Papers authored by Erven A

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Alkali-metal pyrazolate complexes with unusual pyrazolate coordination modes and pseudocubane motifs.
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Beaini S, Deacon GB, Erven AP, Junk PC, and Turner DR
Chemistry, an Asian journal 2(4):539-50, 2007 Apr 2 - Who cited this? | PubMed ID: 17441192 | Fulltext
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Tmc1 is necessary for normal functional maturation and survival of inner and outer hair cells in the mouse cochlea.
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Marcotti W, Erven A, Johnson SL, Steel KP, and Kros CJ
The Journal of physiology 574(Pt 3):677-98, 2006 Aug 1 - Who cited this? | PubMed ID: 16627570 | Fulltext
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Two quantitative trait loci affecting progressive hearing loss in 101/H mice.
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Mashimo T, Erven AE, Spiden SL, Guénet JL, and Steel KP
Mammalian genome : official journal of the International Mammalian Genome Society 17(8):841-50, 2006 Aug - Who cited this? | PubMed ID: 16897347 | Fulltext
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Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disorders.
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Rastan S, Hough T, Kierman A, Hardisty R, Erven A, Gray IC, Voeling S, Isaacs A, Tsai H, Strivens M, Washbourne R, Thornton C, Greenaway S, Hewitt M, McCormick S, Selley R, 
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Genetica 122(1):47, 2004 Sep - Who cited this? | PubMed ID: 15619960 | Fulltext
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An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice.
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Ahituv N, Erven A, Fuchs H, Guy K, Ashery-Padan R, Williams T, de Angelis MH, Avraham KB, and Steel KP
Mammalian genome : official journal of the International Mammalian Genome Society 15(6):424-32, 2004 Jun - Who cited this? | PubMed ID: 15181535 | Fulltext
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The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media.
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Hardisty RE, Erven A, Logan K, Morse S, Guionaud S, Sancho-Oliver S, Hunter AJ, Brown SD, and Steel KP
Journal of the Association for Research in Otolaryngology : JARO 4(2):130-8, 2003 Jun - Who cited this? | PubMed ID: 12943368 | Fulltext
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A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil.
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Erven A, Skynner MJ, Okumura K, Takebayashi S, Brown SD, Steel KP, and Allen ND
The European journal of neuroscience 16(8):1433-41, 2002 Oct - Who cited this? | PubMed ID: 12405956 | Fulltext
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ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis.
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Kiernan AE, Erven A, Voegeling S, Peters J, Nolan P, Hunter J, Bacon Y, Steel KP, Brown SD, and Guénet JL
Mammalian genome : official journal of the International Mammalian Genome Society 13(3):142-8, 2002 Mar - Who cited this? | PubMed ID: 11919684 | Fulltext
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Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.
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Vreugde S, Erven A, Kros CJ, Marcotti W, Fuchs H, Kurima K, Wilcox ER, Friedman TB, Griffith AJ, Balling R, Hrabé De Angelis M, Avraham KB, and Steel KP
Nature genetics 30(3):257-8, 2002 Mar - Who cited this? | PubMed ID: 11850623 | Fulltext
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A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.
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Nolan PM, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray IC, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, 
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Nature genetics 25(4):440, 2000 Aug - Who cited this? | PubMed ID: 10932191 | Fulltext
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The promoter of the strictosidine synthase gene from periwinkle confers elicitor-inducible expression in transgenic tobacco and binds nuclear factors GT-1 and GBF.
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Pasquali G, Erven AS, Ouwerkerk PB, Menke FL, and Memelink J
Plant molecular biology 39(6):1299-310, 1999 Apr - Who cited this? | PubMed ID: 10380815 | Fulltext
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Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness.
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Kenna P, Mansergh F, Millington-Ward S, Erven A, Kumar-Singh R, Brennan R, Farrar GJ, and Humphries P
The British journal of ophthalmology 81(3):207-13, 1997 Mar - Who cited this? | PubMed ID: 9135384 | Fulltext
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Retinopathy induced in mice by targeted disruption of the rhodopsin gene.
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Humphries MM, Rancourt D, Farrar GJ, Kenna P, Hazel M, Bush RA, Sieving PA, Sheils DM, McNally N, Creighton P, Erven A, Boros A, Gulya K, Capecchi MR, and Humphries P
Nature genetics 15(2):216-9, 1997 Feb - Who cited this? | PubMed ID: 9020854 | Fulltext
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