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Afimetoran

New Drug Approvals

11:373-384 (2010)). 10:89-102 (2010)). TLR7-9 are among the set that are endosomally located and respond to single-stranded RNA (TLR7and TLR8) or unmethylated single-stranded DNA containing cytosine-phosphate-guanine (CpG) motifs (TLR9). Nature Immunol., With the exception of TLR3, all TLRs recruit the adaptor molecule MyD88.

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Atlas XIV And Reflections On The VC Math Problem

LifeSciVC

combinatorial chemistry, human genetics, functional genomics, mRNA, I/O, CRISPR, RNA editing, and many others). When I joined in 2005, the “patient” (Atlas) was undergoing surgery and we came out of the decade in 2010 with a small partnership, around one table, in one office in Cambridge.

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A Molecular Portrait of ALS and FTD

Drug Target Review

14 TDP-43 is a DNA and RNA binding protein that regulates the expression and splicing of several target transcripts. Many potential toxic effects have been suggested, including the mis-splicing of the Stathmin-2 RNA transcript. Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis.” Neuron vol. 29 2022, pp.

RNA 98
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The Dangers of Mirrored Life

Codon

DNA and RNA molecules are also built from exclusively right-handed nucleic acids. Across the tree of life, organisms strictly require exactly one of the two chiral forms of their molecular building blocks — amino acids, nucleotides of RNA and DNA. In 2010, researchers at the J.

RNA 104
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Experimental Myotonic Dystrophy Treatment Teams Monoclonal Antibody and siRNA

PLOS: DNA Science

Now Avidity Biosciences has developed a candidate drug that weds a monoclonal antibody (MAb) to a short piece of RNA – a small interfering RNA (siRNA). This novel class of RNA therapeutics is called Antibody Oligonucleotide Conjugates (AOCs™). Father and daughter died within weeks of each other in early 2010.

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Cave Coronavirus in Wuhan Lab Seeded COVID – The Truth Has Always Been Out There, in the Genetics

PLOS: DNA Science

The most compelling evidence for the origin lies in the RNA genome sequence similarities between RaTG13 and SARS-CoV-2 – specifically, a part that encodes the “furin binding site” of the spike protein with which the virus adheres to host cells. RaTG13 likely wasn’t the only stop on the evolutionary road to SARS-CoV-2.

Virus 52
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Codon Digest: Discovering Antibiotics with Deep Learning

Codon

The researchers first compared the editing efficiency of different versions of IscB when coupled with 'ωRNA,' which guides the enzyme to the right spot on the DNA. A particular variant, named IscB*-ωRNA*, had the highest editing efficiency across multiple different sites in the genome. Read more in Nature Methods.

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