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Items: 21

1.

Headcase is a Repressor of Lamellocyte Fate in Drosophila melanogaster.

Varga GIB, Csordás G, Cinege G, Jankovics F, Sinka R, Kurucz É, Andó I, Honti V.

Genes (Basel). 2019 Mar 5;10(3). pii: E173. doi: 10.3390/genes10030173.

2.

Sperm-Leucylaminopeptidases are required for male fertility as structural components of mitochondrial paracrystalline material in Drosophila melanogaster sperm.

Laurinyecz B, Vedelek V, Kovács AL, Szilasi K, Lipinszki Z, Slezák C, Darula Z, Juhász G, Sinka R.

PLoS Genet. 2019 Feb 25;15(2):e1007987. doi: 10.1371/journal.pgen.1007987. eCollection 2019 Feb.

3.

Drosophila small ovary gene is required for transposon silencing and heterochromatin organization, and ensures germline stem cell maintenance and differentiation.

Jankovics F, Bence M, Sinka R, Faragó A, Bodai L, Pettkó-Szandtner A, Ibrahim K, Takács Z, Szarka-Kovács AB, Erdélyi M.

Development. 2018 Dec 4;145(23). pii: dev170639. doi: 10.1242/dev.170639.

4.

Analysis of Drosophila melanogaster testis transcriptome.

Vedelek V, Bodai L, Grézal G, Kovács B, Boros IM, Laurinyecz B, Sinka R.

BMC Genomics. 2018 Sep 24;19(1):697. doi: 10.1186/s12864-018-5085-z.

5.

South Indian Isolates of the Fusarium solani Species Complex From Clinical and Environmental Samples: Identification, Antifungal Susceptibilities, and Virulence.

Homa M, Galgóczy L, Manikandan P, Narendran V, Sinka R, Csernetics Á, Vágvölgyi C, Kredics L, Papp T.

Front Microbiol. 2018 May 23;9:1052. doi: 10.3389/fmicb.2018.01052. eCollection 2018.

6.

Testis-Specific Bb8 Is Essential in the Development of Spermatid Mitochondria.

Vedelek V, Laurinyecz B, Kovács AL, Juhász G, Sinka R.

PLoS One. 2016 Aug 16;11(8):e0161289. doi: 10.1371/journal.pone.0161289. eCollection 2016.

7.

The role of acroblast formation during Drosophila spermatogenesis.

Fári K, Takács S, Ungár D, Sinka R.

Biol Open. 2016 Aug 15;5(8):1102-10. doi: 10.1242/bio.018275.

8.

Reduced expression of CDP-DAG synthase changes lipid composition and leads to male sterility in Drosophila.

Laurinyecz B, Péter M, Vedelek V, Kovács AL, Juhász G, Maróy P, Vígh L, Balogh G, Sinka R.

Open Biol. 2016 Jan;6(1):50169. doi: 10.1098/rsob.150169.

9.

Toward a comprehensive map of the effectors of rab GTPases.

Gillingham AK, Sinka R, Torres IL, Lilley KS, Munro S.

Dev Cell. 2014 Nov 10;31(3):358-373. doi: 10.1016/j.devcel.2014.10.007. Epub 2014 Nov 10.

10.

A genome-wide RNA interference screen identifies two novel components of the metazoan secretory pathway.

Wendler F, Gillingham AK, Sinka R, Rosa-Ferreira C, Gordon DE, Franch-Marro X, Peden AA, Vincent JP, Munro S.

EMBO J. 2010 Jan 20;29(2):304-14. doi: 10.1038/emboj.2009.350. Epub 2009 Nov 26.

11.

Spatial and functional relationship of GGAs and AP-1 in Drosophila and HeLa cells.

Hirst J, Sahlender DA, Choma M, Sinka R, Harbour ME, Parkinson M, Robinson MS.

Traffic. 2009 Nov;10(11):1696-710.

12.

Golgi coiled-coil proteins contain multiple binding sites for Rab family G proteins.

Sinka R, Gillingham AK, Kondylis V, Munro S.

J Cell Biol. 2008 Nov 17;183(4):607-15. doi: 10.1083/jcb.200808018. Epub 2008 Nov 10.

13.

Multiple protein phosphatases are required for mitosis in Drosophila.

Chen F, Archambault V, Kar A, Lio' P, D'Avino PP, Sinka R, Lilley K, Laue ED, Deak P, Capalbo L, Glover DM.

Curr Biol. 2007 Feb 20;17(4):293-303.

14.

Genome-wide survey of protein kinases required for cell cycle progression.

Bettencourt-Dias M, Giet R, Sinka R, Mazumdar A, Lock WG, Balloux F, Zafiropoulos PJ, Yamaguchi S, Winter S, Carthew RW, Cooper M, Jones D, Frenz L, Glover DM.

Nature. 2004 Dec 23;432(7020):980-7.

15.

Autolytic activation and localization in Schneider cells (S2) of calpain B from Drosophila.

Farkas A, Tompa P, Schád E, Sinka R, Jékely G, Friedrich P.

Biochem J. 2004 Mar 1;378(Pt 2):299-305.

16.

The Drosophila homolog of Aut1 is essential for autophagy and development.

Juhász G, Csikós G, Sinka R, Erdélyi M, Sass M.

FEBS Lett. 2003 May 22;543(1-3):154-8.

17.

Molecular cloning and RNA expression of a novel Drosophila calpain, Calpain C.

Spadoni C, Farkas A, Sinka R, Tompa P, Friedrich P.

Biochem Biophys Res Commun. 2003 Mar 28;303(1):343-9.

PMID:
12646209
18.

Hemese, a hemocyte-specific transmembrane protein, affects the cellular immune response in Drosophila.

Kurucz E, Zettervall CJ, Sinka R, Vilmos P, Pivarcsi A, Ekengren S, Hegedüs Z, Ando I, Hultmark D.

Proc Natl Acad Sci U S A. 2003 Mar 4;100(5):2622-7. Epub 2003 Feb 21.

19.

MOESIN crosslinks actin and cell membrane in Drosophila oocytes and is required for OSKAR anchoring.

Jankovics F, Sinka R, Lukácsovich T, Erdélyi M.

Curr Biol. 2002 Dec 10;12(23):2060-5.

20.

poirot, a new regulatory gene of Drosophila oskar acts at the level of the short Oskar protein isoform.

Sinka R, Jankovics F, Somogyi K, Szlanka T, Lukácsovich T, Erdélyi M.

Development. 2002 Jul;129(14):3469-78.

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