John Kamholz - Publications

Molecular Biology and Genetics Wayne State University, Detroit, MI, United States 
Neuroscience Biology, Molecular Biology

113 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
2018 Somayajulu M, Bessert DA, Hüttemann M, Sohi J, Kamholz J, Skoff RP. Insertion of Proteolipid Protein into Mitochondria but not DM20 Regulates Metabolism of Cells. Neuroscience Letters. PMID 29729355 DOI: 10.1016/j.neulet.2018.05.005  0.32
2017 Wang DS, Wu X, Bai Y, Zaidman C, Grider T, Kamholz J, Lupski JR, Connolly AM, Shy ME. PMP22 exon 4 deletion causes ER retention of PMP22 and a gain-of-function allele in CMT1E. Annals of Clinical and Translational Neurology. 4: 236-245. PMID 28382305 DOI: 10.1002/acn3.395  0.4
2016 Laukka JJ, Kamholz J, Bessert D. Novel pathologic findings in patients with Pelizaeus-Merzbacher disease. Neuroscience Letters. PMID 27222925 DOI: 10.1016/j.neulet.2016.05.028  0.6
2015 Jerath NU, Kamholz J, Grider T, Harper A, Swenson A, Shy ME. Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2-p12) deletion. Muscle & Nerve. 52: 905-8. PMID 26012543 DOI: 10.1002/mus.24713  0.72
2014 Laukka JJ, Makki MI, Lafleur T, Stanley J, Kamholz J, Garbern JY. Diffusion tensor imaging of patients with proteolipid protein 1 gene mutations. Journal of Neuroscience Research. 92: 1723-32. PMID 25156430 DOI: 10.1002/jnr.23458  0.72
2014 Parikh S, Goldstein A, Koenig MK, Scaglia F, Enns GM, Saneto R, Anselm I, Collins A, Cohen BH, DeBrosse SD, Dimmock D, Falk MJ, Ganesh J, ... ... Kamholz J, et al. Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges. Mitochondrion. 14: 26-33. PMID 23891656 DOI: 10.1016/j.mito.2013.07.116  0.72
2013 Laukka JJ, Stanley JA, Garbern JY, Trepanier A, Hobson G, Lafleur T, Gow A, Kamholz J. Neuroradiologic correlates of clinical disability and progression in the X-linked leukodystrophy Pelizaeus-Merzbacher disease. Journal of the Neurological Sciences. 335: 75-81. PMID 24139698 DOI: 10.1016/j.jns.2013.08.030  0.72
2012 Patzkó A, Bai Y, Saporta MA, Katona I, Wu X, Vizzuso D, Feltri ML, Wang S, Dillon LM, Kamholz J, Kirschner D, Sarkar FH, Wrabetz L, Shy ME. Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice. Brain : a Journal of Neurology. 135: 3551-66. PMID 23250879 DOI: 10.1093/brain/aws299  0.72
2012 Daffu G, Sohi J, Kamholz J. Proteolipid protein dimerization at cysteine 108: Implications for protein structure. Neuroscience Research. 74: 144-55. PMID 22902553 DOI: 10.1016/j.neures.2012.07.009  0.72
2012 Liu Z, Wang Y, Yedidi RS, Brunzelle JS, Kovari IA, Sohi J, Kamholz J, Kovari LC. Crystal structure of the extracellular domain of human myelin protein zero. Proteins. 80: 307-13. PMID 21971831 DOI: 10.1002/prot.23164  0.72
2009 Kamholz J. Predicting the unpredictable. Annals of Neurology. 65: 480. PMID 19399867 DOI: 10.1002/ana.21650  0.72
2008 Grandis M, Vigo T, Passalacqua M, Jain M, Scazzola S, La Padula V, Brucal M, Benvenuto F, Nobbio L, Cadoni A, Mancardi GL, Kamholz J, Shy ME, Schenone A. Different cellular and molecular mechanisms for early and late-onset myelin protein zero mutations. Human Molecular Genetics. 17: 1877-89. PMID 18337304 DOI: 10.1093/hmg/ddn083  0.72
