ライフサイエンスコーパス: HMT

1 HMT altered the X-ray pattern from A+B-->A.

2 HMT and ANN increased the relative crystallinity but DR

3 HMT and DR altered XRD patterns from B to A and A + B ty

4 HMT clones expressing > or = 9-fold the parental levels

5 HMT has markedly modified the pasting properties and res

6 HMT shows much higher adhesiveness (-78.27 gF.s) compare

7 HMT used alone or in dual modifications promoted the str

8 HMT was associated with a 7% lower relative risk of ADRD

9 HMT, which can yield important molecules for prebiotic c

10 imum conditions were 0.63 (HMT 15) and 1.00 (HMT 25 and 35).

11 -90 min at different moisture levels of 15% (HMT 15-BGS), 25% (HMT 25-BGS) and 35% (HMT 35-BGS).

12 nt moisture levels of 15% (HMT 15-BGS), 25% (HMT 25-BGS) and 35% (HMT 35-BGS).

13 15% (HMT 15-BGS), 25% (HMT 25-BGS) and 35% (HMT 35-BGS).

14 zation, 28 patients were excluded leaving 47 HMT and 43 DUN long-term (55 +/- 35 months) evaluable pa

15 f the obtained optimum conditions were 0.63 (HMT 15) and 1.00 (HMT 25 and 35).

16 t E(z) protein was found to be inactive in a HMT assay.

17 Our results show that all HMT types rapidly transitioned to hypoxic conditions in

18 high and low (i.e., sub-saturating) SAM, all HMTs displayed the highest catalytic efficiency (k(cat)/

19 eration efficiencies (TTN up to 7,700) among HMTs characterized to date.

20 we have gone on to test whether DmHMT-1, an HMT-1 from a new source, Drosophila, whose genome lacks

21 ly, G9a represses PPARgamma expression in an HMT activity-dependent manner but facilitates Wnt10a exp

22 In an HMT-3522 S1 (S1) breast epithelial risk-progression thre

23 This strategy, based at least in part on an HMT-dependent inhibitory histone code, imposes a require

24 phila ovary, and demonstrate in vivo that an HMT, the product of the eggless (egg) gene, is required

25 Using an HMT-modified TFO to direct ICLs to a specific site, we f

26 ion in swelling power observed after ANN and HMT treatment in both varieties corresponds with the pas

27 crease the peak viscosity of single ANN- and HMT-treated starches.

28 RIP140 serves as a scaffold for both DNA and HMT activities to inhibit gene transcription by two key

29 reduced following HMT (222.1 +/- 9.1 g) and HMT-ANN (253.6 +/- 9.3 g), suggesting that dense crystal

30 tro digestibility assays showed that HMT and HMT-ANN treatments increased resistant and slowly digest

31 l gene expression profiles show that MMT and HMT are co-expressed in leaves, roots and reproductive t

32 MMT and HMT together have been proposed to constitute a futile S

33 The oxidised and HMT starches had lower viscosity and swelling power comp

34 The films made of native, oxidised and HMT starches were characterised by thickness, water solu

35 motion within 1 predefined scan period, and HMT is not readily available in the clinic since it typi

36 of risk with age, self-identified race, and HMT type.

37 ots and developing seeds all express MMT and HMTs, and can metabolize [35S]Met to [35S]SMM and vice v

38 these treatments (ANN-HMT, ANN-SNT, HMT-ANN, HMT-SNT, SNT-ANN, SNT-HMT).

39 The ANN, HMT and SNT did not provide visible cracks, notches or g

40 ed by a combination of these treatments (ANN-HMT, ANN-SNT, HMT-ANN, HMT-SNT, SNT-ANN, SNT-HMT).

41 nable techniques, including ANN (annealing), HMT (heat moisture treatment), US (ultrasound), Pregel (

42 ong SET domain proteins known to function as HMTs (reviewed in ).

43 ly binds HCF-1 associated with the Set1/Ash2 HMT complex in the absence of the Sin3 HDAC complex.

