Gpr177/mouse Wntless is essential for Wnt‐mediated craniofacial and brain development
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Wei Hsu | W. Hsu | Jiang Fu | Takamitsu Maruyama | Jiang Fu | Hsiao-Man Ivy Yu | Takamitsu Maruyama | Anthony J Mirando | Hsiao-Man Ivy Yu | Anthony J. Mirando | A. Mirando
[1] Hendrik C Korswagen,et al. The making of Wnt: new insights into Wnt maturation, sorting and secretion , 2007, Development.
[2] F. Costantini,et al. Impaired neural development caused by inducible expression of Axin in transgenic mice , 2007, Mechanisms of Development.
[3] F. Costantini,et al. Development of a unique system for spatiotemporal and lineage-specific gene expression in mice. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[4] A. Joyner,et al. Subtle cerebellar phenotype in mice homozygous for a targeted deletion of the En-2 homeobox. , 1991, Science.
[5] S. Martinez,et al. Modulation of Fgf8 activity during vertebrate brain development , 2005, Brain Research Reviews.
[6] Harukazu Nakamura,et al. Isthmus organizer for midbrain and hindbrain development , 2005, Brain Research Reviews.
[7] A. Berns,et al. Knockout mouse models to study Wnt signal transduction. , 2006, Trends in genetics : TIG.
[8] Mario R. Capecchi,et al. Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development , 1990, Nature.
[9] R. Tjian,et al. Transcription factor AP-2 is expressed in neural crest cell lineages during mouse embryogenesis. , 1991, Genes & development.
[10] C. MacArthur,et al. Fgf-8 expression in the post-gastrulation mouse suggests roles in the development of the face, limbs and central nervous system , 1994, Mechanisms of Development.
[11] Steven J. M. Jones,et al. A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo. , 1999, Development.
[12] A. McMahon,et al. Fate of the mammalian cardiac neural crest. , 2000, Development.
[13] W. Hsu,et al. Reciprocal regulation of Wnt and Gpr177/mouse Wntless is required for embryonic axis formation , 2009, Proceedings of the National Academy of Sciences.
[14] A. Joyner,et al. The midbrain-hindbrain phenotype of Wnt-1− Wnt-1− mice results from stepwise deletion of engrailed-expressing cells by 9.5 days postcoitum , 1992, Cell.
[15] Jiaoti Huang,et al. Co-opted JNK/SAPK Signaling in Wnt/β-catenin-Induced Tumorigenesis , 2008 .
[16] R. Nusse,et al. The Wnt signaling pathway in development and disease. , 2004, Annual review of cell and developmental biology.
[17] Andrew P. McMahon,et al. Engrailed-1 as a target of the Wnt-1 signalling pathway in vertebrate midbrain development , 1996, Nature.
[18] W. Hsu,et al. Expression of Gpr177, a Wnt trafficking regulator, in mouse embryogenesis , 2010, Developmental dynamics : an official publication of the American Association of Anatomists.
[19] Allan Bradley,et al. Requirement for Wnt3 in vertebrate axis formation , 1999, Nature Genetics.
[20] A. McMahon,et al. Wnt signalling required for expansion of neural crest and CNS progenitors , 1997, Nature.
[21] W. Hsu,et al. Craniosynostosis caused by Axin2 deficiency is mediated through distinct functions of beta-catenin in proliferation and differentiation. , 2007, Developmental biology.
[22] W. Hsu,et al. Manipulating gene activity in Wnt1‐expressing precursors of neural epithelial and neural crest cells , 2009, Developmental dynamics : an official publication of the American Association of Anatomists.
[23] R. Lang,et al. Generation of mice with a conditional null allele for Wntless , 2010, Genesis.
[24] N. Ueno,et al. Monounsaturated fatty acid modification of Wnt protein: its role in Wnt secretion. , 2006, Developmental cell.
[25] Philippe Soriano. Generalized lacZ expression with the ROSA26 Cre reporter strain , 1999, Nature Genetics.
[26] Andrew P. McMahon,et al. The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain , 1990, Cell.
[27] Wei Hsu,et al. SUMO-Specific Protease 2 Is Essential for Modulating p53-Mdm2 in Development of Trophoblast Stem Cell Niches and Lineages , 2008, PLoS biology.
[28] A. McMahon,et al. Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis. , 2000, Development.
[29] K. Basler,et al. Helping Wingless take flight: how WNT proteins are secreted , 2007, Nature Reviews Molecular Cell Biology.
[30] A. Joyner,et al. Multiple developmental defects in Engrailed-1 mutant mice: an early mid-hindbrain deletion and patterning defects in forelimbs and sternum. , 1994, Development.
[31] J C Olivo,et al. Two rhombomeres are altered in Hoxa-1 mutant mice. , 1993, Development.
[32] C. Deng,et al. The Balance of WNT and FGF Signaling Influences Mesenchymal Stem Cell Fate During Skeletal Development , 2010, Science Signaling.
[33] A. Joyner,et al. EN and GBX2 play essential roles downstream of FGF8 in patterning the mouse mid/hindbrain region. , 2001, Development.
[34] I. Weissman,et al. Wnt proteins are lipid-modified and can act as stem cell growth factors , 2003, Nature.
[35] Walter Birchmeier,et al. Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of beta-catenin in mice. , 2008, Genes & development.
[36] W. Birchmeier,et al. The role of Axin2 in calvarial morphogenesis and craniosynostosis , 2005, Development.
[37] H. Clevers. Wnt/beta-catenin signaling in development and disease. , 2006, Cell.
[38] A. McMahon,et al. Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development. , 2001, Development.