Peptide Bound Hypohydroxyprolinuria in Handigodu Disease: A Familial Syndrome of Spondylo Epi(meta)physeal Dysplasia

by Mallikarjun Badadani, S. V. Suresh Babu, K. T. Shetty, S. S. Agarwal
Published 2009-01-01

Exercise training reverses skeletal muscle atrophy in an experimental model of VCP disease.

by Angèle Nalbandian, Christopher Nguyen, Veeral Katheria, Katrina J Llewellyn, Mallikarjun Badadani, Vincent Caiozzo, Virginia E Kimonis
Published 2013-01-01

VCP associated inclusion body myopathy and paget disease of bone knock-in mouse model exhibits tissue pathology typical of human disease.

by Mallikarjun Badadani, Angèle Nalbandian, Giles D Watts, Jouni Vesa, Masashi Kitazawa, Hailing Su, Jasmin Tanaja, Eric Dec, Douglas C Wallace, Jogeshwar Mukherjee, Vincent Caiozzo, Matthew Warman, Virginia E Kimonis
Published 2010-10-01

The homozygote VCP(R¹⁵⁵H/R¹⁵⁵H) mouse model exhibits accelerated human VCP-associated disease pathology.

by Angèle Nalbandian, Katrina J Llewellyn, Masashi Kitazawa, Hong Z Yin, Mallikarjun Badadani, Negar Khanlou, Robert Edwards, Christopher Nguyen, Jogeshwar Mukherjee, Tahseen Mozaffar, Giles Watts, John Weiss, Virginia E Kimonis
Published 2012-01-01