1 ses; these are compelling targets for future
functional analyses.
2 and carried out a series of statistical and
functional analyses.
3 a hypothesis-generating resource for further
functional analyses.
4 eractions using structural, biophysical, and
functional analyses.
5 y distant species, affinity purification and
functional analyses.
6 ent immunological diseases and complementing
functional analyses.
7 tate modelling analysis were implemented for
functional analyses.
8 n = 14) and subjected them to phenotypic and
functional analyses.
9 ssue can be cultured for days for subsequent
functional analyses.
10 iles, epigenetic studies, and phenotypic and
functional analyses.
11 bling sensitive motif finding and downstream
functional analyses.
12 e system will enable high resolution in vivo
functional analyses.
13 and by screening of SCN9A for mutations and
functional analyses.
14 o prioritize them for further mutational and
functional analyses.
15 varying lengths and types for structural and
functional analyses.
16 force microscopy, solution biophysical, and
functional analyses.
17 CD4(-)), and characterised by phenotypic and
functional analyses.
18 3) expression, as shown by means of in vitro
functional analyses.
19 d neutralizing antibodies for structural and
functional analyses.
20 Moreover, complementary
functional analyses allowed us to identify and validate
21 Functional analyses also revealed a relative enrichment
22 te mapping, parabiotic, transcriptional, and
functional analyses and demonstrated that the heart cont
23 Pathway, network,
functional analyses and gene family classification were
24 Here we show
functional analyses and structural simulations for three
25 was inferred by combining the results of the
functional analyses and their expression patterns in gra
26 ation with results from a range of in silico
functional analyses and wet bench experiments, our findi
27 Functional analyses are needed to explore the biological
28 ntial for protein secretion, structure-based
functional analyses are required to unravel the mechanis
29 Functional analyses associated these alterations with in
30 address this, we performed computational and
functional analyses at MTMR2 to identify transcriptional
31 Transcriptome and in vitro
functional analyses at the single-cell level reveal a co
32 tion studies using mathematical modeling and
functional analyses,
Cheng et al. suggested that LPS-dri
33 The structure, in combination with
functional analyses,
clearly shows how SEB adopts a wedg
34 Gene expression and
functional analyses comparing senescent and non-senescen
35 Functional analyses confirmed a requirement for ERRalpha
36 Bioinformatic and
functional analyses confirmed that Arg2 mRNA is a direct
37 Functional analyses confirmed that Ave1 activates Ve1-me
38 Our structural and
functional analyses demonstrate that both N-terminal and
39 Combined in silico and
functional analyses demonstrate that envelope glycoprote
40 Our
functional analyses demonstrate that gfi1aa and gfi1b ha
41 Functional analyses demonstrate that Jagged1 overexpress
42 Further biochemical and
functional analyses demonstrate that Mob1 mediates Lats1
43 Our structural data together with
functional analyses demonstrate that plant eIF4G binds t
44 Functional analyses demonstrate that the coiled-coil dom
45 Functional analyses demonstrate that these competitive i
46 Functional analyses demonstrate that these mutations con
47 Functional analyses demonstrated CXXC5 to inhibit leukem
48 Functional analyses demonstrated spontaneous inflammasom
49 Functional analyses demonstrated that ERAP1 allotype pai
50 Posterior
functional analyses demonstrated that more rapid kinetic
51 Our in vivo
functional analyses demonstrated that R293A cannot suppo
52 Structure-based
functional analyses demonstrated that the HMW1C protein
53 Functional analyses demonstrated that this region of HBI
54 Histological and
functional analyses documented the initial degeneration
55 Functional analyses encompassing in vitro growth inhibit
56 Ultrastructural and
functional analyses established that MARK4 kinase activi
57 Functional analyses exist only for a few of the morpholo
58 e (AADD; 2n = 52) makes genetic, genomic and
functional analyses extremely challenging.
59 By conducting
functional analyses for orthologs of the flower meristem
60 considered candidates for future genetic and
functional analyses for rice improvement.
61 Then, we performed in silico
functional analyses for these 11 SNPs by eQTL analysis,
62 Comparative and
functional analyses further indicated that the alternati
63 Dynamic and
functional analyses further indicated that the Az1-induc
64 Structural modeling followed by
functional analyses further revealed that phenylalanine-
65 Functional analyses further supported that CYP6P12 contr
66 Principal component and
functional analyses grouped the samples isolated from fo
67 pproaches and transgenesis-based lineage and
functional analyses have been instrumental in decipherin
68 mutation in these syndromes, and no previous
functional analyses have been performed.
