Search research articles
Contact Us
Filters
Showing results (1-10 of 7) with videos related to
Page
of 1
Sort By:
STAR Protocols
|
September 27, 2023
Using PrISMa to reveal the interactome of the human claudins family
Daniel Perez-Hernandez, Lorena Suarez-Artiles, Mattson S O Jones, et al.
Genes
|
January 5, 2018
Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 Disease
Lorena Suarez-Artiles, Ana Perdomo-Ramirez, Elena Ramos-Trujillo, et al.
BMC Medical Genetics
|
January 10, 2019
Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations
Ana Perdomo-Ramirez, Marian de Armas-Ortiz, Elena Ramos-Trujillo, et al.
Molecular & Cellular Proteomics : MCP
|
August 15, 2021
A Universal Peptide Matrix Interactomics Approach to Disclose Motif-Dependent Protein Binding
Evelyn Ramberger, Lorena Suarez-Artiles, Daniel Perez-Hernandez, et al.
Cell Reports
|
November 9, 2022
Pan-claudin family interactome analysis reveals shared and specific interactions
Lorena Suarez-Artiles, Tilman Breiderhoff, Rossana Girardello, et al.
Biorxiv : the Preprint Server for Biology
|
February 12, 2026
Multi-omics Insight into Cardiac Myofibril Remodeling in Post-Prandial Burmese Pythons
Thomas G Martin, Lorena Suarez-Artiles, Kathleen C Woulfe, et al.
Cell Reports
|
September 6, 2018
Transcriptional and Translational Differences of Microglia from Male and Female Brains
Dilansu Guneykaya, Andranik Ivanov, Daniel Perez Hernandez, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
STAR Protocols
|
September 27, 2023
Using PrISMa to reveal the interactome of the human claudins family
Daniel Perez-Hernandez, Lorena Suarez-Artiles, Mattson S O Jones, et al.
Genes
|
January 5, 2018
Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 Disease
Lorena Suarez-Artiles, Ana Perdomo-Ramirez, Elena Ramos-Trujillo, et al.
BMC Medical Genetics
|
January 10, 2019
Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations
Ana Perdomo-Ramirez, Marian de Armas-Ortiz, Elena Ramos-Trujillo, et al.
Molecular & Cellular Proteomics : MCP
|
August 15, 2021
A Universal Peptide Matrix Interactomics Approach to Disclose Motif-Dependent Protein Binding
Evelyn Ramberger, Lorena Suarez-Artiles, Daniel Perez-Hernandez, et al.
Cell Reports
|
November 9, 2022
Pan-claudin family interactome analysis reveals shared and specific interactions
Lorena Suarez-Artiles, Tilman Breiderhoff, Rossana Girardello, et al.
Biorxiv : the Preprint Server for Biology
|
February 12, 2026
Multi-omics Insight into Cardiac Myofibril Remodeling in Post-Prandial Burmese Pythons
Thomas G Martin, Lorena Suarez-Artiles, Kathleen C Woulfe, et al.
Cell Reports
|
September 6, 2018
Transcriptional and Translational Differences of Microglia from Male and Female Brains
Dilansu Guneykaya, Andranik Ivanov, Daniel Perez Hernandez, et al.
Page
of 1