Day JW, L.J. Schut, M.L. Moseley, and L.P.W. Ranum. Spinocerebellar ataxia type 8 (SCA8) Clinical features of a large family. Neurology 55:649-657, 2000.
Moseley ML, Schut LJ, Bird TD, Koob MD, Day JW, Ranum LP. SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance. Human Molecular Genetics. 9(14):2125-30, 2000.
Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LPW. Myotonic Dystrophy Type 2: Caused by a CCTG Expansion in Intron 1 of ZNF9. Science 293:864-867, 2001.
Day, J.W., K. Ricker, J.F. Jacobsen, L.J. Rasmussen, K.A. Dick, W. Kress C. Schneider, M.C. Koch, G.J. Bielman, A.R. Harrison, J.C. Dalton and L.P.W. Ranum (2003) Myotonic dystrophy type 2: molecular, diagnostic, and clinical spectrum. Neurology 60:657-664.
Liquori, C.L, Y. Ikeda, M. Weatherspoon, K. Ricker, B.G.H. Schoser, J.C. Dalton, J.W. Day, L.P.W. Ranum (2003) Myotonic dystrophy type 2: human founder haplotype and evolutionary conservation of the repeat tract. Am. J. Hum.Genet. 73:849-862.
Day JW, Ricker K, Jacobsen J, Rasmussen L, Dick K, Kress W, Schneider C, Koch M, Beilman G, Harrison A, Dalton J, Ranum L. Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum. Neurol 60:657-64, 2003.
Savkur RS, Philips AV, Cooper TA, Dalton JC, Moseley ML, Ranum LPW, Day JW. Insulin Receptor Splicing Alteration in Myotonic Dystrophy Type 2. Am. J. Hum. Genet. 74:1309–1313, 2004.
Schoser BG, Ricker K, Schneider-Gold C, Hengstenberg C, Durre J, Bultmann B, Kress W, Day JW, Ranum LP. Sudden cardiac death in myotonic dystrophy type 2. Neurology 63(12):2402-4, 2004.
Ikeda, Y., J.C. Dalton, M.L.Moseley, K.L. Gardner, T.D. Bird, T. Ashizawa, W.K. Seltzer, M. Pandolfo, A. Milunsky, N.T. Potter, M. Shoji, , J.B. Vincent, JW Day, L.P.W. Ranum. Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 ataxia families. Am. J. Hum.Genet. 75:3-16, 2004.
Ranum LP, Day JW. Myotonic dystrophy: RNA pathogenesis comes into focus. Am. J. Hum.Gent. 74:793-804, 2004.
Day JW, Ranum, LPW. RNA Pathogenesis of the Myotonic Dystrophies. Neuromuscul. Disord. 15(1):5-16, 2005.
Day JW, Ranum LP. Genetics and molecular pathogenesis of the myotonic dystrophies. Curr Neurol Neurosci Rep. 5(1):55-9. 2005.
Trudeau MM, Dalton JC, Day JW, Ranum LP, Meisler MH. Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia and mental retardation. J Med Genet. 2005.
Ikeda Y, Dick KA, Weatherspoon MR, Gincel D, Armbrust KR, Dalton JC, Stevanin G, Durr A, Zuhlke C, Burk K, Clark HB, Brice A, Rothstein JD, Schut LJ, Day JW, Ranum LP. Spectrin mutations cause spinocerebellar ataxia type 5. Nat Genet. 38(2):184-90. 2006.
Margolis JM, Schoser BG, Moseley ML, Day JW, Ranum LP. DM2 intronic expansions: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expression. Hum Mol Genet. 15(11):1808-15. 2006.
Moseley ML, Zu T, Ikeda Y, Gao W, Mosemiller AK, Daughters RS, Chen G, Weatherspoon MR, Clark HB, Ebner TJ, Day JW, Ranum LP. Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8. Nat Genet. 38(7):758-69. 2006.
Lowe, D.A., B.O. Williams, D.D. Thomas and R.W. Grange. Molecular and cellular contractile dysfunction of dystrophic muscle from young mice. Muscle Nerve 34: 92-100. 2006.
Traaseth, N.J., D.D. Thomas and G. Veglia. Effects of Ser16 phosphorylation on the allosteric transitions of phospholamban/Ca(2+)-ATPase complex. J Mol Biol, in press. 2006.
Karim, C.B., Z. Zhang, E.C. Howard, K.D. Torgersen and D.D. Thomas. Phosphorylation-dependent conformational switch in spin-labeled phospholamban bound to SERCA. J Mol Biol, 358: 1032-40. 2006.
Buffy, J.J., B.A. Buck-Koehntop, F. Porcelli, N.J. Traaseth, D.D. Thomas and G. Veglia. Defining the intramembrane binding mechanism of sarcolipin to calcium ATPase using solution NMR spectroscopy. J Mol Biol, 358: 420-9. 2006.
Traverse J.H., Y. E. Nesmelov, M. Crampton, P. Lindstrom, D. D. Thomas and R. J. Bache. Measurement of myocardial free radical production during exercise using EPR spectrscopy. Am J Physiol Heart Circ Physiol, e-published. 2006.
