Application of Amplitude Spectrum Gradient Attribute in the Prediction of Reservoir Productivity

Wang, X. J.; Wei, Xu; He, Xin; Wang, Z. F.; Cai, J.; Sun, Hedong

doi:10.3997/2214-4609.20148527

Cited by 12 publications

(14 citation statements)

References 2 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…420 The selectivity to SC was improved slightly using tert-butyl hydroperoxide as the oxidant. 421,422 Under optimized reaction conditions, 0.01% Au/R201 (Amberlite IRA-400) exhibited the best performance and 98.1% conversion of styrene with 50.6% selectivity to SC was achieved without additional Lewis-acid catalyst. If Au/Fe(OH) 3 ÀZnBr 2 /Bu 4 NBr was used as the catalyst, the yield to SC reached 53%.…”

Section: Càn Bond Formationmentioning

confidence: 99%

Nano-Gold Catalysis in Fine Chemical Synthesis

et al. 2011

View full text Add to dashboard Cite

Section: Càn Bond Formationmentioning

confidence: 99%

Nano-Gold Catalysis in Fine Chemical Synthesis

et al. 2011

View full text Add to dashboard Cite

“…During this period, a threecomponent catalyst composed of Au/Fe(OH) 3 , ZnBr 2 , and Bu 4 NBr was shown to be very efficient for the direct oxidative carboxylation of styrene to styrene carbonate. 450 In this reaction, CO 2 acts as both reagent and solvent. The same group 451 improved the method by using the strong basic resin R201, containing quaternary ammonium groups, to support the gold.…”

Section: Formation Of Carbonatesmentioning

confidence: 99%

Gold-Catalyzed Carbon−Heteroatom Bond-Forming Reactions

2011

View full text Add to dashboard Cite

“…In addition, a de novo frameshift variant in the highly intolerant DDX1 (pLI 0.994) was identified in a patient with hypogammaglobulinemia, hematopoietic cell lineage abnormalities and recurrent infections. Although a causal genotype-phenotype relationship remains unclear, it has been reported that DDX1 plays a role in NF-κB signalling, type I interferon responses, and the regulation of hematopoietic stem and progenitor cell homeostasis (59,65). Furthermore, the de novo frameshift variant in KMT2C was detected in a patient with combined immunodeficiency and a neurodevelopmental phenotype, displaying partial phenotypic overlap with Kleefstra syndrome type 2 that has already been associated with de novo mutations in KMT2C (60).…”

Section: Discussionmentioning

confidence: 99%

“…DDX1 encodes an RNA helicase, which is part of a double-stranded RNA sensor that activates the NF-κB pathway and type I interferon responses (59). Moreover, DDX1 is involved in the regulation of hematopoietic stem and progenitor cell homeostasis (59,65).…”

Section: Cohort Characteristicsmentioning

confidence: 99%

Trio-based whole exome sequencing in patients with suspected sporadic inborn errors of immunity: a retrospective cohort study

Hebert

Simons

Schuurs-Hoeijmakers

et al. 2022

Preprint

View full text Add to dashboard Cite

<underline>Background</underline> De novo variants (DNVs) are currently not routinely evaluated as part of diagnostic whole exome sequencing (WES) analysis in patients with suspected inborn errors of immunity (IEI).<underline>Methods</underline>This study explored the potential added value of systematic assessment of DNVs in a retrospective cohort of 123 patients with a suspected sporadic IEI who underwent patient-parent trio-based WES.<underline>Results</underline>A likely molecular diagnosis for (part) of the immunological phenotype was achieved in 12 patients with the diagnostic in silico IEI WES gene panel. Exome-wide evaluation of rare, non-synonymous DNVs affecting coding or splice site regions led to the identification of 14 candidate DNVs in genes with an annotated immune function. DNVs were identified in IEI genes (NLRP3 and RELA) and potentially novel candidate genes, including PSMB10, DDX1, KMT2C and FBXW11. The FBXW11 canonical splice site DNV, in a patient with autoinflammatory disease, was shown to lead to defective RNA splicing, increased NF-κB p65 signalling, and elevated IL-1β production in primary immune cells.<underline>Conclusions</underline>This retrospective cohort study advocates the implementation of trio-based sequencing in routine diagnostics of patients with sporadic IEI. Furthermore, we have provided functional evidence supporting a causal role for FBXW11 loss-of-function mutations in autoinflammatory disease.<underline>Funding</underline>This research was supported by grants from the European Union, ZonMW and the Radboud Institute for Molecular Life Sciences.

show abstract

Application of Amplitude Spectrum Gradient Attribute in the Prediction of Reservoir Productivity

Cited by 12 publications

References 2 publications

Nano-Gold Catalysis in Fine Chemical Synthesis

Nano-Gold Catalysis in Fine Chemical Synthesis

Gold-Catalyzed Carbon−Heteroatom Bond-Forming Reactions

Trio-based whole exome sequencing in patients with suspected sporadic inborn errors of immunity: a retrospective cohort study

Contact Info

Product

Resources

About