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

Year Number of Results
2001 1
2002 1
2003 1
2005 3
2006 2
2007 1
2009 1
2011 1
2013 1
2019 2
2020 2
2023 1
2024 0

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14 results

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Page 1
Bottom-gated epitaxial graphene.
Waldmann D, Jobst J, Speck F, Seyller T, Krieger M, Weber HB. Waldmann D, et al. Among authors: krieger m. Nat Mater. 2011 May;10(5):357-60. doi: 10.1038/nmat2988. Epub 2011 Apr 3. Nat Mater. 2011. PMID: 21460820
The sandfish lizard's aerodynamic filtering system.
Stadler AT, Krieger M, Baumgartner W. Stadler AT, et al. Among authors: krieger m. Bioinspir Biomim. 2020 Mar 3;15(3):036003. doi: 10.1088/1748-3190/ab6137. Bioinspir Biomim. 2020. PMID: 31829988
Stark Tuning of the Silicon Vacancy in Silicon Carbide.
Rühl M, Bergmann L, Krieger M, Weber HB. Rühl M, et al. Among authors: krieger m. Nano Lett. 2020 Jan 8;20(1):658-663. doi: 10.1021/acs.nanolett.9b04419. Epub 2019 Dec 16. Nano Lett. 2020. PMID: 31809057
SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndrome.
Krieger M, Roos A, Stendel C, Claeys KG, Sonmez FM, Baudis M, Bauer P, Bornemann A, de Goede C, Dufke A, Finkel RS, Goebel HH, Häussler M, Kingston H, Kirschner J, Medne L, Muschke P, Rivier F, Rudnik-Schöneborn S, Spengler S, Inzana F, Stanzial F, Benedicenti F, Synofzik M, Lia Taratuto A, Pirra L, Tay SK, Topaloglu H, Uyanik G, Wand D, Williams D, Zerres K, Weis J, Senderek J. Krieger M, et al. Brain. 2013 Dec;136(Pt 12):3634-44. doi: 10.1093/brain/awt283. Epub 2013 Oct 30. Brain. 2013. PMID: 24176978 Free article.
Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy.
Senderek J, Krieger M, Stendel C, Bergmann C, Moser M, Breitbach-Faller N, Rudnik-Schöneborn S, Blaschek A, Wolf NI, Harting I, North K, Smith J, Muntoni F, Brockington M, Quijano-Roy S, Renault F, Herrmann R, Hendershot LM, Schröder JM, Lochmüller H, Topaloglu H, Voit T, Weis J, Ebinger F, Zerres K. Senderek J, et al. Among authors: krieger m. Nat Genet. 2005 Dec;37(12):1312-4. doi: 10.1038/ng1678. Epub 2005 Nov 13. Nat Genet. 2005. PMID: 16282977
Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3.
Senderek J, Garvey SM, Krieger M, Guergueltcheva V, Urtizberea A, Roos A, Elbracht M, Stendel C, Tournev I, Mihailova V, Feit H, Tramonte J, Hedera P, Crooks K, Bergmann C, Rudnik-Schöneborn S, Zerres K, Lochmüller H, Seboun E, Weis J, Beckmann JS, Hauser MA, Jackson CE. Senderek J, et al. Among authors: krieger m. Am J Hum Genet. 2009 Apr;84(4):511-8. doi: 10.1016/j.ajhg.2009.03.006. Epub 2009 Apr 2. Am J Hum Genet. 2009. PMID: 19344878 Free PMC article.
14 results