Relevant bibliographies by topics / C-trimer (CT)

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  2. Dissertations / Theses

Academic literature on the topic 'C-trimer (CT)'

Author: Grafiati
Published: 11 March 2023
Last updated: 31 July 2025

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Journal articles on the topic "C-trimer (CT)"

1

Summer, Dominik, Christine Rangger, Maximilian Klingler, et al. "Exploiting the Concept of Multivalency with 68Ga- and 89Zr-Labelled Fusarinine C-Minigastrin Bioconjugates for Targeting CCK2R Expression." Contrast Media & Molecular Imaging 2018 (2018): 1–12. http://dx.doi.org/10.1155/2018/3171794.

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Cholecystokinin-2 receptors (CCK2R) are overexpressed in a variety of malignant diseases and therefore have gained certain attention for peptide receptor radionuclide imaging. Among extensive approaches to improve pharmacokinetics and metabolic stability of minigastrin (MG) based radioligands, the concept of multivalency for enhanced tumour targeting has not been investigated extensively. We therefore utilized fusarinine C (FSC) as chelating scaffold for novel mono-, di-, and trimeric bioconjugates for targeting CCK2R expression. FSC-based imaging probes were radiolabelled with positron emitti
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2

Jarret, R. L., L. C. Merrick, T. Holms, J. Evans, and M. K. Aradhya. "Simple sequence repeats in watermelon (Citrullus lanatus (Thunb.) Matsum. &Nakai)." Genome 40, no. 4 (1997): 433–41. http://dx.doi.org/10.1139/g97-058.

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Simple sequence repeat length polymorphisms were utilized to examine genetic relatedness among accessions of watermelon (Citrullus lanatus (Thunb.) Matsum. &Nakai). A size-fractionated TaqI genomic library was screened for the occurrence of dimer and trimer simple sequence repeats (SSRs). A total of 96 (0.53%) SSR-bearing clones were identified and the inserts from 50 of these were sequenced. The dinucleotide repeats (CT)n and (GA)n accounted for 82% of the SSRs sequenced. PCR primer pairs flanking seven SSR loci were used to amplify SSRs from 32 morphologically variable watermelon genotyp
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3

Denomme, G. A. "An Adenine Trimer Precedes a C/G Polymorphism in the 3′-Amplimer Region of the Human Platelet Glycoprotein IIIa Intron 6 CT Repeat." Human Heredity 48, no. 2 (1998): 115–18. http://dx.doi.org/10.1159/000022790.

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4

Yartsev, V. M. "Complex conductivity of trimerized quasi-one-dimensional CT crystals: Arbitrary trimer." Synthetic Metals 35, no. 1-2 (1990): 29–38. http://dx.doi.org/10.1016/0379-6779(90)90021-c.

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5

Chan, Yee-Peng, Min Lu, Somnath Dutta, et al. "Biochemical, Conformational, and Immunogenic Analysis of Soluble Trimeric Forms of Henipavirus Fusion Glycoproteins." Journal of Virology 86, no. 21 (2012): 11457–71. https://doi.org/10.5281/zenodo.13477310.

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(Uploaded by Plazi for the Bat Literature Project) ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxoviruses discovered in the mid- to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect cells by a pH-independent membrane fusion mechanism facilitated by their attachment (G) and fusion (F) glycoproteins. Here, several soluble forms of henipavirus F (sF) were engineered and characterized. Recombinant sF was produced by deleting the transmembrane (TM) and cytoplasmic tail
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6

Chan, Yee-Peng, Min Lu, Somnath Dutta, et al. "Biochemical, Conformational, and Immunogenic Analysis of Soluble Trimeric Forms of Henipavirus Fusion Glycoproteins." Journal of Virology 86, no. 21 (2012): 11457–71. https://doi.org/10.5281/zenodo.13477310.

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(Uploaded by Plazi for the Bat Literature Project) ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxoviruses discovered in the mid- to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect cells by a pH-independent membrane fusion mechanism facilitated by their attachment (G) and fusion (F) glycoproteins. Here, several soluble forms of henipavirus F (sF) were engineered and characterized. Recombinant sF was produced by deleting the transmembrane (TM) and cytoplasmic tail
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7

Chan, Yee-Peng, Min Lu, Somnath Dutta, et al. "Biochemical, Conformational, and Immunogenic Analysis of Soluble Trimeric Forms of Henipavirus Fusion Glycoproteins." Journal of Virology 86, no. 21 (2012): 11457–71. https://doi.org/10.5281/zenodo.13477310.

