Search Results - "Wu, Baoping"
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High risk and early onset of cancer in Chinese patients with Peutz-Jeghers syndrome
Published in Frontiers in oncology (03-08-2022)“…Peutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disorder associated with a predisposition to a variety of cancers. Previous studies that have…”
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Numerical Analysis of Novel Air-Based Li-Ion Battery Thermal Management
Published in Batteries (Basel) (01-09-2022)“…The lithium-ion battery is considered the primary power supply source for electric vehicles due to its high-energy density, long lifespan, and no memory…”
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Prenatal diagnosis in a hereditary Peutz-Jeghers syndrome family with high cancer risk
Published in BMC medical genetics (02-05-2018)“…Peutz-Jeghers Syndrome (PJS) is a hereditary cancer predisposing syndrome caused by autosomal dominant mutations in the serine/threonine kinase 11 (STK11) gene…”
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Longitudinal parallel compression suture to control postopartum hemorrhage due to placenta previa and accrete
Published in Taiwanese journal of obstetrics & gynecology (01-04-2016)“…Abstract Objective To assess the efficacy and safety of longitudinal parallel compression suture to control heavy postpartum hemorrhage (PPH) in patients with…”
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Aberrant expression of Sonic hedgehog signaling in Peutz-Jeghers syndrome
Published in Human pathology (01-04-2016)“…Summary The SHH signaling pathway is critical for gastrointestinal development and organic patterning, and dysregulation of SHH pathway molecules has been…”
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Reflections on the Concept of "Law" of Shang Yang from the Perspective of Political Philosophy: Function, Value, and Spirit of the "Rule of Law"
Published in Contemporary Chinese thought (02-04-2016)“…This article argues that Shang Yang's philosophy of law was not only a means to enrich the state and strengthen its army, but also envisioned the orderly rule…”
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Development and external validation of a novel nomogram for screening Chinese Lynch syndrome: based on a multicenter, population study
Published in Therapeutic advances in medical oncology (2021)“…Background: This multicenter study aimed to reveal the genetic spectrum of colorectal cancer (CRC) with deficient mismatch repair (dMMR) and build a screening…”
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Adipose-Derived Stem Cells Promote Bone Coupling in Bisphosphonate-Related Osteonecrosis of the Jaw by TGF-β1
Published in Frontiers in cell and developmental biology (12-05-2021)“…This study aimed to investigate molecularly targeted therapy to revive bone remodeling and prevent BRONJ by local adipose-derived stem cells (ADSCs)…”
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A novel mutation in STK11 gene is associated with Peutz-Jeghers syndrome in Chinese patients
Published in BMC genetics (14-12-2011)“…Peutz-Jeghers syndrome (PJS) is caused by mutations in the tumor suppressor gene, STK11, and is characterized by gastrointestinal hamartomas, melanin spots on…”
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A rare case of hematemesis
Published in Gastrointestinal endoscopy (01-11-2023)Get full text
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Changes in the Gut Microbiome Associated with Intussusception in Patients with Peutz-Jeghers Syndrome
Published in Microbiology spectrum (31-01-2023)“…Peutz-Jeghers syndrome (PJS) is a rare hereditary disorder characterized by intestinal polyposis, and intestinal intussusception is one of the most urgent…”
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Long-Term Ozone Exposure and Small Airway Dysfunction: The China Pulmonary Health (CPH) Study
Published in American journal of respiratory and critical care medicine (15-02-2022)“…It remains unknown whether long-term ozone exposure can impair lung function. To investigate the associations between long-term ozone exposure and adult lung…”
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Synthesis, characterization and catalytic application of mesoporous molecular sieves SBA-15 functionalized with phosphoric acid
Published in Journal of porous materials (01-10-2012)“…The phosphoric acid groups has been successfully grafted on the surface of mesoporous molecular sieve SBA-15 to form a solid acid catalyst P-SBA-15 by…”
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The prevalence of germline mutations in Chinese colorectal cancer patients with mismatch repair deficiency
Published in Journal of clinical oncology (20-05-2018)“…Abstract only…”
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STK11 Domain XI Mutations: Candidate Genetic Drivers Leading to the Development of Dysplastic Polyps in Peutz-Jeghers Syndrome
Published in Human mutation (01-07-2014)“…ABSTRACT Peutz–Jeghers syndrome (PJS) is a rare hereditary disorder resulting from mutations in serine/threonine kinase 11 (STK11) and characterized by…”
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Two novel STK11 missense mutations induce phosphorylation of S6K and promote cell proliferation in Peutz-Jeghers syndrome
Published in Oncology letters (01-01-2018)“…Peutz-Jeghers syndrome (PJS) is a rare hereditary disease caused by mutations in serine threonine kinase 11 ( ) and characterized by an increased risk of…”
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Wnt signaling may be activated in a subset of Peutz-Jeghers syndrome polyps closely correlating to LKB1 expression
Published in Oncology reports (01-06-2010)“…The premalignant potential of Peutz-Jeghers syndrome (PJS) hamartomas has not been established. The major gene responsible for PJS is LKB1. LKB1 has a complex…”
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Wnt signaling may be activated in a subset of Peutz-Jeghers syndrome polyps closely correlating to LKB 1 expression
Published in Oncology reports (2010)Get full text
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Exploration technology of integrated air leakage channel of shallow buried coal seam in northern Shaanxi Province
Published in Mei kuang an quan (01-04-2023)“…Taking the fire-threatened mines in the shallow buried coal seam of the Jurassic coalfield in northern Shaanxi Province as the research object, the…”
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