1 ere also markedly attenuated by iPLA(2)gamma
genetic ablation.
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 Genetic ablation and pharmacological inhibition of ASIC1
5 Cell type-specific
genetic ablation and pharmacological inhibition of PDK2
6 3 (NLRP3) inflammasome activation, since the
genetic ablation and pharmacological inhibition using th
7 Using
genetic ablation and pharmacological inhibition, we show
8 Genetic ablation and selective pharmacologic inhibition
9 Genetic ablation and therapeutic blockade of CD24 result
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 Genetic ablation confirms the relevance of this R-loop-c
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 a mitochondrial protein phosphatase whose
genetic ablation in mice results in mitochondria-related
17 vity, whether by pharmacologic inhibition or
genetic ablation,
inhibited proliferation of PPARG-activ
18 nflammatory disease in humans, whereas their
genetic ablation is embryonically lethal in mice.
19 Although
genetic ablation is straightforward, reversible and spec
20 Using a
genetic ablation model, we asked whether pericyte loss a
21 Using a myocyte-selective
genetic ablation mouse model of the essential clock acti
22 Furthermore, ventriculomegaly was rescued by
genetic ablation of 5,10-methylene tetrahydrofolate redu
23 In zebrafish,
genetic ablation of 5-HT production by the raphe reduces
24 Here, we show that
genetic ablation of a receptor tyrosine kinase encoded b
25 Genetic ablation of a single immune-regulatory molecule
26 Moreover,
genetic ablation of a single receptor prevents its cogna
27 Moreover,
genetic ablation of AAVR renders a wide range of mammali
28 hesis to facilitate de novo lipogenesis, and
genetic ablation of ACO2 reduced total lipid content and
29 Genetic ablation of Aldh1a1 substantially increases the
30 a transgenic mouse strain with constitutive
genetic ablation of Aldh7a1.
31 The endothelium-specific
genetic ablation of Alk1 in Ldlr-KO animals leads to les
32 ses to acute light exposure are absent after
genetic ablation of all ipRGCs except a subpopulation th
33 Genetic ablation of alpha3 in established skin tumors ca
34 Genetic ablation of alpha6 in collagen-expressing mesenc
35 To compare the effects of
genetic ablation of Ank, Enpp1, and both factors concurr
36 Genetic ablation of Ank, Enpp1, or both factors increase
37 ediated ADP/ATP exchange promotes mitophagy,
genetic ablation of ANT paradoxically suppresses mitopha
38 ciated with Abeta localizing to synapses and
genetic ablation of APP prevents both Abeta binding and
39 Though
genetic ablation of autophagy strongly attenuates primar
40 However, here we show that
genetic ablation of AXL has no effect on ZIKV entry or Z
41 apacity of insulin-producing cells following
genetic ablation of beta cells.
42 Genetic ablation of beta-arrestin2 markedly ablates tau
43 We find that
genetic ablation of beta-arrestin2, but not beta-arresti
44 ng using Sfrp1, Dkk1, or fibroblast-specific
genetic ablation of beta-catenin strongly decreased the
45 wound and tumor vascularization in mice with
genetic ablation of both integrin subunits alpha1 and al
46 Genetic ablation of Btbd7 in mice disrupts branching mor
47 Genetic ablation of C-terminus of Hsc70-interacting prot
48 Genetic ablation of C2cd4a in beta cells of mice phenoco
49 Genetic ablation of C3 accelerated structural and functi
50 Genetic ablation of Cacna1a in layer VI neurons produced
51 Genetic ablation of CBS in CBS heterozygous mice (CBS(+/
52 reactive oxygen species (ROS) generation or
genetic ablation of CD11b.
53 We show highly efficient
genetic ablation of CD33 antigen using CRISPR/Cas9 techn
54 Genetic ablation of Cd36 in T(reg) cells suppressed tumo
55 Genetic ablation of CD73 compromised HSPC transplantatio
56 Furthermore,
genetic ablation of CDC42 in both murine and human MLL-A
57 Genetic ablation of cell surface sulfation reduces bacte
58 DT, termed BRAINSPAReDT, for tissue-specific
genetic ablation of cells outside the CNS.
