... Schorle H (20 05) The AP -2 family of transcription factors Genome Biol 6, 24 6, doi:10.1186/gb -20 05-6-13 -24 6 12 Moser M, Ruschoff J & Buettner R (1997) Comparative analysis of AP -2 alpha and AP -2 beta ... expression of a new AP -2 transcription factor, AP -2 epsilon Dev Dyn 23 1, 128 –135 Garcia MA, Campillos M, Ogueta S, Valdivieso F & Vazquez J (20 00) Identification of amino acid residues of transcription ... analyses of the regulationof AP -2 and the interactions of the transcription factor with binding partners, as well as of the regulationof target gene expression, have been performed for AP-2a Up...
... Journal 27 3 (20 06) 5333–5346 ª 20 06 The Authors Journal compilation ª 20 06 FEBS Y Ding et al 24 25 26 27 28 29 30 31 32 33 34 35 36 Yoshida T (1995) Heme oxygenase -2 Properties of the heme complex of ... with HO -2 siRNA in HepG2 cells These results indicate that the down -regulation of HO -2 expression is associated with induction of HO-1 expression FEBS Journal 27 3 (20 06) 5333–5346 ª 20 06 The ... 5¢-UAUAAGAGUCAGUACACAUCAUGGAAG-3¢, antisense, 3¢-UAAUAUUCUCAGUCAUGUGUAGUACCU-5¢ Another HO -2- specific siRNA, HO -2 siRNA1 (target base 21 2 23 2) reported by other investigators [ 32] , was also used GAPDH...
... reported that the levels of Fru -2, 6-P2 were Ó FEBS 20 02 significantly increased by adenovirus-mediated overexpression of a mutant form of 6-phosphofructo -2- kinase/ fructose -2, 6-bisphosphatase in ... Physiol 26 6, E796–E803 Roden, M., Perseghin, G., Petersen, K.F., Hwang, J.H., Cline, G.W., Gerow, K., Rothman, D.L & Shulman, G.I (1996) The 4 426 I.-Y Choi et al (Eur J Biochem 26 9) 21 22 23 24 25 26 ... than its inhibition of fructose-1,6bisphosphatase This is a significant observation because it offers the first in vivo assessment of the action of Fru -2, 6-P2 on the 6-phosphofructo-1-kinase/fructose-1,6-bisphosphatase...
... centrifuged Ca2 + and Pi were determined in the pellets corresponding to the mineral structure Symbols corresponding to various Ca2 + concentrations are: n, Ca2 + 2. 5 mM; e, Ca2 + mM; h, Ca2 + 7.5 mM; s, Ca2 + ... the Ca2 + concentration increased from 2. 5 mM to 6–7.5 mM, the mineralization began at 48 h At 144 h the Ca/ Pi ratio was % 1 .2 1.3 At 24 mM Ca2 +, HA crystals were obtained at about 12 h with a Ca/ Pi ... Wavenumber (cm)1) 1 125 –1145 918– 924 10 52 1060 587–600 1038 1 127 741 561–563 575 601–603 960 10 32 10 92 1094 11 12 1116 Origin HPO 42 HPO 42 Ref stretch stretch m3 m4 m3 PO3 stretch in HPO 42 OH libration...
... Acids Res 20 00, 28 :23 5 -24 2 22 Ginalski K, Elofsson A, Fischer D, Rychlewski L: 3D-Jury: a simple approach to improve protein structure predictions Bioinformatics 20 03, 19:1015-1018 23 Proteinkeys ... analysis of a complete Page 12 of 12 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 poxvirus transcriptome reveals an immediate-early class of genes Proc Natl Acad Sci USA 20 08, 105 :21 40 -21 45 ... usually located in poxvirus genomes [25 ,26 ] Eight of the orthologue groups can be found in orthopoxvirus genomes: N1L, N2L, A52R and B15R can González and Esteban Virology Journal 20 10, 7:59...
... leukocyte adhesion in postcapillary venules: in vivo effects 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 with relevance to the acute inflammatory response Proc Natl Acad Sci USA 1981, ... aerated (95% O2, % CO2) PSS of the following composition (mM): NaCl 110.5, KC1 3.4, CaCl2 2. 4, MgSO4 0.8, KH2PO4 1 .2, NaHCO3 25 .7, and dextrose 5.6, as previously described in details [26 ] The serum ... Ca2 +-independent Am J Respir Crit Care Med 20 01, 163(1) :26 6 -27 2 Song P, Milanese M, Crimi E, Rehder K, Brusasco V: Allergen challenge of passively sensitized human bronchi alters M2 and beta2...
... Results 81! 4 .2. 1! Accumulation of mDia2 to nuclear envelope (NE) 81! 4 .2. 2! mDia2 is localized to the cytoplasmic side of NE 84! 4 .2. 3! Co-localization of mDia2 with NPC and importin ... overexpression of mDia2 have been reported to induce human deafness (Lynch et al., 1997; Schoen et al., 20 13) 1 .2. 3 .2 INF2 INF2 has two C-terminal splice variants: the CAAX variant (prenylated, 22 isoform ... 51! 3 .2! Results 52! 3 .2. 1! Force activation induces reversible perinuclear actin polymerization ……………………………………………………………………. 52! 3 .2. 2! The role of calcium 57! 3 .2. 3! The...
... catalytic subunit of PP2A 82 2.4 Co-localization of PP2A-C and Bcl -2 was inhibited in cells with an augmented O2- level 85 v 2. 5 Mitochondrial translocation of PP2A-C was inhibited ... 2A PP2A-A A scaffolding subunit of PP2A PP2AB56α B56α-containing PP2A enzyme PP2AB56γ1 B56γ1-containing PP2A holoenzyme PP2AB56δ B56δ-containing PP2A PP2A-C Catalytic subunit of PP2A pRb Retinoblastoma ... pillared by a large arsenal of antioxidant machineries capable of eradicating H2O2 2.2 Catalase Catalase is a haem-protein responsible for the neutralization of intracellular H2O2 [87, 88] It is widely...
... Vectors 60 2. 1.5 Transformation and Inoculation 60 2. 1.6 Low-yield Purification of Plasmid DNA (Miniprep) 61 2. 1.7 Qualification of Miniprep product 62 2.1.8 DNA Sequencing 62 2 .2 Synthesis of Constructs ... Interference of hSKP1 and hSRB7/MED21 63 2. 2.1 Design of siRNA pSuper Constructs 63 2.2 .2 Annealing of Constructs 63 2. 3 Transfection of High Quality Plasmids into HeLa Cells 64 iv 2. 3.1 Retransformation ... Beads 120 Figure 19: Immunoprecipitation of hCul1 122 Figure 20 : Immunoprecipitation of hMed6 123 Figure 21 : Co-immunoprecipitation of Cul1 by Med6 with Protein A and Protein G 124 Figure 22 : Co-immunoprecipitation...