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1 SBS in NGS is underpinned by 'reversible-terminator chem
2 SBS results were significantly different when AmelxKO an
3 SBS was the major indication for HPN in our cohort.
4 SBSs and insertions/deletions occur predominantly at the
5 SBSs remained relatively stable amongst the UK cohort, w
7 l subjects with intact intestine and from 13 SBS patients dependent on parenteral nutrition because o
9 mportantly, site-directed mutagenesis of 202-SBS or expression of a dominant negative form of STAT3 s
10 AT3 to an oligonucleotide containing the 202-SBS in gel-mobility shift assays and to the 5'-regulator
11 a potential STAT3 DNA-binding site (the 202-SBS) present in the 5'-regulatory region of the Ifi202 g
13 trulline concentrations were lower in type 3 SBS but not significantly different: 15 umol/L (11-25 um
14 e previous methods, DeepMS could discover 37 SBS, 5 DBS, and 9 Indel new signatures, many of which re
16 ence of HVI among patients with an abdominal SBS and negative findings on CT is extremely low, if not
18 ng and observing all patients with abdominal SBS should be reconsidered when a high-quality CT scan i
22 ion with a newly-developed eye mask (Activa, SBS Sistemi, Turin, Italy) immediately followed by IPL t
24 ce the half-life of SMD targets that form an SBS by either intramolecular or intermolecular base-pair
25 tely 355 nm) in 10 sec, we then performed an SBS reaction on a chip that contains a self-priming DNA
28 erodimer (SB) and two heterotrimers (BSB and SBS) by alkyne bridges leads to the formation of coupled
29 rial hypertension, dyslipidemia, cancer, and SBS-CIF caused by radiation enteritis, but fewer cases a
31 main MBS and SBS homomers are different, and SBS homomers are likely to be folded cotranslationally,
32 show that the folds of single-domain MBS and SBS homomers are different, and SBS homomers are likely
35 s(4,5)P(2) and that three lysine residues at SBS I site, Lys-1420, Lys-1432, and Lys-1434, are respon
36 we reported a single-molecule nanopore-based SBS strategy that accurately distinguishes four bases by
45 ubility (SL), shear bond strength to dentin (SBS), and viability of Streptococcus mutans under 14.6 J
46 life seem to be similar to those who develop SBS as adolescents with regards to long-term outcome, de
47 erences between adult patients who developed SBS during early childhood and those who develop this as
48 ised the pediatric group (PG), 37 developing SBS at age 13 to 25 constituted the adolescent group (AG
49 he two groups, pediatric patients developing SBS early in life seem to be similar to those who develo
51 tudy evaluated patients with newly diagnosed SBS-CIF initiating PS between 2015 and 2020 at a nationa
58 hort bowel syndrome with intestinal failure (SBS-IF) is a rare but devastating medical condition.
59 hort-bowel syndrome with intestinal failure (SBS-IF) to gain insight into its mechanism of action.
65 c supplementation as a potential therapy for SBS and describe a xenotransplantation model that provid
66 inical trials as a potential new therapy for SBS and is the only hGLP-2 analogue in clinical testing
68 d with clinically used PA gel yielded higher SBS than the BCA/BPA etchants, it exhibited greater adhe
71 ead length of >30 bases by using this hybrid SBS method on a chip and a four-color fluorescence scann
80 SS OCT can provide useful information in SBS, revealing a wide variety of vitreoretinal interface
83 illus resp. low amounts of Proteobacteria in SBS patients with preservation of colon and ileocecal va
84 hat the evolution of quaternary structure in SBS homomers is significantly influenced by stochastic p
88 s of SI, LPH, and ApN in colonocytes in most SBS patients with large variation and strongest effect f
90 sponding mutants with a single SBS, multiple SBSs probably interact to cause the high affinity bindin
93 nanopore-based sequencing by synthesis (Nano-SBS) strategy that can accurately distinguish four bases
95 pore-based sequencing-by-synthesis (Nanopore-SBS) approach, which used a set of nucleotides with poly
