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Results: 1 to 20 of 94

References for PMC Articles for PubMed (Select 21330364)

1.

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.

Franke A, McGovern DP, Barrett JC, Wang K, Radford-Smith GL, Ahmad T, Lees CW, Balschun T, Lee J, Roberts R, Anderson CA, Bis JC, Bumpstead S, Ellinghaus D, Festen EM, Georges M, Green T, Haritunians T, Jostins L, Latiano A, Mathew CG, Montgomery GW, Prescott NJ, Raychaudhuri S, Rotter JI, Schumm P, Sharma Y, Simms LA, Taylor KD, Whiteman D, Wijmenga C, Baldassano RN, Barclay M, Bayless TM, Brand S, Büning C, Cohen A, Colombel JF, Cottone M, Stronati L, Denson T, De Vos M, D'Inca R, Dubinsky M, Edwards C, Florin T, Franchimont D, Gearry R, Glas J, Van Gossum A, Guthery SL, Halfvarson J, Verspaget HW, Hugot JP, Karban A, Laukens D, Lawrance I, Lemann M, Levine A, Libioulle C, Louis E, Mowat C, Newman W, Panés J, Phillips A, Proctor DD, Regueiro M, Russell R, Rutgeerts P, Sanderson J, Sans M, Seibold F, Steinhart AH, Stokkers PC, Torkvist L, Kullak-Ublick G, Wilson D, Walters T, Targan SR, Brant SR, Rioux JD, D'Amato M, Weersma RK, Kugathasan S, Griffiths AM, Mansfield JC, Vermeire S, Duerr RH, Silverberg MS, Satsangi J, Schreiber S, Cho JH, Annese V, Hakonarson H, Daly MJ, Parkes M.

Nat Genet. 2010 Dec;42(12):1118-25. doi: 10.1038/ng.717.

2.

Family-wide characterization of the DENN domain Rab GDP-GTP exchange factors.

Yoshimura S, Gerondopoulos A, Linford A, Rigden DJ, Barr FA.

J Cell Biol. 2010 Oct 18;191(2):367-81. doi: 10.1083/jcb.201008051. Epub 2010 Oct 11.

3.

Quantitative analysis of synaptic vesicle Rabs uncovers distinct yet overlapping roles for Rab3a and Rab27b in Ca2+-triggered exocytosis.

Pavlos NJ, Grønborg M, Riedel D, Chua JJ, Boyken J, Kloepper TH, Urlaub H, Rizzoli SO, Jahn R.

J Neurosci. 2010 Oct 6;30(40):13441-53. doi: 10.1523/JNEUROSCI.0907-10.2010.

4.

A large-scale, consortium-based genomewide association study of asthma.

Moffatt MF, Gut IG, Demenais F, Strachan DP, Bouzigon E, Heath S, von Mutius E, Farrall M, Lathrop M, Cookson WO; GABRIEL Consortium.

N Engl J Med. 2010 Sep 23;363(13):1211-21. doi: 10.1056/NEJMoa0906312.

5.

Variants of DENND1B associated with asthma in children.

Marat AL, McPherson PS.

N Engl J Med. 2010 Sep 2;363(10):988-9; author reply 989. doi: 10.1056/NEJMc1002262. No abstract available.

6.

The Mon1-Ccz1 complex is the GEF of the late endosomal Rab7 homolog Ypt7.

Nordmann M, Cabrera M, Perz A, Bröcker C, Ostrowicz C, Engelbrecht-Vandré S, Ungermann C.

Curr Biol. 2010 Sep 28;20(18):1654-9. doi: 10.1016/j.cub.2010.08.002.

7.

EHBP-1 functions with RAB-10 during endocytic recycling in Caenorhabditis elegans.

Shi A, Chen CC, Banerjee R, Glodowski D, Audhya A, Rongo C, Grant BD.

Mol Biol Cell. 2010 Aug 15;21(16):2930-43. doi: 10.1091/mbc.E10-02-0149. Epub 2010 Jun 23.

8.

Molecular mechanisms in signal transduction at the membrane.

Groves JT, Kuriyan J.

Nat Struct Mol Biol. 2010 Jun;17(6):659-65. doi: 10.1038/nsmb.1844. Epub 2010 May 23. Review.

9.

Identification of the switch in early-to-late endosome transition.

Poteryaev D, Datta S, Ackema K, Zerial M, Spang A.

Cell. 2010 Apr 30;141(3):497-508. doi: 10.1016/j.cell.2010.03.011.

10.

Regulation of exosome secretion by Rab35 and its GTPase-activating proteins TBC1D10A-C.

Hsu C, Morohashi Y, Yoshimura S, Manrique-Hoyos N, Jung S, Lauterbach MA, Bakhti M, Grønborg M, Möbius W, Rhee J, Barr FA, Simons M.

