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1  of the major landmarks of late 20th century molecular genetics.
2  OCT findings, ERG phenotype, and microscopy/molecular genetics.
3  and excellent experimental tractability for molecular genetics.
4 rs of TACK archaea and have well-established molecular genetics [6-9].
5 hemical markers that serve as surrogates for molecular genetic alterations and identification of char
6                               We showed that molecular genetic alterations in membrane lipid composit
7     These characteristics link the signature molecular genetic alterations present in individuals wit
8                                          The molecular-genetic alterations contributing to the pathog
9 or a more comprehensive understanding of the molecular-genetic alterations pivotal to the development
10                                              Molecular genetic analyses of both point mutants reveal
11                             Structure-guided molecular genetic analyses revealed that it has distinct
12                                     However, molecular genetic analyses suggest that autosomal common
13 ral cognitive ability) are highly heritable, molecular genetic analyses to date have had limited succ
14                 Accordingly, cytogenetic and molecular genetic analyses, such as conventional karyoty
15 morphology, flow cytometry, cytogenetic, and molecular genetic analyses.
16 ensively studied using both quantitative and molecular genetic analysis methods, both approaches lack
17 ally persistent silencing enables a detailed molecular genetic analysis of an inherited epigenetic st
18 mendous advances in our ability to perform a molecular genetic analysis of Chlamydia species.
19    Results of ophthalmologic examination and molecular genetic analysis of CNGB1.
20 hift mutations should greatly accelerate the molecular genetic analysis of development in V. carteri,
21 imaging, full-field electroretinography, and molecular genetic analysis of NR2E3 gene.
22 ssical genetics and three-point crosses with molecular genetic analysis of recombinants to generate t
23                                              Molecular genetic analysis of the RS1 was performed and
24                                              Molecular genetic analysis of the switch-like regulation
25 ssible, the diagnosis should be confirmed by molecular genetic analysis or measurement of levels of f
26                        In this report, using molecular genetics, analytical chemistry, and mass spect
27                                In this work, molecular genetic and biochemical approaches were taken
28                          Here, we review the molecular genetic and clinical features of inherited neu
29 f the cell biology underlying the burgeoning molecular genetic and genomic knowledge of oomycete path
30 minimal/measurable residual disease (MRD) by molecular genetic and/or flow cytometric techniques.
31 rmation derived from clinical research using molecular genetics and advanced imaging techniques has p
32 id dominant plant, is fast becoming a useful molecular genetics and bioinformatics tool due to its ke
33 rrectly read 'Department of Biochemistry and Molecular Genetics and Breast Surgery, Ehime University
34 ng the paradigm of what is possible in wheat molecular genetics and breeding.
35 resolution, we show through a combination of molecular genetics and chemical perturbations that direc
36  manipulation, land-use and habitat surveys, molecular genetics and demographic and spatial modelling
37 rphological features, but recent progress in molecular genetics and embryology has revealed deep simi
38 y interesting regions of the genome for both molecular genetics and evolutionary studies; yet, for mo
39                                        Using molecular genetics and functional genomics, we find that
40 ene, PMP22, the technological advancement in molecular genetics and gene technology has allowed scien
41 ntegrative diagnosis taking histomorphology, molecular genetics and imaging into account are reviewed
42                                 Here we used molecular genetics and in vivo calcium imaging to invest
43                                              Molecular genetics and observational case studies of 2 f
44  recent advances in this field regarding the molecular genetics and pathogenic mechanisms of CDAs, th
45 Technological advancements in fields such as molecular genetics and the human microbiome have resulte
46         Combining emerging technologies with molecular genetics and traditional animal models promise
47 he most fruitful marriage of the advances in molecular genetics and treatment will be the design of a
48                                      We used molecular, genetic and biochemical techniques to examine
49 ng been recognized, but our knowledge of the molecular, genetic and epigenetic requirements that unde
50 se complementary computational, biochemical, molecular, genetic and imaging approaches in Caenorhabdi
51 and discuss the current understanding of the molecular, genetic and physiological mechanisms that con
52       For eukaryotic algae, a combination of molecular, genetic and physiological studies using the m
53  Kcnj2 is expressed in the nascent face; (2) molecular-genetic and biophysical techniques are availab
54 lved mPFC-to-NAc projection displayed unique molecular-genetic and microcircuit-level features concor
55        Using a combination of pharmacologic, molecular genetic, and behavioral studies in mice, we de
56               This study combines in silico, molecular genetics, and biochemical analyses to characte
57 tz crystal microbalance, circular dichroism, molecular genetics, and immunofluorescence to study spec
58 plication of modern chemistry, biochemistry, molecular genetics, and optical physics to these old str
59                          Here, using diverse molecular, genetic, and behavioral approaches in mouse m
60 assessing gene function with high-throughput molecular, genetic, and cellular technologies.
