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Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of C0L8A2 mutations in Fuchs endothelial corneal dystrophy.
Published in:
Journal of Human Genetics, 2014, v. 59, n. 8, p. 444, doi. 10.1038/jhg.2014.55
By:
- 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
Publication type:
Article
Author Correction: In vivo CRISPR screens reveal Serpinb9 and Adam2 as regulators of immune therapy response in lung cancer.
Published in:
2023
By:
- 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
Publication type:
Correction Notice
In vivo CRISPR screens reveal Serpinb9 and Adam2 as regulators of immune therapy response in lung cancer.
Published in:
Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38841-7
By:
- 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
Publication type:
Article
In vivo CRISPR screens reveal Serpinb9 and Adam2 as regulators of immune therapy response in lung cancer.
Published in:
Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38841-7
By:
- 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
Publication type:
Article
Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies.
Published in:
Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-46094-y
By:
- Malhotra, Darpan;
- Loganathan, Sampath K.;
- Chiu, Anthony M.;
- Lukowski, Chris M.;
- Casey, Joseph R.
Publication type:
Article
Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 22, p. 4579, doi. 10.1093/hmg/ddt307
By:
- Vilas, Gonzalo L.;
- Loganathan, Sampath K.;
- Liu, Jun;
- Riau, Andri K.;
- Young, James D.;
- Mehta, Jodhbir S.;
- Vithana, Eranga N.;
- Casey, Joseph R.
Publication type:
Article
Corneal Dystrophy-Causing SLC4 A11 Mutants: Suitability for Folding-Correction Therapy.
Published in:
Human Mutation, 2014, v. 35, n. 9, p. 1082, doi. 10.1002/humu.22601
By:
- Loganathan, Sampath K.;
- Casey, Joseph R.
Publication type:
Article
Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations.
Published in:
Human Mutation, 2012, v. 33, n. 2, p. 419, doi. 10.1002/humu.21655
By:
- Vilas, Gonzalo L.;
- Loganathan, Sampath K.;
- Quon, Anita;
- Sundaresan, Periasamy;
- Vithana, Eranga N.;
- Casey, Joseph
Publication type:
Article
A Novel Bone Morphogenetic Protein 2 Mutant Mouse, nBmp2NLS(tm), Displays Impaired Intracellular Ca(2+) Handling in Skeletal Muscle.
Published in:
2013
By:
- 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
Publication type:
Journal Article
A Novel Bone Morphogenetic Protein 2 Mutant Mouse, nBmp2NLS<sup>tm</sup>, Displays Impaired Intracellular Ca<sup>2+</sup> Handling in Skeletal Muscle.
Published in:
BioMed Research International, 2013, v. 2013, p. 1, doi. 10.1155/2013/125492
By:
- 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.
Publication type:
Article

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