1 of 50 vivax malaria patients where schizonts
were completely absent in 27 isolates, and few schizonts
2 Expression of p18(INK4c)
was completely absent in 43% of GBM primary tumors studi
3 High affinity [3H]5-HT uptake
was completely absent in 5-HTT-/- mice, confirming a phy
4 5-HT via a transporter-dependent mechanism,
was completely absent in 5-HTT-/- mutants.
5 HS2ST activity is present in C. elegans and
is completely absent in a deletion mutant of hst-2, ok59
6 in studies of human AVPR1A diversity, "RS3,"
is completely absent in A. azarai and all other platyrrh
7 eless, CT-induced fluid accumulation in vivo
was completely absent in AC6loxloxVillinCre mice, associ
8 reases dramatically shortly after birth, and
is completely absent in adults across various models of
9 on was evident in the substrate mycelia, but
was completely absent in aerial hyphae.
10 By contrast, pyrrolinone
is completely absent in all MS measurements of comparabl
11 The hypotensive effect of alpha2 agonists
was completely absent in alpha2A-deficient mice.
12 Immune synapse translocation
was completely absent in antigen-specific T cells from P
13 namic regulation of miR398 under salt stress
was completely absent in Arabidopsis, in which miR398 wa
14 , within the developing renal stroma, and it
is completely absent in BF-2 null kidney stroma.
15 rature and concomitant circadian adjustment,
were completely absent in Brn-3.1(-/-) mice.
16 This induction
was completely absent in Car(-/-) mice, but was not affe
17 Both forms of LTD
were completely absent in CB(1) cannabinoid receptor kno
18 ing-catalepsy, hypomobility, and hypothermia
were completely absent in CB1 mutant mice.
19 indicative of loss of ion selectivity, that
was completely absent in cells expressing N604T TRPV1.
20 in the presence of duplication mutations and
was completely absent in cells with deletion mutations.
21 Importantly, both of these changes
were completely absent in Cobl KO mice.
22 at the solvent separated minimum in the bulk
is completely absent in confined water, independent of t
23 BCA-1 (CXCL13)
was completely absent in control biopsy samples from pat
24 REMS) and fever in WT animals, these effects
were completely absent in COX-2 KO mice.
25 mays subspecies parviglumis and mexicana and
is completely absent in domesticated maize.
26 trains revealed that the dominant transcript
is completely absent in each mutant.
27 ontinental populations, and the risk alleles
were completely absent in East Asian populations.
28 tive effects of HMG-CoA reductase inhibitors
are completely absent in eNOS-deficient mice, indicating
29 sts or eNOS inhibitors in wild-type mice and
were completely absent in eNOS-deficient (Nos3(-/-)) mic
30 This effect
was completely absent in eosinophil-deficient dblGATA mi
31 SHP induction by these estrogens
is completely absent in ERalphaKO mice.
32 ay be missed if they have a low frequency or
are completely absent in European populations, especiall
33 -mediated downscaling of synaptic inhibition
is completely absent in Fmr1 knock-out neurons.
34 As previously observed, all effects of CL
were completely absent in gene knockout mice lacking bet
35 expression is restricted to the cortical hem
are completely absent in Gli3(Xt/Xt) embryos, but some e
36 ake of wild-type (WT) C57BL/6J mice only and
was completely absent in global GPR39 knockout mice.
37 sis, a hallmark of adult HK1.fos phenotypes,
was completely absent in HK1.fos-p53 -/- mice.
38 ebellar granule cell layer of wild-type mice
was completely absent in homozygous mice.
39 in response to a secondary recall challenge
was completely absent in ICOS knockout mice.
40 In contrast, the effects of IFN-gamma
were completely absent in ICSBP(-/-) progenitors.
41 mod-induced psoriasis-like skin inflammation
was completely absent in IkappaBzeta-deficient mice, whe
42 while mature B cell numbers were normal, LNs
were completely absent in Ikka(Lyve1) mice.
43 in wild-type mice under the chronic protocol
was completely absent in iNOS(-/-) mice despite persiste
44 BNST), although robust in wild-type animals,
was completely absent in knock-out animals.
45 s fear conditioning, of female offspring but
was completely absent in male offspring of cocaine-expos
46 found in Abeta protofibrils, these contacts
were completely absent in mature Abeta fibrils.
