Literature/Journals/Newsletters


References

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

horizontal line

Original address of this page:
www.retina-international.org/sci-news/usher.htm

nav. button overview overview    nav. button backback  nav. button next next