The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Links

 

Gene Review

HLX  -  H2.0-like homeobox

Homo sapiens

Synonyms: H2.0-like homeobox protein, HB24, HLX1, Homeobox protein HB24, Homeobox protein HLX1
 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

High impact information on HLX1

 

Biological context of HLX1

 

Other interactions of HLX1

  • Real-time polymerase chain reaction quantitation showed reduced HLX1 mRNA levels with advancing gestation age (preterm control placentas, 27 to 35 weeks, 1.1 +/- 0.3, n = 13, versus term placentas 36 to 41 weeks, 0.74 +/- 0.02, n = 12, P < 0.005) [4].
 

Analytical, diagnostic and therapeutic context of HLX1

References

  1. PARP alleles within the linked chromosomal region are associated with systemic lupus erythematosus. Tsao, B.P., Cantor, R.M., Grossman, J.M., Shen, N., Teophilov, N.T., Wallace, D.J., Arnett, F.C., Hartung, K., Goldstein, R., Kalunian, K.C., Hahn, B.H., Rotter, J.I. J. Clin. Invest. (1999) [Pubmed]
  2. Polymorphisms in human homeobox HLX1 and DNA repair RAD51 genes increase the risk of therapy-related acute myeloid leukemia. Jawad, M., Seedhouse, C.H., Russell, N., Plumb, M. Blood (2006) [Pubmed]
  3. Dinucleotide repeat polymorphism for HLX1 gene. Sander, A., Kennedy, M.A., Rayner, J.C., Murray, J.C. Hum. Mol. Genet. (1994) [Pubmed]
  4. Homeobox gene HLX1 expression is decreased in idiopathic human fetal growth restriction. Murthi, P., Doherty, V., Said, J., Donath, S., Brennecke, S.P., Kalionis, B. Am. J. Pathol. (2006) [Pubmed]
  5. Linkage localization of TGFB2 and the human homeobox gene HLX1 to chromosome 1q. Nishimura, D.Y., Purchio, A.F., Murray, J.C. Genomics (1993) [Pubmed]
  6. Genomic structure, promoter sequence, and revised translation of human homeobox gene HLX1. Kennedy, M.A., Rayner, J.C., Morris, C.M. Genomics (1994) [Pubmed]
 
WikiGenes - Universities