1 By analogy with 2,6-di-tert-butylpyridine and its 4-meth
2 By analogy to a baseball glove, the protein "catches" an
3 Designed
by analogy to a protein-folding intermediate, the analog
4 d mechanism for sequence recognition, which,
by analogy with a related process in biomolecular inform
5 the (13)Calpha-atom of glycine was assigned
by analogy with alanine and lactate assuming that the mo
6 n added to the list as a putative metabolite
by analogy to alcohol 6 and ketone 7.
7 and dispersion in chromatography are modeled
by analogy to an effective eddy diffusion process.
8 and variability of a postretinal peak that,
by analogy to animal studies, likely corresponds to the
9 be phosphorylated by PKA in vitro and which,
by analogy to animal studies, may have significance for
10 By analogy with animal cells, we propose that yeast cent
11 By analogy with animal experiments, these regions are li
12 By analogy with Aos1p, we infer that Enr2p functions in
13 redicted from the ionic radius of Ra(2+) and
by analogy with Ba(2+), supporting greater water labilit
14 By analogy with Bcl-2, this phosphorylation may play a c
15 By analogy with biogenic calcite crystals, we associate
16 This model allowed distinguishing,
by analogy with bone development and repair, an outer, c
17 By analogy with C4, where this residue influences the nu
18 rtial cone, 1,2-alternate, and 1,3-alternate
by analogy to calix[4]arene.
19 estimates obtained in the present study and
by analogy to carotenoid-binding sites in other pigment-
20 By analogy with celiac disease and type I diabetes, the
21 n proposed to participate in O(2) activation
by analogy to certain proposals made for cytochrome P450
22 th electron flow from NAD(P)H to oxygen, and
by analogy to chlororespiration (in chloroplasts) and ch
23 By analogy with classic numerical methods, we show that
24 By analogy to classical mechanisms of cell surface recep
25 By analogy to conjugated polyenes, conjugative stabiliza
26 proteins are very similar, indicating that,
by analogy to cp254, cp228 adopts a global folded state.
27 ilX; letE encodes a small novel protein; or,
by analogy to csrB, letE encodes a regulatory RNA that s
28 lycine-alpha-hydroxylating monooxygenase and
by analogy to cytochrome P-450, the accumulation of a re
29 modes of substrate binding have been deduced
by analogy to D-Ala-D-Ala ligase and to pyruvate kinase.
30 By analogy to Dictyostelium Skp1, the mechanism may invo
31 By analogy to DNA repair, we propose that the ability of
32 s that are likely to co-ordinate the cluster
by analogy to DNA2.
33 By analogy with E. coli FimH, we suggest that Salmonella
34 Furthermore,
by analogy with E. coli MglB which interacts with the se
35 lucidation by isotopic labeling experiments,
by analogy with earlier studies of other heme proteins,
36 By analogy with Earth, methane in the Martian atmosphere
37 By analogy with electrical charge drift motion, we defin
38 By analogy to elongation factor Tu (EF-Tu), SelB is expe
39 Most often, EVs,
by analogy to enveloped viruses, are suggested to fuse t
40 By analogy to epigenetic phenomena in several eukaryotes
41 By analogy to eukaryotic histones, this patch could inte
42 inition and abbreviation (ENAC) are proposed
by analogy with extended metal atom chain (EMAC) complex
43 By analogy to femtosecond chemistry and photosynthetic d
44 By analogy with findings in those species, we speculate
45 By analogy with flagella, which are known to exist in di
46 By analogy with functions of the UBR domain in the N-end
47 By analogy to Ga- and Cr-promoted samples, we conclude t
48 By analogy to genetics, there are interference phenotype
49 idue of xanthine oxidase (possibly Glu-1261,
by analogy to Glu-869 in the crystallographically known
50 By analogy with Grignard reagents, these compounds can b
51 By analogy to growth factor receptors, G protein-coupled
52 By analogy with hematopoiesis research, a thorough inves
53 on of change, in ways that can be understood
by analogy to historical El Nino and La Nina events: Nor
54 By analogy to Hofmeister salt effects on protein folding
55 The residual component may be interpreted,
by analogy with horizontal and vertical vergence, as ref
56 By analogy with HSV-1, envelope-associated PRV gD probab
57 By analogy to human RCC in which mutations in the von Hi
58 s, is assumed to be mature frataxin (78-207)
by analogy with human mature frataxin (81-210).
