戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

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 ithout inhibitory feedback is functional but fragile.
2 c patient subgroups, such as the elderly and fragile.
3 s cells are dynamic, chemically diverse, and fragile.
4 pristine matter and coherence was considered fragile.
5  remain at risk and hence the gains made are fragile.
6                                              Fragile 3D floc samples were successfully captured and s
7   However, superhydrophobicity is remarkably fragile and can break down due to the wetting of the sur
8 tivity of bioorthogonal reagents in the most fragile and complex organs.
9 owever, multiparty entanglement is generally fragile and difficult to quantify.
10  cuticle of LmCYP4G102-knockdown locusts was fragile and easier deformable than in control animals.
11 n adopted immunity, although fundamental, is fragile and failing.
12 bers used for in vivo bioanalysis can be too fragile and flexible, which limits suitability for direc
13 population, a situation in which ongoing-but fragile and limited-health cooperation and training arra
14                             Sialic acids are fragile and prone to fragmentation under electrospray io
15  used for these studies, which are large and fragile and remain laboratory instruments.
16                     However, these gains are fragile, and coverage is far from optimal.
17  powerful, on average, they tend to be weak, fragile, and fleeting.
18 es in person perception were generally weak, fragile, and fleeting; (2) Social perceptions were often
19  a PET10 deletion strongly aggregate, appear fragile, and fuse in vivo when cells are cultured in ole
20 uption by noise: redundant codes can be very fragile, and synergistic codes can-in some cases-optimiz
21 ce is lost, the vessels can be malformed and fragile, and they can lose arteriovenous differentiation
22  production, resulting in the formation of a fragile biofilm in Streptococcus sanguinis.
23 nent system in S. sanguinis SK36, produced a fragile biofilm.
24 cal CT analysis--those with osteoporosis or "fragile bone strength"--agreed well against classificati
25 ion named seal was produced, associated with fragile bones and susceptibility to fractures (spine and
26 and alter chromatin structure, especially in fragile cells such as neurons.
27 sible involvement of difficult-to-replicate (fragile) chromosomal sites in this process.
28 lance, thus preventing falls among older and fragile citizens.
29 h promotion and basic first-line services in fragile contexts with weak secondary health service infr
30 grid express interactions among modules with fragile couplings that amplify even small shocks, thus p
31 rms well-ordered crystals, whereas rA6 forms fragile crystalline-like structures, and rA5, rA8 and rA
32       HHT is characterized by development of fragile, direct connections between arteries and veins,
33 ight into why human neoplastic translocation fragile DNA sequences are more prone to enzymes or agent
34  can show stable, divergent, and metastable (fragile) dynamics.
35 nservation efforts aimed at protecting these fragile ecosystems in the face of anthropogenic warming.
36 sions, affecting the climate impact of these fragile ecosystems.
37 n the case of young children and the case of fragile egos.
38   Because PT-symmetry has been thought of as fragile, experimental realisations to date have been usu
39 tection to human telomeres, as well as other fragile genomic sites.
40 te its remote location, the deep sea and its fragile habitats are already being exposed to human wast
41 s-Danlos syndrome (cEDS) is characterized by fragile, hyperextensible skin and hypermobile joints.
42 ow firing rate is surprisingly difficult and fragile in a biological context.
43 ient's blood (e.g., red blood cells are more fragile in patients undergoing chemotherapy) and the car
44    However, existing bioengineered lungs are fragile, in part because of their immature vascular stru
45                       The intensity of these fragile ions gradually disappeared at voltages beyond 50
46 idative damage in lipids and proteins, and a fragile juvenile plumage.
47 rd trials, as mediated by robust priming and fragile learning.
48  that water is a mixture of a high density, "fragile" liquid, and a low density, "strong" liquid, the
49                The change is much greater in fragile liquids, with the activation energy becoming ver
50 n excitations are quite similar indicating a fragile low temperature ground state with respect to the
51 ly significant dichotomous results are often fragile, meaning that a difference of only a couple of e
52 usion-promoting proteins, and deliver large, fragile membrane protein complexes into the target bilay
53 s rarely been analyzed, foremost because the fragile membranous structures in the inner ear are hard
54                                          For fragile models, fluctuations of the single-neuron dynami
55 he experimentally used treatment protocol is fragile (nonrobust) and (ii) discovered an alternative r
56                  Its glassy state is neither fragile nor strong.
57 -encoded nucleosome fragility, we also found fragile nucleosomes at locations where we expected to fi
58                                   Genes with fragile nucleosomes in their promoters tended to be lowl
59  that for nearly all mouse genes, a class of fragile nucleosomes occupies previously designated nucle
60                                              Fragile nucleosomes were defined by nucleosomal DNA frag
61  protein complexes, with little evidence for fragile nucleosomes.
