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GEN – Genetic Engineering and Biotechnology News
Mary Ann Liebert, Inc. Publishers
GEN Edge
Genomics
Genomics in the Clinic: A Candid Conversation with Sema4 CEO Eric…
Circulating Tumor Cell
Illumina Launching Pan-Cancer IVD Test, Cloud-Based Bioinformatics Platform
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Guardant Health Launches Early-Stage Colorectal Cancer ctDNA Assay
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Transcriptomics Reveals Liver Genes and Circadian Clock Crosstalk in Time and…
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Bacteria “Croak” in the Presence of Toadlet Peptide
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Algorithms Designed to Study Language Can Predict Immune “Escape” Mutations for…
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To Treat Alzheimer’s, Try Inciting a More Frenzied Amyloid Dance
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Cytiva Delivers Modular Biologics Factory to Lonza
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Machine Learning for Better Bioprocess Data Analysis
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New Promise for Spinal-Cord Injuries
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Trojan Horse Antidotes Designed to Neutralize Lethal Botulinum Toxin
January 2021 Vol. 41 No. 1
Seven Biopharma Trends to Watch in 2021
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January 2021 Vol. 41 No. 1
Seven Biopharma Trends to Watch in 2021
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Top 15 Best-Selling Drugs Launched in 2020
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Top 50 NIH-Funded Institutions of 2020
July 2020 Vol. 40 No. 7
Top 10 Earners among Women Biopharma Executives
June 2020 Vol. 40 No. 6
In Praise of Lesser-Sung Life Sciences Clusters
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Transcriptomics Reveals Liver Genes and Circadian Clock Crosstalk in Time and…
Drug Discovery
Bacteria “Croak” in the Presence of Toadlet Peptide
Coronavirus
Algorithms Designed to Study Language Can Predict Immune “Escape” Mutations for…
Alzheimers
To Treat Alzheimer’s, Try Inciting a More Frenzied Amyloid Dance
Magazine
January 2021 Vol. 41 No. 1
Seven Biopharma Trends to Watch in 2021
January 2021 Vol. 41 No. 1
Leroy Hood: Reflections on a Legendary Career
January 2021 Vol. 41 No. 1
COVID-19 One Year Later: The Biology and the Business
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Monoclonal Antibodies: Developers Explore New Territories
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Uncharted Territory: Top Challenges Facing Gene Therapy Development
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![Illustration of chromosome 16 showing the 14 fly counterparts of the 25 human genes located in a deletion on the chromosome that is associated with autism risk. Researchers used RNA interference (RNAi) to the reduce the expression of these genes individually and in tandem to test how the interactions of these genes modulate neurodevelopmental symptoms associated with the deletion. Interactions between genes that either enhance or suppress the affect of reduced expression are shown by red or blue lines. [Girirajan Laboratory/Penn State]](https://www.genengnews.com/wp-content/uploads/2018/08/Jul2_2018_PennState_Chromosome16Ilustration4113701011-265x198.jpg "Autism Genetic Complexity Comes to Light")
![Fragile X syndrome (FXS) is the most common inherited form of intellectual disability and a major single-gene cause of autism spectrum disorders. [Peter Saxon/Wikimedia]](https://www.genengnews.com/wp-content/uploads/2018/08/Jul16_2018_Wikimedia_Fragx4324425195-324x160.jpg "Fragile X Symptoms May be Helped with New Pharmacological Approach")
