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1 administered mice and was reduced upon PAR-2 blockage.
2 d hyperexcitable following chronic M-channel blockage.
3 x pump inhibitors (EPIs) to control catheter blockage.
4 d forecasts a danger over one month ahead of blockage.
5 in mouse lungs, which was reduced upon PAR-2 blockage.
6 nocytosine (epsilonC) causes transcriptional blockage.
7 s well as apoptotic cells in the lungs after blockage.
8 escued PDXK disruption induced proliferation blockage.
9 esence of species that do not cause catheter blockage.
10 f Proteus mirabilis infection and subsequent blockage.
11 ertaken to confirm the role of interleukin-1 blockage.
12  provide a clear visual warning of impending blockage.
13 ons or provide warning of impending catheter blockage.
14  proliferation and erythroid differentiation blockage.
15 y 1-10 MPa) that likely stemmed from conduit blockage.
16 ha (GPIbalpha) receptor, thereby causing its blockage.
17 cumulation but may cause irreversible vessel blockage.
18 hindering effect on Hg(0) uptake due to pore blockage.
19  more resilient cake layer and membrane pore blockage.
20 nts (12.7%) had perifimbrial adhesion and/or blockage.
21 d in LUTO etiology as a result of anatomical blockage.
22 ome species have the ability to remove these blockages.
23 s those oriented head-on were severe, stable blockages.
24 ence VAS -10 mm (95% CI -18 to -2) P = 0.02, blockage -0.7 (95% CI -1.3 to -0.1) P = 0.02, with recov
25 st doses: VAS 15 mm (95% CI 4-25) P = 0.009, blockage 1.1 (95% CI 0.5-1.6) P = 0.001.
26                                          The blockage also becomes less pronounced upon reduced RNA p
27 tm1a/tm1a) mice revealed severe nasal airway blockage and abnormal ciliary morphologies in nasal MCCs
28 xazole compound with potent AM2-S31N channel blockage and antiviral activity, in this study we report
29                              Pharmacological blockage and genetic deletion of D2R in DA neurons preve
30 case Rep, resulting in increased replication blockage and thus increased reinitiation away from oriC,
31 miniature coils could be effective in axonal blockage and, if so, what the underlying mechanisms are.
32 II)-catalyzed transformation by surface-site blockage and/or organic Fe(II) complexation.
33 s like a brush layer to prevent SERS-hotspot blockages and fouling by blood-serum proteins.
34 e of alphaHL, resulting in decreased current blockages and slower unzipping.
35 atings provide up to 12h advanced warning of blockage, and are stable both in the absence of infectio
36 influenced by cannabinoid or opioid receptor blockage, and euphoria cannot be studied in mouse models
37 of struvite crystals, catheter encrustation, blockage, and formation of urinary stones.
38 sociated with proliferation, differentiation blockage, and leukemia initiation were differentially ex
39 symptoms (rhinorrhea, mucus in throat, nasal blockage, and sense of smell), patient-reported outcomes
40 ligonucleotide effective charges and current blockages, and between their diffusion constants and DNA
41 omplete evacuation, and a sense of anorectal blockage are just as important as decreased stool freque
42  determined not to cause cardiac ion channel blockage are more likely to pass successfully through cl
43 dicating selective and prolonged replication blockage at 6-4PPs.
44             Bypassing requires translational blockage at a "takeoff codon" immediately upstream of a
45 hin approximately 10 min of replication fork blockage at a site-specific barrier in fission yeast, le
46 nd they suggest that the Gac system senses a blockage at the aconitase step of the tricarboxylic acid
47 queduct are critical for preventing physical blockage between the third and fourth ventricles and the
48 n factor IIS, which is in contrast to pol II blockage by a nucleosome barrier.
49 , the CPP modified drug is released from the blockage by a second triggering agent, while remaining i
50 sign, the electrode surface is less prone to blockage by any formed gas bubbles.
51  asymmetrical extrusion until unidirectional blockage by CTCF that is presumed to occur in mammals.