61                                          The molecular, genetic, and clinical studies are consistent
62 hila melanogaster plays an important role in molecular, genetic, and genomic studies of heredity, dev
63 eterogeneous at the clinical, immunological, molecular, genetic, and microbial levels.
64 n to regulate sleep, and provide anatomical, molecular, genetic, and pharmacological evidence that NP
65             Transgenic, immunohistochemical, molecular-genetic, and fluorescence imaging approaches r
66                          We therefore used a molecular genetic approach and found that PTP was unaffe
67                            Here we explore a molecular genetics approach to restrict the assimilation
68                                        Using molecular genetic approaches in mice of either sex, we i
69                                              Molecular genetic approaches in the mouse have led to th
70 e have used biochemical, cell biological and molecular genetic approaches to demonstrate that beta8 i
71                                        Using molecular genetic approaches to target different neurona
72                             We have employed molecular genetic approaches to understand the domain or
73                               More recently, molecular genetic approaches, including genome-wide stud
74                                              Molecular genetic approaches, including targeted next-ge
75            Using proteomic, biochemical, and molecular genetic approaches, we found that this effect
76                        Using biochemical and molecular genetic approaches, we identified three tropom
77         Here, using comparative genomics and molecular genetic approaches, we reveal that the capacit
78                           The utilization of molecular genetics approaches in examination of panic di
79 ted image identification and developments in molecular genetic assays offer considerable promise for
80        Our results, based on geochemical and molecular genetic assays on sediments from four of the m
81    Examining 20 730 individuals, we report a molecular genetics-based heritability estimate (h(2)SNP)
82 Despite this, very little is known about the molecular genetic bases of tiller development in importa
83          This study provides the first clear molecular genetic basis for an OTCS case, indicates that
84                  Despite its importance, the molecular genetic basis of C(4) leaf development is stil
85 e informs experiments designed to reveal the molecular genetic basis of gene regulatory control, and
86 Additional studies are needed to explore the molecular genetic basis of heterosis and outbreeding dep
87                        To clarify the shared molecular genetic basis of major depressive disorder and
88         Advances in our understanding of the molecular genetic basis of mitochondrial disease have no
89                              We investigated molecular genetic basis of natural variations in thermo-
90     These findings provide insights into the molecular genetic basis of PME and show the role of de n
91        Like most hematological diseases, the molecular genetic basis of the SAs has ridden the wave o
92 enetic and biochemical characterization, the molecular genetic basis underlying the biosynthesis of b
93                                 However, the molecular genetic basis underlying the quantitative vari
94                 These data indicate that the molecular-genetic basis of brain function is shaped by i
95                            To understand the molecular-genetic basis of functional specialization and
96 are yet to have a clear understanding of its molecular-genetic basis.
97                                 Here, we use molecular genetic, behavioral, and anatomical studies in
98         There are significant differences in molecular genetics between pancreatic and extrapancreati
99               Since the utility of classical molecular genetics beyond model species is limited, the
100                                       We use molecular genetics, biochemical analyses, and experiment
101                              However, recent molecular, genetic, biochemical, and genomic studies hav
102                                  We utilized molecular genetics, biochemistry, and cryo-electron micr
103                                  Painstaking molecular genetics, biochemistry, and electron microscop
104                     We used a combination of molecular, genetic, bioinformatic and phylogenetic analy
105 none of these case subjects were linked to a molecular genetic cause.
106   All together, these findings elucidate the molecular genetic causes of UHS and shed light on its pa
107                  In this study we report the molecular genetic characterization of the Arabidopsis mi
108                            Understanding the molecular genetic circuitries underlying thermomorphogen
109 ays, have been defined, leading to the first molecular/genetic classification of the disease.
110 re research for the neuroscience and broader molecular genetics communities.
111 stigations have just begun to illuminate the molecular genetic contributions to major psychiatric ill
112                             Here, we provide molecular, genetic, cytological, and biochemical evidenc
113 (PGC-PTSD) combined genome-wide case-control molecular genetic data across 11 multiethnic studies to
114 idence was based on inferences from twin not molecular genetic data and it is unclear how much geneti
115                                              Molecular genetic data from over 2,000 individuals sampl
116  and discuss the advantages of incorporating molecular genetic data in the diagnosis, classification,
117 ped to provide data analyses for large-scale molecular genetic data, coupled with complex replicated
118                                      The new molecular genetic data, especially those derived from ne
119 o ocular adnexal tumors in light of emerging molecular genetic data.
