The FaceBase Consortium: a comprehensive resource for craniofacial researchers
暂无分享,去创建一个
Carl Kesselman | James F. Brinkley | Axel Visel | Mary L. Marazita | Richard L. Maas | Richard A. Spritz | Harm van Bakel | Kenneth L. Jones | Ophir D. Klein | C. Kesselman | A. Visel | S. Fisher | J. Brinkley | R. Spritz | O. Klein | H. van Bakel | R. Maas | M. Marazita | J. Wysocka | Y. Chai | L. Selleri | J. Hooper | Joanna Wysocka | M. Harris | Shannon Fisher | Matthew P. Harris | Greg Holmes | Joan E. Hooper | Ethylin Wang Jabs | Licia Selleri | Trevor J. Williams | Yang Chai | Greg Holmes | M. Marazita | E. Wang Jabs | Trevor J Williams | T. Williams | James F. Brinkley | Shannon Fisher | Matthew P. Harris | Greg Holmes | Joan E. Hooper | Ethylin Wang Jabs | Kenneth L. Jones | Carl Kesselman | Richard L. Maas | Licia Selleri | Axel Visel | Trevor J. Williams | Joanna Wysocka | Yang Chai | Ophir D. Klein | Licia Selleri | Axel Visel | Greg Holmes | Matthew P. Harris | James F. Brinkley | Shannon Fisher | Joan E. Hooper | Ethylin Wang Jabs | Kenneth L. Jones | Carl Kesselman | Richard L. Maas | Trevor J Williams | Joanna Wysocka | Yang Chai
[1] Seth M. Weinberg,et al. The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community , 2016, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
[2] Kenneth A. Philbrick,et al. BCL11B regulates sutural patency in the mouse craniofacial skeleton. , 2016, Developmental biology.
[3] R. Pelikan,et al. Disruption of the ERK/MAPK pathway in neural crest cells as a potential cause of Pierre Robin sequence , 2015, Development.
[4] F. Alkuraya,et al. Identification of a Recognizable Progressive Skeletal Dysplasia Caused by RSPRY1 Mutations. , 2015, American journal of human genetics.
[5] F. Gage,et al. Enhancer Divergence and cis-Regulatory Evolution in the Human and Chimp Neural Crest , 2015, Cell.
[6] Claude C. Warzecha,et al. The splicing regulators Esrp1 and Esrp2 direct an epithelial splicing program essential for mammalian development , 2015, eLife.
[7] S. Twigg,et al. A Genetic-Pathophysiological Framework for Craniosynostosis. , 2015, American journal of human genetics.
[8] J. Iwata,et al. Integration of comprehensive 3D microCT and signaling analysis reveals differential regulatory mechanisms of craniofacial bone development. , 2015, Developmental biology.
[9] R. Koul. Computer processable classification of craniofacial clefts , 2015, Front. Physiol..
[10] Ingo Ruczinski,et al. Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci. , 2015, American journal of human genetics.
[11] C. Wade,et al. Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate , 2015, PLoS genetics.
[12] E. Jabs,et al. BCL11B expression in intramembranous osteogenesis during murine craniofacial suture development. , 2015, Gene expression patterns : GEP.
[13] Karl Czajkowski,et al. Digital asset management for heterogeneous biomedical data in an era of data-intensive science , 2014, 2014 IEEE International Conference on Bioinformatics and Biomedicine (BIBM).
[14] C. Morton,et al. Functional Analysis of SPECC1L in Craniofacial Development and Oblique Facial Cleft Pathogenesis , 2014, Plastic and reconstructive surgery.
[15] J. Richtsmeier,et al. Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses , 2014, Current Genetic Medicine Reports.
[16] Axel Visel,et al. Identification of Novel Craniofacial Regulatory Domains Located far Upstream of SOX9 and Disrupted in Pierre Robin Sequence , 2014, Human mutation.
[17] Jacinda R. Larson,et al. Facial morphometrics of children with NON-syndromic orofacial clefts in Tanzania , 2014, BMC oral health.
[18] Kyle B. Jones,et al. Craniofacial morphometric analysis of individuals with X-linked hypohidrotic ectodermal dysplasia , 2014, Molecular genetics & genomic medicine.
[19] A. Visel,et al. An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects. , 2014, Human molecular genetics.
[20] J. Mejino,et al. Computer processable classification of craniofacial clefts , 2015, Front. Physiol..
