1 pecific transcriptional coregulator Fog2 for
functional analysis.
2 c, and epigenetic studies, and complementary
functional analysis.
3 s widely adopted in integrated pipelines for
functional analysis.
4 ort was followed at different timepoints for
functional analysis.
5 entification of novel alleles and subsequent
functional analysis.
6 fficult to purify, preventing structural and
functional analysis.
7 sulting gene lists to Enrichr for downstream
functional analysis.
8 me annotation, gene dynamics and comparative
functional analysis.
9 sses pose major challenges to structural and
functional analysis.
10 ng, exome sequencing, Sanger sequencing, and
functional analysis.
11 anscripts can then be extracted for advanced
functional analysis.
12 rther taxonomic profiling and down-streaming
functional analysis.
13 at have been validated with fine-mapping and
functional analysis.
14 is to our knowledge the first structural and
functional analysis,
along with an in-depth comparison,
15 biotechnological applications including gene
functional analysis and antimicrobial target validation
16 e novel methods provide ideal approaches for
functional analysis and biomarker discovery of ECs- and
17 ogy of psoriasis, suggesting new avenues for
functional analysis and improved therapies.
18 Functional analysis and in vitro experiments confirmed g
19 etailed transcriptomic, flow cytometric, and
functional analysis and transcription factor-deficient m
20 assignments, residual dipolar coupling data,
functional analysis,
and a structural model of GCAP1 mut
21 These gaps need to be filled to enable
functional analysis,
and gap-filling choices influence m
22 tion, evolutionary reconstruction, community
functional analysis,
and metabolic engineering.
23 HUS, illustrate the importance of performing
functional analysis,
and support the use of complementar
24 e community was dominated by haloarchaea and
functional analysis attributed most of the autotrophic C
25 hat it not only can reduce the complexity of
functional analysis by grouping thousands of genes into
26 In-depth
functional analysis by subcellular protein localization,
27 Left ventricular
functional analysis can be performed easily and reliably
28 Structural and
functional analysis characterized core enzymes and ident
29 Functional analysis confirmed inactivating CYLD mutation
30 significantly associated with fertility and
functional analysis confirmed that sperm from bulls poss
31 Additional
functional analysis demonstrated increased total carbon
32 Functional analysis demonstrated that c.202G > A and c.6
33 Functional analysis demonstrated that IL-10DC-related so
34 Instead, single-cell molecular and
functional analysis demonstrated that most fetal T-IPs e
35 In vitro
functional analysis demonstrated that the GLRA2(Deltaex8
36 Targeted mutagenesis and
functional analysis demonstrated that the increased GSTP
37 Functional analysis demonstrates that a subset of CSLD g
38 This concerted biophysical and
functional analysis demonstrates that HiGlpG, with a sim
39 Functional analysis determined that DOCK10, ITGA11, DAB2
40 While
functional analysis disfavored the HIF2alpha:ARNT hetero
41 To test this hypothesis by
functional analysis,
double mutants of the flounder SLC3
42 However, a systematic and
functional analysis for an entire family of KMT or KDM e
43 mology search is still a significant step in
functional analysis for genomic data.
44 omprehensive bioinformatics and experimental
functional analysis for the region.
45 Functional analysis found ABTs were enriched in motifs f
46 Functional analysis found that the RNA structure in MYB3
47 Functional analysis further implicates a critical role o
48 In vitro
functional analysis further revealed multiple prometasta
49 Functional analysis further revealed that rifampicin can
50 Our
functional analysis further showed that RAY3 promotes an
51 ntial gene expression, alternative splicing,
functional analysis,
gene fusion detection and eQTL mapp
52 Functional analysis highlighted biological processes str
53 Functional analysis highlighted the roles of interferon
54 Functional analysis identified interferon-related pathwa
55 Our
functional analysis identifies CLUH as a cytosolic messe
56 Cross-sectional clinical, serological and
functional analysis in 25 consecutive participants with
57 Functional analysis in a responding patient demonstrated
58 At this time point,
functional analysis in astrocytes revealed a decrease in
59 elet development for gene identification and
functional analysis in barley (Hordeum vulgare).