120                                       Modern molecular genetic datasets, primarily collected to study
121 rently prevent using this model to study the molecular genetic details before or during tubule induct
122                                              Molecular genetic details of the human coagulation syste
123                                          The molecular genetic determinants of essential tremor are u
124                            Here, we combined molecular, genetic, developmental, and functional studie
125 f anterior vitreous (SLAV), and clinical and molecular genetic diagnoses were documented.
126  the unsolved cases, our assay resulted in a molecular genetic diagnosis for 35 of 139 patients.
127                              The WES-related molecular genetic diagnosis had implications for clinica
128                            The most frequent molecular genetic diagnosis is a P102L mutation of the p
129                The likelihood of detecting a molecular genetic diagnosis was highest for patients wit
130 tients with complex III deficiency without a molecular genetic diagnosis.
131          Our study results should facilitate molecular genetic diagnostics of SRNS, etiologic classif
132 has ushered in a new paradigm for the use of molecular genetic diagnostics to guide targeted therapie
133 tation of non-coding genetic variants in the molecular genetic dissection of brain disorders.
134 Drosophila model will enable a sophisticated molecular genetic dissection of cold nociceptive genes a
135 ap in knowledge, we present the results of a molecular genetic dissection of the TFIID subunit Taf2.
136 ri Matangi population, to find (1) a lack of molecular genetic diversity at a genome-wide level in bo
137 rrent classification system, histopathology, molecular genetics, electrophysiology, and transcriptome
138 rther companion paper was published in Human Molecular Genetics (Ellis et al, 2005 [3]) showing that
139                                              Molecular genetic estimates of Ne computed from linkage
140 We additionally calculated two single-sample molecular genetic estimates of Ne to corroborate the dem
141 lly, we provide structural, biochemical, and molecular genetic evidence identifying the Hsp15 homolog
142                   Here we provide definitive molecular genetic evidence supported by biochemical, cel
143                                              Molecular genetic examination of the CP gene for cerulop
144      Using public data and data from our own molecular genetic experiments (quantitative PCR, Western
145                                              Molecular genetic experiments are revealing how the fly
146                                              Molecular genetic experiments indicate that BnMS5(a) and
147           In a series of pharmacological and molecular genetic experiments, we identify key component
148 ologs in plants by phylogenetic analysis and molecular genetic experiments.
149  delineation of their clinical phenotype and molecular genetic features.
150        To describe the detailed clinical and molecular genetic findings in a series of patients with
151 linical, electrophysiologic, structural, and molecular genetic findings in nonsyndromic inherited ret
152 he combination of clinical, biochemical, and molecular genetic findings must be considered to obtain
153    Here we take advantage of newly available molecular genetics for Cryptosporidium parvum to investi
154                                         This molecular genetic framework of neuronal identity integra
155          Moreover, little is known about the molecular genetic functions of NEUROG3 in human islet de
156                  We discuss recent data from molecular genetic, genomic and functional methods that,
157  in nitrate research, spanning biochemistry, molecular genetics, genomics, and systems biology.
158               As the scope of assays used in molecular genetics has expanded to capture systems-level
159                           The development of molecular genetics has greatly enhanced the study of the
160 nt research using methodological advances in molecular genetics has improved our understanding of the
161                                The advent of molecular genetics has in the past several years aided c
162                           Here we review how molecular genetics have advanced our understanding of th
163                 Second, dramatic advances in molecular genetics have created new possibilities for in
164                  Although recent advances in molecular genetics have enabled improved risk classifica
165               Advances in cell type-specific molecular genetics have now helped to elucidate several
166                              Advancements in molecular genetics have revealed that hybridization may
167                                  Advances in molecular genetics have vastly improved our understandin
168 reater number of models that capture greater molecular/genetic heterogeneity of the cancer type.
169                                            A molecular genetic imaging strategy for noninvasive imagi
170 ls were imaged by both modalities using this molecular genetic imaging strategy.
171 ggesting these cells' utility to dissect T2D molecular genetics in these regions.
172                                              Molecular genetics, in vitro assays, and expression data
173 ade available here afford the best-available molecular genetic index of PTSD-for both European- and A
174 s, categorized by both tumour morphology and molecular genetic information, which led to reduced misc
175 phenotypes that might bridge the gap between molecular genetic inheritance and phenotypic consequence
176                                          The molecular genetic investigation included bidirectional S
177                                              Molecular genetic investigations have revealed mutations
178                           Elucidation of the molecular genetic landscape of HNSCC over the past decad
179 comprehensive characterisation of the entire molecular genetic landscape of meningioma to identify bi
180 ght; however, it is poorly understood at the molecular genetic level.