J Cell Biol. 2010 Apr 19;189(2):223-32. doi: 10.1083/jcb.200911018.

11.

Recycling of the Ca2+-activated K+ channel, KCa2.3, is dependent upon RME-1, Rab35/EPI64C, and an N-terminal domain.

Gao Y, Balut CM, Bailey MA, Patino-Lopez G, Shaw S, Devor DC.

J Biol Chem. 2010 Jun 4;285(23):17938-53. doi: 10.1074/jbc.M109.086553. Epub 2010 Apr 1.

12.

Coordination of Rab8 and Rab11 in primary ciliogenesis.

Knödler A, Feng S, Zhang J, Zhang X, Das A, Peränen J, Guo W.

Proc Natl Acad Sci U S A. 2010 Apr 6;107(14):6346-51. doi: 10.1073/pnas.1002401107. Epub 2010 Mar 22.

13.

The Connecdenn DENN domain: a GEF for Rab35 mediating cargo-specific exit from early endosomes.

Allaire PD, Marat AL, Dall'Armi C, Di Paolo G, McPherson PS, Ritter B.

Mol Cell. 2010 Feb 12;37(3):370-82. doi: 10.1016/j.molcel.2009.12.037.

14.

Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly.

Giannandrea M, Bianchi V, Mignogna ML, Sirri A, Carrabino S, D'Elia E, Vecellio M, Russo S, Cogliati F, Larizza L, Ropers HH, Tzschach A, Kalscheuer V, Oehl-Jaschkowitz B, Skinner C, Schwartz CE, Gecz J, Van Esch H, Raynaud M, Chelly J, de Brouwer AP, Toniolo D, D'Adamo P.

Am J Hum Genet. 2010 Feb 12;86(2):185-95. doi: 10.1016/j.ajhg.2010.01.011.

15.

The connecdenn family, Rab35 guanine nucleotide exchange factors interfacing with the clathrin machinery.

Marat AL, McPherson PS.

J Biol Chem. 2010 Apr 2;285(14):10627-37. doi: 10.1074/jbc.M109.050930. Epub 2010 Feb 12.

16.

Comprehensive screening for novel rab-binding proteins by GST pull-down assay using 60 different mammalian Rabs.

Kanno E, Ishibashi K, Kobayashi H, Matsui T, Ohbayashi N, Fukuda M.

Traffic. 2010 Apr;11(4):491-507. doi: 10.1111/j.1600-0854.2010.01038.x. Epub 2010 Jan 12.

PMID:
20070612
17.

Rab35 mediates transport of Cdc42 and Rac1 to the plasma membrane during phagocytosis.

Shim J, Lee SM, Lee MS, Yoon J, Kweon HS, Kim YJ.

Mol Cell Biol. 2010 Mar;30(6):1421-33. doi: 10.1128/MCB.01463-09. Epub 2010 Jan 11.

18.

Assembly of the biogenesis of lysosome-related organelles complex-3 (BLOC-3) and its interaction with Rab9.

Kloer DP, Rojas R, Ivan V, Moriyama K, van Vlijmen T, Murthy N, Ghirlando R, van der Sluijs P, Hurley JH, Bonifacino JS.

J Biol Chem. 2010 Mar 5;285(10):7794-804. doi: 10.1074/jbc.M109.069088. Epub 2010 Jan 4.

19.

Variants of DENND1B associated with asthma in children.

Sleiman PM, Flory J, Imielinski M, Bradfield JP, Annaiah K, Willis-Owen SA, Wang K, Rafaels NM, Michel S, Bonnelykke K, Zhang H, Kim CE, Frackelton EC, Glessner JT, Hou C, Otieno FG, Santa E, Thomas K, Smith RM, Glaberson WR, Garris M, Chiavacci RM, Beaty TH, Ruczinski I, Orange JS, Allen J, Spergel JM, Grundmeier R, Mathias RA, Christie JD, von Mutius E, Cookson WO, Kabesch M, Moffatt MF, Grunstein MM, Barnes KC, Devoto M, Magnusson M, Li H, Grant SF, Bisgaard H, Hakonarson H.

N Engl J Med. 2010 Jan 7;362(1):36-44. doi: 10.1056/NEJMoa0901867. Epub 2009 Dec 23. Erratum in: N Engl J Med. 2012 Feb 16;366(7):672. Orange, Jordan M [corrected to Orange, Jordan S]. N Engl J Med. 2010 Sep 2;363(10):994.

20.

Disruption of ST5 is associated with mental retardation and multiple congenital anomalies.

Göhring I, Tagariello A, Endele S, Stolt CC, Ghassibé M, Fisher M, Thiel CT, Trautmann U, Vikkula M, Winterpacht A, FitzPatrick DR, Rauch A.

J Med Genet. 2010 Feb;47(2):91-8. doi: 10.1136/jmg.2009.069799. Epub 2009 Oct 19.

PMID:
19843505
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