44 The Set1/Ash2 HMT methylates histone H3 at Lys 4 (K4), but not if the

45 We discuss how an autosomally associated HMT may participate in silencing genes on the X chromoso

46 Second, we mine a family of bacterial HMTs from Pseudomonas species sharing less than 50% sequ

47 i-like sp., Peptoniphilaceae [G-1] bacterium HMT 113, Porphyromonas gingivalis, Fretibacterium fastid

48 , and Saccharibacteria (TM7) [G-1] bacterium HMT 346 were more abundant with increasing severity of p

49 human oral Saccharibacteria (TM7) bacterium, HMT-952, strain TM7x, which is an ultrasmall parasite of

50 adjusting the moisture content to 25% before HMT (100 degrees C, 1h).

51 prevotella increased at night and Bergeyella HMT 206/Haemophilus slowly increased during the daytime.

52 es showed no significant association between HMT and ADRD.

53 ts are sequence-dependent: ozone followed by HMT amplifies changes, while the reverse order gives add

54 l with 1.5% stearic acid (SA) was treated by HMT using infrared (IR) energy (at 110 degrees C for 1,

55 - and race-based associations also varied by HMT type.

56 rees C (native) to 69.35 +/- 0.01 degrees C (HMT-ANN), accompanied by higher enthalpy (DeltaH) values

57 show that ZFPs linked to a minimal catalytic HMT domain affect local methylation of histone H3K9 and

58 2) derived from phenotypically normal cells (HMT-3522) and led to growth arrest in a three-dimensiona

59 human tumorigenic mammary epithelial cells, HMT-3522-T4-2, with those of their immediate premalignan

60 in vivo role of the Saccharomyces cerevisiae HMT, Set2.

61 WDR5, hDPY-30, NCOA6, SET domain-containing HMTs MLL3 and MLL4, and substoichiometric amount of JmjC

62 In contrast, HMT-d(CCGGTACCGG) forms a sequence-dependent junction.

63 0 degrees C for 1, 2 & 3 h) and conventional HMT (at 110 degrees C for 16 h) independently.

64 nd has the potential to replace conventional HMT in the development of lower GI, higher value-added f

65 Infrared HMT is similar to conventional HMT since both treatments resulted in significantly (P <

66 ance in C. elegans demonstrate PC-dependent, HMT-1-mediated heavy metal detoxification not only in S.

67 scherichia coli yagD mutant and by detecting HMT activity in complemented cells.

68 tural reorganisation of starch chains during HMT temperature was influenced by starch chain flexibili

69 Gel hardness was notably reduced following HMT (222.1 +/- 9.1 g) and HMT-ANN (253.6 +/- 9.3 g), sug

70 he first detection of HMT and functionalized HMT species in the carbonaceous chondrites Murchison, Mu

71 sistently, deletion of G9a or inhibiting G9a HMT activity promotes adipogenesis.

72 th samples was the 75 to 79 years age group (HMT, 2721 women [22.0%]; no HMT, 1469 women [22.8%]), an

73 Silencing H3K9 HMT, but not H3K27 HMT, impaired oligodendrocyte differentiation and functi

74 methyltransferases (H3K9 HMT), but not H3K27 HMT, increased more prominently upon exposure to oligode

75 s to Saccharomyces cerevisiae Set2, an H3K36 HMT that prevents the ectopic initiation of transcriptio

76 HP1 and the NuRD complex act with this H3K36 HMT to prevent ectopic transcriptional initiation.

77 hus distinguishing it from other known H3K36 HMTs.

78 met-2 is homologous to human SETDB1, an H3K9 HMT that represses transcription.

79 -25 was antagonized by another maternal H3K9 HMT, MET-2/SETDB1, which works with LIN-65/ATF7IP and AR

80 nd activity of H3K9 methyltransferases (H3K9 HMT), but not H3K27 HMT, increased more prominently upon

81 Silencing H3K9 HMT, but not H3K27 HMT, impaired oligodendrocyte differe

82 Chp1 and Clr4 (H3K9-HMT), bind transcriptionally active heterochromatin, whe

83 plex composed of SUV39H1 and the two H3K9me2 HMTs, G9A and GLP.

