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1                     However, Kif3a and Ift88 genetic ablation also disrupts ependymal cilia, resultin
2 mia (AML), where, using in vitro and in vivo genetic ablation and knockdown experiments in murine mod
3                                      Through genetic ablation and optogenetic activation, we then sho
4                                        Using genetic ablation and pharmacological inactivation of JNK
5                                         PHD2 genetic ablation and pharmacological inhibition attenuat
6                                              Genetic ablation and pharmacological inhibition of ASIC1
7                                              Genetic ablation and rescue experiments demonstrated tha
8                                              Genetic ablation and selective pharmacologic inhibition
9 eminiscent of those elicited by CB1 receptor genetic ablation, and CB1-null mice were resistant to TH
10      Using quantitative whole-mount imaging, genetic ablation, and traction force microscopy and atom
11                                   Fyn or Lyn genetic ablation as well as treatment with SFK inhibitor
12               Conversely, TSP4 antibodies or genetic ablation blocks nociception and changes in synap
13                     Current techniques allow genetic ablation, constitutive silencing, or hyperactiva
14 C1 activity via either chemical inhibitor or genetic ablation enhances VC.
15 change protein directly activated by cAMP 1) genetic ablation (Epac1(-/-)) protects against experimen
16 is restricted to variant PRC1 complexes, and genetic ablation experiments reveal that targeting of th
17                                     However, genetic ablation experiments showed that satellite cells
18                                 Furthermore, genetic ablation (i.e., knockout) of CaMKIIdelta, the pr
19 as a bona fide tumor suppressor and that its genetic ablation in B cells promotes lymphoma developmen
20 antly, pharmacologic blockade of C5aR or its genetic ablation in C5aR-deficient mice were sufficient
21 vity, whether by pharmacologic inhibition or genetic ablation, inhibited proliferation of PPARG-activ
22                                     Although genetic ablation is straightforward, reversible and spec
23 : the hand2 mutant and a myocardial-specific genetic ablation method.
24                                      Using a genetic ablation model, we asked whether pericyte loss a
25                                              Genetic ablation of a master regulator of cellular defen
26                  In this study, we show that genetic ablation of a natural tuner of TCR signaling, mi
27 mediated signaling downstream of PLCgamma by genetic ablation of a negative regulator of diacylglycer
28                           Here, we show that genetic ablation of a receptor tyrosine kinase encoded b
29                                              Genetic ablation of a recycling endosome resident small
30                                              Genetic ablation of a single immune-regulatory molecule
31                                    Moreover, genetic ablation of a single receptor prevents its cogna
32                                    Moreover, genetic ablation of AAVR renders a wide range of mammali
33 cation-dependent gene expression levels, and genetic ablation of ACIII dramatically alters the cilia
34                                              Genetic ablation of ADAM10 and ADAM17 disrupts the devel
35                                              Genetic ablation of AKAP150 protected against these alte
36                                              Genetic ablation of AKAP7 specifically from dentate gran
37                                              Genetic ablation of Akt1, which is known to abrogate end
38                                              Genetic ablation of Aldh1a1 substantially increases the
39                     The endothelium-specific genetic ablation of Alk1 in Ldlr-KO animals leads to les
40                                              Genetic ablation of alpha6 in collagen-expressing mesenc
41 ciated with Abeta localizing to synapses and genetic ablation of APP prevents both Abeta binding and
42                   However, here we show that genetic ablation of AXL has no effect on ZIKV entry or Z
43                    In contrast, knockdown or genetic ablation of beta-arrestin 2 in an insulin-secret
44                                 We find that genetic ablation of beta-arrestin2, but not beta-arresti
45 wound and tumor vascularization in mice with genetic ablation of both integrin subunits alpha1 and al
46                                              Genetic ablation of both sPLA2s improves recovery from i
47                                              Genetic ablation of Btbd7 in mice disrupts branching mor
48                                              Genetic ablation of C-terminus of Hsc70-interacting prot
49                                              Genetic ablation of C/EBP-alpha in podocytes resulted in
50                                              Genetic ablation of Cacna1a in layer VI neurons produced
51 y a specific increase in the gamma wave, and genetic ablation of canonical transient receptor potenti
52                                              Genetic ablation of caspase-1 and -11 from cpdm mice sig
53  attenuation of these changes by blockade or genetic ablation of CB1R suppresses the growth of HCC an
54 ngly, neither pharmacological inhibition nor genetic ablation of CB2 had any effect on CB2 agonist-in
55                                              Genetic ablation of CBS in CBS heterozygous mice (CBS(+/
56 ronate, MPhi Fas-induced apoptosis mice) and genetic ablation of CCR2 and CX3CR1 all inhibited LLC1 t
57 , mice treated with CCR2 antagonist mimicked genetic ablation of CCR2, showing reduced tumor growth a
58                  In this study, we show that genetic ablation of CCR5 prevents microglial activation
59  production by Th17 cells can be overcome by genetic ablation of CD73 or by using IL1beta instead of