59 By analogy with hydroformylation, bulkier ligands ought
60 s have since become known as chalcogen bonds
by analogy to hydrogen and halogen bonds.
61 By analogy to interword separations in language, we hypo
62 d at the tips of espin-elongated microvilli,
by analogy to its location in stereocilia, whereas myosi
63 nMuv genes encode an Rb/DP/E2F complex that,
by analogy with its mammalian and Drosophila counterpart
64 By analogy to known examples of arylamine oxidation, a c
65 By analogy to known proteins of the innate immune system
66 counteracted by the PhrLS20 peptide, which,
by analogy to known Rap/Phr systems, is secreted and tak
67 ressor of currents encoded by the Kv4 family
by analogy to Kv1 channels.
68 of the orotate-reducing flavin and Lys 168 (
by analogy with L. lactis DHODase A).
69 By analogy to large cloning systems in microorganisms, M
70 By analogy with LCTs, we hypothesised that the CHD motif
71 By analogy to linear polymers, shorter T(1) relaxation t
72 By analogy with LLPS in binary solutions, cellular LLPS
73 By analogy to logic processing, we propose programmable
74 s retarded tumor development in mice unless,
by analogy with loss of heterozygosity, the PTEN gene wa
75 a possible alternative cluster ligand Asp13 (
by analogy with M. smegmatis WhiB2) was not.
76 spinal cord might be more easily recognized
by analogy to marionette puppets, another system in whic
77 By analogy to mechanosensitive channels, the force assoc
78 of cellular functions and is often explained
by analogy to membrane phase separation; however, models
79 By analogy with microbial "pathogen-associated molecular
80 By analogy with model organisms, we suggest that stallin
81 biochemical studies, crystal structures, and
by analogy with monooxygenases, we predict that FADH2 re
82 logy is referred to as hole-burning imaging,
by analogy with MRI.
83 By analogy to natural signaling systems, the insights fr
84 paB.IkappaBbeta complex crystals were formed
by analogy to NF-kappaB.
85 air, pointing out areas of commonality, (2)
by analogy to nHCs, argue that climate change may alter
86 These basis functions are related
by analogy to optical filters and offer a pathway to the
87 blast activity has been speculated for years
by analogy to osteoclast biology.
88 By analogy to other armadillo domain proteins, including
89 face protein of pathogenic Leptospira, which
by analogy to other bacterial immunoglobulin superfamily
90 odel of synaptic-vesicle recycling, proposed
by analogy to other cellular endocytic pathways, involve
91 By analogy to other chromosomal protein complexes such a
92 By analogy to other death domain containing proteins, p8
93 idely-expressed transcription factors which,
by analogy to other instances, may be sufficient to expl
94 ES element is not known at present; however,
by analogy to other IRES-containing mRNAs expressed in n
95 By analogy to other La proteins, p43 may function in cha
96 designated FCV replication complexes (RCs),
by analogy to other positive-strand RNA viruses.
97 and Glu-14-->Ala) in the Exo I motif, which,
by analogy to other proofreading exonucleases, is essent
98 date is Sal(A), a putative ABC-F NTPase that-
by analogy to other proteins of this type-may act to pro
99 It is argued
by analogy to other proteins with coiled-coil dimerizati
100 recruitment of these cells are unknown, but
by analogy to other systems, chemokines are likely to be
101 By analogy to other transposons that encode two proteins
102 By analogy to other tumor systems, the identification of
103 By analogy to other two-component systems, NodV and NodW
104 most of these proteins have been established
by analogy to other viruses and by sequence homology to
105 ts of OmpRc can be assigned functional roles
by analogy to other winged-helix DNA-binding proteins.
