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1 iverdin requires oxygen for its synthesis by heme oxygenase.
2  analysis shows upregulation of ferritin and heme oxygenase.
3 m-positive bacteria that possess IsdG-family heme oxygenases.
4 al cytochrome P450 (P450) monooxygenases and heme oxygenases.
5 ikely common intermediate with the canonical heme oxygenases.
6 cts differ from those generated by canonical heme oxygenases.
7 talase, glutathione peroxidase 1 (GPX1), and heme oxygenase 1 (Hmox1) and transcription factor nuclea
8 sapje-like, while upregulating the inducible heme oxygenase 1 (Hmox1) at the protein level.
9  We showed that variation in basal levels of heme oxygenase 1 (HMOX1) contribute to the response to O
10 ed reduced progesterone levels and placental heme oxygenase 1 (Hmox1) expression and increased methyl
11 h regulates the expression of genes encoding heme oxygenase 1 (Hmox1), glutamate-cysteine ligase cata
12 ous Nrf2-regulated genes/proteins, including heme oxygenase 1 (Hmox1).
13                         We hypothesized that heme oxygenase 1 (HMOX1; HO-1), an enzyme responsible fo
14 ession of heat-shock protein 70 (HSP-70) and heme oxygenase 1 (HO-1) and promoted cell survival after
15 nd up-regulation of the antioxidant proteins heme oxygenase 1 (HO-1) and sulfiredoxin 1 (SRXN1).
16                                              Heme oxygenase 1 (HO-1) and the cytochromes P450 (P450s)
17 D2) expression and a delayed upregulation of heme oxygenase 1 (HO-1) expression.
18 ctor erythroid 2-related factor 2 (Nrf2) and heme oxygenase 1 (HO-1) gene proteins in retinal tissues
19 investigated whether up-regulation of DAF by heme oxygenase 1 (HO-1) is an underlying mechanism by us
20                      To assess intracellular heme oxygenase 1 (HO-1) isolated PBMCs were used.
21 e 2 signaling response, downstream of which, heme oxygenase 1 (HO-1) was also found to be time-depend
22              Importantly, mRNA expression of heme oxygenase 1 (HO-1), a potential modulator of immune
23 (hIL-10R) by cmvIL-10 led to upregulation of heme oxygenase 1 (HO-1), an enzyme linked with suppressi
24 overexpression of the heme-degrading enzyme, heme oxygenase 1 (HO-1), has been shown to protect mice
25  NAD(P)H:quinone oxidoreductase 1 (NQO1) and heme oxygenase 1 (HO-1), typical chemoprotective gene pr
26                  AKI induces upregulation of heme oxygenase 1 (HO-1), which exerts cytoprotective eff
27 on a key enzyme involved in heme catabolism, heme oxygenase 1 (HO-1), which, ironically, has been poo
28 ar adiponectin (gAcrp) are mediated by IL-10/heme oxygenase 1 (HO-1)-dependent pathways.
29 d expression of the major antioxidant enzyme heme oxygenase 1 (HO-1).
30 t stimulated MMP-1 expression via activating heme oxygenase 1 (HO-1).
31 catalase, NF-E2-related factor 2 (Nrf2), and heme oxygenase 1 (HO-1).
32                                              Heme oxygenase 1 (P < 0.01), an oxidative stress marker,
33 gets superoxide dismutase 2 (P <= 0.001) and heme oxygenase 1 (P <= 0.001).
34 kers (matrix metalloproteinase 1 [MMP-1] and heme oxygenase 1 [HO-1]), and proinflammatory cytokines
35    The carboxyhemoglobin level (a measure of heme oxygenase 1 activity) has not been assessed in adul
36                        miR-24 also regulated heme oxygenase 1 and H2A histone family, member X, in vi
37 orresponded with increases in cytoprotective heme oxygenase 1 and IL-10 mRNAs, selective reductions i
38 ential for linked antioxidant protection via heme oxygenase 1 and reduced foam cell formation via liv
39                                              Heme oxygenase 1 expression is increased in pediatric pa
40 ion, hypoxia-inducible factor 1alpha-induced heme oxygenase 1 expression resulting in improved surviv
41 with the latter associated with induction of heme oxygenase 1 expression.
