Found: 14
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The natural history of classic galactosemia: lessons from the GalNet registry.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Discovery of novel inhibitors of human galactokinase by virtual screening.
- Published in:
- Journal of Computer-Aided Molecular Design, 2019, v. 33, n. 4, p. 405, doi. 10.1007/s10822-019-00190-3
- By:
- Publication type:
- Article
Deficits of facial emotion recognition and visual information processing in adult patients with classical galactosemia.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Galactose-1-Phosphate Uridyltransferase Activities in Different Genotypes: A Retrospective Analysis of 927 Samples.
- Published in:
- Journal of Applied Laboratory Medicine, 2018, p. 222, doi. 10.1373/jalm.2017.025536
- By:
- Publication type:
- Article
Galactose-1-phosphate uridyltransferase (GalT), an in vivo-induced antigen of Actinobacillus pleuropneumoniae serovar 5b strain L20, provided immunoprotection against serovar 1 strain MS71.
- Published in:
- PLoS ONE, 2018, v. 13, n. 5, p. 1, doi. 10.1371/journal.pone.0198207
- By:
- Publication type:
- Article
HIV replication is associated to inflammasomes activation, IL-1β, IL-18 and caspase-1 expression in GALT and peripheral blood.
- Published in:
- PLoS ONE, 2018, v. 13, n. 3, p. 1, doi. 10.1371/journal.pone.0192845
- By:
- Publication type:
- Article
Using a Personal Glucose Meter and Alkaline Phosphatase for Point-of-Care Quantification of Galactose-1-Phosphate Uridyltransferase in Clinical Galactosemia Diagnosis.
- Published in:
- Chemistry - An Asian Journal, 2015, v. 10, n. 10, p. 2221, doi. 10.1002/asia.201500642
- By:
- Publication type:
- Article
Novel GALT variations and mutation spectrum in the Korean population with decreased galactose-1-phosphate uridyltransferase activity.
- Published in:
- BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/s12881-014-0094-5
- By:
- Publication type:
- Article
Large deletions involving the regulatory upstream regions of A4 GALT give rise to principally novel P1 PK-null alleles.
- Published in:
- Transfusion, 2014, v. 54, n. 7, p. 1831, doi. 10.1111/trf.12543
- By:
- Publication type:
- Article
P<sup>1</sup>/ P<sup>2</sup> genotyping of known and novel null alleles in the P1 PK and GLOB histo-blood group systems.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2928, doi. 10.1111/trf.12355
- By:
- Publication type:
- Article
Galactosemia in the Turkish population with a high frequency of Q188R mutation and distribution of Duarte-1 and Duarte-2 variations.
- Published in:
- Journal of Human Genetics, 2013, v. 58, n. 10, p. 675, doi. 10.1038/jhg.2013.76
- By:
- Publication type:
- Article
Fertility preservation in female classic galactosemia patients.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-107
- By:
- Publication type:
- Article
Molecular simulation and docking studies of Gal1p and Gal3p proteins in the presence and absence of ligands ATP and galactose: implication for transcriptional activation of GAL genes.
- Published in:
- Journal of Computer-Aided Molecular Design, 2012, v. 26, n. 7, p. 847, doi. 10.1007/s10822-012-9579-5
- By:
- Publication type:
- Article
Structural and molecular biology of type I galactosemia: Disease-associated mutations.
- Published in:
- IUBMB Life, 2011, v. 63, n. 11, p. 949, doi. 10.1002/iub.510
- By:
- Publication type:
- Article