106 By analogy with other bacterial pathogens, it is plausib
107 We hypothesize that,
by analogy with other carotenoid oxygenases, the predict
108 From the primary sequence and
by analogy with other channels in this family, PC2 is mo
109 By analogy with other enteric pathogens such as Salmonel
110 ions as an entry mediator or coreceptor and,
by analogy with other herpesviruses, gH is then thought
111 o's tidal axis and may be an impact feature,
by analogy with other large basins in the Solar System.
112 We suggest,
by analogy with other neurodegenerations and from SOD1 A
113 ells is more limited than might be predicted
by analogy with other oncogenic viruses.
114 V F, once triggered by the receptor-bound G,
by analogy with other paramyxovirus F proteins, undergoe
115 It had been assumed,
by analogy with other paramyxoviruses, that the G and F
116 By analogy with other pathogens that utilize fibronectin
117 dered to be the primary polyprotein cleavage
by analogy with other picornaviruses, is mediated by 3C(
118 NTR sequences regulate RNA synthesis and,
by analogy with other segmented negative-sense RNA virus
119 ory system has not been determined it could,
by analogy with other sensory systems, guide the functio
120 el connected to an amphipathic cavity, which
by analogy with other TetR regulators, may serve as a bi
121 function predicted from previous studies and
by analogy with other two-component response regulators.
122 Again,
by analogy with other viruses gH is thought to be critic
123 h two distinct mechanisms: first, CED-9 may,
by analogy with p35, directly inhibit the CED-3 protease
124 By analogy to patched, TRC8 might function as a signalin
125 By analogy with Pavlov's dogs, certain pathogens have ev
126 By analogy to PD-1 and PD-L1 blockade, VISTA blockade ma
127 By analogy with phosphatidylcholine and phosphatidyletha
128 By analogy to phosphorylation cascades that transmit inf
129 By analogy with photoreceptors, and with reference to fi
130 s two [4Fe-4S] clusters named F(A) and F(B),
by analogy with photosystem I (PS I).
131 d has a portal at one fivefold vertex which,
by analogy to portal-containing phages, is believed to m
132 By analogy to previous work on lateral geniculate nucleu
133 By analogy with previous studies of myosin 10, our data
134 By analogy to prior art and from our own observations, w
135 By analogy with procollagen, chylomicrons may drive the
136 By analogy to proteoglycan-mediated regulation of growth
137 This type of elementary reaction could have,
by analogy to proton-coupled electron transfer, an impor
138 By analogy with published crystallographic data, we sugg
139 ons with the y-terpinene isomer limonene and
by analogy to reactions catalyzed by related enzymes.
140 By analogy with recent observations in Antarctica, the r
141 By analogy to related complexes formed by IgE and its ev
142 By analogy with related regulatory systems, we designate
143 By analogy with road construction, which causes temporar
144 By analogy to rodent NSCs, these observations may allow
145 occurs in the lumen of the Golgi apparatus,
by analogy to S. cerevisiae.
146 By analogy to salivary and submucosal glands, where flui
147 By analogy to self-compartmentalising proteases, the tun
148 pace-charge regions generated by mobile ions
by analogy to semiconductor junctions.
149 By analogy with similar sequences in other viral envelop
150 Single-molecule toroics (SMTs) are defined,
by analogy with single-molecule magnets, as bistable mol
151 By analogy to siRNA processing, Ago2 cleavage may facili
152 By analogy with social mobility (a measure of people mov
153 xcited by ATP released during tissue damage,
by analogy to somatic pain-sensing C-fibers.
154 By analogy to spin electronic system, topological concep
155 In addition,
by analogy to square-wave voltammetry, a net differentia
156 By analogy with structures on Earth, we propose here tha
157 By analogy to successful vaccine antigen engineering app
158 ctive, we parse the many forms of cell death
by analogy to suicide, sabotage, and murder, and conside
159 By analogy to the AAA+ ATPases, it can be predicted that
160 ctrometer is established and is rationalized
by analogy to the atmospheric transmission of the common
161 By analogy to the beta-factor from laser physics(10,17-2
162 We propose that
by analogy to the cadherin switch during epithelial-mese
163 By analogy to the coatomer (COPI)-independent transport
164 s used to model the structure of glucokinase
by analogy to the crystal structure of brain hexokinase.
