1 from NEUROG3(-/-) pluripotent stem cells for
functional analyses.
2 and generates testable hypotheses for future
functional analyses.
3 tate modelling analysis were implemented for
functional analyses.
4 e system will enable high resolution in vivo
functional analyses.
5 CD4(-)), and characterised by phenotypic and
functional analyses.
6 3) expression, as shown by means of in vitro
functional analyses.
7 d neutralizing antibodies for structural and
functional analyses.
8 ses; these are compelling targets for future
functional analyses.
9 and carried out a series of statistical and
functional analyses.
10 a hypothesis-generating resource for further
functional analyses.
11 eractions using structural, biophysical, and
functional analyses.
12 y distant species, affinity purification and
functional analyses.
13 ent immunological diseases and complementing
functional analyses.
14 n = 14) and subjected them to phenotypic and
functional analyses.
15 by validation of the hits by biochemical and
functional analyses.
16 gs, this work could be used to guide further
functional analyses.
17 cipient for 1 week and conducted RNA-Seq and
functional analyses.
18 tical step in gene expression and subsequent
functional analyses.
19 of inferior cell lines and a lack of proper
functional analyses.
20 obiota on IBD etiology requires larger-scale
functional analyses.
21 s to interpret metagenome datasets and guide
functional analyses.
22 encing of 111 TAM and 141 ML-DS samples with
functional analyses.
23 Moreover, complementary
functional analyses allowed us to identify and validate
24 Our
functional analyses allowed us to probe the molecular de
25 The structural and
functional analyses,
along with computational studies, r
26 Functional analyses also indicated that GMB lipid metabo
27 Functional analyses also indicated that GMB lipid metabo
28 structures, together with computational and
functional analyses and a mutant channel structure, reve
29 te mapping, parabiotic, transcriptional, and
functional analyses and demonstrated that the heart cont
30 Here we show
functional analyses and structural simulations for three
31 was inferred by combining the results of the
functional analyses and their expression patterns in gra
32 ation with results from a range of in silico
functional analyses and wet bench experiments, our findi
33 of X-ray crystallography, NMR spectroscopy,
functional analyses,
and kinetic modeling to reveal the
34 ing comparative metabolomic, transcriptomic,
functional analyses,
and unsupervised machine learning (
35 While physical and
functional analyses are generally used to determine the
36 Nevertheless,
functional analyses are hindered by incompletely modeled
37 Functional analyses are needed to explore the biological
38 Several
functional analyses are performed on this model to study
39 ntial for protein secretion, structure-based
functional analyses are required to unravel the mechanis
40 Phylogenetic and
functional analyses associated the occurrence of a funct
41 Functional analyses associated these alterations with in
42 address this, we performed computational and
functional analyses at MTMR2 to identify transcriptional
43 Transcriptome and in vitro
functional analyses at the single-cell level reveal a co
44 tion studies using mathematical modeling and
functional analyses,
Cheng et al. suggested that LPS-dri
45 The structure, in combination with
functional analyses,
clearly shows how SEB adopts a wedg
46 Gene expression and
functional analyses comparing senescent and non-senescen
47 Functional analyses confirmed a requirement for ERRalpha
48 Bioinformatic and
functional analyses confirmed that Arg2 mRNA is a direct
49 Our structures, in combination with
functional analyses,
delineate a structural mechanism by
50 Functional analyses demonstrate that Jagged1 overexpress
51 Further biochemical and
functional analyses demonstrate that Mob1 mediates Lats1
52 Our structural data together with
functional analyses demonstrate that plant eIF4G binds t
53 Lineage tracing and
functional analyses demonstrate that the majority of adu
54 Functional analyses demonstrate that these competitive i
55 Functional analyses demonstrate that these mutations con
56 Functional analyses demonstrated CXXC5 to inhibit leukem
57 Functional analyses demonstrated spontaneous inflammasom
58 Functional analyses demonstrated that Eip1p is important
59 Functional analyses demonstrated that in addition the kn
60 Posterior
functional analyses demonstrated that more rapid kinetic
61 ground of 17 Malus species combined with the
functional analyses described above indicate that Ma1 pl
62 Upon
functional analyses during mouse male meiosis, we demons
63 Functional analyses encompassing in vitro growth inhibit
64 SERBP1-binding motif; subsequent genomic and
functional analyses establish SERBP1 regulation role in
65 Functional analyses exist only for a few of the morpholo
66 e (AADD; 2n = 52) makes genetic, genomic and
functional analyses extremely challenging.
