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PLoS Biology, ISSN 1544-9173, 10/2017, Volume 15, Issue 10, pp. e2004045 - e2004045
During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors for neural plate, neural crest, placodes and epidermis. Here, we... 
GENE REGULATORY NETWORK | TRANSCRIPTION FACTORS | XENOPUS-LAEVIS | EXPRESSION ANALYSIS | CANCER GENOMICS | CRANIAL PLACODES | SUPER-ENHANCERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL IDENTITY | BIOLOGY | ZINC-FINGER GENE | MATRIX FACTORIZATION | Ectoderm - embryology | Microdissection | Humans | Databases, Genetic | Neurons - cytology | Gene Expression Profiling | Gene Regulatory Networks | Stem Cells - metabolism | Wnt Proteins - metabolism | Neural Crest - metabolism | Ectoderm - metabolism | Gastrulation - genetics | Neoplasms - genetics | Time Factors | Gene Expression Regulation, Developmental | Xenopus laevis - genetics | Principal Component Analysis | Gene Ontology | Xenopus laevis - embryology | Transcriptome - genetics | Neurulation - genetics | Algorithms | Animals | Neural Crest - embryology | Internet | Cluster Analysis | Visualization | Ectoderm | Wnt protein | Funding | Genomics | Spatial discrimination | Genomes | Biology | Genetic code | Specifications | Genetics | Neural plate | Supervision | Medical research | Developmental biology | Principal components analysis | Epidermis | Grants | Axes (reference lines) | Gene expression | Clustering | Embryos | Neural crest | Vertebrates | Signaling | Spatial data | Stem cells | Data collection | Neural stem cells | Software | Gene mapping | Cancer | Index Medicus | Life Sciences | Quantitative Methods
Journal Article
Science, ISSN 0036-8075, 4/2009, Volume 324, Issue 5926, pp. 522 - 528
Journal Article
by Renfree, Marilyn B and Papenfuss, Anthony T and Deakin, Janine E and Lindsay, James and Heider, Thomas and Belov, Katherine and Rens, Willem and Waters, Paul D and Pharo, Elizabeth A and Shaw, Geoff and Wong, Emily S.W and Lefèvre, Christophe M and Nicholas, Kevin R and Kuroki, Yoko and Wakefield, Matthew J and Zenger, Kyall R and Wang, Chenwei and Ferguson-Smith, Malcolm and Nicholas, Frank W and Hickford, Danielle and Yu, Hongshi and Short, Kirsty R and Siddle, Hannah V and Frankenberg, Stephen R and Chew, Keng Y and Menzies, Brandon R and Stringer, Jessica M and Suzuki, Shunsuke and Hore, Timothy A and Delbridge, Margaret L and Mohammadi, Amir and Schneider, Nanette Y and Hu, Yanqiu and O'Hara, William and Al Nadaf, Shafagh and Wu, Chen and Feng, Zhi-Ping and Cocks, Benjamin G and Wang, Jianghui and Flicek, Paul and Searle, Stephen M.J and Fairley, Susan and Beal, Kathryn and Herrero, Javier and Carone, Dawn M and Suzuki, Yutaka and Sugano, Sumio and Toyoda, Atsushi and Sakaki, Yoshiyuki and Kondo, Shinji and Nishida, Yuichiro and Tatsumoto, Shoji and Mandiou, Ion and Hsu, Arthur and McColl, Kaighin A and Lansdell, Benjamin and Weinstock, George and Kuczek, Elizabeth and McGrath, Annette and Wilson, Peter and Men, Artem and Hazar-Rethinam, Mehlika and Hall, Allison and Davis, John and Wood, David and Williams, Sarah and Sundaravadanam, Yogi and Muzny, Donna M and Jhangiani, Shalini N and Lewis, Lora R and Morgan, Margaret B and Okwuonu, Geoffrey O and Ruiz, San J and Santibanez, Jireh and Nazareth, Lynne and Cree, Andrew and Fowler, Gerald and Kovar, Christie L and Dinh, Huyen H and Joshi, Vandita and Jing, Chyn and Lara, Fremiet and Thornton, Rebecca and Chen, Lei and Deng, Jixin and Liu, Yue and Shen, Joshua Y and Song, Xing-Zhi and Edson, Janette and Troon, Carmen and Thomas, Daniel and Stephens, Amber and Yapa, Lankesha and Levchenko, Tanya and Gibbs, Richard A and Cooper, Desmond W and Speed, Terence P and Fujiyama, Asao and M Graves, Jennifer A and O'Neill, Rachel J and ...
Genome Biology, ISSN 1474-7596, 08/2011, Volume 12, Issue 8, pp. R81 - R81
Journal Article
Journal Article
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 05/2015, Volume 133, Issue 5, p. 511
  Screening for splice site mutation c.828+3A>T in the peripherin 2 (PRPH2) gene should be a high priority in families with highly variable retinal... 
Genetic disorders | Genes | Eye diseases | Mutation | Ophthalmology | Polymorphism
Journal Article
Catalysis Reviews, ISSN 0161-4940, 03/2010, Volume 52, Issue 1, pp. 60 - 105
Journal Article
Translational Psychiatry, ISSN 2158-3188, 02/2014, Volume 4, Issue 2, pp. e358 - e358
Journal Article