Found: 54
Select item for more details and to access through your institution.
Lack of CUL4B in Adipocytes Promotes PPARγ-Mediated Adipose Tissue Expansion and Insulin Sensitivity.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Pterostilbene mediates neuroprotection against oxidative toxicity via oestrogen receptor α signalling pathways.
- Published in:
- Journal of Pharmacy & Pharmacology, 2015, v. 67, n. 5, p. 720, doi. 10.1111/jphp.12360
- By:
- Publication type:
- Article
DNM2 mutations in Chinese Han patients with centronuclear myopathy.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Ankylosing spondylitis: analysis of gene-gene interactions between IL-12β, JAK2, and STAT3 in Han Chinese and Algerian cohorts.
- Published in:
- Central European Journal of Immunology, 2019, v. 44, n. 1, p. 65, doi. 10.5114/ceji.2019.84019
- By:
- Publication type:
- Article
Autophagy Contributes to the Maintenance of Genomic Integrity by Reducing Oxidative Stress.
- Published in:
- Oxidative Medicine & Cellular Longevity, 2020, p. 1, doi. 10.1155/2020/2015920
- By:
- Publication type:
- Article
CUL4B renders breast cancer cells tamoxifen‐resistant via miR‐32‐5p/ER‐α36 axis.
- Published in:
- Journal of Pathology, 2021, v. 254, n. 2, p. 185, doi. 10.1002/path.5657
- By:
- Publication type:
- Article
CUL4B activates Wnt/β-catenin signalling in hepatocellular carcinoma by repressing Wnt antagonists.
- Published in:
- Journal of Pathology, 2015, v. 235, n. 5, p. 784, doi. 10.1002/path.4492
- By:
- Publication type:
- Article
The secreted glycoprotein lubricin protects cartilage surfaces and inhibits synovial cell overgrowth.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Novel PNPLA2 gene mutations in Chinese Han patients causing neutral lipid storage disease with myopathy.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 10, p. 679, doi. 10.1038/jhg.2012.84
- By:
- Publication type:
- Article
Clinical and molecular genetic analysis in Chinese patients with distal myopathy with rimmed vacuoles.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 4, p. 335, doi. 10.1038/jhg.2011.15
- By:
- Publication type:
- Article
Autophagic Flux Unleashes GATA4-NF-κB Axis to Promote Antioxidant Defense-Dependent Survival of Colorectal Cancer Cells under Chronic Acidosis.
- Published in:
- Oxidative Medicine & Cellular Longevity, 2021, p. 1, doi. 10.1155/2021/8189485
- By:
- Publication type:
- Article
Mendelian randomization studies on atherosclerotic cardiovascular disease: evidence and limitations.
- Published in:
- SCIENCE CHINA Life Sciences, 2019, v. 62, n. 6, p. 758, doi. 10.1007/s11427-019-9537-4
- By:
- Publication type:
- Article
MiR-182 overexpression in tumourigenesis of high-grade serous ovarian carcinoma.
- Published in:
- Journal of Pathology, 2012, v. 228, n. 2, p. 204, doi. 10.1002/path.4000
- By:
- Publication type:
- Article
CUL4B orchestrates mesenchymal stem cell commitment by epigenetically repressing KLF4 and C/EBPδ.
- Published in:
- Bone Research, 2023, v. 11, n. 1, p. 1, doi. 10.1038/s41413-023-00263-y
- By:
- Publication type:
- Article
ORMDL3 contributes to the risk of atherosclerosis in Chinese Han population and mediates oxidized low-density lipoprotein-induced autophagy in endothelial cells.
- Published in:
- Scientific Reports, 2015, p. 17194, doi. 10.1038/srep17194
- By:
- Publication type:
- Article
Unfolded Protein Response and Activated Degradative Pathways Regulation in GNE Myopathy.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058116
- By:
- Publication type:
- Article
Lack of Cul4b, an E3 Ubiquitin Ligase Component, Leads to Embryonic Lethality and Abnormal Placental Development.
