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1 oked currents with high intracellular Ca(2+) buffering.
2 MODIS images, to demonstrate hydrogeological buffering.
3 uch as Hsp70 and Hsp90 do not correlate with buffering.
4 er WAT compartment, and had improved glucose buffering.
5 d there is limited evidence of translational buffering.
6 ulting from compromised intracellular Ca(2+) buffering.
7 othelin-1 (ET-1) is important for skin Na(+) buffering.
8 (2+)]i transients and prevented by [Ca(2+)]i buffering.
9 antagonist blocked the effects of the social buffering.
10 of mRNA degradation, resulting in mRNA level buffering.
11  evidence of diminished mitochondrial Ca(2+) buffering.
12 nsitive to the amount of cytoplasmic calcium buffering.
13 extracellular Ca(2+) or intracellular Ca(2+) buffering.
14 s on mNCE activity and mitochondrial calcium buffering.
15 ed currents with modest intracellular Ca(2+) buffering.
16 ith temporally precise intracellular calcium buffering.
17 ced an unobserved stressor, providing social buffering.
18 ins most of its refreezing capacity for now, buffering 22% of the increased meltwater production.
19     This modification did not affect the PEI buffering abilities but enhanced its pH-sensitive aggreg
20 CHA and maximizes its thermo- and structure- buffering abilities.
21  a golden standard polymer owing to its high buffering ability for endosomal escape of gene to be exp
22                                   This novel buffering activity of SLiMs was observed in different ti
23 cg) 1 serves a seminal physiological role in buffering against hypoglycemia, but its poor biophysical
24 nditions within each year-class, and reduced buffering against negative environmental influences.
25 ghlights the neuroprotective role of glial K buffering against seizures and spreading depression, and
26 hortening and thus preventing the clock from buffering against this change in temperature.
27 ting carbon sequestration and storage and by buffering against uncertainty in management, environment
28 ferences in temperature, pH, ionic strength, buffering agent, or other additives can alter chemical e
29 esolution, (ii) the effect of excipients and buffering agents, (iii) the performance of the assay com
30 ptation potential and ecological benefits by buffering alley crops to weather extremes, diversifying
31                                  Demographic buffering allows populations to persist by compensating
32 because of high energy needs and calcium ion buffering along axons to synapses during neurotransmissi
33 ely, land-use change might overwhelm natural buffering and amplify latent climate signals, rendering
34 , with differential effects on matrix Ca(2+) buffering and DeltaPsim recovery.
35 provide new insights into intracellular zinc buffering and may have broad relevance given the presenc
36 ion is mutualistic or commensal, there is no buffering and only monotonic toxic responses are possibl
37 or carbon storage and sequestration [8], for buffering and regulating local climates [9], and for sup
38      In this model, uncoupling impaired K(+) buffering and temporally preceded apoptotic neuronal dea
39 ns in the kinetics of perisynaptic glutamate buffering and uptake contributing to dysfunction of thal
40 gorithm that includes channel gating, Ca(2+) buffering, and Ca(2+) diffusion.
41 EPSP/AP pairing or high intracellular Ca(2+) buffering, and its sign was inverted by GABA-A receptor
42 y extracellular Ca(2+), intracellular Ca(2+) buffering, and membrane potential, by their common effec
43 s, including neurotransmitter clearance, ion buffering, and metabolite delivery.
44 n of supramolecular ring-chain buffering, pH buffering, and molecular titration is presented.
45 imary forests in their potential for thermal buffering, and subsequent ability to retain temperature-
46 tion pipeline facilitating Ca(2+) diffusion, buffering, and synchronicity.
47 actile muscles as a results of their role as buffering, anti-oxidative, and anti-glycation capacities
48 excess buffer approximation (EBA), the rapid buffering approximation (RBA), and the linear approximat
49 te Ciona intestinalis to show that levels of buffering are maternally inherited.
50                             We now show that buffering astrocyte Ca(2+) inhibits neuronally evoked ca
51    It was suppressed by intracellular Ca(2+) buffering at a fixed physiological level, inhibitors of
52  steady-state glutamate uptake and glutamate buffering at the synapse.