96 a nanopore, in combination with the Nanopore-SBS approach, can provide the foundation for a low-cost,
97 d in duodenal and colonic biopsies from nine SBS patients in a late stage of adaptation as well as he
100 175 kcal/d, P = 0.001) and also for the non-SBS group (2393 +/- 445 compared with 1532 +/- 178 kcal/
101 antly lower in the SBS group than in the non-SBS group (P < 0.01); however, predicted TEE did not dif
103 ort the melt-phase self-assembly behavior of SBS triblock copolymers (S = poly(styrene) and B = poly(
105 the abundance of PepT1 mRNA in the colon of SBS patients was more than 5-fold that in control subjec
107 NA template, facilitating the development of SBS as a viable approach for high-throughput DNA sequenc
109 ol reported in indoor air during episodes of SBS; (2) acute exposure to 2,2,4-trimethyl-1,3-pentanedi
110 shown to improve survival and weight gain of SBS mice and increase the proliferation of intestinal cr
113 f administration in relation to the onset of SBS, optimal patient selection for use, duration of trea
114 nfants who have liver failure as a result of SBS are frequently referred for consideration for combin
115 permanent sequelae are rare, the symptoms of SBS can be uncomfortable, even disabling, and whole work
121 t to calculate the total costs for pediatric SBS patients and to provide an in-depth analysis of thes
122 This is particularly true for pediatric SBS patients who receive some of the most complex medica
123 an (+/- SD) total cost of care for pediatric SBS was US$505 250 +/- US$248 398 (corrected for inflati
126 t better prediction of outcomes of pediatric SBS, which may help to direct future management of these
129 ) </= 0.82, we demonstrate that polydisperse SBS triblock copolymers self-assemble into periodic stru
132 cept to being both affordable and practical, SBS needed to overcome a series of challenges, each of w
136 e, we provide the first validation of an RNA-SBS mutational signature by decomposing novel exogenous
138 Recently, RNA single base substitution (RNA-SBS) signatures were defined and described by decomposin
139 luenced by cellular factors, on a fine scale SBSs are influenced by the local DNA sequence-context, a
141 reshold for stimulated Brillouin scattering (SBS) by an order of magnitude, whilst simultaneously con
142 ht-enhanced stimulated Brillouin scattering (SBS) imaging contrast, the signal-to-noise ratio is sign
144 intermodal stimulated Brillouin scattering (SBS) mediated by long-lived flexural acoustic waves.
145 Each participant's sexual behavior score (SBS) was estimated based on the number and type of unpro
146 aly (MHA) and Fechtner (FTNS) and Sebastian (SBS) syndromes are autosomal dominant platelet disorders
148 demonstrate that the SMAD binding sequence (SBS) representing the TGF-beta response element in the r
150 on electron microscopy analyses of seventeen SBS triblock copolymers with poly(1,4-butadiene) volume
152 ions, discovered a new mutational signature (SBS-RT), recognized an oxidative phosphorylation (OXPHOS
154 than the corresponding mutants with a single SBS, multiple SBSs probably interact to cause the high a
159 ate association testing or the site-by-site (SBS) testing may underutilize the longitudinal feature o
161 ) binding to clustered Su(Hw) binding sites (SBSs) and recruitment of the insulator proteins Centroso
162 enome-wide analysis of Su(Hw)-binding sites (SBSs) in the ovary, showing that tissue-specific binding
166 ers, with an adapted solution blow spinning (SBS) device for intercalated placement of aligned reinfo
167 s study employed the solution blow spinning (SBS) technique for the rapid production of smart nanofib
169 ng was compared through shear bond strength (SBS) studies with 2 different systems (etch-and-rinse an
170 tems that can maintain shear bond strengths (SBS) suitable for clinical performance are unable to lim
171 combination of the single-base substitution (SBS) "signatures" observed in germline, soma, and tumors
172 he reduced rate of single-base substitution (SBS) mutations in gene bodies and H3K4me1-rich regions.
