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Select item 12885751.

Haploinsufficiency of ALX4 as a Potential Cause of Parietal Foramina in the 11p11.2 Contiguous Gene–Deletion Syndrome

Yuan-Qing Wu, Jose L. Badano, Christopher McCaskill, Hannes Vogel, Lorraine Potocki, Lisa G. Shaffer

Am J Hum Genet. 2000 Nov; 67(5): 1327–1332. Published online 2000 Oct 3. doi: 10.1016/s0002-9297(07)62963-2

PMCID:: PMC1288575

Abstract Article PDF–634K

Select item 89316712.

A transgenic Alx4-CreER mouse to analyze anterior limb and nephric duct development

Devan M. Rockwell, Amber K. O’Connor, Melissa R. Bentley-Ford, Courtney J. Haycraft, Mandy J. Croyle, Kathryn M. Brewer, Nicolas F. Berbari, Robert A. Kesterson, Bradley K. Yoder

Dev Dyn. Author manuscript; available in PMC 2022 Sep 6.

Published in final edited form as: Dev Dyn. 2022 Sep; 251(9): 1524–1534. Published online 2021 Mar 23. doi: 10.1002/dvdy.328

PMCID:: PMC8931671

Abstract Article PDF–2.0M

Select item 30244243.

Genetic Analysis of Hedgehog Signaling in Ventral Body Wall Development and the Onset of Omphalocele Formation

Daisuke Matsumaru, Ryuma Haraguchi, Shinichi Miyagawa, Jun Motoyama, Naomi Nakagata, Frits Meijlink, Gen Yamada

PLoS One. 2011; 6(1): e16260. Published online 2011 Jan 20. doi: 10.1371/journal.pone.0016260

PMCID:: PMC3024424

Abstract Article PDF–823K

Select item 15713194.

Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation

Ileana Antonopoulou, Lampros A Mavrogiannis, Andrew O M Wilkie, Gillian M Morriss-Kay

J Anat. 2004 Jun; 204(6): 487–499. doi: 10.1111/j.0021-8782.2004.00304.x

PMCID:: PMC1571319

Abstract Article PDF–496K

Select item 24090935.

Impaired meningeal development in association with apical expansion of calvarial bone osteogenesis in the Foxc1 mutant

Philaiporn Vivatbutsiri, Shizuko Ichinose, Marjo Hytönen, Kirsi Sainio, Kazuhiro Eto, Sachiko Iseki

J Anat. 2008 May; 212(5): 603–611. doi: 10.1111/j.1469-7580.2008.00893.x

PMCID:: PMC2409093

Abstract Article PDF–408K

Select item 1553436.

Mutual genetic antagonism involving GLI3 and dHAND prepatterns the vertebrate limb bud mesenchyme prior to SHH signaling

Pascal te Welscher, Marian Fernandez-Teran, Marian A. Ros, Rolf Zeller

Genes Dev. 2002 Feb 15; 16(4): 421–426. doi: 10.1101/gad.219202

PMCID:: PMC155343

Abstract Article PDF–195K

Select item 108208867.

TFAP2 paralogs regulate midfacial development in part through a conserved ALX genetic pathway

Timothy T. Nguyen, Jennyfer M. Mitchell, Michaela D. Kiel, Colin P. Kenny, Hong Li, Kenneth L. Jones, Robert A. Cornell, Trevor J. Williams, James T. Nichols, Eric Van Otterloo

Development. 2024 Jan 1; 151(1): dev202095. Published online 2024 Jan 2. doi: 10.1242/dev.202095

PMCID:: PMC10820886

Abstract Article

Select item 44821108.

A novel allele of Alx4 results in reduced Fgf10 expression and failure of eyelid fusion in mice

Michelle Curtain, Caleb S. Heffner, Dennis M. Maddox, Polyxeni Gudis, Leah Rae Donahue, Stephen A. Murray

Mamm Genome. Author manuscript; available in PMC 2016 Apr 1.

Published in final edited form as: Mamm Genome. 2015 Apr; 26(0): 173–180. Published online 2015 Feb 12. doi: 10.1007/s00335-015-9557-z

PMCID:: PMC4482110

Abstract Article PDF–1.5M

Select item 39252839.

Genetic analysis of the role of Alx4 in the coordination of lower body and external genitalia formation

Daisuke Matsumaru, Ryuma Haraguchi, Anne M Moon, Yoshihiko Satoh, Naomi Nakagata, Ken-ichi Yamamura, Naoki Takahashi, Sohei Kitazawa, Gen Yamada

Eur J Hum Genet. 2014 Mar; 22(3): 350–357. Published online 2013 Aug 14. doi: 10.1038/ejhg.2013.160

PMCID:: PMC3925283

Abstract Article PDF–3.3M

Select item 342406710.

