We are improving our search experience. To check which content you have full access to, or for advanced search, go back to the old search.

Search

Please fill in this field.

Search Results

Showing 1-20 of 350 results
  1. Suppression of the long non-coding RNA LINC01279 triggers autophagy and apoptosis in lung cancer by regulating FAK and SIN3A

    Long non-coding RNAs play critical roles in the development of lung cancer by functioning as tumor suppressors or oncogenes. Changes in the...

    Jiancong Wu, **aobi Huang, ... Wenmei Su in Discover Oncology
    Article Open access 02 January 2024
  2. Berberine chloride suppresses non-small cell lung cancer by deregulating Sin3A/TOP2B pathway in vitro and in vivo

    Purpose

    Berberine chloride (BBC) is a well-known plant isoquinoline alkaloid derived from Berberis aristata . In this study, we aim to explore the...

    Jian Chen, **aofei Huang, ... Zhengzhi Wu in Cancer Chemotherapy and Pharmacology
    Article 30 June 2020
  3. Skeletal muscle and intermuscular adipose tissue gene expression profiling identifies new biomarkers with prognostic significance for insulin resistance progression and intervention response

    Aims/hypothesis

    Although insulin resistance often leads to type 2 diabetes mellitus, its early stages are often unrecognised, thus reducing the...

    Dominik Lutter, Stephan Sachs, ... Susanna M. Hofmann in Diabetologia
    Article Open access 15 February 2023
  4. Sperm-borne microRNA-34c regulates maternal mRNA degradation and preimplantation embryonic development in mice

    Background

    Studies have shown that sperm-borne microRNAs (miRNAs) are involved in mammalian preimplantation embryonic development. In humans,...

    Long Cui, Li Fang, ... Yinghui Ye in Reproductive Biology and Endocrinology
    Article Open access 26 April 2023
  5. Prenatal Diagnosis for a Novel Missense Mutation in X-Linked Intellectual Disability Gene Followed by Favorable Pregnancy Outcome

    Intellectual disability (ID) is still unexplained in 60% of cases and prenatal diagnosis is very challenging for this condition. A second gravida...

    Sangeeta Khatter, Ritika Bajaj, ... Umesh **dal in Journal of Fetal Medicine
    Article 01 July 2021
  6. Deciphering potential causative factors for undiagnosed Waardenburg syndrome through multi-data integration

    Background

    Waardenburg syndrome (WS) is a rare genetic disorder mainly characterized by hearing loss and pigmentary abnormalities. Currently, seven...

    Fengying Sun, Minmin **ao, ... Tieliu Shi in Orphanet Journal of Rare Diseases
    Article Open access 06 June 2024
  7. Abolished clustering of MeCP2T158M can be partially reverted with small molecules

    Rett syndrome (OMIM 312750) is a rare neurodevelopmental disorder caused by de novo mutations in the Methyl-CpG Binding Protein 2 (MeCP2) gene...

    Rodrigo Lata, Liesbeth Steegmans, ... Zeger Debyser in Translational Medicine Communications
    Article Open access 05 June 2024
  8. Functional genomics elucidates regulatory mechanisms of Parkinson’s disease-associated variants

    Background

    Genome-wide association studies (GWASs) have identified multiple risk loci for Parkinson’s disease (PD). However, identifying the...

    Rui Chen, Jiewei Liu, ... **ong-Jian Luo in BMC Medicine
    Article Open access 16 February 2022
  9. hsa-mir-(4328, 4422, 548z and -628-5p) in diabetic retinopathy: diagnosis, prediction and linking a new therapeutic target

    Aims

    Growing evidence suggests that microRNAs (miRNAs) are crucial in controlling how diabetic retinopathy (DR) develops. We intend to mine miRNAs...

    Weijun Liu, Zhanqing Luo, ... Weimin Yang in Acta Diabetologica
    Article 31 March 2023
  10. Alveolar Epithelial Type 2 Cell Dysfunction in Idiopathic Pulmonary Fibrosis

    Idiopathic pulmonary fibrosis (IPF) is a progressive and irreversible pulmonary interstitial disease that seriously affects the patient’s quality of...

