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THRA wt Allele
Known as:
THRA2
, Thyroid Hormone Receptor Alpha Gene
, ERBA1
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Human THRA wild-type allele is located in the vicinity of 17q11.2 and is approximately 31 kb in length. This allele, which encodes thyroid hormone…
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National Institutes of Health
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Related topics
Related topics
15 relations
17q11.2-q12
Biologic Development
Cell Differentiation process
Cell Proliferation
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Broader (1)
THRA gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2005
2005
Thyroid Cancer Susceptibility and THRA1 and BAT-40 Repeats Polymorphisms
A. Baida
,
S. Farrington
,
P. Galofré
,
R. Marcos
,
A. Velázquez
Cancer Epidemiology, Biomarkers and Prevention
2005
Corpus ID: 19003704
Although genetic and environmental factors have been identified in the etiology of thyroid cancer, the specific genetic…
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2002
2002
A targeted thyroid hormone receptor alpha gene dominant-negative mutation (P398H) selectively impairs gene expression in differentiated embryonic stem cells.
Yan-Yun Liu
,
K. Tachiki
,
G. Brent
Endocrinology
2002
Corpus ID: 33580110
Thyroid hormone and retinoic acid (RA) are essential for normal neural development in vivo, yet all in vitro differentiation…
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2002
2002
Expansion of microsatellite in the thyroid hormone receptor-alpha1 gene linked to increased receptor expression and less aggressive thyroid cancer.
M. Onda
,
Dai Li
,
+5 authors
N. Rampino
Clinical Cancer Research
2002
Corpus ID: 37688986
PURPOSE The purpose of this study was to determine whether the length of the THRA1 microsatellite, which resides in a noncoding…
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Highly Cited
2001
Highly Cited
2001
Suppression of the deafness and thyroid dysfunction in Thrb-null mice by an independent mutation in the Thra thyroid hormone receptor alpha gene.
L. Ng
,
A. Rüsch
,
+4 authors
D. Forrest
Human Molecular Genetics
2001
Corpus ID: 39884299
Deletion of thyroid hormone receptor beta (TR beta), a ligand-dependent transcription factor encoded by the Thrb gene, causes…
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1997
1997
Microsatellite instability and loss of heterozygosity in primary breast tumours.
G. Sourvinos
,
H. Kiaris
,
A. Tsikkinis
,
S. Vassilaros
,
D. Spandidos
Tumour biology : the journal of the International…
1997
Corpus ID: 28163851
Allelic imbalance or loss of heterozygosity (LOH) studies have been used extensively to identify regions on chromosomes that may…
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1996
1996
Allele loss of tumour suppressor genes on chromosome 17 in human testicular germ cell tumours.
M. Vanderlooij
,
H. Eid
,
M. Bak
,
I. Bodrogi
,
E. Oláh
International Journal of Oncology
1996
Corpus ID: 30383237
The molecular genetics of testicular germ cell tumours (TGCT) are still largely unknown. We investigated 20 TGCT tumours for…
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1995
1995
Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors.
M. Nagai
,
A. Medeiros
,
+4 authors
L. Mulligan
Oncology
1995
Corpus ID: 46763123
In this study, we analyzed 105 paired sporadic primary breast tumor and normal tissue samples for loss of heterozygosity (LOH) on…
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Highly Cited
1993
Highly Cited
1993
THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21.
A. Bowcock
,
L. Anderson
,
+6 authors
Mary Claire King
American Journal of Human Genetics
1993
Corpus ID: 20351204
In order to pinpoint the locale of the gene for early-onset familial breast and ovarian cancer (BRCA1), polymorphisms were…
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1993
1993
A somatic cell hybrid map of the long arm of human chromosome 17, containing the familial breast cancer locus (BRCA1).
D. Black
,
H. Nicolai
,
J. Borrow
,
E. Solomon
American Journal of Human Genetics
1993
Corpus ID: 34640410
We describe a detailed somatic cell hybrid map of human chromosome 17q11.2-q23, containing the familial breast and ovarian cancer…
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1992
1992
Developmental expression of mRNAs from a rat C-erbA genomic locus.
E. Jannini
,
T. Mitsuhashi
,
V. Nikodem
Biochemical and Biophysical Research…
1992
Corpus ID: 30244117
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