PubMed (OMIM) for id: 321902

Year	Number of Results
1981	1
1997	2
1998	4
1999	3
2000	1
2003	1
2005	1
2024	0

1

A deafness mutation isolates a second role for the tectorial membrane in hearing.

Legan PK, Lukashkina VA, Goodyear RJ, Lukashkin AN, Verhoeven K, Van Camp G, Russell IJ, Richardson GP. Legan PK, et al. Nat Neurosci. 2005 Aug;8(8):1035-42. doi: 10.1038/nn1496. Epub 2005 Jul 3. Nat Neurosci. 2005. PMID: 15995703

2

Distinctive audiometric profile associated with DFNB21 alleles of TECTA.

Naz S, Alasti F, Mowjoodi A, Riazuddin S, Sanati MH, Friedman TB, Griffith AJ, Wilcox ER, Riazuddin S. Naz S, et al. J Med Genet. 2003 May;40(5):360-3. doi: 10.1136/jmg.40.5.360. J Med Genet. 2003. PMID: 12746400 Free PMC article. No abstract available.

3

A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

Legan PK, Lukashkina VA, Goodyear RJ, Kössi M, Russell IJ, Richardson GP. Legan PK, et al. Neuron. 2000 Oct;28(1):273-85. doi: 10.1016/s0896-6273(00)00102-1. Neuron. 2000. PMID: 11087000 Free article.

4

Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypes.

Balciuniene J, Dahl N, Jalonen P, Verhoeven K, Van Camp G, Borg E, Pettersson U, Jazin EE. Balciuniene J, et al. Hum Genet. 1999 Sep;105(3):211-6. doi: 10.1007/s004390051091. Hum Genet. 1999. PMID: 10987647

5

Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss.

Alloisio N, Morlé L, Bozon M, Godet J, Verhoeven K, Van Camp G, Plauchu H, Muller P, Collet L, Lina-Granade G. Alloisio N, et al. Eur J Hum Genet. 1999 Feb-Mar;7(2):255-8. doi: 10.1038/sj.ejhg.5200273. Eur J Hum Genet. 1999. PMID: 10196713

6

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

Mustapha M, Weil D, Chardenoux S, Elias S, El-Zir E, Beckmann JS, Loiselet J, Petit C. Mustapha M, et al. Hum Mol Genet. 1999 Mar;8(3):409-12. doi: 10.1093/hmg/8.3.409. Hum Mol Genet. 1999. PMID: 9949200

7

Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family.

Kirschhofer K, Kenyon JB, Hoover DM, Franz P, Weipoltshammer K, Wachtler F, Kimberling WJ. Kirschhofer K, et al. Cytogenet Cell Genet. 1998;82(1-2):126-30. doi: 10.1159/000015086. Cytogenet Cell Genet. 1998. PMID: 9763681

8

Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family.

Balciuniene J, Dahl N, Borg E, Samuelsson E, Koisti MJ, Pettersson U, Jazin EE. Balciuniene J, et al. Am J Hum Genet. 1998 Sep;63(3):786-93. doi: 10.1086/302012. Am J Hum Genet. 1998. PMID: 9718342 Free PMC article.

9

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.

Verhoeven K, Van Laer L, Kirschhofer K, Legan PK, Hughes DC, Schatteman I, Verstreken M, Van Hauwe P, Coucke P, Chen A, Smith RJ, Somers T, Offeciers FE, Van de Heyning P, Richardson GP, Wachtler F, Kimberling WJ, Willems PJ, Govaerts PJ, Van Camp G. Verhoeven K, et al. Nat Genet. 1998 May;19(1):60-2. doi: 10.1038/ng0598-60. Nat Genet. 1998. PMID: 9590290

10

Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness.

Hughes DC, Legan PK, Steel KP, Richardson GP. Hughes DC, et al. Genomics. 1998 Feb 15;48(1):46-51. doi: 10.1006/geno.1997.5159. Genomics. 1998. PMID: 9503015

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

13 results

Results by year