Zhang, J., B. J. Wallar, C. V. Popescu, D. B. Renner, D. D. Thomas, and J. D. Lipscomb. Methane monooxygenase hydroxylase and B component interactions. Biochemistry, 45: 2913-26. 2006.
Nesmelov, Y. E. and D. D. Thomas. Multibore sample cell increases EPR sensitivity for aqueous samples. J of Magn Reson, 178: 318-24. 2005.
Thompson LV, Durand D, Fugere NA, Ferrington DA. Myosin and actin expression and oxidation in aging muscle. J Appl Physiol. 2006.
Zhong S, Lowe DA, Thompson LV. Effects of hindlimb unweighting and aging on rat semimembranosus muscle and myosin. J Appl Physiol. 2006.
Ahmadzadeh H, Thompson LV, Arriaga EA. On-column labeling for capillary electrophoretic analysis of individual mitochondria directly sampled from tissue cross sections. Anal Bioanal Chem. 384(1):169-74. 2006.
Snow LM, Sanchez OA, McLoon LK, Serfass RC, Thompson LV. Effect of endurance exercise on myosin heavy chain isoform expression in diabetic rats with peripheral neuropathy. J Phys Med Rehabil.84(10):770-9. 2005.
Snow LM, McLoon LK, Thompson LV. Adult and developmental myosin heavy chain isoforms in soleus muscle of aging Fischer Brown Norway rat. nat Rec A Discov Mol Cell Evol Biol. 86(1):866-73. 2005.
J. Ishibashi, R. L. Perry, A. Asakura, M. A. Rudnicki, MyoD induces myogenic differentiation through cooperation of its NH2- and COOH-terminal regions, J. Cell Biol. 171: 471-482, 2005.
C. J. Storbeck, K. Daniel, Y. H. Zhang, J. Lunde, A. Scime, A. Asakura, B. Jasmin, R. G. Korneluk, L. A. Sabourin. Ste20-like kinase SLK displays myofiber type specificity and is involved in C2C12 myoblast differentiation. Muscle Nerve 29, 553-64, 2004.
M. Komaki, A. Asakura, M. A. Rudnicki, S. Cheifetz, J. Sodek. MyoD enhances BMP-induced osteogenic differentiation of myogenic cell cultures. J Cell Sci. 117, 1457-68, 2004.
Laske TG, Skadsberg ND, Hill AJ, Klein GJ, Iaizzo PA: Excitation of the intrinsic conduction system through His and intraventricular septal pacing. Pacing and Clinical Electrophysiology 29:397-405, 2006.
Snedeker JG, Barnstuble BB, Iaizzo PA, Farshad M, Niederer P, Schmidlin FR: A comprehensive renal injury concept based on a validated finite element model of the human abdomen. Journal of Trauma, Injury, Infection, and Critical Care (in press) 2006.
Lohuis T, Harlow HJ, Beck TdI, Iaizzo PA: Hibernating bears conserve muscle strength and maintain fatigue resistance. Physiological and Biochemical Zoology (in press) 2006.
Sola S, Garshelis DL, Amaral JD, Noyce KV, Coy PL, Steer CJ, Iaizzo PA, Rodrigues CMP: Plasma levels of ursodeoxycholic acid in black bears, Ursus americanus: seasonal changes. Comparative Biochemistry and Physiology 143:204-208, 2006.
Xiao YF, TenBroek EM, Wilhelm JJ, Iaizzo PA, Sigg DC: Electrophysiological characterization of murine HL-5 atrial cardiomyocytes. AJP: Cell Physiology (in press) 2006.
Hill AJ, Ahlberg SE, Wilkoff BL, Iaizzo PA: Dynamic obstruction to coronary sinus access: the Thebesian valve. Heart Rhythm (in press) 2006.
Sigg DC, Iaizzo PA: In vivo versus in vitro comparison of swine cardiac performance: Induction of cardiodepression with halothane. European Journal of Pharmacology (in press) 2006.
Chromy CA, Carey MT, Balgaard KG, Iaizzo PA: The potential use of axial spinal unloading in the treatment of adolescent idiopathic scoliosis: A case series. Archive of Physical Medicine and Rehabilitation (in press) 2006.
Firshman AM, Valberg SJ, B Bender JB, Annandale EJ, Hayden DW. Comparison of Histopathologic Criteria and Skeletal Muscle Fixation Techniques for the Diagnosis of Polysaccharide Storage Myopathy in Horses. Vet Pathol. 2006 May;43(3):257-69.
Wagner ML, Valberg SJ, Ames EG, Bauer MM, Wiseman JA, Penedo CT, Kinde H, Abbitt B, and Mickelson JR. Allele Frequency and Likely Impact of the Glycogen Branching Enzyme Deficiency Gene in Quarter Horse and Paint Horse Populations. J Vet Int Med (in press)
Sage AM, Valberg SJ, Hayden DW, Firshman AM and Jacob K, Cor Pulmonale and early right heart failure in a horse with heaves. J Vet Int Med 2006;20:694-696.