53 ands; exposure to 12% CO2 without additional buffering blocked ligand shedding, as well as EGFR and p
54 ults showed a slow pH increase due to strong buffering by Al hydrolysis and precipitation and CO2 upt
55 boratory trials, we demonstrate that thermal buffering by centimetre-thick mussel and seaweed beds el
56 xotomized SNL L5 neurons but enhanced Ca(2+) buffering by neurons in adjacent SNL L4 neurons.
57  the design principles of the supramolecular buffering by ring-chain competition using a combined exp
58  metabolic acid load requiring excretion and buffering by the kidney.
59                                  This social buffering by the male partner on biobehavioral responses
60 acts locally to control the pH by modulating buffering by the NADPH oxidase NOX2.
61 y active positive feedback in the absence of buffering by the negative feedback.
62 Ns, enhanced mGluR1 function is prevented by buffering [Ca(2+)] at normal resting levels while in wil
63 xons from stress and insults, for example by buffering calcium [8].
64                         At both frequencies, buffering calcium prevents LTD induction and LTP results
65 ribe a novel mechanism by which increased Ca buffering can account for changes to systolic Ca(2+) in
66  Furthermore, we predict that supramolecular buffering can be significantly improved using a tetraval
67 ct where even-valent molecules show superior buffering capabilities.
68 at the site, and the depletion of Al mineral buffering capacity after approximately 5 years.
69                                The very high buffering capacity allows the Mediterranean Sea waters t
70 ondria exhibit reduced mitochondrial calcium buffering capacity and are highly sensitive to mitochond
71 n significantly reduced saliva flow rate and buffering capacity and increased mucus acidity.
72 ructure with the potential to extend stretch-buffering capacity and support a revised model for the f
73 tablish a close link between nuclear calcium buffering capacity and the transcription of genes that d
74 f RVH rats, and (2) that a blunted ER Ca(2+) buffering capacity contributes to the altered NMDAR-Delt
75 s also indicated that algae have substantial buffering capacity for free heavy metals in their cytoso
76 tween intermittent contractions and inherent buffering capacity had minimal impact on predicted fatig
77 cell patch-clamp dialysis and quantified its buffering capacity in murine hippocampal slices using co
78 m human brain that suggested loss of calcium buffering capacity in neurons correlated with areas of n
79 r has proven challenging because of a signal buffering capacity inherent in the functionally relevant
80 ticular, it suggests that the Class 1 Ca(2+) buffering capacity is auto-regulated by the rate at whic
81   Mitochondria also buffer Ca(2+), and their buffering capacity is dependent on DeltaPsi Here, we cha
82                 These findings highlight the buffering capacity of developmental systems, allowing ma
83 ty is important for cell uptake and that the buffering capacity of histidine facilitates endosomal me
84 eir virulence varied depending on the pH and buffering capacity of host tissue.
85 er, in a physiological situation, the Ca(2+)-buffering capacity of mitochondria was found not to be e
86 -producing S. gordonii is dominant while the buffering capacity of saliva is valid ( approximately pH
87 vironment can vary depending on the diet and buffering capacity of saliva, materials testing in const
88 ification in the surface ocean decreases the buffering capacity of seawater for CO2, whilst photosynt
89 f biodiesel wastewater and by increasing the buffering capacity of the anode medium.
90                Here we show that the calcium buffering capacity of the cell nucleus in mouse hippocam
91 obal temperature change based on the thermal buffering capacity of the germination phenotype.
92 antitative imaging experiments show that the buffering capacity of the nerve terminal is markedly low
93                 The mechanical stability and buffering capacity of this hydrogel can be adjusted by w
94 n the bacterial cells and facilitated by the buffering capacity of yogurt.
95 ribution of the loss of mitochondrial Ca(2+)-buffering capacity to disease mechanism(s) by eliminatin
96 s of this neurocircuitry maintain sufficient buffering capacity to resist an effect on motivated beha
97                             Reducing HSP90's buffering capacity with inhibitors or febrile temperatur
98 t to the lung, nor a change in eosinophil pH-buffering capacity, allergen-challenged chimeric mice th
99 t SOD1-mediated loss of mitochondrial Ca(2+) buffering capacity, altered mitochondrial morphology, mo
100 ter absorption, nutrient inflow, and luminal buffering capacity, and generates testable predictions o
101  activation, loss of glutamate and potassium buffering capacity, loss of astrocyte coupling, and chan
102            Together they lead to a poor acid buffering capacity, severe acidification and increased c
103 n juxtanuclear ones despite their comparable buffering capacity.
