Results 51 to 60 of about 1,704,122 (259)
Parameterized complexity of fair deletion problems
, 2017 Deletion problems are those where given a graph $G$ and a graph property $\pi$, the goal is to find a subset of edges such that after its removal the graph $G$ will satisfy the property $\pi$. Typically, we want to minimize the number of elements removed.
Masařík, Tomáš, Toufar, Tomáš
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A comprehensive analysis of the importance of translation initiation factors for Haloferax volcanii applying deletion and conditional depletion mutants [PDF]
, 2013 Translation is an important step in gene expression. The initiation of translation is phylogenetically diverse, since currently five different initiation mechanisms are known.
Gäbel, Katrin +4 more
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Molecular bases of circadian magnesium rhythms across eukaryotes
FEBS Letters, EarlyView.Circadian rhythms in intracellular [Mg2+] exist across eukaryotic kingdoms. Central roles for Mg2+ in metabolism suggest that Mg2+ rhythms could regulate daily cellular energy and metabolism. In this Perspective paper, we propose that ancestral prokaryotic transport proteins could be responsible for mediating Mg2+ rhythms and posit a feedback model ...
Helen K. Feord, Gerben van Ooijen
wiley +1 more source
Proximal 4p Deletion Syndrome in an Infant With Multiple Systemic Anomalies
Molecular Genetics & Genomic MedicineBackground Contiguous gene deletion in the short arm of chromosome 4 is linked to various neurodevelopmental disorders. Methods In this study, we conducted peripheral blood chromosome G‐banding karyotyping and whole‐exome sequencing (WES) on a proband ...
Ying Pang +11 more
doaj +1 more source
Meiotic Chromosomal Abnormality Detected in a Heterozygote of Elymus nutans
Frontiers in Plant Science, 2022 Elymus nutans is an allopolyploid with a genome constitution of StStYYHH (2n = 6x = 42). Highly frequent intergenomic translocations and chromosomal variations with repeat amplification and deletions in E.
Bo Liu +5 more
doaj +1 more source
A Note on the Deletion Channel Capacity [PDF]
, 2012 Memoryless channels with deletion errors as defined by a stochastic channel matrix allowing for bit drop outs are considered in which transmitted bits are either independently deleted with probability $d$ or unchanged with probability $1-d$.
Duman, Tolga M., Rahmati, Mojtaba
core
Microarray-based ultra-high resolution discovery of genomic deletion mutations [PDF]
, 2014 BACKGROUND: Oligonucleotide microarray-based comparative genomic hybridization (CGH) offers an attractive possible route for the rapid and cost-effective genome-wide discovery of deletion mutations.
Baban, D. +8 more
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Crosstalk between the ribosome quality control‐associated E3 ubiquitin ligases LTN1 and RNF10
FEBS Letters, EarlyView.Loss of the E3 ligase LTN1, the ubiquitin‐like modifier UFM1, or the deubiquitinating enzyme UFSP2 disrupts endoplasmic reticulum–ribosome quality control (ER‐RQC), a pathway that removes stalled ribosomes and faulty proteins. This disruption may trigger a compensatory response to ER‐RQC defects, including increased expression of the E3 ligase RNF10 ...
Yuxi Huang +8 more
wiley +1 more source
Studies in Chinese Linguistics, 2022 This paper studies echo answers to yes-no questions in Chinese with respect to their distributions, derivations, and typological patterns. We reconsider Simpson’s (2015) verb-raising analyses of verb echo answers (VEAs), finding that his analysis is ...
Wei Ting-Chi
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Frontiers in Genetics, 2022 Background: Thalassemia was the most common monogenic diseases worldwide, which was caused by mutations, deletions or duplications in human globin genes which disturbed the synthesis balance between α- and β-globin chains of hemoglobin.
Guoxing Zhong +9 more
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