Articles with "type mutant" as a keyword



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In vitro antioxidant, antibacterial, in vivo immunomodulatory, antitumor and hematological potential of exopolysaccharide produced by wild type and mutant Lactobacillus delbureckii subsp. bulgaricus

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Published in 2020 at "Heliyon"

DOI: 10.1016/j.heliyon.2020.e03268

Abstract: Biological evaluation of exopolysaccharides (EPS) produced by wild type and mutant Lactobacillus delbureckii (EPSWLD and EPSMLD) was investigated. Varying degrees of functional groups associated with polysaccharides were present thus confirming the EPS. The EPSs had… read more here.

Keywords: epsmld; mutant lactobacillus; produced wild; activity ... See more keywords
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Discovery of a Potent Dual Inhibitor of Wild-Type and Mutant Respiratory Syncytial Virus Fusion Proteins.

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Published in 2020 at "ACS medicinal chemistry letters"

DOI: 10.1021/acsmedchemlett.0c00008

Abstract: A novel series of macrocyclic pyrazolo[1,5-a]pyrimidine derivatives as respiratory syncytial virus (RSV) fusion glycoprotein (F protein) inhibitors were designed and synthesized based on docking studies of acyclic inhibitors. This effort resulted in the discovery of… read more here.

Keywords: respiratory syncytial; syncytial virus; mutant; type mutant ... See more keywords
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In vitro evidence consistent with an interaction between wild‐type and mutant SOD1 protein associated with canine degenerative myelopathy

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Published in 2019 at "European Journal of Neuroscience"

DOI: 10.1111/ejn.14526

Abstract: Canine degenerative myelopathy (DM) is a progressive neurological disorder that may be considered to be a large animal model for specific forms of the fatal human disease, familial amyotrophic lateral sclerosis (fALS). DM is associated… read more here.

Keywords: wild type; type mutant; interaction wild; sod1 ... See more keywords
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SAR439859, a Novel Selective Estrogen Receptor Degrader (SERD), Demonstrates Effective and Broad Antitumor Activity in Wild-Type and Mutant ER-Positive Breast Cancer Models

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Published in 2020 at "Molecular Cancer Therapeutics"

DOI: 10.1158/1535-7163.mct-20-0390

Abstract: Primary treatment for estrogen receptor-positive (ER+) breast cancer is endocrine therapy. However, substantial evidence indicates a continued role for ER signaling in tumor progression. Selective estrogen receptor degraders (SERD), such as fulvestrant, induce effective ER… read more here.

Keywords: type mutant; estrogen receptor; cancer; breast cancer ... See more keywords
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Cancer: From Wild-Type to Mutant Huntingtin

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Published in 2018 at "Journal of Huntington's Disease"

DOI: 10.3233/jhd-180290

Abstract: Huntingtin (HTT) is a scaffold protein mostly known because it gives rise to the severe and incurable inherited neurological disorder Huntington’s disease (HD) when mutated. The Huntingtin gene (HTT) carries a polymorphic trinucleotide expansion of… read more here.

Keywords: mutant htt; type mutant; htt; wild type ... See more keywords
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Opposing Roles of Wild-type and Mutant p53 in the Process of Epithelial to Mesenchymal Transition

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Published in 2022 at "Frontiers in Molecular Biosciences"

DOI: 10.3389/fmolb.2022.928399

Abstract: The central role of an aberrantly activated EMT program in defining the critical features of aggressive carcinomas is well documented and includes cell plasticity, metastatic dissemination, drug resistance, and cancer stem cell-like phenotypes. The p53… read more here.

Keywords: type mutant; mutant p53; p53; roles wild ... See more keywords
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The Osteogenesis Imperfecta Type V Mutant BRIL/IFITM5 Promotes Transcriptional Activation of MEF2, NFATc, and NR4A in Osteoblasts

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Published in 2022 at "International Journal of Molecular Sciences"

DOI: 10.3390/ijms23042148

Abstract: BRIL (bone restricted ifitm-like; also known as IFITM5) is a transmembrane protein expressed in osteoblasts. Although its role in skeletal development and homeostasis is unknown, mutations in BRIL result in rare dominant forms of osteogenesis… read more here.

Keywords: bril; type mutant; mef2 nfatc; osteogenesis imperfecta ... See more keywords
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Discovery of Novel EGFR Inhibitor Targeting Wild-Type and Mutant Forms of EGFR: In Silico and In Vitro Study

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Published in 2023 at "Molecules"

DOI: 10.3390/molecules28073014

Abstract: Targeting L858R/T790M and L858R/T790M/C797S mutant EGFR is a critical challenge in developing EGFR tyrosine kinase inhibitors to overcome drug resistance in non-small cell lung cancer (NSCLC). The discovery of next-generation EGFR tyrosine kinase inhibitors (TKIs)… read more here.

Keywords: type mutant; novel egfr; type; egfr inhibitor ... See more keywords