42 med a systematic review and meta-analysis of heme oxygenase 1 gene (HO-1) promoter polymorphisms and
43 ), intercellular adhesion molecule 1, IL-10, heme oxygenase 1 hypoxia-inducible factor 1 (HIF-1), mon
44 ssion of hypoxia-inducible factor 1alpha and heme oxygenase 1 in the hippocampus was increased in the
45   Cobalt protoporphyrin (CoPP), a well known heme oxygenase 1 inducer, has been used to promote endog
46                                              Heme oxygenase 1 induction, by counteracting the cytotox
47 t upregulation of superoxide dismutase 2 and heme oxygenase 1 protein following hypoxia-reoxygenation
48                                              Heme oxygenase 1, an enzyme upregulated by oxidative str
49 ples for hypoxia-inducible factor 1alpha and heme oxygenase 1, and 4) immunohistochemistry of hippoca
50  H(2)O(2), concomitant with up-regulation of heme oxygenase 1, COX-2, and anti-apoptotic proteins (BC
51 e and iron in liver despite up-regulation of heme oxygenase 1, ferroportin, and ferritins.
52 several genes, including p53, cyclin G1, and heme oxygenase 1, in embryos.
53 on of antioxidant genes, including those for heme oxygenase 1, NAD(P)H quinone oxidoreductase 1, and
54  most robustly increased genes and proteins, heme oxygenase 1, NADPH-quinone oxidoreductase 1, and gr
55 ulation of H2A histone family, member X, and heme oxygenase 1, which were experimentally validated as
56                                        Human heme oxygenases 1 and 2 (HO-1 and HO-2) degrade heme in
57 ncreased inducible nitric oxide synthase and heme-oxygenase 1 expression, and increased MDA and plasm
58 ncreased inducible nitric oxide synthase and heme-oxygenase 1 expression, and increased plasma creati
59 f Bcl-2 (5.5-folds), Bcl-xl (5.5-folds), and heme oxygenase-1 (4.4-folds); decreased expression of IC
60                                              Heme oxygenase-1 (gene HMOX1; protein HO-1) is the induc
61  adenoassociated virus (rAAV)-encoding human heme oxygenase-1 (hHO-1) in attenuating post-ischemic in
62 n (HP), cluster of differentiation (CD) 163, heme oxygenase-1 (HMOX1), and biliverdin reductase A (BL
63                              Inactivation of heme oxygenase-1 (Hmox1), one of the most stringently de
64 otective response relies on the induction of heme oxygenase-1 (HMOX1; HO-1) and ferritin H chain (FTH
65 tional downregulation of the redox regulator heme oxygenase-1 (HO-1 or HMOX1).
66                                     Although heme oxygenase-1 (HO-1) acts downstream of vascular endo
67 f2, NAD(P)H quinone oxidoreductase 1 (NQO1), heme oxygenase-1 (HO-1) and a high ratio of Bcl-2/Bax.
