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NKX2-1 gene

Known as: NK2.1, MOUSE, HOMOLOG OF, TITF1, NKX2A 
This gene plays a role in thyroid gene transcription.
National Institutes of Health

Related topics

Related topics

10 relations
Cell Differentiation processHomo sapiensNK2 Homeobox 1 MeasurementPattern Formation

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NKX2-1 wt Allele

Papers overview

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2018
2018
Sex‐specific responses in neuroanatomy of hatchling American kestrels in response to embryonic exposure to the flame retardants bis(2‐ethylhexyl)‐2,3,4,5‐tetrabromophthalate and 2‐ethylhexyl‐2,3,4,5…
Bis(2‐ethylhexyl)‐2,3,4,5‐tetrabromophthalate (BEH‐TEBP) and 2‐ethylhexyl‐2,3,4,5‐tetrabromobenzoate (EH‐TBB), flame retardant… 
2017
2017
Vehicles as outdoor BFR sources :
• Users may freely distribute the URL that is used to identify this publication. • Users may download and/or print one copy of… 
2014
2014
LKB1 loss by alteration of the NKX2-1/p53 pathway promotes tumor malignancy and predicts poor survival and relapse in lung adenocarcinomas
LKB1 loss is a frequent homozygous deletion and/or gene mutation found in lung adenocarcinomas. However, few cases of LKB1 loss… 
2014
2014
Thyroid transcription factor-1 is a specific marker of benign but not malignant feline lung tumours.
2013
2013
Linking genomic lesions with minimal residual disease improves prognostic stratification in children with T-cell acute lymphoblastic leukaemia.
2011
2011
Secretoglobin 3A2/uteroglobin-related protein 1 is a novel marker for pulmonary carcinoma in mice and humans.
2008
2008
Evaluation of the NK2 Homeobox 1 Gene (NKX2‐1) as a Hirschsprung's Disease Locus 
THIS ARTICLE HAS BEEN RETRACTED
Hirschsprung's disease (HSCR, colonic aganglionosis) is an oligogenic entity that usually requires mutations in RET and other… 
2006
2006
Linear chromosome maintenance in the absence of essential telomere-capping proteins
Telomeres were defined by their ability to cap chromosome ends. Proteins with high affinity for the structure at chromosome ends… 
2006
2006
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause
Benign hereditary chorea (BHC; OMIM 118700) is an autosomal dominant movement disorder. Mutations in the thyroid transcription… 
Highly Cited
1995
Highly Cited
1995
Upstream Enhancer Activity in the Human Surfactant Protein B Gene Is Mediated by Thyroid Transcription Factor 1 (*)
Surfactant protein B (SP-B) is selectively expressed in bronchiolar and alveolar epithelial cells of the lung. We identified an… 
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