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Juergen Reichardt

Affiliations: 
Pharmacy and Molecular Sciences James Cook University 
Website:
http://www.jcu.edu.au/phms/staff/JCUPRD1_070552.html
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"gene discovery"
Mean distance: 9.33
 
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Paul Berg grad student 1989 Stanford
 (Molecular biology of Galactosemia)
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Publications

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Ho G, Reichardt J, Christodoulou J. (2013) In vitro read-through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria. Journal of Inherited Metabolic Disease. 36: 955-9
Tyfield L, Reichardt J, Fridovich-Keil J, et al. (1999) Classical galactosemia and mutations at the galactose-1-phosphate uridyl transferase (GALT) gene. Human Mutation. 13: 417-30
Maceratesi P, Daude N, Dallapiccola B, et al. (1998) Human UDP-galactose 4' epimerase (GALE) gene and identification of five missense mutations in patients with epimerase-deficiency galactosemia. Molecular Genetics and Metabolism. 63: 26-30
Reichardt JK, Berg P. (1988) Conservation of short patches of amino acid sequence amongst proteins with a common function but evolutionarily distinct origins: implications for cloning genes and for structure-function analysis. Nucleic Acids Research. 16: 9017-26
Reichardt JK, Berg P. (1988) Cloning and characterization of a cDNA encoding human galactose-1-phosphate uridyl transferase. Molecular Biology & Medicine. 5: 107-22
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