68 production of antioxidant enzymes, including heme oxygenase-1 (HO-1) and glutathione peroxidase 1 (Gp
69  of the antioxidant/anti-inflammatory enzyme heme oxygenase-1 (HO-1) and increased neuroinflammation
70                                              Heme oxygenase-1 (HO-1) and its metabolic by-product, ca
71                           BACKGROUND & AIMS: Heme oxygenase-1 (HO-1) and its metabolic by-product, ca
72                              ATF-1 coinduces heme oxygenase-1 (HO-1) and Liver X receptor beta (LXR-b
73 d CXCL8 secretion and required activation of heme oxygenase-1 (HO-1) and phosphorylated adenosine mon
74  cells by the regulations of novel molecules heme oxygenase-1 (HO-1) and programmed death-1 ligand 1
75      An ELISA assay for the Nrf2 target gene heme oxygenase-1 (HO-1) and studies using Nrf2 small int
76  a hypoxia-inducible plasmid expressing both heme oxygenase-1 (HO-1) and the Src homology domain-2 co
77              Despite recent data identifying heme oxygenase-1 (HO-1) as a putative autophagy inducer,
78 AC and selected reaction monitoring revealed heme oxygenase-1 (HO-1) as the most significantly up-reg
79 he cytoprotective and antiapoptotic molecule heme oxygenase-1 (HO-1) at the transcriptional level.
80                 Kidney-specific induction of heme oxygenase-1 (HO-1) attenuates the development of an
81                                     The Nrf2/heme oxygenase-1 (HO-1) axis affords significant protect
82                                              Heme oxygenase-1 (HO-1) catalyzes the degradation of hem
83                                              Heme oxygenase-1 (HO-1) concentrations have been recentl
84                                   The enzyme heme oxygenase-1 (HO-1) degrades heme and protects again
85 a, urine, and tissues, which in turn induces heme oxygenase-1 (HO-1) expression in the colonic epithe
86        We investigated the effect of reduced heme oxygenase-1 (HO-1) expression on vaccine response a
87  vitro study showed that adiponectin induced heme oxygenase-1 (HO-1) expression through the peroxisom
88                We tested the hypothesis that heme oxygenase-1 (HO-1) expression, which is protective
89 ase expression, nitric oxide production, and heme oxygenase-1 (HO-1) expression, which was associated
90 nase-1 (PON-1) expression and down-regulated heme oxygenase-1 (HO-1) expression.
91 al injury, and inhibited RPTC Nrf2, Agt, and heme oxygenase-1 (HO-1) gene expression in Akita Cat tra
92                                              Heme oxygenase-1 (HO-1) has potent anti-inflammatory act
93 lective overexpression of the stress protein heme oxygenase-1 (HO-1) in astrocytes of novel GFAP.HMOX
94  the products of the cytoprotective molecule heme oxygenase-1 (HO-1) in cancer cells, has been implic
95  of NO induce the anti-inflammatory effector heme oxygenase-1 (HO-1) in gastric epithelial cells thro
96 of the cytoprotective, heme-degrading enzyme heme oxygenase-1 (HO-1) in neutrophil progenitors in bon
97 e antioxidative and anti-inflammatory enzyme heme oxygenase-1 (HO-1) in the brains of individuals wit
98 ed a hypothesized anti-inflammatory role for heme oxygenase-1 (HO-1) in the development of metabolic
99                                     Although Heme Oxygenase-1 (HO-1) induction in various forms of ki
100                                              Heme oxygenase-1 (HO-1) induction is a crucial defense m
101          Carbon monoxide or the induction of heme oxygenase-1 (HO-1) inhibited the expression of myof
102                                              Heme oxygenase-1 (HO-1) is a cytoprotective protein whos
103                                              Heme oxygenase-1 (HO-1) is a key enzyme triggered by cel
104                                              Heme oxygenase-1 (HO-1) is a microsomal enzyme with anti
105                                              Heme oxygenase-1 (HO-1) is a stress-inducible, anti-infl
106                                              Heme oxygenase-1 (HO-1) is a ubiquitously expressed indu
107                                              Heme oxygenase-1 (HO-1) is an inducible enzyme that exhi
108                                              Heme oxygenase-1 (HO-1) is an inducible stress-response
109                                              Heme oxygenase-1 (HO-1) is an inducible stress-responsiv
110                                              Heme oxygenase-1 (HO-1) is an inducible, detoxifying enz
111 sed expression of the cytoprotective enzyme, heme oxygenase-1 (HO-1) is often found.