181 aches such as this enhance the resolution of molecular genetics, make genome editing easier, and may
182  Firmicutes bacterium that is intractable to molecular genetic manipulation.
183  Chlamydia is experiencing a renaissance for molecular genetic manipulation.
184 uding Chlamydia, are not amenable to routine molecular genetic manipulations.
185                              We consider how molecular-genetic manipulations have been used to probe
186 t decisions are based on a limited number of molecular genetic markers and morphology-based assessmen
187 amental form of learning, yet the underlying molecular genetic mechanisms are not well defined.
188 t is also a complex trait and uncovering the molecular genetic mechanisms controlling fruit firmness
189      For this latter mechanism, two distinct molecular genetic mechanisms have been observed, a tande
190 nderlying SCZ and PD, indicating that common molecular genetic mechanisms may contribute to overlappi
191                            Understanding the molecular genetic mechanisms of development and function
192          Little is known, however, about the molecular genetic mechanisms that control the formation
193 radiation-induced breast carcinogenesis, the molecular genetic mechanisms that underlie cell transfor
194          To obtain new information about the molecular genetic mechanisms underlying carriage of grou
195                                 However, the molecular genetic mechanisms underlying NKTCL remain unc
196 mplex syndrome and the need to explore other molecular genetic mechanisms.
197  genetic variants and could elucidate shared molecular genetic mechanisms.
198 nia and cognitive function, suggesting novel molecular genetic mechanisms.
199  are usually qualitative models derived from molecular-genetic mechanisms for DNA repair, DNA synthes
200                 We propose a simple model of molecular-genetic mechanisms to explain how physiologica
201                                 As a result, molecular genetic methods have become the gold standard
202 ticism; using formal genetic twin models and molecular genetic methods, i.e. polygenic risk scores (P
203 rs in regulating CYP3A4 expression, and used molecular genetics methods (siRNA/shRNA gene knockdown a
204 llutant, on MuSCs by combining in vivo mouse molecular genetic models with ex vivo studies.
205                  However, improved tools for molecular, genetic, morphological and physiological asse
206                         Recent findings from molecular genetics now make it possible to test directly
207  we provide a state-of-the-art review of the molecular genetics of ADHD incorporating evidence from c
208 owerful resource for those investigating the molecular genetics of facial development and facial clef
209 these data provide key new insights into the molecular genetics of form and function in the mammalian
210       Extraordinary progress accomplished in molecular genetics of inherited cardiomyopathies allowed
211                           Here, I review the molecular genetics of meiotic silencing and consider the
212  a major advance in our understanding of the molecular genetics of NCMD and provide insights into the
213             An improved understanding of the molecular genetics of OS may yield new approaches to imp
214                            Research into the molecular genetics of osteoarthritis (OA) has been subst
215 ology in increasing our understanding of the molecular genetics of PAD.
216 stantially advanced our understanding of the molecular genetics of PAH.
217                 Therefore, understanding the molecular genetics of palate development is important fr
218                                          The molecular genetics of panic disorder (PD) with and witho
219 Here, we review the current knowledge of the molecular genetics of replisome dysfunction disorders an
220 ome editing] will be critical to dissect the molecular genetics of T2DM pathogenesis, to build next-g
221 ing data, our findings shed new light on the molecular genetics of uveal melanoma, delineating it as
222 his issue, we took advantage of the power of molecular genetics of yeast.
223 esence of VEGF stimulation was combined with molecular genetics, optical imaging, and biochemistry to
224 utcome despite the inevitable variability at molecular, genetic, or environmental levels.
225   These results broaden our understanding of molecular genetic pathology of tooth enamel formation.
226       This is the first report elucidating a molecular genetic pathway downstream of Lhx in palate de
227                          Here we delineate a molecular-genetic pathway governing LCD in C. elegans.
228                                        Using molecular genetics, plant physiology, hormone analysis a
229       We examined the interactions between a molecular genetic predisposition to various aspects of o
230 which understanding these organism-level and molecular genetic processes can be used for crop plant i
231 ice has led to fundamental insights into the molecular genetic processes that govern cancer initiatio
232                                          The molecular genetic program for root hair development has
233 ical cross-linking mass spectrometry (CXMS), molecular genetics, protein biochemistry, and structural
234                              Here we applied molecular genetics, proteomics, and whole-genome sequenc
235 identified from NGS databases at three large molecular genetics reference laboratories.