60 Functional analysis in both B. oleracea and the model Ar
61 Functional analysis in cultured cells overexpressing FLA
62 Previous studies on structural-
functional analysis in patients with AMD with reticular
63 zation of soybean WRKY gene family and their
functional analysis in resistance to soybean cyst nemato
64 ilin phosphorylation in mammalian cells, and
functional analysis in S. cerevisiae.
65 Functional analysis in the developing zebrafish embryo d
66 ntified by genetic association studies or by
functional analysis in the laboratory, both of which are
67 Functional analysis in vivo revealed impaired monocyte c
68 Functional analysis indicated a whole system response du
69 Functional analysis indicated that TGF-beta3 contributed
70 Functional analysis indicated that the cancer risk allel
71 Functional analysis indicated that the characteristic pr
72 these resources provide key information for
functional analysis,
modeling and simulation both in ind
73 is conserved in the fungus Sordaria However,
functional analysis of 13 mer2 mutants and successive lo
74 Functional analysis of 51 experimentally validated miR-2
75 Here we report the identification and
functional analysis of a Dorsal homologue (MsDorsal) and
76 Here we describe the identification and
functional analysis of a novel PCNA interacting protein
77 Here, we describe the initial
functional analysis of a poorly characterized human lncR
78 g in the patient and parents was followed by
functional analysis of a prioritized candidate gene with
79 Analogous to the human NPSR1 risk isoform,
functional analysis of a synonymous single nucleotide po
80 l annotations we describe will impact on the
functional analysis of a variety of future autism-releva
81 ur approach should enable massively parallel
functional analysis of a wide range of CREs in any organ
82 Functional analysis of AlgG mutants suggests that His(31
83 Here,
functional analysis of aminophenyl-1,3,5-triazine analog
84 Furthermore,
functional analysis of an E809A mutant showed that the c
85 Functional analysis of an indel variant (c.3607+3_6del)
86 n 2 of the 3 patient alleles was observed by
functional analysis of ANGPT1 variants in a combined in
87 comprehensive and improved morphological and
functional analysis of any visualized duct system.
88 across sample cohorts is a prerequisite for
functional analysis of biological processes.
89 monocytes and prompt further ontogenetic and
functional analysis of CD14(+) CD1c(+) and LPS-activated
90 A
functional analysis of ChoA identified 2 amino acids tha
91 We performed extensive phenotypic and
functional analysis of circulating TFH (cTFH) and B cell
92 minal dileucine-like motifs was required for
functional analysis of ClC-3a and ClC-3b.
93 The systematic
functional analysis of combinatorial genetics has been l
94 Functional analysis of concatemeric channels, which perm
95 P and GhSFT expression enabled unprecedented
functional analysis of cotton development.
96 Functional analysis of DEGs in placental and endometrial
97 NA-Seq) is a powerful and versatile tool for
functional analysis of different types of RNA molecules,
98 rams of biological processes widely used for
functional analysis of differentially expressed genes or
99 Functional analysis of differentially expressed miRNAs v
100 Functional analysis of differentially methylated CpG sit
101 These results highlight that
functional analysis of disease-associated SNPs on gene e
102 Here we report
functional analysis of Drosophila Ataxin 2-binding prote
103 Functional analysis of ECONEXIN in glioma cell lines, U8
104 Here we describe
functional analysis of eight previously uncharacterized
105 Functional analysis of essential genes in the malarial p
106 nable sophisticated comparative genomics and
functional analysis of fungal pathogens in silico.
107 e offering a user-friendly interface for the
functional analysis of gene expression and genomic data.
108 Groupwise
functional analysis of gene variants is becoming standar
109 son of multiple genomes provides signals for
functional analysis of genes and the evolutionary proces
110 we describe a strategy for facile and rapid
functional analysis of genes using an approach based on
111 Our unbiased discovery and
functional analysis of genes with regional expression in
112 Functional analysis of genes within these modules reveal
113 yogenesis, to serve as a resource for future
functional analysis of genes, and as a basis for compara
114 d mutagenesis in mice is a powerful tool for
functional analysis of genes.
115 didate functional SNPs within a locus during
functional analysis of genome-wide association studies.
116 Functional analysis of hearing in the resulting Xirp2-nu
117 rovide previously unidentified insights into
functional analysis of HER2 mutations and strategies to
118 Here, we report a molecular and
functional analysis of HMS1, a region of 9.2 kb in chrom
119 Here, we report crystal structures and
functional analysis of human anillin and S. pombe Mid1.