69 In addition, the fact that
functional analyses have been undertaken mainly in trypa
70 Extensive
functional analyses have demonstrated that the pituitary
71 However,
functional analyses have never been performed within a s
72 Functional analyses have revealed that a majority of KID
73 s high-resolution structure and accompanying
functional analyses have revealed the molecular mechanis
74 Genetic, structural, and
functional analyses have uncovered a number of commonali
75 Candidate gene approaches and
functional analyses have yielded insights into large fam
76 NMR, mutagenesis and
functional analyses highlight the key role of calcium in
77 Integrated transcriptomic and
functional analyses identified BCL2/adenovirus E1B 19 kD
78 by in silico protein structure modeling and
functional analyses identified five disease-associated a
79 Temporal transcriptome and
functional analyses identified heat shock protein 27 (HS
80 nd genome-wide transcriptional profiling and
functional analyses identified heterogeneity between TSL
81 Proteomics and
functional analyses identified hypoxia-inducible gene 2
82 Combined gene expression, biochemical, and
functional analyses identified mesenchymal cells as the
83 In addition, further molecular and
functional analyses identified Prmt1 as a key common dow
84 Taken together, our genetic and
functional analyses identified REV7 as a previously unde
85 Functional analyses identified the cytidine deaminase AP
86 Functional analyses identifies epigenetics marks, gene o
87 Furthermore, system-level and
functional analyses identify YAP1 as a downstream effect
88 Functional analyses illustrate that lncOL1 interacts wit
89 Additionally, heterologous
functional analyses in Arabidopsis resulted in flowering
90 ical studies in murine neuronal cultures and
functional analyses in Caenorhabditis elegans revealed t
91 sion studies in human clinical biopsies with
functional analyses in cell lines and mouse models.
92 Notably, RNA deep sequencing and
functional analyses in HuR-deficient PDAC cell lines ide
93 Functional analyses in mammalian cells showed all 4 HIFa
94 e findings are currently being extended with
functional analyses in model organisms and genotype-phen
95 and sOPTiKO provide a unique opportunity for
functional analyses in multiple cell types relevant for
96 ization studies in cells and tissues, and by
functional analyses in neuronal morphogenesis we demonst
97 Therefore, there is a need for
functional analyses in rapid and efficient animal models
98 nomes, and summarizing the progress of their
functional analyses in recent years.
99 Functional analyses in vivo show that the mechanism requ
100 monstrating their loss-of-function effect by
functional analyses in zebrafish embryos and cultured hi
101 Functional analyses included in vitro follicular helper
102 We report comprehensive epigenomic and
functional analyses,
including 12 million differentiall
103 distinct cell types through histological and
functional analyses,
including rare subpallial-derived i
104 These data coupled with binding and
functional analyses indicate that F240 recognizes non-tr
105 Genetic studies on disease associations and
functional analyses indicate that FHR-1 enhances complem
106 Ultrastructural and
functional analyses indicate that LD and CD are homologo
107 Functional analyses indicate that MFSD12 encodes a lysos
108 Functional analyses indicate that these macrophages are
109 Functional analyses indicate that, similarly as myo18a,
110 Here, biochemical and
functional analyses localized the putative mechanosensit
111 Further genomic and
functional analyses may help elucidate mechanisms by whi
112 mic elements, along with transcriptional and
functional analyses,
may help to explain why type III st
113 Based on immunophenotype, migration, and
functional analyses,
MERTK-expressing monocytes migrate
114 In agreement with these
functional analyses,
molecular modeling indicated reduce
115 Genetic and
functional analyses of 120 mouse strains have identified
116 We performed structural, thermodynamic, and
functional analyses of a conserved T-cell receptor (TCR)
117 Functional analyses of a diverse group of genes encoding
118 Here, we report on structural and
functional analyses of a set of N-terminal PilQ deletion
119 Previous structural and
functional analyses of arenavirus nucleoproteins (NPs) r
120 Functional analyses of bir2 mutants show differential im
121 Functional analyses of candidate genes identified in thi
122 Here we performed structural and
functional analyses of centralspindlin using high-speed
123 content of the gastrointestinal microbiome,
functional analyses of common microbial gene sets are re
124 the future this hypothesis can be tested by
functional analyses of Cornus B-class genes.
