1 Significant injuries
were absent in 2,815 of the 2,823 patients assigned low-
2 HPSE2 mutations
were absent in 23 non-neurogenic neurogenic bladder prob
3 n 59 patients (16%; other-LGE group), and it
was absent in 26 patients (no-LGE group).
4 egated with the disease in all pedigrees and
were absent in 300 unrelated controls.
5 red in 7 of 289 men with azoospermia (2.4%),
were absent in 384 controls with normal sperm concentrat
6 nine lesions in DNA and has been reported to
be absent in 5-20% of most tumor types.
7 limb muscle, both in vivo and in vitro, this
was absent in 6 of 6 Kcne3(-/-) mice tested.
8 omotes a tumorigenic phenotype in vitro, and
is absent in 723 other salivary gland tumors.
9 The p.Gly97Arg
was absent in 800 ethnically matched chromosomes and 140
10 This novel outcome-prediction encoding
was absent in a control task, in which actions were rewa
11 4%, indicating that left atrial hypertension
was absent in a majority of patients.
12 females' memory advantage during free recall
was absent in a recognition setting.
13 This transfer effect
was absent in active and sham control groups.
14 ncrease in the fast delta band (2-4 Hz) that
is absent in adults.
15 cellular mechanism of neonatal healing that
is absent in adults.
16 SOCE
was absent in agonist-stimulated sweat glands from Orai1
17 Cilia
are absent in all organs examined, leading to the conclu
18 edly, we show that the phosphorylation motif
is absent in all eukaryotic neuronal VAMPs, but present
19 ecundity in both sexes when leptin signaling
is absent in all other cells and that in females, the ab
20 rapid eye movement (REM) and non-REM sleep,
was absent in all animals in which 5-HT deficiency was v
21 Intraocular antibody production and DNA
was absent in all tested patients.
22 Palisades of Vogt
were absent in all (100.0%) patients, and the cornea-con
23 Notably, methanogen 16S rRNA signatures
were absent in all Illumina libraries and mcrA was not d
24 S cones
were absent in Allocebus trichotis and Cheirogaleus medi
25 importance of this repair pathway, MutS-MutL
are absent in almost all Actinobacteria and many Archaea
26 s of alpha6-containing (alpha6*) nAChRs, and
were absent in alpha6*-nAChR knockout mice.
27 Such complex changes in MN recruitment
were absent in ALS-resistant OMNs.
28 -type mice, but vasoconstriction and rupture
were absent in Amhr2(cre/+)SmoM2 mice in which follicle
29 so inhibited lipid synthesis, an effect that
was absent in AMPK knockout cells and that required phos
30 Left ventricular outflow tract gradients
are absent in an important proportion of patients with h
31 all intestinal lamina propria, this increase
was absent in antibiotic-treated mice.
32 rved within the native range of the host and
was absent in areas where international trade has moved
33 Light-evoked outer retina Delta1/T1rho
was absent in ARR1-null mice and supernormal in overexpr
34 rate laser power, while such optical control
is absent in as-WS2 for all growth substrates investigat
35 ome cell lines expressing an IgG BCR, but it
was absent in BCR(-) B cell lines.
36 entified both structurally and functionally,
was absent in beta cells from human T2D donors and in IN
37 Surprisingly, obestatin-induced GSIS
was absent in beta-cells in which GHS-R was suppressed.
38 To our knowledge, these novel findings
are absent in blood flow in straight tubes, and they und
39 rkers, including CD73, CD49d and CD200, that
are absent in both fibroblasts and iPS cells.
40 tes unusual features in the PX molecule that
are absent in both the molecules to which it is compared
41 In hearing signers, enhanced activation
was absent in both left and right STC during all three t
42 muli were physically identical and the inset
was absent in both, subjects behaved opposite to optimal
43 Deleterious CFTR variants
were absent in both pedigrees.
44 sponsive floral meristem identity gene EaLFY
were absent in both VG and HG plants, suggesting that a
45 es in patients with COPD with emphysema that
is absent in bronchiolitis.
46 However, DNA methylation was considered to
be absent in C. elegans because of the lack of detectabl
47 ed to other nematode species and this effect
is absent in C. elegans daf-22 larvae which are pheromon
48 ila to young levels, and this effect of S107
is absent in calstabin (FK506-BP2) mutants.
49 kade-induced homeostatic synaptic plasticity
is absent in CaN knockout neurons, demonstrating the ess
50 2 is remarkably conserved across species but
is absent in canonical FERM proteins, including talin.