120 efficient procedure that permits large-scale
functional analysis of human disease-linked mutations es
121 This is the first extensive
functional analysis of human FX neurons derived in vitro
122 Functional analysis of identified and unidentified paras
123 the expanding data sets, as well as expanded
functional analysis of implicated proteins and mutations
124 urce for further targeted identification and
functional analysis of in vivo sites.
125 Functional analysis of individual fibroblasts disclosed
126 A lack of tools thus constrains the
functional analysis of influenza virus-encoded proteins.
127 Functional analysis of isolated renal macrophages showed
128 tivity and provides a foundation for further
functional analysis of key phosphosites involved in pres
129 The synthesis and
functional analysis of KL001 derivatives, which are modu
130 protein interactions are urgently needed for
functional analysis of large-scale genomics and proteomi
131 study now provides the basis for a detailed
functional analysis of malignant transformation of matur
132 In the
functional analysis of metagenomes, the features may ref
133 FMAP is a comprehensive tool for providing
functional analysis of metagenomic/metatranscriptomic se
134 Through transcriptional and
functional analysis of murine Kras(G12D) -p53(null) , -p
135 Functional analysis of mutant proteins with missense sub
136 ring the transport cycle, as demonstrated by
functional analysis of mutants with charge-reversed netw
137 Functional analysis of NCKX4-deficient mouse cones revea
138 recently enabled saturation mutagenesis and
functional analysis of nearly all possible variants of r
139 ring locus T-10 (ft-10)) lines were used for
functional analysis of nematode infective and reproducti
140 sults are the first to provide an integrated
functional analysis of neutrophil FcgammaR haplotypes an
141 his dataset provides a framework for further
functional analysis of newly identified IL-4-regulated p
142 Functional analysis of NK cells shows a significant impa
143 In vitro
functional analysis of NKp46+ CD3+ cells confirm that NK
144 Functional analysis of one of these variants, M932L/V991
145 Here we report fine-mapping and
functional analysis of one such locus residing in a 610
146 Functional analysis of osteoclast progenitors isolated f
147 Histopathological and
functional analysis of ovaries from these mutant mice (C
148 results from a global circRNA expression and
functional analysis of patients with hepatocellular carc
149 of circulating avian viruses and for further
functional analysis of PB2.
150 Our studies broadly enable the
functional analysis of physiological RNA structures and
151 Here, we performed a
functional analysis of Plk4's structural domains.
152 We provide here a comparative structural and
functional analysis of pNS3h with respect to its ortholo
153 Functional analysis of PNTs revealed their widespread ro
154 e can be used by data analysis pipelines for
functional analysis of processed genomics data.
155 ighlights the broad applicability of AID for
functional analysis of proteins across the Plasmodium li
156 ts represent the most complete computational
functional analysis of proteins comprising the Prx super
157 Functional analysis of PSD and non-PSD interactomes illu
158 In PBMCs both quantitative and
functional analysis of regulatory T (Treg) and TH17 cell
159 Comparative
functional analysis of reporter constructs reveals that
160 ISPR)-Cas9 platform for in situ high-content
functional analysis of RREs.
161 Functional analysis of rs3731217 suggests it is associat
162 In vitro
functional analysis of selected co-occupied elements ver
163 by depleting E6/E7 in relevant cells and by
functional analysis of selected genes in vitro.
164 Functional analysis of selected lncRNAs with altered exp
165 Functional analysis of selected transcription factors re
166 We further highlight recent applications in
functional analysis of single cells and in label-free de
167 SomamiR 2.0 to make it a better platform for
functional analysis of somatic mutations altering miRNA-
168 y (SD-OCT) technology that enables real-time
functional analysis of sorting microparticles and cells
169 Moreover, ProteoModlR enables
functional analysis of sparsely sampled quantitative mas
170 larization assays, as well as phenotypic and
functional analysis of STAT1-mutated patient cells.