125 also provide a rich database for mining for
functional analyses of cotton improvement or evolution.
126 Functional analyses of cultured GC from these tumors sho
127 munohistochemistry, quantitative RT-PCR, and
functional analyses of cultured Schwann cells.
128 Functional analyses of differentially expressed and diff
129 Functional analyses of differentiated keratinocytes from
130 We performed comparative
functional analyses of disease-associated IFD variants a
131 Functional analyses of disease-linked polymorphic varian
132 Here we present crystallographic and
functional analyses of drug binding to the bacterial hom
133 Functional analyses of EAC-derived mutations in ELMO1 id
134 software tool that enables visualization and
functional analyses of gene clusters would be a great as
135 Moreover, the study demonstrates that
functional analyses of genes carrying DNMs are warranted
136 Topological and
functional analyses of genes in this network uncovered g
137 We also performed
functional analyses of HepG2 cells.
138 Functional analyses of heterozygous KCNQ1 WT:G589D and h
139 e, we have performed detailed structural and
functional analyses of Hhn2b, leading us to identify two
140 Moreover, population and
functional analyses of host-associated nsSNPs for FimH,
141 plantation models, as well as phenotypic and
functional analyses of human biopsy specimens, provide c
142 ment of molecular tools/resources to perform
functional analyses of individuals in isolation and in p
143 Here we present structural and
functional analyses of isolated FlaH and archaellum moto
144 Transcriptomic and
functional analyses of Kras-independent escapers reveal
145 imal and plant proteins, which should enable
functional analyses of lesser characterized SR family me
146 Functional analyses of MADS-box transcription factors in
147 We performed lipidomic and
functional analyses of MFSD2A in mucosal biopsies and pr
148 Here, we present structural and
functional analyses of molecular interactions between hu
149 Here, we present structural and
functional analyses of Mtb TlyA interaction with its obl
150 s, X-ray scattering, biochemical assays, and
functional analyses of mutant PfRad50 complexes show tha
151 The recent discovery and
functional analyses of new classes of noncoding RNAs (nc
152 analysis and next-generation sequencing and
functional analyses of NFKB1 and its mutated alleles.
153 Functional analyses of novel mutations were performed us
154 Here, we report structural and
functional analyses of ObcA, revealing mechanistic featu
155 his study provide a framework for conducting
functional analyses of other NSTs identified in T. bruce
156 Functional analyses of phosphomimetic as well as dimeric
157 These findings provide systematic
functional analyses of PPs in Plasmodium, identify how p
158 Genomic, biochemical and
functional analyses of pre-leukemic thymocytes and tumor
159 Functional analyses of primary samples face at least 3 m
160 c colony assays that enable quantitative and
functional analyses of progenitor-like cells isolated fr
161 f DLBCL and demonstrated their usefulness in
functional analyses of proximal BCR pathway inhibition.
162 Our
functional analyses of PRPS1 mutants uncovered a new che
163 ss of this approach opens the possibility of
functional analyses of ribosomes, with applications in b
164 The results of mutational and
functional analyses of RpLcsB and RpPimA variants led us
165 Functional analyses of selected mutations showed reducti
166 Our study serves as an initial step toward
functional analyses of Sema 1a and Fas I expression duri
167 Through localization studies and
functional analyses of semisynthetic PEGylated Rab1, Rab
168 velopment of a new web based tool to compare
functional analyses of sequence runs within a study.
169 Functional analyses of several in vivo mutants (iv) of t
170 identify a set of candidate genes for future
functional analyses of sex-specific isoform usage.
171 Functional analyses of some of these TFs indicate that t
172 Biochemical, proteomic, and
functional analyses of SVZ NPC-secreted factors revealed
173 power of the approach, performing the first
functional analyses of TBR1 variants identified in spora
174 We use evolutionary and
functional analyses of TfR1 in the rodent clade, where t
175 work for the study of spectral, temporal and
functional analyses of the basal ganglia and lays the fo
176 work for the study of spectral, temporal and
functional analyses of the BG and therefore lays the fou
177 Here, we report the structural and
functional analyses of the Caenorhabditis elegans NXF va
178 Phenotypic and
functional analyses of the cell product were performed b
179 stage is an important element weighting into
functional analyses of the cellular roles of ARF-GEFs.