112                    The cytoprotective enzyme heme oxygenase-1 (HO-1) is often overexpressed in differ
113      Expression of the cytoprotective enzyme heme oxygenase-1 (HO-1) is significantly reduced in the
114                                              Heme oxygenase-1 (HO-1) levels were previously shown to
115   The stress-inducible cytoprotective enzyme heme oxygenase-1 (HO-1) may play a critical role in the
116                                 Induction of heme oxygenase-1 (HO-1) mediates tolerance to the cytoto
117 ukin-8 (IL-8), cyclooxygenase-2 (COX-2), and heme oxygenase-1 (HO-1) mRNA was measured in BEAS-2B cel
118  of inducing the activity of the host enzyme heme oxygenase-1 (HO-1) on hRSV replication and pathogen
119                                 Induction of heme oxygenase-1 (HO-1) or administration of its product
120  overexpression of the cytoprotective enzyme heme oxygenase-1 (HO-1) play a critical role in the grow
121                                              Heme oxygenase-1 (HO-1) protein is an antioxidant enzyme
122 epatocellular injury is the up-regulation of heme oxygenase-1 (HO-1) signaling.
123     Only overexpression of the gene encoding heme oxygenase-1 (HO-1) significantly correlated with in
124            Carbon monoxide (CO) generated by heme oxygenase-1 (HO-1) strongly influences cellular pro
125 y amplified in human breast cancers, induced heme oxygenase-1 (HO-1) through Nrf2 transactivation in
126                      Hepatocytes overinduced heme oxygenase-1 (HO-1) to catabolize free heme in build
127  erythroid 2p45-related factor-2 (Nrf2), and heme oxygenase-1 (HO-1) was tested in both in vitro and
128  up-regulation of the cytoprotective protein heme oxygenase-1 (HO-1) which is capable of mitigating a
129 amplification with pNaKtide and induction of heme oxygenase-1 (HO-1) with cobalt protoporphyrin (CoPP
130 d that PRRSV downregulates the expression of heme oxygenase-1 (HO-1), a pivotal cytoprotective enzyme
131                                              Heme oxygenase-1 (HO-1), a pivotal cytoprotective enzyme
132                                              Heme oxygenase-1 (HO-1), an enzyme that catalyzes the ra
133 ter antioxidant transcription factor, and of heme oxygenase-1 (HO-1), one of its main target genes, i
134 ome solid tumors and myeloid leukemia cells, heme oxygenase-1 (HO-1), the anti-oxidant, anti-inflamma
135 attention as a master protective sentinel is heme oxygenase-1 (HO-1), the rate-limiting step in the c
136                     The wound mRNA levels of heme oxygenase-1 (HO-1), TNF-alpha, the receptor for adv
137     Many cancer cells constitutively express heme oxygenase-1 (HO-1), which catabolizes heme to gener
138 is the up-regulation of the inducible enzyme heme oxygenase-1 (HO-1), which catabolizes heme to gener
139   Intracellular heme levels are regulated by heme oxygenase-1 (HO-1), which catalyzes the degradation
140        We therefore investigated the role of heme oxygenase-1 (HO-1), which catalyzes the degradation
141 ng expression of the stress response protein heme oxygenase-1 (HO-1), which interacts with and thereb
142 ory functions, preclinical studies encourage heme oxygenase-1 (HO-1)-inducing regimens in clinical or
143  (WT) animals, and exhibited upregulation of heme oxygenase-1 (HO-1).
144 ctor erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1).
145 ion of many cytoprotective enzymes including heme oxygenase-1 (HO-1).
146 e antioxidant response and reduces levels of heme oxygenase-1 (HO-1).
147 d upregulation of the heme-degrading enzyme, heme oxygenase-1 (HO-1).
148 wnregulation of the stress-responsive enzyme heme oxygenase-1 (HO-1).
