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Search references for DLX3. Phrases containing DLX3
See searches and references containing DLX3!DLX3
Mammalian protein found in Homo sapiens
that in humans is encoded by the DLX3 gene. Dlx3 is a crucial regulator of hair follicle differentiation and cycling. Dlx3 transcription is mediated through
DLX3
Organ found in mammalian skin
morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: Alternative mode for Dlx3 induction in mouse keratinocytes". Nucleic Acids
Hair_follicle
Medical condition
Tennessee, and North Carolina. The cause of this disease is a mutation in the DLX3 (distal-less 3) gene, which controls hair follicle differentiation and induction
Tricho–dento–osseous_syndrome
Subclass of mammals in the clade Theriiformes
"Theria-Specific Homeodomain and cis-Regulatory Element Evolution of the Dlx3–4 Bigene Cluster in 12 Different Mammalian Species". Journal of Experimental
Theria
ENSG00000115844 Homeodomain Known motif – High-throughput in vitro [143] TAATTR DLX3 ENSG00000064195 Homeodomain Known motif – High-throughput in vitro [144]
List of human transcription factors
List_of_human_transcription_factors
Genes in the DLX family
two-gene clusters (bigene clusters) with each other. There are DLX1-DLX2, DLX3-DLX4, DLX5-DLX6 clusters in vertebrates, linked to Hox gene clusters HOXD
DLX_gene_family
Specialised epithelial tissue in the nasal cavity that detects odours
regulated downstream expression of transcription factors, such as Pax6, Dlx3, Sox2, and others, within the presumptive olfactory placode are crucial for
Olfactory_epithelium
Cell compartment found in the nucleus's interchromatin space
Dispensable No CPSF6 Dispensable No CPSF7 Important No DAZAP1 Essential Yes DLX3 n.d. Yes EWSR1 Dispensable Yes Yes FAM98A Important Yes FIGN Important Yes
Paraspeckle
Medical condition
cause autosomal-recessive Wiedemann-Rautenstrauch syndrome. Am J Hum Genet "DLX3 distal-less homeobox 3 [Homo sapiens (human)]". Gene - National Center for
Wiedemann–Rautenstrauch syndrome
Wiedemann–Rautenstrauch_syndrome
DNA pattern affecting anatomy development
ANTP-like group. Humans have a "distal-less homeobox" family: DLX1, DLX2, DLX3, DLX4, DLX5, and DLX6. Dlx genes are involved in the development of the nervous
Homeobox
Mammalian protein found in Homo sapiens
Wright JT, Pettenati MJ, Hart TC (1998). "Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome". Hum. Mol. Genet. 7
DLX4
HGNC:2911; P36957 4318 DLX1 HGNC:2914; P56177 4319 DLX2 HGNC:2915; Q07687 4320 DLX3 HGNC:2916; O60479 4321 DLX4 HGNC:2917; Q92988 4322 DLX5 HGNC:2918; P56178
List of human protein-coding genes 2
List_of_human_protein-coding_genes_2
imperfecta, hypomaturation-hypoplastic type, with taurodontism; 104510; DLX3 Amelogenesis imperfecta, hypoplastic/hypomaturation type; 301200; AMELX Amelogenesis
List_of_OMIM_disorder_codes
Anatomical entity
the transcription factor ZBTB16 is a target for further investigations. DLX3, a transcription factor, which is related to the induced BMP2 pathway in
Dental_follicle
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