2007 Gaboreanu AM, Hrstka R, Xu W, Shy M, Kamholz J, Lilien J, Balsamo J. Myelin protein zero/P0 phosphorylation and function require an adaptor protein linking it to RACK1 and PKC alpha. The Journal of Cell Biology. 177: 707-16. PMID 17502419 DOI: 10.1083/jcb.200608060  0.72
2007 Shy ME, Kamholz J. Mutations in Schwann cell genes causing inherited neuropathies The Biology of Schwann Cells: Development, Differentiation and Immunomodulation. 126-157. DOI: 10.1017/CBO9780511541605.009  0.72
2007 Kamholz JA, Brucal M, Li J, Shy M. Myelin Protein Zero and CMT1B. A Tale of two Phenotypes Molecular Neurology. 463-474. DOI: 10.1016/B978-012369509-3.50031-7  0.72
2006 Sabet A, Li J, Ghandour K, Pu Q, Wu X, Kamholz J, Shy ME, Cambi F. Skin biopsies demonstrate MPZ splicing abnormalities in Charcot-Marie-Tooth neuropathy 1B Neurology. 67: 1141-1146. PMID 17030746 DOI: 10.1212/01.wnl.0000238499.37764.b1  0.72
2006 Ford CC, Johnson KP, Lisak RP, Panitch HS, Shifronis G, Wolinsky JS. A prospective open-label study of glatiramer acetate: over a decade of continuous use in multiple sclerosis patients. Multiple Sclerosis (Houndmills, Basingstoke, England). 12: 309-20. PMID 16764344 DOI: 10.1191/135248506ms1318oa  0.72
2006 Shy ME, Scavina MT, Clark A, Krajewski KM, Li J, Kamholz J, Kolodny E, Szigeti K, Fischer RA, Saifi GM, Scherer SS, Lupski JR. T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy. Annals of Neurology. 59: 358-64. PMID 16437560 DOI: 10.1002/ana.20777  0.72
2005 Woodward KJ, Cundall M, Sperle K, Sistermans EA, Ross M, Howell G, Gribble SM, Burford DC, Carter NP, Hobson DL, Garbern JY, Kamholz J, Heng H, Hodes ME, Malcolm S, et al. Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination. American Journal of Human Genetics. 77: 966-87. PMID 16380909 DOI: 10.1086/498048  0.72
2005 Kamholz JA, Garbern JY. Neuronal cell injury precedes brain atrophy in multiple sclerosis. Neurology. 64: 176; author reply 17. PMID 15642939 DOI: 10.1212/wnl.64.1.176  0.72
2004 Southwood C, He C, Garbern J, Kamholz J, Arroyo E, Gow A. CNS myelin paranodes require Nkx6-2 homeoprotein transcriptional activity for normal structure. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 11215-25. PMID 15601927 DOI: 10.1523/JNEUROSCI.3479-04.2004  0.72
2004 Kamholz J, Shy ME. Late onset Charcot-Marie-Tooth 2 syndrome caused by two novel mutations in the MPZ gene. Neurology. 63: 194; author reply 19. PMID 15249646  0.72
2004 Huang Y, Rangwala F, Fulkerson PC, Ling B, Reed E, Cox AD, Kamholz J, Ratner N. Role of TC21/R-Ras2 in enhanced migration of neurofibromin-deficient Schwann cells. Oncogene. 23: 368-78. PMID 14724565 DOI: 10.1038/sj.onc.1207075  0.72
2004 Shy ME, Jáni A, Krajewski K, Grandis M, Lewis RA, Li J, Shy RR, Balsamo J, Lilien J, Garbern JY, Kamholz J. Phenotypic clustering in MPZ mutations. Brain : a Journal of Neurology. 127: 371-84. PMID 14711881 DOI: 10.1093/brain/awh048  0.72
2003 Shy ME, Hobson G, Jain M, Boespflug-Tanguy O, Garbern J, Sperle K, Li W, Gow A, Rodriguez D, Bertini E, Mancias P, Krajewski K, Lewis R, Kamholz J. Schwann cell expression of PLP1 but not DM20 is necessary to prevent neuropathy. Annals of Neurology. 53: 354-65. PMID 12601703 DOI: 10.1002/ana.10466  0.72
2003 Hudson LD, Garbern JY, Kamholz JA. Pelizaeus-Merzbacher Disease Myelin Biology and Disorders. 2: 867-885. DOI: 10.1016/B978-012439510-7/50090-5  0.72
