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480 Result(s)
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Open AccessMolecular basis and homeostatic regulation of Zinc taste
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Open AccessCorrection to: Nuclear m6A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos
The original article can be found online at https://doi.org/10.1007/s13238-021-00837-8.
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Open AccessFerroptosis as an important driver of lupus
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Open AccessComprehensive analysis of RNA-seq and whole genome sequencing data reveals no evidence for SARS-CoV-2 integrating into host genome
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Open AccessCardioprotective mechanism of SGLT2 inhibitor against myocardial infarction is through reduction of autosis
Sodium-glucose cotransporter 2 (SGLT2) inhibitors reduce cardiovascular mortality in patients with diabetes mellitus but the protective mechanism remains elusive. Here we demonstrated that the SGLT2 inhibitor,...
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Open AccessHomology-based repair induced by CRISPR-Cas nucleases in mammalian embryo genome editing
Recent advances in genome editing, especially CRISPR-Cas nucleases, have revolutionized both laboratory research and clinical therapeutics. CRISPR-Cas nucleases, together with the DNA damage repair pathway in ...
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Open AccessNuclear peripheral chromatin-lamin B1 interaction is required for global integrity of chromatin architecture and dynamics in human cells
The eukaryotic genome is folded into higher-order conformation accompanied with constrained dynamics for coordinated genome functions. However, the molecular machinery underlying these hierarchically organized...
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Open AccessIdentification of a novel cDC2-committed progenitor within mouse common dendritic cell progenitor population
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Open AccessDrug target inference by mining transcriptional data using a novel graph convolutional network framework
A fundamental challenge that arises in biomedicine is the need to characterize compounds in a relevant cellular context in order to reveal potential on-target or off-target effects. Recently, the fast accumula...
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Open AccessRestoration of FMRP expression in adult V1 neurons rescues visual deficits in a mouse model of fragile X syndrome
Many people affected by fragile X syndrome (FXS) and autism spectrum disorders have sensory processing deficits, such as hypersensitivity to auditory, tactile, and visual stimuli. Like FXS in humans, loss of Fmr1
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Open AccessExosomes from antler stem cells alleviate mesenchymal stem cell senescence and osteoarthritis
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Open AccessCancer biology deciphered by single-cell transcriptomic sequencing
Tumors are complex ecosystems in which heterogeneous cancer cells interact with their microenvironment composed of diverse immune, endothelial, and stromal cells. Cancer biology had been studied using bulk gen...
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Open AccessA pair of transporters controls mitochondrial Zn2+ levels to maintain mitochondrial homeostasis
Zn2+ is required for the activity of many mitochondrial proteins, which regulate mitochondrial dynamics, apoptosis and mitophagy. However, it is not understood how the proper mitochondrial Zn2+ level is achieved ...
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Open AccessMaternal heterozygous mutation in CHEK1 leads to mitotic arrest in human zygotes
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Open AccessEpigenetic integrity of paternal imprints enhances the developmental potential of androgenetic haploid embryonic stem cells
The use of two inhibitors of Mek1/2 and Gsk3β (2i) promotes the generation of mouse diploid and haploid embryonic stem cells (ESCs) from the inner cell mass of biparental and uniparental blastocysts, respectiv...
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Open AccessGenomic instability as a major mechanism for acquired resistance to EGFR tyrosine kinase inhibitors in cancer
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Open AccesscGAS guards against chromosome end-to-end fusions during mitosis and facilitates replicative senescence
As a sensor of cytosolic DNA, the role of cyclic GMP-AMP synthase (cGAS) in innate immune response is well established, yet how its functions in different biological conditions remain to be elucidated. Here, w...
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Open AccessPINK1 kinase dysfunction triggers neurodegeneration in the primate brain without impacting mitochondrial homeostasis
In vitro studies have established the prevalent theory that the mitochondrial kinase PINK1 protects neurodegeneration by removing damaged mitochondria in Parkinson’s disease (PD). However, difficulty in detecting...
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Open AccessIsogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
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Open AccessA tribute to Professor Yong Zhao