104  due to blunted endoplasmic reticulum Ca(2+) buffering capacity.
105 portant for matching local energy and Ca(2+) buffering capacity.
106 ow level of atmospheric CO2 and a high ocean buffering capacity.
107 e, limited hydraulic conductivity, and redox buffering capacity.
108 gentler droplet environment, despite its low buffering capacity.
109  of calcium, increasing the lysosomal Ca(2+) buffering capacity.
110                       Thus, we can realize a buffering-capacity independent monitoring of changes in
111 tensively in many species, and a function in buffering carbon availability or in fueling later growth
112 further suggest a novel role for this Obp in buffering changes in the odor environment, perhaps provi
113 ree buffer concentration for a wide range of buffering conditions.
114 roximation (LIN), each valid for appropriate buffering conditions.
115 ease (IICR) and reduced mitochondrial Ca(2+) buffering, consistent with a reduced mitochondrial densi
116 s for non-local resource access and resource buffering, crucial in the human foraging niche, will inc
117 (DeltaPsim), the role of the mitochondria in buffering cytosolic Ca(2+) signals was investigated.
118                                              Buffering DAMGO-induced changes in [Ca(2+)]i with BAPTA-
119 ight a novel mechanism by which increased Ca buffering decreases systolic Ca(2+) in old atria.
120      However, the exact magnitude of spatial buffering depends upon demographic parameters such as ad
121  nutrient transfer continuum based on soil P buffering, depth to bedrock, and retention within the aq
122                          Bicarbonate-derived buffering did not contribute to buffering of acid loads
123 lic acidosis and that compensation with bone buffering does take place.
124 ed that canopies played an important role in buffering dry Ndep also at the low Ndep site.
125 n channels, maximal conductances, and Ca(2+) buffering each have independent temperature sensitivitie
126 re at ground level within a forest, with the buffering effect being stronger below-ground than one me
127 d differentiate new adipocytes, prevents its buffering effect in obesity and is characterized by expa
128                 Our results suggest that the buffering effect of a geographically wide distribution o
129 tlantic forests of Brazil, we found that the buffering effect of forests reduced maximum outside temp
130                                          The buffering effect of hematite was further supported by a
131 esponses in numerous species, but the stress-buffering effect of status may dissipate or even reverse
132 rvations of plague resistance and reveal the buffering effect of such evolution against environmental
133 r data show how chemical stresses can reduce buffering effects in the ubiquitin proteasome system.
134 tance of microbial community composition for buffering effects of global change in drylands worldwide
135 tbred adults, suggesting that the beneficial buffering effects of maternal care can persist long afte
136                                      Thermal buffering effects of soil can reduce exposure to extreme
137 ricular nucleus oxytocin mediates the social buffering effects on the stress response and thus may be
138 s consistent with a role as flexible rods in buffering elastic power transmission between the domains
139 ults lead to the concept that reduced Ca(2+) buffering enables fast active zone Ca(2+) signaling, sug
140       Furthermore, imaging, simulations, and buffering experiments all support a model whereby fast N
141              An increase in intracellular Ca buffering explains both the decrease in Ca(2+) transient
142                                        These buffering features also occur in other genes in Drosophi
143 e been used as a dietary supplement and risk-buffering food in ancient Teotihuacan (150 B.C. to A.D.
144 l-level variation; b) provides advantages in buffering food risk, and is positively associated with b
145 maintaining balanced hematopoietic output by buffering FOXO3 expression.
146 he initial assembly of metastable structures buffering free monomers and thereby slows the formation
147                                         This buffering function is most visible after fasting, when l
148 nduce zinc efflux by interfering with the Zn-buffering function of BSH.
149                           In addition to its buffering function, AT is also a target of POPs and may
150 arch and policy interventions geared towards buffering future crop production from climate variabilit
151  astrocyte Ca(2+) and Na(+) signalling, K(+) buffering, gap junction coupling and metabolism.