165 y in infinite-layer nickelates was motivated
by analogy to the cuprates, and this perspective has fra
166 nstable hydrolysis intermediate was assigned
by analogy to the degradation product picrotoxic acid.
167 By analogy to the diffraction produced by the scattering
168 By analogy to the E ring, R/2003 U 1 is probably produce
169 By analogy to the ENaCs and the degenerins, which form h
170 By analogy to the Fe(III) trafficking that leads to the
171 By analogy to the first solution structure of an isolate
172 cts of unknown reading frames are attributed
by analogy to the functions of sequence-related proteins
173 It is suggested that,
by analogy to the GTPase activity of p21(ras) and by exa
174 By analogy to the homologous cAMP receptor protein (CRP)
175 By analogy to the hyperfine interactions seen in a homol
176 to form its neuraminidase (NA) active site,
by analogy to the influenza virus neuraminidase protein.
177 By analogy to the KIRs, p91/PIR-B may represent a novel
178 By analogy to the Kjeldahl method, we suggest that the t
179 ture investigations of their polymerization,
by analogy to the known polymerization of Mes-P=CPh(2).
180 We argue,
by analogy to the neural organization of the object reco
181 Structural assignment of the latter was made
by analogy to the NMR properties of the known 3-phosphoh
182 Thus,
by analogy to the Notch receptor, we designate this clea
183 By analogy to the past, we suggest that, without major r
184 By analogy to the past, we suggest today's widespread la
185 By analogy to the patterns of concordant and discordant
186 By analogy to the persistence of a foreign virus, the la
187 By analogy to the plant AP2 proteins and based on the ex
188 We named these isoforms "pre-P"
by analogy to the pre-C and pre-S regions of the core an
189 By analogy to the recently published MscL structure from
190 By analogy to the related focal adhesion kinase, Pyk2 ha
191 By analogy to the related Novel Interactor of JAZ (NINJA
192 By analogy to the retina, we propose that UBCs comprise
193 By analogy to the situation in Saccharomyces cerevisiae,
194 ty) indice according to the standard chosen,
by analogy to the TEAC indice (Trolox Equivalent Antioxi
195 face, separating two 2D colloidal entities),
by analogy to the term "surfactant" (which indicates a m
196 By analogy to the term 'hoxology', which refers to the c
197 phosphoramidate reaction products were made
by analogy to the tetrahydrofurfuryl products.
198 By analogy to the thermodynamics of organometallic compl
199 From the characterization of the mutants and
by analogy to the three-dimensional structure of CheY, w
200 IndInt required for Eiger-mediated signaling
by analogy to the TNF-alpha system, suggesting the prese
201 By analogy to the topologically similar M segment-encode
202 By analogy to the traditional reaction map formed by S,
203 oducts is currently under investigation, but
by analogy to the well-described 12-lipoxygenase pathway
204 By analogy to the yeast Rad55 and Rad57, our results sug
205 By analogy with the "histone code" hypothesis, we propos
206 By analogy with the "Stokes problems" in hydrodynamics (
207 the mouse corneal epithelial cells and thus,
by analogy with the abundant lens crystallins, is consid
208 of ACR1 as the beta-phosphate binding domain
by analogy with the actin/hsp70/hexokinase superfamily,
209 If so,
by analogy with the behavior of colipase, increasing dia
210 By analogy with the better characterized prokaryotic Cu-
211 By analogy with the classical central venous pressure ru
212 aches describe the fusion of cell aggregates
by analogy with the coalescence of liquid droplets and i
213 By analogy with the concept of the 'druggable genome', t
214 By analogy with the desiccation- and radiation-resistant
215 We propose,
by analogy with the diverse crystallins of the eye lens
216 By analogy with the dsDNA bacteriophage we reasoned that
217 We suggest,
by analogy with the effects of SV40, that these changes
218 hydrolytic transition states, respectively,
by analogy with the equivalent complexes of myosin.