51 tumors (P = 5.47 x 10(-17)); TP53 mutations
were absent in carcinomatous elements in nonhypermutated
52 after stress, this increase in connectivity
was absent in carriers of the deletion variant, who inst
53 LTD
was absent in CB1 knock-out mice but preserved in hetero
54 Antiallodynic efficacy of LY2828360
was absent in CB2 knockout (KO) mice.
55 fficacy of systemic administration of AM1710
was absent in CB2KO mice and WT mice receiving the CB2 a
56 ed by a selective CB2R antagonist, AM630, or
was absent in CB2R-KO but not CB1R-KO mice.
57 However, CIH-induced aorta changes
were absent in CD36 knockout mice, Our results provide m
58 mechanism of cell polarization and migration
is absent in cells expressing E- or R-cadherin.
59 TBCK
was absent in cells from affected individuals, and decre
60 gly with intron number, and this correlation
was absent in cells lacking LEDGF.
61 ion were sensitive to Ki-67; these responses
were absent in cells that did not induce p21.
62 These features found in many pathogenic RNAs
are absent in cellular RNAs due to post-transcriptional
63 dvanced and 7% of all primary MDS cases, but
were absent in children with MDS secondary to therapy or
64 Stress-induced IRI protection
was absent in Chrna7 knockout (a7nAChR(-/-)) mice and gr
65 by the quorum sensing regulator HapR, which
is absent in classical biotype strains.
66 y the observation that the anomalous current
is absent in cochlear cells of Piezo2-null mice, even th
67 tant tumor cell lines, and that this benefit
is absent in combinations of formaldehyde and epirubicin
68 This lineage
is absent in contemporary Europeans, although it is foun
69 rrow, hardly circulate in healthy donors and
are absent in cord blood.
70 y isolated human peripheral blood cells that
was absent in corresponding cell lines.
71 n resonance spectroscopy in wild-type PASMCs
was absent in Cox4i2(-/-) PASMCs and was dependent on cy
72 lated shift in the cullin neddylation status
is absent in csn mutants.
73 Despite this association, this entity
is absent in current risk-benefit analysis models, which
74 ) in the aqueous phase after irradiation but
were absent in dark controls.
75 This effect
was absent in DCC-deficient mice.
76 We found that exaggerated skin inflammation
was absent in DeltaLC x CXCR6(-/-) mice.
77 binding is sensitive to digitonin, and which
are absent in DeltaLhca4.
78 ses were abolished by TRPM8 antagonists, and
were absent in DRG and TG neurons isolated from Trpm8(-/
79 atory pool of manganese in B. japonicum that
is absent in E. coli.
80 s large/zona occludens-1 (PDZ) ligand, which
is absent in EAAT2a.
81 rtue of a characteristic lysine patch, which
is absent in EBNA-1 of the Epstein-Barr virus.
82 bind in a structurally distinct pocket that
is absent in eukaryotic IMPDHs.
83 gin of replication, and that such a gradient
is absent in exponentially growing cells.
84 ty-specific anomalies mimic a phenotype that
is absent in extant mice but present in mouse ancestors
85 Cardiac events
were absent in FG+/phenotype-negative relatives; subtle
86 itic signalling, and antidepressant efficacy
are absent in Fmr1-knockout (KO) mice.
87 to the nutrient intake is limited since data
are absent in food composition tables and databases.
88 DP IELs
are absent in germ-free mice, which suggests that their
89 s were similar, whereas secondary bile acids
were absent, in GF mdr2(-/-) mice.
90 ta-hairpin extension of red-type RbcS, which
is absent in green-type RbcS, is critical for efficient
91 offset by an apparent decline in LPB, which
was absent in healthy-weight subjects.
92 aling in both yeast and HEK-293 cells, which
is absent in HEK-293S cells.
93 RIPK3
was absent in hepatocytes, and MLKL-deficient mice, but
94 MitoIK, ATP
was absent in hESC-VCMs.
95 a photosystem I-containing megacomplex that
is absent in high-light-acclimated cells and contains di
96 This salt bridge
was absent in HLA-Bw6 molecules as well as position 83 m
97 anges in structure observed in WT myocardium
were absent in HM myocardium.
98 ultured cells and naked mole rat tissues but
is absent in human and mouse cells.
99 potential as a selective drug target, which
is absent in humans but essential to the survival of man
100 ThyX
is absent in humans, rendering FDTS an attractive antibi
101 shown to be essential in many pathogens and
is absent in humans.