152 t libraries to identify synthetic lethal and buffering gene pairs across multiple cell types, includi
153          In terms of pH regulation, HCO3 (-) buffering has been shown to be important in both glia an
154                              This phenotypic buffering has been theorized to arise from a variety of
155 ss; thus, we focus on the impact that social buffering has on the stress response and the governing e
156 viding evidence that purifying selection and buffering have limited the deleterious impact of regulat
157   Depriving NHEs of intracellular protons by buffering HC cytosol with a pH 9.2 pipette solution elim
158   Oxytocin (OT) is considered to be a stress-buffering hormone, dampening the physiologic effects of
159 ote CO2 removal from the atmosphere, thereby buffering human effects on global radiative forcing.
160                      The addition of a Na(+) buffering hydrogel layer between the SiO2 of the SiNW an
161                                   The social buffering hypothesis conceptualizes one possible mediati
162 r bond broadens the generality of the social buffering hypothesis.
163 , lowers resting [Ca2+]SR and alters SR Ca2+ buffering in a way that copies the functional instabilit
164 out the role and relative importance of zinc buffering in all organisms.
165 , our findings identify failure of potassium buffering in astrocytes as a crucial mechanism in ammoni
166 indings show diminished mitochondrial Ca(2+) buffering in axotomized SNL L5 neurons but enhanced Ca(2
167 ensitive to blockade of mitochondrial Ca(2+) buffering in order to assess mitochondrial contributions
168 n transport on mitochondrial Ca(2+) flux and buffering in Pi-depleted guinea pig cardiac mitochondria
169 esults demonstrate conclusively that calcium buffering in the mitochondrial matrix in live cells occu
170 cid involved in adenosine triphosphate (ATP) buffering, in oligodendrocyte function.
171 g activity had very little effect on thermal buffering, in terms of macroclimate and microclimate tem
172 patic glucose metabolism was not affected by buffering InsP3 in the nucleus.
173 art, enhancing physiological performance and buffering internal organ function while foraging in the
174           Mitochondria play central roles in buffering intracellular Ca(2)(+) transients.
175  when Ca(2+) release sites were uncoupled by buffering intracellular Ca(2+) with EGTA-AM.
176                                              Buffering intracellular calcium with EGTA-AM or BAPTA-AM
177 rocyte [Ca(2+)]i, [Mg(2+)]i and [H(+)]i, and buffering intracellular pH reduces the [Ca(2+)]i and [Mg
178 gulator of SLC4A4 and CFTR, encoding the key buffering ion transporters, in modulating enamel mineral
179 tion, pointing to a role for this protein in buffering iron availability and facilitating iron-sparin
180                                    Molecular buffering is achieved as a result of competition in a ri
181                             This conditional buffering is confined to the scaffold module, but contro
182  we still do not understand how the level of buffering is controlled in natural populations.
183 nsmission, mitochondrial fusion, and calcium buffering, is complex and was differentially regulated a
184 Zn(2+)-binding mutants by binding Zn(2+) and buffering it to a level such that Zn(2+) can repopulate
185 ntransitivity increased with aridity, partly buffering its negative effects on diversity, but was dec
186 e I(2)PS hollow fiber is found to serve as a buffering layer that mitigates hydraulic compression on
187 teins (HSPs) can be used as a measurement of buffering levels, we propose that ER associated chaperon
188 sting that the strength of endogenous Ca(2+) buffering limits the rate of synchronous synaptic transm
189 stress, social support can serve as a potent buffering mechanism that enhances resilience.
190 urrent connections and functions as a strict buffering mechanism that maintains a roughly constant av
191 n of how this may also serve as a biological buffering mechanism.
192 c oxidative stress condition through a redox-buffering mechanism.
193 of gene expression requires the existence of buffering mechanisms that tightly regulate the magnitude
194 ize differences had undermined developmental buffering mechanisms.
195 ort hairpin RNAs (shRNAs) identified the ATP-buffering, mitochondrial creatine kinase CKMT1 as necess
196  and refolding of misfolded species, thereby buffering mutations that compromise protein structure an
197                                 The electron-buffering nitrosyl's role is subtler as a bifunctional e
198 NA)-Nkx2.1 gene duplex that is essential for buffering Nkx2.1 expression, lung epithelial cell identi
199  This also allows us to conclude that Ca(2+) buffering normally controls late release and prevents th
200 the important role astrocytic EAAT2 plays on buffering nTS excitation and overall cardiorespiratory f
201 on regime in which supramolecular ring-chain buffering occurs as well as the maximum concentration of
202 an important piece to the puzzle of how zinc buffering occurs in a large number of microbes and provi
203 l data of several molecular systems in which buffering occurs via competition between cyclization, gr
204       Our analysis shows that supramolecular buffering of a molecule is caused by its participation a
205 nate-derived buffering did not contribute to buffering of acid loads from short (</= 4 s) trains of a
