Works matching DE "ALPHA-galactosidase"
Results: 84
In silico analysis of the α-amylase family GH57: eventual subfamilies reflecting enzyme specificities.
- Published in:
- 3 Biotech, 2018, v. 8, n. 7, p. 1, doi. 10.1007/s13205-018-1325-9
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- Publication type:
- Article
Unexplained left ventricular hypertrophy, arrhythmias and conduction disorders: take into account Anderson-Fabry Disease (AFD). A case report of a diagnosed and under treatment AFD in a heterozygous female, with severe left ventricular hypertrophy and conduction disorders
- Published in:
- 2014
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- Publication type:
- Case Study
Establishing 3-nitrotyrosine as a biomarker for the vasculopathy of Fabry disease.
- Published in:
- Kidney International, 2014, v. 86, n. 1, p. 58, doi. 10.1038/ki.2013.520
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- Publication type:
- Article
Fabry nephropathy: a review - how can we optimize the management of Fabry nephropathy?
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- BMC Nephrology, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2369-15-72
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- Publication type:
- Article
A New α-Galactosidase from Thermoacidophilic Alicyclobacillus sp. A4 with Wide Acceptor Specificity for Transglycosylation.
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- Applied Biochemistry & Biotechnology, 2014, v. 174, n. 1, p. 328, doi. 10.1007/s12010-014-1050-8
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- Publication type:
- Article
Retargeting pre-existing human antibodies to a bacterial pathogen with an alpha-Gal conjugated aptamer.
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- Journal of Molecular Medicine, 2015, v. 93, n. 6, p. 619, doi. 10.1007/s00109-015-1280-4
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- Publication type:
- Article
Scientific Opinion on the safety and efficacy of AGal-Pro BL/BL-L (alpha-galactosidase and endo-1,4-beta-glucanase) as a feed additive for laying hens and minor poultry species for laying.
- Published in:
- EFSA Journal, 2015, v. 13, n. 5, p. 4107, doi. 10.2903/j.efsa.2015.4107
- Publication type:
- Article
Scientific Opinion on the safety and efficacy of AGal-Pro BL-L (alpha-galactosidase and endo-1, 4-beta-glucanase) as a feed additive for chickens for fattening.
- Published in:
- EFSA Journal, 2014, v. 12, n. 11, p. n/a, doi. 10.2903/j.efsa.2014.3897
- Publication type:
- Article
Perturbation of the interaction between Gal4p and Gal80p of the S accharomyces cerevisiae GAL switch results in altered responses to galactose and glucose.
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- Molecular Microbiology, 2014, v. 94, n. 1, p. 202, doi. 10.1111/mmi.12757
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- Publication type:
- Article
Multicentric study on the diagnosis of Fabry's disease using angiokeratoma biopsy registries.
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- International Journal of Dermatology, 2015, v. 54, n. 6, p. e241, doi. 10.1111/ijd.12713
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- Publication type:
- Article
Aspectos de actualidad en enfermedad de Fabry.
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- Medicina Interna de Mexico, 2012, v. 28, n. 2, p. 177
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- Publication type:
- Article
Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant.
- Published in:
- 2016
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- Publication type:
- journal article
Prevalence of Fabry disease in men with tinnitus and sensorineural hearing loss.
- Published in:
- Journal of Applied Biomedicine, 2021, v. 19, n. 1, p. 57, doi. 10.32725/jab.2021.003
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- Publication type:
- Article
Mutational analysis of the GLA gene in Mexican families with Fabry disease.
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- Journal of Genetics, 2017, v. 96, n. 1, p. 161, doi. 10.1007/s12041-017-0744-4
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- Publication type:
- Article
Characterization of two novel heat-active α-galactosidases from thermophilic bacteria.
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- Extremophiles, 2017, v. 21, n. 1, p. 85, doi. 10.1007/s00792-016-0885-z
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- Publication type:
- Article
香菇产α-半乳糖苷酶的液体发酵工艺优化.