84 ts should be treated with hemithyroidectomy (HMT) or with a more extensive procedure.

85 Hexamethylenetetramine (HMT)-incorporated silver and nickel hydroxide carbonate

86 o solve the problem, hexamethylenetetramine (HMT) has not been confirmed in extraterrestrial material

87 ologically, impairment of KLF11-mediated HP1-HMT recruitment abolishes tumor suppression, providing d

88 increasing the specificity of targeting HP1-HMT complexes to gene promoters.

89 pression, providing direct evidence that HP1-HMTs act in a sequence-specific manner to achieve this f

90 The recruitment of the hSETD1A HMT complex confers promoter-associated H3K4me3 that lea

91 )CH(2))(3)N]Mo(NH(3))][BAr'(4)] (Ter = HTBT, HMT, or pBrHIPT and Ar' = 3,5-(CF(3))(2)C(6)H(3))).

92 systemically delivered doxycycline hyclate (HMT; 20 mg, twice a day) plus locally delivered doxycycl

93 In HMT 35-BGS, water absorption capacity was significantly

94 In HMT-3522 cells, the bulk of AZU-1 protein resided in a d

95 ltransferases (HMTs) and its applications in HMT drug discovery, including analyzing the activity of

96 Overexpression of the DG cDNA in HMT-3522-T4-2 cells elevated alpha-DG levels and altered

97 e (9.2 vs 1.8%, P = 0.2) were more common in HMT, mostly because of undiagnosed cancer requiring comp

98 peak and setback viscosities was observed in HMT sample, decreasing from 3278 +/- 33 cP to 1467 +/- 4

99 dium dodecyl sulfate (SDDS) were observed in HMT samples.

100 Infrared HMT is similar to conventional HMT since both treatments

101 These results suggested that infrared HMT changes the functional and nutritional properties of

102 IR-HMT seemed to increase hydrogen bonding between starch p

103 ed evidence of amylose-lipid complexes in IR-HMT starch with SA.

104 ch granular surface for maize starch with IR-HMT plus SA.

105 r MyoD in proliferating muscle cells and its HMT activity, which is associated with MyoD, diminishes

106 ne expression and this property required its HMT activity.

107 y unliganded TR and in so doing requires its HMT activity.

108 Another H3-K27 HMT functions in adult somatic cells, oocytes, and the P

109 we show that the histone 3/lysine 4 (H3/K4) HMT and the transcriptional regulator MLL associate with

110 less than 50% sequence identities with known HMTs and evaluated their activities in SAM regeneration.

111 endogenous PTIP associates with a Set1-like HMT complex of unique subunit composition.

112 omplex that is shared by all human Set1-like HMT complexes.

113 show that the noncancerous mammary cell line HMT-3522 S1, when allowed to spontaneously form cell agg

114 Rap1 activity in malignant HMT-3522 T4-2 cells is appreciably higher than in S1 cel

115 that MES-4 has histone H3 methyltransferase (HMT) activity in vitro, and is required for histone H3K3

116 and inhibits the MLL H3K4 methyltransferase (HMT) activity with an IC50 value of 12.7 nM.

117 a novel protein histidine methyltransferase (HMT).

118 o identify native histone methyltransferase (HMT) activities from Saccharomyces cerevisiae.

119 ains, has similar histone methyltransferase (HMT) activity, and belongs in the same phylogenetic subg

120 possess intrinsic histone methyltransferase (HMT) activity.

121 a small number of histone methyltransferase (HMT) and histone demethylase (HDM) enzymes as regulators

122 is introduced by histone methyltransferase (HMT) and its regulatory scaffolding proteins.

123 , methylated by a histone methyltransferase (HMT) and then bound by a chromodomain-containing protein

124 ferase DNMT3B and histone methyltransferase (HMT) complex components (G9A, Enhancer of Zeste 2 (EZH2)

125 ts of a Set1-like histone methyltransferase (HMT) complex that also contains ASH2L, RBBP5, WDR5, hDPY

126 hanges in cognate histone methyltransferase (HMT) complexes on the Il12p35 and Il12p40 promoters.

