Long J

ORCID: 0000-0002-6889-6195 · 19 papers in corpus
observational 2026
BMC psychology ·doi:10.1186/s40359-026-04235-9

BACKGROUND: Patients undergoing assisted reproductive technology (ART) frequently manifest sleep disturbances and psychological morbidity. This study examined associations between cerebral activation patterns, sleep quality, and psychologic…

lab-animal 2026
Bone research ·doi:10.1038/s41413-026-00573-x

Osteoarthritis (OA) is a widespread degenerative joint disorder manifesting as chronic pain, functional impairment, and progressive disability, imposing a substantial burden on global public health. Despite extensive research, the precise m…

observational 2026
Scientific reports ·doi:10.1038/s41598-026-46566-y

This study aimed to explore the association between leukocyte telomere length (LTL) and premature rupture of membranes (PROM). This cross-sectional study included a total of 170,841 participants from the UK Biobank. Restricted cubic spline …

lab-animal 2026
Molecular immunology ·doi:10.1016/j.molimm.2026.05.008

BACKGROUND: Endometriosis is a chronic inflammatory disease characterized by immune microenvironment dysregulation, with the IL-33/ST2L signaling axis playing a crucial role in macrophage polarization and disease progression. Despite growin…

review 2024
Chinese medicine ·doi:10.1186/s13020-024-00969-z

All types of ginger have common fundamental components, although they possess distinct strengths and inclinations when it comes to effectiveness and medicinal applications. Fresh ginger possesses the ability to effectively stimulate movemen…

observational 2022
Frontiers in endocrinology ·doi:10.3389/fendo.2022.986567

OBJECTIVE: To evaluate HIF2α polymorphisms and glucose metabolism in a group of women with polycystic ovary syndrome (PCOS) or unexplained infertility (UI). PATIENTS: The infertile group (n=148) consisted of 96 women with PCOS, 52 women wi…

lab-animal 2022
Frontiers in physiology ·doi:10.3389/fphys.2022.1042449

Numerous studies have suggested the possibility of explaining the etiology of metabolic syndrome through DNA methylation. DNA methyltransferase 3B (DNMT3B) plays an important role in de novo DNA methylation. There was an alteration in mater…

observational 2022
International journal of general medicine ·doi:10.2147/ijgm.s340629

PURPOSE: miR-500a-3p has been extensively reported to be implicated in the development and progression in several human cancer types. This study aimed to investigate the diagnostic and prognostic significance of miR-500a-3p as a biomarker i…

diagnostic-accuracy 2022
Frontiers in oncology ·doi:10.3389/fonc.2022.949766

OBJECTIVE: This work was designed to investigate the performance of the International Ovarian Tumor Analysis (IOTA) ADNEX (Assessment of Different NEoplasias in the adneXa) model combined with human epithelial protein 4 (HE4) for early ovar…

other 2022
Frontiers in surgery ·doi:10.3389/fsurg.2022.814290

BACKGROUND: The purpose of this study was to report our experience in treating multiple ureteral polyps with transabdominal laparoscopic ureteroureterostomy (LAP-UU) with intraoperative retrograde ureteroscopy (RU)-assisted technique. METH…

qualitative 2021
British journal of pain ·doi:10.1177/2049463720961413

INTRODUCTION: Prior research into endometriosis-related pain has focused on specific aspects of the pain experience such as cyclical pain, emotional aspects of pain and certain types of pain such as dysmenorrhea and dyspareunia. However, re…

meta-analysis 2021
Human reproduction (Oxford, England) ·doi:10.1093/humrep/deab086

STUDY QUESTION: Does the expansion of genome-wide association studies (GWAS) to a broader range of ancestries improve the ability to identify and generalise variants associated with age at menarche (AAM) in European populations to a wider r…

case-report 2021
Annals of surgery open : perspectives of surgical history, education, and clinical approaches ·doi:10.1097/as9.0000000000000041

A minimally invasive approach to partial hepatectomy with transvaginal specimen extraction is safe and feasible with the potential to improve the cosmetic outcome, minimize postoperative narcotic utilization, and shorten hospital length of …

lab-animal 2017
Journal of experimental & clinical cancer research : CR ·doi:10.1186/s13046-017-0568-3

BACKGROUND: miR-500a-3p has been demonstrated to be involved in the development, progression and metastasis in several human cancers. Constitutive activation of JAK/STAT3 signaling pathway has been reported to play an important role in the …

other 2015
Human molecular genetics ·doi:10.1093/hmg/ddu552

Common variants in the hepatocyte nuclear factor 1 homeobox B (HNF1B) gene are associated with the risk of Type II diabetes and multiple cancers. Evidence to date indicates that cancer risk may be mediated via genetic or epigenetic effects …

lab-animal 2014
Oncology research ·doi:10.3727/096504015x14386062091352

Liver cancer is one of the most lethal cancers, but our knowledge of the molecular mechanism underlying this process remains insufficient. Through deep sequencing and expression regulation analysis in liver cancer cells, we identified two n…

lab-animal 2013
Experimental and therapeutic medicine ·doi:10.3892/etm.2013.1458

Endometriosis is a common disease in females of reproductive age and has the classic characteristic of mononuclear cell infiltration into lesions. Shikonin is an anti-inflammatory phytocompound obtained from Lithospermum erythrorhizon whose…

meta-analysis 2012
European journal of obstetrics, gynecology, and reproductive biology ·doi:10.1016/j.ejogrb.2012.05.008

The objective of our study is to assess the association of endometriosis risk and genetic polymorphisms involving biosynthesis of sex steroids and their receptors. A systematic search of three databases was conducted. Twenty-seven studies o…

review 2002
AACN clinical issues ·doi:10.1097/00044067-200211000-00008

The advent of the Human Genome Project has allowed for increased understanding and sophistication in diagnosis, treatment methods, and overall care planning on the part of healthcare providers for children with genetic disorders. Genetics r…