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.