Results 1 -
10
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700
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R -"3-hydroxytetradecanoic" acid
- ... Y, Greenberg DA, Concepcion E, Skrabanek L, Villanueva R, Tomer Y. Amino acid substitutions in the thyroglobulin gene are associated with ...
- ... Costantino G, De Franco F, Passeri D, Pellicciari R, Setchell KD. Synthesis of atypical bile acids for use as investigative tools for the genetic ...
- ... 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 ...
- ... 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 ...
- ... 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. ...
- ... 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 ...
- ... MYOPATHY, INFANTILE, TRANSIENT; MMIT TRANSFER RNA, MITOCHONDRIAL, GLUTAMIC ACID; MTTE NCBI Gene ClinVar Horvath R, Kemp JP, Tuppen HA, Hudson G, Oldfors A, ...
- ... 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. ...
- ... 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 ...
- ... 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: ...