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Geometrically Controlled WNT Activation Drives Intestinal Morphogenesis
Crypt‐villi‐like morphogenesis can be driven and controlled via architectural patterns in colorectal cells with the use of digital light processing printing. The resulting mini tissues exhibit budding structures and functionality, as evidenced by increased mucin expression.
Nathaniel C. Burmas+3 more
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A modular and customizable RNAi therapeutics delivery platform composed of a pseudosymmetric human RNA binding protein‐siRNA complex (SmiRNP) is developed. By fusing a targeting module and an endosomal escape peptide onto the delivery platform, SmiRNP successfully delivered siRNA to silence the KRAS oncogene in a colorectal carcinoma cell line, leading
Nok Yin Tam+9 more
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Redox Biology and Insulin-like Growth Factor-Binding Protein-6: A Potential Relationship. [PDF]
Coda ARD, Liso A, Bellanti F.
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Molecular Biology of ACL Graft Healing: Early Mechanical Loading Perspective. [PDF]
Kacprzak B.
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The Role of Fibroblasts in Melanoma Development: From Tumor Microenvironment Remodeling to Pre-Metastatic Niche Formation. [PDF]
Belviso I+7 more
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Feasibility analysis of Sinomenine alleviating fibrosis of filtering bleb after glaucoma filtering surgery: a mini review. [PDF]
Xun X, Liu X, Zhou P, Wu C, Peng Q.
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Activation of the fibroblast growth factor receptor 3 in bladder cancer
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Fibroblast growth factor receptor-3 in urothelial tumorigenesis
Urologic Oncology: Seminars and Original Investigations, 2013Fibroblast growth factor receptor-3 (FGFR3) is a receptor tyrosine kinase implicated in the tumorigenesis of multiple malignancies, including bladder and other urothelial cancers, multiple myeloma, and cervical cancer. In urothelial carcinoma (UC), constitutive receptor activation occurs most commonly through substitution of a wild-type residue with ...
Matthew I. Milowsky+2 more
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Mutations of the Fibroblast Growth Factor Receptor-3 Gene in Achondroplasia
Hormone Research, 1996Achondroplasia (ACH), the most common cause of chondrodysplasia in man (1 in 15,000 live births), is an autosomal dominant condition of unknown origin characterized by short-limbed dwarfism and macrocephaly. Recently, a gene for ACH has been mapped to chromosome 4p16.3.
J. Bonaventure+7 more
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