amelogenesis

This protein is formed for a short time during amelogenesis.

During tooth development there are strong similarities between keratinization and amelogenesis.

Researchers are looking for mutations in other genes that may also cause amelogenesis imperfecta.

Enamel formation is called amelogenesis and occurs in the crown stage of tooth development.

Answer: There are several conditions that can cause the lack of enamel, including a condition called amelogenesis imperfecta.

There are many different types of Amelogenesis imperfecta.

Another very rare side effect is amelogenesis imperfecta.

Defects in this gene are a cause of amelogenesis imperfecta type 3 (AI3).

Normally, amelogenesis involves a period of enamel matrix formation and a rest period.

The exact incidence of amelogenesis imperfecta is uncertain.

This is because they are formed by entrapment of odontoblast processes between ameloblasts prior to and during amelogenesis.

This protein is formed by ameloblasts during the early secretory to late maturation stages of amelogenesis.

People afflicted with amelogenesis imperfecta have teeth with abnormal color: yellow, brown or grey.

Amelogenin is the name for a series of closely related proteins involved in amelogenesis, the development of enamel.

Mutations in this gene cause autosomal-recessive hypomaturation amelogenesis imperfecta.

Taurodontism is found in association with amelogenesis imperfecta, ectodermal dysplasia and tricho-dento-osseous syndrome.

Enamel mineralisation only occurs once (as ameloblasts die out) therefore after amelogenesis, enamel is final.

Although the precise role of amelogenin(s) in regulating the mineralization process is unknown, it is known that amelogenins are abundant during amelogenesis.

Jalili syndrome is a genetic disorder characterized by the combination of cone-rod dystrophy of the retina and amelogenesis imperfecta.

Mutations in AMELX can cause amelogenesis imperfecta, a disorder of tooth enamel development.

A mutation in FAM20A was reported to be associated with amelogenesis imperfecta, an inherited enamel defect, and gingival hyperplasia syndrome.

The formation of a developing tooth includes the process of dentin formation, (see: Dentinogenesis) and enamel formation, (see: amelogenesis).

A mutation in this gene, which alters the normal splice pattern and results in premature termination of the encoded protein, has been associated with amelogenesis imperfecta.

Mutations in the related AMELX gene on the X chromosome cause X-linked amelogenesis imperfecta.

Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome (TDO) and amelogenesis imperfecta with taurodontism.