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 By analogy with Bcl-2, this phosphorylation may play a c
14 This model allowed distinguishing,
by analogy with bone development and repair, an outer, c
15 By analogy with C4, where this residue influences the nu
16 rtial cone, 1,2-alternate, and 1,3-alternate
by analogy to calix[4]arene.
17 estimates obtained in the present study and
by analogy to carotenoid-binding sites in other pigment-
18 By analogy with celiac disease and type I diabetes, the
19 n proposed to participate in O(2) activation
by analogy to certain proposals made for cytochrome P450
20 th electron flow from NAD(P)H to oxygen, and
by analogy to chlororespiration (in chloroplasts) and ch
21 By analogy to classical mechanisms of cell surface recep
22 By analogy to conjugated polyenes, conjugative stabiliza
23 proteins are very similar, indicating that,
by analogy to cp254, cp228 adopts a global folded state.
24 ilX; letE encodes a small novel protein; or,
by analogy to csrB, letE encodes a regulatory RNA that s
25 lycine-alpha-hydroxylating monooxygenase and
by analogy to cytochrome P-450, the accumulation of a re
26 modes of substrate binding have been deduced
by analogy to D-Ala-D-Ala ligase and to pyruvate kinase.
27 By analogy to Dictyostelium Skp1, the mechanism may invo
28 By analogy with E. coli FimH, we suggest that Salmonella
29 Furthermore,
by analogy with E. coli MglB which interacts with the se
30 lucidation by isotopic labeling experiments,
by analogy with earlier studies of other heme proteins,
31 By analogy with Earth, methane in the Martian atmosphere
32 By analogy to elongation factor Tu (EF-Tu), SelB is expe
33 By analogy to epigenetic phenomena in several eukaryotes
34 inition and abbreviation (ENAC) are proposed
by analogy with extended metal atom chain (EMAC) complex
35 By analogy to femtosecond chemistry and photosynthetic d
36 By analogy with findings in those species, we speculate
37 By analogy with flagella, which are known to exist in di
38 By analogy with functions of the UBR domain in the N-end
39 By analogy to Ga- and Cr-promoted samples, we conclude t
40 By analogy to genetics, there are interference phenotype
41 idue of xanthine oxidase (possibly Glu-1261,
by analogy to Glu-869 in the crystallographically known
42 By analogy to growth factor receptors, G protein-coupled
43 By analogy with hematopoiesis research, a thorough inves
44 By analogy to Hofmeister salt effects on protein folding
45 The residual component may be interpreted,
by analogy with horizontal and vertical vergence, as ref
46 By analogy with HSV-1, envelope-associated PRV gD probab
47 By analogy to human RCC in which mutations in the von Hi
48 By analogy with hydroformylation, bulkier ligands ought
49 s have since become known as chalcogen bonds
by analogy to hydrogen and halogen bonds.
50 d at the tips of espin-elongated microvilli,
by analogy to its location in stereocilia, whereas myosi
51 nMuv genes encode an Rb/DP/E2F complex that,
by analogy with its mammalian and Drosophila counterpart
52 By analogy to known examples of arylamine oxidation, a c
53 By analogy to known proteins of the innate immune system
54 counteracted by the PhrLS20 peptide, which,
by analogy to known Rap/Phr systems, is secreted and tak
55 ressor of currents encoded by the Kv4 family
by analogy to Kv1 channels.
56 of the orotate-reducing flavin and Lys 168 (
by analogy with L. lactis DHODase A).
57 By analogy to large cloning systems in microorganisms, M
58 By analogy to linear polymers, shorter T(1) relaxation t
59 s retarded tumor development in mice unless,
by analogy with loss of heterozygosity, the PTEN gene wa
60 a possible alternative cluster ligand Asp13 (
by analogy with M. smegmatis WhiB2) was not.
61 spinal cord might be more easily recognized
by analogy to marionette puppets, another system in whic
62 By analogy to mechanosensitive channels, the force assoc
63 By analogy with microbial "pathogen-associated molecular
64 By analogy with model organisms, we suggest that stallin
65 biochemical studies, crystal structures, and
by analogy with monooxygenases, we predict that FADH2 re
66 logy is referred to as hole-burning imaging,
by analogy with MRI.
67 By analogy to natural signaling systems, the insights fr
68 paB.IkappaBbeta complex crystals were formed
by analogy to NF-kappaB.
69 These basis functions are related
by analogy to optical filters and offer a pathway to the
70 blast activity has been speculated for years
by analogy to osteoclast biology.
71 By analogy to other armadillo domain proteins, including
72 face protein of pathogenic Leptospira, which
by analogy to other bacterial immunoglobulin superfamily
73 odel of synaptic-vesicle recycling, proposed
by analogy to other cellular endocytic pathways, involve
74 By analogy to other chromosomal protein complexes such a
75 By analogy to other death domain containing proteins, p8
76 idely-expressed transcription factors which,
by analogy to other instances, may be sufficient to expl
77 ES element is not known at present; however,
by analogy to other IRES-containing mRNAs expressed in n
78 By analogy to other La proteins, p43 may function in cha
79 designated FCV replication complexes (RCs),
by analogy to other positive-strand RNA viruses.
