Connection

ZEYNEP COBAN-AKDEMIR to HEK293 Cells

This is a "connection" page, showing publications ZEYNEP COBAN-AKDEMIR has written about HEK293 Cells.
Connection Strength

0.092
  1. Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1. Mol Genet Genomic Med. 2020 01; 8(1):e1023.
    View in: PubMed
    Score: 0.033
  2. Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa. PLoS Genet. 2018 08; 14(8):e1007504.
    View in: PubMed
    Score: 0.030
  3. De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder. Am J Hum Genet. 2017 Nov 02; 101(5):716-724.
    View in: PubMed
    Score: 0.029
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.