- Amelogenin, X
isoform is a
protein that in
humans is
encoded by the
AMELX gene.
AMELX is
located on the X
chromosome and
encodes a set of
isoforms of amelogenin...
-
protein isoforms produced by
alternative splicing or
proteolysis from the
AMELX gene, on the X chromosome, and also the
AMELY gene in males, on the Y chromosome...
-
crystal growth and
enamel mineralization.[citation needed]
Mutations in the
AMELX, ENAM, ACP4, MMP20, KLK-4, FAM83H, WDR72, C4orf26, SLC24A4 LAMB3 and ITGB6...
- arm [Yp]. ZFY ZFX Zinc finger. RPS4Y1 RPS4X
Ribosomal protein S4.
AMELY AMELX Amelogenin. TBL1Y TBL1X PCDH11Y PDCH11X X-transposed
region (XTR) from Xq21...
- HGNC:457 P17707 614 AMDHD1 HGNC:28577 Q96NU7 615 AMDHD2 HGNC:24262 Q9Y303 616
AMELX HGNC:461 Q99217 617
AMELY HGNC:462 Q99218 618 AMER1 HGNC:26837 Q5JTC6 619...
-
Community of Belgium. Amel may also
refer to: Amel (name)
Amelogenin (AMELY and
AMELX), ****
determining DNA
chromosomal markers Amel (river), a
Belgian river...
-
biomineralization during tooth enamel development.
Mutations in the
related AMELX gene on the X
chromosome cause X-linked
amelogenesis imperfecta. GRCh38:...
-
these cells with amelogenin, the main
component of enamel,
encoded by the
AMELX gene,
which has been
already implicated as a
causative factor of Amelogenesis...
- DLX3
Amelogenesis imperfecta, hypoplastic/hypomaturation type; 301200;
AMELX Amelogenesis imperfecta, type 3; 130900; FAM83H
Amelogenesis imperfecta...
