Generation of novel conditional and hypomorphic alleles of the Smad2 gene and the effects of Smad2 removal in environments with elevated retinoid signaling

作者: Maria H. Festing

DOI:

关键词: RetinoidGeneComputational biologyBioinformaticsText miningBiologyAllele

摘要:

参考文章(140)
Roach E, Palmer C, Demyer W, Conneally Pm, Merritt Ad, Holoprosencephaly: birth data, benetic and demographic analyses of 30 families. Birth defects original article series. ,vol. 11, pp. 294- 313 ,(1975)
Hans Jörnvall, Olle Danielsson, Lars Hjelmqvist, Bengt Persson, Jawed Shafqat, The Alcohol Dehydrogenase System Advances in Experimental Medicine and Biology. ,vol. 372, pp. 281- 294 ,(1995) , 10.1007/978-1-4615-1965-2_34
N Ray Dunn, Brigid L M Hogan, How does the mouse get its trunk Nature Genetics. ,vol. 27, pp. 351- 352 ,(2001) , 10.1038/86829
Karen Niederreither, Vemparala Subbarayan, Pascal Dollé, Pierre Chambon, Embryonic retinoic acid synthesis is essential for early mouse post-implantation development. Nature Genetics. ,vol. 21, pp. 444- 448 ,(1999) , 10.1038/7788
Masatoshi Nomura, En Li, Smad2 role in mesoderm formation, left-right patterning and craniofacial development Nature. ,vol. 393, pp. 786- 790 ,(1998) , 10.1038/31693
Joseph L. Napoli, Retinoic acid: its biosynthesis and metabolism. Progress in Nucleic Acid Research and Molecular Biology. ,vol. 63, pp. 139- 188 ,(1999) , 10.1016/S0079-6603(08)60722-9
Karen W. Gripp, David Wotton, Michael C. Edwards, Erich Roessler, Lesley Ades, Peter Meinecke, Antonio Richieri-Costa, Elaine H. Zackai, Joan Massagué, Maximilian Muenke, Stephen J. Elledge, Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination Nature Genetics. ,vol. 25, pp. 205- 208 ,(2000) , 10.1038/76074
Masahiro Kawabata, Mitsuyasu Kato, Tadaichi Kitamura, Kohei Miyazono, Hideyuki Beppu, Hitoshi Okada, Toshiaki Hamamoto, Compound Disruption of Smad2 Accelerates Malignant Progression of Intestinal Tumors in Apc Knockout Mice Cancer Research. ,vol. 62, pp. 5955- 5961 ,(2002)