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Results 1 - 10 of 700 for R -"3-hydroxytetradecanoic" acid
  1. ... Y, Greenberg DA, Concepcion E, Skrabanek L, Villanueva R, Tomer Y. Amino acid substitutions in the thyroglobulin gene are associated with ...
  2. ... Costantino G, De Franco F, Passeri D, Pellicciari R, Setchell KD. Synthesis of atypical bile acids for use as investigative tools for the genetic ...
  3. ... CA, Kuba K, Danilczyk U, Skovby F, Kleta R, Penninger JM, Verrey F. Tissue-specific amino acid transporter partners ACE2 and collectrin differentially interact with ...
  4. ... 7; SLC7A7 NCBI Gene ClinVar Chillaron J, Roca R, Valencia A, Zorzano A, Palacin M. Heteromeric amino acid transporters: biochemistry, genetics, and physiology. Am J Physiol ...
  5. ... Pilz DT, Jungbluth H, Dionisi-Vici C, Carsetti R. The Vici syndrome protein EPG5 regulates intracellular nucleic acid trafficking linking autophagy to innate and adaptive immunity. ...
  6. ... H, Hartlmuller C, Wang Z, Windhager A, Janowski R, Madl T, Jin P, Niessing D. Structural basis of nucleic-acid recognition and double-strand unwinding by the essential ...
  7. ... MYOPATHY, INFANTILE, TRANSIENT; MMIT TRANSFER RNA, MITOCHONDRIAL, GLUTAMIC ACID; MTTE NCBI Gene ClinVar Horvath R, Kemp JP, Tuppen HA, Hudson G, Oldfors A, ...
  8. ... ELOVL4 PubMed ELONGATION OF VERY LONG CHAIN FATTY ACIDS-LIKE 4; ELOVL4 NCBI Gene ClinVar Agbaga MP, Brush RS, Mandal MN, Henry K, Elliott MH, Anderson RE. ...
  9. ... S, Kiss A, Rosa RF, Unger SL, Renella R, Bonafe L, Spranger J, Unger S, Zabel B, Superti-Furga A. Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and ...
  10. ... PHOSPHORYLASE; TYMP NCBI Gene ClinVar Hirano M, Marti R, Spinazzola A, Nishino I, Nishigaki Y. Thymidine phosphorylase deficiency causes MNGIE: an autosomal recessive mitochondrial disorder. Nucleosides Nucleotides Nucleic Acids. 2004 Oct;23(8-9):1217-25. doi: ...
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