62 tead occupied by easily digested, unstable, "fragile" nucleosomes.
63            In regions with scarce resources, fragile or fragmented health systems, cancer contributes
64 , although severe complications can occur in fragile patients.
65 an evolutionary history of hybridization and fragile prezygotic isolating mechanisms.
66 ructural barriers that impede replication at fragile regions in the genome.
67 primary cells steadily accrue macroH2A1.2 at fragile regions, whereas macroH2A1.2 loss in these cells
68 rmation of the apical hook that protects the fragile shoot apical meristem when it breaks through the
69 y reductive amination; (ii) stabilization of fragile sialic acids by carbodiimide coupling; (iii) rel
70 pecific enrichment results as well as highly fragile significances.
71    The magnetic structure in GdPd3 is highly fragile since applied magnetic fields of moderate streng
72     In this study, loss of expression of the fragile site-encoded Wwox protein was found to contribut
73 -to-replicate genomic regions, namely common fragile sites (CFS).
74                                       Common fragile sites (CFSs) are genomic regions that are unstab
75 ves late replication intermediates at common fragile sites (CFSs) during early mitosis to trigger DNA
76 RC sites are strongly associated with common fragile sites and recurrent deletions in cancers.
77 ad of the fork, including stable protein-DNA fragile sites and termination.
78 addition, important genomic elements such as fragile sites and tRNA genes are found to be clustered s
79 construct a statistical model that separates fragile sites from regions showing signatures of positiv
80                  Thus, loop anchors serve as fragile sites that generate DSBs and chromosomal rearran
81 occur either over tumour suppressors or over fragile sites, regions of increased genomic instability.
82 ffected genes overlap with early replicating fragile sites, show elevated levels of gammaH2AX, and su
83 mic loci/regions include centromeres, common fragile sites, subtelomeres, and telomeres.
84  collapse, late origin firing and stabilizes fragile sites.
85 ution view of replication-associated genomic fragile sites.
86 omotes replication of DNA lesions and common fragile sites.
87  lose their biological activity due to their fragile structural conformation during formulation, stor
88 s, phenols, and malonates to be present, and fragile structures are also tolerated.
89 y treated flours suggested the production of fragile structures that broke easily.
90  This presents a difficult situation whereby fragile substrates such as lactone will be hydrolyzed by
91 , however, are anticipated to be exceedingly fragile, suppressed by very small Zeeman energies.
92     Members of the Cryptochiridae are small, fragile, symbiotic crabs that live in domiciles in moder
93                          We observe frequent fragile telomeres in ALT cells, suggesting that telomere
94 ll lines, we show that ALT cells harbor more fragile telomeres representing telomere replication prob
95 ective POT1-TPP1 complex leads to longer and fragile telomeres, which in turn promotes genomic instab
96 ith increased frequencies of deprotected and fragile telomeres.
97 -8) Pa, G(T) and D(T) have super-Arrhenius ("fragile") temperature dependences, but both cross over t
98 es of the brain, and provide rigidity to the fragile tissue while eliminating background interference
99 we find that although human life is somewhat fragile to nearby events, the resilience of Ecdysozoa su
100         Therefore, the CphA active - site is fragile to substitutions, suggesting active-site residue
101 oportion of which explains the anomalies and fragile-to-strong crossover in water.
102                                              Fragile transition metal complex ions such as [Cr(H2O)4C
103 ding and/or the beta-annulus, making it more fragile under neutral/basic pH conditions.
104  materials, which originates from relatively fragile/weak bonds between inorganic and organic constit
105 , optimized for filtration, is intrinsically fragile, whereby local transient biochemical imbalances
106  systems are typically costly, toxic, and/or fragile, with limited chemical versatility.