171 Functional analysis of SWEET2 activity in yeast showed l
172 on of neuronal circuits, a process requiring
functional analysis of synaptic connections and morpholo
173 ies were undertaken, alongside comprehensive
functional analysis of T cells targeted at the natural v
174 Functional analysis of T-cell responses in HIV-infected
175 ase-mediated mutation is a powerful tool for
functional analysis of tandem genes in secondary metabol
176 We carried out a comprehensive
functional analysis of the ADAMTS13 cysteine-rich (Cys-r
177 Epa family, we have performed a large scale
functional analysis of the adhesion (A) domains of 17 Ep
178 We report here an in-depth structural and
functional analysis of the anophelin family member cE5,
179 Functional analysis of the Arg320His mutant channel show
180 Functional analysis of the basic helix-loop-helix (bHLH)
181 We validate our predictions by
functional analysis of the bHLH TF OLIG2.
182 In conclusion, our phenome-based
functional analysis of the C. neoformans TF mutant libra
183 Here, we present a detailed structural and
functional analysis of the Catenulisporales acidiphilia
184 Our results provide the first detailed
functional analysis of the Cav1.4 subunits that form nat
185 Functional analysis of the cleavable RTKs indicated that
186 Functional analysis of the data indicates that there was
187 Functional analysis of the deleterious mutants revealed
188 Functional analysis of the differentially expressed gene
189 Functional analysis of the differentially expressed tran
190 Functional analysis of the FHR1 fraction purified from s
191 re was maintained to the level of class, and
functional analysis of the genes present also displayed
192 The
functional analysis of the HPR motif unveils the existen
193 Surprisingly,
functional analysis of the interaction between eIF3 and
194 Functional analysis of the LASP-1 knockdown cells reveal
195 Functional analysis of the ligands, named ipglycermides,
196 Functional analysis of the MAP3K5 R256C mutation reveale
197 Functional analysis of the module genes revealed four ge
198 Functional analysis of the mutations in MYCN, PTPN14 and
199 gulation is a viable alternative approach to
functional analysis of the P. falciparum genome.
200 using diverse sources of information such as
functional analysis of the pathways and therapeutic uses
201 Here, we have conducted a
functional analysis of the PCSK6 locus combining further
202 lies in non-flowering plants, we performed a
functional analysis of the PEBP gene AcMFT of the MFT cl
203 hods are currently available for large-scale
functional analysis of the Plasmodium falciparum genome.
204 Functional analysis of the predicted mRNA targets of der
205 Both, the expression yields and
functional analysis of the protein were reported.
206 Functional analysis of the R390Q substitution revealed t
207 Functional analysis of the respective genetic signatures
208 Here, we performed an in-depth
functional analysis of the risk locus proximal to the PH
209 Functional analysis of the role of different T-cell subs
210 We therefore undertook a structural and
functional analysis of the role of reactive cysteine res
211 This approach provides a model for
functional analysis of the single subunits within a mult
212 Detailed
functional analysis of the top candidate splicing factor
213 Functional analysis of the transient changes in middle a
214 Functional analysis of the truncated NOR Nlrp1b protein
215 Here, we report structural and
functional analysis of the VQ protein family from soybea
216 ir differentiation that are relevant for the
functional analysis of their different microbiomes, and
217 Functional analysis of these cells revealed a partially
218 This study will facilitate the
functional analysis of these genes and provide new resou
219 Functional analysis of these genes showed that loss of f
220 isomiRs from public NGS data and to provide
functional analysis of these isomiRs is available to dat
221 We additionally present detailed
functional analysis of these loci, identifying a statist
222 Through
functional analysis of these miRNA targets, 12 immune-re
223 The
functional analysis of these processes ideally would be
224 Functional analysis of three PLRV-interacting host prote
225 ed large-scale expression, localization, and
functional analysis of tobacco (Nicotiana tabacum) EXO70
226 Functional analysis of TRPA1 mutants showed that cystein
227 A detailed
functional analysis of two maize (Zea mays) homologs of
228 nscripts into 22 non-overlapping groups, the
functional analysis of which showed enrichment of stress
229 his integrative molecular classification and
functional analysis offers a new approach to understandi
230 Functional analysis on these genes further revealed the
231 Functional analysis,
performed on isolated PSII supercom
232 e we introduce our open-sourced, stand-alone
functional analysis pipeline for analyzing whole metagen
233 The available
functional analysis pipelines lack several key features:
234 ions are consistent with currently available
functional analysis pipelines.
235 In particular, the precise
functional analysis provided here serves as a reference
236 ants with potential disease association, but
functional analysis remains a challenge.
