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22. Functional Diversification of the Four MARCKS Family Members in Zebrafish Neural Development. Prieto D; Zolessi FR J Exp Zool B Mol Dev Evol; 2017 Jan; 328(1-2):119-138. PubMed ID: 27554589 [TBL] [Abstract][Full Text] [Related]
23. Relationship between the major protein kinase C substrates acidic 80-kDa protein-kinase-C substrate (80K) and myristoylated alanine-rich C-kinase substrate (MARCKS). Members of a gene family or equivalent genes in different species. Herget T; Brooks SF; Broad S; Rozengurt E Eur J Biochem; 1992 Oct; 209(1):7-14. PubMed ID: 1396720 [TBL] [Abstract][Full Text] [Related]
24. Expression and regulation of 80K/MARCKS, a major substrate of protein kinase C, in the developing rat heart. McGill CJ; Brooks G Cardiovasc Res; 1997 May; 34(2):368-76. PubMed ID: 9205551 [TBL] [Abstract][Full Text] [Related]
25. Expression of the major protein kinase C substrate, the acidic 80-kilodalton myristoylated alanine-rich C kinase substrate, increases sharply when Swiss 3T3 cells move out of cycle and enter G0. Herget T; Brooks SF; Broad S; Rozengurt E Proc Natl Acad Sci U S A; 1993 Apr; 90(7):2945-9. PubMed ID: 8464911 [TBL] [Abstract][Full Text] [Related]
26. Nanomolar amyloid beta protein activates a specific PKC isoform mediating phosphorylation of MARCKS in Neuro2A cells. Tanimukai S; Hasegawa H; Nakai M; Yagi K; Hirai M; Saito N; Taniguchi T; Terashima A; Yasuda M; Kawamata T; Tanaka C Neuroreport; 2002 Mar; 13(4):549-53. PubMed ID: 11930178 [TBL] [Abstract][Full Text] [Related]
27. Myristoylated alanine-rich C-kinase substrate is phosphorylated and translocated by a phorbol ester-insensitive and calcium-independent protein kinase C isoform in C6 glioma cell membranes. Douglas DN; Fink HS; Ridgway ND; Cook HW; Byers DM Biochim Biophys Acta; 1999 Jan; 1448(3):439-49. PubMed ID: 9990296 [TBL] [Abstract][Full Text] [Related]
28. Amyloid beta protein (25-35) phosphorylates MARCKS through tyrosine kinase-activated protein kinase C signaling pathway in microglia. Nakai M; Hojo K; Yagi K; Saito N; Taniguchi T; Terashima A; Kawamata T; Hashimoto T; Maeda K; Gschwendt M; Yamamoto H; Miyamoto E; Tanaka C J Neurochem; 1999 Mar; 72(3):1179-86. PubMed ID: 10037491 [TBL] [Abstract][Full Text] [Related]
29. Overexpression of the myristoylated alanine-rich C-kinase substrate in Rat1 cells increases sensitivity to calmodulin antagonists. Herget T; Broad S; Rozengurt E Eur J Biochem; 1994 Oct; 225(2):549-56. PubMed ID: 7957169 [TBL] [Abstract][Full Text] [Related]
30. Effects of insulin and phorbol esters on MARCKS (myristoylated alanine-rich C-kinase substrate) phosphorylation (and other parameters of protein kinase C activation) in rat adipocytes, rat soleus muscle and BC3H-1 myocytes. Arnold TP; Standaert ML; Hernandez H; Watson J; Mischak H; Kazanietz MG; Zhao L; Cooper DR; Farese RV Biochem J; 1993 Oct; 295 ( Pt 1)(Pt 1):155-64. PubMed ID: 8216211 [TBL] [Abstract][Full Text] [Related]
31. A role for MARCKS, the alpha isozyme of protein kinase C and myosin I in zymosan phagocytosis by macrophages. Allen LH; Aderem A J Exp Med; 1995 Sep; 182(3):829-40. PubMed ID: 7650489 [TBL] [Abstract][Full Text] [Related]
32. Mice lacking the ski proto-oncogene have defects in neurulation, craniofacial, patterning, and skeletal muscle development. Berk M; Desai SY; Heyman HC; Colmenares C Genes Dev; 1997 Aug; 11(16):2029-39. PubMed ID: 9284043 [TBL] [Abstract][Full Text] [Related]
33. Activation of protein kinase C-alpha and translocation of the myristoylated alanine-rich C-kinase substrate correlate with phorbol ester-enhanced noradrenaline release from SH-SY5Y human neuroblastoma cells. Goodall AR; Turner NA; Walker JH; Ball SG; Vaughan PF J Neurochem; 1997 Jan; 68(1):392-401. PubMed ID: 8978751 [TBL] [Abstract][Full Text] [Related]
34. Neural tube defects and abnormal brain development in F52-deficient mice. Wu M; Chen DF; Sasaoka T; Tonegawa S Proc Natl Acad Sci U S A; 1996 Mar; 93(5):2110-5. PubMed ID: 8700893 [TBL] [Abstract][Full Text] [Related]
35. Microglial signaling by amyloid beta protein through mitogen-activated protein kinase mediating phosphorylation of MARCKS. Hasegawa H; Nakai M; Tanimukai S; Taniguchi T; Terashima A; Kawamata T; Fukunaga K; Miyamoto E; Misaki K; Mukai H; Tanaka C Neuroreport; 2001 Aug; 12(11):2567-71. PubMed ID: 11496150 [TBL] [Abstract][Full Text] [Related]
36. The human myristoylated alanine-rich C kinase substrate (MARCKS) gene (MACS). Analysis of its gene product, promoter, and chromosomal localization. Harlan DM; Graff JM; Stumpo DJ; Eddy RL; Shows TB; Boyle JM; Blackshear PJ J Biol Chem; 1991 Aug; 266(22):14399-405. PubMed ID: 1860846 [TBL] [Abstract][Full Text] [Related]
37. Characterization of a selective protein kinase C substrate derived from the MARCKS phosphorylation site domain for use in brain tissue homogenates. Mundy WR; Sutton LD Anal Biochem; 2000 Feb; 278(2):185-91. PubMed ID: 10660461 [TBL] [Abstract][Full Text] [Related]
38. Development-associated myristoylated alanine-rich C kinase substrate phosphorylation in rat brain. Hamada H; Zhang YL; Kawai A; Li F; Hibino Y; Hirashima Y; Kurimoto M; Hayashi N; Kato I; Endo S; Hiraga K Childs Nerv Syst; 2003 Mar; 19(3):152-8. PubMed ID: 12644866 [TBL] [Abstract][Full Text] [Related]
39. Arginine vasopressin (AVP) causes the reversible phosphorylation of the myristoylated alanine-rich C kinase substrate (MARCKS) protein in the ovine anterior pituitary: evidence that MARCKS phosphorylation is associated with adrenocorticotropin (ACTH) secretion. Liu JP; Engler D; Funder JW; Robinson PJ Mol Cell Endocrinol; 1994 Nov; 105(2):217-26. PubMed ID: 7859929 [TBL] [Abstract][Full Text] [Related]
40. Arginine vasopressin (AVP) causes the reversible phosphorylation of the myristoylated alanine-rich C kinase substrate (MARCKS) protein in the ovine anterior pituitary: evidence that MARCKS phosphorylation is associated with adrenocorticotropin (ACTH) secretion. Liu JP; Engler D; Funder JW; Robinson PJ Mol Cell Endocrinol; 1994 May; 101(1-2):247-56. PubMed ID: 9397959 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]