107                            The population is fragile, with no growth projected under current conditio
108 hildren with a disability as a result of the Fragile X (FX) premutation, a genetic abnormality in FMR
109 athophysiology of FXS.SIGNIFICANCE STATEMENT Fragile X (FXS) individuals have a range of sensory rela
110 ngs identify RSK as a therapeutic target for fragile X and suggest the therapeutic potential of drugs
111 enic syndromes highly comorbid with autism - fragile X and tuberous sclerosis types 1 and 2 syndromes
112 related protein 1 (FXR1P) is a member of the fragile X family of RNA-binding proteins, which includes
113 e a long-standing unanswered question in the fragile X field, which is also relevant to autism pathog
114 lb circuits exhibited axonal localization of Fragile X granules (FXGs), structures that comprise ribo
115 l translational machinery is associated with Fragile X granules (FXGs), which are restricted to axons
116                                        FXGs (Fragile X granules) are axonal RNPs present in a stereot
117 cortex and hippocampus in wild-type (WT) and fragile X knockout (FMR1-KO) mice during the first 5 wee
118                                 Silencing of fragile X mental retardation 1 (FMR1) gene and loss of f
119 00 CGG repeat expansion in the 5'-UTR of the fragile X mental retardation 1 (FMR1) gene is known as a
120 e sensory abilities disrupted by loss of the Fragile X Mental Retardation 1 (Fmr1) gene.
121 to rescue the dendritic spine defects of the Fragile X Mental Retardation 1 gene KO neurons.
122                        Finally, upregulating fragile X mental retardation 1 protein (Fmr1, also calle
123 rative molecular analysis converged on FMR1 (Fragile X Mental Retardation 1), an important negative r
124               The expression levels of FXR1 (fragile X mental retardation autosomal homolog 1), an RN
125 e biology: it has a regulatory loop with the fragile X mental retardation homologue FXR1 and regulate
126  Pum2 display RNA-dependent interaction with fragile X mental retardation protein (FMRP) and bind to
127  pathophysiology associated with the loss of fragile X mental retardation protein (FMRP) and haploins
128 nnel open probability was reduced by loss of fragile X mental retardation protein (FMRP) and that FMR
129 es, mRNA, and RNA binding proteins including Fragile X mental retardation protein (FMRP) and the rela
130 mental retardation 1 (FMR1) gene and loss of fragile X mental retardation protein (FMRP) cause fragil
131                                      Loss of fragile X mental retardation protein (FMRP) causes fragi
132 es to understand how the loss of function of fragile X mental retardation protein (FMRP) causes fragi
133  brain.SIGNIFICANCE STATEMENT The absence of Fragile X Mental Retardation Protein (FMRP) from birth r
134                              How the loss of fragile X mental retardation protein (FMRP) in different
135 ndrome (FXS) is caused by the absence of the Fragile X Mental Retardation Protein (FMRP) in neurons.
136                                              Fragile X mental retardation protein (FMRP) is a multifu
137                                              Fragile X mental retardation protein (FMRP) is thought t
138 tic protein synthesis resulting from loss of fragile X mental retardation protein (FMRP) is thought t
139        In fragile X syndrome, the absence of fragile X mental retardation protein (FMRP) leads to def
140                                              Fragile X mental retardation protein (FMRP) loss causes
141      Here we show that the effect of loss of fragile X mental retardation protein (FMRP) on these pat
142  expected, P = .0062) and for targets of the fragile X mental retardation protein (FMRP) pathway (10
143 opic glutamate receptor signaling though the fragile X mental retardation protein (FMRP) pathway may
144                                          The fragile X mental retardation protein (FMRP) plays an imp
145            The tandem Agenet domain (TAD) of fragile X mental retardation protein (FMRP) protein is c
146                                              Fragile X mental retardation protein (FMRP) sculpts syna
147                               More recently, fragile X mental retardation protein (FMRP), an RNA-bind
148 ires protein translation and is dependent on fragile X mental retardation protein (FMRP), the protein
149                                              Fragile X mental retardation protein (FMRP), the protein
150     FXS results from the loss of function of fragile X mental retardation protein (FMRP), which repre
151 rum disorder (ASD), results from the loss of Fragile X mental retardation protein (FMRP).
152  mutation that disrupts the transcription of Fragile X Mental Retardation Protein (FMRP).
153 of the mRNA-binding translational suppressor Fragile X Mental Retardation Protein (FMRP).
