コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 cific dietary fats and cell fates are poorly understood.
2 ity of their function is achieved are poorly understood.
3 the salt dissolution behavior should be well understood.
4 ease features, and pathophysiology is poorly understood.
5 the genetic etiology of NTDs remains poorly understood.
6 of relative sea level rise (RSLR) is poorly understood.
7 o and development in metazoans remains to be understood.
8 how gamma-TuRC nucleates a MT remains poorly understood.
9 e signaling pathways in plants remain poorly understood.
10 cts the response to immunotherapy are poorly understood.
11 R139 and its signaling mechanisms are poorly understood.
12 s, but their release properties are not well understood.
13 ffect substrate conformations remains poorly understood.
14 nts, yet how this is achieved remains poorly understood.
15 mibiotrophic fungal infection remains poorly understood.
16 wide activity drive action selection is less understood.
17 pathologically relevant conditions is poorly understood.
18 h in Huntington's disease (HD) are not fully understood.
19 n safely operate, but is not comprehensively understood.
20 contributes to PDAC progression is not well understood.
21 e overlooked and their impacts remain poorly understood.
22 nt which significance for immunity is poorly understood.
23 -driven tumor metastasis needs to be further understood.
24 wever, their specific functions are not well-understood.
25 o the migraine phenotype remain incompletely understood.
26 analyses of neural populations are not well understood.
27 monsoonal precipitation and runoff is poorly understood.
28 t the drivers of these patterns are not well understood.
29 these are implemented in the brain is poorly understood.
30 echanisms underlying this process are poorly understood.
31 h taste receptors, processes that are poorly understood.
32 c neovascularization after injury are poorly understood.
33 robial community response has not been fully understood.
34 atory micro-environments remain incompletely understood.
35 cale hydroclimate variability remains poorly understood.
36 up in the cortical hierarchy remains poorly understood.
37 calcium fluctuations are hitherto not fully understood.
38 rain as this learning takes place are poorly understood.
39 ible for these phenomena remain incompletely understood.
40 d in the evolution of bat immunity is poorly understood.
41 the dynamics of PIC components are not fully understood.
42 chanisms that underlie these defects are not understood.
43 reased TB susceptibility in T2D are not well understood.
44 to suppress host innate immunity is not well understood.
45 and consequences thereof are so far not well understood.
46 cell responses is complex and only partially understood.
47 evelopment and function remains incompletely understood.
48 te exposure on an immune system are not well understood.
49 which plants sense temperature are not well understood.
50 ics underlying these phenomena are not fully understood.
51 this function to tumor suppression is poorly understood.
52 contribute to their formation are not fully understood.
53 al selection in normal tissues remain poorly understood.
54 failure for Mycoplasma genitalium is poorly understood.
55 nisms underlying this pathology are not well understood.
56 op-associated genomic stress is still poorly understood.
57 in part because its pathogenesis is not well understood.
58 its pharmacology, however, remains scarcely understood.
59 mechanism of transport into plants is poorly understood.
60 patterns for grants and grantees are poorly understood.
61 6 activity and endosomal function are poorly understood.
65 ation initiation by OCM opens new avenues to understand alternative translation mechanisms involved i
67 we discuss current challenges for biological understanding and future requirements to overcome them.
