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Introduction: According to the World Health Organization, 44 million people worldwide suffer from Alzheimer's disease. Abnormal movements are atypical symptoms of Alzheimer's disease.

Case Description: An 87-year-old woman, followed for Alzheimer's disease, experienced abnormal movements.

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Introduction: Lymphedema, a debilitating characterized by localized fluid retention and tissue swelling, results from abnormalities in the lymphatic system. In the case of primary lymphedema, this condition is attributed to malformations in lymphatic vessels or nodes, and it is marked by a relentless progression leading to irreversible tissue fibrosis after repetitive inflammation. Many questions regarding its treatment, such as the choice of the type of intervention and the timing, still remain unanswered.

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Background: Genetically modified mouse models have provided a vital understanding of the Alzheimer's disease (AD) mechanisms, but these models were generally focused on familial AD and do not recapitulate the late-onset human AD pathophysiology. To circumvent the complications of existing AD mice models, we are investigating a novel non-mutant humanized amyloid beta (Aβ) expressing mouse line that expresses the humanized mouse App gene within the Aβ peptide sequence METHOD: This study aims to investigate the learning and memory function in this novel human Aβ knock-in (h-Aβ KI) mice of different age and sex groups using behavioral tests, neuronal circuitry, and long-term potentiation experiments.

Result: Behavioral studies revealed age and sex specific phenotype: 12 and 18 months old female h-Aβ KI mice demonstrated reduced locomotor and exploration activities along with pronounced deficits in the preference for social novelty.

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Background: Apolipoprotein E4 (apoE4) has been identified as the major genetic risk factor for late onset Alzheimer's disease (AD). Our lab has demonstrated that chronic administration of Aβ12-28P, a synthetic peptide that blocks apoE4/Aβ binding, in middle-aged transgenic AD mice significantly ameliorates pathology progression, resulting in reduced Aβ plaques deposition and cerebral amyloid angiopathy (CAA) along with improved memory and cognition. However, whether blocking apoE4/Aβ interaction by Aβ12-28P also has an ameliorating effect on the neuronal and cognitive function of old AD mice where Aβ pathology has been extensively developed remains unknown.

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Single-cell analysis unveils cell subtypes of acral melanoma cells at the early and late differentiation stages.

J Cancer

January 2025

Department of Plastic and Reconstructive Surgery, Shanghai 9th People's Hospital, School of Medicine, Shanghai Jiao Tong University, 639 Zhi Zao Ju Rd, Shanghai, 200011, China.

Background: Melanoma, a malignant neoplasm originating from melanocytes, is a form of skin cancer with rapidly increasing global incidence, often exacerbated by UV radiation[1]. Particularly, acral melanoma, characterized by its swift metastasis and poor prognosis, underscores the significance of further research into its heterogeneity. Single-cell sequencing has been widely utilized in the study of tumor heterogeneity; however, research related to melanoma remains to be further refined.

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