2002 Shy ME, Garbern JY, Kamholz J. Hereditary motor and sensory neuropathies: a biological perspective. The Lancet. Neurology. 1: 110-8. PMID 12849515 DOI: 10.1016/S1474-4422(02)00042-X  0.72
2002 Paulson HL, Garbern JY, Hoban TF, Krajewski KM, Lewis RA, Fischbeck KH, Grossman RI, Lenkinski R, Kamholz JA, Shy ME. Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease. Annals of Neurology. 52: 429-34. PMID 12325071 DOI: 10.1002/ana.10305  0.72
2002 Uhler J, Garbern J, Yang L, Kamholz J, Mellerick DM. Nk6, a novel Drosophila homeobox gene regulated by vnd. Mechanisms of Development. 116: 105-16. PMID 12128210 DOI: 10.1016/S0925-4773(02)00155-7  0.72
2002 Awatramani R, Shumas S, Kamholz J, Scherer SS. TGFbeta1 modulates the phenotype of Schwann cells at the transcriptional level. Molecular and Cellular Neurosciences. 19: 307-19. PMID 11906205 DOI: 10.1006/mcne.2001.1094  0.72
2002 Garbern JY, Yool DA, Moore GJ, Wilds IB, Faulk MW, Klugmann M, Nave KA, Sistermans EA, van der Knaap MS, Bird TD, Shy ME, Kamholz JA, Griffiths IR. Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation. Brain : a Journal of Neurology. 125: 551-61. PMID 11872612  0.72
2001 Shy ME, Balsamo J, Lilien J, Kamholz J. A molecular basis for hereditary motor and sensory neuropathy disorders Current Neurology and Neuroscience Reports. 1: 77-88. PMID 11898503  0.72
2001 Khan OA, Tselis AC, Kamholz JA, Garbern JY, Lewis RA, Lisak RP. A prospective, open-label treatment trial to compare the effect of IFNβ-1a (Avonex®), IFNβ-1b (Betaseron®), and glatiramer acetate (Copaxone®) on the relapse rate in relapsing-remitting multiple sclerosis: Results after 18 months of therapy Multiple Sclerosis. 7: 349-353. PMID 11795454 DOI: 10.1191/135245801701567041  0.72
2001 Menichella DM, Arroyo EJ, Awatramani R, Xu T, Baron P, Vallat JM, Balsamo J, Lilien J, Scarlato G, Kamholz J, Scherer SS, Shy ME. Protein zero is necessary for E-cadherin-mediated adherens junction formation in Schwann cells. Molecular and Cellular Neurosciences. 18: 606-18. PMID 11749037 DOI: 10.1006/mcne.2001.1041  0.72
2001 Garbern J, Shy M, Krajewski K, Kamholz J, Hobson G, Cambi F, Schiffmann R, Moore DF, Freir K, Choir B, Patronas N, Virta A, Buespflüg-Tanguy O, Tedeschi G. Evidence for neuroaxonal injury in patients with proteolipid gene mutations[2] (multiple letter) Neurology. 57: 1938-1939. PMID 11723304 DOI: 10.1212/WNL.57.10.1938-a  0.72
2001 Xu W, Shy M, Kamholz J, Elferink L, Xu G, Lilien J, Balsamo J. Mutations in the cytoplasmic domain of P0 reveal a role for PKC-mediated phosphorylation in adhesion and myelination. The Journal of Cell Biology. 155: 439-46. PMID 11673479 DOI: 10.1083/jcb.200107114  0.72
2001 Khan OA, Zvartau-Hind M, Caon C, Din MU, Cochran M, Lisak D, Tselis AC, Kamholz JA, Garbern JY, Lisak RP. Effect of monthly intravenous cyclophosphamide in rapidly deteriorating multiple sclerosis patients resistant to conventional therapy Multiple Sclerosis. 7: 185-188. PMID 11475443 DOI: 10.1191/135245801678438429  0.72
2001 Khan OA, Tselis AC, Kamholz JA, Garbern JY, Lewis RA, Lisak RP. A prospective, open-label treatment trial to compare the effect of IFN β-1a (Avonex), IFNβ-1b (Betaseron), and glatiramer acetate (Copaxone) on the relapse rate in relapsing-remitting multiple sclerosis European Journal of Neurology. 8: 141-148. PMID 11284992 DOI: 10.1046/j.1468-1331.2001.00189.x  0.72
