Results 61 to 70 of about 2,520 (267)

Importin 7 mediates the nuclear import of HIV‐1 integrase via a specific interacting interface

open access: yesFEBS Open Bio, EarlyView.
HIV‐1 integrase enables viral DNA integration into the host genome. By binding to the core domain of the host protein Importin 7 via its C‐terminal domain, the integrase is transported across the nuclear membrane into the nucleus, where integration of the viral genome into host DNA takes place. This translocation is a critical step for subsequent viral
Juana Bana   +5 more
wiley   +1 more source

Dual native G‐quadruplex folding is associated with chromatin looping at the MYC locus

open access: yesFEBS Open Bio, EarlyView.
BG4‐detectable G‐quadruplex (G4) in HaCaT and NHEK keratinocytes identified folded and unfolded G4s enriched at promoters/TSSs and active enhancers, whereas unfolded G4s also overlapped weak/poised enhancers. At MYC–PVT1, 3C‐qPCR detected enhancer–promoter looping only when G4s were simultaneously folded at both regulatory elements under native ...
Dieila Giomo de Lima   +7 more
wiley   +1 more source

Chronobiology of Cancer: How Aging Fuels Oncogenesis at the Molecular Level

open access: yesAging and Cancer, EarlyView.
This graphical abstract illustrates the key biological pathways linking aging with cancer development and progression. In the upper left, cumulative exposure to ultraviolet radiation, toxins, and reactive oxygen species (ROS) causes DNA damage and genomic instability, whereas age‐related decline in repair mechanisms, such as ATM/ATR, BER, and NER ...
Anu Singh, Aroonima Misra, Sufian Zaheer
wiley   +1 more source

Identity of Linaria × versicolor (Antirrhineae, Plantaginaceae) and typification of its basionym

open access: yesMediterranean Botany
The identity of Linaria ×versicolor (Jacq.) Chaz. is discussed, supporting a hybrid origin in cultivation that involved species of the North African clade of Linaria subsect. Versicolores as parents.
Nicolas Ruch   +2 more
doaj   +1 more source

Detecção de cepas patogênicas pela PCR multiplex e avaliação da sensibilidade a antimicrobianos de Escherichia coli isoladas de leitões diarréicos Detection of pathogenic strains by multiplex PCR and antimicrobial sensitivity of Escherichia coli isolated from piglets

open access: yesArquivo Brasileiro de Medicina Veterinária e Zootecnia, 2007
Avaliou-se a freqüência dos genes de fímbrias (K88, K99, 987P, F18 e F41) e toxinas (LT, Stb, StaP e Stx2e) de cepas de E. coli isoladas de leitões com diarréia usando a técnica de PCR multiplex com primers específicos para esses genes, e estudou-se o ...
N.R. Macêdo   +5 more
doaj   +1 more source

Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone   +8 more
wiley   +1 more source

Lectotype designation of the Macaronesian endemic Gymnosporia cassinoides (Celastraceae)

open access: yesAnales del Jardín Botánico de Madrid
The typification of the name Celastrus cassinoides, currently accepted as Gymnosporia cassinoides (Celastraceae), is discussed. This species is a plant endemic to the Canary Islands, traditionally known as Maytenus canariensis. A lectotype is designated
P. Pablo Ferrer-Gallego
doaj   +1 more source

Fiction et typification

open access: yesMethodos, 2005
How are cognitive elements of experience available for the continuation of ego’s action, and how are they passed on to alter ? In the social phenomenology of Alfred Schutz for instance, these questions are related back to generalisation and stabilisation
Nathalie Zaccaï-Reyners
doaj   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

FABACEAE: THE TYPIFICATION OF HAEMATOXYLUM DINTERI

open access: yesBothalia: African Biodiversity & Conservation, 1976
THE TYPIFICATION OF HAEMATOXYLUM ...
J. H. Ross
doaj   +1 more source

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