4 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2007 Wu JI, Centilli MA, Vasquez G, Young S, Scolnick J, Durfee LA, Spearow JL, Schwantz SD, Rennebeck G, Artzt K. Tint maps to mouse chromosome 6 and may interact with a notochordal enhancer of Brachyury. Genetics. 177: 1151-61. PMID 17954925 DOI: 10.1534/genetics.107.079715  0.572
1998 Rennebeck G, Kleymenova EV, Anderson R, Yeung RS, Artzt K, Walker CL. Loss of function of the tuberous sclerosis 2 tumor suppressor gene results in embryonic lethality characterized by disrupted neuroepithelial growth and development Proceedings of the National Academy of Sciences of the United States of America. 95: 15629-15634. PMID 9861021 DOI: 10.1073/pnas.95.26.15629  0.456
1998 Rennebeck G, Lader E, Fujimoto A, Lei EP, Artzt K. Mouse Brachyury the second (T2) is a gene next to classical T and a candidate gene for tct Genetics. 150: 1125-1131. PMID 9799264  0.624
1995 Rennebeck GM, Lader E, Chen Q, Bohm RA, Cai ZS, Faust C, Magnuson T, Pease LR, Artzt K. Is There aBrachyury the Second?Analysis of a Transgenic Mutation Involved in Notochord Maintenance in Mice Developmental Biology. 172: 206-217. PMID 7589801 DOI: 10.1006/Dbio.1995.0016  0.624
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