180 art these forces is an important step toward
functional analyses of the different components of CRNs,
181 Functional analyses of the eVP30-eNP interface identify
182 Our
functional analyses of the Gryllus Blimp-1 ortholog reve
183 ion for performing equivalent structural and
functional analyses of the H17 HA protein.
184 Subsequent bioinformatics and
functional analyses of the human H2-Ob homolog, HLA-DOB,
185 Extensive
functional analyses of the identified mutations in cell
186 In conclusion, these structural and
functional analyses of the industrially favored XynCDBFV
187 of colorectal cancer and performed in vitro
functional analyses of the mutant forms of FAN1 identifi
188 Functional analyses of the mutant proteins revealed a pa
189 Here we have performed structural and
functional analyses of the organic microrings and organi
190 Here, we report structural and
functional analyses of the prototypical molecular bridge
191 Here, we report the structural and
functional analyses of the SOE SorT from Sinorhizobium m
192 Extended
functional analyses of the Stachel sequences and derived
193 Our follow up topological and
functional analyses of the subnetwork revealed that six
194 Functional analyses of the TUBB mutants show multiple de
195 We have performed
functional analyses of the two Arabidopsis (Arabidopsis
196 Functional analyses of these compounds suggest a wide ar
197 Functional analyses of these distinct MP subsets have be
198 Functional analyses of these genes and their pathogenic
199 Functional analyses of these genes revealed an interconn
200 analysis promotes further developmental and
functional analyses of this important system of neurons.
201 ides a basis for experimental validation and
functional analyses of this novel candidate leanness and
202 type diet using RNA sequencing and in silico
functional analyses of transcriptome data.
203 Enrichment
functional analyses of transcriptome profiles drove us t
204 targeted gene sequencing and phenotypic and
functional analyses of Treg cells.
205 Protein-protein interaction and
functional analyses of XND1 deletion mutants were used t
206 We performed
functional analyses on a few widely expressed fusions, a
207 By overlaying these
functional analyses on a phylogenetic framework of Vpr a
208 We carried out targeted
functional analyses on Et skeletogenesis to identify the
209 Importantly,
functional analyses performed in vivo using adoptive tra
210 Functional analyses performed on both affected individua
211 For
functional analyses,
primary cultures of fibroblasts wer
212 This viral catalog and
functional analyses provide a necessary foundation for t
213 Association and
functional analyses provide evidence that the best candi
214 sed single-cell transcriptomics coupled with
functional analyses provides novel insights into how neu
215 The structure, combined with
functional analyses,
provides insight into the mechanism
216 Biochemical and
functional analyses reveal that Fxr1 is a direct substra
217 Furthermore, our genomic and in vivo
functional analyses reveal that retrotransposon sequence
218 Structural and
functional analyses reveal that somatic mutations in FWR
219 Integrated mRNA-miRNA
functional analyses reveal that: 1) several very highly
220 Functional analyses revealed a higher intensity for the
221 Microarray and
functional analyses revealed a reduced ability of mif(-/
222 Transcriptome and
functional analyses revealed alterations in MSC differen
223 The follow-up
functional analyses revealed lower IL-2RA expression upo
224 Functional analyses revealed slight reductions in freque
225 e mining for potential symbiosis factors and
functional analyses revealed that a type 2 secretion sys
226 Functional analyses revealed that amiloride-insensitive,
227 Functional analyses revealed that CnAIP2 plays important
228 High-resolution live imaging and
functional analyses revealed that endodermal cells reach
229 Functional analyses revealed that expression of p63 and
230 However,
functional analyses revealed that PTL treatment prevente
231 Genome-wide transcriptional profiling and
functional analyses revealed that RORgammat(+) ILCs expr
232 Functional analyses revealed that rs800292 was associate
233 Genetic and
functional analyses revealed that the accumulation of SH
234 Functional analyses revealed that the lymphocyte homing
235 Site-directed mutagenesis and
functional analyses revealed that the lysine (K) residue
236 Functional analyses revealed that the risk allele of the
237 Functional analyses revealed that TUBA4A mutants destabi
238 Phylogenetic and
functional analyses revealed the functional conservation
239 System-level and
functional analyses revealed the TGF-beta pathway as a k
240 The combination of structural and
functional analyses reveals that binding avidity dictate
241 Functional analyses show a wider range of effector contr
242 Our structural and
functional analyses show no evidence that the DH domain
243 Functional analyses show six genes that have recurrent c