59 Furthermore, after
genetic ablation of cholinergic Pitx2(+) interneurons, M
60 Genetic ablation of circadian clock function or environm
61 In contrast,
genetic ablation of claustral neurons attenuated SW acti
62 Genetic ablation of Cobra1, which encodes a Pol II-pausi
63 Genetic ablation of complement C3 or its inactivation wi
64 Pharmacological blockade of gap junctions or
genetic ablation of connexin 36 (Cx36) subunits eliminat
65 hown that pharmacological blockade of GJs or
genetic ablation of connexin 36 (Cx36) subunits, which a
66 cadian clock via nighttime light exposure or
genetic ablation of core clock components impairs immune
67 Genetic ablation of CRIg exacerbated islet inflammation
68 Furthermore,
genetic ablation of DNAJB9 in WT mice increased CFTR exp
69 d from DNA-hypomethylated 2i/L ES cells with
genetic ablation of Dnmt3a or Dnmt3b.
70 Genetic ablation of DOCK8 in human NK cells attenuated c
71 odies prevented Notch-driven metastasis, and
genetic ablation of EC Notch signaling inhibited periton
72 Here, we found that global
genetic ablation of EHD2 in mice leads to increased lipi
73 RagA translation are strongly attenuated by
genetic ablation of eIF4E phosphorylation, MNK1 eliminat
74 Genetic ablation of either CASP3 or ENDOG prevented Myc-
75 Genetic ablation of either CD24 or Siglec-10, as well as
76 Genetic ablation of either IFN-gamma signaling or T-bet
77 ormalization of pulmonary STAT3 activity, by
genetic ablation of either Il6 or Stat3, suppressed the
78 The
genetic ablation of either of these downstream effectors
79 independent of TNF-TNFR1 signaling since the
genetic ablation of either Tnf or Tradd did not rescue t
80 Indeed,
genetic ablation of endocardially derived macrophages ca
81 Genetic ablation of Epha2 or Ptgs2 in preclinical models
82 0325901 (MEK1/2 inhibitor) in the tongue and
genetic ablation of Erk1 or Calhm1 genes impaired prefer
83 We induced
genetic ablation of exon 11 in the Brca1 gene specifical
84 Endothelial
genetic ablation of Fgfbp1 results in transient hypervas
85 Here, we found that
genetic ablation of GABA(B) receptors in medial prefront
86 Notably,
genetic ablation of gammadelta T cells in ETBF-colonized
87 Genetic ablation of Gli1(+) cells abolished BMF and resc
88 Genetic ablation of Gli1(+) cells before induction of ki
89 Furthermore, we show that
genetic ablation of GLUT4 leads to an arrest of synaptic
90 We now document that liver-conditional
genetic ablation of gp78/AMFR in male mice disrupts P450
91 ired by either inhibiting SCFA production or
genetic ablation of GPR43.
92 Mice with brown adipose tissue-specific
genetic ablation of HDAC3 become severely hypothermic an
93 Genetic ablation of hepatic p38a increases simple steato
94 Here, we show that
genetic ablation of HSP70 markedly impairs HCC initiatio
95 Genetic ablation of Id2 delayed tumor-induced mortality,
96 Genetic ablation of Idol increases low-density lipoprote
97 ride (LPS)-induced lethality is prevented by
genetic ablation of IFN signaling genes such as IFNAR1 a
98 jection of wild type but not SA fibroblasts,
genetic ablation of IFNAR1 in fibroblasts also accelerat
99 We show that
genetic ablation of IFT20 in vitro slows keratinocyte mi
100 orming upon loss of the tumor suppressor Apc
Genetic ablation of Ikkepsilon in beta-catenin-driven mo
101 Germ-free environment improves, and
genetic ablation of IL-22 restores normal growth in mice
102 interleukin-27 receptor (IL-27R) in AAA, as
genetic ablation of IL-27R protects mice from the diseas
103 Importantly,
genetic ablation of Il33 potentiated the therapeutic eff
104 t the hepatocyte-specific deletion of Stat3,
genetic ablation of Il6, treatment with a neutralizing a
105 Selective
genetic ablation of ILC2 in Ldlr(-/-) mice accelerates t
106 mouse model of CLL in which B-cell-specific
genetic ablation of ILK resulted in decelerated leukemia
107 Importantly, pharmacological or
genetic ablation of innervation preserved NK cell functi
108 inhibit glucagon secretion is lost following
genetic ablation of insulin receptors in the somatostati
109 We also demonstrate that
genetic ablation of integrin beta6 impedes colorectal CI
110 Genetic ablation of interleukin-1 ligands or receptor in
111 Mechanistically,
genetic ablation of iPLA(2)gamma markedly decreased the
112 Genetic ablation of IRE1alpha prevented the colitis-asso
113 In this study, after
genetic ablation of Itga4 in DCs and monocytes in mice v
