Stanley Appel - Publications

Duke University, Durham, NC 

39 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2013 Ravits J, Appel S, Baloh RH, Barohn R, Brooks BR, Elman L, Floeter MK, Henderson C, Lomen-Hoerth C, Macklis JD, McCluskey L, Mitsumoto H, Przedborski S, Rothstein J, Trojanowski JQ, et al. Deciphering amyotrophic lateral sclerosis: what phenotype, neuropathology and genetics are telling us about pathogenesis. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 14: 5-18. PMID 23678876 DOI: 10.3109/21678421.2013.778548  0.364
2005 Vigh L, Smith RG, Soós J, Engelhardt JI, Appel SH, Siklós L. Sublethal dose of 4-hydroxynonenal reduces intracellular calcium in surviving motor neurons in vivo. Acta Neuropathologica. 109: 567-75. PMID 15933871 DOI: 10.1007/S00401-004-0977-1  0.306
2002 Mohamed HA, Mosier DR, Zou LL, Siklós L, Alexianu ME, Engelhardt JI, Beers DR, Le WD, Appel SH. Immunoglobulin Fc gamma receptor promotes immunoglobulin uptake, immunoglobulin-mediated calcium increase, and neurotransmitter release in motor neurons. Journal of Neuroscience Research. 69: 110-6. PMID 12111822 DOI: 10.1002/Jnr.10271  0.7
2002 Simpson EP, Mosier D, Appel SH. Mechanisms of disease pathogenesis in amyotrophic lateral sclerosis. A central role for calcium. Advances in Neurology. 88: 1-19. PMID 11908220  0.685
2001 Beers DR, Ho BK, Siklós L, Alexianu ME, Mosier DR, Mohamed AH, Otsuka Y, Kozovska ME, McAlhany RE, Smith RG, Appel SH. Parvalbumin overexpression alters immune-mediated increases in intracellular calcium, and delays disease onset in a transgenic model of familial amyotrophic lateral sclerosis. Journal of Neurochemistry. 79: 499-509. PMID 11701753 DOI: 10.1046/J.1471-4159.2001.00582.X  0.707
2001 Appel SH, Beers D, Siklos L, Engelhardt JI, Mosier DR. Calcium: the Darth Vader of ALS. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 2: S47-54. PMID 11465925 DOI: 10.1080/146608201300079418  0.708
2000 Siklós L, Engelhardt JI, Reaume AG, Scott RW, Adalbert R, Obál I, Appel SH. Altered calcium homeostasis in spinal motoneurons but not in oculomotor neurons of SOD-1 knockout mice. Acta Neuropathologica. 99: 517-24. PMID 10805095 DOI: 10.1007/S004010051154  0.305
2000 Mosier DR, Siklós L, Appel SH. Resistance of extraocular motoneuron terminals to effects of amyotrophic lateral sclerosis sera. Neurology. 54: 252-5. PMID 10636164 DOI: 10.1212/Wnl.54.1.252  0.702
1999 Siklós L, Engelhardt JI, Adalbert R, Appel SH. Calcium-containing endosomes at oculomotor terminals in animal models of ALS. Neuroreport. 10: 2539-45. PMID 10574366 DOI: 10.1097/00001756-199908200-00019  0.345
1999 Le W, Conneely OM, Zou L, He Y, Saucedo-Cardenas O, Jankovic J, Mosier DR, Appel SH. Selective agenesis of mesencephalic dopaminergic neurons in Nurr1-deficient mice. Experimental Neurology. 159: 451-8. PMID 10506516 DOI: 10.1006/Exnr.1999.7191  0.644
1998 Siklós L, Engelhardt JI, Alexianu ME, Gurney ME, Siddique T, Appel SH. Intracellular calcium parallels motoneuron degeneration in SOD-1 mutant mice. Journal of Neuropathology and Experimental Neurology. 57: 571-87. PMID 9630237 DOI: 10.1097/00005072-199806000-00005  0.33
