User profiles for Yangfan Liu
Yangfan LiuGraduate Student, Stanford University Verified email at stanford.edu Cited by 14 |
Radiotherapy targeting cancer stem cells “awakens” them to induce tumour relapse and metastasis in oral cancer
Y Liu, M Yang, J Luo, H Zhou - International journal of oral science, 2020 - nature.com
Radiotherapy is one of the most common treatments for oral cancer. However, in the clinic,
recurrence and metastasis of oral cancer occur after radiotherapy, and the underlying …
recurrence and metastasis of oral cancer occur after radiotherapy, and the underlying …
Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response
JM Gerdes, Y Liu, NA Zaghloul, CC Leitch… - Nature …, 2007 - nature.com
Primary cilia and basal bodies are evolutionarily conserved organelles that mediate
communication between the intracellular and extracellular environments. Here we show that bbs1, …
communication between the intracellular and extracellular environments. Here we show that bbs1, …
Persistent accumulation of therapy-induced senescent cells: an obstacle to long-term cancer treatment efficacy
J Luo, T Sun, Z Liu, Y Liu, J Liu, S Wang… - International Journal of …, 2025 - nature.com
In the ever-evolving landscape of cancer therapy, while cancer treatments such as
chemotherapy, radiotherapy, and targeted therapy aim to eradicate malignant cells, they also …
chemotherapy, radiotherapy, and targeted therapy aim to eradicate malignant cells, they also …
DNMT1-targeting remodeling global DNA hypomethylation for enhanced tumor suppression and circumvented toxicity in oral squamous cell carcinoma
Y Liu, Y Sun, J Yang, D Wu, S Yu, J Liu, T Hu, J Luo… - Molecular cancer, 2024 - Springer
Background The faithful maintenance of DNA methylation homeostasis indispensably
requires DNA methyltransferase 1 (DNMT1) in cancer progression. We previously identified …
requires DNA methyltransferase 1 (DNMT1) in cancer progression. We previously identified …
CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290
…, H Özyurek, S Dibooglu, EA Otto, Y Liu… - The American Journal of …, 2008 - cell.com
Joubert syndrome and related disorders (JSRD) are primarily autosomal-recessive conditions
characterized by hypotonia, ataxia, abnormal eye movements, and intellectual disability …
characterized by hypotonia, ataxia, abnormal eye movements, and intellectual disability …
Loss of δ-catenin function in severe autism
Autism is a multifactorial neurodevelopmental disorder affecting more males than females;
consequently, under a multifactorial genetic hypothesis, females are affected only when they …
consequently, under a multifactorial genetic hypothesis, females are affected only when they …
Short‐lived air pollutants and climate forcers through the lens of the COVID‐19 pandemic
Dramatic reductions in anthropogenic emissions during the lockdowns of the COVID‐19
pandemic provide an unparalleled opportunity to assess responses of the Earth system to …
pandemic provide an unparalleled opportunity to assess responses of the Earth system to …
Genetic drivers of kidney defects in the DiGeorge syndrome
E Lopez-Rivera, YP Liu, M Verbitsky… - … England Journal of …, 2017 - Mass Medical Soc
Background The DiGeorge syndrome, the most common of the microdeletion syndromes,
affects multiple organs, including the heart, the nervous system, and the kidney. It is caused by …
affects multiple organs, including the heart, the nervous system, and the kidney. It is caused by …
Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators
Cilia are critical mediators of paracrine signaling; however, it is unknown whether proteins
that contribute to ciliopathies converge on multiple paracrine pathways through a common …
that contribute to ciliopathies converge on multiple paracrine pathways through a common …
Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene
KM Nishiguchi, RG Tearle, YP Liu, EC Oh… - Proceedings of the …, 2013 - pnas.org
We performed whole genome sequencing in 16 unrelated patients with autosomal recessive
retinitis pigmentosa (ARRP), a disease characterized by progressive retinal degeneration …
retinitis pigmentosa (ARRP), a disease characterized by progressive retinal degeneration …