2001 Shy ME, Balsamo J, Lilien J, Kamholz J. Inherited demyelinating neuropathies: Clues to pathogenesis Acta Myologica. 20: 9-20.  0.72
2000 Awatramani R, Beesley J, Yang H, Jiang H, Cambi F, Grinspan J, Garbern J, Kamholz J. Gtx, an oligodendrocyte-specific homeodomain protein, has repressor activity. Journal of Neuroscience Research. 61: 376-87. PMID 10931524 DOI: 10.1002/1097-4547(20000815)61:4<376::AID-JNR4>3.0.CO;2-#  0.72
2000 Jiang H, Duchala CS, Awatramani R, Shumas S, Carlock L, Kamholz J, Garbern J, Scherer SS, Shy ME, Macklin WB. Proteolipid protein mRNA stability is regulated by axonal contact in the rodent peripheral nervous system. Journal of Neurobiology. 44: 7-19. PMID 10880128 DOI: 10.1002/1097-4695(200007)44:1<7::AID-NEU2>3.0.CO;2-A  0.72
2000 Krajewski KM, Lewis RA, Fuerst DR, Turansky C, Hinderer SR, Garbern J, Kamholz J, Shy ME. Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A Brain. 123: 1516-1527. PMID 10869062  0.72
2000 Xu W, Manichella D, Jiang H, Vallat JM, Lilien J, Baron P, Scarlato G, Kamholz J, Shy ME. Absence of P0 leads to the dysregulation of myelin gene expression and myelin morphogenesis. Journal of Neuroscience Research. 60: 714-24. PMID 10861783 DOI: 10.1002/1097-4547(20000615)60:6<714::AID-JNR3>3.0.CO;2-1  0.72
2000 Hodes ME, Woodward K, Spinner NB, Emanuel BS, Enrico-Simon A, Kamholz J, Stambolian D, Zackai EH, Pratt VM, Thomas IT, Crandall K, Dlouhy SR, Malcolm S. Additional copies of the proteolipid protein gene causing Pelizaeus- Merzbacher disease arise by separate integration in to the X chromosome American Journal of Human Genetics. 67: 14-22. PMID 10827108 DOI: 10.1086/302965  0.72
2000 Dyer CA, Kendler A, Jean-Guillaume D, Awatramani R, Lee A, Mason LM, Kamholz J. GFAP-positive and myelin marker-positive glia in normal and pathologic environments. Journal of Neuroscience Research. 60: 412-26. PMID 10797544 DOI: 10.1002/(SICI)1097-4547(20000501)60:3<412::AID-JNR16>3.0.CO;2-E  0.72
2000 Kamholz J, Menichella D, Jani A, Garbern J, Lewis RA, Krajewski KM, Lilien J, Scherer SS, Shy ME. Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapy. Brain : a Journal of Neurology. 123: 222-33. PMID 10648431  0.72
1999 Kamholz J, Awatramani R, Menichella D, Jiang H, Xu W, Shy M. Regulation of Myelin-Specific Gene Expression: Relevance to CMT1. Annals of the New York Academy of Sciences. 883: 91-108. PMID 29086995 DOI: 10.1111/j.1749-6632.1999.tb08572.x  0.48
1999 Shy ME, Kamholz J, Lovelace RE. Introduction to the Third International Symposium on Charcot-Marie-Tooth Disorders. Annals of the New York Academy of Sciences. 883: xiii-xviii. PMID 29086991 DOI: 10.1111/j.1749-6632.1999.tb08559.x  0.4
1999 Krajewski K, Turansky C, Lewis R, Garbern J, Hinderer S, Kamholz J, Shy ME. Correlation between Weakness and Axonal Loss in Patients with CMT1A. Annals of the New York Academy of Sciences. 883: 490-492. PMID 29086958 DOI: 10.1111/j.1749-6632.1999.tb08618.x  0.4
