Toronto, Canada

Brenda L Gallie


Average Co-Inventor Count = 1.9

ph-index = 2

Forward Citations = 15(Granted Patents)


Company Filing History:


Years Active: 1982-2000

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3 patents (USPTO):Explore Patents

Title: Brenda L Gallie: Innovator in Genetic Testing

Introduction

Brenda L Gallie is a prominent inventor based in Toronto, Canada. She has made significant contributions to the field of genetic testing, particularly in the diagnosis of mutations in the RB1 gene. With a total of 3 patents, her work has advanced the understanding and detection of genetic disorders.

Latest Patents

One of her latest patents focuses on a method, reagents, and kit for reliable and cost-effective testing for mutations in the RB1 gene. This innovative approach involves quantitatively amplifying exons of the sample RB1 gene using primers that are complementary to intron regions flanking each exon. The lengths and/or quantities of the amplification products for each exon are then determined and compared to those obtained from a wild-type RB1 gene. Differences in length between the amplified sample exon and the corresponding wild-type exon indicate the presence of insertion or deletion mutations. Additionally, differences in quantity can reflect the complete absence of an exon or heterozygosity for a mutant exon. The nucleic acid sequence of each exon with identified mutations is subsequently determined, enhancing the diagnostic capabilities in genetic testing.

Career Highlights

Brenda has worked with notable organizations such as Visible Genetics Inc. and the University of Toronto. Her experience in these institutions has allowed her to collaborate with leading experts in the field and contribute to groundbreaking research in genetic diagnostics.

Collaborations

Some of her notable coworkers include James M Dunn and John K Stevens. Their collaborative efforts have furthered advancements in genetic testing methodologies.

Conclusion

Brenda L Gallie's innovative work in genetic testing has made a significant impact on the diagnosis of genetic disorders. Her contributions continue to influence the field and improve patient outcomes through advanced testing techniques.

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