Results 91 to 100 of about 2,885,338 (147)

The (trans)national Russian religious imagination in exile: Iulia de Beausobre (1893‐1977)

Modern Theology, EarlyView.
Abstract The article offers a case study of how Russian Orthodox who migrated from the Soviet Union after the Bolshevik Revolution of 1917 reimagined their religious identity and their church in a transnational setting. Iulia de Beausobre (1893‐1977) was a Russian aristocrat who fell victim to the Stalinist purges but survived the Soviet prison system ...
Ruth Coates
wiley   +1 more source

U-rich elements drive pervasive cryptic splicing in 3’ UTR massively parallel reporter assays

Nature Communications
Untranslated RNA sequences play essential roles in orchestrating gene expression. However, the sequence codes and mechanisms underpinning post-transcriptional regulation remain incompletely understood.
Khoa Dao, Courtney F. Jungers, Sergej Djuranovic, Anthony M. Mustoe   +3 more
doaj   +1 more source

A method for identifying alternative or cryptic donor splice sites within gene and mRNA sequences. Comparisons among sequences from vertebrates, echinoderms and other groups

BMC Genomics, 2009
Background As the amount of genome sequencing data grows, so does the problem of computational gene identification, and in particular, the splicing signals that flank exon borders.
Florea Liliana D, Buckley Katherine M, Smith L Courtney   +2 more
doaj   +1 more source

City of God and the Duty of Just Memory

Modern Theology, EarlyView.
Abstract In a recent essay, Richard Miller claims that Augustine presumes a duty to remember justly in his City of God. However, Miller's brief reference to a presumed duty of “just memory” does not fully explain how Augustine conceptualizes this duty or how it relates to his theological concerns.
Zachary J. Taylor
wiley   +1 more source

An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sites

, 2005
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder associated with gastrointestinal polyposis and an increased cancer risk. PJS is caused by germline mutations in the tumor suppressor gene LKB1. One such mutation, IVS2+1A>G, alters the second
Nicoletta Resta, Guanti G, Traum, D., STELLA, Alessandro, RESTA, Nicoletta, Michelle L Hastings, Daniel Traum, Ginevra Guanti, Krainer, A. R., Guanti, G., Stella, A., Krainer AR, Alessandro Stella, Hastings ML, Adrian R Krainer, Hastings, M. L., Resta, N., Traum D   +17 more
core   +1 more source

Application of Computational Methods to Study the Selection of Authentic and Cryptic Splice Sites [PDF]

, 2017
Proteins are building blocks of the bodies of eukaryotes, and the process of synthesizing proteins from DNA is crucial for the good health of an organism [13].
Dey, Tapomay
core   +1 more source

The Reverb of Divine Revelation: Theological Poetics in John of the Cross

Modern Theology, EarlyView.
Abstract This article examines the theological poetics of John of the Cross, investigating both the conditions under which contemplative experience gives rise to speech and the theological status of that speech within John's account of divine revelation.
Michael C. Costas
wiley   +1 more source

The main WAP isoform usually found in camel milk arises from the usage of an improbable intron cryptic splice site in the precursor to mRNA in which a GC-AG intron occurs

BMC Genetics, 2019
Background Whey acidic protein (WAP) is a major protein identified in the milk of several mammalian species with cysteine-rich domains known as four-disulfide cores (4-DSC).
Alma Ryskaliyeva, Céline Henry, Guy Miranda, Bernard Faye, Gaukhar Konuspayeva, Patrice Martin   +5 more
doaj   +1 more source

Cryptic splicing sites are differentially utilized in vivo.

, 2008
It has long been considered that cryptic splice sites are ignored by the splicing machinery in the context of intact genuine splice sites. In the present study, it is shown that cryptic splice sites are utilized in all circumstances, when the authentic ...
Deguillien, Mireille, Ben Chibani, Jemni, Baklouti, Faouzi, Haj Khelil, Amel, Morinière, Madeleine   +4 more
core   +1 more source

Deep intronic ANK1 variants causing pseudo‐exon inclusion in hereditary spherocytosis: Whole‐genome sequencing and functional assessment

British Journal of Haematology, EarlyView.
Victor Marin, Alexandre Janin, Céline Renoux, Yoann Huguenin, AURAGEN consortium, Stéphanie Dulucq, Louis Lebreton, Philippe Joly, Julian Boutin   +8 more
wiley   +1 more source