52                                  Replication blockage by DPC did not produce damaged forks or detecta
53       The channel activity is susceptible to blockage by known drugs and structurally diverse compoun
54 bited new protein synthesis, indicating that blockage by NPPB enhances the degradation of ABCB transp
55 o found using PAGE mass assay that metabolic blockage by phosphate starvation surprisingly increased
56 r tetramethylrhodamine (TMR)-dextran and its blockage by the Na(+)/H(+) exchanger ethylisopropyl amil
57 he results provide information regarding how blockage caused by 1-MCP may be circumvented at the meta
58 nsing mechanism was based on the nanochannel blockage caused by MS2 binding to immobilized capture an
59                                    Capillary blockages colocalised strongly with pericytes, where cap
60                          Pharmacological xCT blockage counteracts NAC prophylactic effects.
61 il identified significant differences in the blockage current and the unzipping duration between the
62 urrent fluctuations that reflects a discrete blockage current level structure.
63  translocation times, ion-current noise, and blockage currents.
64               The phenotypic results of this blockage define patterns of communication among distant
65 stis biofilm formation that is important for blockage-dependent plague transmission from fleas to mam
66            Surprisingly, the effect of ACAT1 blockage does not alter mTOR signaling or endoplasmic re
67 ation of the nanochannels (20 nm pore sized) blockage due to the immunocomplex formation.
68 rent methods to detect drought-induced xylem blockages (e.g., embolisms) and quantify corresponding d
69 ctrical approaches, the underlying geometric blockage effect provides a robust and sensitive signal,
70 rases (Pols) in ameliorating the replication blockage effects elicited by the straight- and branched-
71 ation, and other nBu-PTEs displayed moderate blockage effects, with none of them being mutagenic.
72                By providing reversible nerve blockage, electric stimulation with an implanted electro
73                                GCGR antibody blockage expanded alpha-cell mass 5.7-fold, and S961 had
74 tion with optogenetics, reveal that pericyte blockage facilitates axonal regeneration and neuronal in
75  diffusion constants and DNA-induced current blockage fluctuations.
76 s agencies, leakage for indigenous lands but blockage for federal PAs, suggesting a stronger external
77  m(-1) to 15.1+/-2.6 bar m(-1) due to spacer blockage from the developing biofilm.
78                               Amount of UV-A blockage from windshields and side windows.
79                             We confirmed the blockage function of Tbf1 using synthetic promoters.
80 y tuft input and (simulated) calcium-channel blockage functionally acts as a composite sigmoidal func
81             A high level of side-window UV-A blockage (>90%) was found in 4 of 29 automobiles (13.8%)
82 whether congenital LUTO caused by anatomical blockage has a monogenic cause.
83 ased pumping energy requirements from spacer blockage highlight the serious challenges of using high
84 active cancer vaccination, immune checkpoint blockage (ICB) and chimeric antigen receptor (CAR) for T
85 some to overcome the translation termination blockage imposed by an arrest peptide.
86 iated by tumor associated macrophages, whose blockage improves the effect of CI ablation.
87                 Further analysis indicates a blockage in autophagic flux associated with lysosomal dy
88                            Furthermore, this blockage in cell surface expression was correlated with
89 onstruct markedly reduced APP-induced axonal blockage in Drosophila.
90  antiviral activity based on percent channel blockage in electrophysiological assays.
91  leading edge, the latter is consistent with blockage in membrane trafficking.
92 y and ELISA experiments revealed that GM-CSF blockage in monocytes stimulated production of the chemo
93 ed conditional reduced growth, near complete blockage in PSII supercomplex formation, and concomitant
94 high temperatures is not able to reverse the blockage in ripening.
95                            Chronic autophagy blockage in several conditions, including DRPLA and Vici
96 ilm formation in vitro and biofilm-dependent blockage in the oriental rat flea Xenopsylla cheopis res
97                              betaIII-Tubulin blockage in vivo reduced tumor incidence and growth.
98 h Chlamydia trachomatis may lead to fibrotic blockage in women's upper genital tracts, resulting in t
99 bidopsis (Arabidopsis thaliana) mutants with blockages in the pathway simply redirect carbon flux to
100                                              Blockages in this network stabilize ligand-activated EGF
101 at losses in pedicel kh were associated with blockages in vessel elements, whereas air embolisms were
102  correlated with direct competition and pore blockage indicators.
