FAM83H gene

Known as: family with sequence similarity 83 member H, FAMILY WITH SEQUENCE SIMILARITY 83, MEMBER H, FLJ46072 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Recently, the roles of FAM83H in tumorigenesis have been interested and increased expression of FAM83H and MYC in hepatocellular… (More)
  • figure 1
  • table 1
  • table 2
  • figure 2
  • figure 3
Is this relevant?
2017
2017
Whole transcriptome analyses of next generation RNA sequencing (RNA-Seq) data from human cancer samples reveled thousands of… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2017
2017
The long non-coding RNA, FAM83H antisense RNA 1 (head to head) (FAM83H-AS1), has exhibited a functional role as an oncogene in a… (More)
Is this relevant?
2016
2016
Truncation mutations in FAM83H (family with sequence similarity 83, member H) cause autosomal dominant hypocalcified amelogenesis… (More)
Is this relevant?
2015
2015
OBJECTIVE Amelogenesis imperfecta (AI) is a group of clinically and genetically heterogeneous inherited conditions, causing… (More)
  • table 1
  • figure 1
  • figure 2
  • table 2
Is this relevant?
2014
2014
BACKGROUND Amelogenesis Imperfecta (AI) is a disorder of tooth development where there is an abnormal formation of enamel or the… (More)
  • figure 1
  • figure 2
  • table 2
Is this relevant?
2013
2013
OBJECTIVE The aim of this study was to determine if FAM83H over-expression causes dentine or enamel malformations. MATERIALS… (More)
  • table 1
  • figure 1
  • figure 2
  • table 2
  • table 3
Is this relevant?
2013
2013
Keratin filaments form cytoskeletal networks in epithelial cells. Dynamic rearrangement of keratin filament networks is required… (More)
Is this relevant?
2012
2012
The domestic dog (Canis familiaris) segregates more naturally-occurring diseases and phenotypic variation than any other species… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2011
2011
Mutations in a family with sequence similarity 83 member H (FAM83H) cause autosomal-dominant hypocalcification amelogenesis… (More)
Is this relevant?