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 |
0.428 |
|
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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