127 a core subunit of histone methyltransferase (HMT) complexes.

128 c deletion of the histone methyltransferase (HMT) Ezh2 from all retinal progenitors resulted in progr

129 repression of the histone methyltransferase (HMT) G9a has recently been implicated in transcriptional

130 nesis regulators, histone methyltransferase (HMT) G9a-mediated repressive epigenetic mark H3K9me2 is

131 d inactivation of histone methyltransferase (HMT) multiple myeloma SET domain (MMSET) in mouse B cell

132 MMSET/WHSC1 is a histone methyltransferase (HMT) overexpressed in t(4;14)+ multiple myeloma (MM) pat

133 that the H3K9me3 histone methyltransferase (HMT) suppressor of variegation 3-9 homolog 1 (SUV39H1) i

134 Histone methyltransferase (HMT)(1) class enzymes that methylate lysine residues of

135 an H3-K9-specific histone methyltransferase (HMT), SUV39H1.

136 related Set1/Ash2 histone methyltransferase (HMT).

137 e of plants, homocysteine methyltransferase (HMT) catalyzes the formation of two molecules of methion

138 talyzed by homocysteine S-methyltransferase (HMT).

139 lysine-9 (H3-K9) specific methyltransferase (HMT) that is associated with gene silencing through chro

140 > Met reaction (SMM:Hcy S-methyltransferase, HMT) were identified by homology and authenticated by co

141 etylases (HDAC), histone methyltransferases (HMT) and histone demethylases.

142 (TrxG) family of histone methyltransferases (HMT) that methylate H3K4 at promoters of active genes.

143 Halide methyltransferases (HMTs) provide an effective way to regenerate S-adenosyl

144 ward identifying histone methyltransferases (HMTs) and elucidating the consequences of histone methyl

145 ection assay for histone methyltransferases (HMTs) and its applications in HMT drug discovery, includ

146 A number of histone methyltransferases (HMTs) are known to influence telomeric chromatin status;

147 Defects in histone methyltransferases (HMTs) are major contributing factors in neurodevelopment

148 Histone methyltransferases (HMTs) catalyze the S-adenosylmethionine (AdoMet)-depende

149 operties of H3K9 histone methyltransferases (HMTs) contribute to this epigenetic persistence.

150 out the roles of histone methyltransferases (HMTs) in the establishment of heterochromatin, little is

151 embly of DNA and histone methyltransferases (HMTs) on the Ucp1 enhancer and leads to methylation of s

152 ts of inhibitory histone methyltransferases (HMTs) to impose gene-specific gatekeeper functions that

153 ta in recruiting histone methyltransferases (HMTs) to specific gene targets, such as Hoxc8.

154 he expression of histone methyltransferases (HMTs) was inversely correlated to the activity of NNMT,

155 mia (MLL) family histone methyltransferases (HMTs), revealing a unique regulatory feature for the MLL

156 eracting to H3K9 histone methyltransferases (HMTs), such as SUV39H1, which methylate this residue on

157 teins are histone lysine methyltransferases (HMTs) that play essential roles in development.

158 ses [HDACs], and histone methyltransferases [HMTs]), evidence points to the use of chromatin remodele

159 GS were found to be 80 degrees C for 30 min (HMT 15), 105.74 degrees C for 30 min (HMT 25), and 113.1

160 0 min (HMT 15), 105.74 degrees C for 30 min (HMT 25), and 113.16 degrees C for 30 min (HMT 35).

161 n (HMT 25), and 113.16 degrees C for 30 min (HMT 35).

162 oped and optimized a new AlphaLISA-based MLL HMT functional assay to facilitate the functional evalua

163 A hierarchical multi-tasking network model (HMT-Net) was developed using conjunctival images, and th

164 modified by annealing (ANN), heat-moisture (HMT) or sonication (SNT) treatments.

165 rived from cells transfected with DNA MTase (HMT) expressed 1- to 50-fold the level of DNA MTase prot

166 nd Wellbeing - National Core Study (LHW-NCS) HMT/UKRI/MRC.

