Literature DB >> 6029472

Impaired intestinal transport of proline in a patient with familial iminoaciduria.

S I Goodman, C A McIntyre, D O'Brien.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1967        PMID: 6029472     DOI: 10.1016/s0022-3476(67)80081-7

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


× No keyword cloud information.
  6 in total

1.  Hartnup disease.

Authors:  M D Milne
Journal:  Biochem J       Date:  1969-02       Impact factor: 3.857

2.  Iminoglycinuria in a child in Czechoslovakia.

Authors:  B Blehová; N Păzoutová; J Hyánek; J Jirásek
Journal:  Humangenetik       Date:  1973-07-20

3.  Renal tubular transport of proline, hydroxyproline, and glycine. 3. Genetic basis for more than one mode of transport in human kidney.

Authors:  C R Scriver
Journal:  J Clin Invest       Date:  1968-04       Impact factor: 14.808

4.  Iminoglycinuria--a "harmless" inborn error of metabolism?

Authors:  G R Fraser; A I Friedmann; V M Patton; D N Wade; L I Woolf
Journal:  Humangenetik       Date:  1968

Review 5.  The molecular basis of neutral aminoacidurias.

Authors:  Angelika Bröer; Juleen A Cavanaugh; John E J Rasko; Stefan Bröer
Journal:  Pflugers Arch       Date:  2005-07-29       Impact factor: 3.657

6.  Delineation of sodium-stimulated amino acid transport pathways in rabbit kidney brush border vesicles.

Authors:  A K Mircheff; I Kippen; B Hirayama; E M Wright
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.