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Results:
1-7
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Results: 7
Authors:
Herskovits, AA
Seluanov, A
Rajsbaum, R
ten Hagen-Jongman, CM
Henrichs, R
Bochkareva, ES
Phillips, GJ
Probst, FJ
Nakae, T
Ehrmann, M
Luirink, J
Bibi, E
Citation: Aa. Herskovits et al., Evidence for coupling of membrane targeting and function of the signal recognition particle (SRP) receptor FtsY, EMBO REP, 2(11), 2001, pp. 1040-1046
Authors:
Anderson, DW
Probst, FJ
Belyantseva, IA
Fridell, RA
Beyer, L
Martin, DM
Wu, D
Kachar, B
Friedman, TB
Raphael, Y
Camper, SA
Citation: Dw. Anderson et al., The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells, HUM MOL GEN, 9(12), 2000, pp. 1729-1738
Authors:
Beyer, LA
Odeh, H
Probst, FJ
Lambert, EH
Dolan, DF
Camper, SA
Kohrman, DC
Raphael, Y
Citation: La. Beyer et al., Hair cells in the inner ear of the pirouette and shaker 2 mutant mice, J NEUROCYT, 29(4), 2000, pp. 227-239
Authors:
Martin, DM
Probst, FJ
Camper, SA
Petty, EM
Citation: Dm. Martin et al., Characterisation and genetic mapping of a new X linked deafness syndrome, J MED GENET, 37(11), 2000, pp. 836-841
Authors:
Liang, Y
Wang, AH
Belyantseva, IA
Anderson, DW
Probst, FJ
Barber, TD
Miller, W
Touchman, JW
Jin, L
Sullivan, SL
Sellers, JR
Camper, SA
Lloyd, RV
Kachar, B
Friedman, TB
Fridell, RA
Citation: Y. Liang et al., Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2, GENOMICS, 61(3), 1999, pp. 243-258
Authors:
Probst, FJ
Chen, KS
Zhao, Q
Wang, AH
Friedman, TB
Lupski, JR
Camper, SA
Citation: Fj. Probst et al., A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2), GENOMICS, 55(3), 1999, pp. 348-352
Authors:
Probst, FJ
Camper, SA
Citation: Fj. Probst et Sa. Camper, The role of mouse mutants in the identification of human hereditary hearing loss genes, HEARING RES, 130(1-2), 1999, pp. 1-6
Risultati:
1-7
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