检索结果 - Ehsan, Mehroz

When signalling goes wrong: pathogenic variants in structural and signalling proteins causing cardiomyopathies 由 Ehsan, Mehroz, Jiang, He, L.Thomson, Kate, Gehmlich, Katja

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Urinary neutrophil gelatinase-associated lipocalin (NGAL) can potentially predict vascular complications and reliably risk stratify patients with peripheral arterial disease 由 Ehsan, Mehroz, Syed, Muzammil H., Zamzam, Abdelrahman, Jahanpour, Niousha, Singh, Krishna K., Abdin, Rawand, Qadura, Mohammad

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Pravastatin‐induced changes in expression of long non‐coding and coding RNAs in endothelial cells 由 Singh, Shweta, Nguyen, Hien C., Ehsan, Mehroz, Michels, David C. R., Singh, Priyanka, Qadura, Mohammad, Singh, Krishna K.

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BReast CAncer susceptibility gene 2 deficiency exacerbates oxidized LDL‐induced DNA damage and endothelial apoptosis 由 Singh, Shweta, Nguyen, Hien, Michels, David, Bazinet, Hannah, Matkar, Pratiek N., Liu, Zongyi, Esene, Lilian, Adam, Mohamed, Bugyei‐Twum, Antoinette, Mebrahtu, Elizabeth, Joseph, Jameela, Ehsan, Mehroz, Chen, Hao H., Qadura, Mohammad, Singh, Krishna K.

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Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion 由 Ehsan, Mehroz, Kelly, Matthew, Hooper, Charlotte, Yavari, Arash, Beglov, Julia, Bellahcene, Mohamed, Ghataorhe, Kirandeep, Poloni, Giulia, Goel, Anuj, Kyriakou, Theodosios, Fleischanderl, Karin, Ehler, Elisabeth, Makeyev, Eugene, Lange, Stephan, Ashrafian, Houman, Redwood, Charles, Davies, Benjamin, Watkins, Hugh, Gehmlich, Katja

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The Essential Autophagy Gene ATG7 Modulates Organ Fibrosis via Regulation of Endothelial-to-Mesenchymal Transition 由 Singh, Krishna K., Lovren, Fina, Pan, Yi, Quan, Adrian, Ramadan, Azza, Matkar, Pratiek N., Ehsan, Mehroz, Sandhu, Paul, Mantella, Laura E., Gupta, Nandini, Teoh, Hwee, Parotto, Matteo, Tabuchi, Arata, Kuebler, Wolfgang M., Al-Omran, Mohammed, Finkel, Toren, Verma, Subodh

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Endothelial-specific Loss of IFT88 Promotes Endothelial-to-Mesenchymal Transition and Exacerbates Bleomycin-induced Pulmonary Fibrosis 由 Singh, Shweta, Adam, Mohamed, Matkar, Pratiek N., Bugyei-Twum, Antoinette, Desjardins, Jean-Francois, Chen, Hao H., Nguyen, Hien, Bazinet, Hannah, Michels, David, Liu, Zongyi, Mebrahtu, Elizabeth, Esene, Lillian, Joseph, Jameela, Ehsan, Mehroz, Qadura, Mohammad, Connelly, Kim A., Leong-Poi, Howard, Singh, Krishna K.

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Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant 由 Jiang, He, Hooper, Charlotte, Kelly, Matthew, Steeples, Violetta, Simon, Jillian N., Beglov, Julia, Azad, Amar J., Leinhos, Lisa, Bennett, Pauline, Ehler, Elisabeth, Kalisch-Smith, Jacinta I., Sparrow, Duncan B., Fischer, Roman, Heilig, Raphael, Isackson, Henrik, Ehsan, Mehroz, Patone, Giannino, Huebner, Norbert, Davies, Benjamin, Watkins, Hugh, Gehmlich, Katja

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