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Understanding the mechanism of muscle gene expression is an important first step for improving skeletal muscle function. We hypothesized that shear stress would induce a gene expression profile similar to that observed after stretching. Here, we aimed to evaluate the effect of cyclic stretching on muscle gene expression. In this study, a previously established nonlinear viscoelastic biomechanical stretch apparatus (NLV) was used for stretching to minimize shear stress. Adult Wistar rats were either stretched for 1 or 3 h on day 1 of the training week and the trained and untrained legs were separated for subsequent analysis. Differentially expressed genes were identified using GeneChip technology. Of the genes upregulated by stretching (372), the majority were involved in cell differentiation and organization and ion transport. Of the genes downregulated by stretching (26), the majority were involved in the mitochondria. In addition, stretching altered the extracellular matrix and axon guidance. Finally, a few differentially expressed genes were involved in transcription and circadian rhythm. In conclusion, cyclic stretching significantly upregulates a large number of gene transcripts in skeletal muscle.The 2nd Quarter just started. By now, you’ve spent some time on the links and you’re adding a new content to your website, right? Well, today I’m going to give you some tips to boost your SEO.

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A case of metastatic malignant melanoma with lung, liver, brain, and skin involvement, including a subcutaneous nodule at the inferior aspect of the left temporal scalp, is reported. The lung metastases were extensive and required resection. Histologically the lung nodule was composed of the typical malignant melanoma. The metastases in the liver and other sites were found to be composed of the same malignant melanoma. The metastasis at the scalp was composed of spindle cells with immunoreactivity for S-100 protein. These cells had an identical histopathologic and immunohistochemical pattern to those in the primary scalp lesion. This is, to our knowledge, the first reported case of par

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A study conducted at the University of Hawaii shows that the big pills called Tamoxifen and Arimidex block the action of hormones like estrogen, progesterone and testosterone. That means they may pose a risk for breast cancer survivors.

The study is known as a “risk-benefit” analysis.

University of Hawaii scientists studied the effects of using Tamoxifen or Arimidex for five years. They found that the longer you use them, the greater the risk for a different, but serious, condition called abnormal bone growth.

“Tamoxifen is well-known as a breast cancer drug, but there is also growing awareness that it can have side effects that are relevant to bone health,” said Timothy Peters, lead author of the study and a researcher in the Graduate Program in Toxicology at the UH Mānoa College of Pharmacy. “Our study reinforces this and suggests that, in some circumstances, it may be a good thing to use tamoxifen for a longer period of time, so there is enough time to monitor these side effects.”

Peters warns that estrogen and testosterone levels may be higher for people who take both Tamoxifen and Arimidex.

“This is a very important work. It is important because they are both often used for breast cancer treatment and it’s important for women to know that these drugs may have some extra effects,” said Dr. Maria S. Belfort-Rodriguez, professor of the College of Medicine and leader of the UH Mānoa Molecular Oncology Research Program at the UH Cancer Research Center. “We are still in the beginning phases of this work, and we’d love to have more funding in order to do some long-term research.”

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