DR and AJD were FCT research grantees (PIC/IC/82822/2007)Development of a simple mutation directed method in order to allow lowering the cost of mutation testing using an easily obtainable biological material. Assessment of the feasibility of such method was tested using a GC-rich amplicon. A method of denaturing high-performance liquid chromatography (dHPLC) was improved and implemented as a technique for the detection of variants in exon 9 of the IDUA gene. The optimized method was tested in 500 genomic DNA samples obtained from dried blood spots (DBS). With this dHPLC approach it was possible to detect different variants, including the common p.Trp402Ter mutation in the IDUA gene. The high GC content did not interfere with the resolution...
Detection of mutations by DNA sequencing can be facilitated by scanning methods to identify amplicon...
Aims: Quinolone antibiotics are the agents of choice for treating systemic Salmonella infections. Re...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
Copyright © 2013 Diogo Ribeiro et al. This is an open access article distributed under the Creative ...
DHPLC is an efficient method for candidate gene scanning with a high level of automation. Single-bas...
Denaturing high-performance liquid chromatography (DHPLC) is a novel high-capacity technique for det...
Mutations in the ABCA1 gene are the cause of familial high density lipoprotein deficiency (FHD). Bec...
Beta-thalassemia is a common inherited disease, resulting from one or more of a total of more than 2...
The manifestation of hemophilia A, a common hereditary bleeding disorder in humans, is caused by abn...
The inherited disorders of hemoglobin represent the most common Mendelian disease worldwide, with a ...
The inherited disorders of hemoglobin represent the most common Mendelian disease worldwide, with a ...
Abstract Denaturing high performance liquid chromatography is a relatively new method by which heter...
Denaturing high-performance liquid chromatography (DHPLC), which has recently been developed as an a...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
Background The G71R mutation in the UGT1A1 gene has been associated with neonatal jaundice and ...
Detection of mutations by DNA sequencing can be facilitated by scanning methods to identify amplicon...
Aims: Quinolone antibiotics are the agents of choice for treating systemic Salmonella infections. Re...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
Copyright © 2013 Diogo Ribeiro et al. This is an open access article distributed under the Creative ...
DHPLC is an efficient method for candidate gene scanning with a high level of automation. Single-bas...
Denaturing high-performance liquid chromatography (DHPLC) is a novel high-capacity technique for det...
Mutations in the ABCA1 gene are the cause of familial high density lipoprotein deficiency (FHD). Bec...
Beta-thalassemia is a common inherited disease, resulting from one or more of a total of more than 2...
The manifestation of hemophilia A, a common hereditary bleeding disorder in humans, is caused by abn...
The inherited disorders of hemoglobin represent the most common Mendelian disease worldwide, with a ...
The inherited disorders of hemoglobin represent the most common Mendelian disease worldwide, with a ...
Abstract Denaturing high performance liquid chromatography is a relatively new method by which heter...
Denaturing high-performance liquid chromatography (DHPLC), which has recently been developed as an a...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
Background The G71R mutation in the UGT1A1 gene has been associated with neonatal jaundice and ...
Detection of mutations by DNA sequencing can be facilitated by scanning methods to identify amplicon...
Aims: Quinolone antibiotics are the agents of choice for treating systemic Salmonella infections. Re...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...