User profiles for Huili Hu
Huili HuHubrecht Institute and SDU Verified email at hubrecht.eu Cited by 2588 |
[PDF][PDF] Long-term expansion of functional mouse and human hepatocytes as 3D organoids
The mammalian liver possesses a remarkable regenerative ability. Two modes of damage
response have been described: (1) The "oval cell" response emanates from the biliary tree …
response have been described: (1) The "oval cell" response emanates from the biliary tree …
High-resolution 3D imaging of fixed and cleared organoids
…, PR Jamieson, AM Vonk, GD Amatngalim, H Hu… - Nature protocols, 2019 - nature.com
In vitro 3D organoid systems have revolutionized the modeling of organ development and
diseases in a dish. Fluorescence microscopy has contributed to the characterization of the …
diseases in a dish. Fluorescence microscopy has contributed to the characterization of the …
[PDF][PDF] Building consensus on definition and nomenclature of hepatic, pancreatic, and biliary organoids
Hepatic, pancreatic, and biliary (HPB) organoids are powerful tools for studying development,
disease, and regeneration. As organoid research expands, the need for clear definitions …
disease, and regeneration. As organoid research expands, the need for clear definitions …
[HTML][HTML] In vitro grafting of hepatic spheroids and organoids on a microfluidic vascular bed
…, R Dinkelberg, SB García, B Kramer, T Olivier, H Hu… - Angiogenesis, 2022 - Springer
With recent progress in modeling liver organogenesis and regeneration, the lack of vasculature
is becoming the bottleneck in progressing our ability to model human hepatic tissues in …
is becoming the bottleneck in progressing our ability to model human hepatic tissues in …
[PDF][PDF] CRL4B catalyzes H2AK119 monoubiquitination and coordinates with PRC2 to promote tumorigenesis
We reported that Cullin4B-Ring E3 ligase complex (CRL4B) is physically associated with
Polycomb-repressive complex 2 (PRC2). We showed that CRL4B possesses an intrinsic …
Polycomb-repressive complex 2 (PRC2). We showed that CRL4B possesses an intrinsic …
[PDF][PDF] Probing the tumor suppressor function of BAP1 in CRISPR-engineered human liver organoids
The deubiquitinating enzyme BAP1 is a tumor suppressor, among others involved in
cholangiocarcinoma. BAP1 has many proposed molecular targets, while its Drosophila homolog is …
cholangiocarcinoma. BAP1 has many proposed molecular targets, while its Drosophila homolog is …
[PDF][PDF] A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42)
P Lin, J Li, Q Liu, F Mao, J Li, R Qiu, H Hu… - The American Journal of …, 2008 - cell.com
Hereditary spastic paraplegias (HSPs), characterized by progressive and bilateral spasticity
of the legs, are usually caused by developmental failure or degeneration of motor axons in …
of the legs, are usually caused by developmental failure or degeneration of motor axons in …
Establishment of human fetal hepatocyte organoids and CRISPR–Cas9-based gene knockin and knockout in organoid cultures from human liver
The liver is composed of two epithelial cell types: hepatocytes and liver ductal cells. Culture
conditions for expansion of human liver ductal cells in vitro as organoids were previously …
conditions for expansion of human liver ductal cells in vitro as organoids were previously …
[HTML][HTML] MiR-135b-5p and MiR-499a-3p promote cell proliferation and migration in atherosclerosis by directly targeting MEF2C
Z Xu, Y Han, J Liu, F Jiang, H Hu, Y Wang, Q Liu… - Scientific Reports, 2015 - nature.com
Proliferation and migration of endothelial cells (ECs) and vascular smooth muscle cells (VSMCs)
are critical processes involved in atherosclerosis. Recent studies have revealed that …
are critical processes involved in atherosclerosis. Recent studies have revealed that …
A combined model of human iPSC‐derived liver organoids and hepatocytes reveals ferroptosis in DGUOK mutant mtDNA depletion syndrome
…, F Bao, L Yang, H Shi, M Gao, L Zheng, H Hu… - Advanced …, 2021 - Wiley Online Library
Mitochondrial DNA depletion syndrome (MDS) is a group of severe inherited disorders caused
by mutations in genes, such as deoxyribonucleoside kinase (DGUOK). A great majority of …
by mutations in genes, such as deoxyribonucleoside kinase (DGUOK). A great majority of …