Erratum to: Zebrafish phenotypic screen identifies novel Notch antagonists
Sign Up to like & getrecommendations! Published in 2017 at "Investigational New Drugs"
DOI: 10.1007/s10637-017-0437-0
Abstract: The authors would like to note that in the original online first version of this article, the symbol ɣ is missing from the text where ɣ-secretase is stated. Also, labels to figures in the Results… read more here.
Keywords: zebrafish phenotypic; phenotypic screen; identifies novel; screen identifies ... See more keywords
WITHDRAWN: Whole genome sequencing identifies novel NOTCH3 mutations for leukoaraiosis.
Sign Up to like & getrecommendations! Published in 2018 at "Biochemical and biophysical research communications"
DOI: 10.1016/j.bbrc.2018.02.074
Abstract: This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause. The full Elsevier Policy on Article Withdrawal can be found at https://www.elsevier.com/about/our-business/policies/article-withdrawal. read more here.
Keywords: withdrawn whole; whole genome; identifies novel; novel notch3 ... See more keywords
Pan-Genomic Illumination of Tomato Identifies Novel Gene-Trait Interactions.
Sign Up to like & getrecommendations! Published in 2019 at "Trends in plant science"
DOI: 10.1016/j.tplants.2019.08.001
Abstract: A recent study by Gao et al., (Nat. Genet., 2019) presents a tomato pan-genome that was constructed using genome sequences of 725 phylogenetically and geographically representative accessions. The study revealed 4873 genes that are absent… read more here.
Keywords: identifies novel; genomic illumination; tomato identifies; novel gene ... See more keywords
Functional metagenomics identifies novel genes ABCTPP, TMSRP1 and TLSRP1 among human gut enterotypes
Sign Up to like & getrecommendations! Published in 2018 at "Scientific Reports"
DOI: 10.1038/s41598-018-19862-5
Abstract: Every niche in the biosphere is touched by the seemingly endless capacity of microbes to transform the world around them by adapting swiftly and flexibly to the environmental changes, likewise the gastrointestinal tract is no… read more here.
Keywords: gut; human gut; identifies novel; functional metagenomics ... See more keywords
Exome sequencing identifies novel mutation signatures of UV radiation and trichostatin A in primary human keratinocytes
Sign Up to like & getrecommendations! Published in 2020 at "Scientific Reports"
DOI: 10.1038/s41598-020-61807-4
Abstract: Canonical ultraviolet (UV) mutation type and spectra are traditionally defined by direct sequencing-based approaches to map mutations in a limited number of representative DNA elements. To obtain an unbiased view of genome wide UV mutation… read more here.
Keywords: exome sequencing; identifies novel; novel mutation; human keratinocytes ... See more keywords
A yeast two-hybrid screening identifies novel Atg8a interactors in Drosophila
Sign Up to like & getrecommendations! Published in 2022 at "Autophagy"
DOI: 10.1080/15548627.2022.2045535
Abstract: ABSTRACT Macroautophagy/autophagy-related protein Atg8/LC3 is important for autophagosome biogenesis and required for selective degradation of various substrates. In our recent study, we performed a yeast two-hybrid screening to identify proteins that interact with Atg8a, the… read more here.
Keywords: hybrid screening; two hybrid; novel atg8a; screening identifies ... See more keywords
A proteomic atlas of the neointima identifies novel druggable targets for preventive therapy
Sign Up to like & getrecommendations! Published in 2021 at "European Heart Journal"
DOI: 10.1093/eurheartj/ehab140
Abstract: Abstract Aims In-stent restenosis is a complication after coronary stenting associated with morbidity and mortality. Here, we sought to investigate the molecular processes underlying neointima formation and to identify new treatment and prevention targets. Methods… read more here.
Keywords: neointima identifies; identifies novel; formation; proteomic atlas ... See more keywords
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Sign Up to like & getrecommendations! Published in 2018 at "Genome Biology"
DOI: 10.1186/s13059-018-1457-6
Abstract: BackgroundGenome-wide association studies conducted on QRS duration, an electrocardiographic measurement associated with heart failure and sudden cardiac death, have led to novel biological insights into cardiac function. However, the variants identified fall predominantly in non-coding… read more here.
Keywords: identifies novel; analysis; novel loci; exome chip ... See more keywords
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive
Sign Up to like & getrecommendations! Published in 2017 at "F1000Research"
DOI: 10.12688/f1000research.12102.1
Abstract: Microcephaly is a genetically heterogeneous disorder and is one of the frequently notable conditions in paediatric neuropathology which exists either as a single entity or in association with other co-morbidities. More than a single gene… read more here.
Keywords: exome sequencing; identifies novel; sequencing identifies; autosomal recessive ... See more keywords
Whole-Exome Sequencing Identifies Novel SCN1A and CACNB4 Genes Mutations in the Cohort of Saudi Patients With Epilepsy
Sign Up to like & getrecommendations! Published in 2022 at "Frontiers in Pediatrics"
DOI: 10.3389/fped.2022.919996
Abstract: Epilepsy is a neurological disorder described as recurrent seizures mild to severe convulsions along with conscious loss. There are many different genetic anomalies or non-genetic conditions that affect the brain and cause epilepsy. The exact… read more here.
Keywords: whole exome; saudi patients; identifies novel; sequencing identifies ... See more keywords