Structure, mapping and expression of the human gene encoding the homeodomain protein, SIX2
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference23 articles.
1. A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family;Abdelhak;Nat. Genet.,1997
2. A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat;Boucher;Hum. Mol. Genet.,1995
3. Cloning of the human SIX1 gene and its assignment to chromosome 14;Boucher;Genomics,1996
4. The Drosophila sine oculis locus encodes a homeodomain-containing protein required for the development of the entire visual system;Cheyette;Neuron,1994
5. Purification of CpG islands using a methylated DNA binding column;Cross;Nat. Genet.,1994
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2. Renal Autologous Cell Therapy to Stabilize Function in Diabetes-Related Chronic Kidney Disease: Corroboration of Mechanistic Action With Cell Marker Analysis;Kidney International Reports;2022-07
3. Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment;PLOS ONE;2022-06-16
4. Smarcd1 antagonizes the apoptosis of injured MES23.5 DA cells by enhancing the effect of Six2 on GDNF expression;Neuroscience Letters;2021-08
5. A Novel p.Tyr129His Variant in SIX1 Leads to Dominant, Delayed-onset Hearing Loss with Possible Association with Congenital Anosmia;BIOMED ENVIRON SCI;2021
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