Some Novel Rare Earth Metal Ions complexes: Synthesis, Characterization, Luminescence and Biocidal Efficiency.
Sign Up to like & getrecommendations! Published in 2020 at "Analytical biochemistry"
DOI: 10.1016/j.ab.2020.113645
Abstract: New lanthanide complexes (1-3) of the general formulae [Ln(L)(NO3)(H2O)] have been synthesized by reaction of Ln(NO3)3.xH2O {Ln = La (1), Sm (2) and Yb (3)} with 2,2'-(((1E,1'E)-thiophene-2,5-diylbis(methaneylylidene))bis(azaneylylidene))diphenol (H2L). Based on elemental analysis and spectroscopic analysis… read more here.
Keywords: earth metal; complexes synthesis; metal ions; novel rare ... See more keywords
Novel rare earth Dy doping impact on physical properties of PbI2 nanostructures synthesized by microwave route for optoelectronics
Sign Up to like & getrecommendations! Published in 2020 at "Materials Characterization"
DOI: 10.1016/j.matchar.2020.110688
Abstract: Abstract Dysprosium (Dy) doped lead iodide (PbI2) nanostructures (Dy@PbI2 NSs) were facilely synthesized via microwave-assisted route for the first time and studied by state-of-art experimental tools. Energy dispersive X-ray spectroscopy/scanning electron microscopy (EDX/SEM) elemental-mapping confirm… read more here.
Keywords: novel rare; rare earth; route; pbi2 nanostructures ... See more keywords
Targeted next-generation sequencing reveals novel and rare variants in Indian patients with amyotrophic lateral sclerosis
Sign Up to like & getrecommendations! Published in 2018 at "Neurobiology of Aging"
DOI: 10.1016/j.neurobiolaging.2018.05.012
Abstract: Studies on genetic aberrations among Indian amyotrophic lateral sclerosis (ALS) patients are limited to C9orf72 and ATXN2 repeat expansions and mutations in the SOD1 gene. In this study, we used targeted next-generation sequencing to analyze… read more here.
Keywords: targeted next; novel rare; amyotrophic lateral; rare variants ... See more keywords
A novel rare earth-salt bath nitriding of TC21-DT titanium alloy
Sign Up to like & getrecommendations! Published in 2018 at "Surface Engineering"
DOI: 10.1080/02670844.2016.1213035
Abstract: ABSTRACT A novel rare earth (RE)-salt bath nitriding of TC21-DT titanium alloy was primarily developed by adding certain amount of RE cerium oxide (CeO2) in KNO3 and NaNO3 salt bath, heated to temperatures in the… read more here.
Keywords: novel rare; rare earth; salt bath; earth salt ... See more keywords
Novel Rare Genetic Variants Associated with Airflow Obstruction in the General Population.
Sign Up to like & getrecommendations! Published in 2019 at "American journal of respiratory and critical care medicine"
DOI: 10.1164/rccm.201909-1868le
Abstract: Citation for published version (APA): de Vries, M., van der Plaat, D. A., Nedeljkovic, I., van der Velde, K. J., Amin, N., van Duijn, C. M., Vonk, J. M., Boezen, H. M., & van Diemen,… read more here.
Keywords: rare genetic; medicine; variants associated; associated airflow ... See more keywords
Novel rare genetic variants in idiopathic pulmonary fibrosis
Sign Up to like & getrecommendations! Published in 2020 at "European Respiratory Journal"
DOI: 10.1183/13993003.03252-2020
Abstract: Idiopathic pulmonary fibrosis (IPF) is a rare disease of epithelial injury leading to persistent fibrosis, remodelling of the lung parenchyma, and chronic respiratory failure [1]. IPF can be differentiated from other forms of interstitial fibrosis… read more here.
Keywords: fibrosis; idiopathic pulmonary; genetic variants; novel rare ... See more keywords
Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing
Sign Up to like & getrecommendations! Published in 2023 at "Open Life Sciences"
DOI: 10.1515/biol-2022-0593
Abstract: Abstract Pulmonary atresia (PA) is a severe cyanotic congenital heart disease. Although some genetic mutations have been described to be associated with PA, the knowledge of pathogenesis is insufficient. The aim of this research was… read more here.
Keywords: pulmonary atresia; whole exome; novel rare; rare genetic ... See more keywords
Clinical and molecular characteristics of a novel rare de novo variant in PPP2CA in a patient with a developmental disorder, autism, and epilepsy
Sign Up to like & getrecommendations! Published in 2022 at "Frontiers in Cell and Developmental Biology"
DOI: 10.3389/fcell.2022.1059938
Abstract: PP2A-related (neuro) developmental disorders are a family of genetic diseases caused by a heterozygous alteration in one of several genes encoding a subunit of type 2A protein phosphatases. Reported affected genes, so far, are PPP2R5D,… read more here.
Keywords: characteristics novel; novel rare; molecular characteristics; ppp2ca ... See more keywords
Novel and Rare Fusion Transcripts Involving Transcription Factors and Tumor Suppressor Genes in Acute Myeloid Leukemia
Sign Up to like & getrecommendations! Published in 2019 at "Cancers"
DOI: 10.3390/cancers11121951
Abstract: Approximately 18% of acute myeloid leukemia (AML) cases express a fusion transcript. However, few fusions are recurrent across AML and the identification of these rare chimeras is of interest to characterize AML patients. Here, we… read more here.
Keywords: rare fusion; myeloid leukemia; novel rare; acute myeloid ... See more keywords