80 and Glu-14-->Ala) in the Exo I motif, which,
by analogy to other proofreading exonucleases, is essent
81 It is argued
by analogy to other proteins with coiled-coil dimerizati
82 recruitment of these cells are unknown, but
by analogy to other systems, chemokines are likely to be
83 By analogy to other transposons that encode two proteins
84 By analogy to other tumor systems, the identification of
85 By analogy to other two-component systems, NodV and NodW
86 most of these proteins have been established
by analogy to other viruses and by sequence homology to
87 ts of OmpRc can be assigned functional roles
by analogy to other winged-helix DNA-binding proteins.
88 By analogy with other bacterial pathogens, it is plausib
89 We hypothesize that,
by analogy with other carotenoid oxygenases, the predict
90 From the primary sequence and
by analogy with other channels in this family, PC2 is mo
91 By analogy with other enteric pathogens such as Salmonel
92 ions as an entry mediator or coreceptor and,
by analogy with other herpesviruses, gH is then thought
93 o's tidal axis and may be an impact feature,
by analogy with other large basins in the Solar System.
94 We suggest,
by analogy with other neurodegenerations and from SOD1 A
95 ells is more limited than might be predicted
by analogy with other oncogenic viruses.
96 V F, once triggered by the receptor-bound G,
by analogy with other paramyxovirus F proteins, undergoe
97 It had been assumed,
by analogy with other paramyxoviruses, that the G and F
98 By analogy with other pathogens that utilize fibronectin
99 dered to be the primary polyprotein cleavage
by analogy with other picornaviruses, is mediated by 3C(
100 ory system has not been determined it could,
by analogy with other sensory systems, guide the functio
101 el connected to an amphipathic cavity, which
by analogy with other TetR regulators, may serve as a bi
102 function predicted from previous studies and
by analogy with other two-component response regulators.
103 Again,
by analogy with other viruses gH is thought to be critic
104 h two distinct mechanisms: first, CED-9 may,
by analogy with p35, directly inhibit the CED-3 protease
105 By analogy to patched, TRC8 might function as a signalin
106 By analogy to PD-1 and PD-L1 blockade, VISTA blockade ma
107 By analogy with phosphatidylcholine and phosphatidyletha
108 By analogy with photoreceptors, and with reference to fi
109 s two [4Fe-4S] clusters named F(A) and F(B),
by analogy with photosystem I (PS I).
110 d has a portal at one fivefold vertex which,
by analogy to portal-containing phages, is believed to m
111 By analogy to previous work on lateral geniculate nucleu
112 By analogy with previous studies of myosin 10, our data
113 By analogy with procollagen, chylomicrons may drive the
114 By analogy to proteoglycan-mediated regulation of growth
115 By analogy with published crystallographic data, we sugg
116 By analogy with recent observations in Antarctica, the r
117 By analogy to related complexes formed by IgE and its ev
118 By analogy with related regulatory systems, we designate
119 By analogy to rodent NSCs, these observations may allow
120 occurs in the lumen of the Golgi apparatus,
by analogy to S. cerevisiae.
121 By analogy to salivary and submucosal glands, where flui
122 By analogy to self-compartmentalising proteases, the tun
123 pace-charge regions generated by mobile ions
by analogy to semiconductor junctions.
124 By analogy with similar sequences in other viral envelop
125 Single-molecule toroics (SMTs) are defined,
by analogy with single-molecule magnets, as bistable mol
126 By analogy to siRNA processing, Ago2 cleavage may facili
127 xcited by ATP released during tissue damage,
by analogy to somatic pain-sensing C-fibers.
128 By analogy with structures on Earth, we propose here tha
129 By analogy to the AAA+ ATPases, it can be predicted that
130 ctrometer is established and is rationalized
by analogy to the atmospheric transmission of the common
131 We propose that
by analogy to the cadherin switch during epithelial-mese
132 By analogy to the coatomer (COPI)-independent transport
133 s used to model the structure of glucokinase
by analogy to the crystal structure of brain hexokinase.
134 By analogy to the diffraction produced by the scattering
135 By analogy to the E ring, R/2003 U 1 is probably produce
136 By analogy to the ENaCs and the degenerins, which form h
137 By analogy to the Fe(III) trafficking that leads to the
138 By analogy to the first solution structure of an isolate
139 cts of unknown reading frames are attributed
by analogy to the functions of sequence-related proteins
140 It is suggested that,
by analogy to the GTPase activity of p21(ras) and by exa
141 By analogy to the homologous cAMP receptor protein (CRP)
142 By analogy to the hyperfine interactions seen in a homol
143 to form its neuraminidase (NA) active site,
by analogy to the influenza virus neuraminidase protein.