60                           Here, we show that genetic ablation of Cdc42 exclusively in the B cell line
61                                 Furthermore, genetic ablation of CDC42 in both murine and human MLL-A
62                    Here, we demonstrate that genetic ablation of Cdk5 in PV interneurons in mouse bra
63             Consistent with this notion, the genetic ablation of Cdkn1a in FOG-2(R3K5A) mice leads to
64                                              Genetic ablation of cell surface sulfation reduces bacte
65 DT, termed BRAINSPAReDT, for tissue-specific genetic ablation of cells outside the CNS.
66                            Here we show that genetic ablation of cGas in Trex1(-/-) mice eliminated a
67                                              Genetic ablation of circadian clock function or environm
68                                   Concurrent genetic ablation of CK1alpha and IFNAR1 leads to intesti
69                                              Genetic ablation of claudin-14 or the use of a loop diur
70                                              Genetic ablation of Cobra1, which encodes a Pol II-pausi
71                                              Genetic ablation of complement C3 or its inactivation wi
72 Pharmacological blockade of gap junctions or genetic ablation of connexin 36 (Cx36) subunits eliminat
73 hown that pharmacological blockade of GJs or genetic ablation of connexin 36 (Cx36) subunits, which a
74 cadian clock via nighttime light exposure or genetic ablation of core clock components impairs immune
75                                              Genetic ablation of CPEB3 impairs the maintenance of bot
76         We therefore studied consequences of genetic ablation of Cplx1 in the mouse calyx of Held syn
77                                              Genetic ablation of CRIg exacerbated islet inflammation
78                                              Genetic ablation of cyclooxygenases (COX) or prostagland
79 P were increased in heterozygous hearts, but genetic ablation of cyclophilin-D in these hearts signif
80                                    Moreover, genetic ablation of Dclk1 revealed that DCLK1(+) tuft ce
81 unction experiments using pharmacological or genetic ablation of DEGS1 in preadipocytes prevented adi
82                                              Genetic ablation of DOCK8 in human NK cells attenuated c
83 ox/flox);3(+/-) mouse, we show that compound genetic ablation of Dvls causes hydrocephalus.
84 odies prevented Notch-driven metastasis, and genetic ablation of EC Notch signaling inhibited periton
85                                              Genetic ablation of either CASP3 or ENDOG prevented Myc-
86                              However, single genetic ablation of either E-cyclin or Cdk2 does not aff
87 ot undergo sensitization to necroptosis upon genetic ablation of either FADD or caspase-8 and that th
88                                              Genetic ablation of either IFN-gamma signaling or T-bet
89 ormalization of pulmonary STAT3 activity, by genetic ablation of either Il6 or Stat3, suppressed the
90 independent of TNF-TNFR1 signaling since the genetic ablation of either Tnf or Tradd did not rescue t
91 inhibition of NAADP-evoked Ca(2+) release or genetic ablation of endolysosomal TPC1 or TPC2 channels
92 0325901 (MEK1/2 inhibitor) in the tongue and genetic ablation of Erk1 or Calhm1 genes impaired prefer
93          In this study, we demonstrated that genetic ablation of FcRn and excess irrelevant human IgG
94 d into FCRN-humanized mice as effectively as genetic ablation of FcRn, thus preventing the glomerular
95                                              Genetic ablation of Fhl1 in HCM mice was deleterious, wh
96               Pharmacological inhibition and genetic ablation of FoxO1 in smooth muscle cells reprodu
97                                    Selective genetic ablation of Gad2-expressing interneurons severel
98                                     Notably, genetic ablation of gammadelta T cells in ETBF-colonized
99  Consistent with this biochemical mechanism, genetic ablation of GATOR1 nullifies the mTORC1-inhibiti
100           Nevertheless, neither constitutive genetic ablation of Girk1 or Girk2, nor the selective ab
101                                              Genetic ablation of Gli1(+) cells abolished BMF and resc
102                                              Genetic ablation of Gli1(+) cells before induction of ki
103                    Furthermore, we show that genetic ablation of GLUT4 leads to an arrest of synaptic
104 ired by either inhibiting SCFA production or genetic ablation of GPR43.