102 lysaccharides among them galactofuran, which
is absent in humans.
103 in Hb1- and Hb2-infected wild-type (WT) mice
was absent in IL-13Ralpha1(-/-)mice.
104 rved in response to Hb2 infection in WT mice
were absent in IL-13Ralpha1(-/-)mice.
105 Here we show that although signs of colitis
are absent in IL10R-deficient mice during the first two
106 arette smoke, as observed in wild-type mice,
was absent in Il17a(-/-) mice and in mice treated with a
107 In contrast, Th17 response
was absent in immunized IL-23R(-/-) mice that failed to
108 Evidence of stronger CTL selection
was absent in infants with severe immunosuppression.
109 ntractile deficits, whereas chamber dilation
was absent in IPAH (+37+/-10% versus +1+/-8%, P=0.004, a
110 dicative of the presence of xylan, but these
were absent in irx9l These data, together with the spg p
111 induced enhancement of the allergen response
was absent in isolated airways from mice lacking the IL-
112 ns at least four independent HGT tracts that
are absent in its nearest relative.
113 These pro-apoptotic events
were absent in KI mice and were attenuated in WTs co-adm
114 This effect
is absent in kif3a;IFT double mutants, indicating that I
115 rientation in our knock-in mouse line, which
are absent in knockout animals.
116 This allele
was absent in known databases and segregated with the pa
117 ased Tb without affecting LMA; these effects
were absent in KO mice and potentiated in OE mice.
118 uses and parasites are common in humans, but
are absent in laboratory mice, and thus represent potent
119 akes place in planar membranes, and thus, it
is absent in liposomes and not detectable in calorimetri
120 ion-limited growth regime in colonies, which
is absent in liquid cultures.
121 cells in livers of chronic HCV patients that
is absent in liver tissues from nonviral hepatitis or he
122 8(+) T cells increased with tumor growth but
was absent in lymphoid organs.
123 is an ideal characteristic that is known to
be absent in macro-scale transmission lines.
124 onic endocannabinoid release in females that
is absent in males.
125 Although the HNMT-like gene
is absent in mammalian genomes, the activity of carnosin
126 environmental stimuli to adaptive responses,
are absent in mammals, and are embedded in various patho
127 e (His) in a similar, multistep pathway that
is absent in mammals.
128 the envelope (E) protein, is polymorphic; it
is absent in many of the African isolates but present in
129 Because the inducer
is absent in mice and their diets, Bacteroides gene expr
130 mucosa of mice that depends on cysLTs, as it
is absent in mice deficient in the terminal enzyme for c
131 SCFA-induced reduction of hepatic steatosis
was absent in mice lacking hepatic PPARgamma.
132 ucose 6-phosphatase (G6Pase) and this effect
was absent in mice lacking liver estrogen receptor alpha
133 observed following chronic hypoxic exposure
was absent in mice with pulmonary endothelial HIF-2alpha
134 aled typical Randall-type renal lesions that
were absent in mice expressing the complete human HC.
135 These effects of rosiglitazone
were absent in mice lacking adiponectin but having norma
136 ibrosis; these cells and concurrent fibrosis
were absent in mice lacking tumor necrosis factor recept
137 osphorylation, and synaptic pathology, which
were absent in mice treated with zileuton.
138 eight and stimulation of insulin sensitivity
were absent in mice with adipose-specific disruption of
139 The reactivation of plasticity by LRx
is absent in Mmp9(-/-) mice, and is rescued by hyaluroni
140 netics in short time-scale measurements that
are absent in more typical long time-scale experiments a
141 ne (10 mg/kg per day i.p. x 12 days), but it
was absent in morphine-tolerant CB2KO mice.
142 at a frequency of 76.2% in our sample while
being absent in most other populations, and we found str
143 of PMPs also requires PEX16, a protein that
is absent in most yeast species.
144 Because EYS
is absent in mouse and rat, and the structure of the ret
145 ocyte inflammatory responses- a pathway that
is absent in mouse monocytes.
146 nd macrosteatosis; however, these phenotypes
are absent in mutant p53(R172H) or IL27RA(-/-) mice.
147 RGPRX2, and that injection-site inflammation
is absent in mutant mice.
148 ch is independent of glutamate receptors and
is absent in neurons from ASIC1a(-/-) mice.
149 -18 were mediated by the IL-18R because they
were absent in neurons from animals null for IL-18Ralpha
150 current and ABA-enhanced slow anion current
were absent in nia1nia2.
