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Page 1
Osteocyte control of bone formation via sclerostin, a novel BMP antagonist.
Winkler DG, Sutherland MK, Geoghegan JC, Yu C, Hayes T, Skonier JE, Shpektor D, Jonas M, Kovacevich BR, Staehling-Hampton K, Appleby M, Brunkow ME, Latham JA. Winkler DG, et al. EMBO J. 2003 Dec 1;22(23):6267-76. doi: 10.1093/emboj/cdg599. EMBO J. 2003. PMID: 14633986 Free PMC article.
A novel mutation in CD83 results in the development of a unique population of CD4+ T cells.
García-Martínez LF, Appleby MW, Staehling-Hampton K, Andrews DM, Chen Y, McEuen M, Tang P, Rhinehart RL, Proll S, Paeper B, Brunkow ME, Grandea AG 3rd, Howard ED, Walker DE, Charmley P, Jonas M, Shaw S, Latham JA, Ramsdell F. García-Martínez LF, et al. Among authors: staehling hampton k. J Immunol. 2004 Sep 1;173(5):2995-3001. doi: 10.4049/jimmunol.173.5.2995. J Immunol. 2004. PMID: 15322158
A point mutation in the murine Hem1 gene reveals an essential role for Hematopoietic protein 1 in lymphopoiesis and innate immunity.
Park H, Staehling-Hampton K, Appleby MW, Brunkow ME, Habib T, Zhang Y, Ramsdell F, Liggitt HD, Freie B, Tsang M, Carlson G, Friend S, Frevert C, Iritani BM. Park H, et al. Among authors: staehling hampton k. J Exp Med. 2008 Nov 24;205(12):2899-913. doi: 10.1084/jem.20080340. Epub 2008 Nov 17. J Exp Med. 2008. PMID: 19015308 Free PMC article.
A role for Ebi in neuronal cell cycle control.
Boulton SJ, Brook A, Staehling-Hampton K, Heitzler P, Dyson N. Boulton SJ, et al. EMBO J. 2000 Oct 16;19(20):5376-86. doi: 10.1093/emboj/19.20.5376. EMBO J. 2000. PMID: 11032805 Free PMC article.
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes.
Asai-Coakwell M, French CR, Ye M, Garcha K, Bigot K, Perera AG, Staehling-Hampton K, Mema SC, Chanda B, Mushegian A, Bamforth S, Doschak MR, Li G, Dobbs MB, Giampietro PF, Brooks BP, Vijayalakshmi P, Sauvé Y, Abitbol M, Sundaresan P, van Heyningen V, Pourquié O, Underhill TM, Waskiewicz AJ, Lehmann OJ. Asai-Coakwell M, et al. Among authors: staehling hampton k. Hum Mol Genet. 2009 Mar 15;18(6):1110-21. doi: 10.1093/hmg/ddp008. Epub 2009 Jan 6. Hum Mol Genet. 2009. PMID: 19129173
Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome.
Cornier AS, Staehling-Hampton K, Delventhal KM, Saga Y, Caubet JF, Sasaki N, Ellard S, Young E, Ramirez N, Carlo SE, Torres J, Emans JB, Turnpenny PD, Pourquié O. Cornier AS, et al. Among authors: staehling hampton k. Am J Hum Genet. 2008 Jun;82(6):1334-41. doi: 10.1016/j.ajhg.2008.04.014. Epub 2008 May 15. Am J Hum Genet. 2008. PMID: 18485326 Free PMC article.
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