219 rg residue in the transmembrane region that,
by analogy with the FcalphaR relative, suggests the pote
220 Hence,
by analogy with the fetal state, we posit the existence
221 er to these fish GCs as spot detectors (SDs)
by analogy with the frog SD.
222 op of Cdc42Hs, but from biochemical data and
by analogy with the G-protein subunit G(i alpha1), we pr
223 By analogy with the genetic organization of the Escheric
224 re' sequence for an anion-selective ion pore
by analogy with the homologous GYG sequence that is esse
225 By analogy with the inhibition of the Rb/E2F regulatory
226 By analogy with the key role of beta-blockers in the man
227 By analogy with the known actions of agouti, these data
228 RS-S(O)-NH(2)) formation, a pathway expected
by analogy with the known reactivity of HNO with thiol.
229 By analogy with the larger neurofilament chains, we post
230 By analogy with the other two members of the tenascin fa
231 By analogy with the prokaryotic small subunit, this chan
232 By analogy with the properties of the ferricyanide-oxidi
233 By analogy with the random assignment of treatment in ra
234 By analogy with the rat pol beta structure, it is sugges
235 ' anion, [BeCp](-), to an organic substrate,
by analogy with the reactivity of sp(2)-sp(3) diboranes.
236 By analogy with the roles of 4.1R in red blood cells, 4.
237 enotypes differ markedly from those expected
by analogy with the S. griseus A-factor system.
238 By analogy with the site elucidated in the gammaC domain
239 istent with singlet phosphinidene reactivity
by analogy with the Skell hypothesis for singlet carbene
240 We call them 'small-world' networks,
by analogy with the small-world phenomenon (popularly kn
241 on is supported by computational methods and
by analogy with the solid-state behavior of an analogous
242 e altered at the position of Trp-676, which,
by analogy with the structure of rat CPR, is close to th
243 By analogy with the structure of ribonuclease inhibitor
244 We call them ST-motifs,
by analogy with the term Asx-motif we suggested for the
245 By analogy with the three cryptic inscriptions of the cl
246 By analogy with the three-signal model required to activ
247 By analogy with the trypsin model, it was proposed that
248 By analogy with the yeast-mouse dyad, this green pair ha
249 s, 2.9316(2) to 3.101(4) A) were synthesized
by analogy with their bromine analogues.
250 By analogy with their functions in other cell systems, i
251 expressed in complementary rhombomeres and,
by analogy with their roles in axon pathfinding, could m
252 By analogy with these comparable terrestrial rocks, Jake
253 By analogy with these, we propose that the RAMP-FGFR1 fu
254 By analogy to thioredoxin, Rdx proteins can use catalyti
255 in water with complex structure and dynamics
by analogy with those found in nature.
256 ain building blocks may be understood easily
by analogy with three-orbital four-electron "hypervalent
257 By analogy to thymidylate synthase, which also uses CH(2
258 Subsequent studies revealed that
by analogy to TIRAP, TcpB interacts with phosphoinositid
259 braries of sarafotoxin variants or suggested
by analogy with tissue inhibitors of metalloproteinases,
260 By analogy to Tolman cone angles in cation coordination
261 By analogy to transistors in classical electronic circui
262 By analogy with transport phenomena we show that, counte
263 By analogy to tumor suppressor genes, which restrain cel
264 By analogy with type 1 copper proteins, putative superex
265 In this scheme,
by analogy with variational autoencoders (VAEs), the gen
266 Golgi membrane are predicted to be required,
by analogy to vesicle budding from other membranes.
267 otein cages is by now fairly well understood
by analogy to viral protein shells in terms of Caspar an
268 By analogy with viral trimeric coiled-coil class I membr
269 nd the carboxyl terminus but not as expected
by analogy with voltage-dependent K+ channels, in H5.
270 By analogy to well-characterized bacteriophage systems,
271 the elaboration of anion organic frameworks,
by analogy with well-known MOF derivatives.