Lorena Suarez-Artiles
Overview
Explore the profile of Lorena Suarez-Artiles including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
5
Citations
30
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Perez-Hernandez D, Suarez-Artiles L, Jones M, Dittmar G
STAR Protoc
. 2023 Sep;
4(4):102549.
PMID: 37756153
Here, we provide a protocol for the systematic screening of protein-protein interactions mediated by short linear motifs using the Protein Interaction Screen on a peptide Matrix (PrISMa) technique. We describe...
2.
Suarez-Artiles L, Breiderhoff T, Girardello R, Gonschior H, Rodius S, Lesur A, et al.
Cell Rep
. 2022 Nov;
41(6):111588.
PMID: 36351382
Claudins are a family of transmembrane proteins expressed in epithelial tissues and are the major components of tight junctions (TJs), which define barrier properties in epithelia and maintain cell polarity....
3.
Ramberger E, Suarez-Artiles L, Perez-Hernandez D, Haji M, Popp O, Reimer U, et al.
Mol Cell Proteomics
. 2021 Aug;
20:100135.
PMID: 34391889
Protein-protein interactions mediated by intrinsically disordered regions are often based on short linear motifs (SLiMs). SLiMs are implicated in signal transduction and gene regulation yet remain technically laborious and notoriously...
4.
Perdomo-Ramirez A, de Armas-Ortiz M, Ramos-Trujillo E, Suarez-Artiles L, Claverie-Martin F
BMC Med Genet
. 2019 Jan;
20(1):6.
PMID: 30621608
Background: Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis type 1 is an autosomal recessive disease characterized by excessive renal magnesium and calcium excretion, bilateral nephrocalcinosis, and progressive chronic renal failure. This...
5.
Suarez-Artiles L, Perdomo-Ramirez A, Ramos-Trujillo E, Claverie-Martin F
Genes (Basel)
. 2018 Jan;
9(1).
PMID: 29300302
Mutations in the gene are associated with both Lowe syndrome and Dent-2 disease. Patients with Lowe syndrome present congenital cataracts, mental disabilities and a renal proximal tubulopathy, whereas patients with...