67 By conducting
functional analyses for orthologs of the flower meristem
68 considered candidates for future genetic and
functional analyses for rice improvement.
69 Then, we performed in silico
functional analyses for these 11 SNPs by eQTL analysis,
70 Dynamic and
functional analyses further indicated that the Az1-induc
71 Structural modeling followed by
functional analyses further revealed that phenylalanine-
72 Functional analyses further supported that CYP6P12 contr
73 Principal component and
functional analyses grouped the samples isolated from fo
74 mutation in these syndromes, and no previous
functional analyses have been performed.
75 mary afferents has been well described, most
functional analyses have focused on the regulation of tr
76 However,
functional analyses have never been performed within a s
77 Functional analyses have revealed that a majority of KID
78 s high-resolution structure and accompanying
functional analyses have revealed the molecular mechanis
79 Genetic, structural, and
functional analyses have uncovered a number of commonali
80 Candidate gene approaches and
functional analyses have yielded insights into large fam
81 NMR, mutagenesis and
functional analyses highlight the key role of calcium in
82 Finally, comparative and
functional analyses identified 351 sites hypervariable a
83 by in silico protein structure modeling and
functional analyses identified five disease-associated a
84 Proteomics and
functional analyses identified hypoxia-inducible gene 2
85 In addition, further molecular and
functional analyses identified Prmt1 as a key common dow
86 Taken together, our genetic and
functional analyses identified REV7 as a previously unde
87 Functional analyses identified the cytidine deaminase AP
88 Functional analyses identifies epigenetics marks, gene o
89 Our
functional analyses identify a Ctf19c(CCAN)-dependent ki
90 Furthermore, system-level and
functional analyses identify YAP1 as a downstream effect
91 Functional analyses illustrate that lncOL1 interacts wit
92 Here, we report genetic and
functional analyses implicating the rat sarcoma signalin
93 We combined lineage tracing and
functional analyses in a sequential dual-recombinase app
94 We performed
functional analyses in a zebrafish popdc3 knockdown mode
95 Additionally, heterologous
functional analyses in Arabidopsis resulted in flowering
96 ementation, and behavioral, biochemical, and
functional analyses in Caenorhabditis elegans As capsaic
97 ical studies in murine neuronal cultures and
functional analyses in Caenorhabditis elegans revealed t
98 sion studies in human clinical biopsies with
functional analyses in cell lines and mouse models.
99 Notably, RNA deep sequencing and
functional analyses in HuR-deficient PDAC cell lines ide
100 Functional analyses in mammalian cells showed all 4 HIFa
101 e findings are currently being extended with
functional analyses in model organisms and genotype-phen
102 yloid toxicity and forms a basis for further
functional analyses in model organisms and translation t
103 and sOPTiKO provide a unique opportunity for
functional analyses in multiple cell types relevant for
104 (CRISPR)-CRISPR-associated protein 9 (Cas9)
functional analyses in Parhyale, we show that a gene net
105 Therefore, there is a need for
functional analyses in rapid and efficient animal models
106 nomes, and summarizing the progress of their
functional analyses in recent years.
107 sing cryo-electron microscopy and a range of
functional analyses in vitro.
108 monstrating their loss-of-function effect by
functional analyses in zebrafish embryos and cultured hi
109 ro tail-anchored protein insertion assay and
functional analyses in zebrafish.
110 Functional analyses included in vitro follicular helper
111 es (1,456 IPF cases and 11,874 controls) and
functional analyses (
including statistical fine-mapping,
112 We report comprehensive epigenomic and
functional analyses,
including 12 million differentially
113 distinct cell types through histological and
functional analyses,
including rare subpallial-derived i
114 These data coupled with binding and
functional analyses indicate that F240 recognizes non-tr
115 Genetic studies on disease associations and
functional analyses indicate that FHR-1 enhances complem
116 Ultrastructural and
functional analyses indicate that LD and CD are homologo
117 Functional analyses indicate that MFSD12 encodes a lysos
118 Functional analyses indicate that Pol theta/TMEJ addicti
119 Functional analyses indicate that, similarly as myo18a,
120 Initial
functional analyses indicated that the interaction with
121 Interestingly, our
functional analyses indicated that this particular noncy
122 Here, biochemical and
functional analyses localized the putative mechanosensit
123 mic elements, along with transcriptional and
functional analyses,
may help to explain why type III st
124 Based on immunophenotype, migration, and
functional analyses,
MERTK-expressing monocytes migrate
125 In agreement with these
functional analyses,
molecular modeling indicated reduce
126 Genetic and
functional analyses of 120 mouse strains have identified
127 Functional analyses of a diverse group of genes encoding
128 Here we carried out
functional analyses of a flagellar axonemal inner-arm dy
129 her a gene of interest is essential, perform
functional analyses of a lethal gene, and analyze corres
130 we present phylogenetic, biogeographic, and
functional analyses of a previously unrecognized RepL-ty
131 Previous structural and
functional analyses of arenavirus nucleoproteins (NPs) r
132 ption and serves as a resource to aid future
functional analyses of ASFV genes which are essential to
133 der to elucidate the mechanism, we performed
functional analyses of B4GALNT1-overexpressing cells.
