Longitudinal analysis of electroencephalography pattern changes in an infant with Schaaf‐Yang syndrome and a novel mutation in melanoma antigen L2 (MAGEL2)
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DOI: 10.1002/mgg3.1932
Abstract: Schaaf‐Yang syndrome (SYS) is a rare hereditary disease caused by truncating point mutations of the paternal allele of melanoma antigen L2 (MAGEL2), one of five protein‐coding genes within the Prader‐Willi syndrome (PWS) critical domain. SYS… read more here.
Keywords: schaaf yang; melanoma antigen; antigen magel2; yang syndrome ... See more keywords
Evolution of Melanoma Antigen-A11 (MAGEA11) During Primate Phylogeny
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DOI: 10.1007/s00239-018-9838-8
Abstract: Melanoma antigen-A11 (MAGE-A11) is an X-linked and primate-specific steroid hormone receptor transcriptional coregulator and proto-oncogenic protein whose increased expression promotes the growth of prostate cancer. The MAGEA11 gene is expressed at low levels in normal… read more here.
Keywords: mage a11; evolution; a11; melanoma antigen ... See more keywords