Dranchak PK, Ekenstedt KJ, Valberg SJ, Chowdhary BP, Raudsepp T, and Mickelson J R.Chromosomal assignments for the equine AMPK family genes Anima Genetics (in press)
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Dranchak PK, Valberg SJ, Gary W. Onan GW, Gallant EM, Binns MM,. Swinburne JE and James R. Mickelson JR. Exclusion of Linkage of Recurrent Exertional Rhabdomyolysis in Thoroughbred Horses to the RYR1, CACNA1S and ATP2A1 Genes. (in press)
Firshman AM, Valberg SJ, Finno C. Sensitivity to insulin test for the early detection of polysaccharide storage myopathy in Quarter Horses. (submitted)
Finno CM, Valberg SJ, Wunschmann A and Murphy M. Pasture Myopathy in 14 horses in the Midwestern USA. J Am Vet Med Assoc (in press)
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McCue, M, Ribiero W, Lewis S and Valberg SJ. Prevalence of polysaccharide storage myopathy in horses with neuromuscular disorders. Equine Veterinary Journal Suppl. (in press).
Christiansen SP, McLoon LK. The effect of resection on satellite cell activity in extraocular muscle. Invest. Ophthalmol. Vis. Sci. 47: 605-613, 2006.
Shinners MJ, Goding GS, McLoon LK. Effect of recurrent laryngeal nerve section on the laryngeal muscles of adult rabbits. Otolaryngol. Head Neck Surg. 134: 413-418, 2006.
Anderson BC, Christiansen SP, Grandt S, Grange RW, McLoon LK. Increased extraocular muscle strength with direct injection of insulin-like growth factor-I. Invest. Ophthalmol. Vis. Sci. 47: 2461-2467, 2006.
Harrison AR, McLoon LK. Reduction in touch sensitivity and hyperinnervation in vesicant-injured rabbit eyelid by direct injection of corticotropin releasing factor. Neurosci. Lett. 400:30-34, 2006.
Danylkova NO, Pomeranz HD, Alcala SR, McLoon LK. Histological and morphometric evaluation of transient retinal and optic nerve ischemia in rat. Brain Res. 1096:20-29, 2006.
Christiansen SP, Anderson BC, McLoon LK. Increasing muscle strength as a treatment for strabismus: Sustained release of insulin growth factor-1 results in stronger extraocular muscle. J AAPOS 10: in press, 2006.
McLoon LK, Thorstenson KM, Solomon A, Lewis MP. Myogenic precursor cells in craniofacial muscles. Oral Sci. In press, 2006.
Danylkova NO, Pomeranz HD, Alcala SR, McLoon LK. Neuroprotective effects of brimonidine treatment in a rodent model of ischemic optic neuropathy. Exp. Eye Res. In press, 2006.
Moran, A.L., G.L. Warren, D.A. Lowe. Soleus and EDL muscle contractility across the lifespan of female C57BL/6 mice. Exp. Gerontol. 40: 966-975, 2005. DOI 10.1016/j.exger.2005.09.005
Moran, A.L., G.L. Warren, D.A. Lowe. Removal of ovarian hormones detrimentally affects soleus and extensor digitorum longus muscle contractile function and myosin in mice. J. Appl. Physiol. 100: 548-559, 2006. DOI 10.1152/japplphysiol.01029.2005
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Gorzek, J.F., K.C. Hendrickson, J.P. Forstner, J.L. Rixen, A.L. Moran, D.A. Lowe. Estradiol and tamoxifen reverse ovariectomy-induced physical inactivity in C57BL/6 mice. Med. Sci. Sport Exerc. (In Press)
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Dranchak PK, Valberg SJ, Onan GW, Gallant EM, Binns MM, Swinburne JE and Mickelson JR. (2006). Exclusion of Linkage of Recurrent Exertional Rhabdomyolysis in Thoroughbred Horses to the RYR1, CACNA1S and ATP2A1 Genes. Am J Vet Res 67, 1395-1400.
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Wagner ML, Raudsepp T, Goh G, Agarwala R, Schäffer AA, Dranchak PK, Brinkmeyer-Langford C, Skow LC, Chowdhary BP, and Mickelson JR. (2006). A 1.3-Mb interval map of equine homologs of HSA2. Cytogenetics and Genome Research 112, 227-234.
Dranchak PK, Ekenstedt KJ, Valberg SJ, Chowdhary BP, Raudsepp T, and Mickelson JR. (2006). Chromosomal assignments for the equine AMPK family genes. Animal Genetics 27, 293-294.
Dranchak PK, Valberg SJ, Onan GW, Gallant EM, Binns MM, Swinburne JE and Mickelson JR. (2006). Exclusion of Linkage of Recurrent Exertional Rhabdomyolysis in Thoroughbred Horses to the RYR1, CACNA1S and ATP2A1 Genes. Am J Vet Res 67, 1395-1400.
Taylor DA, Ott HC. (2006) Cardiovascular Cell Therapy – What are Realistic Targets in 2006? Nature Clin Prac Cardiovasc Med (in press).
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