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Results: 1-25/31
Authors:
Holme, RH
Steel, KP
Citation: Rh. Holme et Kp. Steel, Pictures in molecular medicine - Hair cell function - it's all a matter oforganization, TRENDS MO M, 7(3), 2001, pp. 138-138
Authors:
Steel, KP
Kros, CJ
Citation: Kp. Steel et Cj. Kros, A genetic approach to understanding auditory function, NAT GENET, 27(2), 2001, pp. 143-149
Authors:
Di Palma, F
Holme, RH
Bryda, EC
Belyantseva, IA
Pellegrino, R
Kachar, B
Steel, KP
Noben-Trauth, K
Citation: F. Di Palma et al., Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D, NAT GENET, 27(1), 2001, pp. 103-107
Authors:
Chaudhry, SS
Gazzard, J
Baldock, C
Dixon, J
Rock, MJ
Skinner, GC
Steel, KP
Kielty, CM
Dixon, MJ
Citation: Ss. Chaudhry et al., Mutation of the gene encoding fibrillin-2 results in syndactyly in mice, HUM MOL GEN, 10(8), 2001, pp. 835-843
Authors:
Tsai, H
Hardisty, RE
Rhodes, C
Kiernan, AE
Roby, P
Tymowska-Lalanne, Z
Mburu, P
Rastan, S
Hunter, AJ
Brown, SDM
Steel, KP
Citation: H. Tsai et al., The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelialpatterning in the organ of Corti, HUM MOL GEN, 10(5), 2001, pp. 507-512
Authors:
Libby, RT
Steel, KP
Citation: Rt. Libby et Kp. Steel, Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved. in human Usher syndrome type 1B, INV OPHTH V, 42(3), 2001, pp. 770-778
Authors:
Kiernan, AE
Ahituv, N
Fuchs, H
Balling, R
Avraham, KB
Steel, KP
de Angelis, MH
Citation: Ae. Kiernan et al., The Notch ligand Jagged1 is required for inner ear sensory development, P NAS US, 98(7), 2001, pp. 3873-3878
Authors:
Alavizadeh, A
Kiernan, AE
Nolan, P
Lo, C
Steel, KP
Bucan, M
Citation: A. Alavizadeh et al., The Wheels mutation in the mouse causes vascular, hindbrain, and inner eardefects, DEVELOP BIO, 234(1), 2001, pp. 244-260
Authors:
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, XH
McCormack, S
Pickford, K
Selley, R
Wells, C
Tymowska-Lalanne, Z
Roby, P
Glenister, P
Thornton, C
Thaung, C
Stevenson, JA
Arkell, R
Mburu, P
Hardisty, R
Kiernan, A
Erven, H
Steel, KP
Voegeling, S
Guenet, JL
Nickols, C
Sadri, R
Naase, M
Isaacs, A
Davies, K
Browne, M
Fisher, EMC
Martin, J
Rastan, S
Brown, SDM
Hunter, J
Citation: Pm. Nolan et al., A systematic, genome-wide, phenotype-driven mutagenesis programme for genefunction studies in the mouse, NAT GENET, 25(4), 2000, pp. 440-443
Authors:
Steel, KP
Citation: Kp. Steel, A take on the tectorial membrane, NAT GENET, 24(2), 2000, pp. 104-104
Authors:
Liu, XZ
Xia, XJ
Xu, LR
Pandya, A
Liang, CY
Blanton, SH
Brown, SDM
Steel, KP
Nance, WE
Citation: Xz. Liu et al., Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss, HUM MOL GEN, 9(1), 2000, pp. 63-67
Authors:
Steel, KP
Citation: Kp. Steel, Science, medicine, and the future - New interventions in hearing impairment, BR MED J, 320(7235), 2000, pp. 622-625
Authors:
Paige, AJW
Kiernan, BW
Varela, A
Rogers, MJC
