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Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder.
Nemirovsky SI, Córdoba M, Zaiat JJ, Completa SP, Vega PA, González-Morón D, Medina NM, Fabbro M, Romero S, Brun B, Revale S, Ogara MF, Pecci A, Marti M, Vazquez M, Turjanski A, Kauffman MA. Nemirovsky SI, et al. Among authors: turjanski a. PLoS One. 2015 Feb 3;10(2):e0116358. doi: 10.1371/journal.pone.0116358. eCollection 2015. PLoS One. 2015. PMID: 25646853 Free PMC article.
Oculocutaneous albinism type 1B associated with a functionally significant tyrosinase gene polymorphism detected with Whole Exome Sequencing.
Mendez R, Iqbal S, Vishnopolska S, Martinez C, Dibner G, Aliano R, Zaiat J, Biagioli G, Fernandez C, Turjanski A, Campbell AJ, Mercado G, Marti MA. Mendez R, et al. Among authors: turjanski a. Ophthalmic Genet. 2021 Jun;42(3):291-295. doi: 10.1080/13816810.2021.1888129. Epub 2021 Feb 18. Ophthalmic Genet. 2021. PMID: 33599182
Aromatic clusters in protein-protein and protein-drug complexes.
Lanzarotti E, Defelipe LA, Marti MA, Turjanski AG. Lanzarotti E, et al. Among authors: turjanski ag. J Cheminform. 2020 May 8;12(1):30. doi: 10.1186/s13321-020-00437-4. J Cheminform. 2020. PMID: 33431014 Free PMC article.
Biased Docking for Protein-Ligand Pose Prediction.
Arcon JP, Turjanski AG, Martí MA, Forli S. Arcon JP, et al. Among authors: turjanski ag. Methods Mol Biol. 2021;2266:39-72. doi: 10.1007/978-1-0716-1209-5_3. Methods Mol Biol. 2021. PMID: 33759120 Free PMC article.
97 results