- Published in:
- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037070
- By:
- Publication type:
- Article
Berberine Radiosensitizes Human Esophageal Cancer Cells by Downregulating Homologous Recombination Repair Protein RAD51.
- Published in:
- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023427
- By:
- Publication type:
- Article
Replication Stress Induces Micronuclei Comprising of Aggregated DNA Double-Strand Breaks.
- Published in:
- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0018618
- By:
- Publication type:
- Article
A novel deletion mutation in GJB1 causes X-linked Charcot-Marie-Tooth disease in a Han Chinese family.
- Published in:
- Muscle & Nerve, 2010, v. 42, n. 6, p. 922, doi. 10.1002/mus.21790
- By:
- Publication type:
- Article
Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in <bold>NEFH</bold> in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in <bold>NEFH</bold> for Charcot-Marie-Tooth 2.
- Published in:
- Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 74, doi. 10.1159/000487754
- By:
- Publication type:
- Article
Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 9, p. 1105, doi. 10.1038/ejhg.2014.7
- By:
- Publication type:
- Article
CUL4B Promotes Temozolomide Resistance in Gliomas by Epigenetically Repressing CDNK1A Transcription.
- Published in:
- Frontiers in Oncology, 2021, v. 11, p. N.PAG, doi. 10.3389/fonc.2021.638802
- By:
- Publication type:
- Article
ETS1 variants confer susceptibility to ankylosing spondylitis in Han Chinese.
- Published in:
- Arthritis Research & Therapy, 2014, v. 16, n. 2, p. 1, doi. 10.1186/ar4530
- By:
- Publication type:
- Article
Serum withdrawal up-regulates human SIRT1 gene expression in a p53-dependent manner.
- Published in:
- Journal of Cellular & Molecular Medicine, 2009, v. 13, n. 10, p. 4176, doi. 10.1111/j.1582-4934.2008.00468.x
- By:
- Publication type:
- Article
Sp1 and KLF15 regulate basal transcription of thehuman LRP5 gene.
- Published in:
- BMC Genetics, 2010, v. 11, p. 12, doi. 10.1186/1471-2156-11-12
- By:
- Publication type:
- Article
Signal transducer and activator of transcription 6 directly regulates human ORMDL3 expression.
- Published in:
- FEBS Journal, 2013, v. 280, n. 9, p. 2014, doi. 10.1111/febs.12225
- By:
- Publication type:
- Article
CUL4B facilitates HBV replication by promoting HBx stabilization.
- Published in:
- Cancer Biology & Medicine, 2022, v. 19, n. 1, p. 120, doi. 10.20892/j.issn.2095-3941.2020.0468
- By:
- Publication type:
- Article
RECQL4 regulates DNA damage response and redox homeostasis in esophageal cancer.
- Published in:
- Cancer Biology & Medicine, 2021, v. 18, n. 1, p. 120, doi. 10.20892/j.issn.2095-3941.2020.0105
- By:
- Publication type:
- Article
Lack of CUL4B leads to increased abundance of GFAP-positive cells that is mediated by PTGDS in mouse brain.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 16, p. 4686, doi. 10.1093/hmg/ddv200
- By:
- Publication type:
- Article
Zebrafish cul4a, but not cul4b, modulates cardiac and forelimb development by upregulating tbx5a expression.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 3, p. 853, doi. 10.1093/hmg/ddu503
- By:
- Publication type:
- Article
HBV suppresses ZHX2 expression to promote proliferation of HCC through miR‐155 activation.
- Published in:
- International Journal of Cancer, 2018, v. 143, n. 12, p. 3120, doi. 10.1002/ijc.31595
- By:
- Publication type:
- Article
Exposure to blue light stimulates the proangiogenic capability of exosomes derived from human umbilical cord mesenchymal stem cells.
- Published in:
- Stem Cell Research & Therapy, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13287-019-1472-x
- By:
- Publication type:
- Article
CUL4B mutations impair human cortical neurogenesis through PP2A-dependent inhibition of AKT and ERK.