154 sulting from the partial or complete loss of fragile X mental retardation protein (FMRP).
155                The process is antagonized by fragile X mental retardation protein (FMRP).
156 ts (SNVs; P=5.4 x 10(-4)) and targets of the Fragile X mental retardation protein (P=0.0018).
157                     The resulting absence of fragile X mental retardation protein 1 (FMRP) leads to b
158 crucially on protein synthesis controlled by fragile X mental retardation protein and on Arc signalin
159                                  Loss of the Fragile X mental retardation protein leads to excessive
160 trated that hYVH1 co-localizes with YB-1 and fragile X mental retardation protein on stress granules
161 anslational regulatory complex that includes fragile X mental retardation protein, DEAD box helicase
162 including Y box-binding protein 1 (YB-1) and fragile X mental retardation protein, proteins that func
163  analyzed 15 synaptic proteins in normal and Fragile X mental retardation syndrome (FXS) model mouse
164                       Here, we show that the fragile X mental retardation-related protein 2 (FXR2P) c
165 ing networks are altered in the neocortex of fragile X mice such that S6 phosphorylation receives abe
166                              We show that in fragile X mice, S6 is regulated by ERK via the "alternat
167 R) signaling is elevated in the neocortex of fragile X mice.
168 ces susceptibility to audiogenic seizures in fragile X mice.
169 itive phenotypes displayed by the Drosophila fragile X model, and thus reveal a metabolic pathway tha
170 cal, and behavioral symptoms observed in the fragile X mouse.
171 G repeat RAN translation in the 5' leader of fragile X mRNA, FMR1.
172 ior and to rescue the memory deficits in the fragile X mutant fly.
173 d by new and already approved drugs to treat fragile X patients.
174                              Improvements in fragile X phenotypes have been observed following chroni
175 ) complexes results in the identification of fragile X protein family (FMRP, Fxr1 and Fxr2) as bindin
176 intact brain that contain one or more of the Fragile X related (FXR) proteins (FMRP, FXR2P, and FXR1P
177                                              Fragile X related protein 1 (FXR1P) is a member of the f
178  and its inhibition by overexpression of the fragile X retardation protein Fmr1.
179 here that in mouse models PFC dysfunction in Fragile X Syndrome (FX) can be attributed to the continu
180                                              Fragile X Syndrome (FX) is generally considered a develo
181 ptors (mGlu1/5) is a core pathophysiology of fragile X syndrome (FX); however, the differentially tra
182           Autism spectrum disorder (ASD) and Fragile X syndrome (FXS) are developmental disorders.
183 e behavioral and anatomical deficits seen in fragile X syndrome (FXS) are widely believed to result f
184 e X mental retardation protein (FMRP) causes fragile X syndrome (FXS) have largely focused on neurons
185                                              Fragile X syndrome (FXS) is a leading genetic cause of i
186                                              Fragile X syndrome (FXS) is a neurodevelopmental disease
187                                              Fragile X syndrome (FXS) is a neurodevelopmental disorde
188                                              Fragile X syndrome (FXS) is an undertreated neurodevelop
189                                              Fragile X syndrome (FXS) is caused by the absence of the
190                                              Fragile X syndrome (FXS) is characterized by sensory hyp
191                                              Fragile X syndrome (FXS) is the leading monogenic cause
192                                              Fragile X syndrome (FXS) is the most common form of inhe
193                                              Fragile X syndrome (FXS) is the most common form of inhe
194                                              Fragile X syndrome (FXS) is the most common heritable ca
195 ssing deficits in FXS.SIGNIFICANCE STATEMENT Fragile X Syndrome (FXS) is the most common inheritable
196 specially in non-neuron glial cells, induces fragile X syndrome (FXS) phenotypes has just begun to be
197                                              Fragile X syndrome (FXS) results from a repeat expansion
198 le X mental retardation protein (FMRP) cause fragile X syndrome (FXS), a genetic disorder characteriz
199                                              Fragile X syndrome (FXS), a heritable intellectual and a
200 ental retardation protein (FMRP) loss causes Fragile X syndrome (FXS), a major disorder characterized
201  autism spectrum disorders (ASDs), including fragile X syndrome (FXS), and frequently leads to tactil
202                                              Fragile X syndrome (FXS), caused by the loss of function
203                                              Fragile X syndrome (FXS), due to mutations of the FMR1 g
204 ty (ID) and autism spectrum disorders (ASD), Fragile X syndrome (FXS), is caused by loss of the mRNA-
205 trum disorder (ASD), including in those with fragile X syndrome (FXS), one of the most common genetic
206                                              Fragile X syndrome (FXS), the most common form of inheri
207 get for diseases affecting synapses, such as fragile X syndrome (FXS), the most common heritable auti
208               FMR1 gene silencing results in fragile X syndrome (FXS), the most common heritable caus
209                        One such condition is fragile X syndrome (FXS), which is considered to be caus
210 e X mental retardation protein (FMRP) causes fragile X syndrome (FXS), yet the mechanisms underlying
211 rited form of mental retardation and autism, fragile X syndrome (FXS).
