Results 141 to 150 of about 30,834 (284)

Isolation of cytoplasmic non‐ribosomal ribonucleoprotein particles (informosomes) [PDF]

open access: bronze, 1972
J. Kempf   +5 more
openalex   +1 more source

Single‐cell spatial transcriptomic sequencing and machine learning models uncover molecular mechanisms and diagnostic biomarkers of Peyronie's disease formation in rats

open access: yesVIEW, EarlyView.
Peyronie's disease (PD) is a common male reproductive system disorder. The exact etiology of PD remains unclear. This study aimed to investigate molecular and cellular changes in PD using single‐cell spatial transcriptomics. Abstract Peyronie's disease (PD), commonly known as penile induration, is a prevalent male reproductive system disorder with ...
Keyuan Lou   +6 more
wiley   +1 more source

Strand displacement‐driven CRISPR/Cas12a framework enables precise identification of low‐abundance point mutations

open access: yesVIEW, EarlyView.
We established an engineered CRISPR/Cas12a point mutation detection strategy (E‐CRISPR) for low‐abundance point mutations detection. By integrating the precise regulatory mechanism of strand displacement reaction (SDR) with the local high‐concentration probe microenvironment created by tetrahedral DNA frameworks (TDFs), it has achieved simultaneous ...
Jiaxi Mo   +11 more
wiley   +1 more source

CRISPR vs. nematodes: A new era of genetic solutions for potato crop protection

open access: yesAnnals of Applied Biology, EarlyView.
This review highlights the impact of nematodes on potato production and explores CRISPR/Cas genome editing as a breakthrough strategy for enhancing resistance. We discuss the potential, challenges, and future directions of CRISPR‐based approaches in developing resilient potato cultivars.
Karam Mostafa   +6 more
wiley   +1 more source

CRISPR Technology in Disease Management: An Updated Review of Clinical Translation and Therapeutic Potential

open access: yesCell Proliferation, EarlyView.
CRISPR‐Cas systems offer transformative genome editing capabilities for precise manipulation of cellular genes. This enables two main therapeutic avenues: ex vivo modification of patient cells for re‐transplantation or direct in vivo gene targeting via advanced delivery methods.
Bahareh Farasati Far   +4 more
wiley   +1 more source

In vivo modeling of lethal congenital contracture syndrome 1 suggests pathomechanisms in cellular stress responses

open access: yesThe FEBS Journal, EarlyView.
Gle1 knockout mice fail to segregate cell lineages at the blastocyst stage, resulting in very early embryonic lethality. Gle1 knock‐in (KI) mice harboring a pathogenic variant giving rise to lethal congenital contracture syndrome 1 show both known and novel innervation defects, supportive of multiorgan pathology in human fetuses.
Tomáš Zárybnický   +22 more
wiley   +1 more source

SYNCAS‐mediated CRISPR‐Cas9 genome editing in the Jewel wasp, Nasonia vitripennis

open access: yesInsect Molecular Biology, EarlyView.
Maternal injection of Cas9 RNP together with BAPC and saponins (SYNCAS) results in efficient gene editing of Nasonia vitripennis offspring. The timing of injection and egg collection is important for maximising efficiency and reducing screening effort.
Filippo Guerra   +2 more
wiley   +1 more source

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