144 By analogy to the KIRs, p91/PIR-B may represent a novel
145 We argue,
by analogy to the neural organization of the object reco
146 Structural assignment of the latter was made
by analogy to the NMR properties of the known 3-phosphoh
147 Thus,
by analogy to the Notch receptor, we designate this clea
148 By analogy to the past, we suggest today's widespread la
149 By analogy to the patterns of concordant and discordant
150 By analogy to the persistence of a foreign virus, the la
151 By analogy to the plant AP2 proteins and based on the ex
152 We named these isoforms "pre-P"
by analogy to the pre-C and pre-S regions of the core an
153 By analogy to the recently published MscL structure from
154 By analogy to the related focal adhesion kinase, Pyk2 ha
155 By analogy to the related Novel Interactor of JAZ (NINJA
156 By analogy to the retina, we propose that UBCs comprise
157 By analogy to the situation in Saccharomyces cerevisiae,
158 ty) indice according to the standard chosen,
by analogy to the TEAC indice (Trolox Equivalent Antioxi
159 face, separating two 2D colloidal entities),
by analogy to the term "surfactant" (which indicates a m
160 By analogy to the term 'hoxology', which refers to the c
161 phosphoramidate reaction products were made
by analogy to the tetrahydrofurfuryl products.
162 By analogy to the thermodynamics of organometallic compl
163 From the characterization of the mutants and
by analogy to the three-dimensional structure of CheY, w
164 By analogy to the topologically similar M segment-encode
165 By analogy to the traditional reaction map formed by S,
166 oducts is currently under investigation, but
by analogy to the well-described 12-lipoxygenase pathway
167 By analogy to the yeast Rad55 and Rad57, our results sug
168 By analogy with the "histone code" hypothesis, we propos
169 By analogy with the "Stokes problems" in hydrodynamics (
170 the mouse corneal epithelial cells and thus,
by analogy with the abundant lens crystallins, is consid
171 of ACR1 as the beta-phosphate binding domain
by analogy with the actin/hsp70/hexokinase superfamily,
172 If so,
by analogy with the behavior of colipase, increasing dia
173 By analogy with the better characterized prokaryotic Cu-
174 By analogy with the desiccation- and radiation-resistant
175 We propose,
by analogy with the diverse crystallins of the eye lens
176 By analogy with the dsDNA bacteriophage we reasoned that
177 We suggest,
by analogy with the effects of SV40, that these changes
178 hydrolytic transition states, respectively,
by analogy with the equivalent complexes of myosin.
179 rg residue in the transmembrane region that,
by analogy with the FcalphaR relative, suggests the pote
180 Hence,
by analogy with the fetal state, we posit the existence
181 op of Cdc42Hs, but from biochemical data and
by analogy with the G-protein subunit G(i alpha1), we pr
182 By analogy with the genetic organization of the Escheric
183 re' sequence for an anion-selective ion pore
by analogy with the homologous GYG sequence that is esse
184 By analogy with the inhibition of the Rb/E2F regulatory
185 By analogy with the key role of beta-blockers in the man
186 By analogy with the known actions of agouti, these data
187 By analogy with the larger neurofilament chains, we post
188 By analogy with the other two members of the tenascin fa
189 By analogy with the prokaryotic small subunit, this chan
190 By analogy with the properties of the ferricyanide-oxidi
191 By analogy with the rat pol beta structure, it is sugges
192 By analogy with the roles of 4.1R in red blood cells, 4.
193 enotypes differ markedly from those expected
by analogy with the S. griseus A-factor system.
194 By analogy with the site elucidated in the gammaC domain
195 istent with singlet phosphinidene reactivity
by analogy with the Skell hypothesis for singlet carbene
196 We call them 'small-world' networks,
by analogy with the small-world phenomenon (popularly kn
197 on is supported by computational methods and
by analogy with the solid-state behavior of an analogous
198 e altered at the position of Trp-676, which,
by analogy with the structure of rat CPR, is close to th
199 By analogy with the structure of ribonuclease inhibitor
200 We call them ST-motifs,
by analogy with the term Asx-motif we suggested for the
201 By analogy with the three cryptic inscriptions of the cl
202 By analogy with the trypsin model, it was proposed that
203 By analogy with the yeast-mouse dyad, this green pair ha
204 s, 2.9316(2) to 3.101(4) A) were synthesized
by analogy with their bromine analogues.
205 By analogy with their functions in other cell systems, i
206 expressed in complementary rhombomeres and,
by analogy with their roles in axon pathfinding, could m
207 By analogy with these comparable terrestrial rocks, Jake
208 By analogy with these, we propose that the RAMP-FGFR1 fu
209 By analogy to thioredoxin, Rdx proteins can use catalyti
210 ain building blocks may be understood easily
by analogy with three-orbital four-electron "hypervalent
211 By analogy to thymidylate synthase, which also uses CH(2
212 Subsequent studies revealed that
by analogy to TIRAP, TcpB interacts with phosphoinositid
213 braries of sarafotoxin variants or suggested
by analogy with tissue inhibitors of metalloproteinases,
214 By analogy to transistors in classical electronic circui
215 By analogy to tumor suppressor genes, which restrain cel
216 By analogy with type 1 copper proteins, putative superex
217 By analogy with viral trimeric coiled-coil class I membr
218 nd the carboxyl terminus but not as expected
by analogy with voltage-dependent K+ channels, in H5.
219 By analogy to well-characterized bacteriophage systems,
220 the elaboration of anion organic frameworks,
by analogy with well-known MOF derivatives.