149                                          The heme oxygenase-1 (HO-1)/CO pathway modulates cellular re
150 is generated by the stress-responsive enzyme heme oxygenase-1 (HO-1, encoded by Hmox1), which is high
151                                              Heme oxygenase-1 (HO-1, Hmox1) regulates viability, prol
152                             The induction of heme oxygenase-1 (HO-1; Hmox1) by inflammation, for inst
153                                              Heme oxygenase-1 (HO-1; Hmox1) is critical in maintainin
154  quality control is regulated in part by the heme oxygenase-1 (HO-1; Hmox1) system through the redox-
155               In diabetics, up-regulation of heme oxygenase-1 (HO1) in gastric macrophages protects a
156 mL; CO-E-CPR, 89 +/- 26 pg/mL; p < 0.05) and heme oxygenase-1 (sham, 1 +/- 0.1; cardiopulmonary resus
157 kers Kim-1, p21, and the cytoprotective gene heme oxygenase-1 accompanied this.
158 ranofin displayed synergistic lethality with heme oxygenase-1 and glutamate-cysteine ligase inhibitor
159  via Nrf2 pathway, enhancing GSH/GSSG ratio, heme oxygenase-1 and glyoxalase 1 in liver tissue.
160 e discuss here new insights into the role of heme oxygenase-1 and heme on cardiovascular health, and
161 ontractility rather than passive stretch via heme oxygenase-1 and histone deacetylase signalling.
162 d4 to Nrf2-binding sites on the promoters of heme oxygenase-1 and NADPH quinone oxidoreductase 1.
163 rf2 or DJ-1 attenuated Cu((II))ATSM-mediated heme oxygenase-1 and NADPH quinone oxidoreductase-1 indu
164  into the nucleus to induce transcription of heme oxygenase-1 and other cytoprotective enzymes throug
165 and reendothelialization via upregulation of heme oxygenase-1 and SDF-1alpha.
166 result of the upregulation of cytoprotective heme oxygenase-1 and sirtuin-1 (SIRT1).
167 arkable cardioprotective effects ascribed to heme oxygenase-1 are best evidenced by its ability to re
168               We also show data to implicate heme oxygenase-1 as a potential molecular link between N
169 nhancing expression of the IL-10 target gene heme oxygenase-1 by mechanisms dependent on p38 MAPK act
170 -1beta and FAS concentrations, and increased heme oxygenase-1 concentration.
171                             Macrophages from heme oxygenase-1 deficient mice (Hmox1(-/-)) had increas
172  enhances its paracine effects on RIII via a heme oxygenase-1 dependent mechanism, which may help us
173 a, IL-1beta and nitric oxide partially via a heme oxygenase-1 dependent mechanism.
174 s, whereas treatment with carbon monoxide, a heme oxygenase-1 enzymatic product, abrogated this effec
175 als treated with tin protoporphyrin (SnPP, a heme oxygenase-1 enzyme inhibitor), even after Ad.Trx1 t
176 at abrogated the Nrf2-dependent induction of heme oxygenase-1 expression by nitro-oleic acid.
177 -induced oxidative stress by down-regulating heme oxygenase-1 expression via nuclear factor (erythroi
178 nd molecular markers (caspase-3 activity and heme oxygenase-1 expression) were analyzed.
179 nosine thymidine dinucleotide repeats in the heme oxygenase-1 gene promoter in 386 patients with coro
180 nosine thymidine dinucleotide repeats in the heme oxygenase-1 gene promoter is associated with cardio
181 nosine thymidine dinucleotide repeats in the heme oxygenase-1 gene promoter is associated with higher
182                                              Heme oxygenase-1 has been implicated in regulating DC ma
183                                          The Heme Oxygenase-1 in renal Transplantation study was a ra
184 duced expression of the Nrf2 target protein, heme oxygenase-1 in the skin and protected against UVB-i
185 e (HbSS), corresponding with elevated plasma heme oxygenase-1 in this group.