1998 Alexianu ME, Robbins E, Carswell S, Appel SH. 1Alpha, 25 dihydroxyvitamin D3-dependent up-regulation of calcium-binding proteins in motoneuron cells. Journal of Neuroscience Research. 51: 58-66. PMID 9452309 DOI: 10.1002/(Sici)1097-4547(19980101)51:1<58::Aid-Jnr6>3.0.Co;2-K  0.306
1997 Colom LV, Alexianu ME, Mosier DR, Smith RG, Appel SH. Amyotrophic lateral sclerosis immunoglobulins increase intracellular calcium in a motoneuron cell line. Experimental Neurology. 146: 354-60. PMID 9270044 DOI: 10.1006/Exnr.1997.6541  0.709
1997 Engelhardt JI, Siklos L, Appel SH. Altered calcium homeostasis and ultrastructure in motoneurons of mice caused by passively transferred anti-motoneuronal IgG. Journal of Neuropathology and Experimental Neurology. 56: 21-39. PMID 8990126 DOI: 10.1097/00005072-199701000-00003  0.32
1996 Siklós L, Engelhardt J, Harati Y, Smith RG, Joó F, Appel SH. Ultrastructural evidence for altered calcium in motor nerve terminals in amyotropic lateral sclerosis. Annals of Neurology. 39: 203-16. PMID 8967752 DOI: 10.1002/Ana.410390210  0.338
1996 Smith RG, Siklos L, Alexianu ME, Engelhardt JI, Mosier DR, Colom L, Habib Mohamed A, Appel SH. Autoimmunity and ALS. Neurology. 47: S40-5; discussion S4. PMID 8858050 DOI: 10.1212/Wnl.47.4_Suppl_2.40S  0.702
1995 Mosier DR, Baldelli P, Delbono O, Smith RG, Alexianu ME, Appel SH, Stefani E. Amyotrophic lateral sclerosis immunoglobulins increase Ca2+ currents in a motoneuron cell line. Annals of Neurology. 37: 102-9. PMID 7818241 DOI: 10.1002/Ana.410370119  0.718
1993 Llinás R, Sugimori M, Cherksey BD, Smith RG, Delbono O, Stefani E, Appel S. IgG from amyotrophic lateral sclerosis patients increases current through P-type calcium channels in mammalian cerebellar Purkinje cells and in isolated channel protein in lipid bilayer. Proceedings of the National Academy of Sciences of the United States of America. 90: 11743-7. PMID 8265620 DOI: 10.1073/Pnas.90.24.11743  0.403
1981 Merickel M, Gray R, Chauvin P, Appel S. Cultured muscle from myotonic muscular dystrophy patients: Altered membrane electrical properties Proceedings of the National Academy of Sciences of the United States of America. 78: 648-652. PMID 6941262 DOI: 10.1073/Pnas.78.1.648  0.31
1977 McNamara JO, Appel SH. Biochemical approaches to dementia. Contemporary Neurology Series. 15: 155-68. PMID 144584  0.361
1977 McNamara JO, Appel SH. Myelin basic protein phosphatase activity in rat brain. Journal of Neurochemistry. 29: 27-35. PMID 69679 DOI: 10.1111/J.1471-4159.1977.Tb03920.X  0.427
1976 Roses AD, Roses MJ, Miller SE, Hull KL, Appel SH. Carrier detection in Duchenne muscular dystrophy. The New England Journal of Medicine. 294: 193-8. PMID 1244534 DOI: 10.1056/Nejm197601222940404  0.395
1976 Roses AD, Appel SH. Erythrocyte spectrin peak II phosphorylation in Duchenne muscular dystrophy. Journal of the Neurological Sciences. 29: 185-93. PMID 978207 DOI: 10.1016/0022-510X(76)90170-2  0.399
1976 Butterfield DA, Roses AD, Appel SH, Chesnut DB. Electron spin resonance studies of membrane proteins in erythrocytes in myotonic muscular dystrophy. Archives of Biochemistry and Biophysics. 177: 226-34. PMID 187121 DOI: 10.1016/0003-9861(76)90432-X  0.39
