檢索結果 - Conrad C. Weihl

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  1. 1
    Motor neuron disease associated with copper deficiency

    Motor neuron disease associated with copper deficiency 由 Conrad C. Weihl, Glenn Lopate

    出版 2006
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  2. 2
    The VCP/p97 system at a glance: connecting cellular function to disease pathogenesis

    The VCP/p97 system at a glance: connecting cellular function to disease pathogenesis 由 Hemmo Meyer, Conrad C. Weihl

    出版 2014
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  3. 3
    Regulation of SQSTM1/p62 via UBA domain ubiquitination and its role in disease

    Regulation of SQSTM1/p62 via UBA domain ubiquitination and its role in disease 由 Youjin Lee, Conrad C. Weihl

    出版 2017
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  4. 4
    p97/VCP at the intersection of the autophagy and the ubiquitin proteasome system

    p97/VCP at the intersection of the autophagy and the ubiquitin proteasome system 由 Jeong-Sun Ju, Conrad C. Weihl

    出版 2010
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  5. 5
    Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy

    Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy 由 Jeong-Sun Ju, Conrad C. Weihl

    出版 2010
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  6. 6
    Valosin-containing protein disease: Inclusion body myopathy with Paget’s disease of the bone and fronto-temporal dementia

    Valosin-containing protein disease: Inclusion body myopathy with Paget’s disease of the bone and fronto-temporal dementia 由 Conrad C. Weihl, Alan Pestronk, Virginia Kimonis

    出版 2009
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  7. 7
    Molecular and cellular basis of genetically inherited skeletal muscle disorders

    Molecular and cellular basis of genetically inherited skeletal muscle disorders 由 James J. Dowling, Conrad C. Weihl, Melissa J. Spencer

    出版 2021
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  8. 8
    Quantitation of "autophagic flux" in mature skeletal muscle

    Quantitation of "autophagic flux" in mature skeletal muscle 由 Jeong-Sun Ju, Arun S. Varadhachary, Sara Miller, Conrad C. Weihl

    出版 2010
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  9. 9
    Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice

    Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice 由 Conrad C. Weihl, Sara Miller, Phyllis I. Hanson, Alan Pestronk

    出版 2007
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  10. 10
    Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation

    Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation 由 Conrad C. Weihl, Seema Dalal, Alan Pestronk, Phyllis I. Hanson

    出版 2005
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  11. 11
    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 由 Usha P. Andley, Paul D. Hamilton, Nathan Ravi, Conrad C. Weihl

    出版 2011
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  12. 12
    Impaired Protein Aggregate Handling and Clearance Underlie the Pathogenesis of p97/VCP-associated Disease

    Impaired Protein Aggregate Handling and Clearance Underlie the Pathogenesis of p97/VCP-associated Disease 由 Jeong-Sun Ju, Sara Miller, Phyllis I. Hanson, Conrad C. Weihl

    出版 2008
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  13. 13
    Acute and Bilateral Blindness Due to Optic Neuropathy Associated With Copper Deficiency

    Acute and Bilateral Blindness Due to Optic Neuropathy Associated With Copper Deficiency 由 Robert T. Naismith, James Shepherd, Conrad C. Weihl, Nhial T. Tutlam, Anne H. Cross

    出版 2009
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  14. 14
    Myofibrillar disruption and RNA-binding protein aggregation in a mouse model of limb-girdle muscular dystrophy 1D

    Myofibrillar disruption and RNA-binding protein aggregation in a mouse model of limb-girdle muscular dystrophy 1D 由 Rocío Bengoechea, Sara K. Pittman, E.P. Tuck, Heather L. True, Conrad C. Weihl

    出版 2015
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  15. 15
    Myopathy-causing Mutations in an HSP40 Chaperone Disrupt Processing of Specific Client Conformers

    Myopathy-causing Mutations in an HSP40 Chaperone Disrupt Processing of Specific Client Conformers 由 Kevin C. Stein, Rocío Bengoechea, Matthew B. Harms, Conrad C. Weihl, Heather L. True

    出版 2014
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  16. 16
    VCP maintains lysosomal homeostasis and TFEB activity in differentiated skeletal muscle

    VCP maintains lysosomal homeostasis and TFEB activity in differentiated skeletal muscle 由 Khalid Arhzaouy, Chrisovalantis Papadopoulos, Nina Schulze, Sara K. Pittman, Hemmo Meyer, Conrad C. Weihl

    出版 2019
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  17. 17
    Mutant Presenilin-1 Induces Apoptosis and Downregulates Akt/PKB

    Mutant Presenilin-1 Induces Apoptosis and Downregulates Akt/PKB 由 Conrad C. Weihl, Ghanashyam D. Ghadge, Scott Kennedy, Nissim Hay, Richard Miller, Raymond P. Roos

    出版 1999
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  18. 18
    p62 expression and autophagy in αB-crystallin R120G mutant knock-in mouse model of hereditary cataract

    p62 expression and autophagy in αB-crystallin R120G mutant knock-in mouse model of hereditary cataract 由 Jonathan A. Wignes, Joshua W. Goldman, Conrad C. Weihl, Matthew G. Bartley, Usha P. Andley

    出版 2013
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  19. 19
    Keap1/Cullin3 Modulates p62/SQSTM1 Activity via UBA Domain Ubiquitination

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

    出版 2017
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  20. 20
    Desmin forms toxic, seeding-competent amyloid aggregates that persist in muscle fibers

    Desmin forms toxic, seeding-competent amyloid aggregates that persist in muscle fibers 由 Niraja Kedia, Khalid Arhzaouy, Sara K. Pittman, Yuanzi Sun, Mark Batchelor, Conrad C. Weihl, Jan Bieschke

    出版 2019
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