• Thumbnail for DLX1
    Homeobox protein DLX-1 is a protein that in humans is encoded by the DLX1 gene. This gene encodes a member of a homeobox transcription factor gene family...
    5 KB (544 words) - 01:49, 3 December 2023
  • Thumbnail for Rat
    Retrieved 2006-11-24. Katerji, Suhair (1 May 2009). "Expression of Msx1 and Dlx1 during Dumbo rat head development: correlation with morphological features"...
    64 KB (6,915 words) - 22:54, 6 August 2024
  • Thumbnail for Ectrodactyly
    (Xq26), SHFM3 (FBXW4/DACTYLIN at 10q24), SHFM4 (TP63 at 3q27), and SHFM5 (DLX1 and DLX 2 at 2q31). SHFM3 is unique in that it is caused by submicroscopic...
    29 KB (3,025 words) - 12:02, 28 July 2024
  • in human and mice, numbered DLX1 to DLX6. They form two-gene clusters (bigene clusters) with each other. There are DLX1-DLX2, DLX3-DLX4, DLX5-DLX6 clusters...
    10 KB (1,073 words) - 20:30, 7 November 2023
  • from similar protein – In vivo/Misc source [141] VCRBNYYCGKGDRYTTCCGDVDNNB DLX1 ENSG00000144355 Homeodomain Known motif – High-throughput in vitro [142]...
    374 KB (81 words) - 02:10, 23 September 2023
  • Thumbnail for Homeobox
    into a large ANTP-like group. Humans have a "distal-less homeobox" family: DLX1, DLX2, DLX3, DLX4, DLX5, and DLX6. Dlx genes are involved in the development...
    41 KB (4,385 words) - 07:06, 25 July 2024
  • Thumbnail for DLX5
    findings, and orofacial clefting. In mice, the targeted disruption of DLX1, DLX2, DLX1/2, or DLX5 orthologs yields craniofacial, bone, and vestibular defects...
    9 KB (1,108 words) - 14:57, 8 January 2024
  • HGNC:2909 Q9NYJ7 4322 DLL4 HGNC:2910 Q9NR61 4323 DLST HGNC:2911 P36957 4324 DLX1 HGNC:2914 P56177 4325 DLX2 HGNC:2915 Q07687 4326 DLX3 HGNC:2916 O60479 4327...
    277 KB (17 words) - 23:17, 27 April 2024
  • Thumbnail for Ganglionic eminence
    differentiation and specification of interneurons and oligodendrocytes, including: Dlx1, Dlx2, Gsh1, Mash1, Gsh2, Nkx2.1, Nkx5.1, Isl1, Six3 and Vax1. The induced...
    16 KB (1,940 words) - 18:37, 25 November 2023
  • Retinal dystrophy, iris coloboma and comedogenic acne syndrome (RDCCAS) DLX1, DLX2 AD Split-hand/foot malformation type V C12orf57 AR Temtamy syndrome...
    13 KB (538 words) - 09:46, 18 March 2024