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

Year Number of Results
2000 1
2004 1
2005 2
2006 4
2008 3
2009 1
2010 1
2011 1
2012 1
2015 3
2016 1
2017 2
2018 1
2019 1
2020 1
2021 1
2022 0
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25 results
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Page 1
smORFer: a modular algorithm to detect small ORFs in prokaryotes.
Bartholomäus A, Kolte B, Mustafayeva A, Goebel I, Fuchs S, Benndorf D, Engelmann S, Ignatova Z. Bartholomäus A, et al. Among authors: goebel i. Nucleic Acids Res. 2021 Sep 7;49(15):e89. doi: 10.1093/nar/gkab477. Nucleic Acids Res. 2021. PMID: 34125903 Free PMC article.
Dynamic m6A methylation facilitates mRNA triaging to stress granules.
Anders M, Chelysheva I, Goebel I, Trenkner T, Zhou J, Mao Y, Verzini S, Qian SB, Ignatova Z. Anders M, et al. Among authors: goebel i. Life Sci Alliance. 2018 Jul 3;1(4):e201800113. doi: 10.26508/lsa.201800113. eCollection 2018 Aug. Life Sci Alliance. 2018. PMID: 30456371 Free PMC article.
Dysfunction of the MDM2/p53 axis is linked to premature aging.
Lessel D, Wu D, Trujillo C, Ramezani T, Lessel I, Alwasiyah MK, Saha B, Hisama FM, Rading K, Goebel I, Schütz P, Speit G, Högel J, Thiele H, Nürnberg G, Nürnberg P, Hammerschmidt M, Zhu Y, Tong DR, Katz C, Martin GM, Oshima J, Prives C, Kubisch C. Lessel D, et al. Among authors: goebel i. J Clin Invest. 2017 Oct 2;127(10):3598-3608. doi: 10.1172/JCI92171. Epub 2017 Aug 28. J Clin Invest. 2017. PMID: 28846075 Free PMC article.
MTHFR C677T polymorphism and migraine with aura.
Todt U, Freudenberg J, Goebel I, Netzer C, Heinze A, Heinze-Kuhn K, Göbel H, Kubisch C. Todt U, et al. Among authors: goebel i. Ann Neurol. 2006 Nov;60(5):621-2; author reply 622-3. doi: 10.1002/ana.20911. Ann Neurol. 2006. PMID: 16800002 No abstract available.
Identification of two novel ALS2 mutations in infantile-onset ascending hereditary spastic paraplegia.
Daud S, Kakar N, Goebel I, Hashmi AS, Yaqub T, Nürnberg G, Nürnberg P, Morris-Rosendahl DJ, Wasim M, Volk AE, Kubisch C, Ahmad J, Borck G. Daud S, et al. Among authors: goebel i. Amyotroph Lateral Scler Frontotemporal Degener. 2016;17(3-4):260-5. doi: 10.3109/21678421.2015.1125501. Epub 2016 Jan 11. Amyotroph Lateral Scler Frontotemporal Degener. 2016. PMID: 26751646
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
Borck G, Ur Rehman A, Lee K, Pogoda HM, Kakar N, von Ameln S, Grillet N, Hildebrand MS, Ahmed ZM, Nürnberg G, Ansar M, Basit S, Javed Q, Morell RJ, Nasreen N, Shearer AE, Ahmad A, Kahrizi K, Shaikh RS, Ali RA, Khan SN, Goebel I, Meyer NC, Kimberling WJ, Webster JA, Stephan DA, Schiller MR, Bahlo M, Najmabadi H, Gillespie PG, Nürnberg P, Wollnik B, Riazuddin S, Smith RJ, Ahmad W, Müller U, Hammerschmidt M, Friedman TB, Riazuddin S, Leal SM, Ahmad J, Kubisch C. Borck G, et al. Among authors: goebel i. Am J Hum Genet. 2011 Feb 11;88(2):127-37. doi: 10.1016/j.ajhg.2010.12.011. Epub 2011 Jan 20. Am J Hum Genet. 2011. PMID: 21255762 Free PMC article.
25 results