1 37 participants (23 HTT mutation carriers and 14 controls),
we further assessed whether concentrations of NfL in plasma c
2 We further demonstrate a concurrent increase in NF-kappaB sig
3 We further demonstrate an important role for non-adrenergic s
4 We further demonstrate that application of this conjugation c
5 We further demonstrate that in the presence of membrane-assoc
6 We further demonstrate that this Kirkendall cavitation proces
7 We further demonstrated that deletion of ami1 leads to increa
8 We further demonstrated that the conformational cross-talk be
9 We further demonstrated that, upon CREB activation, HDAC2 rep
10 We further describe postinvasion morphologic and rheologic al
11 We further detected novel cardiac chemical signatures related
12 We further developed a method, iMAAPs, to infer multiple-wave
13 Additionally,
we further developed the NTA methodology to explore its suita
14 We further discuss perspectives on overcoming limitations of
15 We further elucidated the signaling downstream of Gq and iden
16 We further establish that BONCAT can be coupled to tandem liq
17 We further established that FI-HSV-2 alone or in combination
18 We further examine the interaction of PorB with outer membran
19 We further find initial evidence for home-lab links: common n
20 We further find that effects of Tel1 are distinct but partial
21 We further find that this G-actin pool functions in spine dev
22 We further found that all mutations affecting auto-phosphoryl
23 We further found that FA induced the disassembly of 26S immun
24 We further found that PA increased the production of reactive
25 We further found that the block of CD74 degradation in CatS(-
26 We further functionally identified EgWRI1-1, one of three EgW
27 We further identified SYK as a critical kinase that phosphory
28 We further identify a naturally polymorphic site at Nef posit
29 Herein,
we further investigate the underlying mechanism of this confo
30 We further performed whole-genome sequencing of nosocomial MD
31 We further show that 4-PBA triggers the secretion of a KDEL-t
32 We observed the same patterns in human transcriptomes and
we further show that AS rates correlate with the fitness cost
33 We further show that cross-links dominate entanglement dynami
34 We further show that deubiquitination of ILV cargoes is inhib
35 We further show that neuron numbers impact overall interconne
36 We further show that PF-06446846 reduces plasma PCSK9 and tot
37 We further show that the input of (236)U by the Elbe River is
38 We further show that the optimal dual drug conjugate more eff
39 We further show that this synaptic rearrangement requires the
40 We further show that, when SCs become myelinating, they downr
41 We further showed that disruption of original cysteine pairs
42 We further showed that Tnc expression is repressed by the tra
43 Here,
we further stabilized pre-F by adding both disulfide and cavi
44 We further studied 1536 samples obtained from 3 independent c
45 We further uncover that several P2X receptors, including thos
46 We further utilize an improved CD34+ culture system to engine
47 ing accuracy and peptide detection capability of PECAN, and
we further validate its detection with data-dependent acquisi
48 We further validate our findings through assessing the power
49 parameters, with genomic DNA sequence being the only input,
we further validate that the nonconsensus nucleotide triplet
50 We further verified the inhibitory and stimulatory functions