167 years age group (HMT, 2721 women [22.0%]; no HMT, 1469 women [22.8%]), and the majority of women in b

168 fied as White (HMT, 10 904 women [88.3%]; no HMT, 5622 women [87.1%]).

169 homologs regulate vulval development, but no HMT is known to act in this process.

170 (23.7%) of HMT users and 1802 (27.9%) of non-HMT users developed ADRD.

171 cation and characterization of Set2, a novel HMT that is site-specific for lysine 36 (Lys36) of the H

172 ge of 12 years of follow-up, 2926 (23.7%) of HMT users and 1802 (27.9%) of non-HMT users developed AD

173 the part-per-billion level concentration of HMT in Murchison and Tagish Lake is comparable to other

174 Here we report the first detection of HMT and functionalized HMT species in the carbonaceous c

175 say allows rapid and facile determination of HMT kinetics and can be adapted to measure the enzymatic

176 age 75 years, while the protective effect of HMT diminished with age and varied by race in women.

177 e enzyme, and applied it to the evolution of HMT from Paraburkholderia xenovorans.

178 our current understanding of the function of HMT-1 proteins and invoke a PC-independent role for thes

179 heless, the dominant structural influence of HMT in reducing SDS often outweighs the positive effects

180 We show that a generic inhibitor of HMT activity, DzNep, phenocopies expression of an induci

181 ction in previous studies due to the loss of HMT during the extraction processes.

182 ar structure of starch during the process of HMT was suggested.

183 l scanning calorimetry thermal properties of HMT 15, 25 and 35-BGS.

184 rch content decreased at all temperatures of HMT, whereas resistant starch content increased at HMT80

185 For these three types of HMT, oxygen and hydrobiological profiles were measured d

186 se proteins are members of a small family of HMTs that contain bifurcated SET domains.

187 nse interest in elucidating the functions of HMTs in transcriptional regulation, these enzymes have r

188 ns, selectivity profiling against a panel of HMTs, and studying mode of action of select hits.

189 Thirty percent of HMTs developed hypothyroidism and required long-term T4

190 on, little is known about the recruitment of HMTs to regulatory regions of chromatin.

191 To investigate the role of HMTs and specifically H3K9 methylation in gene repressio

192 Most of our knowledge of the role of HMTs in trimethylating lysine 4 of histone H3 (H3K4me3)

193 To characterize the substrate specificity of HMTs, we have developed a coupled-fluorescence-based ass

194 Structural changes on HMT were monitored by microscopy, HPAEC-PAD, ATR-FTIR, W

195 rystallites and acid hydrolysis decreased on HMT.

196 anoxia between day 2 and day 7 depending on HMT type.

197 s it decreased slightly in other starches on HMT.

198 bution remained unchanged in all starches on HMT.

199 ith FIR and with HMT using Vicra (an optical HMT device), which can be considered the gold standard.

200 The optimum HMT conditions for BGS were found to be 80 degrees C for

201 drothermal modifications followed the order: HMT>dual modifications>ANN.

202 ut the mechanism by which ATX1, or any other HMT of plant origin, affects transcription.

203 Our best performing HMT from P. aeruginosa, PaHMT, displays the highest SAM

204 Plant HMT is known to transfer the pro-R methyl group of SMM.

205 methyl-p-terphenyl polymethylbenzimidazoles (HMT-PMBI), charge balanced by hydroxide ions (IEC from 2

206 lycomb repressive complex (PRC) 2, possesses HMT activity with specificity for Lys 9 (K9) and Lys 27

207 of their immediate premalignant progenitors, HMT-3522-S2.

208 We surveyed all 38 putative HMT genes in C. elegans and identified met-1 and met-2 a

209 hin a reconstituted basement membrane (rBM), HMT-3522 cells form polarized and growth-arrested tissue

210 dentify patients who did and did not receive HMT treatment within 3 years after the initial diagnosis

211 tween 2007 and 2009, 12 356 (65.7%) received HMT within 3 years after diagnosis, while 6452 (34.3%) d

212 ared with 64.9 months for those who received HMT ( P < .001).