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- Acta Edulis Fungi, 2018, v. 25, n. 2, p. 79, doi. 10.16488/j.cnki.1005-9873.2018.02.011
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- Publication type:
- Article
Biocatalytic characterization of Aspergillus oryzae β-galactosidase immobilized on functionalized multi-walled carbon nanotubes.
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- Biocatalysis & Biotransformation, 2017, v. 35, n. 4, p. 260, doi. 10.1080/10242422.2017.1323886
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- Publication type:
- Article
Effects of reduction in the alpha-gal antigen on bony union: a model of xenobone graft using GalT knockout mouse.
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- Xenotransplantation, 2014, v. 21, n. 3, p. 267, doi. 10.1111/xen.12092
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- Publication type:
- Article
Alpha-Gal detectors in xenotransplantation research: a word of caution.
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- Xenotransplantation, 2012, v. 19, n. 4, p. 215, doi. 10.1111/j.1399-3089.2012.00714.x
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- Publication type:
- Article
Pig xenogeneic antigen modification with green coffee bean α-galactosidase.
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- Xenotransplantation, 1999, v. 6, n. 4, p. 238, doi. 10.1034/j.1399-3089.1999.00035.x
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- Publication type:
- Article
Relative bioavailability and the effect of meal type and timing on the pharmacokinetics of migalastat in healthy volunteers.
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- Clinical Pharmacology in Drug Development, 2015, v. 4, n. 3, p. 193, doi. 10.1002/cpdd.147
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- Publication type:
- Article
Diagnosing Fabry disease--delays and difficulties within discordant siblings.
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- QJM: An International Journal of Medicine, 2015, v. 108, n. 7, p. 585, doi. 10.1093/qjmed/hct024
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- Publication type:
- Article
Characterization of Properties and Transglycosylation Abilities of Recombinant α-Galactosidase from Cold-Adapted Marine Bacterium Pseudoalteromonas KMM 701 and Its C494N and D451A Mutants.
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- Marine Drugs, 2018, v. 16, n. 10, p. 349, doi. 10.3390/md16100349
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- Publication type:
- Article
Familial hypertrophic obstructive cardiomyopathy with the GLA E66Q mutation and zebra body.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Pathologic endothelial response and impaired function of circulating angiogenic cells in patients with Fabry disease.
- Published in:
- Basic Research in Cardiology, 2013, v. 108, n. 1, p. 1, doi. 10.1007/s00395-012-0311-3
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- Publication type:
- Article
Retrospective Evaluation of Clinical and Molecular Characteristics of Patients with Fabry Disease Being Followed-Up in Our Clinic.
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- Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2021, v. 15, n. 2, p. 117, doi. 10.12956/tchd.820757
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- Publication type:
- Article
Case report of concurrent Fabry disease and amyotrophic lateral sclerosis supports a common pathway of pathogenesis.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Fabry disease, a complex pathology not easy to diagnose.
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- Cardiogenetics, 2015, v. 5, n. 1, p. 17, doi. 10.4081/cardiogenetics.2015.5612
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- Publication type:
- Article
Fabry disease presenting with sudden hearing loss and otosclerosis: a case report.
- Published in:
- 2012
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- Publication type:
- journal article
Clinical utility gene card for: Fabry disease.
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- European Journal of Human Genetics, 2012, v. 20, n. 2, p. 1, doi. 10.1038/ejhg.2011.178
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- Publication type:
- Article
Legislation.
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- European Food & Feed Law Review, 2024, v. 19, n. 2, p. 87
- Publication type:
- Article
Challenging popular tools for the annotation of genetic variations with a real case, pathogenic mutations of lysosomal alpha-galactosidase.
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- BMC Bioinformatics, 2018, v. 19, n. 15, p. 39, doi. 10.1186/s12859-018-2416-7
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- Publication type:
- Article
Increased expression of Trpv1 in peripheral terminals mediates thermal nociception in Fabry disease mouse model.
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- Molecular Pain, 2016, v. 12, p. N.PAG, doi. 10.1177/1744806916663729
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- Publication type:
- Article
Comprehensive and differential long-term characterization of the alpha-galactosidase A deficient mouse model of Fabry disease focusing on the sensory system and pain development.
