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Results 1 - 10 of 50 for Biochemistry
  1. ... D. Molecular determinants of heritable vitamin E deficiency. Biochemistry. 2004 Apr 13;43(14):4143-9. doi: ... heritable mutations in the alpha-tocopherol transfer protein. Biochemistry. 2006 Jul 11;45(27):8236-42. doi: ...
  2. ... small heat shock proteins and human congenital diseases. Biochemistry (Mosc). 2012 Dec;77(13):1500-14. doi: ... Small Heat Shock Proteins and Distal Hereditary Neuropathies. Biochemistry (Mosc). 2015 Dec;80(13):1734-47. doi: ...
  3. ... small heat shock proteins and human congenital diseases. Biochemistry (Mosc). 2012 Dec;77(13):1500-14. doi: ... Small Heat Shock Proteins and Distal Hereditary Neuropathies. Biochemistry (Mosc). 2015 Dec;80(13):1734-47. doi: ...
  4. ... of five disease-associated human adenylosuccinate lyase mutants. Biochemistry. 2009 Jun 16;48(23):5291-302. doi: ... ADSL) and the R303C ADSL deficiency-associated mutation. Biochemistry. 2012 Aug 21;51(33):6701-13. doi: ...
  5. ... 1007/s10545-005-0081-2. Citation on PubMed Biochemistry (fifth edition, 2002): Ammonium Ion is Converted into ... intragenic complementation at the human argininosuccinate lyase locus. Biochemistry. 2001 Dec 25;40(51):15581-90. doi: ...
  6. ... isovaleryl-CoA dehydrogenase in patients with isovaleric acidemia. Biochemistry. 1998 Jul 14;37(28):10325-35. doi: ...
  7. ... PubMed Wanders RJ, Waterham HR. Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders. Clin Genet. ...
  8. ... GLUCOSE-6-PHOSPHATE DEHYDROGENASE; G6PD NCBI Gene ClinVar Biochemistry (fifth edition, 2002): Glucose 6-Phosphate Dehydrogenase Plays ...
  9. ... aggregation-prevention activity of p97/valosin-containing protein. Biochemistry. 2007 Dec 25;46(51):14889-98. doi: ...
  10. ... a simple route to the treatment of Hawkinsinuria. Biochemistry. 2010 Aug 24;49(33):7218-26. doi: ...
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