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

Year Number of Results
1991 1
1994 2
1995 1
1996 2
1997 1
1998 1
1999 2
2000 6
2001 4
2002 7
2003 2
2004 4
2005 6
2006 1
2007 3
2008 3
2009 4
2010 2
2011 1
2013 2
2014 2
2015 2
2016 1
2019 2
2020 5
2021 3
2022 2
2024 0

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68 results

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Page 1
FCHO controls AP2's initiating role in endocytosis through a PtdIns(4,5)P2-dependent switch.
Zaccai NR, Kadlecova Z, Dickson VK, Korobchevskaya K, Kamenicky J, Kovtun O, Umasankar PK, Wrobel AG, Kaufman JGG, Gray SR, Qu K, Evans PR, Fritzsche M, Sroubek F, Höning S, Briggs JAG, Kelly BT, Owen DJ, Traub LM. Zaccai NR, et al. Among authors: honing s. Sci Adv. 2022 Apr 29;8(17):eabn2018. doi: 10.1126/sciadv.abn2018. Epub 2022 Apr 29. Sci Adv. 2022. PMID: 35486718 Free PMC article.
Temporal Ordering in Endocytic Clathrin-Coated Vesicle Formation via AP2 Phosphorylation.
Wrobel AG, Kadlecova Z, Kamenicky J, Yang JC, Herrmann T, Kelly BT, McCoy AJ, Evans PR, Martin S, Müller S, Salomon S, Sroubek F, Neuhaus D, Höning S, Owen DJ. Wrobel AG, et al. Among authors: honing s. Dev Cell. 2019 Aug 19;50(4):494-508.e11. doi: 10.1016/j.devcel.2019.07.017. Dev Cell. 2019. PMID: 31430451 Free PMC article.
Temporal Ordering in Endocytic Clathrin-Coated Vesicle Formation via AP2 Phosphorylation.
Wrobel AG, Kadlecova Z, Kamenicky J, Yang JC, Herrmann T, Kelly BT, McCoy AJ, Evans PR, Martin S, Müller S, Salomon S, Sroubek F, Neuhaus D, Höning S, Owen DJ. Wrobel AG, et al. Among authors: honing s. Dev Cell. 2020 Mar 9;52(5):673. doi: 10.1016/j.devcel.2020.02.010. Dev Cell. 2020. PMID: 32155440 Free PMC article. No abstract available.
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway.
Asif M, Kaygusuz E, Shinawi M, Nickelsen A, Hsieh TC, Wagle P, Budde BS, Hochscherf J, Abdullah U, Höning S, Nienberg C, Lindenblatt D, Noegel AA, Altmüller J, Thiele H, Motameny S, Fleischer N, Segal I, Pais L, Tinschert S, Samra NN, Savatt JM, Rudy NL, De Luca C; Italian Undiagnosed Diseases Network; Paola Fortugno, White SM, Krawitz P, Hurst ACE, Niefind K, Jose J, Brancati F, Nürnberg P, Hussain MS. Asif M, et al. Among authors: honing s. HGG Adv. 2022 Apr 18;3(3):100111. doi: 10.1016/j.xhgg.2022.100111. eCollection 2022 Jul 14. HGG Adv. 2022. PMID: 35571680 Free PMC article.
Syntaxin binding mechanism and disease-causing mutations in Munc18-2.
Hackmann Y, Graham SC, Ehl S, Höning S, Lehmberg K, Aricò M, Owen DJ, Griffiths GM. Hackmann Y, et al. Among authors: honing s. Proc Natl Acad Sci U S A. 2013 Nov 19;110(47):E4482-91. doi: 10.1073/pnas.1313474110. Epub 2013 Nov 5. Proc Natl Acad Sci U S A. 2013. PMID: 24194549 Free PMC article.
68 results