Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

NKX2-1 wt Allele

Known as: NK-2, BCH, TITF1 
Human NKX2-1 wild-type allele is located in the vicinity of 14q13 and is approximately 4 kb in length. This allele, which encodes thyroid… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2013
Highly Cited
2013
Abstract Background and objectives. Birth size curves are needed for clinical and epidemiological purposes. We constructed birth… Expand
Is this relevant?
Highly Cited
2013
Highly Cited
2013
BACKGROUND L-type amino acid transporters (LATs) uptake neutral amino acids including L-leucine into cells, stimulating mammalian… Expand
  • figure 5
Is this relevant?
Highly Cited
2010
Highly Cited
2010
OBJECT Chronic subdural hematoma (CSDH), a condition much more common in the elderly, presents an increasing challenge as the… Expand
  • table 1
  • figure 1
  • table 2
  • table 4
  • table 3
Is this relevant?
Highly Cited
2008
Highly Cited
2008
Lung cancer is a leading cause of cancer death, where the amplification of oncogenes contributes to tumorigenesis. Genomic… Expand
  • figure 1
  • figure 2
Is this relevant?
Highly Cited
2005
Highly Cited
2005
We have previously described a multiprotein complex termed the BHC or BRAF–HDAC complex, which is required for the repression of… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
2005
Highly Cited
2005
Thyroid dysgenesis (TD) is responsible for most cases of congenital hypothyroidism, a condition that affects about one in 4000… Expand
Is this relevant?
Highly Cited
2003
Highly Cited
2003
Thyroid transcription factor-1 (TTF-1) is a 43-kDa, phosphorylated member of the Nkx2 family of homeodomain-containing proteins… Expand
  • figure 1
  • table I
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
2002
Highly Cited
2002
BRAF35, a structural DNA-binding protein, initially was identified as a component of a large BRCA2-containing complex… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2002
Highly Cited
2002
Benign hereditary chorea (BHC) (MIM 118700) is an autosomal dominant movement disorder. The early onset of symptoms (usually… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2001
Highly Cited
2001
Andrographis paniculata (AP) treatment prevents BHC induced increase in the activities of enzymes y-Glutamyl transpeptidase… Expand
  • table 2
Is this relevant?