206  CPu axons, and evidence for endogenous fast buffering of Ca(2+) in NAc.
207 ogical resilience was associated with marked buffering of CTRA activation such that PTSD-affected for
208  mitochondria play a major role in the rapid buffering of cytosolic calcium, we hypothesized that alt
209 ronal excitability via transporter-dependent buffering of extracellular glutamate (Glu).
210                        The amplification and buffering of fire-climate relationships by humans unders
211                               Mfn2 increased buffering of intracellular Ca(2+), an effect mediated th
212      Thus, we found evidence for demographic buffering of life histories, but also evidence of mechan
213 p expression in l-LNvs may contribute to the buffering of light-driven arousal in wild-type flies.
214 cts is limited, and thus there is incomplete buffering of ploidy variation despite a common cytosol.
215 (or a combination of them) provide efficient buffering of size variations.
216 t abundance, but we lack evidence of spatial buffering of temporal variability in demographic rates s
217       We therefore find evidence for spatial buffering of temporal variability in early juvenile surv
218 lation of uptake and efflux transporters and buffering of the free metal concentration by low-molecul
219  reported an organocatalytic system in which buffering of the molecular catalyst by supramolecular in
220 itutions in their substrates, likely through buffering of their destabilizing effects.
221  modification of endogenous BiP enhancing ER buffering of unfolded protein stress in mammalian cells,
222                                           By buffering offspring against environmental perturbation w
223 s reduced by increasing intracellular Ca(2+) buffering or by reducing Ca(2+) influx but did not appea
224 this forest but also plays a central role in buffering or exacerbating impacts of climate fluctuation
225 ner effects occur only during stress (social buffering) or generally throughout daily life (main effe
226 an be partially rescued by improving calcium buffering, or decreasing action potential-evoked calcium
227 g throughout the species' latitudinal range, buffering overall performance across a range of temperat
228 g compensatory increases in alterative redox-buffering pathways.
229 f available calcite plays a critical role in buffering pH; (3) high salinity in general hinders As re
230 side comparison of supramolecular ring-chain buffering, pH buffering, and molecular titration is pres
231 nce Ca2(+)-activated K(+) (BKCa) channels in buffering phenylephrine-induced vasoconstrictions was de
232                               In addition to buffering plants from water stress during severe drought
233                                      Thermal buffering potential is broadly determined by: (i) the di
234 map that used the soil and hydrogeological P buffering potential of the watershed as key assumptions
235 tio of flux and [Ca2+] gradient) and SR Ca2+ buffering power (B).
236 e phagosomes of M1 macrophages had a similar buffering power and proton (equivalent) leakage permeabi
237                                          The buffering power, B, of the sarcoplasmic reticulum (SR),
238                                  The calcium buffering power, binding capacity and non-linear binding
239 s not increase the total acidity and reduces buffering power, tartaric acid shows the opposite behavi
240 mplicating RNA structural remodelling in the buffering process.
241 ed modeling revealed that the low endogenous buffering promotes fast clearance of Ca(2+) from the act
242 ion, treatment with the mitochondrial Ca(2+)-buffering protein parvalbumin significantly suppressed R
243 rin1 (CSQ1), a sarcoplasmic reticulum Ca(2+) buffering protein, inhibits SOCE, but the mechanism of a
244      In the presence of calretinin, a Ca(2+)-buffering protein, the amplitude of cytosolic spikes dur
245                     Our finding of tensional buffering, rather than homeostasis, allows cells to tran
246 o affect both the Ca(2+) uptake rate and the buffering reaction, but the role of anion transport in d
247 e assembly location, providing a wide Ca(2+) buffering regime while maintaining membrane stabilizatio
248  architecture and special energy and calcium-buffering requirements at the synapse.
249 n to localized energy production and calcium buffering requirements.