244 Biochemical and
functional analyses show that adenosine, but not typical
245 Functional analyses show that C1q-mediated inhibition of
246 Our in-vitro and in-vivo
functional analyses show that silencing OPN expression i
247 These structures, together with
functional analyses,
show that 2CARD(RIG-I) acts as a te
248 Functional analyses showed a range of biological pathway
249 Functional analyses showed that Bmal1(lox/lox)/Ren1(d)Cr
250 Functional analyses showed that CHD1 is an essential tum
251 Functional analyses showed that L35P abrogates the PALB2
252 Functional analyses showed that overexpression of AK0173
253 Functional analyses showed that Pla2g16 knockdown decrea
254 Genome-wide location and
functional analyses showed that Tfe3 directly integrates
255 The
functional analyses showed that the mutation results in
256 Here, biochemical and
functional analyses showed that the PulM interaction def
257 of REST encoding the DNA-binding domain, and
functional analyses showed that these mutations compromi
258 ng anthracycline-related cardiotoxicity, and
functional analyses suggest that these genes are influen
259 In another patient, structural and
functional analyses suggested that cones had degenerated
260 We performed computational and
functional analyses that revealed two cis-acting regulat
261 ing technology, permitting compositional and
functional analyses that were previously an unrealistic
262 we show, using X-ray crystal structures and
functional analyses,
that a single molecule of borrelidi
263 e we show, using proteomic, cytological, and
functional analyses,
that autophagosomes are spatially,
264 In
functional analyses the p.R157X variant caused proteasom
265 In
functional analyses,
the mutant FHR-1 protein strongly c
266 the crystal structure of YfcM and performed
functional analyses to determine the hydroxylation mecha
267 y including genetic mapping, sequencing, and
functional analyses to elucidate a mutation to explain t
268 on of genomic information with complementary
functional analyses to identify oncogenic targets and re
269 mbine molecular evolution and structural and
functional analyses to investigate further the high numb
270 of genomics technology, bioinformatics, and
functional analyses to provide new insights into our und
271 Here, we use biophysical and
functional analyses to show that the isolated EAL domain
272 We used immunostaining and
functional analyses to study the hematopoietic compartme
273 non-Watson-Crick pairing) forms, along with
functional analyses,
to show that Pol X uses multiple un
274 Mutagenesis and
functional analyses using agonists to map the odorant-bi
275 Functional analyses using mutant forms of Sarah showed t
276 By a combination of biochemical and
functional analyses we show e37b promotes a form of ubiq
277 By transcriptional and
functional analyses,
we demonstrate that a pool of polyc
278 Using mutagenesis coupled with
functional analyses,
we determined residues of actin and
279 With histological, flow cytometric and
functional analyses,
we find that CPCs remain undifferen
280 bination with a multitude of biophysical and
functional analyses,
we find that Pseudomonas FliD exhib
281 Through mutagenesis and
functional analyses,
we found that the R(340)R(341)GR(34
282 Based on our structural and
functional analyses,
we present the hypothesis that neur
283 On the basis of our structural and
functional analyses,
we propose that CarD functions by f
284 ral insight combined with bioinformatics and
functional analyses,
we show that naturally occurring ca
285 Using a combination of bioinformatics and
functional analyses,
we show that the rate of amplificat
286 Based on our structural and
functional analyses,
we suggest that Na(+) triggers mult
287 th and histological, biochemical, and visual
functional analyses were performed at the end of the exp
288 Functional analyses were performed in Xenopus laevis ooc
289 Genetic, molecular, and
functional analyses were performed to characterize an in
290 Genetic, molecular, and
functional analyses were performed to characterize the L
291 Functional analyses were performed using transport activ
292 se demonstrated >98% correlation and overall
functional analyses were similar.
293 Functional analyses were subsequently conducted using In
294 Genetic, molecular, and
functional analyses were used to identify and characteri
295 Genetic, immunologic, protein, and cellular
functional analyses were used to identify and characteri
296 very similar to AURKB, based on sequence and
functional analyses,
why germ cells express AURKC is unc
297 8-mediated virus inhibition and suggest that
functional analyses will be important for determining wh
298 an Leeuwenhoek"-like cataloguing, as well as
functional analyses,
will likely accelerate as DNA and R
299 at integrating global phosphoproteomics with
functional analyses with kinase inhibitors can identify
300 By combining
functional analyses with RNA sequencing, we explain why