anemia | GenomeWeb

anemia

VISION aims to provide validated regulatory modules, quantitative models for gene regulation, and guides for translating research from mouse models to human.

A modified version of a commercially available magnetic bead cell sorting instrument from Miltenyi Biotec could be deployed to areas without cGMP facilities.

The team at Cincinnati Children’s Hospital Medical Center was able to override errors in the FA DNA repair pathway, allowing the cells to grow normally.

This Week in PNAS

In PNAS this week: decreased DOCK4 expression in myelodysplastic syndromes plus anemia, hepatitis A evolution, and more.

Researchers sequenced samples from hundreds of individuals with aplastic anemia to narrow in on somatic mutation and clonal evolution patterns in the disease.

The Global Globin 2020 Challenge will promote the collection and sharing of genomic data, especially in low- and middle-income countries most affected by hemolytic anemias.

This article has been updated to correct the name of Intrinsic's CEO.

Alnylam Pharmaceuticals this week provided an update to its research and development activities, adding a new preclinical program to its pipeline with ALN-AS1 for acute intermittent porphyria while dropping its refractory anemia drug ALN-HPN in order to focus on “higher priority”

Researchers using exome sequencing to study ADHD found rare mutations they think may be causing a patient's anemia, raising the question of how to handle unrelated findings in sequencing studies.

The assay, which its developers claim can measure telomere length in less than half the time of other PCR-based methods while using 20-fold less genetic material, will be deployed as part of a clinical study designed to monitor changes in telomere length in response to certain therapies in patients with telomere diseases.

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An opinion piece in the New York Times urges lawmakers to keep genetic protections in place.

Research funding in Canada is to remain mostly the same, ScienceInsider reports.

In Science this week: random DNA replication errors play role in cancer, and more.

The Bill and Melinda Gates Foundation embarks on an open-access publishing path.