103 as risking injuries due to gastro-intestinal blockage, ingestion of foamed PS exposes animals to harm
104 nfocal microscopy to show that the secretion blockage is due to the stabilization of open fusion pore
105 during recovery from arterial restriction or blockage is essential for health, but mechanisms are poo
106                                Notably, this blockage is exacerbated in Cockayne Syndrome and xeroder
107                           This transcription blockage is much less pronounced for a C-rich sequence,
108                              Remarkably, the blockage is not pronounced if transcription is performed
109 om control experiments, we conclude that the blockage is primarily due to the formation of stable RNA
110 ts prevent ion currents indicating that pore blockage is primarily responsible.
111                     Detailed analysis of the blockage kinetics of VDAC reconstituted into planar lipi
112 "leakage," more deforestation elsewhere, to "blockage," less deforestation elsewhere.
113                        Comparison of current-blockage levels of each protein yields volumetric inform
114       We further presented evidence that the blockage mechanism is widely used among genome-wide DGPs
115 biosynthesis pathway by chemical and genetic blockage mimicked these transcriptional responses, indic
116 nfer identical defects, including late onset blockage near the terminal cell-stalk cell junction and
117 human cancer cells that evade the cell cycle blockage normally imposed by DNA damage experience susta
118                    In vitro assays indicated blockage of (11)C-sarcosine uptake into PC-3 and LNCaP t
119                                          The blockage of androgen receptor significantly increased ra
120 s in attenuation of caspase 3 activation and blockage of apoptosis.
121 features were phenocopied by pharmacological blockage of Arf6 activation.
122 opQ targets host-cell V-ATPase, resulting in blockage of autophagic flux and neutralization of acidic
123 duced alterations in autophagy result from a blockage of autophagosome degradation rather than an inc
124                                              Blockage of autophagy upregulated radiation-induced cyto
125                                              Blockage of Axl gene expression by small interfering RNA
126 vide an interesting alternative for electric blockage of axonal conductance in clinical settings.
127 f thymus and bone marrow, and stage-specific blockage of B cell development.
128                                              Blockage of B cell-specific PD-L1 restored Th1 responses
129 h p62-dependent inclusion body formation and blockage of Bardet-Biedl syndrome 4 (BBS4) entrance into
130  and the potential benefits arising from the blockage of both inflammation-related enzymes were thoro
131 -6 trans-signaling pathway, but not combined blockage of both, the classical and trans-signaling path
132                                              Blockage of canonical signaling using Sfrp1, Dkk1, or fi
133 ity for its own better survival; conversely, blockage of caspases strongly reduces the severity of th
134 estigate whether the enhancement of ADCML by blockage of CD59 function is mediated by nAbs, non-nAbs,
135                                        After blockage of CD59 function, the reactive Abs, regardless
136  have led to different models, including (i) blockage of cell wall synthesis, (ii) membrane pore form
137 erve in real-time formation of the thrombus, blockage of cerebral perfusion and eventually stroke les
138                                We found that blockage of Ces3 by WWL229 or siRNA dramatically attenua
139                                 Furthermore, blockage of CMA leads to hyperphosphorylation and destab
140                                     Specific blockage of Cx43 HC function by TAT-Gap19, a Cx43 mimeti
141                                 Induction or blockage of CYP3A1 by a miR-23b inhibitor or mimic could
142 m the ER, a process that correlates with LFG blockage of cytochrome c release to the cytosol and casp
143                                    Moreover, blockage of D1R or D2R signaling could alleviate normal
144                                              Blockage of Delta-like 4 (DLL4)-directed Notch signaling
145 ive strain that fails to remove Pxr-mediated blockage of development and reintroduced variably trunca
146 ting in uncontrolled cell proliferation, and blockage of differentiation and chondrodysplasia in mice
147 tional twin-boundary (TB) strengthening from blockage of dislocations impinging on TBs, coupled with
148 this inhibition is primarily mediated by the blockage of DL-glyceraldehyde binding to ALR2.
149                                              Blockage of DNA recognition by the innate immune system
150 yl-DL-tyrosine methyl ester hydrochloride or blockage of DOP1 receptor with antagonist SCH23390 impai
151 lerotic action in vivo via the AMPK-mediated blockage of Drp1-mediated mitochondrial fission.
152 tical for PTHrP action in chondrogenesis, as blockage of ECM1 nearly abolishes PTHrP regulation of ch
153  of both enzymes appears more promising than blockage of either protein alone.
