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Items: 20

1.

Identification of EMS-induced mutations in Drosophila melanogaster by whole-genome sequencing.

Blumenstiel JP, Noll AC, Griffiths JA, Perera AG, Walton KN, Gilliland WD, Hawley RS, Staehling-Hampton K.

Genetics. 2009 May;182(1):25-32. doi: 10.1534/genetics.109.101998. Epub 2009 Mar 23.

2.

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.

Hum Mol Genet. 2009 Mar 15;18(6):1110-21. doi: 10.1093/hmg/ddp008. Epub 2009 Jan 6.

PMID:
19129173
3.

Aneuploidy underlies rapid adaptive evolution of yeast cells deprived of a conserved cytokinesis motor.

Rancati G, Pavelka N, Fleharty B, Noll A, Trimble R, Walton K, Perera A, Staehling-Hampton K, Seidel CW, Li R.

Cell. 2008 Nov 28;135(5):879-93. doi: 10.1016/j.cell.2008.09.039.

4.

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.

J Exp Med. 2008 Nov 24;205(12):2899-913. doi: 10.1084/jem.20080340. Epub 2008 Nov 17.

5.

A comprehensive library of histone mutants identifies nucleosomal residues required for H3K4 methylation.

Nakanishi S, Sanderson BW, Delventhal KM, Bradford WD, Staehling-Hampton K, Shilatifard A.

Nat Struct Mol Biol. 2008 Aug;15(8):881-8. doi: 10.1038/nsmb.1454. Epub 2008 Jul 11.

6.

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.

Am J Hum Genet. 2008 Jun;82(6):1334-41. doi: 10.1016/j.ajhg.2008.04.014. Epub 2008 May 15.

7.

Characterization of Cullin-box sequences that direct recruitment of Cul2-Rbx1 and Cul5-Rbx2 modules to Elongin BC-based ubiquitin ligases.

Mahrour N, Redwine WB, Florens L, Swanson SK, Martin-Brown S, Bradford WD, Staehling-Hampton K, Washburn MP, Conaway RC, Conaway JW.

J Biol Chem. 2008 Mar 21;283(12):8005-13. doi: 10.1074/jbc.M706987200. Epub 2008 Jan 10.

8.

RDH10 is essential for synthesis of embryonic retinoic acid and is required for limb, craniofacial, and organ development.

Sandell LL, Sanderson BW, Moiseyev G, Johnson T, Mushegian A, Young K, Rey JP, Ma JX, Staehling-Hampton K, Trainor PA.

Genes Dev. 2007 May 1;21(9):1113-24.

9.

Sterile and disposable fluidic subsystem suitable for clinical high speed fluorescence-activated cell sorting.

Jayasinghe SM, Wunderlich J, McKee A, Newkirk H, Pope S, Zhang J, Staehling-Hampton K, Li L, Haug JS.

Cytometry B Clin Cytom. 2006 Sep 15;70(5):344-54.

10.

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.

J Immunol. 2004 Sep 1;173(5):2995-3001.

11.

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.

EMBO J. 2003 Dec 1;22(23):6267-76.

12.

A 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch population.

Staehling-Hampton K, Proll S, Paeper BW, Zhao L, Charmley P, Brown A, Gardner JC, Galas D, Schatzman RC, Beighton P, Papapoulos S, Hamersma H, Brunkow ME.

Am J Med Genet. 2002 Jun 15;110(2):144-52.

PMID:
12116252
13.

A role for Ebi in neuronal cell cycle control.

Boulton SJ, Brook A, Staehling-Hampton K, Heitzler P, Dyson N.

EMBO J. 2000 Oct 16;19(20):5376-86.

14.

A genetic screen for modifiers of E2F in Drosophila melanogaster.

Staehling-Hampton K, Ciampa PJ, Brook A, Dyson N.

Genetics. 1999 Sep;153(1):275-87.

15.
16.

Drosophila Dpp signaling is mediated by the punt gene product: a dual ligand-binding type II receptor of the TGF beta receptor family.

Letsou A, Arora K, Wrana JL, Simin K, Twombly V, Jamal J, Staehling-Hampton K, Hoffmann FM, Gelbart WM, Massagué J, et al.

Cell. 1995 Mar 24;80(6):899-908.

17.

dpp induces mesodermal gene expression in Drosophila.

Staehling-Hampton K, Hoffmann FM, Baylies MK, Rushton E, Bate M.

Nature. 1994 Dec 22-29;372(6508):783-6.

PMID:
7997266
19.

Identification of two bone morphogenetic protein type I receptors in Drosophila and evidence that Brk25D is a decapentaplegic receptor.

Penton A, Chen Y, Staehling-Hampton K, Wrana JL, Attisano L, Szidonya J, Cassill JA, Massagué J, Hoffmann FM.

Cell. 1994 Jul 29;78(2):239-50.

PMID:
8044838
20.

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