1999 Garbern JY, Cambi F, Lewis R, Shy M, Sima A, Kraft G, Vallat JM, Bosch EP, Hodes ME, Dlouhy S, Raskind W, Bird T, Macklin W, Kamholz J. Peripheral Neuropathy Caused by Proteolipid Protein Gene Mutations. Annals of the New York Academy of Sciences. 883: 351-365. PMID 29086946 DOI: 10.1111/j.1749-6632.1999.tb08597.x  0.4
1999 Menichella DM, Xu W, Jiang H, Sohi J, Vallat JM, Baron P, Kamholz J, Shy M. The Absence of Myelin P0 Protein Produces a Novel Molecular Phenotype in Schwann Cell. Annals of the New York Academy of Sciences. 883: 281-293. PMID 29086945 DOI: 10.1111/j.1749-6632.1999.tb08590.x  0.4
1999 Jani A, Menichella D, Jiang H, Chbihi T, Acsadi G, Kamholz J, Shy ME. Overcoming Cellular Immunity to Prolong Adenoviral-Mediated Gene Expression in Sciatic Nerve. Annals of the New York Academy of Sciences. 883: 397-414. PMID 29086944 DOI: 10.1111/j.1749-6632.1999.tb08601.x  0.4
1999 Tang XM, Beesley JS, Grinspan JB, Seth P, Kamholz J, Cambi F. Cell cycle arrest induced by ectopic expression of p27 is not sufficient to promote oligodendrocyte differentiation Journal of Cellular Biochemistry. 76: 270-279. PMID 10618643 DOI: 10.1002/(SICI)1097-4644(20000201)76:2<270::AID-JCB10>3.0.CO;2-6  0.72
1999 Krajewski K, Turansky C, Lewis R, Garbern J, Hinderer S, Kamholz J, Shy ME. Correlation between weakness and axonal loss in patients with CMT1A Annals of the New York Academy of Sciences. 883: 490-492. PMID 10586281  0.72
1999 Jani A, Menichella D, Jiang H, Chbihi T, Acsadi G, Kamholz J, Shy ME. Overcoming cellular immunity to prolong adenoviral-mediated gene expression in sciatic nerve Annals of the New York Academy of Sciences. 883: 397-414. PMID 10586264  0.72
1999 Garbern JY, Cambi F, Lewis R, Shy M, Sima A, Kraft G, Vallat JM, Bosch EP, Hodes ME, Dlouhy S, Raskind W, Bird T, Macklin W, Kamholz J. Peripheral neuropathy caused by proteolipid protein gene mutations. Annals of the New York Academy of Sciences. 883: 351-65. PMID 10586260  0.72
1999 Menichella DM, Xu W, Jiang H, Sohi J, Vallat JM, Baron P, Kamholz J, Shy M. The absence of myelin P0 protein produces a novel molecular phenotype in Schwann cells. Annals of the New York Academy of Sciences. 883: 281-93. PMID 10586253  0.72
1999 Kamholz J, Awatramani R, Menichella D, Jiang H, Xu W, Shy M. Regulation of myelin-specific gene expression. Relevance to CMT1. Annals of the New York Academy of Sciences. 883: 91-108. PMID 10586235  0.72
1999 Shy ME, Kamholz J, Lovelace RE. Introduction to the third international symposium on Charcot-Marie-Tooth disorders Annals of the New York Academy of Sciences. 883. PMID 10586222  0.72
1999 Garbern J, Cambi F, Shy M, Kamholz J. The molecular pathogenesis of Pelizaeus-Merzbacher disease Archives of Neurology. 56: 1210-1214. PMID 10520936 DOI: 10.1001/archneur.56.10.1210  0.72
1999 Jani A, Menichella D, Jiang H, Chbihi T, Acsadi G, Shy ME, Kamholz J. Modulation of cell-mediated immunity prolongs adenovirus-mediated transgene expression in sciatic nerve Human Gene Therapy. 10: 787-800. PMID 10210146 DOI: 10.1089/10430349950018544  0.72
1998 Taveggia C, Pizzagalli A, Feltri ML, Grinspan JB, Kamholz J, Wrabetz L. MEBA derepresses the proximal myelin basic protein promoter in oligodendrocytes Journal of Biological Chemistry. 273: 27741-27748. PMID 9765312 DOI: 10.1074/jbc.273.42.27741  0.72