151 s likely, as low frequency auditory function
is absent in noise exposed Foxo3KO/KOs even though all c
152 This population
was absent in nondiseased liver tissues and peripheral b
153 were detectable for 72 h after exposure and
were absent in nonexposed control animals.
154 store-operated Ca(2+) entry, a process that
is absent in normal heart cells.
155 Y (RNA-binding motif on Y chromosome), which
is absent in normal hepatocytes but present in male HCC
156 sis of a human breast TMA showed that LASP-1
is absent in normal human breast epithelium but the expr
157 IL30
was absent in normal mammary ducts, ductules, and acini
158 try demonstrates that cochlear amplification
is absent in Nptn mutant mice, which is consistent with
159 Strikingly, this oscillation in acetylation
is absent in old mice while CR robustly rescues global p
160 Fe minerals
are absent in/
on all organically preserved cell walls.
161 ructural variants (SV) cluster in HGSOC, but
are absent in one ultramutated tumor, providing insights
162 Microplastics
were absent in one brand while others contained between
163 ASM from non-asthmatics and asthmatics, and
were absent in OR51E2-deleted primary human ASM.
164 Since the redox sensor of Orai1 (Cys-195)
is absent in Orai3, the Orai1/Orai3 ratio in T cells det
165 cation is based on diffraction features that
are absent in ordinary cubic (c-) diamond (space group:
166 This motif
is absent in other ACAT families, suggesting that EutT e
167 Conversely, BRAF-V600E
is absent in other B-cell neoplasms, including mimickers
168 onnection of the top and bottom surfaces and
is absent in other two-dimensional systems such as graph
169 s operating within its most sensitive range,
is absent in outer and inner hair cells from homozygous
170 (e.g., proestrus vs estrus), (2) pLTF would
be absent in ovariectomized (OVX) rats and in physiologi
171 zes acylation at the R3' position in tomato,
is absent in P. axillaris Furthermore, where putative or
172 motor cortex and the inferior frontal gyrus
was absent in Parkinson's disease patients on placebo (d
173 res than whites, but that this disparity may
be absent in patients who spend time in the ICU during t
174 These data provide evidence that FHR3, which
is absent in patients with the autoimmune form of hemoly
175 his reward modulation of attentional priming
was absent in patients with VMF damage.
176 consistent change in HAs during contraction
was absent in patients.
177 evere hypoglycemia and diabetic ketoacidosis
were absent in patients with functioning graft.
178 Truncating FLNC mutations
were absent in patients with other phenotypes, including
179 Notably, mutations in GATA2
were absent in patients with therapy-related MDS or acqu
180 structures found in the center of normal PD
were absent in PD containing VP37-tubules.
181 This alveolar macrophage phenotype
was absent in peritoneal and bone marrow-derived macroph
182 The degradation of IFI16
was absent in phosphonoacetic acid-treated cells, which
183 linked cluster of thrum-specific genes that
are absent in pins.
184 development of animals and Dictyostelium but
are absent in plants and yeast.
185 Although TRP channels seem to
be absent in plants, C. reinhardtii possesses genomic se
186 This RNA
is absent in plants where the psbN gene is not transcrib
187 t with the 99-hairpin loop of trypsin, which
is absent in plasmin.
188 body opsonization and antigen expression and
was absent in platelets with low or minimal HLA expressi
189 cular lamina and basilar membrane vibrations
are absent in postmortem cochleae.
190 ly 70 nucleotides upstream of rrn23 and ndhA
are absent in ppr53 mutants, and the translational effic
191 This effect
was absent in primary auditory cortex and did not occur
192 The initial wave of fetal B-1 development
was absent in PU.1 hypomorphic mice, while subsequent fe
193 or the relaxation of disorder in spinel that
are absent in pyrochlore.
194 Mitomycin C (MMC) -sensitive hematopoiesis),
were absent in Rad18(-/-) mice.
195 hysiological correlate of successful recall,
was absent in rats with degraded PNNs in V2L.
196 hypertension (PH) in rats, but these effects
were absent in rats treated with imatinib, another BCR-A
197 d components during heat treatment, while it
is absent in raw foodstuffs.
198 pansion (maximum in glycolytic cells), which
was absent in reduced or OMM-detached cristae of OPA1- a
199 n CTCL cell lines and primary CTCL cells but
is absent in resting T cells from healthy donors and B-c
200 glutamate levels in response to hypoglycemia
is absent in RH animals.