105 56 and its ligand collagen type III, whereas genetic ablation of GPR56 expression attenuates overload
106                           Here, we show that genetic ablation of Grb2 in MKs and platelets did not in
107 cal blockade of the CGRP or GRPR pathway, or genetic ablation of Grpr, led to a drastically attenuate
108  spontaneous metastasis models, we show that genetic ablation of haematopoietic FAK does not affect p
109      Mice with brown adipose tissue-specific genetic ablation of HDAC3 become severely hypothermic an
110                                              Genetic ablation of HDAC9 improves adipogenic differenti
111                                              Genetic ablation of hmox-1 in H. pylori-infected mice in
112                    We also show that partial genetic ablation of hypothalamic radial glia or their pr
113                                              Genetic ablation of Id2 delayed tumor-induced mortality,
114          Further, inhibition of autophagy or genetic ablation of Ido1 or Gcn2 converted Ab-induced, s
115 ride (LPS)-induced lethality is prevented by genetic ablation of IFN signaling genes such as IFNAR1 a
116 orming upon loss of the tumor suppressor Apc Genetic ablation of Ikkepsilon in beta-catenin-driven mo
117 ot the key effector of this program, because genetic ablation of IKZF1 did not phenocopy pomalidomide
118 t the hepatocyte-specific deletion of Stat3, genetic ablation of Il6, treatment with a neutralizing a
119                                    Selective genetic ablation of ILC2 in Ldlr(-/-) mice accelerates t
120                                              Genetic ablation of ILC2s, however, enhanced IL-1beta, T
121  mouse model of CLL in which B-cell-specific genetic ablation of ILK resulted in decelerated leukemia
122              Importantly, pharmacological or genetic ablation of innervation preserved NK cell functi
123 echanism was confirmed in mice and rats with genetic ablation of insulin signaling and mice lacking a
124                     We demonstrate here that genetic ablation of Ire1alpha in IECs leads to spontaneo
125                                              Genetic ablation of IRE1alpha prevented the colitis-asso
126 in vivo half-life of collagen type VII using genetic ablation of its expression and therapeutic intro
127                  The parasite can counteract genetic ablation of its glucose transporter by increasin
128                                     Finally, genetic ablation of Jnk1 and Jnk2 from cortical interneu
129 n N-terminal kinase (JNK) and c-Jun and that genetic ablation of JNK1 or JNK2 decreased ATZ levels in
130         Heart-specific depletion of SF3B1 or genetic ablation of Khk, but not Khk-A alone, in mice, s
131                       Herein, we report that genetic ablation of Klotho in mice results in a signific
132                                    Moreover, genetic ablation of Kmt2d in mice overexpressing Bcl2 in
133                                     Although genetic ablation of ku or ligD abolishes NHEJ and sensit
134   Furthermore, pharmacological inhibition or genetic ablation of LAL in murine liver largely reduced
135                                              Genetic ablation of Lgr6(+) cells impairs airway injury
136              In this study, we show that the genetic ablation of LHA glutamatergic neurons enhances c
137                                              Genetic ablation of LHA glutamatergic neurons increased
138 CNS specific Nestin promoter to restrict the genetic ablation of Lpd to the central nervous system.
139                                    Selective genetic ablation of LSD1n led to deficits in spatial lea
140 nflammatory phenotype that was suppressed by genetic ablation of lymphocytes.
141                                              Genetic ablation of MasR prevented ischemia-induced mobi
142  is blocked by pharmacological inhibition or genetic ablation of matrix metalloproteinase-9 (MMP-9).
143                                              Genetic ablation of MBP in shiverer mice and mutagenesis
144                                              Genetic ablation of MET signaling in mouse dorsal palliu
145                                              Genetic ablation of Mfsd2a results in a leaky BBB from e
146 tem cells (NSCs), whereas blockade of IL6 or genetic ablation of microglial miR-155 restores neural d
147                                              Genetic ablation of miR-142 caused impaired megakaryocyt
148                                              Genetic ablation of miR-155 increased survival in SOD1 m
149                                     Finally, genetic ablation of miR-223 in mice resulted in increase
150                                     However, genetic ablation of mitosis by knockdown of Cyclin A or
151  protein claudin-3, which was ameliorated by genetic ablation of MMP8.
