These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 18550821)

  • 21. Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin-Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning.
    Zeniou M; Ding T; Trivier E; Hanauer A
    Hum Mol Genet; 2002 Nov; 11(23):2929-40. PubMed ID: 12393804
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ataxia telangiectasia mutated proteins, MAPKs, and RSK2 are involved in the phosphorylation of STAT3.
    Zhang Y; Cho YY; Petersen BL; Bode AM; Zhu F; Dong Z
    J Biol Chem; 2003 Apr; 278(15):12650-9. PubMed ID: 12562765
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Coffin-Lowry syndrome.
    Pereira PM; Schneider A; Pannetier S; Heron D; Hanauer A
    Eur J Hum Genet; 2010 Jun; 18(6):627-33. PubMed ID: 19888300
    [TBL] [Abstract][Full Text] [Related]  

  • 24. ARF6 regulates the synthesis of fusogenic lipids for calcium-regulated exocytosis in neuroendocrine cells.
    Béglé A; Tryoen-Tóth P; de Barry J; Bader MF; Vitale N
    J Biol Chem; 2009 Feb; 284(8):4836-45. PubMed ID: 19124467
    [TBL] [Abstract][Full Text] [Related]  

  • 25. betaPIX-activated Rac1 stimulates the activation of phospholipase D, which is associated with exocytosis in neuroendocrine cells.
    Momboisse F; Lonchamp E; Calco V; Ceridono M; Vitale N; Bader MF; Gasman S
    J Cell Sci; 2009 Mar; 122(Pt 6):798-806. PubMed ID: 19261846
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Selective alteration of adult hippocampal neurogenesis and impaired spatial pattern separation performance in the RSK2-deficient mouse model of Coffin-Lowry syndrome.
    Castillon C; Lunion S; Desvignes N; Hanauer A; Laroche S; Poirier R
    Neurobiol Dis; 2018 Jul; 115():69-81. PubMed ID: 29627578
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Phospholipase D1 production of phosphatidic acid at the plasma membrane promotes exocytosis of large dense-core granules at a late stage.
    Zeniou-Meyer M; Zabari N; Ashery U; Chasserot-Golaz S; Haeberlé AM; Demais V; Bailly Y; Gottfried I; Nakanishi H; Neiman AM; Du G; Frohman MA; Bader MF; Vitale N
    J Biol Chem; 2007 Jul; 282(30):21746-57. PubMed ID: 17540765
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Regulated exocytosis in chromaffin cells. Translocation of ARF6 stimulates a plasma membrane-associated phospholipase D.
    Caumont AS; Galas MC; Vitale N; Aunis D; Bader MF
    J Biol Chem; 1998 Jan; 273(3):1373-9. PubMed ID: 9430671
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Phospholipase D1: a key factor for the exocytotic machinery in neuroendocrine cells.
    Vitale N; Caumont AS; Chasserot-Golaz S; Du G; Wu S; Sciorra VA; Morris AJ; Frohman MA; Bader MF
    EMBO J; 2001 May; 20(10):2424-34. PubMed ID: 11350931
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Contrasting roles of neuronal Msk1 and Rsk2 in Bad phosphorylation and feedback regulation of Erk signalling.
    Clark CJ; McDade DM; O'Shaughnessy CT; Morris BJ
    J Neurochem; 2007 Aug; 102(4):1024-34. PubMed ID: 17663748
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation.
    Field M; Tarpey P; Boyle J; Edkins S; Goodship J; Luo Y; Moon J; Teague J; Stratton MR; Futreal PA; Wooster R; Raymond FL; Turner G
    Clin Genet; 2006 Dec; 70(6):509-15. PubMed ID: 17100996
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Phospholipase D1 produces phosphatidic acid at sites of secretory vesicle docking and fusion.
    Bills BL; Hulser ML; Knowles MK
    Mol Biol Cell; 2024 Mar; 35(3):ar39. PubMed ID: 38117597
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome.
    Zeniou M; Gattoni R; Hanauer A; Stévenin J
    Nucleic Acids Res; 2004; 32(3):1214-23. PubMed ID: 14973203
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The historical Coffin-Lowry syndrome family revisited: identification of two novel mutations of RPS6KA3 in three male patients.
    Nishimoto HK; Ha K; Jones JR; Dwivedi A; Cho HM; Layman LC; Kim HG
    Am J Med Genet A; 2014 Sep; 164A(9):2172-9. PubMed ID: 25044551
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel RSK2 (RPS6KA3) gene mutation associated with abnormal brain MRI findings in a family with Coffin-Lowry syndrome.
    Wang Y; Martinez JE; Wilson GL; He XY; Tuck-Muller CM; Maertens P; Wertelecki W; Chen TJ
    Am J Med Genet A; 2006 Jun; 140(12):1274-9. PubMed ID: 16691578
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Essential role of RSK2 in c-Fos-dependent osteosarcoma development.
    David JP; Mehic D; Bakiri L; Schilling AF; Mandic V; Priemel M; Idarraga MH; Reschke MO; Hoffmann O; Amling M; Wagner EF
    J Clin Invest; 2005 Mar; 115(3):664-72. PubMed ID: 15719069
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification of a plasma membrane-associated guanine nucleotide exchange factor for ARF6 in chromaffin cells. Possible role in the regulated exocytotic pathway.
    Caumont AS; Vitale N; Gensse M; Galas MC; Casanova JE; Bader MF
    J Biol Chem; 2000 May; 275(21):15637-44. PubMed ID: 10748097
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ribosomal S6 Kinase 2 (RSK2) maintains genomic stability by activating the Atm/p53-dependent DNA damage pathway.
    Lim HC; Xie L; Zhang W; Li R; Chen ZC; Wu GZ; Cui SS; Tan EK; Zeng L
    PLoS One; 2013; 8(9):e74334. PubMed ID: 24086335
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Bacterial Expression, Purification and In Vitro Phosphorylation of Full-Length Ribosomal S6 Kinase 2 (RSK2).
    Utepbergenov D; Hennig PM; Derewenda U; Artamonov MV; Somlyo AV; Derewenda ZS
    PLoS One; 2016; 11(10):e0164343. PubMed ID: 27732676
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Phosphatidylinositol (3,4,5)-trisphosphate specifically interacts with the phox homology domain of phospholipase D1 and stimulates its activity.
    Lee JS; Kim JH; Jang IH; Kim HS; Han JM; Kazlauskas A; Yagisawa H; Suh PG; Ryu SH
    J Cell Sci; 2005 Oct; 118(Pt 19):4405-13. PubMed ID: 16179605
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.