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TECTA wt Allele
Known as:
DFNB21
, DFNA8
, Tectorin, Alpha Gene
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Human TECTA wild-type allele is located within 11q22-q24 and is approximately 90 kb in length. This allele, which encodes alpha-tectorin protein, is…
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National Institutes of Health
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Related topics
Related topics
8 relations
Cell Adhesion
Cell Movement
Hearing
Morphogenesis
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2004
Highly Cited
2004
A Genotype-Phenotype Correlation with Gender-Effect for Hearing Impairment Caused by TECTA Mutations
M. Pfister
,
H. Thiele
,
+10 authors
S. Kupka
Cellular Physiology and Biochemistry
2004
Corpus ID: 42513598
Background: Alpha-tectorin is a noncollagenous component of the tectorial membrane which plays an essential role in auditory…
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Highly Cited
2003
Highly Cited
2003
Distinctive audiometric profile associated with DFNB21 alleles of TECTA
S. Naz
,
F. Alasti
,
+5 authors
E. Wilcox
Journal of medical genetics
2003
Corpus ID: 35014353
enetic factors are thought to account for approximately one half of cases of childhood hearing loss, the majority of which is non…
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1999
1999
Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
K. Verhoeven
Nature Genetics
1999
Corpus ID: 13334481
Kristien Verhoeven et al. Nature Genet. 19, 60–62 (1998). The nucleotide numbering of the mouse gene was used for the human…
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Highly Cited
1999
Highly Cited
1999
Alpha-tectorin involvement in hearing disabilities: one gene – two phenotypes
J. Balciuniene
,
N. Dahl
,
+5 authors
E. Jazin
Human Genetics
1999
Corpus ID: 21559396
Abstract. The human α-tectorin (TECTA) gene has recently been cloned and proposed to be involved in autosomal dominant non…
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Highly Cited
1999
Highly Cited
1999
Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss
N. Alloisio
,
L. Morlé
,
+7 authors
G. Lina-Granade
European Journal of Human Genetics
1999
Corpus ID: 2025000
A gene responsible for autosomal dominant non-syndromic hearing impairment in two families (DFNA8 and DFNA12) has recently been…
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Highly Cited
1998
Highly Cited
1998
Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
K. Verhoeven
,
L. Laer
,
+17 authors
G. Camp
Nature Genetics
1998
Corpus ID: 24814696
The tectorial membrane is an extracellular matrix of the inner ear that contacts the stereocilia bundles of specialized sensory…
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Highly Cited
1998
Highly Cited
1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.
K. Verhoeven
,
L. Van Laer
,
+17 authors
G. Van Camp
Nature genetics
1998
Corpus ID: 32069001
The tectorial membrane is an extracellular matrix of the inner ear that contacts the stereocilia bundles of specialized sensory…
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Highly Cited
1998
Highly Cited
1998
Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family.
J. Balciuniene
,
N. Dahl
,
+4 authors
E. Jazin
American journal of human genetics
1998
Corpus ID: 46278891
We investigated a Swedish family with nonsyndromic progressive bilateral sensorineural hearing loss. Thirteen candidate loci for…
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1998
1998
Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family
K. Kirschhofer
,
J. Kenyon
,
+4 authors
W. Kimberling
Cytogenetic and Genome Research
1998
Corpus ID: 46792102
A four-generation family suffering from an autosomal-dominant, congenital, nonprogressive, nonsyndromic hearing loss was found in…
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Highly Cited
1997
Highly Cited
1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.
K. Verhoeven
,
G. Van Camp
,
+10 authors
P. Willems
American journal of human genetics
1997
Corpus ID: 41838586
We performed linkage analysis in a Belgian family with autosomal dominant midfrequency hearing loss, which has a prelingual onset…
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