Signaling pathways crucial for craniofacial development revealed by endothelin-A receptor-deficient mice.
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M. Yanagisawa | J. Richardson | S. Williams | D. Clouthier | M. Wieduwilt | H. Yanagisawa | S. Williams | David E. Clouthier | S.Clay Williams | Hiromi Yanagisawa | Matthew Wieduwilt | James A. Richardson | Masashi Yanagisawa | Matthew Wieduwilt
[1] D. Srivastava,et al. A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects. , 1999, Science.
[2] G. Robinson,et al. Placental failure in mice lacking the homeobox gene Dlx3. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[3] P. Sharpe,et al. Fgf-8 determines rostral-caudal polarity in the first branchial arch. , 1999, Development.
[4] D. Srivastava,et al. A signaling cascade involving endothelin-1, dHAND and msx1 regulates development of neural-crest-derived branchial arch mesenchyme. , 1998, Development.
[5] R. Hammer,et al. Role of Endothelin-1/Endothelin-A receptor-mediated signaling pathway in the aortic arch patterning in mice. , 1998, The Journal of clinical investigation.
[6] R. Ladher,et al. Signalling interactions during facial development , 1998, Mechanisms of Development.
[7] R. Hammer,et al. Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice. , 1998, Development.
[8] D. Bowden,et al. Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome. , 1998, Human molecular genetics.
[9] R. Hammer,et al. Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene. , 1998, Development.
[10] S. Keränen,et al. The life history of an embryonic signaling center: BMP-4 induces p21 and is associated with apoptosis in the mouse tooth enamel knot. , 1998, Development.
[11] Philippe Soriano. The PDGF alpha receptor is required for neural crest cell development and for normal patterning of the somites. , 1997, Development.
[12] D. Srivastava,et al. Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND , 1997, Nature Genetics.
[13] J. Rubenstein,et al. Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches. , 1997, Developmental biology.
[14] A. Lumsden,et al. Rhombencephalic neural crest segmentation is preserved throughout craniofacial ontogeny. , 1996, Development.
[15] A. McMahon,et al. Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2 , 1996, Nature.
[16] R. Jaenisch,et al. Transcription factor AP-2 essential for cranial closure and craniofacial development , 1996, Nature.
[17] S. Elledge,et al. Cdk inhibitors in development and cancer. , 1996, Current opinion in genetics & development.
[18] N. Copeland,et al. Sequence analysis, chromosomal location, and developmental expression of the mouse preproendothelin-1 gene. , 1996, Genomics.
[19] D. Srivastava,et al. A Subclass of bHLH Proteins Required for Cardiac Morphogenesis , 1995, Science.
[20] J. Rubenstein,et al. Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain. , 1995, Genes & development.
[21] P. Thorogood,et al. Bone morphogenetic protein-2 and -4 expression during murine orofacial development. , 1995, Archives of oral biology.
[22] G. Lyons,et al. Expression of the novel basic helix-loop-helix gene eHAND in neural crest derivatives and extraembryonic membranes during mouse development. , 1995, Developmental biology.
[23] M. Capecchi,et al. The role of Hoxa-3 in mouse thymus and thyroid development. , 1995, Development.
[24] Adriana C. Gittenberger-de Groot,et al. Expression patterns of the paired-related homeobox genes MHox/Prx1 and S8/Prx2 suggest roles in development of the heart and the forebrain , 1995, Mechanisms of Development.
[25] J. Martín,et al. The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages. , 1995, Genes & development.
[26] M. Mark,et al. Barx1, a new mouse homeodomain transcription factor expressed in cranio-facial ectomesenchyme and the stomach , 1995, Mechanisms of Development.
[27] R. Hammer,et al. Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice , 1994, Cell.
[28] G. Robinson,et al. Differential and overlapping expression domains of Dlx-2 and Dlx-3 suggest distinct roles for Distal-less homeobox genes in craniofacial development , 1994, Mechanisms of Development.
[29] M. Yanagisawa,et al. ECE-1: A membrane-bound metalloprotease that catalyzes the proteolytic activation of big endothelin-1 , 1994, Cell.
[30] Y. Ouchi,et al. Elevated blood pressure and craniofaclal abnormalities in mice deficient in endothelin-1 , 1994, Nature.
[31] R. Maas,et al. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development , 1994, Nature Genetics.
[32] Pierre Chambon,et al. A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene , 1993, Cell.
[33] Moisés Mallo,et al. Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest , 1993, Cell.
[34] P. Scambler,et al. DiGeorge syndrome: part of CATCH 22. , 1993, Journal of medical genetics.
[35] U. Eriksson,et al. Non-overlapping expression of CRBP I and CRABP I during pattern formation of limbs and craniofacial structures in the early mouse embryo. , 1993, Development.
[36] S. Ben‐Sasson,et al. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation , 1992, The Journal of cell biology.
[37] S. Fraser,et al. Vital dye analysis of cranial neural crest cell migration in the mouse embryo. , 1992, Development.
[38] E. Olson,et al. MHox: a mesodermally restricted homeodomain protein that binds an essential site in the muscle creatine kinase enhancer. , 1992, Development.
[39] A. Graham,et al. Segmental origin and migration of neural crest cells in the hindbrain region of the chick embryo. , 1991, Development.
[40] M. Ferguson,et al. Hox-7 expression during murine craniofacial development. , 1991, Development.
[41] V. Giguère,et al. Molecular cloning of cDNA encoding a second cellular retinoic acid-binding protein. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[42] M. Justice,et al. A new family of mouse homeo box-containing genes: molecular structure, chromosomal location, and developmental expression of Hox-7.1. , 1989, Genes & development.
[43] D. Noden. Interactions and fates of avian craniofacial mesenchyme. , 1988, Development.
[44] B. Hall. Mandibular morphogenesis and craniofacial malformations. , 1982, Journal of craniofacial genetics and developmental biology.
[45] B. Hall,et al. Epithelial influences on skeletogenesis in the mandible of the embryonic chick , 1977, The Anatomical record.