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

Year Number of Results
1993 2
1996 3
1997 2
1998 2
1999 4
2000 1
2001 2
2002 1
2003 2
2004 1
2005 4
2006 4
2007 2
2008 2
2009 2
2010 1
2011 6
2012 2
2013 4
2014 8
2015 3
2016 6
2017 6
2018 6
2019 5
2020 12
2021 3
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92 results
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A colorimetric RT-LAMP assay and LAMP-sequencing for detecting SARS-CoV-2 RNA in clinical samples.
Dao Thi VL, Herbst K, Boerner K, Meurer M, Kremer LP, Kirrmaier D, Freistaedter A, Papagiannidis D, Galmozzi C, Stanifer ML, Boulant S, Klein S, Chlanda P, Khalid D, Barreto Miranda I, Schnitzler P, Kräusslich HG, Knop M, Anders S. Dao Thi VL, et al. Among authors: knop m. Sci Transl Med. 2020 Aug 12;12(556):eabc7075. doi: 10.1126/scitranslmed.abc7075. Epub 2020 Jul 27. Sci Transl Med. 2020. PMID: 32719001 Free PMC article.
ESCRT machinery mediates selective microautophagy of endoplasmic reticulum in yeast.
Schäfer JA, Schessner JP, Bircham PW, Tsuji T, Funaya C, Pajonk O, Schaeff K, Ruffini G, Papagiannidis D, Knop M, Fujimoto T, Schuck S. Schäfer JA, et al. Among authors: knop m. EMBO J. 2020 Jan 15;39(2):e102586. doi: 10.15252/embj.2019102586. Epub 2019 Dec 5. EMBO J. 2020. PMID: 31802527 Free PMC article.
While dedicated machinery for macro-ER-phagy has been discovered, the molecules and mechanisms mediating micro-ER-phagy remain unknown. Here, we first show that micro-ER-phagy in yeast involves the conversion of stacked cisternal ER into multilamellar ER whorls during micr …
While dedicated machinery for macro-ER-phagy has been discovered, the molecules and mechanisms mediating micro-ER-phagy remain unknown. Here …
A versatile toolbox for PCR-based tagging of yeast genes: new fluorescent proteins, more markers and promoter substitution cassettes.
Janke C, Magiera MM, Rathfelder N, Taxis C, Reber S, Maekawa H, Moreno-Borchart A, Doenges G, Schwob E, Schiebel E, Knop M. Janke C, et al. Among authors: knop m. Yeast. 2004 Aug;21(11):947-62. doi: 10.1002/yea.1142. Yeast. 2004. PMID: 15334558 Free article.
Tagging of genes by chromosomal integration of PCR amplified cassettes is a widely used and fast method to label proteins in vivo in the yeast Saccharomyces cerevisiae. This strategy directs the amplified tags to the desired chromosomal loci due to flanking h …
Tagging of genes by chromosomal integration of PCR amplified cassettes is a widely used and fast method to label proteins in vivo in the …
CDK1 couples proliferation with protein synthesis.
Haneke K, Schott J, Lindner D, Hollensen AK, Damgaard CK, Mongis C, Knop M, Palm W, Ruggieri A, Stoecklin G. Haneke K, et al. Among authors: knop m. J Cell Biol. 2020 Mar 2;219(3):e201906147. doi: 10.1083/jcb.201906147. J Cell Biol. 2020. PMID: 32040547 Free PMC article.
Exploring whole-genome duplicate gene retention with complex genetic interaction analysis.
Kuzmin E, VanderSluis B, Nguyen Ba AN, Wang W, Koch EN, Usaj M, Khmelinskii A, Usaj MM, van Leeuwen J, Kraus O, Tresenrider A, Pryszlak M, Hu MC, Varriano B, Costanzo M, Knop M, Moses A, Myers CL, Andrews BJ, Boone C. Kuzmin E, et al. Among authors: knop m. Science. 2020 Jun 26;368(6498):eaaz5667. doi: 10.1126/science.aaz5667. Science. 2020. PMID: 32586993 Free PMC article.