212 on heritable autism spectrum disorder (ASD), fragile X syndrome (FXS).
213 ing causes of abnormal sensory processing in Fragile X syndrome (FXS).
214 tual deficits and sensory dysfunction in the fragile X syndrome (FXS).
215 dult Fmr1 knock-out mice, the mouse model of fragile X syndrome (FXS).
216  receptor might hold therapeutic benefits in Fragile X syndrome (FXS).
217 f the prevalent symptoms in individuals with Fragile X syndrome (FXS).
218 man's syndrome (34%), CHARGE syndrome (30%), fragile X syndrome (male individuals only 30%; mixed sex
219 f several neurological conditions, including Fragile X syndrome and Alzheimer's disease.
220 everal individuals clinically diagnosed with fragile X syndrome and autism spectrum disorder.
221 t of the neocortex, an area affected in both fragile X syndrome and autism spectrum disorder.
222 lem in the Fmr1-knockout (KO) mouse model of Fragile X syndrome and describe potentially treatable un
223                Recent evidence suggests that Fragile X syndrome and other types of autism are associa
224 hysiology of Autism Spectrum Disorder (ASD), Fragile X Syndrome and Tuberous Sclerosis, the role of o
225 pression) relevant to the pathophysiology of fragile X syndrome as well as neural correlates of cogni
226 tion patterns at specific genomic regions in fragile X syndrome cells, and identified dysregulated ge
227        Studies performed on animal models of fragile X syndrome have revealed links between modificat
228 entiated to dorsal forebrain cell fates, our fragile X syndrome human pluripotent stem cell lines exh
229 analysed the early stages of neurogenesis in fragile X syndrome human pluripotent stem cells.
230                                    ABSTRACT: Fragile X syndrome is the most common form of inherited
231    This finding is of high relevance because Fragile X syndrome is the most common monogenetic cause
232 tism spectrum disorder patients, among which fragile X syndrome is the primary monogenic cause.
233                               The Drosophila Fragile X Syndrome model has long generated insights int
234 tion has been most well characterized in the fragile X syndrome mouse model, the Fmr1 knock-out (KO)
235                                              Fragile X syndrome results from loss of FMR1 expression.
236 ulated gene- and network-level correlates of fragile X syndrome that are associated with developmenta
237   We then describe what we have learned from fragile X syndrome that may be applicable to other psych
238                          Specifically, Fmr1 (fragile X syndrome) and Ube3a (Angelman syndrome) are tr
239 e expansion disorders (Friedreich ataxia and fragile X syndrome), and cancer.
240    This form of plasticity is deregulated in Fragile X Syndrome, a monogenic form of autism in humans
241  comprehensive manner, we begin by selecting fragile X syndrome, a neurogenetic disease with cognitiv
242 or fly models of Alzheimer's disease and the Fragile X syndrome, allowing applications such as geneti
243 evelopmental disorders, Rett syndrome (RTT), fragile X syndrome, and CDKL5 syndrome, also affects fem
244 in myotonic dystrophy, and (CGG)n repeats in fragile X syndrome, are also subject to double-strand br
245 otein (FMRP), the protein that is lacking in fragile X syndrome, binds neuroligin-1 and -3 mRNA.
246 cess that is deficient in the mouse model of Fragile X Syndrome, Fmr1 KO.
