Literature DB >> 4950283

Human genetics of membrane transport with emphasis on amino acids.

C R Scriver, P Hechtman.   

Abstract

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Year:  1970        PMID： 4950283     DOI： 10.1007/978-1-4684-0958-1_4

Source DB:  PubMed          Journal:  Adv Hum Genet        ISSN： 0065-275X


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  4 in total

1.  Localization of the membrane defect in transepithelial transport of taurine by parallel studies in vivo and in vitro in hypertaurinuric mice.

Authors:  R W Chesney; C R Scriver; F Mohyuddin
Journal:  J Clin Invest       Date:  1976-01       Impact factor: 14.808

2.  Developmental aspects ofL-valine uptake by mouse intestine.

Authors:  Christos S Bartsocas; Emmanuel Kavazarakis
Journal:  Wilehm Roux Arch Dev Biol       Date:  1981-09

3.  Hyperglycinuria with nephrolithiasis.

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

4.  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 in total

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