134 Functional analyses of bir2 mutants show differential im
135 Functional analyses of candidate genes identified in thi
136 Here we performed structural and
functional analyses of centralspindlin using high-speed
137 In this study,
functional analyses of CpRbp1 were performed by construc
138 Functional analyses of cultured GC from these tumors sho
139 munohistochemistry, quantitative RT-PCR, and
functional analyses of cultured Schwann cells.
140 Functional analyses of differentiated keratinocytes from
141 We performed comparative
functional analyses of disease-associated IFD variants a
142 Here we present crystallographic and
functional analyses of drug binding to the bacterial hom
143 Transcriptomic and
functional analyses of ECs following SOX7 depletion esta
144 Moreover, the study demonstrates that
functional analyses of genes carrying DNMs are warranted
145 Topological and
functional analyses of genes in this network uncovered g
146 However, previous
functional analyses of Grin1 variants have been done usi
147 We also performed
functional analyses of HepG2 cells.
148 e, we have performed detailed structural and
functional analyses of Hhn2b, leading us to identify two
149 Moreover, population and
functional analyses of host-associated nsSNPs for FimH,
150 ttering (SAXS), coupled with biochemical and
functional analyses of human RSV (hRSV) N(Delta30) mutan
151 In addition, genetic and
functional analyses of I-ribosomes and target mRNAs sugg
152 ment of molecular tools/resources to perform
functional analyses of individuals in isolation and in p
153 To address this, we performed detailed
functional analyses of insulin granules purified from ce
154 at agreed well with previous biochemical and
functional analyses of IRR.
155 Here we present structural and
functional analyses of isolated FlaH and archaellum moto
156 Transcriptomic and
functional analyses of Kras-independent escapers reveal
157 ermore, in trans complementation allowed for
functional analyses of lethal orthologs.
158 Functional analyses of MADS-box transcription factors in
159 Detailed
functional analyses of many fundamentally important plan
160 Functional analyses of meiosis-specific interactors of M
161 these transporters, previous structural and
functional analyses of members of the MATE subfamily Din
162 We performed lipidomic and
functional analyses of MFSD2A in mucosal biopsies and pr
163 Here, we present structural and
functional analyses of molecular interactions between hu
164 Here, we present structural and
functional analyses of Mtb TlyA interaction with its obl
165 s, X-ray scattering, biochemical assays, and
functional analyses of mutant PfRad50 complexes show tha
166 The recent discovery and
functional analyses of new classes of noncoding RNAs (nc
167 analysis and next-generation sequencing and
functional analyses of NFKB1 and its mutated alleles.
168 x vivo, in vivo, and in vitro phenotypic and
functional analyses of patients' CD4(+) T cells and a no
169 These data imply that further
functional analyses of PITG_04584 may contribute to new
170 These findings provide systematic
functional analyses of PPs in Plasmodium, identify how p
171 f DLBCL and demonstrated their usefulness in
functional analyses of proximal BCR pathway inhibition.
172 Our
functional analyses of PRPS1 mutants uncovered a new che
173 Expression and
functional analyses of PunPgp-2 and PunPgp-9 in Saccharo
174 Our data call for
functional analyses of putative cancer drivers to guide
175 The results of mutational and
functional analyses of RpLcsB and RpPimA variants led us
176 velopment of a new web based tool to compare
functional analyses of sequence runs within a study.
177 Functional analyses of several in vivo mutants (iv) of t
178 identify a set of candidate genes for future
functional analyses of sex-specific isoform usage.