154                                  Conversely, blockage of endogenous GM-CSF with antibody treatment no
155 DAMB-231 and MDAMB-468 cells and resulted in blockage of ER stress-mediated GRP78 up-regulation.
156                                              Blockage of ETAE distinguishes Fe(III) reduction of laye
157                            Hydrosalpinx, the blockage of fallopian tubes, can result from pelvic infl
158 ose tissues (KLB AdipoKO) or pharmacological blockage of FGF21 signaling.
159 led glucose or glutamine revealed a dramatic blockage of flux of these two metabolites into nucleotid
160                              Pharmacological blockage of fructose uptake ameliorates leukemic phenoty
161  are relevant to RTT because pharmacological blockage of GAT3 can normalize tonic inhibition and intr
162                                              Blockage of glutaminolysis had the same inhibitory effec
163                                          The blockage of H4R could be a new therapeutic modality for
164 fore, S. flexneri infection induces a global blockage of host cell intracellular transport, affecting
165  of influenza NS1 protein that causes potent blockage of host gene expression and contributes to inhi
166 duction of reconstitution potential due to a blockage of HSC differentiation.
167 naptic connectivity; chronic pharmacological blockage of Ih channels reproduced these phenotypes, sug
168 The results of this small study suggest that blockage of IL-1beta using gevokizumab may be beneficial
169                                     However, blockage of IL-1R signaling did not abolish the deleteri
170 ioprotective effects against DCM through the blockage of inflammation, oxidative stress, and apoptosi
171 se results provide a basis for a therapeutic blockage of inhibitory guidance molecules to improve vas
172                                              Blockage of integrin alpha5beta1 with ATN161 abolished t
173 in, suggesting inhibition occurs by physical blockage of its allosteric activation, preventing the al
174  p53 expression, which in turn, leads to the blockage of key apoptotic molecules.
175 erol accumulation, we propose that AnxA6 and blockage of LE cholesterol transport are critical for en
176                     Based on these analyses, blockage of lignin monomer methylation by down-regulatio
177                                          The blockage of m(6)A inhibited splicing of the pre-mRNA enc
178 aging, while systemic or V2a neuron-specific blockage of Mc4r promotes locomotion.
179            Coprecipitation led to a complete blockage of mineral surface sites and pores with >/=177
180                                    Moreover, blockage of miR-30b or 378 by locked nucleic acid inhibi
181 ntribution to peroxide metabolism during the blockage of mitochondrial electron transport.
182                                              Blockage of more than one oncoprotein or pathway is now
183      Improving potencies through concomitant blockage of multiple epitopes and avid binding by fusing
184 ed secretory response to HTS treatment after blockage of neuronal activity.
185                                              Blockage of NOS activity with the inhibitor L-NG-nitroar
186 ling that was more potent than pharmacologic blockage of Notch activation via gamma-secretase inhibit
187                                 Furthermore, blockage of nSMase in monocytes/macrophages inhibited th
188                                     Further, blockage of nuclear export of p27 by inhibition of Expor
189                                   Therefore, blockage of one of these molecules might represent a nov
190 eighbor directly overhead, possibly to avoid blockage of overhead light needed for orientation.
191                                              Blockage of P-selectin by administration of anti-P-selec
192 technologies, including genetic tracking and blockage of pericytes in combination with optogenetics,
193 enhanced in Itk(-/-)Btk(-/-) mast cells, and blockage of phosphatidylinositol-4,5-bisphosphate 3-kina
194 static synaptic plasticity elicited by acute blockage of postsynaptic receptors.
195 meliorated the inflammatory response through blockage of proliferation of activated B cells, inhibiti
196                                  Conversely, blockage of proteolipid protein production exacerbated m
197                                        Thus, blockage of RCA function represents a novel approach to
198 olution resulting in complete and incomplete blockage of reproductive tract in infertile and fertile
199 an be substantially reduced by an additional blockage of residual free cysteine residues with 2,2'-di
200                                              Blockage of sclerostin accelerates the PDLSCs lineage co
201 moval of mature microRNAs or pharmacological blockage of signalling pathways drives PSCs into a low-n
202                                              Blockage of some ion channels and in particular, the hER
203 l to vitamin A-deficient (VAD) mice; (2) the blockage of spermatogonial differentiation by impaired r
204 -pool is gradually silenced, leading to full blockage of synaptic transmission.
