Publications by authors named "R Aurora"

Article Synopsis
  • Endovascular repair for abdominal aortic aneurysms (AAA) has been the preferred method since 1991, with new techniques like contralateral gate cannulation being developed to enhance the process.
  • A new device called the Taofan and Kang (T&K) bidirectional endovascular aortic repair (B-EVAR) was introduced, utilizing a unique approach to deploy stent grafts through both femoral arteries while ensuring safety and effectiveness.
  • In a pilot study involving six patients, the T&K B-EVAR showed promising results with no complications or prolonged hospital stays, indicating it simplifies the AAA repair process and could be beneficial for a wider range of patients.
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The human microbiota, a community of microorganisms in our bodies, is crucial for our health. This paper explores its development from birth through old age, highlighting some of the unique roles at key life stages-infancy, adulthood, and in the elderly years. Understanding the significant health impacts and consequences of changes in the microbiota offers insights for both the public and clinicians.

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Milk production during lactation places a high demand for calcium that is fulfilled both from maternal bone resorption and diet. While it is known that mammary gland-derived PTHrP drives bone resorption during lactation, the impact of postpartum estrogen loss on bone has been unclear. We used a case-control study design to test the effect of estrogen loss in lactating mice.

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Adult T cell leukaemia (ATL), caused by infection with human T- lymphotropic virus type 1 (HTLV-1), is often complicated by hypercalcemia and osteolytic lesions. Therefore, we studied the communication between patient-derived ATL cells (ATL-PDX) and HTLV-1 immortalized CD4+ T cell lines (HTLV/T) with osteoclasts and their effects on bone mass in mice. Intratibial inoculation of some HTLV/T leads to a profound local decrease in bone mass similar to marrow-replacing ATL-PDX, despite the fact that few HTLV/T cells persisted in the bone.

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Background: In breast cancer, ErbB receptors play a critical role, and overcoming drug resistance remains a major challenge in the clinic. However, intricate regulatory mechanisms of ErbB family genes are poorly understood. Here, we demonstrate SON as an ErbB-regulatory splicing factor and a novel therapeutic target for ErbB-positive breast cancer.

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