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Identification and Diagnosis of Complete Haptoglobin Gene Deletion, One of the Genes Responsible for Adverse Posttransfusion Reactions.
- Published in:
- Biomedicines, 2024, v. 12, n. 4, p. 790, doi. 10.3390/biomedicines12040790
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- Publication type:
- Article
FUT1 variants responsible for Bombay or para-Bombay phenotypes in a database.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-44731-1
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- Publication type:
- Article
Detection of c.375A>G, c.385A>T, c.571C>T, and se del2 of FUT2 via Real-Time PCR in a Single Tube.
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- Diagnostics (2075-4418), 2023, v. 13, n. 12, p. 2022, doi. 10.3390/diagnostics13122022
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- Publication type:
- Article
Estimation of Lewis Blood Group Status by Fluorescence Melting Curve Analysis in Simultaneous Genotyping of c.385A>T and Fusion Gene in FUT2 and c.59T>G and c.314C>T in FUT3.
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- Diagnostics (2075-4418), 2023, v. 13, n. 5, p. 931, doi. 10.3390/diagnostics13050931
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- Publication type:
- Article
Fluorescence Melting Curve Analysis for Concurrent Genotyping of Three Tag SNPs in FUT3.
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- Diagnostics (2075-4418), 2022, v. 12, n. 12, p. 3039, doi. 10.3390/diagnostics12123039
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- Publication type:
- Article
Duplex dual‐labeled fluorescence probe‐based melting curve and endpoint genotyping assays for genotyping of rs2000999 and haptoglobin gene deletion.
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- Electrophoresis, 2022, v. 43, n. 23/24, p. 2436, doi. 10.1002/elps.202200202
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- Publication type:
- Article
Rapid genotyping of 508G>A (rs3745635) and 1067T>A (rs3894326) of FUT3 by a duplex Eprobe‐mediated melting curve analysis.
- Published in:
- Vox Sanguinis, 2022, v. 117, n. 5, p. 741, doi. 10.1111/vox.13251
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- Publication type:
- Article
Estimation of Lewis‐negative alleles by high‐resolution melting analysis of three tag SNPs of FUT3.
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- Vox Sanguinis, 2022, v. 117, n. 2, p. 282, doi. 10.1111/vox.13168
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- Publication type:
- Article
Rapid detection of phenotypes Bombay sedel and nonsecretor rs200157007 SNP (302C > T) by real-time PCR-based methods.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-94659-7
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- Publication type:
- Article
Detection of the weak‐secretor rs1047781 (385A>T) single nucleotide polymorphism using an unlabeled probe high‐resolution melting‐based method.
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- Electrophoresis, 2021, v. 42, n. 12, p. 1362, doi. 10.1002/elps.202000386
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- Publication type:
- Article
Effect of tolvaptan on renal involvement in patients with autosomal dominant polycystic kidney disease according to different gene mutations.
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- Clinical & Experimental Nephrology, 2021, v. 25, n. 3, p. 251, doi. 10.1007/s10157-020-01988-4
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- Article
Survey and characterization of nonfunctional alleles of FUT2 in a database.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-82895-w
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- Publication type:
- Article
High‐resolution melting analysis for detection of fusion allele of FUT2.
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- Electrophoresis, 2021, v. 42, n. 3, p. 315, doi. 10.1002/elps.202000241
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- Publication type:
- Article
Haptoglobin polymorphisms in Latin American populations.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-70755-y
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- Publication type:
- Article
Genetic variation of FUT2 in a Peruvian population: identification of a novel LTR-mediated deletion and characterization of 4 nonsynonymous single-nucleotide polymorphisms.
- Published in:
- 2019
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- Publication type:
- journal article
Discoveries and application of prostate-specific antigen, and some proposals to optimize prostate cancer screening.
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- Cancer Management & Research, 2016, v. 8, p. 45, doi. 10.2147/CMAR.S98326
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- Publication type:
- Article
Haptoglobin promoter polymorphism rs5472 as a prognostic biomarker for peptide vaccine efficacy in castration-resistant prostate cancer patients.
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- Cancer Immunology, Immunotherapy, 2015, v. 64, n. 12, p. 1565, doi. 10.1007/s00262-015-1756-7
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- Publication type:
- Article
Genetic variation of FUT2 in a Vietnamese population: identification of two novel Se enzyme-inactivating mutations.