69 This study highlights the significance of understanding and optimizing the effects of liposomal na
71 e underlying molecular mechanisms are poorly understood and warrant investigation given the inadequac
72 omote tissue remodelling are beginning to be understood and will be an important research focus in th
73 The pathophysiology of disease is not fully understood, and it may vary by presentation and clinical
74 underlying these processes are incompletely understood, and were proposed to differ between mouse an
77 on behavior of the solvent molecules must be understood because the electrochemical properties of a s
78 tions supporting this control is crucial for understanding both the nature of computations needed to
79 and centipedes, is a fascinating but poorly understood branch of life, including species with a high
83 century-scale) climatic profiles, and better understand coral persistence, particularly as coral comm
84 mplex process are not well defined and their understanding could offer potential new therapies for CR
85 ion centres and catalytic turnover, but also understanding degradation processes of the photocatalyti
87 ectures using electronic materials with well-understood electronic transport within such structures w
88 powerful new toolbox they can use to better understand environmental effects, and we illustrate this
90 lex 4 (AP-4) lead to prototypical yet poorly understood forms of childhood-onset and complex heredita
91 lying changes in soil C storage are not well understood, hampering long-term predictions of climate C
94 al problem in axon growth and guidance is to understand how cytoplasmic signaling modulates the cytos
100 des in the atmosphere, and it is critical to understand how soil greenhouse gas (GHG) emissions and u
102 bjected to control, thus, it is important to understand how the reduction of this scavenger guild inf
105 ecord provides a window through which we can understand how tree size and traits shape growth respons
106 hese complementary systems is fundamental to understanding how cone-mediated vision is sustained in v
107 properties, which may provide some clues to understanding how melatonin protects against Abeta, and
113 however, are not fully understood, nor is it understood how microstructure and mechanics change with
116 ian BST-2 with avian viruses is important in understanding innate antiviral defenses in birds.IMPORTA
117 cular level can provide valuable insights in understanding intrinsic reaction pathways, for affording
119 tiology of type 1 diabetes (T1D) is not well understood, it is believed to comprise both genetic and
120 ve heterochromatin state are reasonably well understood, less is known about the requirements for its
123 e importance of different memory systems for understanding maladaptive use, clinical research parsing
126 espectively, which may provide insights into understanding miRNA signaling underlying cancer cell met
127 echanical properties, however, are not fully understood, nor is it understood how microstructure and
129 length scales, are used to gain fundamental understanding of all processes leading to catalytic acti
132 for developing a vastly improved mechanistic understanding of animal movements and their roles in eco
133 ar, there have been numerous advances in our understanding of arrhythmia mechanisms, diagnosis, and n
134 is finding has implications not only for our understanding of basic mechanisms of iron biology but al
135 al function of most SMs remains obscure, but understanding of both the activation of silent gene clus
141 th the primary objective of gaining a better understanding of determinants of house dust Pb bioavaila
142 e informative for developing a more profound understanding of disease pathogenesis and ultimately tar
143 non-invasive polysomnography; however, basic understanding of dog sleep patterns remains poorly chara
144 ns of immune-relevant proteins; however, our understanding of electrophile-sensitive cysteines in the
145 e model's substantial complexity informs our understanding of false memories or of the development of
146 and optoelectronic devices, yet fundamental understanding of film formation, key to optimizing these
148 ional connectivity methods for improving our understanding of functional neuroanatomy and disruptions
149 PR/Cas9 technologies have revolutionized our understanding of gene function in complex biological set
151 enabled biochemical studies that deepen our understanding of how bacterial cell wall enzymes coopera
154 dies supporting this function, a mechanistic understanding of how Msp1 extracts its substrates is sti
157 ponses to perceptual figures, we have a poor understanding of how the early visual system contributes
158 . microporus should contribute to the better understanding of how the fungus is able to facilitate wo
159 al models with brain activity and pushes our understanding of human brain function further along the
161 ex, which has important implications for our understanding of information processing across different
162 ny areas of cancer research and improved our understanding of intratumor heterogeneity, the tumor mic
165 sly by oxidative catabolism of heme, and the understanding of its spatial and temporal sensing at the
166 studies have implications in furthering our understanding of JAM in cancer and provide a paradigm fo
175 protein-binding residues (PBRs) improves our understanding of protein-protein interactions, contribut
