about
Evaluation of reference-based two-color methods for measurement of gene expression ratios using spotted cDNA microarrays.Carriers of the Complex Allele HFE c.[187C>G;340+4T>C] Have Increased Risk of Iron Overload in São Miguel Island Population (Azores, Portugal)Low frequency of CD4+CD25+ Treg in SLE patients: a heritable trait associated with CTLA4 and TGFbeta gene variants.HLA Class I and II profiles in São Miguel Island (Azores): genetic diversity and linkage disequilibrium.Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease.Human leptospirosis: seroreactivity and genetic susceptibility in the population of São Miguel Island (Azores, Portugal)Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplicationThree multiplex snapshot assays for SNP genotyping in candidate innate immune genes.Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy.A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.Paternal Transmission of Small Supernumerary Marker Chromosome 15 Identified in Prenatal Diagnosis Due to Advanced Maternal Age.Mitochondrial DNA analysis of Tunisians reveals a mosaic genetic structure with recent population expansion.Cross-protection to new drifted influenza A(H3) viruses and prevalence of protective antibodies to seasonal influenza, during 2014 in Portugal.First isolation of human Leptospira strains, Azores, Portugal.Molecular diagnosis of infectious diseases in São Miguel Island (Azores, Portugal): A hospital-based descriptive study.Genetic variants involved in oxidative stress, base excision repair, DNA methylation, and folate metabolism pathways influence myeloid neoplasias susceptibility and prognosis.Azores Islands: genetic origin, gene flow and diversity pattern.Physical mapping of 49 microsatellite markers on chromosome 19 and correlation with the genetic linkage map.Multiple nevoid basal cell carcinoma syndrome associated with congenital orbital teratoma, caused by a PTCH1 frameshift mutation.Transcriptional and translational mechanisms of cytochrome b5 reductase isoenzyme generation in humans.UGT1A1, UGT1A6 and UGT1A7 genetic analysis: repercussion for irinotecan pharmacogenetics in the São Miguel Island Population (Azores, Portugal).Oxidative stress and mitochondrial dysfunction play a role in myelodysplastic syndrome development, diagnosis, and prognosis: A pilot study.A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report.Genealogical and molecular analysis of a family-based cohort of congenital heart disease patients from the São Miguel Island (Azores, Portugal).Heterogeneity of the rat NADH-cytochrome-b5-reductase transcripts resulting from multiple alternative first exons.Oxidative stress levels are correlated with P15 and P16 gene promoter methylation in myelodysplastic syndrome patients.Clinical and Genetic Spectrum of Bartter Syndrome Type 3.Disease knowledge and attitudes toward predictive testing and prenatal diagnosis in families with Machado-Joseph disease from the Azores Islands (Portugal).Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions.MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.Genetic risk assessment for cardiovascular disease in Azoreans (Portugal): a general population-based study.A new PAX8 mutation causing congenital hypothyroidism in three generations of a family is associated with abnormalities in the urogenital tract.Genetic variation in key genes associated with statin therapy in the Azores Islands (Portugal) healthy population.Evaluation of linkage disequilibrium on the Xq13.3 region: comparison between the Azores islands and mainland Portugal.Epidemiological characterization of congenital heart disease in São Miguel Island, Azores, Portugal.International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation.Failure to find alpha-synuclein gene dosage changes in 190 patients with familial Parkinson disease.A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?Diagnosis of Human Leptospirosis in a Clinical Setting: Real-Time PCR High Resolution Melting Analysis for Detection of Leptospira at the Onset of Disease.Genetic signature of the São Miguel island population (Azores) assessed by 21 microsatellite loci
P50
Q25255703-4C347B9D-DCF9-41A7-AB13-C2F1E72A34ABQ28550491-9F9CEA07-CA15-4B36-ACA0-A96D377D3958Q33403373-86AF450F-EA95-41F2-AB59-CB0216DBD4EBQ33576275-F7954B1B-1368-4065-BE0F-3D4FDBAD2F61Q33853344-5E861ECF-89FB-4170-8575-45BF2F620A8EQ34257487-76B6E71E-A68D-4F17-96E8-AA916C70BD4CQ34491810-C9209986-46E8-4E38-A3C0-F9EF9E9FE113Q34580271-E73BC1FF-1474-459D-A6CE-14FD7AC38EF7Q34660184-DA4395BF-ACFF-43D8-95B2-6972ED075EDAQ35752792-B0E12282-0D68-432F-8E9F-59F275F02F27Q36212709-994AAF80-3E8E-49D7-B41D-E0CE3BB7F261Q38609603-E7DB43C4-8DC8-415A-BBC2-5E6E878880E1Q38894141-D3166218-AD0C-4803-8A88-8585B9F08EBCQ39028206-1E5C0EA4-E222-4671-BDF4-8CD9AB801BC1Q39330467-390384AC-0440-4FC8-AF75-9FAC907285BEQ39942266-35A3475A-BB6C-4BEB-9F3D-66199EB2D872Q40123941-19CC9A1E-3C0F-45A1-91D7-BAA61F733835Q41215140-9D833C12-50C9-4DC9-B1DA-4D0DF68C2875Q42463840-8D74A06B-F968-43A5-A1F9-8C9C63509AE4Q42999049-0667566D-B5C5-4ADA-86CA-8E1CFDDC0D16Q43284930-675A584E-0608-4CF5-AAF7-D501BA66B811Q46729480-960A2DCF-528F-4003-930C-15DA057F80A8Q47551057-D0B8A607-35D6-4421-B2C6-6863F06B60C2Q47627491-BB609218-7052-4005-BA91-FB1ADD4C5DF5Q48084151-8AD73193-3D5D-417C-9C8A-61B3DD6159FBQ48186090-F08273FE-A192-4853-8246-B44567786B76Q48524640-A11FCC18-4867-4778-984A-2031AC4D8B1EQ48667440-7BC9E368-1C6C-4513-9FF7-52FF4224F921Q50312499-ACB17340-D8FB-483F-85AC-C6E12027E983Q50313885-680F3FF7-06B8-4DF9-BCEF-5A25C9D6E686Q50772685-61508E49-45A2-480D-A8EB-77C2D7468491Q51017169-0B450FC8-20A8-44EF-A62D-F7AB7DA0C0BFQ52801124-4BBCD9FA-4788-457E-A595-0046EEF548A6Q52804607-DB2FA6D4-4F82-4F8E-A4F7-7D3064835E4EQ52805477-8D282724-40E8-4528-859C-704BAD72E4A4Q53171003-71B2934E-DDE0-4136-801C-E5A24CE5713FQ54685674-BC24F8DA-33EB-4A7A-9F37-929005DC107EQ55263855-A4722750-7EDE-4A69-B50A-2DA27170D16DQ55347845-A72980EB-3607-4D18-85E8-3CE7E08BA12BQ60607750-5E0FCE21-CCAA-4516-AF84-F0CC48BB3B18
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Luisa Mota-Vieira
@ast
Luisa Mota-Vieira
@en
Luisa Mota-Vieira
@es
Luisa Mota-Vieira
@nl
Luisa Mota-Vieira
@sl
type
label
Luisa Mota-Vieira
@ast
Luisa Mota-Vieira
@en
Luisa Mota-Vieira
@es
Luisa Mota-Vieira
@nl
Luisa Mota-Vieira
@sl
altLabel
L Mota-Vieira
@en
Mota-Vieira, Luisa
@en
prefLabel
Luisa Mota-Vieira
@ast
Luisa Mota-Vieira
@en
Luisa Mota-Vieira
@es
Luisa Mota-Vieira
@nl
Luisa Mota-Vieira
@sl
P1053
I-5909-2013
P106
P1153
9435079600
P1960
FRZwqIUAAAAJ
P2038
Luisa_Mota-Vieira
P21
P2798
P31
P3829
P496
0000-0003-1451-6705