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  1. Systemic interindividual DNA methylation variants in cattle share major hallmarks with those in humans

    Background

    We recently identified ~ 10,000 correlated regions of systemic interindividual epigenetic variation (CoRSIVs) in the human genome. These...

    Wen-Jou Chang, Maria S. Baker, ... Robert A. Waterland in Genome Biology
    Article Open access 15 July 2024
  2. YAP/TAZ interacts with RBM39 to confer resistance against indisulam

    The Hippo pathway and its downstream effectors, Yes-associated protein/transcriptional coactivator with PDZ-binding motif (YAP/TAZ), are essential...

    Toshinori Ando, Kento Okamoto, ... Mikihito Kajiya in Oncogenesis
    Article Open access 15 July 2024
  3. PIM1/NF-κB/CCL2 blockade enhances anti-PD-1 therapy response by modulating macrophage infiltration and polarization in tumor microenvironment of NSCLC

    Elevated infiltration of tumor-associated macrophages (TAMs) drives tumor progression and correlates with poor prognosis for various tumor types. Our...

    **uqiong Chen, **g Zhou, ... Richeng Jiang in Oncogene
    Article 14 July 2024
  4. Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies

    Background

    Childhood epilepsies are caused by heterogeneous underlying disorders where approximately 40% of the origins of epilepsy can be attributed...

    Marina Andjelkovic, Kristel Klaassen, ... Maja Stojiljkovic in Molecular Diagnosis & Therapy
    Article Open access 14 July 2024
  5. Heterotopic ovarian transplantation instead hormonal replacement therapy after radical hysterectomy for cervical cancer: case report and review of literature

    Purpose

    Only a few case reports have described heterotopic ovarian tissue transplantation (OTT) with the only objective of restoring ovarian function.

    ...
    Blandine Courbiere, Laura Miquel, ... Catherine Metzler-Guillemain in Journal of Assisted Reproduction and Genetics
    Article 14 July 2024
  6. Computational Insights into Papaveroline as an In Silico Drug Candidate for Alzheimer’s Disease via Fyn Tyrosine Kinase Inhibition

    Alzheimer’s disease (AD) poses a significant global health challenge, necessitating the exploration of novel therapeutic strategies. Fyn Tyrosine...

    Shreya Satyanarayan Bhat, Spoorthi R. Kulkarni, ... Vidya Niranjan in Molecular Biotechnology
    Article 14 July 2024
  7. Psychological and ethical issues raised by genomic in paediatric care pathway, a qualitative analysis with parents and childhood cancer patients

    In paediatric oncology, genomics raises new ethical, legal and psychological issues, as somatic and constitutional situations intersect throughout...

    Marion Droin-Mollard, Sandrine de Montgolfier, ... Khadija Lahlou-Laforêt in European Journal of Human Genetics
    Article Open access 13 July 2024
  8. Effect of α7 nAChR-autophagy axis of deciduous tooth pulp stem cells in regulating IL-1β in the process of physiological root resorption of deciduous teeth

    Abstract

    Physiological root resorption of deciduous teeth is a normal phenomenon occurring during the developmental stages of children. Previous...

    Tiankai Di, Yujiang Chen, ... Lulu Wang in Journal of Molecular Medicine
    Article 13 July 2024
  9. Antibody MYH9 and Antibiotic Lidamycin Inhibit the Growth and Proliferation of Lung Cancer Cells and Induce Their Apoptosis

    The aim of this study was to investigate the impact of the antibiotic lidamycin (LDM) and the targeted therapy with the antibody Myosin heavy chain 9...

    Jie Jiang, Ruoyu Hu, ... Wei He in Molecular Biotechnology
    Article 13 July 2024
  10. Total gonadotropin dose did not affect euploid blastocyst rates: an analysis of more than 19,000 oocytes

    Background

    To evaluate whether increasing total gonadotropin (Gn) dose is associated with changes in euploid blastocyst rate in preimplantation...

    Jun Shuai, Weiwei Liu, ... Hong Ye in Journal of Assisted Reproduction and Genetics
    Article 13 July 2024
  11. Susceptibility gene mutations in germline and tumors of patients with HER2-negative advanced breast cancer

    Germline mutations in BRCA1 and BRCA2 (g BRCA1/2 ) are required for a PARP inhibitor therapy in patients with HER2-negative (HER2−) advanced breast...

    Peter A. Fasching, Chunling Hu, ... Fergus J. Couch in npj Breast Cancer
    Article Open access 13 July 2024
  12. First Insight into the Phylogenetic Diversity of Bovicola caprae Infesting Goats of Different Agro-climatic Locations in India

    Bovicola caprae is an important obligate ectoparasite of goats worldwide including India. The present study aimed at the molecular confirmation,...

    Aman D. Moudgil, Anil K. Nehra, ... Sukhdeep Vohra in Biochemical Genetics
    Article 13 July 2024
  13. Comprehensive Quality Analysis of Conventional and Novel Biomarkers in Diagnosing and Predicting Prognosis of Coronary Artery Disease, Acute Coronary Syndrome, and Heart Failure, a Comprehensive Literature Review

    Coronary artery disease (CAD), acute coronary syndrome (ACS), and heart failure (HF) are major global health issues with high morbidity and mortality...

    Muhammad Abubakar, Umema Irfan, ... Farea Ahmed in Journal of Cardiovascular Translational Research
    Article 12 July 2024
  14. Protective defunctioning stoma in bowel segmental resection at the time of total hysterectomy for endometriosis: when less is more

    Purpose

    To compare postoperative complications in women undergoing total hysterectomy with segmental resection (TH-SR) for intestinal endometriosis...

    Carolina Dolci, Yohan Kerbage, ... Chrystèle Rubod in Archives of Gynecology and Obstetrics
    Article Open access 12 July 2024
  15. Gut Microbiota in Primary Osteoporosis: a Systematic Review

    The link between gut microbiota (GM) and primary osteoporosis has garnered substantial attention. In this study, we conducted a systematic review...

    Jiangxun Ji, Feihong Cai, ... Yongjun Wang in Phenomics
    Article Open access 12 July 2024
  16. Fragile X Syndrome and FMR1 premutation: results from a survey on associated conditions and treatment priorities in Italy

    Background and objectives

    Fragile X Syndrome (FXS) is the most common cause of inherited intellectual disability, caused by CGG-repeat expansions...

    Federica Alice Maria Montanaro, Paolo Alfieri, ... Stefano Vicari in Orphanet Journal of Rare Diseases
    Article Open access 12 July 2024
  17. Mesomelia-synostoses syndrome: contiguous deletion syndrome, SULF1 haploinsufficiency or enhancer adoption?

    Background

    Mesomelia-Synostoses Syndrome (MSS)(OMIM 600,383) is a rare autosomal dominant disorder characterized by mesomelic limb shortening, acral...

    Ingrid Bendas Feres Lima, Lúcia de Fátima Marques de Moraes, ... Elenice Ferreira Bastos in Molecular Cytogenetics
    Article Open access 12 July 2024
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