201 coid-inducible kinase 1 (SGK1) and PKC-alpha
was absent in Rictorfl/fl Ksp-Cre mice, indicating a fun
202 Vdelta2 T cells
are absent in rodents but readily populate the human int
203 (such as cats and ferrets) and primates but
are absent in rodents.
204 8 T, while Human uses terminal exon 9, which
is absent in rodents.
205 n and Caucasian ethnicity whereas L. gasseri
was absent in samples from Black women.
206 c atmosphere, aerobic metabolic VC oxidation
was absent in sediments with high total organic carbon (
207 ion of peptidergic nociceptors, whereas DPP6
is absent in sensory neurons.
208 mmatory genes induced in wild-type mice that
was absent in Serpinb3a-null mice.
209 olished by the TRPV4 antagonist HC067047 and
were absent in SGCs from Trpv4(-/-) mice.
210 m corneum of skin permeated with CYnLIP that
were absent in skin hydrated with water.
211 to enhance hippocampal LTP, and this effect
is absent in slices treated with either a glial toxin or
212 nt action of midazolam at low concentrations
was absent in slices from GABAA receptor alpha1(H101R)mu
213 ion and release of IL-1beta, a response that
is absent in SMG cells isolated from mice deficient in P
214 ge surrounds the active site of SNM1A, which
is absent in SNM1B and explains the greater apparent pro
215 ing catalytically active {110} facets, which
are absent in solution-grown controls.
216 istributed in eukaryotes, but key components
are absent in some lineages.
217 rning to associate odours with a food reward
is absent in species that feed individually, such as mas
218 chains of ovoid, nonseparated bacteria, but
was absent in spherical, single cocci.
219 tion of Ly6C(lo) monocytes during resolution
was absent in stabilin-1 knockouts leading to persistenc
220 Endosomes were strikingly rare and lysosomes
were absent in striatal axons, in which there was little
221 the trigeminal and dorsal root ganglia, but
was absent in sympathetic neurons of superior cervical g
222 which can be revealed in wild-type mice but
is absent in Syt7 knockout mice.
223 conserved in TgALD1, key catalytic residues
are absent in TgDPA.
224 The H3T3ph signals
are absent in the afd1 (absence of first division) and s
225 oth the secondary cell wall layer and the OR
are absent in the exo70H4 mutants.
226 us genes with other parasitic nematodes that
are absent in the free-living nematode C. elegans, it ha
227 ocots; however, AtHYH (HY5 homolog) homologs
are absent in the monocots analyzed.
228 riety of three-dimensional morphologies that
are absent in the native block copolymer phase diagram.
229 bit a range of novel physical phenomena that
are absent in the parent compounds.
230 M1L
is absent in the attenuated modified vaccinia virus Anka
231 FDY
is absent in the closest relatives of D. melanogaster, a
232 e strained film, which undergoes an MIT, but
is absent in the compressively strained film.
233 This interaction
is absent in the corresponding BINOL-derived systems, an
234 A similar trend
is absent in the corresponding metal complexes, as exemp
235 e is only observed in the hydrated state and
is absent in the dry fibrils, highlighting the role of s
236 The increase in CREB phosphorylation
is absent in the fasted RIIbeta KO hypothalamus.
237 3)) exposes cryptic PG binding activity that
is absent in the full-length domain.
238 al models of diabetic nephropathy since Nox5
is absent in the mouse genome.
239 Here we show that m(6)A
is absent in the mRNA of Drosophila lacking Ime4.
240 uction of new astrocytes from nestin(+) NPCs
is absent in the normal adult cortex, striatum, and spin
241 clear filaments in infected cells, the motif
is absent in the NSs proteins of other Bunyaviridae-fami
242 hydration level investigated here (0.04 g/g)
is absent in the temperature range we studied in this wo
243 K16 expression
is absent in the thinned footpads of irhom2(-/-) mice co
244 in, suggesting that amino group coordination
is absent in the two-nitrogen coordinate form of SliLPMO
245 By contrast, the 4-amino acid deletion
is absent in the VQ22 protein from wild soybean species
246 ith stromal cells or near blood vessels, but
was absent in the amnion.
247 On the other hand, extracellular FAM20C
was absent in the conditioned media of mouse embryonic f
248 a metastatic RCC (mRCC), while the mutation
was absent in the corresponding primary RCC (pRCC).
