Gene cluster regulation by CAMTAs. CAMTA1 to CAMTA6 are divided in two... | Download Scientific Diagram
Identification of a Disease-Defining Gene Fusion in Epithelioid Hemangioendothelioma | Science Translational Medicine
Jerad Gardner, MD on X: "Epithelioid hemangioendothelioma: WWTR1-CAMTA1 or YAP-TFE3 gene fusion -Dr. Shon #ASDP2014 #dermpath #pathologists http://t.co/ULjhYDbAbp" / X
Cancers | Free Full-Text | Unraveling the Biology of Epithelioid Hemangioendothelioma, a TAZ–CAMTA1 Fusion Driven Sarcoma
CAMTA1 Gene - GeneCards | CMTA1 Protein | CMTA1 Antibody
CAMTA 1 regulates drought responses in Arabidopsis thaliana | BMC Genomics | Full Text
TAZ-CAMTA1 and YAP-TFE3 alter the TAZ/YAP transcriptome by recruiting the ATAC histone acetyltransferase complex | eLife
CAMTA1 Antibody (NBP1-93620): Novus Biologicals
CAMTA1 Polyclonal Antibody (PA5-103686)
Mechanism of action of a WWTR1(TAZ)-CAMTA1 fusion oncoprotein | Oncogene
CAMTA1 Antibody (NBP1-93620): Novus Biologicals
Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability | Journal of Medical Genetics
Fig. S1. Deletion of CAMTA1 in mice. ( A ) Generation of CAMTA1... | Download Scientific Diagram
CAMTA1 antibody | Biorbyt
JAZF1-CAMTA1 Dual Fusion/Translocation FISH Probe Kit - CytoTest
Anti-CAMTA1 antibody (ab64119) | Abcam
CAMTA1 antibody | anti CAMTA1 antibody | Biorbyt
Cancers | Free Full-Text | Unraveling the Biology of Epithelioid Hemangioendothelioma, a TAZ–CAMTA1 Fusion Driven Sarcoma
Identifying the 5'End of the CAMTA1 Genes in Zebrafish
Identification of a Disease-Defining Gene Fusion in Epithelioid Hemangioendothelioma | Science Translational Medicine
Expression of CAMTA1 in mouse cerebellum. In situ hybridization... | Download Scientific Diagram
Anti-CAMTA1 antibody (ab199116) | Abcam
WWTR1(TAZ)-CAMTA1 gene fusion is sufficient to dysregulate YAP/TAZ signaling and drive epithelioid hemangioendothelioma tumorigenesis. - Abstract - Europe PMC
CAMTA1 Break Apart FISH Probe Kit - CytoTest
Calmodulin-binding transcription activator 1 - Wikipedia
De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability | European Journal of Human Genetics
