Tuesday, May 24, 2016

Some relevant papers on RPS23 and ribosomopathies

Hydroxylation of the eukaryotic ribosomal decoding center affects translational accuracy

Pubmed


OGFOD1 catalyzes prolyl hydroxylation of RPS23 and is involved in translation control and stress granule formation
Pubmed


Sudestada1, a Drosophila ribosomal prolyl-hydroxylase required for mRNA translation, cell homeostasis, and organ growth

Growing with the wind 

Ribosomal protein hydroxylation and cell growth

Ribosomopathies: how a common root can cause a tree of pathologies

Ribosomopathies and the paradox of cellular hypo- to hyperproliferation

Ribosomal Protein Mutations Induce Autophagy through S6 Kinase Inhibition of the Insulin Pathway


Mysterious Ribosomopathies


Ribosomopathies: Global process, tissue specific defects



The role of ribosomal proteins in the regulation of cell proliferation, tumorigenesis, and genomic integrity
Springer

Wednesday, March 16, 2016

First scientific publication released today on the RPS23 mutation.


Structural Abnormalities in the Hair of a Patient with a Novel Ribosomopathy


http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0149619

In this study the physical properties of Vincent's hair are analyzed in comparison to the rest of our family.

More papers will follow.

Tuesday, March 1, 2016

Rare Disease Day 29th of February

Very nice article written by Ricki Lewis Ph.D. A geneticist, blogger and publisher of genetics textbooks and the author of the book "The Forever Fix" Gene therapy and the boy who saved it.

Vincent's Story: Discovery of a New Autism Spectrum Disorder



http://www.raredr.com/contributor/ricki-lewis-phd/2016/02/vincents-story-discovery-of-a-new-autism-spectrum-disorder