Rare driver mutations in head and neck squamous cell carcinomas converge on NOTCH signaling von Loganathan, Sampath K., Schleicher, Krista, Malik, Ahmad, Quevedo, Rene, Langille, Ellen, Teng, Katie, Oh, Robin H., Rathod, Bhavisha, Tsai, Ricky, Samavarchi-Tehrani, Payman, Pugh, Trevor J., Gingras, Anne-Claude, Schramek, Daniel

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Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies von Malhotra, Darpan, Loganathan, Sampath K., Chiu, Anthony M., Lukowski, Chris M., Casey, Joseph R.

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Corneal Dystrophy-Causing SLC4A11 Mutants: Suitability for Folding-Correction Therapy von Loganathan, Sampath K., Casey, Joseph R.

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Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases von Vilas, Gonzalo L, Loganathan, Sampath K, Liu, Jun, Riau, Andri K, Young, James D, Mehta, Jodhbir S, Vithana, Eranga N, Casey, Joseph R

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In vivo CRISPR screens reveal Serpinb9 and Adam2 as regulators of immune therapy response in lung cancer von Dervovic, Dzana, Malik, Ahmad A., Chen, Edward L. Y., Narimatsu, Masahiro, Adler, Nina, Afiuni-Zadeh, Somaieh, Krenbek, Dagmar, Martinez, Sebastien, Tsai, Ricky, Boucher, Jonathan, Berman, Jacob M., Teng, Katie, Ayyaz, Arshad, Lü, YiQing, Mbamalu, Geraldine, Loganathan, Sampath K., Lee, Jongbok, Zhang, Li, Guidos, Cynthia, Wrana, Jeffrey, Valipour, Arschang, Roux, Philippe P., Reimand, Jüri, Jackson, Hartland W., Schramek, Daniel

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Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies von Loganathan, Sampath K, Schneider, Hans-Peter, Morgan, Patricio E, Deitmer, Joachim W, Casey, Joseph R

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High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy-Causing Mutants of SLC4A11 von Chiu, Anthony M, Mandziuk, Jake J, Loganathan, Sampath K, Alka, Kumari, Casey, Joseph R

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Author Correction: In vivo CRISPR screens reveal Serpinb9 and Adam2 as regulators of immune therapy response in lung cancer von Dervovic, Dzana, Malik, Ahmad A., Chen, Edward L. Y., Narimatsu, Masahiro, Adler, Nina, Afiuni-Zadeh, Somaieh, Krenbek, Dagmar, Martinez, Sebastien, Tsai, Ricky, Boucher, Jonathan, Berman, Jacob M., Teng, Katie, Ayyaz, Arshad, Lü, YiQing, Mbamalu, Geraldine, Loganathan, Sampath K., Lee, Jongbok, Zhang, Li, Guidos, Cynthia, Wrana, Jeffrey, Valipour, Arschang, Roux, Philippe P., Reimand, Jüri, Jackson, Hartland W., Schramek, Daniel

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Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy von Soumittra, Nagasamy, Loganathan, Sampath K, Madhavan, Dharanija, Ramprasad, Vedam L, Arokiasamy, Tharigopala, Sumathi, Sundaram, Karthiyayini, Thirumalai, Rachapalli, Sudhir R, Kumaramanickavel, Govindasamy, Casey, Joseph R, Rajagopal, Rama

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The cytoplasmic domain is essential for transport function of the integral membrane transport protein SLC4A11 von Loganathan, Sampath K, Lukowski, Chris M, Casey, Joseph R

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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 von Michmerhuizen, Nicole L., Heenan, Caitlin, Wang, Jiayu, Leonard, Elizabeth, Bellile, Emily, Loganathan, Sampath K., Wong, Sunny Y., Lei, Yu L., Brenner, J. Chad

