S. Loganathan

发表

A Novel Bone Morphogenetic Protein 2 Mutant Mouse, nBmp2NLStm, Displays Impaired Intracellular Ca2+ Handling in Skeletal Muscle

Joshua D Yates, L. Bridgewater, Jeffery R. Barrow, 2013, BioMed research international.

2 Functional Assessment of SLC 4 A 11 , an Integral Membrane Protein Mutated in Corneal 3 Dystrophies 4 5

P. Morgan, J. Casey, J. Deitmer, 2016 .

High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy-Causing Mutants of SLC4A11.

J. Casey, K. Alka, S. Loganathan, 2015, Investigative ophthalmology & visual science.

Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations

J. Casey, E. Vithana, Periasamy Sundaresan, 2012, Human mutation.

Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases

J. Mehta, J. Casey, E. Vithana, 2013, Human molecular genetics.

Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies

J. Casey, S. Loganathan, Darpan Malhotra, 2019, Scientific Reports.

Corneal Dystrophy‐Causing SLC4A11 Mutants: Suitability for Folding‐Correction Therapy

J. Casey, S. Loganathan, 2014, Human mutation.

A biochemical framework for SLC4A11, the plasma membrane protein defective in corneal dystrophies.

P. Morgan, J. Casey, A. Quon, 2011, Biochemistry.

In vivo CRISPR screens reveal Serpinb9 and Adam2 as regulators of immune therapy response in lung cancer

J. Reimand, J. Wrana, A. Valipour, 2022, bioRxiv.

Loss of epigenetic regulation disrupts lineage integrity, reactivates multipotency and promotes breast cancer

G. Wahl, Gary D. Bader, J. Wrana, 2021, bioRxiv.

Increased water flux induced by an aquaporin-1/carbonic anhydrase II interaction

G. Calamita, J. Casey, G. Tamma, 2015, Molecular biology of the cell.

In vivo screening unveils pervasive RNA-binding protein dependencies in leukemic stem cells and identifies ELAVL1 as a therapeutic target.

J. Dick, M. Minden, L. D. de Rooij, 2023, Blood cancer discovery.

Rare driver mutations in head and neck squamous cell carcinomas converge on NOTCH signaling

Anne-Claude Gingras, Trevor J. Pugh, Trevor J Pugh, 2020, Science.

The cytoplasmic domain is essential for transport function of the integral membrane transport protein SLC4A11.

J. Casey, S. Loganathan, C. Lukowski, 2016, American journal of physiology. Cell physiology.

Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy

Dharanija Madhavan, J. Casey, N. Soumittra, 2014, Journal of Human Genetics.

Follicular Adenomatoid Odontogenic Tumor

R. Veerakumar, H. Srinvasan, S. Loganathan, 2013 .

The NOTCH-RIPK4-IRF6-ELOVL4 Axis Suppresses Squamous Cell Carcinoma

G. Gish, D. Schramek, Yue Yan, 2023, Cancers.

Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies

J. Casey, S. Loganathan, Darpan Malhotra, 2019, Scientific Reports.

In vivo CRISPR screens reveal Serpinb9 and Adam2 as regulators of immune therapy response in lung cancer

J. Reimand, J. Wrana, A. Valipour, 2023, Nature communications.

In vivo CRISPR screens reveal potent driver mutations in head and neck cancers

D. Schramek, S. Loganathan, 2020, Molecular & cellular oncology.

The cytoplasmic domain is essential for transport function of the integral membrane transport protein SLC4A11.

J. Casey, S. Loganathan, C. Lukowski, 2016, American journal of physiology. Cell physiology.

Corneal Dystrophy‐Causing SLC4A11 Mutants: Suitability for Folding‐Correction Therapy

J. Casey, S. Loganathan, 2014, Human mutation.

Combined Pik3ca-H1047R and loss-of-function Notch1 alleles decrease survival time in a 4-nitroquinoline N-oxide-driven head and neck squamous cell carcinoma model.

E. Bellile, N. Michmerhuizen, J. Brenner, 2022, Oral oncology.

Loss of epigenetic regulation disrupts lineage integrity, induces aberrant alveogenesis and promotes breast cancer.

Gary D Bader, T. Sørlie, D. Cescon, 2022, Cancer discovery.

Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies.

P. Morgan, J. Casey, J. Deitmer, 2016, American journal of physiology. Cell physiology.

In Vivo CRISPR/Cas9 Screening to Simultaneously Evaluate Gene Function in Mouse Skin and Oral Cavity.

D. Schramek, Chen Luxenburg, Ellen Langille, 2020, Journal of visualized experiments : JoVE.