114 in vivo half-life of collagen type VII using
genetic ablation of its expression and therapeutic intro
115 The parasite can counteract
genetic ablation of its glucose transporter by increasin
116 n N-terminal kinase (JNK) and c-Jun and that
genetic ablation of JNK1 or JNK2 decreased ATZ levels in
117 Indeed, pharmacologic inhibition and
genetic ablation of JNKs, as well as silencing of expres
118 These mice were generated with
genetic ablation of L-type Ca(v)1.3 (Ca(v)1.3(-/-)), T-t
119 Furthermore, pharmacological inhibition or
genetic ablation of LAL in murine liver largely reduced
120 Pharmacological or
genetic ablation of large conductance Ca(2+)-activated K
121 Genetic ablation of Lgr6(+) cells impairs airway injury
122 Genetic ablation of LHA glutamatergic neurons increased
123 CNS specific Nestin promoter to restrict the
genetic ablation of Lpd to the central nervous system.
124 icular, it has been shown that mechanical or
genetic ablation of LRC cells affect meristem size [7, 8
125 Chemical blockade or
genetic ablation of LRRC8A/SWELL1, a VRAC subunit, resul
126 Lsd1 are unable to drive tumorigenesis, and
genetic ablation of Lsd1 markedly impairs tumor growth i
127 nflammatory phenotype that was suppressed by
genetic ablation of lymphocytes.
128 Genetic ablation of MasR prevented ischemia-induced mobi
129 is blocked by pharmacological inhibition or
genetic ablation of matrix metalloproteinase-9 (MMP-9).
130 ssion of small GTPase proteins in cells upon
genetic ablation of METTL3 (the catalytic subunit of the
131 Finally,
genetic ablation of MFS2 increased fly life span, sugges
132 This action of FGF23 is blocked by
genetic ablation of MFS2.
133 a repressive role at stress response genes,
genetic ablation of Mi-2beta did not prevent reestablish
134 Genetic ablation of microglia inhibits astrocyte death,
135 Antisense targeting and
genetic ablation of miR-128-1 in mouse metabolic disease
136 protein claudin-3, which was ameliorated by
genetic ablation of MMP8.
137 l matrix uptake of Ca(2+) We also found that
genetic ablation of MPC1 in hepatocytes and mouse embryo
138 Genetic ablation of MsrB1 did not preclude LPS-induced i
139 Genetic ablation of MST1 in mouse embryonic fibroblasts
140 cological suppression or epithelial-specific
genetic ablation of Myc in tubular epithelial cells amel
141 Genetic ablation of N-cadherin (N-cad KO) caused hyperpr
142 SUDEP-prone Kcna1-/- mice with partial
genetic ablation of Nav1.2 channels (i.e. Scn2a+/-; Kcna
143 and spine density in mature neurons, whereas
genetic ablation of neurogenesis increased EPSCs in matu
144 Using mice with
genetic ablation of neuronal PPARgamma (PPARgamma(Nestin
145 f neural circuits is a topic of some debate;
genetic ablation of neurotransmitter release by deletion
146 Blockade or
genetic ablation of Notch1 and mitogen-activated protein
147 First, we showed that
genetic ablation of Nox4 in Dahl salt-sensitive (SS) rat
148 S-mutant melanomas can acquire resistance to
genetic ablation of NRAS or combination MEK1/2 and CDK4/
149 Genetic ablation of NRF1 or NRF2 results in vastly diffe
150 In Krt16-/- mice,
genetic ablation of Nrf2 worsened spontaneous skin lesio
151 Genetic ablation of Nsd1 and its paralogue Nsd2 in mouse
152 Genetic ablation of Ocrl in mice failed to recapitulate
153 Genetic ablation of OGT in mouse livers reduces autophag
154 Pharmacologic and
genetic ablation of OPN inhibited debris-stimulated tumo
155 zes tumor cells to gemcitabine in vitro, and
genetic ablation of p110gamma protects against Kras-indu
156 Muscle-specific
genetic ablation of p21-activated kinase (PAK)2, but not
157 Genetic ablation of p311 resulted in a significant decre
158 Interfering with CPH by either
genetic ablation of P4H subunit alpha-2 (P4HA2) or pharm
159 ation of the premature senescence program by
genetic ablation of p53 and p16(INK4a) (Trp53(-/-)Cdkn2a
160 However, because there was no phenotype with
genetic ablation of PAK1 alone, consequently, the relati
161 Genetic ablation of Panx1 in microglia abolished the spi
162 Here, we report that
genetic ablation of PD-1H in mice blocks the differentia
163 Pharmacological inhibition and
genetic ablation of PDE3B prevented autoimmune disease a
164 chemical prevention of centriole assembly or
genetic ablation of pericentrin attenuated interleukin-6
165 esult at variance with experimentation using
genetic ablation of PGR signaling.