186  vivo and IRAK-M(-/-) AECs in vitro with the heme oxygenase-1 inhibitor, tin protoporphyrin, substant
187 a 7-day doxycycline treatment sustained high heme oxygenase-1 levels during the entire period of hypo
188 T6 recruits BAF170 to enhancer region of the Heme oxygenase-1 locus and promotes recruitment of RNA p
189                                              Heme oxygenase-1 may confer protection from HPH by effec
190               Experimental data suggest that heme oxygenase-1 protects against kidney disease.
191 related with CO in the breath were levels of heme oxygenase-1 protein in serum and HMOX1 transcripts
192 ted bitransgenic mice that overexpress human heme oxygenase-1 under doxycycline control in an inducib
193          Antioxidant capacity and muscularis heme oxygenase-1 upregulation are possible protective me
194          Anti-inflammatory and antiapoptotic heme oxygenase-1 was significantly upregulated in the hy
195 tide phosphate:quinone oxidoreductase 1, and heme oxygenase-1 were lower in group 2 than group 3.
196                                        HO-1 (heme oxygenase-1) is an inducible microsomal enzyme that
197 based proteomics screen, we identified HO-1 (heme oxygenase-1), the rate-limiting enzyme in the degra
198 ) mice have increased expression/activity of heme oxygenase-1, a phase II antioxidant, and NF (erythr
199 aimed to investigate the mechanisms by which heme oxygenase-1, an anti-inflammatory enzyme, is protec
200 , despite significantly higher expression of heme oxygenase-1, an antioxidant and cytoprotective enzy
201 ntioxidant systems such as peroxiredoxins-1, heme oxygenase-1, and anti-apoptotic factors, including
202 ed anti-inflammatory factors interleukin-10, heme oxygenase-1, and Hsp70 in macrophages stimulated or
203 ing IL-1ra, IL-10, and PGE(2), but not IL-6, heme oxygenase-1, and NO, attenuated 5-FU-MSC-induced im
204 II, chemokine (C-C motif) ligand 22 (CCL22), heme oxygenase-1, and TSG6.
205 lation of the oxidative stress response gene heme oxygenase-1, and we demonstrated that NF-kappaB inh
206                Mitochondrial accumulation of heme oxygenase-1, another heme protein, was also regulat
207 lial NOS (eNOS), Nrf2, and Phase II enzymes (heme oxygenase-1, catalase, superoxide dismutase-1) in a
208 ation of the CBS inhibitor, CO, a product of heme oxygenase-1, flip the operating preference of CSE f
209  expression of Nrf2-dependent genes, such as heme oxygenase-1, glutamate-cysteine ligase catalytic su
210 tor-kappaB, hypoxia-inducible factor-1alpha, heme oxygenase-1, inducible nitric oxide synthase, B-cel
211 itochondrial superoxide dismutase (SOD), and heme oxygenase-1, mucosal receptors such as the Toll-lik
212 e regulation of key Nrf2 target genes (i.e., heme oxygenase-1, NAD(P)H dehydrogenase, quinone 1, glut
213 ificantly upregulates Nrf2-responsive genes, heme oxygenase-1, NAD(P)H quinone oxidoreductase 1, and
214 n and expression of the antioxidant proteins heme oxygenase-1, NADPH quinone oxidoreductase 1, and gl
215  such as superoxide dismutase, nitric oxide, heme oxygenase-1, neutrophil infiltration, cysteamine, m
216 es that impair liver regeneration, including heme oxygenase-1, programmed cell death 4, and the cycli
217 pression levels of survival genes, Bcl-2 and heme oxygenase-1, were analyzed by gene array analysis a
218 + monocytes expressed higher basal levels of heme oxygenase-1.
219 cyte anti-inflammatory heme-degrading enzyme heme oxygenase-1.
220 er two important molecules: nitric oxide and heme oxygenase-1.
221 f pathogenic CD8(+) T cells and induction of heme oxygenase-1.
222 n, the release of heme, and the induction of heme oxygenase-1.