213 dian PFS was superior for those who received HMT (81.1 v 30.0 months; P < .001 and 38.1 v 15.2 months

214 o IV low-grade serous carcinoma who received HMT after primary treatment had significantly longer PFS

215 Women who received HMT had a significantly lower risk of disease progressio

216 ts-133 who underwent OBS and 70 who received HMT-were seen at our institution.

217 a preexisting diagnosis of ADRD or receiving HMT before the diagnosis of breast cancer were excluded.

218 PTIP complex carries robust HMT activity and specifically methylates lysine 4 (K4) o

219 ANN-treated starches and decreased in single HMT- and SNT-treated starches.

220 ation of these treatments (ANN-HMT, ANN-SNT, HMT-ANN, HMT-SNT, SNT-ANN, SNT-HMT).

221 HMT, ANN-SNT, HMT-ANN, HMT-SNT, SNT-ANN, SNT-HMT).

222 Combination therapy, including SRP, HMT, and TAT, provided significantly greater clinical be

223 valuate a combination therapy involving SRP, HMT, and TAT in the treatment of moderate to severe CP.

224 In all starches, HMT increased crystallinity and gelatinisation temperatu

225 inger transcription factors (ZFPs) to target HMT activity to a specific endogenous gene.

226 Homemade manure tea (HMT) is commonly used in North Africa to enhance crop yi

227 izations and theoretical studies reveal that HMT promotes *CO(2) hydrogenation/*CO desorption for acc

228 The FTIR analysis revealed that HMT and CAT increased the degree of order and the degree

229 y, in vitro digestibility assays showed that HMT and HMT-ANN treatments increased resistant and slowl

230 Our results suggest that HMT-3522 S1 spheroids are useful as an in vitro model sy

231 udies in C. elegans, however, suggested that HMT-1 and PCS-1 do not necessarily act in concert in met

232 covery and with our previous suggestion that HMT-1 and PCS-1 do not operate in a simple linear metal

233 The HMT (18%-60min) promoted an increase in resistant starch

234 The HMT activity of PRC2 is dependent on an intact SET domai

235 The HMT activity of the MES complex appears to be dependent

236 The HMT catalytic SET domains of both MET-2 and SET-25 were

237 The HMT model can be initialized to learn a user-defined num

238 The HMT promoted a reduction of the amylose content, the swe

239 The HMT starch increased the tensile strength and WVP of the

240 The HMT-adduct of d(CCGCTAGCGG) forms a psoralen-induced Hol

241 increase in resistant starch content and the HMT (16%-60min) caused an increase in the slowly digesti

242 Our findings suggest a role for the HMT MMSET in promoting AID-mediated DNA breaks during CS

243 In the HMT clones, methylation reached nearly 100% at susceptib

244 xamined 12 endogenous CpG island loci in the HMT clones.

245 Constraining the directionality in the HMT model leads to a reduction in precursor diversity fo

246 oportionally with increasing moisture in the HMT.

247 he results showed that the enthalpies of the HMT and the CAT samples along with the onset, peak, and

248 e gel elasticity and the adhesiveness of the HMT and the CAT starches were also greater than the NLS

249 The full posterior of the HMT parameters is determined and the underflow problems

250 ule ATP-binding cassette transporters of the HMT-1 (heavy metal tolerance factor 1) subfamily are req

251 The performance of the HMT-Net model was significantly better than that of opht

252 t of this repression is mediated through the HMT activity of the SET domain.

253 e crucial to the control of flux through the HMT reaction and the SMM cycle.

254 hermore, amino acid substitutions within the HMT that ablate its catalytic activity effectively elimi

255 ssociated with hormonal maintenance therapy (HMT) compared with routine observation (OBS) after prima

256 Hormone-modulating therapy (HMT) is a widely accepted treatment for hormone receptor

257 studies showed that host modulation therapy (HMT) or topical antimicrobial therapy (TAT) provided sig

258 maize have one MMT gene, and at least three HMT genes that belong to two anciently diverged classes

259 3 years) were included and randomized: 65 to HMT and 53 to DUN.