- Published in:
- Molecular Pain, 2016, v. 12, p. N.PAG, doi. 10.1177/1744806916646379
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- Publication type:
- Article
Increased expression of Trpv1 in peripheral terminals mediates thermal nociception in Fabry disease mouse model.
- Published in:
- Molecular Pain, 2016, v. 12, p. 1, doi. 10.1177/1744806916663729
- By:
- Publication type:
- Article
Comprehensive and differential long-term characterization of the alpha-galactosidase A deficient mouse model of Fabry disease focusing on the sensory system and pain development.
- Published in:
- Molecular Pain, 2016, v. 12, p. 1, doi. 10.1177/1744806916646379
- By:
- Publication type:
- Article
Functional Analysis of the 5′-Regulatory Region of the Maize ALKALINE ALPHA- GALACTOSIDASE1 Gene.
- Published in:
- Plant Molecular Biology Reporter, 2015, v. 33, n. 5, p. 1361, doi. 10.1007/s11105-014-0840-z
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- Publication type:
- Article
The Proliferation Mechanism of Lactobacillus plantarum RB1 Stimulated by Stachyose.
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- Current Microbiology, 2017, v. 74, n. 6, p. 732, doi. 10.1007/s00284-017-1229-7
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- Publication type:
- Article
New mutations in the GLA gene in Brazilian families with Fabry disease.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 6, p. 347, doi. 10.1038/jhg.2012.32
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- Publication type:
- Article
Gastrointestinal involvement in Fabry disease. So important, yet often neglected.
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- Clinical Genetics, 2016, v. 89, n. 1, p. 5, doi. 10.1111/cge.12673
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- Publication type:
- Article
Fabry disease and enzyme replacement therapy in classic patients with same mutation: different formulations -- different outcome?
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- Clinical Genetics, 2016, v. 89, n. 1, p. 88, doi. 10.1111/cge.12590
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- Publication type:
- Article
Diagnostic dilemmas in Fabry disease: a case series study on GLA mutations of unknown clinical significance.
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- Clinical Genetics, 2015, v. 88, n. 2, p. 161, doi. 10.1111/cge.12449
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- Publication type:
- Article
Intrafamilial phenotypic variability in four families with Anderson-Fabry disease.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 3, p. 258, doi. 10.1111/cge.12261
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- Publication type:
- Article
Misdiagnosis of familial Mediterranean fever in patients with Anderson-Fabry disease.
- Published in:
- Clinical Genetics, 2013, v. 83, n. 6, p. 576, doi. 10.1111/j.1399-0004.2012.01940.x
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- Publication type:
- Article
Fabry disease: polymorphic haplotypes and a novel missense mutation in the GLA gene.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 3, p. 224, doi. 10.1111/j.1399-0004.2011.01689.x
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- Publication type:
- Article
Genome-wide microarray analysis leads to identification of genes in response to herbicide, metribuzin in wheat leaves.
- Published in:
- PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0189639
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- Publication type:
- Article
UM CASO DE AEROPARESTESIAS. ASTENIA E FEBRE. UMA NOVA MUTAÇÃO EM DOENÇA DE FABRY.
- Published in:
- Acta Reumatológica Portuguesa, 2011, v. 36, n. 4, p. 399
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- Publication type:
- Article
Variations in plasma and urinary lipids in response to enzyme replacement therapy for Fabry disease patients by nanoflow UPLC-ESI-MS/MS.
- Published in:
- Analytical & Bioanalytical Chemistry, 2016, v. 408, n. 9, p. 2265, doi. 10.1007/s00216-016-9318-1
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- Publication type:
- Article
Phenotype and Genotype Characterization and Twin Association in Patients with Anderson-Fabry Cardiomyopathy.
- Published in:
- Cardiology, 2012, v. 121, n. 2, p. 71, doi. 10.1159/000336168
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- Publication type:
- Article
Diverse phenotypic expression associated with the same genetic variant in female heterozygote patients of Anderson–Fabry disease: a case series.
- Published in:
- 2021
- By:
- Publication type:
- Case Study