BÁO CÁO KHOA HỌC: "EXPRESSION OF NITRIC OXIDE SYNTHASE ISOFORMS IN THE PORCINE OVARY DURING FOLLICULAR DEVELOPMENT" PPSX

JOURNAL OFVeterinary ScienceJ. Vet. Sci. (2005), 6(2), 97–101Expression of nitric oxide synthase isoforms in the porcine ovary during follicular developmentHeechul Kim , Changjong Moon , Meejung Ahn , Yongduk Lee , H[r]

rpsA operon and is required for normal replication rate inEscherichia coli. J. Bacteriol. 177, 517–523.22. Jordan, A., Pontis, E., Aslund, F., Hellman, U., Gibert, I. &Reichard, P. (1996) The ribonucleotide reductase system of Lac-tococcus lactis. Characterization of an[r]

it was thereby established that nNOS was the mostsensitive substrate; eNOS was slightly more resistant,whereas HSP90, independently from its source, wasfive- to ten-fold less susceptible (Fig. 4D). A similardegradation pattern was obtained with m-calpain iso-lated from rat brain (data not show[r]

high-throughput molecular profiling of tumor specimens. Nat Med 1998, 4:844-847.15. Kobel M, Kalloger SE, Boyd N, McKinney S, Mehl E, Palmer C, Leung S, Bowen NJ, Ionescu DN, Rajput A, et al.: Ovarian carcinoma subtypes are different diseases implications for biomarker studies. PLoS Med 2008,[r]

FEBS Journal 277 (2010) 466–476 ª 2009 The Authors Journal compilation ª 2009 FEBS 475mice by systemically administered myostatin. Science296, 1486–1488.10 Reardon KA, Davis J, Kapsa RM, Choong P & ByrneE (2001) Myostatin, insulin-like growth factor-1, andleukemia inhibitory factor mR[r]

Preparation of TMA-BSA conjugateThe TMA-BSA conjugate was prepared under aseptic con-ditions by dissolving 10 mg/ml of BSA in 0.1 M sodiumborate buffer (pH 9.4), adding approximately 1.5 mgTMA per ml BSA-solution and stirring at room tempera-ture. After 1 h the same amoun[r]

Davies PJ: Coordinate regulation of the production and signaling ofretinoic acid by estrogen in the human endometrium. J Clin EndocrinolMetab 2003, 88:2157-2163.27. Clagett-Dame M, DeLuca HF: The role of vitamin A in mammalianreproduction and embryoni[r]

vascular diseases.In atherosclerotic plaques, cytokines such as tumornecrosis factor-a (TNF-a) and interleukin-1 secreted frommacrophages and foam cells have been implicated in thepathogenetic events [24]. On the other hand, because thesecytokines are responsible for iNOS exp[r]

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He SY (2006) Plant stomata function in innate immu-nity against bacterial invasion. Cell 126, 969–980.44 Bredt DS & Snyder SH (1989) Nitric oxide mediatesglutamate-linked enhancement of cGMP levels in thecerebellum. Proc Natl Acad Sci USA 86, 9030–9033.45 T[r]

cular growth and are crucial for the survi val of ovarianfollicles [26,27]. These mice showed morphological signof regression particularly in the granulosa cells of antralfollicles, since GnRH receptor is mainly localized onthese cells [3,4]. GnRH-Ag trea tment als[r]

changes in inducible NO synthase. Biochemistry 35,5883–5892.17 Raman CS, Li H, Martasek P, Southan G, Masters BS& Poulos TL (2001) Crystal structure of nitric oxidesynthase bound to nitro indazole reveals a novel inacti-vation mechanism. Biochemistry 40, 13448–134[r]

nNOS active amphibian peptides (Table 1) are unique newmolecular p robes f or the functioning of nNOS. We intendto carry out further s tructural s tudies on each of the threegroups of active peptides listed in Table 1, i n order to probethe r elationship b e[r]

ment of octamer-binding factor-1 (Oct-1), another oct-amer-binding protein, cannot be excluded in the LPS-induced expression of iNOS and G-CSF, it is verylikely that Oct-2 plays a more important role, as thelevel of expression of iNOS and G-CSF[r]

mediator protein-2 in signalling pathways that regulatethe proliferation of non-neuronal cells. Biochem BiophysRes Commun 340, 1244–1250.16 Manohar CF, Salwen HR, Furtado MR & Cohn SL(1996) Up-regulation of HOXC6, HOXD1, andHOXD8 homeobox gene expression in[r]

35. Okamura, H., Kashiwamura, S., Tsutsui, H., Yoshimoto, T. &Nakanishi, K. (1998) Regulation of interferon-c production byIL-12 and IL-18. Curr. Opin. Immunol. 10, 259–264.36. Nakahira,M.,Ahn,H J.,Park,W R.,Gao,P.,Tomura,M.,Park,C S.,Hamaoka,T.,Ohta,T.,Kurimoto,M.&Fujiwara,H.[r]

(A). Structures are derived from the PDB1NIW [21]. CaM residues 4–75 peptidebackbone, Ca2+ions, and eNOS peptidebackbone are shown in red, yellow, andblue, respectively. Peptide residues V503,K504, and A507 are shown in grey. Struc-tures were visualized using WebLab Viewer-Lite[r]

age less than 18 or greater than 35 years; a body massindex (BMI, kg/m2) less than 18 or greater than 25;major medical disorders and/or curr ent or previous useof hormonal and/or metabolic drugs; tubal or m ale fac-tor infertility or sub-fertility investigated with hysterosal-pingography and standar[r]

Ó FEBS 2004 Kinetic and thermodynamic properties of nNOS FAD domains (Eur. J. Biochem. 271) 2559the uniform binding energy used to discriminate between NADPHand NADH. Biochemistry 32, 11548–11558.24. Olteanu, H. & Banerjee, R. (2001) Human methionine synthasereductase, a solubl[r]

constant of 50 s)1, most likely representing the tail ofthe ferrous oxygen complex band. These rate constantsare only descriptive because the reaction sequence istoo complex to be modeled with a few exponentials(see simulations in Fig. 5B, and in Fig. 7B below).Aft[r]

Although it is well known that androstenol is a phero-mone in the pig, its role in the human is still ill-defined.Recent findings show that androstenol is able to modulatethe expression of certain cytochrome P450s and alcoholdehydrogenases through interactions[r]