179 Biochemical, proteomic, and
functional analyses of SVZ NPC-secreted factors revealed
180 , combined with deep-phenotypic, spatial and
functional analyses of synovial biopsy fluorescent activ
181 work for the study of spectral, temporal and
functional analyses of the basal ganglia and lays the fo
182 work for the study of spectral, temporal and
functional analyses of the BG and therefore lays the fou
183 , lymphocyte characterization, molecular and
functional analyses of the DNA polymerase delta (Poldelt
184 Functional analyses of the eVP30-eNP interface identify
185 Our
functional analyses of the Gryllus Blimp-1 ortholog reve
186 Subsequent bioinformatics and
functional analyses of the human H2-Ob homolog, HLA-DOB,
187 Extensive
functional analyses of the identified mutations in cell
188 In conclusion, these structural and
functional analyses of the industrially favored XynCDBFV
189 of colorectal cancer and performed in vitro
functional analyses of the mutant forms of FAN1 identifi
190 Functional analyses of the mutant proteins revealed a pa
191 Here we have performed structural and
functional analyses of the organic microrings and organi
192 Here, we report structural and
functional analyses of the prototypical molecular bridge
193 Here, we report the structural and
functional analyses of the SOE SorT from Sinorhizobium m
194 Extended
functional analyses of the Stachel sequences and derived
195 Functional analyses of the TUBB mutants show multiple de
196 Our
functional analyses of the ZFX family provides important
197 Functional analyses of these compounds suggest a wide ar
198 Functional analyses of these genes and their pathogenic
199 Comprehensive
functional analyses of these genes confirmed the previou
200 Functional analyses of these genes revealed an interconn
201 Post-GWAS
functional analyses of these loci revealed their potenti
202 Functional analyses of these miRNAs indicated that their
203 analysis promotes further developmental and
functional analyses of this important system of neurons.
204 ides a basis for experimental validation and
functional analyses of this novel candidate leanness and
205 Our biochemical and
functional analyses of this vertebrate-specific protein
206 type diet using RNA sequencing and in silico
functional analyses of transcriptome data.
207 targeted gene sequencing and phenotypic and
functional analyses of Treg cells.
208 Protein-protein interaction and
functional analyses of XND1 deletion mutants were used t
209 We performed
functional analyses on a few widely expressed fusions, a
210 We carried out targeted
functional analyses on Et skeletogenesis to identify the
211 Functional analyses performance (i.e. urea and albumin p
212 Importantly,
functional analyses performed in vivo using adoptive tra
213 Functional analyses predicted a reduced frequency of sig
214 Functional analyses predicted that gene expression chang
215 For
functional analyses,
primary cultures of fibroblasts wer
216 This viral catalog and
functional analyses provide a necessary foundation for t
217 In silico
functional analyses provide evidence for a role of T cel
218 Association and
functional analyses provide evidence that the best candi
219 Functional analyses reveal both sponge-associated microb
220 Biochemical and
functional analyses reveal that Fxr1 is a direct substra
221 Significantly, gene array and
functional analyses reveal that iPSC-derived fibroblasts
222 Furthermore, our genomic and in vivo
functional analyses reveal that retrotransposon sequence
223 The structure together with
functional analyses reveal that the B56gamma (B'gamma) s
224 Our cryo-EM, biochemical, and
functional analyses reveal the binding mode of three che
225 Microarray and
functional analyses revealed a reduced ability of mif(-/
226 Transcriptome and
functional analyses revealed alterations in MSC differen
227 Genome-wide analyses combined to
functional analyses revealed an increase of mitochondria
228 Functional analyses revealed improved systolic performan
229 The follow-up
functional analyses revealed lower IL-2RA expression upo
230 Structural and
functional analyses revealed that both elements promote
231 Functional analyses revealed that ectopic expression of
232 High-resolution live imaging and
functional analyses revealed that endodermal cells reach
233 Functional analyses revealed that expression of p63 and
234 Functional analyses revealed that homotypic interactions
235 Functional analyses revealed that overrepresented pathwa
236 Genetic and
functional analyses revealed that the accumulation of SH
237 Functional analyses revealed that the lymphocyte homing
238 Site-directed mutagenesis and
functional analyses revealed that the lysine (K) residue
239 Phylogenetic and
functional analyses revealed the functional conservation
240 Further phenotypic and
functional analyses revealed the identity of this B220(+
241 System-level and
functional analyses revealed the TGF-beta pathway as a k
242 Functional analyses reveals that ARID4B is required for
