Publications by authors named "Luisa M Reyes-Cortes"

Article Synopsis
  • Biofabrication of living tissues with hollow channels is essential for creating thicker tissues, but traditional methods struggle with channels smaller than hundreds of micrometers.! -
  • The study introduces a new technique using co-extrusion of cell-laden hydrogels and sacrificial materials to produce thin filaments (1 mm in diameter) with tiny channels that improve cell growth and alignment.! -
  • Results show that these hollow channels enhance cell viability, promote muscle-specific markers, and lead to better tissue engineering outcomes, providing a promising method for developing pre-vascularized tissues.!
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Cancer continues to be a leading cause of mortality in modern societies; therefore, improved and more reliablecancer models are needed to expedite fundamental research and anti-cancer drug development. Here, we describe the use of a miniaturized continuous stirred tank reactor (mCSTR) to first fabricate and mature cancer spheroids (i.e.

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Background: The presence of clinically relevant mutations in KRAS and NRAS genes determines the response of anti-epidermal growth factor receptor antibody therapy for metastatic colorectal cancer (mCRC). The only quantitative polymerase chain reaction (qPCR)-based diagnostic tests approved by the Food and Drug Administration (FDA) screen merely for mutations in codons 12 and 13 of KRAS.

Objective: The objective of the study was to study the frequency of clinically relevant mutations in KRAS and NRAS genes that are not included in FDA-approved qPCR tests.

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The treatment of Type 2 Diabetes Mellitus (T2DM) consists primarily of oral antidiabetic drugs (OADs) that stimulate insulin secretion, such as sulfonylureas (SUs) and reduce hepatic glucose production (e.g., biguanides), among others.

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Background: Current metastatic colorectal cancer (mCRC) therapy uses monoclonal antibodies against the epidermal growth factor receptor. This treatment is only useful in the absence of K-RAS gene mutations; therefore the study of such mutations is part of a personalized treatment. The aim of this work is to determine the frequency and type of the most common K-RAS mutations in Mexican patients with metastatic disease by nucleotide sequencing.

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