- Published in:
- Cell Death & Disease, 2024, v. 15, n. 2, p. 1, doi. 10.1038/s41419-024-06501-3
- By:
- Publication type:
- Article
Anastasis enhances metastasis and chemoresistance of colorectal cancer cells through upregulating cIAP2/NFκB signaling.
- Published in:
- Cell Death & Disease, 2023, v. 14, n. 6, p. 1, doi. 10.1038/s41419-023-05916-8
- By:
- Publication type:
- Article
Cul4a promotes zebrafish primitive erythropoiesis via upregulating scl and gata1 expression.
- Published in:
- Cell Death & Disease, 2019, v. 10, n. 6, p. N.PAG, doi. 10.1038/s41419-019-1629-7
- By:
- Publication type:
- Article
Inhibition of DYRK1A-EGFR axis by p53-MDM2 cascade mediates the induction of cellular senescence.
- Published in:
- Cell Death & Disease, 2019, v. 10, n. 4, p. 1, doi. 10.1038/s41419-019-1521-5
- By:
- Publication type:
- Article
Berberine downregulates CDC6 and inhibits proliferation via targeting JAK-STAT3 signaling in keratinocytes.
- Published in:
- Cell Death & Disease, 2019, v. 10, n. 4, p. 1, doi. 10.1038/s41419-019-1510-8
- By:
- Publication type:
- Article
Human SNF2L Gene Is Regulated Constitutively and Inducibly in Neural Cells via a cAMP-Response Element.
- Published in:
- Yonsei Medical Journal, 2013, v. 54, n. 3, p. 772, doi. 10.3349/ymj.2013.54.3.772
- By:
- Publication type:
- Article
Novel deletion of SPAST in a Chinese family with hereditary spastic paraplegia.
- Published in:
- 2013
- By:
- Publication type:
- journal article
A novel homozygous C-terminal deletion in BTG4 causes zygotic cleavage failure and female infertility.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
Isoliensinine induces apoptosis in triple-negative human breast cancer cells through ROS generation and p38 MAPK/JNK activation.
- Published in:
- Scientific Reports, 2015, p. 12579, doi. 10.1038/srep12579
- By:
- Publication type:
- Article
MiR-135b-5p and MiR-499a-3p Promote Cell Proliferation and Migration in Atherosclerosis by Directly Targeting MEF2C.
- Published in:
- Scientific Reports, 2015, p. 12276, doi. 10.1038/srep12276
- By:
- Publication type:
- Article
A Functional Polymorphism in the TIM-1 Gene Is Associated with Asthma in a Chinese Han Population.
- Published in:
- International Archives of Allergy & Immunology, 2007, v. 144, n. 3, p. 197, doi. 10.1159/000103992
- By:
- Publication type:
- Article
Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia ( SPG42) caused by SLC33A1 mutation in a Chinese kindred.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 5, p. 485, doi. 10.1002/pd.2485
- By:
- Publication type:
- Article
Identification and Functional Analysis of a SLC33 A1: c.339 T> G (p. Ser113 Arg) Variant in the Original SPG42 Family.
- Published in:
- Human Mutation, 2015, v. 36, n. 2, p. 240, doi. 10.1002/humu.22732
- By:
- Publication type:
- Article
Whole-Exome Sequencing Identifies a Variant in TMEM132 E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99.
- Published in:
- Human Mutation, 2015, v. 36, n. 1, p. 98, doi. 10.1002/humu.22712
- By:
- Publication type:
- Article
Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis.
- Published in:
- Nature Genetics, 1999, v. 21, n. 3, p. 302, doi. 10.1038/6821
- By:
- Publication type:
- Article
Chemokine receptor CXCR2 is transactivated by p53 and induces p38-mediated cellular senescence in response to DNA damage.
- Published in:
- Aging Cell, 2013, v. 12, n. 6, p. 1110, doi. 10.1111/acel.12138
- By:
- Publication type:
- Article
Chemotherapy-induced executioner caspase activation increases breast cancer malignancy through epigenetic de-repression of CDH12.
- Published in:
- Oncogenesis, 2023, v. 12, n. 1, p. 1, doi. 10.1038/s41389-023-00479-x
- By:
- Publication type:
- Article