236  onset of high blood pressure; however their molecular genetic relationship (s) and sex-specific dete
237                                          The molecular genetic relationship between esophageal adenoc
238 cal manifestations, laboratory findings, and molecular genetic results of 215 patients referred as po
239 sotope and isotopomer signatures, as well as molecular genetic results, also point towards a major sh
240 c insights into airway defense and a general molecular/genetic roadmap for internal organ sensation b
241 (HSVtk) gene, which has a dual function as a molecular-genetic sensor/reporter and a cell suicide-ind
242 ausing variants in the CHM gene confirmed by molecular genetic sequencing were characterized clinical
243                             In addition, the molecular genetic status was evaluated through next-gene
244 g of actin gene transcription, combined with molecular genetics, stochastic simulation and probabilis
245                                              Molecular genetic studies and twin studies have confirme
246 espite recent insights from quantitative and molecular genetic studies demonstrating considerable ple
247                                              Molecular genetic studies have also shown that common ph
248                                              Molecular genetic studies have identified transduction a
249                                              Molecular genetic studies have now linked multiple human
250                              Several limited molecular genetic studies have reached opposing conclusi
251                                              Molecular genetic studies have revealed the functional b
252 rved between yeast and other eukaryotes, and molecular genetic studies in budding yeast have provided
253              Here, using lineage-tracing and molecular genetic studies in the roots of Arabidopsis th
254                                              Molecular genetic studies of model plants in the past fe
255                                 Clinical and molecular genetic studies over the course of the last 50
256                            We demonstrate by molecular genetic studies that SEEDSTICK (STK), a transc
257 d individuals is widely used in clinical and molecular genetics studies.
258 surveillance and further epidemiological and molecular genetic study of this potential emergent antim
259 large part due to a paucity of resources for molecular genetics, such as a reference genome.
260                                This provides molecular genetic support for a paradigm shift in theori
261 ericans (AAs), but little is known about the molecular genetic susceptibility.
262                       Over the past 20 years molecular genetic techniques have provided a new approac
263                              Using different molecular genetic techniques, we identified 20 patients
264                                              Molecular genetics techniques are an essential diagnosti
265                         Although advances in molecular genetic technologies have enabled highly sensi
266 ulinaemic hypoglycaemia include use of rapid molecular genetic testing for the disease, application o
267 ude ADPKD particularly in younger donors and molecular genetic testing is advised.
268 throcyte protoporphyrin (ePPIX) testing, and molecular genetic testing.
269 oretinography (ERG), and both microscopy and molecular genetic testing.
270           Results of clinical assessment and molecular genetic testing.
271 ce, OCT), electrophysiologic assessment, and molecular genetic testing.
272            Amassing greater knowledge on the molecular genetics that underlie tree form can benefit t
273                  Here we investigated, using molecular genetics, the conservation and diversification
274                     We exploited Arabidopsis molecular genetics to define the mechanism and regulatio
275                                 Here we used molecular genetics to dissect the neuronal circuits by w
276         Here, we employed bioinformatics and molecular genetics to identify and characterize MATE tra
277  genomics, bioinformatics, metabolomics, and molecular genetics to identify and validate molecular ne
278                                      We used molecular genetics to probe the required functions of th
279                                 Here, we use molecular genetics to show that the moss Physcomitrella
280               In order to apply the tools of molecular genetics to this question, we have adapted a b
281 ed evolutionary theory, genome sequences and molecular genetics to understand the selection response
282  review summarizes the current status of the molecular genetic toolbox for Chlamydia species and high
283                                          The molecular genetic toolkit of the Mexican axolotl, a clas
284                                              Molecular genetic tools have had a profound impact on ne
285          This method lays the foundation for molecular genetic tools needed to establish ecological m
286 enomic information, together with increasing molecular genetic tools, a large number of reverse genet
287  without the development of species-specific molecular genetic tools.
288 ontinuous culture, facile animal models, and molecular genetic tools.
289                           MPRAs are powerful molecular genetics tools that can be used to screen thou
290                  Furthermore, several viral, molecular-genetic tools will require the use of cre/loxP
291                                   New viral, molecular-genetic tools will soon allow a more detailed
292 ns, we understand little about the bacterial molecular genetic underpinnings of this phenomenon.
293                                 Estimates of molecular genetic variation are often used as a cheap an
294 sufficient for characterising a population's molecular genetic variation at comparable markers.
295           However, this evidence is based on molecular genetic variation poorly predicting estimates
296     By combining computational modeling with molecular genetics, we show that boundary formation is d
297                                        Using molecular genetics, we then mapped at which point in the
298                                        Using molecular genetics, we unexpectedly found that genetic d
299 in this series of reports as advancements in molecular genetics, whole-genome sequencing, and studies
300                                    Combining molecular genetics with target-based approaches, we esta

 
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