173 ciated, mutational single-base substitution (SBS) signature in nonmalignant mammary cells or patient-
174 es for various DNA single base substitution (SBS) signatures and their associations with different ca
176 ational signatures single-base substitution (SBS)2 and SBS13 were present in 88% and 91% of cases, re
178 54 signatures for single base substitutions (SBSs), 11 for doublet base substitutions (DBSs) and 16 f
182 dications for HPN were short bowel syndrome (SBS) (59%), PNDD (14%), congenital enteropathies (10%),
183 t for the treatment of short bowel syndrome (SBS) and potentially other intestinal diseases (e.g., IB
186 posed in patients with short-bowel syndrome (SBS) as a rehabilitative therapy, but its effects on abs
190 testinal adaptation in short bowel syndrome (SBS) includes morphologic processes and functional mecha
194 ediatric patients with short bowel syndrome (SBS) is now possible because of parenteral nutrition and
200 SRSB) in patients with short bowel syndrome (SBS) who were "permanently" dependent on parenteral nutr
201 olume in patients with short bowel syndrome (SBS) with intestinal failure, increasing intestinal wet
210 ms (often denoted as sick building syndrome (SBS)), chronic respiratory symptoms, and respiratory inf
213 te a version of the Sequencing by Synthesis (SBS) chemistry that potentially can become a preferred t
216 port four-color DNA sequencing by synthesis (SBS) on a chip, using four photocleavable fluorescent nu
219 d with in situ cDNA sequencing by synthesis (SBS) to identify 80,408 single guide RNAs (sgRNAs) in 10
222 by using Illumina's sequencing-by-synthesis (SBS) technology, which allowed us to characterize the co
223 hnologies, based on sequencing-by-synthesis (SBS), are starting to deliver large amounts of DNA seque
225 to use the solution blow spinning technique (SBS) to rapidly produce colorimetric nonwoven indicators
226 atory arthritis (chondrocalcinosis) and that SBS patients may be prone to develop extreme hypomagnesa
227 e in rapidly dividing cells, suggesting that SBS signature 1 is driven by rounds of DNA replication o
232 nsequently, smart nanofibers produced by the SBS technique, using PCL and anthocyanins from agro-indu
233 nificantly higher than predicted TEE for the SBS group (1875 +/- 276 compared with 1517 +/- 175 kcal/
234 Measured TEE was significantly lower in the SBS group than in the non-SBS group (P < 0.01); however,
239 veral surgical options for management of the SBS, including construction of intestinal valves or reve
246 ithstanding the substantial success of these SBS platforms, challenges continue to limit the ability
248 ore UPF1 and ~two- to fivefold more of those SBS-containing mRNAs that were tested, and it comparably
249 onators are achieved to overcome barriers to SBS in the visible, including 1 dB/meter waveguide losse
254 turn out to be ubiquitous across cell types: SBS signature 1, which consists primarily of transitions
256 ed ultra-narrow linewidth visible wavelength SBS lasers opens the door to compact quantum and atomic
257 qualitatively different from monomers, while SBS homomers are much less distinct, supporting the hypo
258 TEE was measured in 22 participants, 11 with SBS and 11 sex-, age-, and body mass index (BMI)-matched
259 ime HPN was feasible and safe in adults with SBS and, compared with overnight HPN, improved subjectiv
264 e total charges incurred by 41 children with SBS over the past decade, encompassing both inpatient an
269 rom a contemporary cohort of 49 infants with SBS and cholestasis whose PN course included soybean ILE
270 l of a fish oil-based ILE in 42 infants with SBS who developed cholestasis (serum direct bilirubin >2
271 the management of a 60 year old patient with SBS and recurrent joint attacks was for different medica
274 0.5% [n = 2/19]), whereas most patients with SBS and vascular or other diseases had colon-in-continui
275 al energy expenditure (TEE) in patients with SBS by using the doubly labeled water (DLW) method to in
279 ndomized, controlled trials in patients with SBS support the safety and efficacy of teduglutide as an
283 , double-blind, phase 3 trial, patients with SBS with intestinal failure requiring PS >=3 d/wk were r
284 Glepaglutide treatment in patients with SBS with intestinal failure resulted in clinically relev
285 We collected data from 85 patients with SBS with intestinal failure, according to the European S
287 stimate energy requirements of patients with SBS, and revision is needed to prevent underfeeding and
288 the effects of teduglutide on patients with SBS, we associated reduced parenteral support volume wit
290 el modifications at imaging in patients with SBS-CIF receiving TED and to assess their predictive val
291 retrospective study including patients with SBS-CIF treated with TED from 2009 to 2018 with availabl
293 e performed a 24-week study of patients with SBS-IF who were given subcutaneous teduglutide (0.05 mg/