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- Transfusion, 2012, v. 52, n. 6, p. 1268, doi. 10.1111/j.1537-2995.2011.03485.x
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- Publication type:
- Article
Nonsynonymous Single-Nucleotide Polymorphisms of the Human Apoptosis-Related Endonuclease - DNA Fragmentation Factor Beta Polypeptide, Endonuclease G, and Flap Endonuclease-1 - Genes Show a Low Degree of Genetic Heterogeneity.
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- DNA & Cell Biology, 2012, v. 31, n. 1, p. 36, doi. 10.1089/dna.2011.1293
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- Publication type:
- Article
High prevalence of an anti-hypertriglyceridemic variant of the MLXIPL gene in Central Asia.
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- Journal of Human Genetics, 2011, v. 56, n. 12, p. 828, doi. 10.1038/jhg.2011.109
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- Publication type:
- Article
Confirmation that SNPs in the high mobility group-A2 gene ( HMGA2) are associated with adult height in the Japanese population; wide-ranging population survey of height-related SNPs in HMGA2.
- Published in:
- Electrophoresis, 2011, v. 32, n. 14, p. 1844, doi. 10.1002/elps.201100128
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- Publication type:
- Article
Functional and Genetic Survey of All Known Single-Nucleotide Polymorphisms Within the Human Deoxyribonuclease I Gene in Wide-Ranging Ethnic Groups.
- Published in:
- DNA & Cell Biology, 2011, v. 30, n. 4, p. 205, doi. 10.1089/dna.2010.1120
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- Publication type:
- Article
TaqMan-based real-time polymerase chain reaction for detection of FUT2 copy number variations: identification of novel Alu-mediated deletion.
- Published in:
- Transfusion, 2011, v. 51, n. 4, p. 762, doi. 10.1111/j.1537-2995.2010.02895.x
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- Publication type:
- Article
First survey of the three gene polymorphisms (PON1 Q192R, eNOS E298D and eNOS C-786T) potentially associated with coronary artery spasm in African populations and comparison with worldwide data.
- Published in:
- Cell Biochemistry & Function, 2011, v. 29, n. 2, p. 156, doi. 10.1002/cbf.1721
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- Publication type:
- Article
Global analysis of single nucleotide polymorphisms in the exons of human deoxyribonuclease I-like 1 and 2 genes.
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- Electrophoresis, 2010, v. 31, n. 21, p. 3552, doi. 10.1002/elps.201000319
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- Publication type:
- Article
Development and validation of a SYBR Green I–based real-time polymerase chain reaction method for detection of haptoglobin gene deletion in clinical materials.
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- Transfusion, 2010, v. 50, n. 6, p. 1322, doi. 10.1111/j.1537-2995.2009.02581.x
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- Publication type:
- Article
Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations.
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- Journal of Human Genetics, 2010, v. 55, n. 1, p. 18, doi. 10.1038/jhg.2009.113
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- Publication type:
- Article
Simple and Sensitive Method for Identification of Human DNA by Allele-Specific Polymerase Chain Reaction of FOXP2.
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- Journal of Forensic Sciences, 2009, v. 54, n. 4, p. 857, doi. 10.1111/j.1556-4029.2009.01063.x
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- Publication type:
- Article
Genetic variation of FUT3 in Ghanaians, Caucasians, and Mongolians.
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- Transfusion, 2009, v. 49, n. 5, p. 959, doi. 10.1111/j.1537-2995.2008.02069.x
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- Publication type:
- Article
Sequence Analysis of Human TRPV6 Suggests Positive Selection Outside Africa.
- Published in:
- Biochemical Genetics, 2009, v. 47, n. 1-2, p. 147, doi. 10.1007/s10528-009-9222-x
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- Publication type:
- Article
Gln222Arg (A2317G) polymorphism in the deoxyribonuclease I gene exhibits ethnic and functional differences.
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- Clinical Chemistry & Laboratory Medicine, 2009, v. 47, n. 1, p. 51, doi. 10.1515/CCLM.2009.002
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- Publication type:
- Article
Genetic variation of FUT2 in Ovambos, Turks, and Mongolians.
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- Transfusion, 2008, v. 48, n. 7, p. 1423, doi. 10.1111/j.1537-2995.2008.01710.x
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- Publication type:
- Article
Reply.