47 In contrast, these proteins
were completely absent in mature neutrophils, indicating
48 opamine receptor-mediated product on of cAMP
is completely absent in membranes of D1A-deficient mice,
49 This response
was completely absent in mice deficient in PDE4B but not
50 xtreme cold-plate stimulation (-5 degrees C)
was completely absent in mice lacking Na(V)1.8.
51 This form was found in native pancreas but
was completely absent in monolayer beta-cells.
52 , endodermal, and hypodermal cells appear to
be completely absent in most embryos, however, all of th
53 We document here that Ram-1 expression
is completely absent in murine yolk sac cells from days
54 In contrast, whereas haplogroup D
is completely absent in Nepal, it accounts for 50.6% of
55 In addition, these puncta signals
were completely absent in neuronal cultures derived from
56 he SNc from wild-type mice, but this current
was completely absent in neurons from GIRK2 knock-out mi
57 Concomitantly, HMGA2 protein, which
was completely absent in normal myometria, was expressed
58 includes dinosaur groups that became rare or
were completely absent in North America around the final
59 x, AP duration, and ICa,L, and these effects
were completely absent in NPR-C(-/-) myocytes.
60 ript, the transcriptional coregulator Vgll2,
is completely absent in older animals.
61 When SMC5/6 complexes
were completely absent in oocytes during meiotic resumpt
62 own toxin, and the receptor-binding domain 2
is completely absent in other well-studied heptameric to
63 -dependent rolling after P-selectin blockade
is completely absent in P-selectin glycoprotein ligand-1
64 This effect of AZD8529
was completely absent in P rats lacking functional mGluR
65 The fIJP
was completely absent in P2ry1(-/-) mice and the P2Y1 re
66 Strikingly, IgG4
was completely absent in patients without FVIII inhibito
67 Moreover, apical Cl(-) channel activity
was completely absent in principal cells from transgenic
68 viral challenge, cutaneous papilloma growth
was completely absent in rabbits immunized with either C
69 early half of the CEN4 monomers was found to
be completely absent in rice centromere 8 (CEN8), sugges
70 re CC progenitors originate, and these cells
are completely absent in sog mutants.
71 lly disappeared at voltages beyond 500 V and
are completely absent in standard high-voltage ionizatio
72 proliferation and migration, but this effect
was completely absent in SY5Y-TrkA cells.
73 Such tubules
are completely absent in temperature-blocked cells.
74 ion of Fas induced Th17 cell death; and AICD
was completely absent in Th17 cells differentiated from
75 des studied present pi-pi interactions which
are completely absent in the nonoxidized analogue.
76 Schwann cells
are completely absent in the peripheral nerves.
77 chlear base but sensory epithelium formation
is completely absent in the apex and all three cristae o
78 eficient cells, and that activation of c-Abl
is completely absent in the DNA mismatch repair-deficien
79 ontain a conserved 50-52 residue insert that
is completely absent in the homologous alpha-glycerophos
80 antum paraelectric SrTiO(3), a property that
is completely absent in the pristine material.
81 This increase
was completely absent in the calcium-restricted mice.
82 ced ROMK inhibition by WNK4; this inhibition
was completely absent in the double mutant WNK4(Y1092/10
83 Expression
was completely absent in the inferior olivary nucleus.
84 activity ratio in WT mice, but this response
was completely absent in the KO mice.
85 the wild-type (WT) rat, Cyp3a1/2 expression
was completely absent in the liver of the KO rat.
86 , the corresponding protein for desmoglein 3
was completely absent in the oral mucosal epithelium of
87 ast, in Wnt3a null embryos, Nrarp expression
was completely absent in the presomitic mesoderm.
88 glycosylated form of EGI, hyperglycosylation
was completely absent in the YlPMR1-disrupted mutant.
89 RubA and PS I electron transport activity
were completely absent in the mutant, although PS II act
90 The responses induced by these agonists
were completely absent in the P2Y(2)-R(-/-) fibroblasts.
91 Also, pancreatic preproinsulin mRNA
was completely absent in these icv leptin-treated T1D mi
92 Mdr1a
was completely absent in tissues, including brain and sm
93 n normal skin and increase post-wounding but
are completely absent in TSG-6-null mice.
94 of rhabdoid tumors in which SMARCB1 protein
is completely absent in tumor cells.
95 arbohydrate binding by the low affinity site
is completely absent in two mutants bearing three or fou
96 Methylation
was completely absent in uninfected and EBV-infected PBM
97 ved in PsaA proteins from Synechococcus, but
is completely absent in viral PsaA proteins from the psa