223 l abrogated by pharmacological inhibition of heme oxygenase-1.
224 ement of NF-erythroid 2-related factor 2 and heme oxygenase-1.
225 em macrophages through coregulation of HO-1 (heme oxygenase-1; HMOX1) and lipid homeostasis genes.
226  the CX3CR1 receptor induced upregulation of heme-oxygenase-1 (HMOX-1), an antioxidant and anti-infla
227 Q61L) mutant induced the anti-oxidant enzyme heme-oxygenase-1 (HO-1) through activation of NRF2.
228 stress by upregulating the stress-responsive heme-oxygenase-1 (HO-1).
229 xidant defenses, including the expression of heme-oxygenase-1 (HO-1).
230  reverses vitamin C-induced up-regulation of heme-oxygenase-1 and ferritin in KRAS-mutant cancer cell
231 ntrol animals, and inhibiting the HIF target heme-oxygenase-1 before IR reduced GFR in STN animals.
232 p-regulation of the stress-inducible protein heme-oxygenase-1.
233 with higher substrate affinity of the enzyme heme oxygenase 2, whereas SH rats present lower substrat
234       Here, we report that mice deficient in heme oxygenase-2 (HO-2), which generates the gaseous mol
235                                              Heme oxygenase-2 (HO2) and -1 (HO1) catalyze heme degrad
236          The C-terminal tail region of human heme oxygenase-2 (HO2) contains two HRMs whose cysteine
237 ate binding site within the cellular protein heme oxygenase-2 that acts as a trap to inhibit N-myrist
238 the circular muscle layer from wild-type and heme oxygenase-2-knockout (HO-2-KO) mice.
239 vel cytotoxic isoflavone is shown to inhibit heme oxygenase, a desirable yet elusive target that disr
240 by the liver mainly through the induction of heme oxygenase activity.
241 s sp. strain PCC 7002 comprises two enzymes: heme oxygenase and phycocyanobilin synthase (PcyA).
242      Tetrapyrrole substrates and products of heme oxygenase are potent inhibitors of hepatitis C viru
243 xide synthase, type 1 heme oxygenase, type 2 heme oxygenase, Bax, and Bcl-2 protein and mRNA expressi
244 on of genes encoding bacteriophytochromes or heme oxygenase clearly show that both bacteriophytochrom
245  metabolic shift to the PPP is controlled by heme oxygenase-dependent generation of carbon monoxide (
246 , homologs of which have been proposed to be heme oxygenases, did not eliminate (13)C-BV IXdelta and
247 H, through the FAD and FMN cofactors, to the heme oxygenase domain, the site of NO generation.
248 electrons from the FAD-binding domain to the heme oxygenase domain.
249 antibacterial effects while CO, generated by heme oxygenases, enhances phagocytosis of macrophages.
250  acquires the following characteristics of a heme oxygenase enzyme: (a) donation by His429 of an addi
251                   In contrast, the canonical heme oxygenase family degrades heme that is bound with m
252          Here we show that the Aedes aegypti heme oxygenase gene (AeHO - AAEL008136) is expressed in
253 her outbreak isolates were found to harbor a heme oxygenase gene (hemO)-containing gene cluster.
254 ve previously shown the catalytic actions of heme oxygenase (HemO) along with the cytoplasmic heme tr
255 stant infections, such as the iron-regulated heme oxygenase (HemO) of Pseudomonas aeruginosa, due to
256 nt for delivering heme to the iron regulated heme oxygenase (HemO).
257 ired for interaction with the iron-regulated heme oxygenase (HemO).
258 is a homolog of the Bradyrhizobium japonicum heme oxygenases HmuD and HmuQ.