- Published in:
- 2008
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- Publication type:
- Letter
Associations of Protein Tyrosine Phosphatase Nonreceptor 22 (PTPN22) Gene Polymorphisms with Susceptibility to Graves' Disease in a Japanese Population.
- Published in:
- Thyroid, 2008, v. 18, n. 6, p. 625, doi. 10.1089/thy.2007.0353
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- Publication type:
- Article
Extremely high prevalence of DNASE1*1 allele in African populations.
- Published in:
- Cell Biochemistry & Function, 2008, v. 26, n. 2, p. 151, doi. 10.1002/cbf.1414
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- Publication type:
- Article
Sec1-FUT2-Sec1 hybrid allele generated by interlocus gene conversion.
- Published in:
- Transfusion, 2008, v. 48, n. 3, p. 488, doi. 10.1111/j.1537-2995.2007.01553.x
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- Publication type:
- Article
Distinct single nucleotide polymorphism pattern at the FUT2 promoter among human populations.
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- Annals of Hematology, 2008, v. 87, n. 1, p. 19, doi. 10.1007/s00277-007-0362-y
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- Publication type:
- Article
The distribution of haptoglobin-gene deletion ( Hp<sup> del</sup>) is restricted to East Asians.
- Published in:
- 2007
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- Publication type:
- Letter
Genetic variation of FUT2 in a Ghanaian population: identification of four novel mutations and inference of balancing selection.
- Published in:
- Annals of Hematology, 2007, v. 86, n. 3, p. 199, doi. 10.1007/s00277-006-0203-4
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- Publication type:
- Article
Population differences of two coding SNPs in pigmentation-related genes SLC24A5 and SLC45A2.
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- International Journal of Legal Medicine, 2007, v. 121, n. 1, p. 36
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- Publication type:
- Article
Lack of Association of Interleukin-18 Gene Polymorphisms with Susceptibility of Japanese Populations to Graves' Disease or Graves' Ophthalmopathy.
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- Thyroid, 2006, v. 16, n. 3, p. 243, doi. 10.1089/thy.2006.16.243
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- Publication type:
- Article
Haptoglobin Gene Promoter Polymorphism and Haplotypes Are Unique in Different Populations.
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- Human Biology, 2006, v. 78, n. 1, p. 121, doi. 10.1353/hub.2006.0029
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- Article
Evidence for Recent Positive Selection at the Human AIM1 Locus in a European Population.
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- Molecular Biology & Evolution, 2006, v. 23, n. 1, p. 179, doi. 10.1093/molbev/msj018
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- Publication type:
- Article
Denaturing high-performance liquid chromatography–based genotyping and genetic variation of FUT2 in Sri Lanka.
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- Transfusion, 2005, v. 45, n. 12, p. 1934, doi. 10.1111/j.1537-2995.2005.00651.x
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- Publication type:
- Article
Interleukin-13 Gene Polymorphisms Confer the Susceptibility of Japanese Populations to Graves’ Disease.
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- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 1, p. 296, doi. 10.1210/jc.2004-0931
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- Publication type:
- Article
Enhanced Expression of Interleukin-18 and its Receptor in Idiopathic Pulmonary Fibrosis.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2004, v. 31, n. 6, p. 619, doi. 10.1165/rcmb.2003-0306OC
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- Publication type:
- Article
A Novel Tetrameric Short Tandem Repeat Located in the 3′ Flanking Region of the Human ABO-Secretor Gene (FUT2) and Association Between FUT2 and FUT2/01 Loci.
- Published in:
- Human Biology, 2004, v. 76, n. 5, p. 789, doi. 10.1353/hub.2005.0008
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- Publication type:
- Article
A novel I247T missense mutation in the haptoglobin 2 β-chain decreases the expression of the protein and is associated with ahaptoglobinemia.
- Published in:
- Human Genetics, 2004, v. 114, n. 5, p. 499, doi. 10.1007/s00439-004-1098-6
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- Publication type:
- Article
DNA sequence variation of the human ABO-secretor locus (FUT2) in New Guinean populations: possible early human migration from Africa.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 534, doi. 10.1007/s00439-003-1013-6
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- Publication type:
- Article
Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.
- Published in:
- British Journal of Haematology, 2002, v. 117, n. 1, p. 220, doi. 10.1046/j.1365-2141.2002.03368.x
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- Publication type:
- Article