249 s a specific substrate of DHHC13 and that it
was absent in the CUH and CE structures of the affected
250 atory element in the GmWRI1a promoter, which
was absent in the GmWRI1b promoter, resulting in reducti
251 TDP-O immunoreactivity
was absent in the hippocampus of HS patients despite abu
252 ated tumors with ELTSLs, but this phenomenon
was absent in the LTSL, NTSL, and ENTSL groups.
253 This signature
was absent in the majority of asymptomatic individuals w
254 -induced shift in fear and neural processing
was absent in the MR-blocked groups.
255 ense mutation in uhpA The expression of uhpT
was absent in the mutant strains with uhpT deletion and
256 sic cerebellar connectivity seen in controls
was absent in the patients.
257 apeutic effect and thermal parameters, which
was absent in the previous mouse studies.
258 ted pathologic and molecular features, which
was absent in the primary HCC tumors.
259 -resistant acid phosphatase staining notably
was absent in the subarticular regions of the cartilage
260 n the proliferating embryonal mass, while it
was absent in the suspensor cells.
261 Glutamate
was absent in the vitreous and presented low levels in t
262 Osteoclasts
were absent in the allografts and there was no expressio
263 Wild-type ketocarotenoids
were absent in the beak and tarsus of yellowbeak birds.
264 These modifications
were absent in the closely related S. enterica serovar T
265 These effects
were absent in the depressed suicide completers with no
266 These changes
were absent in the dexamethasone-treated animals.
267 cytes in the diabetic WT mice, these changes
were absent in the diabetic TxNIP(-/-) mice.
268 Racial/ethnic disparities in survival
were absent in the IHS.
269 ation resistance occurred when Clostridiales
were absent in the neonatal microbiota.
270 at highly conserved amino acid residues and
were absent in the normal population.
271 In contrast, these associations
were absent in the obese group.
272 B, neuregulin 1, NR1 and GABA alpha1 subunit
were absent in the PFC of young adult P2rx7-/- animals.
273 d with increasing load, whereas load effects
were absent in the posterior PIC.
274 ces harboring 1737 protein-coding genes that
were absent in the reference assembly, revealing variant
275 r major bleedings and vascular complications
were absent in the S3-THV group (0% versus 7.7%, P=0.15)
276 ive genes, such as Msh homeobox (Msx) genes,
are absent in this animal group.
277 ity in the colonic epithelia of WT mice that
was absent in tissues from PAR2(-/-) mice.
278 accumulated in nasal respiratory tissues but
were absent in tissues distant to the site of contact.
279 gulates cell proliferation and this capacity
is absent in Tm5NM1 KO cells.
280 yndrome protein homology 2 (WH2) domain that
is absent in Tmods.
281 itro requires Prnp-Grm5 genetic interaction,
being absent in transheterozygous loss-of-function, but
282 ies were inhibited by a TRPA1 antagonist and
were absent in TRPA1-null mice.
283 hairpin RNA (shRNA) in wild-type VSMCs, and
was absent in TRPC1(-/-) VSMCs.
284 strong thermal hyperalgesia, an effect that
was absent in TRPV1 knock-out mice, and was blocked by t
285 st HC067047 (IC50 approximately 0.9 muM) and
were absent in Trpv4(-/-) NPE.
286 pha, owing to the head-tail interaction that
is absent in tRXRalpha.
287 articles on approaching the glass transition
is absent in two dimensions, whereas it is very pronounc
288 host defense function of endogenous BAF may
be absent in U2OS cells but can be recovered through eit
289 phy (SFC), unexpected results are seen which
are absent in ultrafast liquid chromatography.
290 trata cropping out in the northern Andes but
is absent in underlying lower Miocene and Oligocene stra
291 Moreover, collagen IV
is absent in unicellular sister-groups.
292 endently in dozens of multicellular taxa but
is absent in unicellular species.
293 scleroderma without known specificities and
is absent in unrelated autoimmune diseases.
294 ic l-malic acid catabolism in ABSA 1014 that
was absent in UPSA 807.
295 By contrast, similar regulation of LTP
is absent in ventral CA1 neurons.
296 ing immune-activating potential for EVT that
was absent in VT.
297 to niobium atoms in the support; this mixing
is absent in weakly binding metals, such as Ag and Au, a
298 nockout (KO) mice aged 16 months or more but
are absent in wild-type or FE65 KO mice.
299 This phenomenon
was absent in WT mice with experimentally induced chroni
300 sense transcription of the mouse Hoxa11 gene
is absent in zebrafish, which, together with the largely