1998 Garbay B, Boiron-Sargueil F, Shy M, Chbihi T, Jiang H, Kamholz J, Cassagne C. Regulation of oleoyl-CoA synthesis in the peripheral nervous system: Demonstration of a link with myelin synthesis Journal of Neurochemistry. 71: 1719-1726. PMID 9751207 DOI: 10.1046/j.1471-4159.1998.71041719.x  0.72
1998 Gabrielli O, Coppa GV, Carloni I, Salvolini U, Loevner LA, Overhauser J, Kamholz J, Becker LE. 18q - Syndrome and white matter alterations American Journal of Neuroradiology. 19: 398-399. PMID 9504506  0.72
1998 Wrabetz L, Taveggia C, Feltri ML, Quattrini A, Awatramani R, Scherer SS, Messing A, Kamholz J. A minimal human MBP promoter-lacZ transgene is appropriately regulated in developing brain and after optic enucleation, but not in shiverer mutant mice. Journal of Neurobiology. 34: 10-26. PMID 9469615 DOI: 10.1002/(SICI)1097-4695(199801)34:1<10::AID-NEU2>3.0.CO;2-F  0.72
1997 Ferraresi S, Lorenzetti I, Nemni R, Kamholz J, Feltri ML, Wrabetz L. Toward a transgenic mouse model of remyelination Multiple Sclerosis. 3: 80-83. PMID 9291158  0.72
1997 Awatramani R, Scherer S, Grinspan J, Collarini E, Skoff R, O'Hagan D, Garbern J, Kamholz J. Evidence that the homeodomain protein Gtx is involved in the regulation of oligodendrocyte myelination. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 6657-68. PMID 9254678  0.72
1997 Garbern JY, Cambi F, Tang XM, Sima AA, Vallat JM, Bosch EP, Lewis R, Shy M, Sohi J, Kraft G, Chen KL, Joshi I, Leonard DG, Johnson W, Raskind W, ... ... Kamholz J, et al. Proteolipid protein is necessary in peripheral as well as central myelin. Neuron. 19: 205-18. PMID 9247276 DOI: 10.1016/S0896-6273(00)80360-8  0.72
1997 Shy ME, Arroyo E, Sladky J, Menichella D, Jiang H, Xu W, Kamholz J, Scherer SS. Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP). Journal of Neuropathology and Experimental Neurology. 56: 811-21. PMID 9210878  0.72
1996 Kamholz JA. Regulation of myelin development Multiple Sclerosis (Houndmills, Basingstoke, England). 2: 236-240. PMID 9050362  0.72
1996 Loevner LA, Shapiro RM, Grossman RI, Overhauser J, Kamholz J. White matter changes associated with deletions of the long arm of chromosome 18 (18q- syndrome): A dysmyelinating disorder? American Journal of Neuroradiology. 17: 1843-1848. PMID 8933867  0.72
1996 Shy ME, Shi Y, Wrabetz L, Kamholz J, Scherer SS. Axon-Schwann cell interactions regulate the expression of c-jun in Schwann cells. Journal of Neuroscience Research. 43: 511-25. PMID 8833086 DOI: 10.1002/(SICI)1097-4547(19960301)43:5<511::AID-JNR1>3.0.CO;2-L  0.72
1996 Mahr RN, Moberg PJ, Overhauser J, Strathdee G, Kamholz J, Loevner LA, Campbell H, Zackai EH, Reber ME, Mozley DP, Brown L, Turetsky BI, Shapiro RM. Neuropsychiatry of 18q- syndrome. American Journal of Medical Genetics. 67: 172-8. PMID 8723044 DOI: 10.1002/(SICI)1096-8628(19960409)67:2<172::AID-AJMG7>3.0.CO;2-U  0.72
1995 Wrabetz L, Feltri ML, Kim H, Daston M, Kamholz J, Scherer SS, Ratner N. Regulation of neurofibromin expression in rat sciatic nerve and cultured Schwann cells. Glia. 15: 22-32. PMID 8847098 DOI: 10.1002/glia.440150104  0.72
1995 Strathdee G, Zackai EH, Shapiro R, Kamholz J, Overhauser J. Analysis of clinical variation seen in patients with 18q terminal deletions American Journal of Medical Genetics. 59: 476-483. PMID 8585568 DOI: 10.1002/ajmg.1320590414  0.72
