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342 results
  1. AVP gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/avp
    ... PubMed Catalog of Genes and Diseases from OMIM ARGININE VASOPRESSIN; AVP Gene and Variant Databases NCBI Gene ClinVar References Christensen JH, Rittig S. Familial neurohypophyseal diabetes insipidus--an ...
  2. GATM gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/gatm
    ... Catalog of Genes and Diseases from OMIM L-ARGININE:GLYCINE AMIDINOTRANSFERASE; GATM Gene and Variant Databases NCBI Gene ClinVar References Beard E, Braissant O. Synthesis and transport of ...
  3. Asparagine Synthetase Deficiency - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK525916
    ... impaired synthesis of asparagine. Insufficient physiologic levels of arginine cause neurologic impairment [ Ruzzo et al 2013 , Alfadhel et al 2015 ]. References Literature Cited Alfadhel M, Alrifai MT, Trujillano D, ...
  4. RERE gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/rere
    ... PubMed Catalog of Genes and Diseases from OMIM ARGININE-GLUTAMIC ACID DIPEPTIDE REPEATS; RERE Gene and Variant Databases NCBI Gene ClinVar References Fregeau B, Kim BJ, Hernandez-Garcia A, Jordan ...
  5. AVPR2 gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/avpr2
    ... PubMed Catalog of Genes and Diseases from OMIM ARGININE VASOPRESSIN RECEPTOR 2; AVPR2 NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NSIAD Gene and Variant Databases NCBI Gene ClinVar References Arthus MF, Lonergan M, Crumley MJ, Naumova AK, ...
  6. NLM Digital Collections - Physiologic involution in normal aging man : a bibliography of literature, 1956-1960 
    Publication: Washington, D.C. : U.S. Dept. of Health, Education, and Welfare, [1960]
    resource.nlm.nih.gov/60030780R
    ... la paroi abdominale, tendon d'Achille. [Acide glucuronique, arginine, typrosine et hydroxyproline. ] Gerontologia (Basel) 4:39-59, 1960. 38 references. 3 types of connective tissue from subjects ranging ...
  7. Hypokalemic Periodic Paralysis - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1338
    ... an amino acid change that turns positively charged arginines of voltage sensor S4 segments into other ... Change Reference Sequences c.664C>G p.Arg222Gly NM_000334 ​. ...
  8. Arginine:glycine amidinotransferase deficiency | MedlinePlus Genetics 
    https://medlineplus.gov/...nineglycine-amidinotransferase-deficiency
    ... deficiency Genetic and Rare Diseases Information Center L-Arginine:glycine amidinotransferase ... References Beard E, Braissant O. Synthesis and transport of ...
  9. PADI3 gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/padi3
    ... deiminase III protein-arginine deiminase type III protein-arginine deiminase type-3 Additional Information & ... References Calderon P, Otberg N, Shapiro J. Uncombable hair ...
  10. ZAP70-Related Combined Immunodeficiency - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK20221
    ... have been reported. A pathogenic variant in the arginine residue (p.Arg465Cys) of the DLAARN motif of ... Protein Change Reference Sequences c.239C>A (448C>A) p.Pro80Gln ...
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