1. Adato, A., Weil, D., Kalinski, H., Pelor, Y., Ayadi, H.,
Petit, C., Korostishevsky, M., and Bonnetamir, B. Mutation Profile Of All 49 Exons
Of The Human Myosin VIIA Gene, And Haplotype Analysis, In Usher 1b Families From
Diverse Origins. 1997; Am.J.Hum.Genet. 61: 813 - 821.
Goto Top
2. Ayyagari, R., Nestorowicz, A., Li, Y., Smith, R.J.H.,
Kaiser-Kupfer, M., Permutt, M.A., and Heijmancik, J.F. A chromosome 11p14-15.1 YAC
contig that encompasses the Usher Syndrome Type 1C locus. 1995; Am.J.Hum.Genet.
57: A256
Goto Top
3. Chaib, H., Kaplan, J., Gerber, S., Vincent, C., Ayadi,
H., Slim, R., Munnich, A., Weissenbach, J., and Petit, C. A newly identified locus
for Usher syndrome type I, USH1E, maps to chromosome 21q21 A newly identified
locus for Usher syndrome type I, USH1E, maps to chromosome 21q21. 1997;
Hum.Mol.Genet. 6: 27 - 31.
Goto Top
Link to PudMed
4. Cremers, F.P.M., Molloy, C.M., van de Pol, D.J.R., van
den Hurk, J.A.J.M., Bach, I., van Kessel, A.H.M.G., Ropers, H.H., Cremers, F.P.,
van de Pol, D.J., van den Hurk, J.A., and Geurts van Kessel, A.H. An autosomal
homologue of the choroideremia gene colocalizes with the Usher syndrome type II
locus on the distal part of chromosome 1q. 1992; Hum.Mol.Genet. 1: 71 - 75.
Goto Top
Link to PudMed
5. DeAngelis, M., Donaldson, C., Buckley, L., Doucet, J.,
Sherry, S., Den, Z., Pelias, M., Deininger, P., Keats, B., and Batzer, M. In
search of the gene responsible for Acadian Usher syndrome (USH1C) on 11p. 1998;
Am.J.Hum.Genet. 63: A357
Goto Top
6. El Amraoui, A., Sahly, I., Picaud, S., Sahel, J.,
Abitbol, M., and Petit, C. Human Usher 1B/mouse shaker-1: the retinal phenotype
discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor
cells. 1996; Hum.Mol.Genet. 5: 1171 - 1178.
Goto Top
7. Espinos, C., Najera, C., Millan, J.M., Ayuso, C., Baiget,
M., Perez Garrigues, H., Rodrigo, O., Vilela, C., and Beneyto, M. Linkage analysis
in Usher syndrome type I (USH1) families from Spain. 1998; J.Med.Genet. 35: 391 -
398.
Goto Top
Link to PudMed
8. Eudy, J.D., Weston, M.D., Yao, S., Hoover, D.M., Rehm,
H.L., Ma Edmonds, M., Yan, D., Ahmad, I., Cheng, J.J., Ayuso, C., Cremers, C.,
Davenport, S., Moller, C., Talmadge, C.B., Beisel, K.W., Tamayo, M., Morton, C.C.,
Swaroop, A., Kimberling, W.J., and Sumegi, J. Mutation of a gene encoding a
protein with extracellular matrix motifs in Usher syndrome type IIa. 1998;
Science. 280: 1753 - 1757.
Goto Top
Link to PudMed
9. Gerber, S., Larget Piet, D., Rozet, J.M., Bonneau, D.,
Mathieu, M., Der Kaloustian, V., Munnich, A., and Kaplan, J. Evidence for a fourth
locus in Usher syndrome type I. 1996; J.Med.Genet. 33: 77 - 79.
Goto Top
Link to PudMed
10. Jain, P.K., Lalwani, A.K., Li, X.C., Singleton, T.L.,
Smith, T.N., Chen, A., Deshmukh, D., Verma, I.C., Smith, R.J., and Wilcox, E.R. A
gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the
chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene. 1998;
Genomics. 50: 290 - 292.
Goto Top
Link to PudMed
11. Joensuu, T., Blanco, G., Pakarinen, L., Sistonen, P.,
Kaariainen, H., Brown, S., Chapelle, A., and Sankila, E.M. Refined mapping of the
Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and
identification of the putative mouse homologous region. 1996; Genomics. 38: 255 -
263.
Goto Top
Link to PudMed
12. Joensuu, T.H., Hämäläinen, R.H.,
Lehesjoki, A.E., de la Chapelle, A., and Sankila, E.M. Refined physical and
partial transcript map of the Usher syndrome type III region. 1998;
Am.J.Hum.Genet. 63: A250
Goto Top
13. Kaplan, J., Gerber, S., Bonneau, D., Rozet, J.M.,
Delrieu, O., Briard, M.L., Dollfus, H., Ghazi, I., Dufier, J.L., and Frezal, J. A
gene for Usher syndrome type I (USH1A) maps to chromosome 14q. 1992; Genomics. 14:
979 - 987.
Goto Top
14. Keats, B.J., Nouri, N., Pelias, M.Z., Deininger, P.L.,
and Litt, M. Tightly linked flanking microsatellite markers for the Usher syndrome
type I locus on the short arm of chromosome 11. 1994; Am.J.Hum.Genet. 54: 681 -
686.