Hughes, D
Steel, KP
Brown, SDM
Citation: Ajw. Paige et al., A deletion on Chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate, MAMM GENOME, 11(1), 2000, pp. 51-57
Authors:
Gazzard, J
Chaudhry, SS
Sampson, N
Schulte, BA
Dixon, MJ
Steel, KP
Citation: J. Gazzard et al., Mutation in the basolateral secretory Na+-K+-2Cl(-) co-transporter slc12a2causes deafness and vestibular dysfunction in the mouse, BR J AUDIOL, 34(2), 2000, pp. 83-84
Authors:
Holme, RH
Steel, KP
Citation: Rh. Holme et Kp. Steel, Abnormal hair cell differentiation in the cochlea of Waltzer mice, BR J AUDIOL, 34(2), 2000, pp. 84-84
Authors:
Kiernan, AE
Erven, A
Fuchs, H
de Angelis, MH
Balling, R
Guenet, J
Ahituv, N
Avraham, KB
Tang, A
Cheah, K
Tease, C
Nolan, P
Peters, J
Brown, SDM
Steel, KP
Citation: Ae. Kiernan et al., Several new mouse mutations affect semicircular canal morphogenesis of theinner ear, BR J AUDIOL, 34(2), 2000, pp. 85-86
Authors:
Erven, A
Kiernan, AE
de Angelis, MH
Fuchs, H
Balling, R
Guenet, JL
Avraham, KB
Ben-David, O
Vreugde, S
Nolan, P
Peters, J
Cattanach, B
Skynner, M
Allen, N
Brown, SDM
Steel, KP
Citation: A. Erven et al., Phenotypic analysis of new deaf and vestibular mouse mutants, BR J AUDIOL, 34(2), 2000, pp. 85-85
Authors:
Hardisty, RE
Varela, A
Mburu, P
Tsai, HT
Paige, AJW
Kiernan, BW
Holme, RH
Fleming, J
Rogers, MJC
Steel, KP
Brown, SDM
Citation: Re. Hardisty et al., Progress towards the identification of the whirler deafness gene, BR J AUDIOL, 34(2), 2000, pp. 86-86
Authors:
Tamagawa, Y
Kitamura, K
Ishida, T
Nishizawa, M
Liu, XZ
Walsh, J
Steel, KP
Brown, SDM
Citation: Y. Tamagawa et al., Sensorineural hearing impairment, non-syndromic, dominant DFNA11, ADV OTO-RH, 56, 2000, pp. 103-106
Authors:
Kiernan, AE
Steel, KP
Citation: Ae. Kiernan et Kp. Steel, Mouse homologues for human deafness, ADV OTO-RH, 56, 2000, pp. 233-243
Authors:
Dixon, MJ
Gazzard, J
Chaudhry, SS
Sampson, N
Schulte, BA
Steel, KP
Citation: Mj. Dixon et al., Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness inmice, HUM MOL GEN, 8(8), 1999, pp. 1579-1584
Authors:
Holme, RH
Steel, KP
Citation: Rh. Holme et Kp. Steel, Genes involved in deafness, CUR OP GEN, 9(3), 1999, pp. 309-314
Authors:
Rogers, MJC
Fleming, J
Kiernan, BW
Mburu, P
Varela, A
Brown, SDM
Steel, KP
Citation: Mjc. Rogers et al., Genetic mapping of the whirler mutation, MAMM GENOME, 10(5), 1999, pp. 513-519
Authors:
Tucker, JB
Mackie, JB
Bussoli, TJ
Steel, KP
Citation: Jb. Tucker et al., Cytoskeletal integration in a highly ordered sensory epithelium in the organ of Corti: reponse to loss of cell partners in the Bronx waltzer mouse, J NEUROCYT, 28(12), 1999, pp. 1017-1034
Authors:
Kiernan, AE
Zalzman, M
Fuchs, H
de Angelis, MH
Balling, R
Steel, KP
Avraham, KB
Citation: Ae. Kiernan et al., Tailchaser (Tlc): A new mouse mutation affecting hair bundle differentiation and hair cell survival, J NEUROCYT, 28(10-11), 1999, pp. 969-985