205  high levels of Dio3 provides double-pronged blockage of T3 action during glial lineage commitment.
206                                              Blockage of TEAD activity by TEADi in human keratinocyte
207                                              Blockage of tetrapyrrole biosynthesis in the AtHEMN1 mut
208                          To permit selective blockage of the accessory site, alpha4 threonine 126 loc
209 ly used in the clinics, and most of them use blockage of the active site for their mode of inhibition
210 hibition that until now has mainly relied on blockage of the active site or occupation of a regulator
211 iers inactivating the proviral promoter, and blockage of the assembly of the host elongation factor P
212 iting phosphoinositide production leads to a blockage of the autophagy flux in LSD chondrocytes.
213 sidue 132 with phenylalanine caused a steric blockage of the B-type channel and no other material str
214  data, for the first time, demonstrated that blockage of the biological function of RCA members rende
215                                              Blockage of the biological function of RCA members, part
216 t obstruction (LUTO) is caused by anatomical blockage of the bladder outflow tract or by functional i
217 f circumventing the physical and biochemical blockage of the blood-brain barrier, could be a precious
218                                              Blockage of the c-met/hepatocyte growth factor axis atte
219 evated oxidative stress, cellular death, and blockage of the cell cycle.
220 occlusion (RVO) can cause vision loss due to blockage of the central retinal vein (CRVO) or a branch
221                              Transient, ~95% blockage of the channel current by alpha-syn was observe
222  could be retarded due to competition and/or blockage of the CYP2D6 enzyme by Amphetamine; We also fo
223 s a pivotal role in cell cycle regulation by blockage of the G1-to-S-phase transition.
224 iated interruption of the GABA signaling and blockage of the GABAA receptor by the specific inhibitor
225          In 2 mouse models of AAA, selective blockage of the IL-6 trans-signaling pathway, but not co
226 accumulation of autophagosomes occurs due to blockage of the lysosomal degradation process.
227 lication of reverse voltages or irreversible blockage of the macroscopic conductance of lysenin chann
228 lated to external mechanisms due to complete blockage of the membrane surface followed by cake format
229   Nonetheless, the consequences of sustained blockage of the mesoaccumbal circuit for motivation and
230                     Remarkably a single-time blockage of the mGluR5 resulted in chronic neuropathic p
231                                              Blockage of the mGluRs alone only modestly reduced the m
232 ation in mitochondria, which is prevented by blockage of the mitochondrial calcium uniporter.
233                                              Blockage of the mTORC2 signal pathway prevented cytokine
234                                     Complete blockage of the nanopore with Pt metal forms a closed bi
235 our previous studies showing that concurrent blockage of the NF-kappaB and Akt signaling pathways sen
236  unveils that PL enhancement arises from the blockage of the optically excited electron transfer from
237 ses chemoresistance, which is accompanied by blockage of the PD-L1 immune checkpoint.
238 tion for a substrate analogous inhibitor and blockage of the predicted ubiquinone binding site provid
239 at selective, unidirectional, and reversible blockage of the primarily dopaminergic mesoaccumbal circ
240  the hematopoietic compartment resulted in a blockage of the progenitor B-cell-to-precursor B-cell de
241                                 In addition, blockage of the STIM1-Orai pathway effectively abolishes
242  Inhibition of TLR4 resulted in differential blockage of the targets.
243                                          The blockage of the translation in CD14(+) monocytes protect
244 th four affected individuals with anatomical blockage of the urethra identified a rare nonsense varia
245  of dendritic beading during pharmacological blockage of these cotransporters.
246                                              Blockage of these pathways may improve muscle quality an
247                                Pharmacologic blockage of these target pathways reduced CSLCs, and thi
248 transmission of TCR signals, a developmental blockage of thymocytes at the transition from double-neg
249                                              Blockage of TREM-1 signaling caused a more severe proinf
250 s as a dual-targeting agent that invokes the blockage of two signal transduction pathways that are ce
251                                              Blockage of ubiquitination at Lys124 was proposed to abr
252  activate the NRF2 signaling pathway through blockage of ubiquitylation and degradation of NRF2 in a
253 he Ba(2+) and hydroxide ions, as well as the blockage of unwanted pathways by adding methanol.
254 ihydroorotate dehydrogenase (DHODH), and the blockage of uridine transport into cells.