250                      For DBRHs, we show that buffering requires helicase activity, implicating RNA st
251      These results suggest a possible Ca(2+) buffering role for lysosomes and shed new light on lysos
252 ning of caveolae (known for their mechanical buffering role) associated with integrin diffusion and t
253 plemented-also offer water filtration, flood buffering, soil health, biodiversity habitat, and enhanc
254 ) to the pseudo-EF-hand mitochondrial SCaMCs buffering/solute transport proteins.
255                                          The buffering solution approach is simpler than the standard
256 on external calibration in the presence of a buffering solution containing 5 mg L(-1) Na, K, Ca, Mg a
257 accelerated Li-ion transport, and sufficient buffering space for volume change during electrochemical
258 ffering roles of species and clade ranges in buffering species from background and mass extinctions.
259 exist in continental Antarctica beyond 2099, buffering species-wide declines.
260  through undifferentiated cells by providing buffering storage for excess calcium before final excret
261 ata are informative in developing new Ca(2+) buffering strategies for the failing heart.
262  [Ca(2+) ]i transient, increased fast Ca(2+) buffering strength, shortened action potentials and redu
263 elease per [Ca2+]i transient, increased Ca2+ buffering strength, shortened action potentials, and red
264 d Ca2+ release due to an increased cytosolic buffering strength.
265 s serve very different biological functions, buffering surplus lipids for subsequent oxidation or exp
266 tion with important implications for calcium buffering, synaptic plasticity, and protein-membrane ass
267  most significantly by the cytosolic calcium buffering system and changes in diastolic Ca(2+) .
268 e glutathione pathway, an efficient cellular buffering system that counteracts reactive oxygen specie
269 parvalbumin are part of the cellular calcium buffering system that determines intracellular calcium d
270 support a model in which LDs provide a lipid buffering system that sequesters FAs released during the
271 mRNPs and establishes a post-transcriptional buffering system to facilitate SSC homeostasis in the fl
272        Our results demonstrate that distinct buffering systems are dedicated to particular Ca(2+) sou
273 e Ca(2+) transport, the intracellular Ca(2+) buffering systems expressed in ameloblasts and provides
274 emediation by providing microbially mediated buffering systems for the associated microbial and/or ch
275 t that incorporates diffusion, intracellular buffering systems, and stochastically gated ion channels
276 ation is a result of intrinsic developmental buffering that ensures phenotypic robustness under genet
277 bustness requires a process of developmental buffering that is largely not understood, but which can
278  fat storage in excess of levels optimal for buffering - that is, obesity.
279 with the silicate melt, both responsible for buffering the chlorine (Cl) concentration.
280 '-5' linkages, with the flanking nucleotides buffering the disruptive effects of the isomeric linkage
281 over were also highly protected, potentially buffering the effects of global change.
282 atically search for well individuals who are buffering the effects of rare, highly penetrant, deleter
283 racts with SES, potentially exacerbating and buffering the effects of stress, to predict anthropometr
284 tion and adaptation, acting as CO2 sinks and buffering the impacts of rising sea level.
285 O(2), neutralizing entering protons and thus buffering the periplasm to a pH of roughly 6.1 even in g
286 g the sample for 5 min, adjusting the pH and buffering the sample prior to the immunochemical analysi
287 nhancers that have opposite effects, thereby buffering their impact on enhancer activity.
288  cells that grow more than their neighbours, buffering their influence on organ size and shape.
289 upports their pluripotency, while apparently buffering them against pro-differentiation stimuli.
290 might possess inducible pesticide tolerance, buffering them from agrochemical exposure.
291                                              Buffering therefore distinguishes asynchronous vesicles
292 naturally occurring compound involved in the buffering, transport, and regulation of cellular energy,
293                                              Buffering upward arrow[Ca(2+)]i in endothelial cells doe
294 en engineering approach to improve molecular buffering using multivalent ring-chain systems.
295 vated CA1 pyramidal neuron were reduced when buffering was augmented by exogenous carbonic anhydrase
296 utations that are deleterious and subject to buffering when introduced individually into the ancestra
297          However, strong postsynaptic Ca(2+) buffering with BAPTA abolished the potentiation and sele
298             Increasing intraterminal calcium buffering with EGTA-AM or decreasing calcium influx with
299 type Ca(2+) current and blocked by strong pH buffering with HEPES or TABS.
300 lost across the Eukarya, pointing to genetic buffering within the essential NMD pathway.

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