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Results 1 - 10 of 1,115 for 20S -"19,20,22,23-TETRAHYDRO-19-OXO-5H,21H-18,20-ETHANO-12,14-ETHENO-6,10-METHENOBENZ[D]IMIDAZO[4,3-L][1,6,9,13]OXATRIAZACYCLONOADECOSINE-9-CARBONITRILE"
Did you mean 20S -"19,20,22,23-tetra hydro-19-OXO-5H,21H-18,20-than-12,14-then-6,10-METHENOBENZ[D]IMIDAZO[4,3-L][1,6,9,13]OXATRIAZACYCLONOADECOSINE-9-CARBONITRILE"?
  1. 17 alpha-hydroxylase/17,20-lyase deficiency 
    17 alpha(α)-hydroxylase/17,20-lyase deficiency is a condition that affects the function of certain hormone-producing glands called the gonads (ovaries in ...
    https://medlineplus.gov/...-alpha-hydroxylase-17-20-lyase-deficiency - Genetics
  2. Ring chromosome 20 syndrome 
    Ring chromosome 20 syndrome is a condition that affects the normal development and function of the brain. The most common feature ... also appear to be characteristic of ring chromosome 20 syndrome. These episodes involve confusion and behavioral changes. ...
    https://medlineplus.gov/.../condition/ring-chromosome-20-syndrome - Genetics
  3. Chromosome 20 
    ... divided into 23 pairs. Two copies of chromosome 20, one copy inherited from each parent, form one of the pairs. Chromosome 20 spans about 63 million DNA building blocks (base ...
    https://medlineplus.gov/genetics/chromosome/20 - Genetics
  4. MMP20 gene 
    ... About This Health Condition enamel metalloproteinase matrix metallopeptidase 20 (enamelysin) matrix metalloproteinase 20 MMP-20 MMP20_HUMAN Tests of MMP20 PubMed ...
    https://medlineplus.gov/genetics/gene/mmp20 - Genetics
  5. SPART gene 
    ... About This Health Condition KIAA0610 SPARTIN spastic paraplegia 20 spastic paraplegia 20 (Troyer syndrome) spastic paraplegia 20, spartin (Troyer syndrome) ...
    https://medlineplus.gov/genetics/gene/spart - Genetics
  6. SLC20A2 gene 
    ... sodium-dependent phosphate transporter 2 solute carrier family 20 (phosphate transporter), member 2 Tests of SLC20A2 PubMed SOLUTE CARRIER FAMILY 20 (PHOSPHATE TRANSPORTER), MEMBER 2; SLC20A2 NCBI Gene ClinVar ...
    https://medlineplus.gov/genetics/gene/slc20a2 - Genetics
  7. CYP17A1 gene 
    ... glucocorticoids and sex hormones. CYP17A1 also has 17,20-lyase activity, which converts 17-hydroxypregnenolone to dehydroepiandrosterone ( ... have been found to cause 17α-hydroxylase/17,20-lyase deficiency. This condition affects the function of ...
    https://medlineplus.gov/genetics/gene/cyp17a1 - Genetics
  8. WNK1 gene 
    ... HSN2 KDP p65 PPP1R167 PRKWNK1 prostate-derived sterile 20-like kinase protein kinase with no lysine 1 ... S A. 2006 Jan 31;103(5):1615-20. doi: 10.1073/pnas.0510609103. Epub 2006 Jan ...
    https://medlineplus.gov/genetics/gene/wnk1 - Genetics
  9. SLC25A20 gene 
    ... solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 Tests of SLC25A20 PubMed SOLUTE CARRIER FAMILY 25 (CARNITINE/ACYLCARNITINE TRANSLOCASE), MEMBER 20; SLC25A20 NCBI Gene ClinVar Costa C, Costa JM, ...
    https://medlineplus.gov/genetics/gene/slc25a20 - Genetics
  10. NSD1 gene 
    ... N-methyltransferase, H3 lysine-36 and H4 lysine-20 specific NR-binding SET domain containing protein NSD1_ ... protein lysine methyltransferase NSD1. Chem Biol. 2014 Feb 20;21(2):226-37. doi: 10.1016/j. ...
    https://medlineplus.gov/genetics/gene/nsd1 - Genetics
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