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Abstract:
(Uploaded by Plazi for the Bat Literature Project) ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxoviruses discovered in the mid- to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect cells by a pH-independent membrane fusion mechanism facilitated by their attachment (G) and fusion (F) glycoproteins. Here, several soluble forms of henipavirus F (sF) were engineered and characterized. Recombinant sF was produced by deleting the transmembrane (TM) and cytoplasmic tail
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8

Chan, Yee-Peng, Min Lu, Somnath Dutta, et al. "Biochemical, Conformational, and Immunogenic Analysis of Soluble Trimeric Forms of Henipavirus Fusion Glycoproteins." Journal of Virology 86, no. 21 (2012): 11457–71. https://doi.org/10.5281/zenodo.13477310.

Full text
Abstract:
(Uploaded by Plazi for the Bat Literature Project) ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxoviruses discovered in the mid- to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect cells by a pH-independent membrane fusion mechanism facilitated by their attachment (G) and fusion (F) glycoproteins. Here, several soluble forms of henipavirus F (sF) were engineered and characterized. Recombinant sF was produced by deleting the transmembrane (TM) and cytoplasmic tail
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9

Chan, Yee-Peng, Min Lu, Somnath Dutta, et al. "Biochemical, Conformational, and Immunogenic Analysis of Soluble Trimeric Forms of Henipavirus Fusion Glycoproteins." Journal of Virology 86, no. 21 (2012): 11457–71. https://doi.org/10.5281/zenodo.13477310.

Full text
Abstract:
(Uploaded by Plazi for the Bat Literature Project) ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxoviruses discovered in the mid- to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect cells by a pH-independent membrane fusion mechanism facilitated by their attachment (G) and fusion (F) glycoproteins. Here, several soluble forms of henipavirus F (sF) were engineered and characterized. Recombinant sF was produced by deleting the transmembrane (TM) and cytoplasmic tail
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10

Ma, Gary S., Nicolas Aznar, Nicholas Kalogriopoulos, et al. "Therapeutic effects of cell-permeant peptides that activate G proteins downstream of growth factors." Proceedings of the National Academy of Sciences 112, no. 20 (2015): E2602—E2610. http://dx.doi.org/10.1073/pnas.1505543112.

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In eukaryotes, receptor tyrosine kinases (RTKs) and trimeric G proteins are two major signaling hubs. Signal transduction via trimeric G proteins has long been believed to be triggered exclusively by G protein-coupled receptors (GPCRs). This paradigm has recently been challenged by several studies on a multimodular signal transducer, Gα-Interacting Vesicle associated protein (GIV/Girdin). We recently demonstrated that GIV’s C terminus (CT) serves as a platform for dynamic association of ligand-activated RTKs with Gαi, and for noncanonical transactivation of G proteins. However, exogenous manip
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Dissertations / Theses on the topic "C-trimer (CT)"

1

VOTTARIELLO, FRANCESCA. "OLIGOMERIZATION OF RNase A:a) A STUDY OF THE INFLUENCE OF SERINE 80 RESIDUE ON THE 3D DOMAIN SWAPPING MECHANISMb) “ZERO-LENGTH” DIMERS OF RNase A AND THEIR CATIONIZATION WITH PEI." Doctoral thesis, 2010. http://hdl.handle.net/11562/344075.

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"Zero-length" dimers of ribonuclease A, a novel type of dimers formed by two RNase A molecules bound to each other through a zero-length amide bond [Simons, B.L. et al. (2007) Proteins 66, 183-195], were analyzed, and tested for their possible in vitro cytotoxic activity. Results: (i) Besides dimers, also trimers and higher oligomers can be identified among the products of the covalently linking reaction. (ii) The "zero-length" dimers prepared by us appear not to be a unique species, as was instead reported by Simons et al. The product is heterogeneous, as shown by the involvement in the amide
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