Found: 10
Select item for more details and to access through your institution.
Successful treatment of phenylketonuria with tetrahydrobiopterin.
- Published in:
- 2001
- By:
- Publication type:
- Letter
The structure of the anti-c-myc antibody 9E10 Fab fragment/epitope peptide complex reveals a novel binding mode dominated by the heavy chain hypervariable loops.
- Published in:
- Proteins, 2008, v. 73, n. 3, p. 552, doi. 10.1002/prot.22080
- By:
- Publication type:
- Article
Phage display screening for peptidic chitinase inhibitors.
- Published in:
- Journal of Molecular Recognition, 2008, v. 21, n. 6, p. 401, doi. 10.1002/jmr.911
- By:
- Publication type:
- Article
Structure of an anti-cholera toxin antibody Fab in complex with an epitope-derived D-peptide: a case of polyspecific recognition.
- Published in:
- Journal of Molecular Recognition, 2007, v. 20, n. 4, p. 263, doi. 10.1002/jmr.838
- By:
- Publication type:
- Article
Mutational spectrum in German patients with phenylalanine hydroxylase deficiency (For the PKU Special Issue) Online Citation: Human Mutation, Mutation in Brief #587 (2002) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/587.pdf).
- Published in:
- Human Mutation, 2003, v. 21, n. 4, p. 399, doi. 10.1002/humu.9116
- By:
- Publication type:
- Article
Mutational spectrum in German patients with phenylalanine hydroxylase deficiencyFor the PKU Special IssueOnline Citation: Human Mutation, Mutation in Brief #587 (2002) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/587.pdf.
- Published in:
- Human Mutation, 2003, v. 21, n. 4, p. 399, doi. 10.1002/humu.9116
- By:
- Publication type:
- Article
Identification of a novel missense mutation (G314E) in exon 7 of the cystic fibrosis transmembrane conductance regulator gene identified in a CF patient with pancreatic sufficiency.
- Published in:
- Human Mutation, 1994, v. 3, n. 1, p. 67, doi. 10.1002/humu.1380030112
- By:
- Publication type:
- Article
Analysis of exon 7 of the human phenylalanine hydroxylase gene: A mutation hot spot?
- Published in:
- Human Mutation, 1992, v. 1, n. 2, p. 138, doi. 10.1002/humu.1380010209
- By:
- Publication type:
- Article
In frame deletion (ΔF311) within a short trinucleotide repeat of the first transmembrane region of the cystic fibrosis gene.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 12, p. 2173
- By:
- Publication type:
- Article
Phenylalanine hydroxylase gene: silent mutation uncovers evolutionary origin of different alleles.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 4, p. 270, doi. 10.1111/j.1399-0004.1990.tb03580.x
- By:
- Publication type:
- Article