This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Roberts-sc Phocomelia Syndrome
Information about Roberts-sc Phocomelia Syndrome: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Roberts-sc Phocomelia Syndrome
Most recent studies have shown that Roberts-sc Phocomelia Syndrome shares some biological mechanisms with aneuploidy, aplasia-nos, cleft-lip, cleft-palate, congenital-abnormality, cornelia-de-lange-syndrome, craniofacial-abnormalities, cytogenetic-abnormality, dysplasia, fetal-diseases, growth-disorders, growth-retardation, hemangioma, limb-defect, limb-deformities-congenital, orbital-separation-excessive, skeletal-dysplasia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Roberts-sc Phocomelia Syndrome, and have been seen in publications frequently: Aging, Anaphase, Cell Cycle, Cell Death, Cell Division, Cell Proliferation, Centromere Separation, Chromosome Condensation, Chromosome Segregation, Dna Repair, Dna Replication, Hypersensitivity, Interphase, Localization, Metaphase, Mitosis, Pathogenesis, S Phase, Sister Chromatid Cohesion, Translation
Quite a number of genes have been found to play important roles in Roberts-sc Phocomelia Syndrome, such as ARR3, AURKB, CDCA5, DDX11, DNAH5, ERCC2, ERMAP, ESCO1, ESCO2, MTSS1, NIPBL, PCNA, RET, SMC1A, SMC3, SPG7, TWIST1, ZNF143, ZWINT. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.