    Weiwei Zhu, Chunting Tan, Jie Zhang in Lung
    Article 22 September 2022
  11. Retrospective evaluation of neonates with fatal congenital lung malformation: A single center 15-year forensic autopsy experience

    Congenital lung malformation (CLM) is a leading cause of infant mortality. Clinical methods for diagnosing CLM mainly rely on computed tomography,...

    Tingting Wang, Yishu Liu, ... Jifeng Cai in Forensic Science, Medicine and Pathology
    Article 20 June 2024
  12. Proteomic analysis implicates that postovulatory aging leads to aberrant gene expression, biosynthesis, RNA metabolism and cell cycle in mouse oocytes

    Background

    In mammals, oocytes display compromised quality after experiencing a process of postovulatory aging. However, the mechanisms underlying are...

    Chuanxin Zhang, Xueqi Dong, ... Keliang Wu in Journal of Ovarian Research
    Article Open access 14 October 2022
  13. A genetic profiling guideline to support diagnosis and clinical management of lymphomas

    The new lymphoma classifications (International Consensus Classification of Mature Lymphoid Neoplasms, and 5th World Health Organization...

    Margarita Sánchez-Beato, Miriam Méndez, ... Mariano Provencio in Clinical and Translational Oncology
    Article Open access 06 September 2023
  14. Genome-wide transcriptomics of the amygdala reveals similar oligodendrocyte-related responses to acute and chronic alcohol drinking in female mice

    Repeated excessive alcohol consumption is a risk factor for alcohol use disorder (AUD). Although AUD has been more common in men than women, women...

    Sharvari Narendra, Claudia Klengel, ... Junghyup Suh in Translational Psychiatry
    Article Open access 12 November 2022
  15. Circulating tumor cells clusters and their role in Breast cancer metastasis; a review of literature

    Breast cancer is a significant and deadly threat to women globally. Moreover, Breast cancer metastasis is a complicated process involving multiple...

    Zeinab S. Sayed, Mohamed G. Khattap, ... Mohamed H. Nafady in Discover Oncology
    Article Open access 01 April 2024
  16. Hypoxia-induced signaling in the cardiovascular system: pathogenesis and therapeutic targets

    Hypoxia, characterized by reduced oxygen concentration, is a significant stressor that affects the survival of aerobic species and plays a prominent...

    Yongchao Zhao, Weidong **ong, ... Junbo Ge in Signal Transduction and Targeted Therapy
    Article Open access 20 November 2023
  17. Prognostic and clinicopathological values of LINC00665 in cancers: a systematic review and China population-based meta-analysis

    Background

    Recent studies have uncovered that the aberrant expression of LINC00665 contributes to the malignant pathological process of various...

    Ze **, Ya-Jun Meng, ... Zhi-Fan **ong in Clinical and Experimental Medicine
    Article 11 October 2022
  18. Investigation of shared genetic features and related mechanisms between diabetes and tuberculosis

    Objective

    This study aimed to integrate bioinformatics technology to explore shared hub genes and related mechanisms between diabetes and tuberculosis...

    Lifei Huang, Zhihao Liu, ... Yahong Sun in International Urology and Nephrology
    Article 21 March 2024
  19. Zinc finger myeloid Nervy DEAF-1 type (ZMYND) domain containing proteins exert molecular interactions to implicate in carcinogenesis

    Morphogenesis and organogenesis in the low organisms have been found to be modulated by a number of proteins, and one of such factor, deformed...

    Longji Wu, **g Huang, ... **angning Zhang in Discover Oncology
    Article Open access 15 December 2022
  20. TET (Ten-eleven translocation) family proteins: structure, biological functions and applications

    Ten-eleven translocation (TET) family proteins (TETs), specifically, TET1, TET2 and TET3, can modify DNA by oxidizing 5-methylcytosine (5mC)...

    **nchao Zhang, Yue Zhang, ... Xu Wang in Signal Transduction and Targeted Therapy
    Article Open access 11 August 2023
Did you find what you were looking for? Share feedback.