Hasil Pencarian - Conrad C. Weihl

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  1. 1
    Client processing is altered by novel myopathy-causing mutations in the HSP40 J domain.

    Client processing is altered by novel myopathy-causing mutations in the HSP40 J domain. oleh Melanie Y Pullen, Conrad C Weihl, Heather L True

    Diterbitkan 2020-01-01
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  2. 2
    A knock-in mouse model for the R120G mutation of αB-crystallin recapitulates human hereditary myopathy and cataracts.

    A knock-in mouse model for the R120G mutation of αB-crystallin recapitulates human hereditary myopathy and cataracts. oleh Usha P Andley, Paul D Hamilton, Nathan Ravi, Conrad C Weihl

    Diterbitkan 2011-03-01
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  3. 3
    Comparisons of ELISA and Western blot assays for detection of autophagy flux

    Comparisons of ELISA and Western blot assays for detection of autophagy flux oleh Sung-hee Oh, Yong-bok Choi, June-hyun Kim, Conrad C. Weihl, Jeong-sun Ju

    Diterbitkan 2017-08-01
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  4. 4
    LGMDD1 natural history and phenotypic spectrum: Implications for clinical trials

    LGMDD1 natural history and phenotypic spectrum: Implications for clinical trials oleh Andrew R. Findlay, Sarah E. Robinson, Stephanie Poelker, Michelle Seiffert, Rocio Bengoechea, Conrad C. Weihl

    Diterbitkan 2023-02-01
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  5. 5
    Keap1/Cullin3 Modulates p62/SQSTM1 Activity via UBA Domain Ubiquitination

    Keap1/Cullin3 Modulates p62/SQSTM1 Activity via UBA Domain Ubiquitination oleh YouJin Lee, Tsui-Fen Chou, Sara K. Pittman, Amy L. Keith, Babak Razani, Conrad C. Weihl

    Diterbitkan 2017-08-01
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  6. 6
    Keap1/Cullin3 Modulates p62/SQSTM1 Activity via UBA Domain Ubiquitination

    Keap1/Cullin3 Modulates p62/SQSTM1 Activity via UBA Domain Ubiquitination oleh YouJin Lee, Tsui-Fen Chou, Sara K. Pittman, Amy L. Keith, Babak Razani, Conrad C. Weihl

    Diterbitkan 2017-04-01
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  7. 7
    Disease-associated mutations within the yeast DNAJB6 homolog Sis1 slow conformer-specific substrate processing and can be corrected by the modulation of nucleotide exchange factors

    Disease-associated mutations within the yeast DNAJB6 homolog Sis1 slow conformer-specific substrate processing and can be corrected by the modulation of nucleotide exchange factors oleh Ankan K. Bhadra, Michael J. Rau, Jil A. Daw, James A. J. Fitzpatrick, Conrad C. Weihl, Heather L. True

    Diterbitkan 2022-08-01
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  8. 8
    Comprehensive functional characterization of SGCB coding variants predicts pathogenicity in limb-girdle muscular dystrophy type R4/2E

    Comprehensive functional characterization of SGCB coding variants predicts pathogenicity in limb-girdle muscular dystrophy type R4/2E oleh Chengcheng Li, Jackson Wilborn, Sara Pittman, Jil Daw, Jorge Alonso-Pérez, Jordi Díaz-Manera, Conrad C. Weihl, Gabe Haller

    Diterbitkan 2023-06-01
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  9. 9
    Phenotypic diversity in an international Cure VCP Disease registry

    Phenotypic diversity in an international Cure VCP Disease registry oleh Chiseko Ikenaga, Andrew R. Findlay, Michelle Seiffert, Allison Peck, Nathan Peck, Nicholas E. Johnson, Jeffrey M. Statland, Conrad C. Weihl

    Diterbitkan 2020-09-01
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  10. 10
    The p97-UBXD8 complex regulates ER-Mitochondria contact sites by altering membrane lipid saturation and composition

    The p97-UBXD8 complex regulates ER-Mitochondria contact sites by altering membrane lipid saturation and composition oleh Rakesh Ganji, Joao A. Paulo, Yuecheng Xi, Ian Kline, Jiang Zhu, Christoph S. Clemen, Conrad C. Weihl, John G. Purdy, Steve P. Gygi, Malavika Raman

    Diterbitkan 2023-02-01
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  11. 11
    Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation

    Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation oleh Nivedita U. Jerath, Cameron D. Crockett, Steven A. Moore, Michael E. Shy, Conrad C. Weihl, Tsui-Fen Chou, Tiffany Grider, Michael A. Gonzalez, Stephan Zuchner, Andrea Swenson