We describe a systematic complex genetic interaction analysis with yeast paralogs derived from the whole-genome duplication event. Mapping of digenic interactions for a deletion mutant of each paralog, and of trigenic interactions for the double mutant, provides insight in …
We describe a systematic complex genetic interaction analysis with yeast paralogs derived from the whole-genome duplication event. Ma …
Tandem fluorescent protein timers for in vivo analysis of protein dynamics.
Khmelinskii A, Keller PJ, Bartosik A, Meurer M, Barry JD, Mardin BR, Kaufmann A, Trautmann S, Wachsmuth M, Pereira G, Huber W, Schiebel E, Knop M. Khmelinskii A, et al. Among authors: knop m. Nat Biotechnol. 2012 Jun 24;30(7):708-14. doi: 10.1038/nbt.2281. Nat Biotechnol. 2012. PMID: 22729030
Here we describe tandem fluorescent protein timers (tFTs), fusions of two single-color fluorescent proteins that mature with different kinetics, which we use to analyze protein turnover and mobility in living cells. We fuse tFTs to proteins in yeast to study the longevity, …
Here we describe tandem fluorescent protein timers (tFTs), fusions of two single-color fluorescent proteins that mature with different kinet …
SARS-CoV-2 RNA Extraction Using Magnetic Beads for Rapid Large-Scale Testing by RT-qPCR and RT-LAMP.
Klein S, Müller TG, Khalid D, Sonntag-Buck V, Heuser AM, Glass B, Meurer M, Morales I, Schillak A, Freistaedter A, Ambiel I, Winter SL, Zimmermann L, Naumoska T, Bubeck F, Kirrmaier D, Ullrich S, Barreto Miranda I, Anders S, Grimm D, Schnitzler P, Knop M, Kräusslich HG, Dao Thi VL, Börner K, Chlanda P. Klein S, et al. Among authors: knop m. Viruses. 2020 Aug 7;12(8):863. doi: 10.3390/v12080863. Viruses. 2020. PMID: 32784757 Free PMC article.
CRISPR-Cas12a-assisted PCR tagging of mammalian genes.
Fueller J, Herbst K, Meurer M, Gubicza K, Kurtulmus B, Knopf JD, Kirrmaier D, Buchmuller BC, Pereira G, Lemberg MK, Knop M. Fueller J, et al. Among authors: knop m. J Cell Biol. 2020 Jun 1;219(6):e201910210. doi: 10.1083/jcb.201910210. J Cell Biol. 2020. PMID: 32406907 Free PMC article.
YeastRGB: comparing the abundance and localization of yeast proteins across cells and libraries.
Dubreuil B, Sass E, Nadav Y, Heidenreich M, Georgeson JM, Weill U, Duan Y, Meurer M, Schuldiner M, Knop M, Levy ED. Dubreuil B, et al. Among authors: knop m. Nucleic Acids Res. 2019 Jan 8;47(D1):D1245-D1249. doi: 10.1093/nar/gky941. Nucleic Acids Res. 2019. PMID: 30357397 Free PMC article.
The ability to measure the abundance and visualize the localization of proteins across the yeast proteome has stimulated hypotheses on gene function and fueled discoveries. While the classic C' tagged GFP yeast library has been the only resource for over a decade, t …
The ability to measure the abundance and visualize the localization of proteins across the yeast proteome has stimulated hypotheses o …
Pooled clone collections by multiplexed CRISPR-Cas12a-assisted gene tagging in yeast.
Buchmuller BC, Herbst K, Meurer M, Kirrmaier D, Sass E, Levy ED, Knop M. Buchmuller BC, et al. Among authors: knop m. Nat Commun. 2019 Jul 4;10(1):2960. doi: 10.1038/s41467-019-10816-7. Nat Commun. 2019. PMID: 31273196 Free PMC article.
Clone collections of modified strains ("libraries") are a major resource for systematic studies with the yeast Saccharomyces cerevisiae. Construction of such libraries is time-consuming, costly and confined to the genetic background of a specific yeast
Clone collections of modified strains ("libraries") are a major resource for systematic studies with the yeast Saccharomyces
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