Browse our TRPS1 (TRPS1) ELISA Kits

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Trichorhinophalangeal Syndrome I ELISA Kits (TRPS1)
On are 0 Trichorhinophalangeal Syndrome I (TRPS1) ELISA Kits from different suppliers available. Additionally we are shipping TRPS1 Antibodies (22) and and many more products for this protein. A total of 26 TRPS1 products are currently listed.
AI115454, AI447310, D15Ertd586e, GC79, LGCR
list all ELISA KIts Gene Name GeneID UniProt
Rat TRPS1 TRPS1 299897  
Human TRPS1 TRPS1 7227 Q9UHF7
Mouse TRPS1 TRPS1 83925  

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More ELISA Kits for TRPS1 Interaction Partners

Human Trichorhinophalangeal Syndrome I (TRPS1) interaction partners

  1. in this kindred support the previous genotype-phenotype results suggesting that patients with more pronounced facial characteristics and more severe shortening of hands and feet are more likely to have mutation in exon 6 of TRPS1

  2. Down-regulation of TRPS1 by miR (show MLXIP ELISA Kits)-373, acting as a transcriptional activator, promotes epithelial-mesenchymal transition (EMT (show ITK ELISA Kits)) and metastasis by repressing FOXA1 (show FOXA1 ELISA Kits) transcription, expanding upon its previously reported role as a transcription repressor.

  3. TRPS1 gene was responsible for most of the TRPS phenotype

  4. Data show that co-silencing of tricho-rhino (show RHNO1 ELISA Kits)-phalangeal-syndrome (TRPS1) and cathepsin D (show CTSD ELISA Kits) (Cath-D) in breast cancer cells (BCC) affects the transcription of cell cycle and proliferation.

  5. Trps1 plays a crucial role in osteosarcoma angiogenesis, metastasis and clinical surgical stage.

  6. Single nucleotide polymorphisms in TRPS1 gene is associated with Coronary Artery Disease.

  7. Missense mutations are located exclusively in exon 6 and 7 of TRPS1 in patients with tricho-rhino (show RHNO1 ELISA Kits)-phalangeal syndrome.

  8. TRPS1 haploinsufficiency results in STAT3 (show STAT3 ELISA Kits) and SOX9 (show SOX9 ELISA Kits) mRNA expression in Trichorhinophalangeal syndrome.

  9. Trps1 is involved in non-anastomotic biliary structure pathogenesis following liver transplantation and negatively correlates with biliary epithelial cell epithelial-mesenchymal transition and biliary fibrosis in liver grafts.

  10. our study proposes that TRPS1 acts as a central hub in the control of cell cycle and proliferation during cancer development

Mouse (Murine) Trichorhinophalangeal Syndrome I (TRPS1) interaction partners

  1. our findings partially explain why patients with TRPS show a broad range of congenital cardiac defects, although Trps1 expression is observed in a more restricted fashion.

  2. Taken together, these results show that hair follicle development in Trps1 KO embryos is impaired directly or indirectly by decreased Noggin (show NOG ELISA Kits) expression.

  3. association between SNP within TRPS1 and BMD (show BEST1 ELISA Kits)

  4. Trps1 acts as a regulator of hdac1 (show HDAC1 ELISA Kits) and hdac4 (show HDAC5 ELISA Kits) histone deacetylases during mitosis.

  5. The loss of Trps1 suppresses ureteric bud branching because of the activation of TGF-beta (show TGFB1 ELISA Kits) signaling.

  6. We found that Trps1 directly represses expression of the hair follicle stem cell regulator Sox9 (show SOX9 ELISA Kits) to control proliferation of the follicle epithelium.

  7. Trps1 is identified as a potent inhibitor of Dspp (show DSPP ELISA Kits) expression and the subsequent mineralization of dentin.

  8. analysis of control of mesenchymal lineage progression by microRNAs targeting skeletal gene regulators Trps1 and Runx2 (show RUNX2 ELISA Kits)

  9. These observations underscore the indispensable role played by Trps1 in normal temporomandibular joint development.

  10. Genetic variation in TRPS1 may regulate hip geometry as well as bone mineral density

TRPS1 Antigen Profile

Antigen Summary

This gene encodes a transcription factor that represses GATA-regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in this gene are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III.

Alternative names and synonyms associated with TRPS1

  • trichorhinophalangeal syndrome I (Trps1) Elisa Kit
  • trichorhinophalangeal syndrome I (TRPS1) Elisa Kit
  • trichorhinophalangeal syndrome I (trps1) Elisa Kit
  • trichorhinophalangeal syndrome I (human) (Trps1) Elisa Kit
  • AI115454 Elisa Kit
  • AI447310 Elisa Kit
  • D15Ertd586e Elisa Kit
  • GC79 Elisa Kit
  • LGCR Elisa Kit

Protein level used designations for TRPS1

trichorhinophalangeal syndrome I homolog , zinc finger transcription factor Trps1 , tricho-rhino-phalangeal syndrome type I protein , zinc finger protein GC79 , atypical GATA protein TRPS1

299897 Rattus norvegicus
7227 Homo sapiens
399173 Xenopus laevis
83925 Mus musculus
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