179 spital episodes in Scotland has enhanced our understanding of secular trends of EGS, including demogr
182 nd de novo immunity will be critical for our understanding of susceptibility to and the natural cours
185 gh there is still much to learn, our current understanding of tetrapyrrole biogenesis represents a re
186 ptome, and functional assays advance general understanding of the Antarctic green algae and offer pot
187 n coordination complexes affords us a better understanding of the assembly and function of metalloclu
189 equencing revolutionized the epidemiological understanding of the clusters; it also underlined the ri
190 lly viable devices, but it also sharpens our understanding of the design problems solved by evolution
191 tic resistance, together with our increasing understanding of the detrimental effects conferred by br
192 meningiomas is presented alongside existing understanding of the embryological origins for the menin
193 information lays the groundwork for improved understanding of the endogenous opioid system that will
196 oach and results thus contribute to a deeper understanding of the evolutionary dynamics resulting fro
197 servations in the hope of achieving a better understanding of the fate and impact of micro- and/or na
198 lved complex cognitive skills but a detailed understanding of the full scope of their cognition was,
199 wn about the existence of T-R conflicts, our understanding of the genetic and temporal nature of how
211 NA chaperone, significant gaps remain in our understanding of the molecular mechanisms ProQ uses to i
213 s study offers an interesting outlook in the understanding of the necessity of epitope clusters for e
215 terogeneous pigment remain unknown, limiting understanding of the properties of its light-responsive
217 le to reovirus infection and expands current understanding of the receptors on microglial cells that
218 ysing these data but must be applied with an understanding of the relevant biological and computation
219 nate immunity, and may have relevance to our understanding of the responses of ecologically important
224 hin the OFC is fundamental for a mechanistic understanding of the sequelae for several psychiatric di
225 ed XPA missense mutations, and contribute to understanding of the structure and mechanical action of
226 Progress in these reports provides a further understanding of the structure-function relationships of
227 ost terrestrial ecosystem processes, we lack understanding of their interactive effects on ecosystem
228 BsAbs' epitopes not only allows for detailed understanding of their mechanism of actions but also gui
231 and reverse genetics have contributed to our understanding of this important class of microalgae in t
234 stems Immunology' has already influenced our understanding of tumor immunology and immunotherapy.
235 lation and highlight opportunities to better understand OSN modulation mechanisms and their relations
237 (MCI) and Alzheimer's disease (AD) is poorly understood, particularly at early stages preceding neuro
242 ecific manner, which is vital for accurately understanding protein function in cellular processes.
250 diagnosis and environmental microbiology, to understand the contribution of metabolically active bact
252 8,457 somatic structural variations (SVs) to understand the distributions and effects of SVs across T
255 ew highlights future opportunities to better understand the functional significance of genetic varian
258 ges for a variety of brain regions; and (ii) understand the mechanism through which verubecestat migh
259 efficient cause-effect experimental model to understand the mechanisms of direct virus-induced neural
261 er, no study has systematically attempted to understand the molecular basis of imaging traits based o
262 pathogenesis has hampered efforts to better understand the molecular interactions governing disease
263 rend in CNS disease biology is to attempt to understand the neural-cell-immune interaction to investi
265 alyses of viral transcript levels to further understand the roles of these decay pathways in KSHV gen
267 This study will enable other researchers in understanding the B. microti biology, host modulation an
268 A heuristic neurobiological framework for understanding the bidirectional relationship between abn
272 epression symptomatology and a more complete understanding the diversity of molecular changes that oc
279 nces in animal models that are important for understanding the pathogenesis of SARS-CoV-2, vaccine de
280 pathogenesis, there is increased interest in understanding the potential clinical utility of a geneti
283 egulate reward, motivation, and food intake, understanding the role of opioid signaling within the OF
286 direct imaging of EpiSCs after MI to better understand their biology, but also may permit the cell-s
288 cence and floral development is essential to understand their role in the evolutionary origin of deve
293 lls, which offers new perspectives to better understand virus-glycan interactions in physiologically
298 e findings have significant implications for understanding why a hypomorphic loss of BCCIP functions
299 moting excessive activation are incompletely understood, with limited experimental models to investig
300 des, which advance fundamental knowledge for understanding xenon chemistry and physics mechanisms for