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New Study Suggests Pregnant Women Should Avoid Caffeine Altogether. Here’s Why

XTalks

The results did not differ based on fast or slow caffeine metabolism genotype. Until we learn more, our results suggest it might be prudent to limit or forego caffeine-containing beverages during pregnancy,” Dr. Grantz said in a news release from the NIH.

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Why Proviral DNA Drug Resistance Testing is Useful in Guiding Treatment Decisions for HIV-1 Patients

XTalks

Proviral DNA Genotyping. Moreover, drug-resistant virus in proviral DNA could lead to viral rebound if latently infected cells containing drug-resistant proviral DNA become activated. In other words, what is the concordance between proviral resistance results and the historical archive by traditional virus genotyping?

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Type 1 Diabetes Vaccine: Does Diamyd Have a Winning Formula?

XTalks

Specifically, the vaccine contains human recombinant glutamate decarboxylase 65 (GAD65) protein conjugated to aluminum hydroxide (GAD-alum). The vaccine triggers an immune response against pro-inflammatory processes resulting from autoimmune attack of the pancreas – the inflammation helps to destroy the insulin-producing ?-islet

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HFpEF vs. HFrEF: How To Improve Heart Failure Drug Development

XTalks

For example, the sequence environment around the ADRA2B gene contains many other nearby genes, so a simple approach to SNP selection would generate spurious results. Though the HERMES, and the related 2010 CHARGE study, performed large heart failure genomic association analysis, both consortia relied on genotyping and self-reported data.

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BridgeBio Pharma’s Nulibry Approved as First Treatment for Molybdenum Cofactor Deficiency Type A

XTalks

Molybdopterins are a class of cofactors found in most molybdenum-containing and all tungsten-containing enzymes. In the analysis involving 31 patients, 13 were treated with Nulibry and compared to 18 genotype-matched untreated patients from the history control group.

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10 Key Learnings from Successful Cellular and Gene Therapy Trials for Rare Diseases

XTalks

These are, in my view, the most valid comparisons, particularly in inherited diseases where the genotype is obviously the same in each individual patient, and as a consequence, the difference in phenotype after gene therapy is a true difference,” he adds. As a result, there are several EU regulations and directives to follow.

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Rare Disease Diagnosis: Why Tackling the Genomic Analysis Bottleneck is Key to Advancing Precision Medicine

XTalks

We know that users don’t want to report false negatives caused by poor-quality data, which is why we’ve also introduced a genotyping feature for all curated variants contained within any gene panels of interest. HS: At Congenica, we understand the importance of quality.

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