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Loss of Epigenetic Regulation Disrupts Lineage Integrity, Induces Aberrant Alveogenesis, and Promotes Breast Cancer von Langille, Ellen, Al-Zahrani, Khalid N, Ma, Zhibo, Liang, Minggao, Uuskula-Reimand, Liis, Espin, Roderic, Teng, Katie, Malik, Ahmad, Bergholtz, Helga, Ghamrasni, Samah El, Afiuni-Zadeh, Somaieh, Tsai, Ricky, Alvi, Sana, Elia, Andrew, Lü, YiQing, Oh, Robin H, Kozma, Katelyn J, Trcka, Daniel, Narimatsu, Masahiro, Liu, Jeff C, Nguyen, Thomas, Barutcu, Seda, Loganathan, Sampath K, Bremner, Rod, Bader, Gary D, Egan, Sean E, Cescon, David W, Sørlie, Therese, Wrana, Jeffrey L, Jackson, Hartland W, Wilson, Michael D, Witkiewicz, Agnieszka K, Knudsen, Erik S, Pujana, Miguel Angel, Wahl, Geoffrey M, Schramek, Daniel

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Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations von Vilas, Gonzalo L., Loganathan, Sampath K., Quon, Anita, Sundaresan, Periasamy, Vithana, Eranga N., Casey, Joseph

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A Biochemical Framework for SLC4A11, the Plasma Membrane Protein Defective in Corneal Dystrophies von Vilas, Gonzalo L, Morgan, Patricio E, Loganathan, Sampath K, Quon, Anita, Casey, Joseph R

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A Novel Bone Morphogenetic Protein 2 Mutant Mouse, , Displays Impaired Intracellular Handling in Skeletal Muscle von Bridgewater, Laura C., Mayo, Jaime L., Evanson, Bradley G., Whitt, Megan E., Dean, Spencer A., Yates, Joshua D., Holden, Devin N., Schmidt, Alina D., Fox, Christopher L., Dhunghel, Saroj, Steed, Kevin S., Adam, Michael M., Nichols, Caitlin A., Loganathan, Sampath K., Barrow, Jeffery R., Hancock, Chad R.

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In Vivo Screening Unveils Pervasive RNA-Binding Protein Dependencies in Leukemic Stem Cells and Identifies ELAVL1 as a Therapeutic Target von Vujovic, Ana, de Rooij, Laura, Chahi, Ava Keyvani, Chen, He Tian, Yee, Brian A, Loganathan, Sampath K, Liu, Lina, Chan, Derek C H, Tajik, Amanda, Tsao, Emily, Moreira, Steven, Joshi, Pratik, Xu, Joshua, Wong, Nicholas, Balde, Zaldy, Jahangiri, Soheil, Zandi, Sasan, Aigner, Stefan, Dick, John E, Minden, Mark D, Schramek, Daniel, Yeo, Gene W, Hope, Kristin J

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A novel bone morphogenetic protein 2 mutant mouse, nBmp2NLS(tm), displays impaired intracellular Ca2+ handling in skeletal muscle von Bridgewater, Laura C, Mayo, Jaime L, Evanson, Bradley G, Whitt, Megan E, Dean, Spencer A, Yates, Joshua D, Holden, Devin N, Schmidt, Alina D, Fox, Christopher L, Dhunghel, Saroj, Steed, Kevin S, Adam, Michael M, Nichols, Caitlin A, Loganathan, Sampath K, Barrow, Jeffery R, Hancock, Chad R

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Mice bearing a targeted inactivation of nBmp2 show decreased muscle strength von Schmidt, Alina D, Loganathan, Sampath K, Adam, Mike M, Nichols, Caitlin A, Mayo, Jaime L, Felin, Jenny E, Capecchi, Mario R, Barrow, Jeffery R, Bridgewater, Laura C

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A Novel Bone Morphogenetic Protein 2 Mutant Mouse, nBmp2NLStm, Displays Impaired Intracellular Ca2+ Handling in Skeletal Muscle von Fox, Christopher L., Dhunghel, Saroj, Adam, Michael M., Nichols, Caitlin A., Loganathan, Sampath K., Barrow, Jeffery R., Hancock, Chad R., Schmidt, Alina D., Holden, Devin N., Yates, Joshua D., Dean, Spencer A., Whitt, Megan E., Evanson, Bradley G., Mayo, Jaime L., Bridgewater, Laura C., Steed, Kevin S.

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Ear detection using geomorphic metric and convolutional neural networks von Sampath, T., Raj, P. T. Vasanth, Balashenbagam, Kumar, Manoj

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