255           Results demonstrated a significant blockage of VEGF-VEGFR binding by bevacizumab.
256 everse transcription stalls, consistent with blockage of viral reverse transcriptase at gRNA branch p
257 ns must occur without fault to prevent fatal blockages of the airway.
258 NA-PKcs is necessary to relieve the physical blockage on end-ligation imposed by the DNA-PKcs protein
259 pped on the paper leads to the ion diffusion blockage on microelectrodes, therefore cell concentratio
260                                              Blockage or activation of TREM-1 signaling lowered or ra
261 n with C. muridarum readily induces fibrotic blockage or hydrosalpinx in mice and is used for investi
262 stinal tract while inducing oviduct fibrotic blockage or hydrosalpinx.
263                              Pharmacological blockage or knockdown of STIM1 or ORAI1 reduced ENO-1-de
264  be a promising approach to control catheter blockage, or biofilm formation on other medical devices.
265 dinated apical constriction nor its complete blockage prevent internalization and tube formation, alt
266 mbination of antiretroviral therapy with RCA blockage, provirus activators, and therapeutic vaccines
267 of accessible focusing parameters, including blockage ratio, volumetric flow rate, cell concentration
268                                   P-selectin blockage resulted in a marked reduction of PASMC prolife
269 ase in internal resistance and physical pore blockage resulting from extensive cycling may be importa
270 activation pharmacological protein synthesis blockage results in mnemonic failure in hippocampus-depe
271 tion (D1(-/-) , D2(-/-) ) or pharmacological blockage (SCH23390: 0.1 mg/kg/day/5 days; Raclopride: 0.
272 ence between doxazosin and placebo for nasal blockage score and heart rate after single but not chron
273        Nasal visual analogue scale (VAS) and blockage scores were worse between baseline vs. first do
274                The joining of a durable PD-1 blockage significantly boosted the efficacy of PTX@HSST
275 ion of several inflammatory markers, and its blockage significantly increases bone loss.
276 citive device is able to detect and forecast blockages, similar to early detection procedures in canc
277 established based on the results of antibody blockage, siRNA depletion of Mincle and its adaptor sple
278 ardly removable old hemorrhagic clot as self-blockage site of posterior scleral penetrating trauma, a
279              We found multiple transcription blockage sites adjacent to and within sequences engaged
280 (starvation or mammalian target of rapamycin blockage) stimulated RACK1-ATG5 interaction.
281      Analysis of the detailed pattern of the blockage suggests that RNA polymerase is sterically hind
282 low inhibitory activity in hERG K(+) channel blockage testing, negativity in the Ames test, and 5/5 c
283 port into alpha-cells link glucagon receptor blockage to alpha-cell hyperplasia.
284     However, the beneficial actions of ACAT1 blockage to treat Alzheimer's disease remained not well
285  inhibition of JNK was, similar to NF-kappaB blockage, toxic to autonomously proliferating CARD11(L22
286               Triplex-mediated transcription blockage varied significantly with changes in ambient co
287 itochondrial outer membrane permeabilization blockage via BCL2 overexpression or BAX deletion.
288  average percentage of front-windshield UV-A blockage was 96% (range, 95%-98% [95% CI, 95.7%-96.3%])
289 y of the networks was not achieved if IL-17A blockage was delayed two or more hours postreperfusion.
290                                         This blockage was not observed in DM1 fibroblasts, demonstrat
291                                         This blockage was quantified by measuring the oxidation curre
292  by FFSS was blocked by PGE2 and CM and this blockage was reversed by U0126 and the CM depleted of PG
293 ogressive increase in sIgG(4) levels and FAB blockage were also found.
294 ted with the replication fork were transient blockages, whereas those oriented head-on were severe, s
295 r than the average percentage of side-window blockage, which was 71% (range, 44%-96% [95% CI, 66.4%-7
296 perturbed axonal transport by causing axonal blockages, which were enhanced by reduction of kinesin-1
297  were 49 patients (10.9%) with cornual tubal blockage, while 57 patients (12.7%) had perifimbrial adh
298 low emissive CDs was quenched due to analyte blockage, while that of the blue emissive CDs stayed alm
299                           Furthermore, PAPPA blockage with antibody inhibited embryo implantation in
300 ring ischemia of various severity or channel blockage with realistic timescales.

 
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