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pmx retroviral vectors c-myc  (Addgene inc)


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    Addgene inc pmx retroviral vectors c-myc
    A summary of all established human pluripotent stem cell lines for Marfan syndrome that are described in peer-reviewed articles, or deposited in online stem cell registries, being NIH stem cell registry and hPSC registry. For each line, the pathogenic variant and patient information is summarized, if available. Also, original cell source, cell types obtained by directed differentiations for disease model, method of reprogramming, availability of isogenic (ISO) control, the generator of the line and the year of publication or deposition. Abbreviations: NA (not available), United States (United States of America).
    Pmx Retroviral Vectors C Myc, supplied by Addgene inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pmx retroviral vectors c-myc/product/Addgene inc
    Average 90 stars, based on 1 article reviews
    pmx retroviral vectors c-myc - by Bioz Stars, 2026-02
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    1) Product Images from "Human stem cell models for Marfan syndrome: a brief overview of the rising star in disease modelling"

    Article Title: Human stem cell models for Marfan syndrome: a brief overview of the rising star in disease modelling

    Journal: Frontiers in Cell and Developmental Biology

    doi: 10.3389/fcell.2024.1498669

    A summary of all established human pluripotent stem cell lines for Marfan syndrome that are described in peer-reviewed articles, or deposited in online stem cell registries, being NIH stem cell registry and hPSC registry. For each line, the pathogenic variant and patient information is summarized, if available. Also, original cell source, cell types obtained by directed differentiations for disease model, method of reprogramming, availability of isogenic (ISO) control, the generator of the line and the year of publication or deposition. Abbreviations: NA (not available), United States (United States of America).
    Figure Legend Snippet: A summary of all established human pluripotent stem cell lines for Marfan syndrome that are described in peer-reviewed articles, or deposited in online stem cell registries, being NIH stem cell registry and hPSC registry. For each line, the pathogenic variant and patient information is summarized, if available. Also, original cell source, cell types obtained by directed differentiations for disease model, method of reprogramming, availability of isogenic (ISO) control, the generator of the line and the year of publication or deposition. Abbreviations: NA (not available), United States (United States of America).

    Techniques Used: Variant Assay, Control, Transduction, Retroviral, Expressing, Dissection, Plasmid Preparation, CRISPR, TALENs, Knock-Out, Virus, Functional Assay, shRNA, Biomarker Discovery

    Summary of in vitro cellular models for Marfan syndrome established with pluripotent stem cells to model various aspects of the disease, including aortopathy, skeletal phenotype and Marfan-related cardiomyopathy.
    Figure Legend Snippet: Summary of in vitro cellular models for Marfan syndrome established with pluripotent stem cells to model various aspects of the disease, including aortopathy, skeletal phenotype and Marfan-related cardiomyopathy.

    Techniques Used: In Vitro, Variant Assay, Knock-Out, Expressing, Over Expression, Activation Assay, Control, Phospho-proteomics



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    A summary of all established human pluripotent stem cell lines for Marfan syndrome that are described in peer-reviewed articles, or deposited in online stem cell registries, being NIH stem cell registry and hPSC registry. For each line, the pathogenic variant and patient information is summarized, if available. Also, original cell source, cell types obtained by directed differentiations for disease model, method of reprogramming, availability of isogenic (ISO) control, the generator of the line and the year of publication or deposition. Abbreviations: NA (not available), United States (United States of America).

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Human stem cell models for Marfan syndrome: a brief overview of the rising star in disease modelling

    doi: 10.3389/fcell.2024.1498669

    Figure Lengend Snippet: A summary of all established human pluripotent stem cell lines for Marfan syndrome that are described in peer-reviewed articles, or deposited in online stem cell registries, being NIH stem cell registry and hPSC registry. For each line, the pathogenic variant and patient information is summarized, if available. Also, original cell source, cell types obtained by directed differentiations for disease model, method of reprogramming, availability of isogenic (ISO) control, the generator of the line and the year of publication or deposition. Abbreviations: NA (not available), United States (United States of America).

    Article Snippet: MFSiPS cell line (proband FB1592) , Frameshift variant c.1642del3ins20bp , Severe reduction in FBN1 expression , Fibroblast , Osteogenic and chondrogenic fates , pMX retroviral vectors SOX2 , OCT4 , KLF4 , and c- MYC (Addgene) , No , Stanford University (United States) , 2012 , .

    Techniques: Variant Assay, Control, Transduction, Retroviral, Expressing, Dissection, Plasmid Preparation, CRISPR, TALENs, Knock-Out, Virus, Functional Assay, shRNA, Biomarker Discovery

    Summary of in vitro cellular models for Marfan syndrome established with pluripotent stem cells to model various aspects of the disease, including aortopathy, skeletal phenotype and Marfan-related cardiomyopathy.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Human stem cell models for Marfan syndrome: a brief overview of the rising star in disease modelling

    doi: 10.3389/fcell.2024.1498669

    Figure Lengend Snippet: Summary of in vitro cellular models for Marfan syndrome established with pluripotent stem cells to model various aspects of the disease, including aortopathy, skeletal phenotype and Marfan-related cardiomyopathy.

    Article Snippet: MFSiPS cell line (proband FB1592) , Frameshift variant c.1642del3ins20bp , Severe reduction in FBN1 expression , Fibroblast , Osteogenic and chondrogenic fates , pMX retroviral vectors SOX2 , OCT4 , KLF4 , and c- MYC (Addgene) , No , Stanford University (United States) , 2012 , .

    Techniques: In Vitro, Variant Assay, Knock-Out, Expressing, Over Expression, Activation Assay, Control, Phospho-proteomics