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Dan Wells - Publications

Affiliations: 
Biology and Biochemistry University of Houston, Houston, TX, United States 
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7 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
2011 Zak BM, Schuksz M, Koyama E, Mundy C, Wells DE, Yamaguchi Y, Pacifici M, Esko JD. Compound heterozygous loss of Ext1 and Ext2 is sufficient for formation of multiple exostoses in mouse ribs and long bones. Bone. 48: 979-87. PMID 21310272 DOI: 10.1016/J.Bone.2011.02.001  0.357
2009 Abu-Daya A, Sater AK, Wells DE, Mohun TJ, Zimmerman LB. Absence of heartbeat in the Xenopus tropicalis mutation muzak is caused by a nonsense mutation in cardiac myosin myh6. Developmental Biology. 336: 20-9. PMID 19769958 DOI: 10.1016/J.Ydbio.2009.09.019  0.34
2009 Khokha MK, Krylov V, Reilly MJ, Gall JG, Bhattacharya D, Cheung CY, Kaufman S, Lam DK, Macha J, Ngo C, Prakash N, Schmidt P, Tlapakova T, Trivedi T, Tumova L, ... ... Wells DE, et al. Rapid gynogenetic mapping of Xenopus tropicalis mutations to chromosomes. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 238: 1398-46. PMID 19441086 DOI: 10.1002/Dvdy.21965  0.306
2008 Tan Y, DeBruyne J, Cahill GM, Wells DE. Identification of a mutation in the Clock1 gene affecting zebrafish circadian rhythms. Journal of Neurogenetics. 22: 149-66. PMID 18569451 DOI: 10.1080/01677060802049738  0.344
2005 Hilton MJ, Gutiérrez L, Martinez DA, Wells DE. EXT1 regulates chondrocyte proliferation and differentiation during endochondral bone development Bone. 36: 379-386. PMID 15777636 DOI: 10.1016/j.bone.2004.09.025  0.364
2004 DeBruyne J, Hurd MW, Gutiérrez L, Kaneko M, Tan Y, Wells DE, Cahill GM. Isolation and phenogenetics of a novel circadian rhythm mutant in zebrafish. Journal of Neurogenetics. 18: 403-28. PMID 15763996 DOI: 10.1080/01677060490894540  0.406
2002 Hilton MJ, Sawyer JM, Gutiérrez L, Hogart A, Kung TC, Wells DE. Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes. Journal of Human Genetics. 47: 103-6. PMID 11950061 DOI: 10.1007/s100380200010  0.366
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