152 t within 48 h of a spinal lesion or specific genetic ablation of motor neurons at 72 hpf, the pMN dom
153                                              Genetic ablation of MPOA galanin neurons results in mark
154                                              Genetic ablation of MsrB1 did not preclude LPS-induced i
155                                     In vivo, genetic ablation of murine cGAS reveals its requirement
156                       Cancer cell-restricted genetic ablation of murine TRAIL-R in autochthonous KRAS
157                                              Genetic ablation of N-cadherin (N-cad KO) caused hyperpr
158       SUDEP-prone Kcna1-/- mice with partial genetic ablation of Nav1.2 channels (i.e. Scn2a+/-; Kcna
159                                     Although genetic ablation of Nedd9 does not independently influen
160         We have examined the consequences of genetic ablation of Nedd9 in the MMTV-HER2/ERBB2/neu mou
161 and spine density in mature neurons, whereas genetic ablation of neurogenesis increased EPSCs in matu
162                              Using mice with genetic ablation of neuronal PPARgamma (PPARgamma(Nestin
163 f neural circuits is a topic of some debate; genetic ablation of neurotransmitter release by deletion
164 n by using small nidogen-derived peptides or genetic ablation of nidogens prevented the binding of Te
165                                  Conversely, genetic ablation of NLRP12 promoted NIK stabilization, R
166            Upon selective pharmacological or genetic ablation of nociceptors, DDCs failed to produce
167                                  Blockade or genetic ablation of Notch1 and mitogen-activated protein
168                Here we provide evidence that genetic ablation of NOX2 (the prototypical member of NAD
169 gic inhibition of NOX2 in human platelets or genetic ablation of NOX2 in murine platelets.
170                                              Genetic ablation of NRF1 or NRF2 results in vastly diffe
171                            In Krt16-/- mice, genetic ablation of Nrf2 worsened spontaneous skin lesio
172                                              Genetic ablation of Ocrl in mice failed to recapitulate
173                                              Genetic ablation of OGT in AgRP neurons inhibits neurona
174                                              Genetic ablation of OGT in mouse livers reduces autophag
175               Further analysis revealed that genetic ablation of only p18(INK4c) alleviated the requi
176 e, to our knowledge for the first time, that genetic ablation of P2RX7 in the DMD model mouse produce
177                                              Genetic ablation of p311 resulted in a significant decre
178 ation of the premature senescence program by genetic ablation of p53 and p16(INK4a) (Trp53(-/-)Cdkn2a
179             In agreement with these results, genetic ablation of p62 delays HER2-induced mammary tumo
180                                              Genetic ablation of Panx1 in microglia abolished the spi
181                         Here, we report that genetic ablation of PD-1H in mice blocks the differentia
182                                              Genetic ablation of Pdgfra mimics the effect of Nkx2.2 o
183 chemical prevention of centriole assembly or genetic ablation of pericentrin attenuated interleukin-6
184                             Conversely, both genetic ablation of periostin and administration of a pe
185 esult at variance with experimentation using genetic ablation of PGR signaling.
186                     We also demonstrate that genetic ablation of Phd2 and Phd3 was sufficient to prot
187 ansforms human mammary epithelial cells, and genetic ablation of Pik3r1 accelerates a mouse model of
188                       Here, we show that the genetic ablation of PLD1 in mice induces NAFLD due to an
189                                              Genetic ablation of Plin2 in Akita mice leads to mitigat
190                                     Although genetic ablation of Porcn in mouse has provided insight
191                                              Genetic ablation of RAB7L1or C9orf72 in SH-SY5Y cells re
192                                 We find that genetic ablation of radial glia in zebrafish larvae lead
193                                HBC-selective genetic ablation of RelA (p65), the transcriptional acti
194                     Surprisingly, concurrent genetic ablation of RGS4 partially rescued some deficits
195  In a HER2/Neu mouse model of breast cancer, genetic ablation of Rictor decreased cell survival and p
196                                     Although genetic ablation of Rip3 normalizes reticulocyte maturat
197                                              Genetic ablation of ripk1 causes postnatal lethality, wh
198  in Lrat(-) (/-), a murine model for LCA, by genetic ablation of S-opsin.
