Literature DB >> 817205

Purification of inactive phenylalanine hydroxylase protein from liver in classical phenylketonuria.

R G Cotton, D M Danks.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1976        PMID： 817205     DOI： 10.1038/260063a0

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


× No keyword cloud information.
  6 in total

1.  Genetics of the mammalian phenylalanine hydroxylase system. II. Immunological and two-dimensional gel electrophoretic studies of phenylalanine hydroxylase in cultured normal and mutant rat hepatoma cells.

Authors:  K H Choo; R G Cotton
Journal:  Biochem Genet       Date:  1979-10       Impact factor: 1.890

2.  Phenylketonuria and its variants.

Authors:  L I Woolf
Journal:  West J Med       Date:  1979-10

3.  Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria.

Authors:  K H Choo; R G Cotton; D M Danks; I G Jennings
Journal:  Biochem J       Date:  1979-08-01       Impact factor: 3.857

4.  Genetics of mammalian phenylalanine hydroxylase system. IV. Evidence of phenylalanine hydroxylase in a cultured human hepatoma cell line.

Authors:  K H Choo; R G Cotton; I G Jennings; K Fowler; D M Danks
Journal:  Biochem Genet       Date:  1980-10       Impact factor: 1.890

5.  Observations indicating the nature of the mutation in phenylketonuria.

Authors:  K H Choo; R G Cotton; I G Jennings; D M Danks
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

6.  Phenylketonuria: clinical and experimental considerations revealed by the use of animal models.

Authors:  J D Lane; V Neuhoff
Journal:  Naturwissenschaften       Date:  1980-05
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.