166 The
genetic ablation of Phc2 in mice causes a severe defect
167 ansforms human mammary epithelial cells, and
genetic ablation of Pik3r1 accelerates a mouse model of
168 Here, we show that the
genetic ablation of PLD1 in mice induces NAFLD due to an
169 Genetic ablation of Plin2 in Akita mice leads to mitigat
170 Genetic ablation of POLR1A-high cell population imposes
171 Genetic ablation of Ppp1r3a in mice impaired binding of
172 In male mice,
genetic ablation of Pramef12 arrests spermatogenesis and
173 eloped a GBM tumor model wherein conditional
genetic ablation of prolyl 4-hydroxylase subunit beta (P
174 Here, we reveal that
genetic ablation of pS-STAT3 in the gp130 (F/F) spontane
175 Genetic ablation of RAB7L1or C9orf72 in SH-SY5Y cells re
176 We find that
genetic ablation of radial glia in zebrafish larvae lead
177 HBC-selective
genetic ablation of RelA (p65), the transcriptional acti
178 Although
genetic ablation of Rip3 normalizes reticulocyte maturat
179 Genetic ablation of Ripk1 results in perinatal lethality
180 In this study, we show that
genetic ablation of Sema3E in mice results in increased
181 Genetic ablation of sensors of apoptotic cells impaired
182 Genetic ablation of serine protease inhibitor SerpinB9 (
183 In both fly and mouse models,
genetic ablation of Sestrins prevents organisms from acq
184 in mitochondrial NADPH production pathway or
genetic ablation of SHMT2 causes strong increases in inf
185 pe of Stat3(SA/SA) mice was phenocopied upon
genetic ablation of signaling by the cytokine IL-11, whi
186 Genetic ablation of SIN3A abolishes nutrient regulation
187 Genetic ablation of Slc6a2 in SAMs increases brown adipo
188 Genetic ablation of SLMAP in human cells leads to sponta
189 Genetic ablation of smooth muscle TRPC3 channels shorten
190 sruption of paracrine Hedgehog signaling via
genetic ablation of Smoothened (Smo) in stromal fibrobla
191 Defective retrograde transport by
genetic ablation of snapin in mice recapitulates late en
192 hat give rise to both acinar and duct cells,
genetic ablation of SOX2 results in a failure to establi
193 Genetic ablation of Sox2 suppresses neuroendocrine diffe
194 ed SVZ cells to exit the cell cycle, whereas
genetic ablation of SOX5/6/21 dramatically increased the
195 Specifically,
genetic ablation of Sox8 and Sox9 prevents ovarian-to-te
196 In contrast, intersectional
genetic ablation of spinal Grp neurons does not affect i
197 Genetic ablation of SPRED genes in mice leads to behavio
198 Genetic ablation of SREBP activity in myeloid cells or t
199 Genetic ablation of SREBP function shifted the balance o
200 e lineage cells produced glucocorticoids and
genetic ablation of steroidogenesis in these cells as we
201 Genetic ablation of STK11/LKB1 resulted in accumulation
202 Genetic ablation of synchronous release was previously s
203 Genetic ablation of T cell steroidogenesis restricts pri
204 ndent on the transcription factor T-BET, and
genetic ablation of T-BET increased the onset and penetr
205 In this study, we show that whereas
genetic ablation of Tcf1 in mice greatly diminished T(FH
206 Strikingly,
genetic ablation of Tet2 in mice cooperated with oncogen
207 Genetic ablation of TFEB and TFE3 in mice results in der
208 Consistently,
genetic ablation of TGF-beta signaling in the absence of
209 Conditional, bilateral
genetic ablation of the 175 Cdh9/Dbx1 double-positive pr
210 Genetic ablation of the Cdkn2a locus restored muscle ste
211 duced PMN transepithelial migration in vitro
Genetic ablation of the cPLA2 isoform cPLA2alpha dramati
212 Loss of PGE2 signaling by specific
genetic ablation of the EP4 receptor in MuSCs impairs re