199                  In this study, we show that genetic ablation of Sema3E in mice results in increased
200                                              Genetic ablation of sensors of apoptotic cells impaired
201                                              Genetic ablation of SIN3A abolishes nutrient regulation
202                                              Genetic ablation of Slc6a2 in SAMs increases brown adipo
203                                              Genetic ablation of SLMAP in human cells leads to sponta
204 sruption of paracrine Hedgehog signaling via genetic ablation of Smoothened (Smo) in stromal fibrobla
205            Defective retrograde transport by genetic ablation of snapin in mice recapitulates late en
206                                              Genetic ablation of some BC neighbors resulted in increa
207 hat give rise to both acinar and duct cells, genetic ablation of SOX2 results in a failure to establi
208 ed SVZ cells to exit the cell cycle, whereas genetic ablation of SOX5/6/21 dramatically increased the
209                 In contrast to the skeleton, genetic ablation of Spp1, the gene encoding OPN, did not
210                                              Genetic ablation of STK11/LKB1 resulted in accumulation
211                                  Conversely, genetic ablation of sympathetic inputs onto fat pads blo
212 ndent on the transcription factor T-BET, and genetic ablation of T-BET increased the onset and penetr
213                                              Genetic ablation of TALK-1 results in beta-cell membrane
214                                              Genetic ablation of tau prevents neuronal overexcitation
215                                Consistently, genetic ablation of TGF-beta signaling in the absence of
216                       Conditional, bilateral genetic ablation of the 175 Cdh9/Dbx1 double-positive p
217  of mouse pancreatic tumors was inhibited by genetic ablation of the alternative p38 pathway, and tra
218                                              Genetic ablation of the clock gene Bmal1 (also called Ar
219 duced PMN transepithelial migration in vitro Genetic ablation of the cPLA2 isoform cPLA2alpha dramati
220           Loss of PGE2 signaling by specific genetic ablation of the EP4 receptor in MuSCs impairs re
221      We also describe ex vivo procedures for genetic ablation of the epicardium, cell proliferation a
222                                     In mice, genetic ablation of the estrogen receptor 1 (Esr1) gene
223                                              Genetic ablation of the H2S-synthesizing enzyme cystathi
224 ucial modulator of hyphal development, since genetic ablation of the HIR complex subunit Hir1 decreas
225 -directed transport is largely unaffected by genetic ablation of the Hook complex adapting early endo
226                                              Genetic ablation of the IFN-alphabeta receptor (IFNAR) o
227                                 Furthermore, genetic ablation of the IL-27 receptor (Il27Ra(-/-)) att
228                                              Genetic ablation of the IL-33 signaling pathway was suff
229                                              Genetic ablation of the IL2Rbeta chain on CD8(+) T cells
230 d attenuating podocyte insulin signalling by genetic ablation of the insulin receptor or the regulato
231                         Here, we demonstrate genetic ablation of the master cytoprotective transcript
232                                 Furthermore, genetic ablation of the miR-143/145 cluster prevented th
233                                              Genetic ablation of the miR-21 stem loop attenuated neoi
234                                              Genetic ablation of the Nod/Ripk2 signaling pathway prot
235                            In murine models, genetic ablation of the NOTCH pathway accelerated bladde
236 n of TGF-beta signaling in vivo in mice, and genetic ablation of the nox4 gene in mice, protected aga
237 xpressing cells are exquisitely sensitive to genetic ablation of the pathway.
