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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.
2019
2019
Upregulation of the long non-coding RNA FAM83H-AS1 in gastric cancer and its clinical significance.
2018
2018
Amelogenesis imperfecta: A novel FAM83H mutation and characteristics of periodontal ligament cells.
OBJECTIVE To delineate orodental features, dental mineral density, genetic aetiology and cellular characteristics associated with… 
Review
2015
Review
2015
Ultrastructural analysis of the teeth affected by amelogenesis imperfecta resulting from FAM83H mutations and review of the literature.
2014
2014
Missense Mutation in Fam83H Gene in Iranian Patients with Amelogenesis Imperfecta
Background: Amelogenesis Imperfecta (AI) is a disorder of tooth development where there is an abnormal formation of enamel or the… 
2011
2011
Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation.
BACKGROUND.  Autosomal dominant hypocalcified amelogenesis imperfecta (ADHCAI) is a disease with severe dental manifestations… 
2011
2011
imperfecta in a Danish five-gen Limited phenotypic variation of hypocalcified amelogenesis eration family with a novel FAM 83 H nonsense mutation
DORTE HAUBEK, HANS GJØRUP, LILLIAN G. JENSEN, INGER JUNCKER, METTE NYEGAARD, ANDERS D. BØRGLUM, SVEN POULSEN & JENS M. HERTZ… 
2009
2009
Fam83h is Associated with Intracellular Vesicles and ADHCAI
Defects in FAM83H on human chromosome 8q24.3 cause autosomal-dominant hypocalcified amelogenesis imperfecta (ADHCAI). FAM83H does… 
2009
2009
Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta.
AIM To determine the underlying molecular genetic aetiology of a family with the hypocalcified form of amelogenesis imperfecta… 
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