213 Genetic ablation of the FA-associated scaffold protein H
214 es or the central nervous system (CNS) using
genetic ablation of the FGF21 co-receptor beta-klotho in
215 Specifically,
genetic ablation of the Gbetagamma dimer or loss of the
216 Genetic ablation of the H2S-synthesizing enzyme cystathi
217 ucial modulator of hyphal development, since
genetic ablation of the HIR complex subunit Hir1 decreas
218 Genetic ablation of the HLA-DR alpha-chain rendered cell
219 -directed transport is largely unaffected by
genetic ablation of the Hook complex adapting early endo
220 Genetic ablation of the IFN-alphabeta receptor (IFNAR) o
221 Furthermore,
genetic ablation of the IL-27 receptor (Il27Ra(-/-)) att
222 Genetic ablation of the IL2Rbeta chain on CD8(+) T cells
223 Genetic ablation of the Lamc1 gene in adult mice was rap
224 Here, we demonstrate
genetic ablation of the master cytoprotective transcript
225 Furthermore,
genetic ablation of the miR-143/145 cluster prevented th
226 Acute pharmacological inhibition or
genetic ablation of the mitochondrial deubiquitinase (DU
227 xpressing cells are exquisitely sensitive to
genetic ablation of the pathway.
228 re and after remission of disease, mice with
genetic ablation of the podocyte (Podocyte Apoptosis Thr
229 end on distinct p53 downstream activities as
genetic ablation of the pro-apoptotic gene Puma reverts
230 t that pharmacological inhibition as well as
genetic ablation of the protein kinase CK2 (CK2) amelior
231 platform, including rapamycin treatment and
genetic ablation of the Ragulator subunit LAMTOR4, revea
232 Lack of sialylated glycans due to
genetic ablation of the Sia-activating enzyme CMP-sialic
233 An exception is the
genetic ablation of the TRP channel TRPM7, which results
234 Genetic ablation of these APs in vivo, using Ca(V) 1.3(-
235 cause tissue damage in lupus-prone mice, as
genetic ablation of these cells via beta2 m deficiency d
236 aling through IFNLR, it is not known whether
genetic ablation of these cytokines phenotypically recap
237 ated by in vivo ethanol consumption and that
genetic ablation of these neurons decreases ethanol cons
238 Here we use
genetic ablation of this enzyme to induce indolence in t
239 Genetic ablation of Thorase in DAT(+) neurons produced i
240 th that observation, we found that mice with
genetic ablation of Tnf in basophils exhibited reduced s
241 cantly elevated in Traf2-deficient mice, and
genetic ablation of TNFR1 largely abrogated pathological
242 Interestingly, inhibiting apoptosis by
genetic ablation of TNFr1 significantly increased cell s
243 Genetic ablation of TPL2 in the mouse ameliorates liver
244 TPL2 kinase inhibitor mirrors the effects of
genetic ablation of TPL2 in vivo and uncovers ERK and Ak
245 Herein, we report that
genetic ablation of transient receptor potential vanillo
246 Genetic ablation of Trem2 in mice globally inhibits the
247 brain development by using lineage-specific
genetic ablation of TRF2, an essential component of the
248 Genetic ablation of TRIM21 in mice confers protection fr
249 Genetic ablation of TrkB in neural stem/progenitor cells
250 Interestingly,
genetic ablation of TRPML1 in mice (Mcoln1 (-/-) ) induc
251 1 channels protect the skin inflammation, as
genetic ablation of TRPV1 function or pharmacological ab
252 USP7 in neuroblastoma cancer cell lines, or
genetic ablation of Usp7 in the mouse brain, destabilize
253 mic administration of anti-VCAM1 antibody or
genetic ablation of Vcam1 in BECs counteracts the detrim
254 lear cell renal cell carcinomas (ccRCC), but
genetic ablation of Vhl alone in mouse models is insuffi
