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439 results
  1. CSNK2B-Related Neurodevelopmental Disorder - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK606532
    ... subunit of casein kinase II (CK2), a serine/threonine kinase implicated in many diverse cellular functions. The ...
  2. Amino acids 
    https://medlineplus.gov/ency/article/002222.htm
    ... acids are: histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan , and valine. NONESSENTIAL AMINO ACIDS Nonessential means ...
  3. KPTN-Related Disorder - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK605495
    ... response to cellular amino acid levels. The serine/threonine protein kinase mTORC1 is within the canonical phosphoinositide ...
  4. Aminoaciduria 
    https://medlineplus.gov/ency/article/003366.htm
    ... Serine: 0 to 9 Taurine: 18 to 89 Threonine: 13 to 587 Tyrosine: 3 to 14 Valine: ...
  5. CDKL5 Deficiency Disorder - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK602610
    ... kinase-like 5 (CDKL5), a 115-kD serine-threonine kinase and member of the CMGC family, which ...
  6. Plasma amino acids 
    https://medlineplus.gov/ency/article/003361.htm
    ... Children: 11 to 120 Adults: 45 to 130 Threonine: Children: 67 to 150 Adults: 92 to 240 ...
  7. Classic Isovaleric Acidemia - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK601614
    ... SLC25A13 Citrin deficiency AR Hyperammonemia ↑ citrulline, arginine, methionine, threonine, tyrosine, & lysine in plasma ↑ liver enzymes 1, 4 ...
  8. Okur-Chung Neurodevelopmental Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK581083
    ... 500 genes as a member of the serine/threonine kinase family of proteins [ Borgo et al 2021 ]. ...
  9. CTNNB1 Neurodevelopmental Disorder - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK580527
    ... hot spots in exon 3 that encode serine-threonine phosphorylation sites for glycogen synthase kinase 3-beta, ...
  10. Fibrodysplasia Ossificans Progressiva - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK558090
    ... Molecular Pathogenesis ACVR1 encodes ACVR1, a transmembrane serine/threonine kinase. All individuals with FOP have overactive bone ...
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