260 When HHP was applied to HMT starches, the peak viscosities, setback, and final v

261 d on neck ultrasonography were randomized to HMT or Dunhill (DUN).

262 DUN appears superior to HMT for the treatment of AMG in terms of early reoperati

263 Rb-mutant cancers show increased total HMT activity and down-regulation of NNMT.

264 ng real-time hardware-based motion tracking (HMT) information.

265 ndria via horizontal mitochondrial transfer (HMT) to restore respiration.

266 of Suvar39h, the histone methyl transferase (HMT) responsible for heterochromatic H3-K9 trimethylatio

267 n [PB]) starches were heat-moisture treated (HMT) at 80, 100 and 120 degrees C for 12h at a moisture

268 roperties of infrared heat-moisture treated (HMT) maize meal with stearic acid were studied.

269 native, oxidised and heat-moisture treated (HMT) starches were evaluated.

270 (Ultra-sonication, heat-moisture treatment (HMT) and acid hydrolysis) on the functional properties,

271 difications such as heat-moisture treatment (HMT) and citric acid treatment (CAT).

272 to 18.5-23.9% after heat-moisture treatment (HMT) and to 19.5-26.9% after annealing treatment (ANN).

273 the effects of the heat-moisture treatment (HMT) applied to paddy rice grains on the physicochemical

274 S were subjected to heat-moisture treatment (HMT) at 80-120 degrees C for 30-90 min at different mois

275 zers applied during heat-moisture treatment (HMT) on the properties of canna starch were investigated

276 the association of heat moisture treatment (HMT) with high hydrostatic pressure (HHP) and evaluated

277 dified using ozone, heat-moisture treatment (HMT), and their sequential combinations.

278 The effect of heat moisture treatment (HMT), annealing (ANN), and dual retrogradation (DR) on f

279 ostly influenced by Heat-moisture treatment (HMT).

280 s (VBEMS) algorithm for hidden Markov trees (HMT) is proposed for incomplete tree structured data.

281 ine learning method for Hidden Markov Trees (HMTs), which can be applied to large datasets to classif

282 d 4'-hydroxymethyl-4,5',8-trimethylpsoralen (HMT) and scored for normal passage into mitosis.

283 4'-(hydroxymethyl)-4,5',8-trimethylpsoralen (HMT) ICLs by the UvrABC nuclease.

284 y 4'-hydroxymethyl-4,5',8-trimethylpsoralen (HMT).

285 4'-(hydroxymethyl)-4,5',8-trimethylpsoralen (HMT).

286 le or even better performance than the Vicra HMT method in both static and dynamic studies.

287 e-thaw stability (0.03 % syneresis), whereas HMT has the opposite effect.

288 ed event and provides one mechanism by which HMTs can be recruited to chromatin to activate gene expr

289 ly digestible starch (SDS) to 24.64 %, while HMT elevates rapidly digestible starch (RDS) to 34.17 %

290 men in both groups self-identified as White (HMT, 10 904 women [88.3%]; no HMT, 5622 women [87.1%]).

291 d compared its performance with FIR and with HMT using Vicra (an optical HMT device), which can be co

292 The reduction in ADRD risk associated with HMT was greatest for women aged 65 to 74 years who self-

293 Risk of ADRD associated with HMT; associations of risk with age, self-identified race

294 6% +/- 10.9% in K (i) value as compared with HMT, whereas NMC and FIR yielded -18.0% +/- 39.2% and -2

295 +/- 5.2% differences in V (T) compared with HMT, whereas NMC and FIR yielded -20.0% +/- 12.5% and -5

296 3.7% +/- 5.4% for (11)C-UCB-J) compared with HMT, whereas no motion correction (NMC) and FIR yielded

297 s association of ATP-remodeling factors with HMT CARM1 defines a new component of regulation in the n

298 pared to those of the samples processed with HMT alone.

299 NN but changed to a more porous surface with HMT and DR, thereby increasing the digestibility.

300 ability to utilize AdoMet or SMM to a yeast HMT mutant.