S. Ramachandran

发表

PLUNC is a secreted product of neutrophil granules

P. McCray, J. Bartlett, Benjamin J Hicks, 2008, Journal of leukocyte biology.

A genomic signature approach to rescue ΔF508-cystic fibrosis transmembrane conductance regulator biosynthesis and function.

M. Welsh, P. McCray, S. Ramachandran, 2014, American journal of respiratory cell and molecular biology.

Microarray mRNA expression profiling to study cystic fibrosis.

T. Scheetz, L. Clarke, M. Amaral, 2011, Methods in molecular biology.

Integrative genomic meta-analysis reveals novel molecular insights into cystic fibrosis and ΔF508-CFTR rescue

J. Dudley, Li Li, P. McCray, 2020, Scientific Reports.

Cis-acting single nucleotide polymorphisms alter MicroRNA-mediated regulation of human brain-expressed transcripts

Ryan M Spengler, B. Davidson, S. Ramachandran, 2016, Human molecular genetics.

Efficient delivery of RNA interference oligonucleotides to polarized airway epithelia in vitro.

Ashley M. Jacobi, B. Davidson, A. Jacobi, 2013, American journal of physiology. Lung cellular and molecular physiology.

General Anxiety Is Associated with Problematic Initial Recovery After Carpal Tunnel Release

D. Ring, S. Ramachandran, C. Ryan, 2022, Clinical orthopaedics and related research.

Pancreatic damage in fetal and newborn cystic fibrosis pigs involves the activation of inflammatory and remodeling pathways.

D. Meyerholz, M. Welsh, D. Stoltz, 2012, The American journal of pathology.

Post-transcriptional regulation of cystic fibrosis transmembrane conductance regulator expression and function by microRNAs.

Ashley M. Jacobi, M. Welsh, M. Behlke, 2013, American journal of respiratory cell and molecular biology.

A microRNA network regulates expression and biosynthesis of wild-type and ΔF508 mutant cystic fibrosis transmembrane conductance regulator

Ashley M. Jacobi, M. Welsh, M. Behlke, 2012, Proceedings of the National Academy of Sciences.

Reduced Airway Surface pH Impairs Bacterial Killing in the Porcine Cystic Fibrosis Lung

M. Welsh, T. Moninger, C. Wohlford-Lenane, 2012, Nature.

Manipulation of Cell Physiology Enables Gene Silencing in Well-differentiated Airway Epithelia

B. Davidson, M. Behlke, S. Krishnamurthy, 2012, Molecular therapy. Nucleic acids.

Translating in vitro CFTR rescue into small molecule correctors for cystic fibrosis using the Library of Integrated Network‐based Cellular Signatures drug discovery platform

A. Subramanian, A. Liberzon, R. Bridges, 2021, CPT: pharmacometrics & systems pharmacology.

Integrative chemogenomic analysis identifies small molecules that partially rescue ΔF508‐CFTR for cystic fibrosis

J. Dudley, R. Bridges, P. McCray, 2021, CPT: pharmacometrics & systems pharmacology.

Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense.

D. Meyerholz, M. Welsh, A. Comellas, 2016, American journal of physiology. Lung cellular and molecular physiology.

microRNA expression profiling of endometrial endometrioid adenocarcinomas and serous adenocarcinomas reveals profiles containing shared, unique and differentiating groups of microRNAs.

M. Goodheart, E. Devor, K. Leslie, 2011, Oncology reports.

Adherens junction protein nectin-4 (PVRL4) is the epithelial receptor for measles virus

K. Cichutek, P. Sinn, P. McCray, 2011, Nature.

Cystic Fibrosis Pigs Develop Lung Disease and Exhibit Defective Bacterial Eradication at Birth

S. Richter, D. Meyerholz, M. Welsh, 2010, Science Translational Medicine.

The long non-coding RNA NEAT1 is elevated in polyglutamine repeat expansion diseases and protects from disease gene-dependent toxicities

Ryan M Spengler, B. Davidson, S. Ramachandran, 2018, Human molecular genetics.

SYVN1, NEDD8, and FBXO2 Proteins Regulate ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Ubiquitin-mediated Proteasomal Degradation*

Ashley M. Jacobi, M. Behlke, P. McCray, 2016, The Journal of Biological Chemistry.

Newborn Cystic Fibrosis Pigs Have a Blunted Early Response to an Inflammatory Stimulus.

D. Meyerholz, M. Welsh, C. Wohlford-Lenane, 2016, American journal of respiratory and critical care medicine.

Transcriptome sequencing reveals aberrant alternative splicing in Huntington's disease.

Yi Xing, Shihao Shen, Olga Pletnikova, 2016, Human molecular genetics.

Integrated gene expression analysis of controls across datasets available of the genes implicated in type 2 diabetes mellitus complications

S. Ramachandran, R. Rashmi, 2017 .

Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children.

G. McLennan, A. R. Smith, D. Meyerholz, 2010, American journal of respiratory and critical care medicine.

Modulating membrane fluidity corrects Batten disease phenotypes in vitro and in vivo

B. Davidson, E. Lysenko, L. Tecedor, 2018, Neurobiology of Disease.

Global dysregulation of the chromosome 14q32 imprinted region in uterine carcinosarcoma.

M. Goodheart, E. Devor, K. Leslie, 2012, Experimental and therapeutic medicine.

A microRNA network regulates expression and biosynthesis of wild-type and ΔF508 mutant cystic fibrosis transmembrane conductance regulator

Ashley M. Jacobi, M. Welsh, M. Behlke, 2012, Proceedings of the National Academy of Sciences.