Goto Top
Link to PudMed
15. Kimberling, W.J., Aarem van, A., Sumegi, J., Connoly,
C., Weston, M.D., Cremers, C.W.R.J., Suy, P.S., Martini, A., Milana, M., Tamayo,
M.L., Bernal, J., Greenberg, J., Ayuso, C., Moller, C., van Aarem, A., Cremers,
C.W., Ing, P.S., Connolly, C., Milani, M., and et al. Gene mapping of Usher
Syndrome Type IIa: Localisation of the gene to a 2.1 cM segment on chromosome
1q41. 1995; Am.J.Hum.Genet. 56: 216 - 223.
Goto Top
Link to PudMed
16. Levy, G., Leviacobas, F., Blanchard, S., Gerber, S.,
Largetpiet, D., Chenal, V., Liu, X.Z., Newton, V., Steel, K.P., Brown, S.D.M.,
Munnich, A., Kaplan, J., Petit, C., Weil, D., Levi Acobas, F., Larget Piet, D.,
and Brown, S.D. Myosin VIIa Gene: Heterogeneity Of The Mutations Responsible For
Usher Syndrome Type Ib. 1997; Hum.Mol.Genet. 6: 111 - 116.
Goto Top
Link to PudMed
17. Mansergh, F.C., Millington-Ward, S., Kennan, A., Kiang,
A.S., Humphries, M., Farrar, G.J., Humphries, P., and Kenna, P.F. Retinitis
Pigmentosa and Progressive Sensorineural Hearing Loss Caused by a C12258A Mutation
in the Mitochondrial MTTS2 Gene. 1999; Am.J.Hum.Genet. 64: 971 - 985.
Goto Top
18. Pieke Dahl, S., Kimberling, W.J., Gorin, M.B., Weston,
M.D., Furman, J.M., Pikus, A., and Moller, C. Genetic heterogeneity of Usher
syndrome type II. 1993; J.Med.Genet. 30: 843 - 848.
Goto Top
Link to PudMed
19. Sankila, E.M., Pakarinen, L., Kaariainen, H.,
Aittomaki, K., Karjalainen, S., Sistonen, P., and de la Chapelle, A. Assignment of
an Usher syndrome type III (USH3) gene to chromosome 3q. 1995; Hum.Mol.Genet. 4:
93 - 98.
Goto Top
Link to PudMed
20. Slim, R., Mansour, A., Bou Moglabey, Y., El Zir, E.,
Mustapha, M., and Loiselet, J. The Usher syndrome in the Lebanese population:
evidence of further genetic heterogeneity in type I and III. 1998; Am.J.Hum.Genet.
63: A309
Goto Top
21. Smith, R.J., Lee, E.C., Kimberling, W.J., Daiger, S.P.,
Pelias, M.Z., Keats, B.J.B., Jay, M., Bird, A.C., Reardon, W., Guest, M.,
Ayyagari, R., Hejtmancik, J.F., Keats, B.J., Bird, A., and et al. Localization of
two genes for Usher syndrome type I to chromosome 11. 1992; Genomics. 14: 995 -
1002.
Goto Top
Link to PudMed
22. Sumegi, J., Wang, J.Y., Zhen, D.K., Eudy, J.D.,
Talmadge, C.B., Li, B.F., Berglund, P., Weston, M.D., Yao, S.F., Ma Edmonds, M.,
Overbeck, L., Kelley, P.M., Zabarovsky, E., Uzvolgyi, E., Stanbridge, E.J., Klein,
G., and Kimberling, W.J. The construction of a yeast artificial chromosome (YAC)
contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41. 1996;
Genomics. 35: 79 - 86.
Goto Top
Link to PudMed
23. Wayne, S., Der Kaloustian, V.M., Schloss, M., Polomeno,
R., Scott, D.A., Hejtmancik, J.F., Sheffield, V.C., and Smith, R.J. Localization
of the Usher syndrome type ID gene (Ush1D) to chromosome 10. 1996; Hum.Mol.Genet.
5: 1689 - 1692.
Goto Top
Link to PudMed
24. Wayne, S., Lowry, R.B., Mcleod, D.R., Knaus, R., Farr,
C., and Smith, R.J.H. Localization of the Usher syndrome zype 1F (Ush1F) to
chromosome 10. 1997; Am.J.Hum.Genet. 61: A300
Goto Top
25. Weil, D., Blanchard, S., Kaplan, J., Guilford, P.,
Gibson, F., Walsh, J., Mburu, P., Varela, A., Levilliers, J., Weston, M.D.,
Kelley, P.M., Kimberling, W.J., Wagenaar, M., Levi Acobas, F., Larget-Piet, D.,
Munnich, A., Steel, K.P., Brown, S.D.M., Petit, C., and et al. Defective myosin
VIIA gene responsible for Usher syndrome type 1B. 1995; Nature. 374: 60 - 61.
Goto Top
Link to PudMed
26. Weil, D., Kussel, P., Blanchard, S., Levy, G., Levi
Acobas, F., Drira, M., Ayadi, H., and Petit, C. The autosomal recessive isolated
deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA
gene. 1997; Nat.Genet. 16: 191 - 193.
Goto Top
Link to PudMed
Original address of this page:
www.retina-international.org/sci-news/usher.htm