1976 Butterfield DA, Chesnut DB, Appel SH, Roses AD. Spin label study of erythrocyte membrane fluidity in myotonic and Duchenne muscular dystrophy and congenital myotonia. Nature. 263: 159-61. PMID 184394 DOI: 10.1038/263159A0  0.41
1976 Roses AD, Herbstreith M, Metcalf B, Appel SH. Increased phosphorylated components of erythrocyte membrane spectrin band II with reference to Duchenne muscular dystrophy. Journal of the Neurological Sciences. 30: 167-78. PMID 10352 DOI: 10.1016/0022-510X(76)90264-1  0.358
1976 Miller SE, Roses AD, Appel SH. Scanning electron microscopy studies in muscular dystrophy. Archives of Neurology. 33: 172-4. PMID 3154 DOI: 10.1001/Archneur.1976.00500030028005  0.381
1975 Miller SE, Roses AD, Appel SH. Letter: Erythrocytes in human muscular dystrophy. Science (New York, N.Y.). 188: 1131. PMID 1215993 DOI: 10.1126/Science.1215993  0.335
1975 Roses AD, Herbstreith MH, Appel SH. Membrane protein kinase alteration in Duchenne muscular dystrophy. Nature. 254: 350-1. PMID 1118019 DOI: 10.1038/254350A0  0.394
1975 Roses AD, Appel SH, Butterfield DA, Miller SE, Chesnut DB. Specificity of biochemical and biophysical tests in Duchenne and myotonic muscular dystrophy, carrier states, and congenital myotonia. Transactions of the American Neurological Association. 100: 131-4. PMID 179179  0.341
1975 Roses AD, Butterfield A, Appel SH, Chestnut DB. Phenytoin and membrane fluidity in myotonic dystrophy. Archives of Neurology. 32: 535-8. PMID 168843 DOI: 10.1001/Archneur.1975.00490500055006  0.393
1975 Roses AD, Appel SH. Phosphorylation of component a of the human erythrocyte membrane in myotonic muscular dystrophy. The Journal of Membrane Biology. 20: 51-8. PMID 123592 DOI: 10.1007/Bf01870627  0.41
1974 Butterfield DA, Roses AD, Cooper ML, Appel SH, Chesnut DB. A comparative electron spin resonance study of the erythrocyte membrane in myotonic muscular dystrophy. Biochemistry. 13: 5078-82. PMID 4373028  0.374
1974 Butterfield DA, Chesnut DB, Roses AD, Appel SH. Electron spin resonance studies of erythrocytes from patients with myotonic muscular dystrophy. Proceedings of the National Academy of Sciences of the United States of America. 71: 909-13. PMID 4362637 DOI: 10.1073/Pnas.71.3.909  0.408
1974 Roses AD, Appel SH. Muscle membrane protein kinase in myotonic muscular dystrophy. Nature. 250: 245-7. PMID 4277586 DOI: 10.1038/250245A0  0.423
1974 Roses AD, Appel SH. Letter: Muscular dystrophies. Lancet (London, England). 2: 1400. PMID 4143368  0.355
1973 Andrew CG, Roses AD, Almon RR, Appel SH. Phosphorylation of muscle membranes: identification of a membrane-bound protein kinase. Science (New York, N.Y.). 182: 927-9. PMID 4355523 DOI: 10.1126/Science.182.4115.927  0.404
1973 Roses AD, Appel SH. Protein kinase activity in erythrocyte ghosts of patients with myotonic muscular dystrophy. Proceedings of the National Academy of Sciences of the United States of America. 70: 1855-9. PMID 4352659 DOI: 10.1073/Pnas.70.6.1855  0.419
1973 Roses AD, Appel SH. Erythrocyte protein phosphorylation. The Journal of Biological Chemistry. 248: 1408-11. PMID 4346955  0.354
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