Page last updated: 2024-11-08

serine and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

serine has been researched along with Autosomal Recessive Emery-Dreifuss Muscular Dystrophy in 2 studies

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

Research Excerpts

ExcerptRelevanceReference
"Emerin was strongly phosphorylated in an M-phase Xenopus egg cell-free system, and five phosphorylated sites, Ser49, Ser66, Thr67, Ser120, and Ser175, were identified on analysis of chymotryptic and tryptic emerin peptides using a phosphopeptide-concentrating system coupled with a Titansphere column, which specifically binds phosphopeptides, and tandem mass spectrometry sequencing."1.33Dissociation of emerin from barrier-to-autointegration factor is regulated through mitotic phosphorylation of emerin in a xenopus egg cell-free system. ( Furukawa, K; Hirano, Y; Horigome, T; Ouchi, FS; Segawa, M; Takeyasu, K; Yamakawa, Y, 2005)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hirano, Y1
Segawa, M1
Ouchi, FS1
Yamakawa, Y1
Furukawa, K1
Takeyasu, K1
Horigome, T1
Menache, CC1
Brown, CA1
Donnelly, JH1
Shapiro, F1
Darras, BT1

Other Studies

2 other studies available for serine and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

ArticleYear
Dissociation of emerin from barrier-to-autointegration factor is regulated through mitotic phosphorylation of emerin in a xenopus egg cell-free system.
    The Journal of biological chemistry, 2005, Dec-02, Volume: 280, Issue:48

    Topics: Animals; Cell Cycle; Cell-Free System; Chromatin; Chymotrypsin; Cytosol; DNA-Binding Proteins; Gluta

2005
Identification of a novel truncating mutation (S171X) in the Emerin gene in five members of a Caucasian American family with Emery-Dreifuss muscular dystrophy.
    Human mutation, 2000, Volume: 16, Issue:1

    Topics: Alternative Splicing; Amino Acid Substitution; Humans; Membrane Proteins; Muscular Dystrophy, Emery-

2000