Neogenin regulates Sonic hedgehog pathway activity during digit patterning

Mingi Hong, Karen A. Schachter, Guoying Jiang, Robert S. Krauss

Dev Dyn. Author manuscript; available in PMC 2013 Mar 1.

Published in final edited form as: Dev Dyn. 2012 Mar; 241(3): 627–637. doi: 10.1002/dvdy.23745

PMCID:: PMC3424067

Abstract Article PDF–3.8M

Select item 159257511.

Satb2 Haploinsufficiency Phenocopies 2q32-q33 Deletions, whereas Loss Suggests a Fundamental Role in the Coordination of Jaw Development

Olga Britanova, Michael J. Depew, Manuela Schwark, Bethan L. Thomas, Isabelle Miletich, Paul Sharpe, Victor Tarabykin

Am J Hum Genet. 2006 Oct; 79(4): 668–678. Published online 2006 Aug 30. doi: 10.1086/508214

PMCID:: PMC1592575

Abstract Article PDF–5.9M

Select item 378456912.

A Critical Role for PDGFRα Signaling in Medial Nasal Process Development

Fenglei He, Philippe Soriano

PLoS Genet. 2013 Sep; 9(9): e1003851. Published online 2013 Sep 26. doi: 10.1371/journal.pgen.1003851

PMCID:: PMC3784569

Abstract Article PDF–18M

Select item 343268713.

Limb anterior-posterior polarity integrates activator and repressor functions of GLI2 as well as GLI3

Megan Bowers, Liane Eng, Zhimin Lao, Rowena K. Turnbull, Xiaozhong Bao, Elyn Riedel, Susan Mackem, Alexandra L. Joyner

Dev Biol. Author manuscript; available in PMC 2013 Oct 1.

Published in final edited form as: Dev Biol. 2012 Oct 1; 370(1): 110–124. Published online 2012 Jul 25. doi: 10.1016/j.ydbio.2012.07.017

PMCID:: PMC3432687

Abstract Article PDF–4.1M

Select item 292767314.

Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1

Terence D. Capellini, Giulia Vaccari, Elisabetta Ferretti, Sebastian Fantini, Mu He, Massimo Pellegrini, Laura Quintana, Giuseppina Di Giacomo, James Sharpe, Licia Selleri, Vincenzo Zappavigna

Development. 2010 Aug 1; 137(15): 2559–2569. doi: 10.1242/dev.048819

PMCID:: PMC2927673

Abstract Article

Select item 272755915.

DNA binding-dependent and -independent functions of the Hand2 transcription factor during mouse embryogenesis

Ning Liu, Ana C. Barbosa, Shelby L. Chapman, Svetlana Bezprozvannaya, Xiaoxia Qi, James A. Richardson, Hiromi Yanagisawa, Eric N. Olson

Development. 2009 Mar 15; 136(6): 933–942. Published online 2009 Feb 11. doi: 10.1242/dev.034025

PMCID:: PMC2727559

Abstract Article

Select item 123174316.

The interfrontal bone and mutant genes in the mouse.

D R Johnson

J Anat. 1976 Jul; 121(Pt 3): 507–513.

PMCID:: PMC1231743

Summary Page Browse PDF–591K

Select item 648100717.

Crucial and Overlapping Roles of Six1 and Six2 in Craniofacial Development

Z. Liu, C. Li, J. Xu, Y. Lan, H. Liu, X. Li, P. Maire, X. Wang, R. Jiang

J Dent Res. 2019 May; 98(5): 572–579. Published online 2019 Mar 24. doi: 10.1177/0022034519835204

PMCID:: PMC6481007

Abstract Article PDF–890K

Select item 560734218.

Mllt10 knockout mouse model reveals critical role of Af10-dependent H3K79 methylation in midfacial development

Honami Ogoh, Kazutsune Yamagata, Tomomi Nakao, Lisa L. Sandell, Ayaka Yamamoto, Aiko Yamashita, Naomi Tanga, Mai Suzuki, Takaya Abe, Issay Kitabayashi, Toshio Watanabe, Daisuke Sakai

Sci Rep. 2017; 7: 11922. Published online 2017 Sep 20. doi: 10.1038/s41598-017-11745-5

PMCID:: PMC5607342

Abstract Article PDF–8.7M

Select item 435651119.

T396I Mutation of Mouse Sufu Reduces the Stability and Activity of Gli3 Repressor

Shigeru Makino, Olena Zhulyn, Rong Mo, Vijitha Puviindran, Xiaoyun Zhang, Takuya Murata, Ryutaro Fukumura, Yuichi Ishitsuka, Hayato Kotaki, Daisuke Matsumaru, Shunsuke Ishii, Chi-Chung Hui, Yoichi Gondo

PLoS One. 2015; 10(3): e0119455. Published online 2015 Mar 11. doi: 10.1371/journal.pone.0119455