259  final round, we discovered that deletion of heme oxygenase (HMX1) increases total heme concentration
260 ies production and upregulated expression of heme oxygenase HO-1 (HMOX1), an indicator of oxidative s
261      We hypothesize that in beta-thalassemia heme oxygenase (HO) 1 could play a pathogenic role in th
262 ibited activity of the renoprotective enzyme heme oxygenase (HO) and determined the effects on renal
263                                              Heme oxygenase (HO) catalyzes heme degradation, a proces
264                                              Heme oxygenase (HO) catalyzes the rate-limiting step in
265                                              Heme oxygenase (HO) cleaves hemin into biliverdin, iron,
266                                              Heme oxygenase (HO) enzymes could proceed through hetero
267                                              Heme oxygenase (HO) is a ubiquitous enzyme responsible f
268                                              Heme oxygenase (HO), from the pathogenic bacterium N. me
269 n), astrocyte activation, IgG extravasation, heme oxygenase (HO), iron deposition, oxidative end prod
270                  Free heme is metabolized by heme oxygenase (HO), resulting in the generation of carb
271 uman macrophages, SPM (10 pM-10 nM) elevated heme oxygenase (HO)-1 ( approximately 50%, 8 h).
272      Carbon monoxide (CO), an end-product of heme oxygenase (HO)-1 activity, can confer anti-inflamma
273    At the molecular level, the expression of heme oxygenase (HO)-1 and the secretion of stromal cell-
274                                              Heme oxygenase (HO)-1 overexpression or induction has be
275 the expression of antioxidant genes, such as heme oxygenase (HO)-1, that protect parasites from oxida
276 , IL-4, and IL-6 and oxidative stress marker heme oxygenase (HO)-1, were higher in WD+VDD versus WD a
277 imental colitis in IL-10(-/-) mice through a heme oxygenase (HO)-1-dependent pathway.
278                                              Heme oxygenase (HO)-2 deficiency impairs wound healing a
279           Recent in vitro experiments with a heme oxygenase (HO)-like protein from Plasmodium falcipa
280 embrane potential and increases in cytosolic heme oxygenase (HO-1) expression and mitochondrial coloc
281 set of pre-messenger RNAs (mRNAs), including heme oxygenase (HO-1) mRNA.
282 s that interact with HIV-1 MA, we found that heme oxygenase (HO-2) specifically binds the myristate m
283 nduces expression of the CO-producing enzyme heme oxygenase (HO1) and that CO is sensed by M. tubercu
284 ological mechanism of heme degradation is by heme oxygenases (HOs).
285 hing IsdG as a pathophysiologically relevant heme oxygenase in S. lugdunensis.
286 mmatory, and antioxidant (enzymes, including heme oxygenase isoforms [HO-1, HO-2]) markers.
287                   Our data support roles for heme oxygenase isoforms in modulating recovery from syna
288                         The enzyme's central heme-oxygenase-like (HO-like) domain sequentially hydrox
289 ray crystal structure showed that UndA has a heme-oxygenase-like fold, thus associating it with a str
290 used by the massive induction by arsenite of heme oxygenase mRNA (HMOX1; 68-fold increase), the rate-
291 mparable in both types of donors, the type 1 heme oxygenase mRNA expression and antioxidant enzyme ac
292  flux of extracellular heme through the HemO heme oxygenase, resulting in more-efficient heme utiliza
293                    Six compounds that target heme oxygenase signaling were found to rescue the abnorm
294                                          The heme oxygenase system (HO-1 and HO-2) represents an intr
295 nsis expresses an iron-regulated IsdG-family heme oxygenase that binds and degrades heme.
296       Heme-iron utilization involves HmuO, a heme oxygenase that degrades cytosolic heme, resulting i
297  that B. abortus 2308 has at least one other heme oxygenase that works in concert with BhuQ to allow
298                                       Unlike heme oxygenases, this intermediate does not form with ad
299 ase, inducible nitric oxide synthase, type 1 heme oxygenase, type 2 heme oxygenase, Bax, and Bcl-2 pr
300 n the kidneys, whereas high levels of C3 and heme oxygenase were identified in pancreas biopsies.

 
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