Midbrain-Rhombomere 1 Region
Dmitri Chilov, Natalia Sinjushina, Jonna Saarimäki-Vire, Makoto M. Taketo, Juha Partanen
PLoS One. 2010; 5(6): e10881. Published online 2010 Jun 3. doi: 10.1371/journal.pone.0010881
PMCID:
PMC2880587
AbstractArticlePDF–6.2M
11.
Genome-wide microarray comparison reveals downstream genes of Pax6 in the developing mouse cerebellum
Thomas J. Ha, Douglas J. Swanson, Roumyana Kirova, Joanna Yeung, Kunho Choi, Yiai Tong, Elissa J. Chesler, Daniel Goldowitz
Eur J Neurosci. Author manuscript; available in PMC 2014 Oct 8.
Published in final edited form as: Eur J Neurosci. 2012 Oct; 36(7): 2888–2898. Published online 2012 Jul 22. doi: 10.1111/j.1460-9568.2012.08221.x
PMCID:
PMC4189819
AbstractArticlePDF–1.4M
12.
Stromal β-catenin activation impacts nephron progenitor differentiation in the developing kidney and may contribute to Wilms tumor
Keri A. Drake, Christopher P. Chaney, Amrita Das, Priti Roy, Callie S. Kwartler, Dinesh Rakheja, Thomas J. Carroll
Development. 2020 Nov 1; 147(21): dev189597. Published online 2020 Jul 31. doi: 10.1242/dev.189597
PMCID:
PMC7406317
AbstractArticle
13.
Transcription Factors YAP/TAZ and SRF Cooperate To Specify Renal Myofibroblasts in the Developing Mouse Kidney
Keri A. Drake, Christopher Chaney, Mohita Patel, Amrita Das, Julia Bittencourt, Martin Cohn, Thomas J. Carroll
J Am Soc Nephrol. 2022 Sep; 33(9): 1694–1707. Published online 2022 Sep. doi: 10.1681/ASN.2021121559
Correction in:
J Am Soc Nephrol. 2023 Mar; 34(3): 515–516.
PMCID:
PMC9529188
AbstractArticle
14.
Comparative gene expression analysis of genital tubercle development reveals a putative appendicular Wnt7 network for the epidermal differentiation
Han Sheng Chiu, John C. Szucsik, Kylie M. Georgas, Julia L. Jones, Bree A. Rumballe, Dave Tang, Sean M. Grimmond, Alfor G. Lewis, Bruce J. Aronow, James L. Lessard, Melissa H. Little
Dev Biol. Author manuscript; available in PMC 2011 Aug 15.
Published in final edited form as: Dev Biol. 2010 Aug 15; 344(2): 1071–1087. Published online 2010 May 24. doi: 10.1016/j.ydbio.2010.05.495
PMCID:
PMC3154616
AbstractArticlePDF–2.3M
15.
Fibroblast Growth Factor Receptors Cooperate to Regulate Neural Progenitor Properties in the Developing Midbrain and Hindbrain
Jonna Saarimäki-Vire, Paula Peltopuro, Laura Lahti, Thorsten Naserke, Alexandra A. Blak, Daniela M. Vogt Weisenhorn, Kai Yu, David M. Ornitz, Wolfgang Wurst, Juha Partanen
J Neurosci. 2007 Aug 8; 27(32): 8581–8592. doi: 10.1523/JNEUROSCI.0192-07.2007
PMCID:
PMC6672929
AbstractArticlePDF–981K
16.
Transcriptional Analysis of Gli3 Mutants Identifies Wnt Target Genes in the Developing Hippocampus
Kerstin Hasenpusch-Theil, Dario Magnani, Eleni-Maria Amaniti, Lin Han, Douglas Armstrong, Thomas Theil
Cereb Cortex. 2012 Dec; 22(12): 2878–2893. Published online 2012 Jan 10. doi: 10.1093/cercor/bhr365
PMCID:
PMC3491769
AbstractArticlePDF–5.1M
17.
Foxl2 functions in sex determination and histogenesis throughout mouse ovary development
José Elias Garcia-Ortiz, Emanuele Pelosi, Shakib Omari, Timur Nedorezov, Yulan Piao, Jesse Karmazin, Manuela Uda, Antonio Cao, Steve W Cole, Antonino Forabosco, David Schlessinger, Chris Ottolenghi
BMC Dev Biol. 2009; 9: 36. Published online 2009 Jun 18. doi: 10.1186/1471-213X-9-36
PMCID:
PMC2711087
AbstractArticlePDF–656K
18.
Genome-wide expression profiling of mid-gestation placenta and embryo using a 15,000 mouse developmental cDNA microarray
Tetsuya S. Tanaka, Saied A. Jaradat, Meng K. Lim, George J. Kargul, Xiaohong Wang, Marija J. Grahovac, Serafino Pantano, Yuri Sano, Yulan Piao, Ramaiah Nagaraja, Hirofumi Doi, William H. Wood, III, Kevin G. Becker, Minoru S. H. Ko
Proc Natl Acad Sci U S A. 2000 Aug 1; 97(16): 9127–9132. doi: 10.1073/pnas.97.16.9127
PMCID:
PMC16833
AbstractArticlePDF–847K
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
AbstractArticlePDF–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
AbstractArticlePDF–1.1M

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