Biblio

Author Title [ Type(Desc)] Year
Filters: Author is Childers, Martin K  [Clear All Filters]
Journal Article
J Pioner M, Guan X, Klaiman JM, Racca AW, Pabon L, Muskheli V, Macadangdang J, Ferrantini C, Hoopmann MR, Moritz RL, et al. Absence of full-length dystrophin impairs normal maturation and contraction of cardiomyocytes derived from human induced pluripotent stem cells. Cardiovasc Res. 2019.
Mack DL, Guan X, Wagoner A, Walker SJ, Childers MK. Disease-in-a-Dish: The Contribution of Patient-Specific Induced Pluripotent Stem Cell Technology to Regenerative Rehabilitation. Am J Phys Med Rehabil. 2014.
Goddard MA, Burlingame E, Beggs AH, Buj-Bello A, Childers MK, Marsh AP, Kelly VE. Gait characteristics in a canine model of X-linked myotubular myopathy. J Neurol Sci. 2014.
Childers MK, Beggs AH, Buj-Bello A. Gene replacement rescues severe muscle pathology and prolongs survival in myotubularin-deficient mice and dogs. Ann Transl Med. 2015;3(17):257.
Braun R, Wang Z, Mack DL, Childers MK. Gene Therapy for Inherited Muscle Diseases: Where Genetics Meets Rehabilitation Medicine. Am J Phys Med Rehabil. 2014;93(11 Suppl 3):S97-S107.
Guan X, Goddard MA, Mack DL, Childers MK. Gene therapy in monogenic congenital myopathies. Methods. 2015.
Sarwal A, Cartwright MS, Mitchell E, Williams K, Walker FO, Childers MK. Guiding Intramuscular Diaphragm Injections Using Real-time Ultrasound & Electromyography. Muscle Nerve. 2014.
Goddard MA, Mack DL, Czerniecki SM, Kelly VE, Snyder JM, Grange RW, Lawlor MW, Smith BK, Beggs AH, Childers MK. Muscle pathology, limb strength, walking gait, respiratory function and neurological impairment establish disease progression in the p.N155K canine model of X-linked myotubular myopathy. Ann Transl Med. 2015;3(18):262.
Guan X, Wang Z, Czerniecki S, Mack D, François V, Blouin V, Moullier P, Childers MK. Use of Adeno-Associated Virus to Enrich Cardiomyocytes Derived from Human Stem Cells. Hum Gene Ther Clin Dev. 2015.