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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 1
2004 1
2005 1
2007 2
2010 1
2011 1
2012 2
2013 4
2014 8
2015 5
2016 3
2017 9
2018 5
2019 12
2020 3
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53 results
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Page 1
Integrated Genomic Characterization of Pancreatic Ductal Adenocarcinoma.
Cancer Genome Atlas Research Network. Electronic address: andrew_aguirre@dfci.harvard.edu; Cancer Genome Atlas Research Network. Cancer Genome Atlas Research Network. Electronic address: andrew_aguirre@dfci.harvard.edu, et al. Cancer Cell. 2017 Aug 14;32(2):185-203.e13. doi: 10.1016/j.ccell.2017.07.007. Cancer Cell. 2017. PMID: 28810144 Free PMC article.
Single-Cell Genomics.
Paolillo C, Londin E, Fortina P. Paolillo C, et al. Among authors: londin e. Clin Chem. 2019 Aug;65(8):972-985. doi: 10.1373/clinchem.2017.283895. Epub 2019 Mar 14. Clin Chem. 2019. PMID: 30872376 Review.
Small RNA Sequencing across Diverse Biofluids Identifies Optimal Methods for exRNA Isolation.
Srinivasan S, Yeri A, Cheah PS, Chung A, Danielson K, De Hoff P, Filant J, Laurent CD, Laurent LD, Magee R, Moeller C, Murthy VL, Nejad P, Paul A, Rigoutsos I, Rodosthenous R, Shah RV, Simonson B, To C, Wong D, Yan IK, Zhang X, Balaj L, Breakefield XO, Daaboul G, Gandhi R, Lapidus J, Londin E, Patel T, Raffai RL, Sood AK, Alexander RP, Das S, Laurent LC. Srinivasan S, et al. Among authors: londin e. Cell. 2019 Apr 4;177(2):446-462.e16. doi: 10.1016/j.cell.2019.03.024. Cell. 2019. PMID: 30951671 Free PMC article.
The Sustained Induction of c-MYC Drives Nab-Paclitaxel Resistance in Primary Pancreatic Ductal Carcinoma Cells.
Parasido E, Avetian GS, Naeem A, Graham G, Pishvaian M, Glasgow E, Mudambi S, Lee Y, Ihemelandu C, Choudhry M, Peran I, Banerjee PP, Avantaggiati ML, Bryant K, Baldelli E, Pierobon M, Liotta L, Petricoin E, Fricke ST, Sebastian A, Cozzitorto J, Loots GG, Kumar D, Byers S, Londin E, DiFeo A, Narla G, Winter J, Brody JR, Rodriguez O, Albanese C. Parasido E, et al. Among authors: londin e. Mol Cancer Res. 2019 Sep;17(9):1815-1827. doi: 10.1158/1541-7786.MCR-19-0191. Epub 2019 Jun 4. Mol Cancer Res. 2019. PMID: 31164413 Free PMC article.
CRISPR Knockout of the HuR Gene Causes a Xenograft Lethal Phenotype.
Lal S, Cheung EC, Zarei M, Preet R, Chand SN, Mambelli-Lisboa NC, Romeo C, Stout MC, Londin E, Goetz A, Lowder CY, Nevler A, Yeo CJ, Campbell PM, Winter JM, Dixon DA, Brody JR. Lal S, et al. Among authors: londin e. Mol Cancer Res. 2017 Jun;15(6):696-707. doi: 10.1158/1541-7786.MCR-16-0361. Epub 2017 Feb 27. Mol Cancer Res. 2017. PMID: 28242812 Free PMC article.
TRNA-derived fragments as sex-dependent circulating candidate biomarkers for Parkinson's disease.
Magee R, Londin E, Rigoutsos I. Magee R, et al. Among authors: londin e. Parkinsonism Relat Disord. 2019 Aug;65:203-209. doi: 10.1016/j.parkreldis.2019.05.035. Epub 2019 May 25. Parkinsonism Relat Disord. 2019. PMID: 31402278
Murine MPDZ-linked hydrocephalus is caused by hyperpermeability of the choroid plexus.
Yang J, Simonneau C, Kilker R, Oakley L, Byrne MD, Nichtova Z, Stefanescu I, Pardeep-Kumar F, Tripathi S, Londin E, Saugier-Veber P, Willard B, Thakur M, Pickup S, Ishikawa H, Schroten H, Smeyne R, Horowitz A. Yang J, et al. Among authors: londin e. EMBO Mol Med. 2019 Jan;11(1):e9540. doi: 10.15252/emmm.201809540. EMBO Mol Med. 2019. PMID: 30518636 Free PMC article.
Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy.
Vahidnezhad H, Youssefian L, Saeidian AH, Mahmoudi H, Touati A, Abiri M, Kajbafzadeh AM, Aristodemou S, Liu L, McGrath JA, Ertel A, Londin E, Kariminejad A, Zeinali S, Fortina P, Uitto J. Vahidnezhad H, et al. Among authors: londin e. Matrix Biol. 2018 Mar;66:22-33. doi: 10.1016/j.matbio.2017.11.003. Epub 2017 Nov 11. Matrix Biol. 2018. PMID: 29138120
Validation of a Miniaturized Permeability Assay Compatible with CRISPR-Mediated Genome-Wide Screen.
Simonneau C, Yang J, Kong X, Kilker R, Edelstein L, Fortina P, Londin E, Horowitz A. Simonneau C, et al. Among authors: londin e. Sci Rep. 2019 Oct 2;9(1):14238. doi: 10.1038/s41598-019-50588-0. Sci Rep. 2019. PMID: 31578372 Free PMC article.
Whole exome sequencing identifies a germline MET mutation in two siblings with hereditary wild-type RET medullary thyroid cancer.
Sponziello M, Benvenuti S, Gentile A, Pecce V, Rosignolo F, Virzì AR, Milan M, Comoglio PM, Londin E, Fortina P, Barnabei A, Appetecchia M, Marandino F, Russo D, Filetti S, Durante C, Verrienti A. Sponziello M, et al. Among authors: londin e. Hum Mutat. 2018 Mar;39(3):371-377. doi: 10.1002/humu.23378. Epub 2017 Dec 20. Hum Mutat. 2018. PMID: 29219214
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