238 re and after remission of disease, mice with genetic ablation of the podocyte (Podocyte Apoptosis Thr
239 end on distinct p53 downstream activities as genetic ablation of the pro-apoptotic gene Puma reverts
240 t that pharmacological inhibition as well as genetic ablation of the protein kinase CK2 (CK2) amelior
241  contrast with this model, we show here that genetic ablation of the PSC does not cause an increase i
242 ing leptin deficiency, diet-induced obesity, genetic ablation of the secreted frizzled-related protei
243                                    Selective genetic ablation of the SIRT1 deacetylase domain in skel
244             This phenotype was attenuated by genetic ablation of the TNF receptor TNF-R1 in NEMO(Delt
245                          An exception is the genetic ablation of the TRP channel TRPM7, which results
246                                              Genetic ablation of these cells substantially ameliorate
247  cause tissue damage in lupus-prone mice, as genetic ablation of these cells via beta2 m deficiency d
248 petitive and consummatory behaviors, whereas genetic ablation of these neurons reduced these phenotyp
249                                              Genetic ablation of these neutrophil proteases protected
250                                              Genetic ablation of this small cell population resulted
251                                              Genetic ablation of Thorase in DAT(+) neurons produced i
252                                              Genetic ablation of TLR4 improved stroke outcome in Apoe
253 cantly elevated in Traf2-deficient mice, and genetic ablation of TNFR1 largely abrogated pathological
254       Interestingly, inhibiting apoptosis by genetic ablation of TNFr1 significantly increased cell s
255                                              Genetic ablation of TPL2 in the mouse ameliorates liver
256 TPL2 kinase inhibitor mirrors the effects of genetic ablation of TPL2 in vivo and uncovers ERK and Ak
257  brain development by using lineage-specific genetic ablation of TRF2, an essential component of the
258                                              Genetic ablation of TRIM21 in mice confers protection fr
259                                              Genetic ablation of TrkB in neural stem/progenitor cells
260                                      Indeed, genetic ablation of Trp53, or pharmacological inhibition
261 1 channels protect the skin inflammation, as genetic ablation of TRPV1 function or pharmacological ab
262                                              Genetic ablation of TRPV4 did not affect the distributio
263                                          The genetic ablation of Tweak in SOD1(G93A) mice significant
264 V strain TB40/E, pharmacological blockade or genetic ablation of UL97 significantly reduced the level
265  USP7 in neuroblastoma cancer cell lines, or genetic ablation of Usp7 in the mouse brain, destabilize
266                                              Genetic ablation of VEGF in myeloid cells or pharmacolog
267 lear cell renal cell carcinomas (ccRCC), but genetic ablation of Vhl alone in mouse models is insuffi
268                                              Genetic ablation of WD repeat domain, phosphoinositide-i
269                                  Conversely, genetic ablation of Whsc1 prevented tumor progression in
270                                              Genetic ablation of Wnt7b enhanced the proliferation of
271                            Podocyte-specific genetic ablation of XBP1 or inducible expression of ATF6
272                                              Genetic ablation of Zbtb7b impaired cold-induced transcr
273 of browning murine visceral WAT by selective genetic ablation of Zfp423, a transcriptional suppressor
274             Mouse embryonic fibroblasts with genetic ablations of TSC2 or 4E-BP1/2 express less Egr1
275                  We previously reported that genetic ablation ofCul4ain mice led to male infertility
276                                              Genetic ablation or antibody blockade of DC-HIL delays t
277                      miR-155 was targeted by genetic ablation or by peripheral or centrally administe
278 heir obligatory role in regulating appetite, genetic ablation or chemogenetic inhibition of AgRP neur
279                  Loss of RECON activity, via genetic ablation or inhibition by cdNs, increased NF-kap
280                                              Genetic ablation or inhibition of CXCR2 abrogated metast
281 verexpression of the monooxygenase CYP2C8 or genetic ablation or inhibition of the soluble epoxide hy
282                                              Genetic ablation or pharmacologic inhibition of CC chemo
283                                 Furthermore, genetic ablation or pharmacologic inhibition of Hsp70 su
284 ing cholesterol esterification in T cells by genetic ablation or pharmacological inhibition of ACAT1,
285                         We hypothesized that genetic ablation or pharmacological inhibition of MMP8 w
286                                              Genetic ablation or pharmacological inhibition of tankyr
287 cripts were similarly reduced in response to genetic ablation or pharmacological inhibition of TF-PAR
288                      Here, we tested whether genetic ablation or pharmacological inhibition of the mu
289                                 Furthermore, genetic ablation or reduction of DNA methylation in embr
290                        Loss of Ubiquilins by genetic ablation or sequestration in polyglutamine aggre
291 ing was partly mediated by TRPV4 channels as genetic ablation, or pharmacological blockade impaired i
292 gnaling pathway through antibody blockade or genetic ablation prevented lethal GVHD in multiple murin
293               Furthermore, CK2 inhibition or genetic ablation prevents TH17 cell development and prom
294                                    Moreover, genetic ablation revealed that TGFBI was required for no
295 armaceutical blockade (citalopram dosing) or genetic ablation (SERT(-/-)) of SERT function in vivo le
296                                         Elp3 genetic ablation strongly impaired invasion and metastas
297     Here we show through lineage tracing and genetic ablation that BMI1(+) CSCs mediate invasive grow
298 ow NUDT15 limits thiopurine efficacy and how genetic ablation via the R139C missense mutation confers
299                         Through cellular and genetic ablation we show that epithelial cell death is e
300 lenocytes from mice deficient in NK cells by genetic ablation were used as donors.

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