237 ontinues to catalog new compounds, but their
functional analysis remains technically challenging, and
238 In situ molar occlusion and a
functional analysis reveal a new mode of dental occlusio
239 Functional analysis revealed a reduced proliferative cap
240 Our
functional analysis revealed a statistically significant
241 and thyroid hormone and their structural and
functional analysis revealed an evolutionarily conserved
242 Functional analysis revealed defective IL-2 and TNF prod
243 s were detected upstream of 646 genes, whose
functional analysis revealed enrichment for Gene Ontolog
244 Further,
functional analysis revealed introgressed genes that are
245 However,
functional analysis revealed profoundly reduced C3b bind
246 The
functional analysis revealed significant phosphorylation
247 multiple algorithms coupled with systematic
functional analysis revealed specific interactions of mi
248 To conclude, structural, computational, and
functional analysis revealed striking differences betwee
249 Comparative
functional analysis revealed that cAMP signalling in D.
250 Functional analysis revealed that LCE3 proteins, and LCE
251 Functional analysis revealed that mutations in these PPR
252 Further
functional analysis revealed that STAT4 overexpression i
253 In vitro
functional analysis revealed that the IFIH1 c.2465G>A mu
254 Functional analysis revealed that the p.A39E mutant show
255 Functional analysis revealed that these regions are link
256 Further
functional analysis revealed that three genes, NRG1, MST
257 Functional analysis revealed the likely pathogenicity of
258 Importantly,
functional analysis reveals a role for Runx2 in mammary
259 Functional analysis reveals that a2NTD can act as a chem
260 Functional analysis reveals these mutations ablate canon
261 Structural and
functional analysis show that 2'-O methylation at N2, an
262 Functional analysis showed reduced channel activity and
263 Functional analysis showed that an implicated variant in
264 Extensive
functional analysis showed that intrinsic cell parameter
265 Functional analysis showed that such a reduced respirato
266 Functional analysis showed that this HLA-C*06:02-present
267 Functional analysis showed that treatment of endothelial
268 Functional analysis showed that VLVs induced the express
269 Functional analysis showed upregulation in processes rel
270 Functional analysis shows essential roles for TZPs in mo
271 Functional analysis shows that rs662463 is a cis-eQTL fo
272 diseases and functions were generated using
functional analysis software.
273 phase-specific expression patterns, although
functional analysis suggested that many have overlapping
274 A
functional analysis suggested that the abundance of prot
275 Functional analysis suggests that pre-S1 loop residues H
276 variation in bovine beta-defensin genes and
functional analysis supports a role for beta-defensins i
277 rk of depression and metabolic disorders for
functional analysis,
the interactome-based system-level
278 In a
functional analysis,
there were no changes in bile acids
279 ling of proximity interactions combined with
functional analysis thus provides a rich resource for be
280 tation, predicted by structural modeling and
functional analysis to be responsive to carbamazepine, w
281 hus, GWAS are useful "roadmaps" that require
functional analysis to establish the genetic and mechani
282 ons in the number of samples and the lack of
functional analysis to examine the effect of these haplo
283 Here, we use a combined ultrastructural and
functional analysis to examine the relationship between
284 millet, which could be deployed for further
functional analysis to extrapolate their precise roles i
285 Our study provides a foundation for further
functional analysis to reveal the roles that CIPKs and m
286 iological assays, and RNA interference-based
functional analysis to understand different components o
287 a part of the CNS amenable to structural and
functional analysis,
to investigate the constitutive rol
288 established directly from these results, the
functional analysis together with the genetic informatio
289 valuable addition to the currently available
functional analysis toolbox.
290 Here, we provide a
functional analysis,
using CRISPR/Cas9 and fate mapping,
291 Functional analysis was performed for novel TP53 variant
292 Mitochondrial
functional analysis was then performed in primary and cy
293 Using electron microscopy and
functional analysis we demonstrated that C. shasta tubul
294 By combining clinical data with in vitro
functional analysis,
we demonstrate how the X-linked RHO
295 Through site-directed mutagenesis and
functional analysis,
we found that NLS2 is also monopart
296 To provide an additional basis for
functional analysis,
we identified, by matrix-assisted l
297 In this study, genome and
functional analysis were performed to verify whether the
298 Functional analysis with miRNA mimics in cellular models
299 Functional analysis with RNA-seq for one of the families
300 of the fenestrae have so far prohibited any
functional analysis with standard and advanced light mic