Steel KP - Search Results

1

Multiple mutations in mouse Chd7 provide models for CHARGE syndrome.

Bosman EA, Penn AC, Ambrose JC, Kettleborough R, Stemple DL, Steel KP. Bosman EA, et al. Among authors: steel kp. Hum Mol Genet. 2005 Nov 15;14(22):3463-76. doi: 10.1093/hmg/ddi375. Epub 2005 Oct 5. Hum Mol Genet. 2005. PMID: 16207732

2

Study of smell and reproductive organs in a mouse model for CHARGE syndrome.

Bergman JE, Bosman EA, van Ravenswaaij-Arts CM, Steel KP. Bergman JE, et al. Among authors: steel kp. Eur J Hum Genet. 2010 Feb;18(2):171-7. doi: 10.1038/ejhg.2009.158. Epub 2009 Oct 7. Eur J Hum Genet. 2010. PMID: 19809474 Free PMC article.

3

Catweasel mice: a novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome.

Bosman EA, Quint E, Fuchs H, Hrabé de Angelis M, Steel KP. Bosman EA, et al. Among authors: steel kp. Dev Biol. 2009 Apr 15;328(2):285-96. doi: 10.1016/j.ydbio.2009.01.030. Epub 2009 Feb 2. Dev Biol. 2009. PMID: 19389353 Free PMC article.

4

Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1.

Bosman EA, Estabel J, Ismail O, Podrini C, White JK, Steel KP. Bosman EA, et al. Among authors: steel kp. Mamm Genome. 2013 Feb;24(1-2):44-53. doi: 10.1007/s00335-012-9438-7. Epub 2012 Nov 17. Mamm Genome. 2013. PMID: 23160729 Free PMC article.

5

Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study.

Le Quesne Stabej P, Saihan Z, Rangesh N, Steele-Stallard HB, Ambrose J, Coffey A, Emmerson J, Haralambous E, Hughes Y, Steel KP, Luxon LM, Webster AR, Bitner-Glindzicz M. Le Quesne Stabej P, et al. Among authors: steel kp. J Med Genet. 2012 Jan;49(1):27-36. doi: 10.1136/jmedgenet-2011-100468. Epub 2011 Dec 1. J Med Genet. 2012. PMID: 22135276 Free PMC article.

6

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice.

Randall V, McCue K, Roberts C, Kyriakopoulou V, Beddow S, Barrett AN, Vitelli F, Prescott K, Shaw-Smith C, Devriendt K, Bosman E, Steffes G, Steel KP, Simrick S, Basson MA, Illingworth E, Scambler PJ. Randall V, et al. Among authors: steel kp. J Clin Invest. 2009 Nov;119(11):3301-10. doi: 10.1172/JCI37561. Epub 2009 Oct 12. J Clin Invest. 2009. PMID: 19855134 Free PMC article.

7

Mutations and altered expression of SERPINF1 in patients with familial otosclerosis.

Ziff JL, Crompton M, Powell HR, Lavy JA, Aldren CP, Steel KP, Saeed SR, Dawson SJ. Ziff JL, et al. Among authors: steel kp. Hum Mol Genet. 2016 Jun 15;25(12):2393-2403. doi: 10.1093/hmg/ddw106. Epub 2016 Apr 7. Hum Mol Genet. 2016. PMID: 27056980 Free PMC article.

8

Genetic deafness--progress with mouse models.

Brown SD, Steel KP. Brown SD, et al. Among authors: steel kp. Hum Mol Genet. 1994;3 Spec No:1453-6. doi: 10.1093/hmg/3.suppl_1.1453. Hum Mol Genet. 1994. PMID: 7849737 Review.

9

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti.

Tsai H, Hardisty RE, Rhodes C, Kiernan AE, Roby P, Tymowska-Lalanne Z, Mburu P, Rastan S, Hunter AJ, Brown SD, Steel KP. Tsai H, et al. Among authors: steel kp. Hum Mol Genet. 2001 Mar 1;10(5):507-12. doi: 10.1093/hmg/10.5.507. Hum Mol Genet. 2001. PMID: 11181574

10

Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.

Steel KP, Smith RJ. Steel KP, et al. Nat Genet. 1992 Sep;2(1):75-9. doi: 10.1038/ng0992-75. Nat Genet. 1992. PMID: 1303254

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