255 Genetic ablation of WD repeat domain, phosphoinositide-i
256 Conversely,
genetic ablation of Whsc1 prevented tumor progression in
257 Genetic ablation of Wnt7b enhanced the proliferation of
258 Pharmacological inhibition of FAO or
genetic ablation of YAP suppressed LN metastasis in mice
259 Genetic ablation of Zbtb7b impaired cold-induced transcr
260 of browning murine visceral WAT by selective
genetic ablation of Zfp423, a transcriptional suppressor
261 We previously reported that
genetic ablation ofCul4ain mice led to male infertility
262 Genetic ablation or antibody blockade of Siglec-15 ampli
263 Genetic ablation or blockade of components of IL-6-STAT3
264 Genetic ablation or blocking of 4-1BBL signaling by Ab o
265 Genetic ablation or chemical inhibition of AMPK activity
266 Loss of RECON activity, via
genetic ablation or inhibition by cdNs, increased NF-kap
267 Genetic ablation or inhibition of CXCR2 abrogated metast
268 verexpression of the monooxygenase CYP2C8 or
genetic ablation or inhibition of the soluble epoxide hy
269 Genetic ablation or manual removal of ROCs blocks regene
270 Genetic ablation or pharmaceutical blockade of IRE1alpha
271 Genetic ablation or pharmacologic inhibition of CC chemo
272 Furthermore,
genetic ablation or pharmacologic inhibition of Hsp70 su
273 Genetic ablation or pharmacologic inhibition of RAGE blo
274 ing cholesterol esterification in T cells by
genetic ablation or pharmacological inhibition of ACAT1,
275 IO-RhoA non-canonical Galphaq-signaling, and
genetic ablation or pharmacological inhibition of FAK in
276 We hypothesized that
genetic ablation or pharmacological inhibition of MMP8 w
277 Genetic ablation or pharmacological inhibition of PERK s
278 Genetic ablation or pharmacological inhibition of tankyr
279 Genetic ablation or pharmacological inhibition of the he
280 Here, we tested whether
genetic ablation or pharmacological inhibition of the mu
281 Genetic ablation or pharmacological inhibition of USP7 r
282 Either
genetic ablation or pharmacological inhibition of WWP1 t
283 Furthermore,
genetic ablation or reduction of DNA methylation in embr
284 In mice,
genetic ablation or selective pharmacological inhibition
285 We find that
genetic ablation or therapeutic inactivation of mast cel
286 ing was partly mediated by TRPV4 channels as
genetic ablation,
or pharmacological blockade impaired i
287 kinase inhibitors fail to recapitulate ERK5
genetic ablation phenotypes, suggesting kinase-independe
288 gnaling pathway through antibody blockade or
genetic ablation prevented lethal GVHD in multiple murin
289 Furthermore, CK2 inhibition or
genetic ablation prevents TH17 cell development and prom
290 Using
genetic ablation,
quantitative imaging, mechanochemical
291 Liver-specific gp78/AMFR
genetic ablation results in functional protein stabiliza
292 Moreover,
genetic ablation revealed that TGFBI was required for no
293 armaceutical blockade (citalopram dosing) or
genetic ablation (
SERT(-/-)) of SERT function in vivo le
294 Elp3
genetic ablation strongly impaired invasion and metastas
295 Employing conditional lineage-specific
genetic ablation studies in mice, we found that loss of
296 Here we show through lineage tracing and
genetic ablation that BMI1(+) CSCs mediate invasive grow
297 Enzymatic removal of cell surface GAGs and
genetic ablation that diminishes GAG expression reduced
298 ow NUDT15 limits thiopurine efficacy and how
genetic ablation via the R139C missense mutation confers
299 By VTA cell-type-specific
genetic ablation,
we found that ablation of glutamate, b
300 lenocytes from mice deficient in NK cells by
genetic ablation were used as donors.