    Diterbitkan 2015-01-01
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  12. 12
    Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD study

    Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD study oleh Amy Doody, Lindsay Alfano, Jordi Diaz-Manera, Linda Lowes, Tahseen Mozaffar, Katherine D. Mathews, Conrad C. Weihl, Matthew Wicklund, Man Hung, Jeffrey Statland, Nicholas E. Johnson, On behalf of the GRASP-LGMD Consortium

    Diterbitkan 2024-03-01
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  13. 13
    Gentiacaulein inhibits glucose transport to induce PRKAA1-mediated autophagy to clear amyloid beta and associated inflammation in primary astrocytes

    Gentiacaulein inhibits glucose transport to induce PRKAA1-mediated autophagy to clear amyloid beta and associated inflammation in primary astrocytes oleh Ankita Sharma, Sukhleen Kaur, Abubakar Wani, Dilpreet Kour, Mehboob Ali, Syed Mudassir Ali, Lakhvinder Singh, Abhishek Gour, Utpal Nandi, Manish Datt, Parduman Raj Sharma, Conrad C Weihl, Gurdarshan Singh, Ajay Kumar

    Diterbitkan 2024-12-01
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  14. 14
    DNAJB6 isoform specific knockdown: Therapeutic potential for limb girdle muscular dystrophy D1

    DNAJB6 isoform specific knockdown: Therapeutic potential for limb girdle muscular dystrophy D1 oleh Andrew R. Findlay, May M. Paing, Jil A. Daw, Meade Haller, Rocio Bengoechea, Sara K. Pittman, Shan Li, Feng Wang, Timothy M. Miller, Heather L. True, Tsui-Fen Chou, Conrad C. Weihl

    Diterbitkan 2023-06-01
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  15. 15
    A metastable subproteome underlies inclusion formation in muscle proteinopathies

    A metastable subproteome underlies inclusion formation in muscle proteinopathies oleh Prajwal Ciryam, Matthew Antalek, Fernando Cid, Gian Gaetano Tartaglia, Christopher M. Dobson, Anne-Katrin Guettsches, Britta Eggers, Matthias Vorgerd, Katrin Marcus, Rudolf A. Kley, Richard I. Morimoto, Michele Vendruscolo, Conrad C. Weihl

    Diterbitkan 2019-12-01
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  16. 16
    Clinical utility of anti‐cytosolic 5’‐nucleotidase 1A antibody in idiopathic inflammatory myopathies

    Clinical utility of anti‐cytosolic 5’‐nucleotidase 1A antibody in idiopathic inflammatory myopathies oleh Chiseko Ikenaga, Andrew R. Findlay, Namita A. Goyal, Sarah Robinson, Jonathan Cauchi, Yessar Hussain, Leo H. Wang, Joshua C. Kershen, Brent A. Beson, Michael Wallendorf, Robert C. Bucelli, Tahseen Mozaffar, Alan Pestronk, Conrad C. Weihl

    Diterbitkan 2021-03-01
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  17. 17
    Exploiting macrophage autophagy-lysosomal biogenesis as a therapy for atherosclerosis

    Exploiting macrophage autophagy-lysosomal biogenesis as a therapy for atherosclerosis oleh Ismail Sergin, Trent D. Evans, Xiangyu Zhang, Somashubhra Bhattacharya, Carl J. Stokes, Eric Song, Sahl Ali, Babak Dehestani, Karyn B. Holloway, Paul S. Micevych, Ali Javaheri, Jan R. Crowley, Andrea Ballabio, Joel D. Schilling, Slava Epelman, Conrad C. Weihl, Abhinav Diwan, Daping Fan, Mohamed A. Zayed, Babak Razani

    Diterbitkan 2017-06-01
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  18. 18
    Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks

    Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks oleh Melanie Meister-Broekema, Rebecca Freilich, Chandhuru Jagadeesan, Jennifer N. Rauch, Rocio Bengoechea, William W. Motley, E. F. Elsiena Kuiper, Melania Minoia, Gabriel V. Furtado, Maria A. W. H. van Waarde, Shawn J. Bird, Adriana Rebelo, Stephan Zuchner, Peter Pytel, Steven S. Scherer, Federica F. Morelli, Serena Carra, Conrad C. Weihl, Steven Bergink, Jason E. Gestwicki, Harm H. Kampinga

    Diterbitkan 2018-12-01
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