[21] R. Pelikan,et al. TGFβ regulates epithelial-mesenchymal interactions through WNT signaling activity to control muscle development in the soft palate , 2014, Development.
[22] F. Collins,et al. Policy: NIH plans to enhance reproducibility , 2014, Nature.
[23] A. Visel,et al. Rapid and Pervasive Changes in Genome-wide Enhancer Usage during Mammalian Development , 2013, Cell.
[24] J F Brinkley,et al. American Journal of Medical Genetics Part C (seminars in Medical Genetics) the Ontology of Craniofacial Development and Malformation for Translational Craniofacial Research , 2022 .
[25] Bing Ren,et al. Fine Tuning of Craniofacial Morphology by Distant-Acting Enhancers , 2013, Science.
[26] R. Pelikan,et al. Noncanonical Transforming Growth Factor β (TGFβ) Signaling in Cranial Neural Crest Cells Causes Tongue Muscle Developmental Defects*♦ , 2013, The Journal of Biological Chemistry.
[27] Linda G. Shapiro,et al. Human Development Domain of the Ontology of Craniofacial Development and Malformation , 2013, ICBO.
[28] T. Williams,et al. Separation of mouse embryonic facial ectoderm and mesenchyme. , 2013, Journal of visualized experiments : JoVE.
[29] Alexander Hoischen,et al. Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis , 2013, Proceedings of the National Academy of Sciences.
[30] Michael J. Parsons,et al. Skeletogenic Fate of Zebrafish Cranial and Trunk Neural Crest , 2012, PloS one.
[31] Alvaro Rada-Iglesias,et al. Epigenomic annotation of enhancers predicts transcriptional regulators of human neural crest. , 2012, Cell stem cell.
[32] J. Hacia,et al. Modulation of noncanonical TGF-β signaling prevents cleft palate in Tgfbr2 mutant mice. , 2012, The Journal of clinical investigation.
[33] E. Furlong,et al. Tissue-specific analysis of chromatin state identifies temporal signatures of enhancer activity during embryonic development , 2012, Nature Genetics.
[34] Anne E. Trefethen,et al. Toward interoperable bioscience data , 2012, Nature Genetics.
[35] S. Lewis,et al. Uberon, an integrative multi-species anatomy ontology , 2012, Genome Biology.
[36] S. Robertson,et al. Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid. , 2011, American journal of human genetics.
[37] Harry Hochheiser,et al. The FaceBase Consortium: a comprehensive program to facilitate craniofacial research. , 2011, Developmental biology.
[38] Ryan A. Flynn,et al. A unique chromatin signature uncovers early developmental enhancers in humans , 2011, Nature.
[39] Mehmet Gonullu,et al. Department of Computer Science and Engineering , 2011 .
[40] S. Bellusci,et al. Gli3Xt-J/Xt-J mice exhibit lambdoid suture craniosynostosis which results from altered osteoprogenitor proliferation and differentiation. , 2010, Human molecular genetics.
[41] Holger Schwender,et al. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 , 2010, Nature Genetics.
[42] J. Helms,et al. CHD7 cooperates with PBAF to control multipotent neural crest formation , 2010, Nature.
[43] Trevor Williams,et al. Spatial and Temporal Analysis of Gene Expression during Growth and Fusion of the Mouse Facial Prominences , 2009, PloS one.
[44] Fan Yang,et al. Abnormalities in cartilage and bone development in the Apert syndrome FGFR2+/S252W mouse , 2005, Development.
[45] S. Fisher,et al. Radiographic analysis of zebrafish skeletal defects. , 2003, Developmental biology.
[46] J. Hecksher-Sørensen,et al. Optical Projection Tomography as a Tool for 3D Microscopy and Gene Expression Studies , 2002, Science.
[47] Roy T. Fielding,et al. Principled design of the modern Web architecture , 2000, Proceedings of the 2000 International Conference on Software Engineering. ICSE 2000 the New Millennium.
[48] A. Wilkie,et al. Expression patterns of Twist and Fgfr1, -2 and -3 in the developing mouse coronal suture suggest a key role for Twist in suture initiation and biogenesis , 2000, Mechanisms of Development.
[49] Paula M. Mabee,et al. Development of the cranium and paired fins in the zebrafish Danio rerio (Ostariophysi, Cyprinidae) , 1996, Journal of morphology.
[50] R. Behringer,et al. twist is required in head mesenchyme for cranial neural tube morphogenesis. , 1995, Genes & development.
[51] C. Lunn. The Soft Palate , 1872, Hall's journal of health.