243 The combination of structural and
functional analyses reveals that binding avidity dictate
244 h detailed ultrastructural, biochemical, and
functional analyses reveals the distinct composition of
245 Our structural and
functional analyses show no evidence that the DH domain
246 Functional analyses show six genes that have recurrent c
247 Biochemical and
functional analyses show that adenosine, but not typical
248 Functional analyses showed that Bmal1(lox/lox)/Ren1(d)Cr
249 Expression and
functional analyses showed that GmSHMT genes display man
250 Functional analyses showed that L35P abrogates the PALB2
251 Computational, crystal structural, and gene
functional analyses showed that one of these 48 proteins
252 Functional analyses showed that overexpression of AK0173
253 munopurification, mass spectrometry and gene
functional analyses showed that Sir2 levels responded to
254 ith the results of transcriptomic profiling,
functional analyses showed that the cMSC secretome suppr
255 Finally,
functional analyses showed that the downregulation of CD
256 The
functional analyses showed that the mutation results in
257 Here, biochemical and
functional analyses showed that the PulM interaction def
258 of REST encoding the DNA-binding domain, and
functional analyses showed that these mutations compromi
259 p.Gln72Leu), have been found in cancers; our
functional analyses showed that these three changes indu
260 Functional analyses suggest that LumP and PrU cells have
261 Our structural and
functional analyses suggest that rho, and other terminat
262 ng anthracycline-related cardiotoxicity, and
functional analyses suggest that these genes are influen
263 Functional analyses suggest: (1) cellular metabolic flux
264 Functional analyses suggested stronger donor-reactive im
265 esidue Glu(49) of TatB from Escherichia coli
Functional analyses suggested that by interacting with t
266 and a series of multidisciplinary structural/
functional analyses that dissect the various states of t
267 - angstrom resolution and used this to guide
functional analyses that reveal how AcaB binds to DNA.
268 ing technology, permitting compositional and
functional analyses that were previously an unrealistic
269 we show, using X-ray crystal structures and
functional analyses,
that a single molecule of borrelidi
270 In
functional analyses the p.R157X variant caused proteasom
271 In
functional analyses,
the mutant FHR-1 protein strongly c
272 combining computational, morphological, and
functional analyses,
this study relates latent markers o
273 of genomics technology, bioinformatics, and
functional analyses to provide new insights into our und
274 We used immunostaining and
functional analyses to study the hematopoietic compartme
275 In addition,
functional analyses uncovered detrimental effects of man
276 Mutagenesis and
functional analyses using agonists to map the odorant-bi
277 Functional analyses using cell lines provide supporting
278 Functional analyses using CRISPR/dead(d)Cas9 targeting o
279 Using comparative sequence, structural, and
functional analyses,
we characterize the evolution and m
280 Using single-cell RNA sequencing and
functional analyses,
we find that neonatal microglia are
281 bination with a multitude of biophysical and
functional analyses,
we find that Pseudomonas FliD exhib
282 Through mutagenesis and
functional analyses,
we found that the R(340)R(341)GR(34
283 Utilizing bioinformatic and
functional analyses,
we identified over 100 genes with c
284 creening a yeast mutant library, followed by
functional analyses,
we identified the glutamine permeas
285 Through structural and
functional analyses,
we identify variable structural fea
286 Based on our structural and
functional analyses,
we present the hypothesis that neur
287 ral insight combined with bioinformatics and
functional analyses,
we show that naturally occurring ca
288 Using a combination of bioinformatics and
functional analyses,
we show that the rate of amplificat
289 Functional analyses were additionally performed in a gen
290 Functional analyses were performed in Xenopus laevis ooc
291 Thus, to confirm this finding, supportive
functional analyses were performed on Shroom3 in mice us
292 Genetic, molecular, and
functional analyses were performed to characterize an in
293 Functional analyses were performed using transport activ
294 se demonstrated >98% correlation and overall
functional analyses were similar.
295 Genetic, molecular, and
functional analyses were used to identify and characteri
296 Genetic, immunologic, protein, and cellular
functional analyses were used to identify and characteri
297 exciting results are discovered through such
functional analyses,
which offer new insights about what
298 an Leeuwenhoek"-like cataloguing, as well as
functional analyses,
will likely accelerate as DNA and R
299 By combining transcriptomic and
functional analyses with a chimeric AD mouse model, we f
300 By combining
functional analyses with RNA sequencing, we explain why