Literature DB >> 4685850

Familial hyperglycinuria. New defect in renal tubular transport of glycine and imino acids.

M L Greene, P S Lietman, L E Rosenberg, J E Seegmiller.   

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Year:  1973        PMID： 4685850     DOI： 10.1016/0002-9343(73)90232-5

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  4 in total

1.  Phenylketonuria with familial hyperglycinuria.

Authors:  J M Marques
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

2.  Hyperglycinuria with nephrolithiasis.

Authors:  V Oberiter; Z Puretić; V Fabecić-Sabadi
Journal:  Eur J Pediatr       Date:  1978-04-20       Impact factor: 3.183

3.  Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters.

Authors:  Stefan Bröer; Charles G Bailey; Sonja Kowalczuk; Cynthia Ng; Jessica M Vanslambrouck; Helen Rodgers; Christiane Auray-Blais; Juleen A Cavanaugh; Angelika Bröer; John E J Rasko
Journal:  J Clin Invest       Date:  2008-11-06       Impact factor: 14.808

4.  Hypertension and impaired glycine handling in mice lacking the orphan transporter XT2.

Authors:  Hui Quan; Krairerk Athirakul; William C Wetsel; Gonzalo E Torres; Robert Stevens; Y T Chen; Thomas M Coffman; Marc G Caron
Journal:  Mol Cell Biol       Date:  2004-05       Impact factor: 4.272
  4 in total

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