247  expansions, including those associated with fragile X syndrome, Friedreich's ataxia, and Huntington'
248 gh incidence of autistic behaviours, such as fragile X syndrome, has the potential to identify genes
249 expansions in diseases such as hemophilia A, fragile X syndrome, Hunter syndrome, and Friedreich's at
250 ause amyotrophic lateral sclerosis (ALS) and fragile X syndrome, is challenging for short-read whole-
251  of disorders where it is disrupted, such as Fragile X syndrome, Rett syndrome, epilepsy, major depre
252                                           In fragile X syndrome, the absence of fragile X mental reta
253                     Among these disorders is fragile X syndrome, the most common cause of inherited i
254                                              Fragile X syndrome, the most common known monogenic caus
255 he impairment in spinogenesis, a hallmark in Fragile X syndrome, thereby linking the regulation of ac
256 onic dystrophy, spinal muscular atrophy, and fragile X syndrome, with broader implications for other
257                                        These fragile X syndrome-aberrant networks are significantly e
258 omised in a severe monogenic form of autism, Fragile X Syndrome.
259 lated in autism spectrum disorder as well as fragile X syndrome.
260 nal regulation of a distinct set of genes in fragile X syndrome.
261 iology in 16p11.2 microdeletion syndrome and fragile X syndrome.
262 ysfunctional prefrontal cortex processing in fragile X syndrome.
263 l of the developmental neurological disorder Fragile X syndrome.
264 s primary contributors to the development of fragile X syndrome.
265 tions, including nociception, addiction, and fragile X syndrome.
266 of intellectual disability and autism called fragile X syndrome.
267 ated in autism spectrum disorders, including Fragile X syndrome.
268  brain disorders including schizophrenia and fragile X syndrome.
269 e and behavioural phenotypes associated with fragile X syndrome.
270 al and neuropsychiatric disorders, including fragile X syndrome.
271               There is currently no cure for fragile X, although medications targeting specific FXS s
272 othesis of shared pathophysiology of RTT and fragile X, another monogenic cause of autism and intelle
273 omised in a Drosophila melanogaster model of Fragile X, highlighting intriguing new mechanistic conne
274                In brains of a mouse model of fragile X, mGlu5 is less associated with its binding par
275                                           In fragile X, the loss of the mRNA translational repressor
276                                              Fragile X-associated disorders are a family of genetic c
277  to the phenotypes observed in patients with fragile X-associated disorders.
278                                              Fragile X-associated tremor/ataxia syndrome (FXTAS) is a
279                                              Fragile X-associated tremor/ataxia syndrome (FXTAS) is a
280                                              Fragile X-associated tremor/ataxia syndrome (FXTAS) is o
281  are associated with FMR1 overexpression and Fragile X-associated tremor/ataxia syndrome (FXTAS), a l
282 e affected by the neurodegenerative disorder fragile X-associated tremor/ataxia syndrome (FXTAS), pri
283 gnitive deficits are common in patients with fragile X-associated tremor/ataxia syndrome (FXTAS), wit
284 sent in a 5' untranslated region that causes fragile X-associated tremor/ataxia syndrome (FXTAS).
285  that translation of expanded CGG repeats in fragile X-associated tremor/ataxia syndrome is initiated
286 AN translation of the CGG repeats that cause fragile X-associated tremor/ataxia syndrome, revealing s
287                          The review includes fragile X-associated tremor/ataxia syndrome, spinocerebe
288 mentia (C9RAN) and at CGG repeats that cause fragile X-associated tremor/ataxia syndrome.
289  neurodegenerative disorders such as ALS and fragile X-associated tremor/ataxia syndrome.
290 e locus involvement may resolve up to 58% of Fragile X-negative cases.
291 nown to contribute to hippocampal defects in fragile X.
292  in response to ethanol treatment, requiring fragile-X mental retardation protein (FMRP).
293 m disorder due to silencing of the X-linked, fragile-X mental retardation-1 (FMR1) gene.
294                Thus, two consequences of the Fragile-X mutation converge on plasticity at one site in
295                                              Fragile-X syndrome (FXS) patients display intellectual d
296  BPN14770 may be useful for the treatment of fragile-X syndrome and other disorders with decreased cA
297 rtex of Fmr1 knock-out (KO) mice, a model of Fragile-X Syndrome, to test the E/I imbalance theory.
298  in the remaining 43% (1% were found to have Fragile-X).
299              Here, we have transferred human fragile zones into S. cerevisiae in the context of a gen
300 double-strand breaks (DSBs) occurring within fragile zones of less than 200 base pairs account for th

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top