1995 Jacobs AJ, Kamholz J, Selzer ME. The single lamprey neurofilament subunit (NF-180) lacks multiphosphorylation repeats and is expressed selectively in projection neurons. Brain Research. Molecular Brain Research. 29: 43-52. PMID 7770000 DOI: 10.1016/0169-328X(94)00227-6  0.72
1995 Shy ME, Tani M, Shi YJ, Whyatt SA, Chbihi T, Scherer SS, Kamholz J. An adenoviral vector can transfer lacZ expression into Schwann cells in culture and in sciatic nerve. Annals of Neurology. 38: 429-36. PMID 7668829 DOI: 10.1002/ana.410380313  0.72
1994 Scherer SS, Wang DY, Kuhn R, Lemke G, Wrabetz L, Kamholz J. Axons regulate Schwann cell expression of the POU transcription factor SCIP. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 14: 1930-42. PMID 8158248  0.72
1994 Cheng Y, Li X, Kamholz J, Burns FR. Organization of the mouse GP42/Basigin gene: a member of the Ig superfamily Bba - Gene Structure and Expression. 1217: 307-311. PMID 8148376 DOI: 10.1016/0167-4781(94)90290-9  0.72
1994 Kamholz J, Shy M, Scherer S, Yoshikawa H, Nishimura T, Sakoda S, Yanagihara T. Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A [5] Annals of Neurology. 36: 451-452. PMID 8080259 DOI: 10.1002/ana.410360326  0.72
1994 Feltri ML, Scherer SS, Nemni R, Kamholz J, Vogelbacker H, Scott MO, Canal N, Quaranta V, Wrabetz L. Beta 4 integrin expression in myelinating Schwann cells is polarized, developmentally regulated and axonally dependent. Development (Cambridge, England). 120: 1287-301. PMID 8026337  0.72
1994 Scherer SS, Braun PE, Grinspan J, Collarini E, Wang DY, Kamholz J. Differential regulation of the 2',3'-cyclic nucleotide 3'-phosphodiesterase gene during oligodendrocyte development. Neuron. 12: 1363-75. PMID 8011341 DOI: 10.1016/0896-6273(94)90451-0  0.72
1994 Scherer SS, Xu YT, Roling D, Wrabetz L, Feltri ML, Kamholz J. Expression of growth-associated protein-43 kD in Schwann cells is regulated by axon-Schwann cell interactions and cAMP. Journal of Neuroscience Research. 38: 575-89. PMID 7815473 DOI: 10.1002/jnr.490380510  0.72
1994 Baron P, Shy M, Kamholz J, Scarlato G, Pleasure D. Expression of P0 protein mRNA along rat sciatic nerve during development Developmental Brain Research. 83: 285-288. PMID 7535206 DOI: 10.1016/0165-3806(94)00149-9  0.72
1994 Cambi F, Kamholz J. Transcriptional regulation of the rat PLP promoter in primary cultures of oligodendrocytes Neurochemical Research. 19: 1055-1060. PMID 7528350 DOI: 10.1007/BF00968716  0.72
1994 Baron P, Shy M, Honda H, Sessa M, Kamholz J, Pleasure D. Developmental expression of P0 mRNA and P0 protein in the sciatic nerve and the spinal nerve roots of the rat Journal of Neurocytology. 23: 249-257. PMID 7518505 DOI: 10.1007/BF01275529  0.72
1994 Li X, Wrabetz L, Cheng Y, Kamholz J. A novel cyclic AMP response element, CACTTGATC, mediates forskolin induction of the myelin basic protein promoter in the rat Schwannoma line, D6P2T Journal of Neurochemistry. 63: 28-40. PMID 7515947  0.72
1993 Kline AD, White ME, Wapner R, Rojas K, Biesecker LG, Kamholz J, Zackai EH, Muenke M, Scott CI, Overhauser J. Molecular analysis of the 18q- syndrome--and correlation with phenotype. American Journal of Human Genetics. 52: 895-906. PMID 8488839  0.72
1993 Scherer SS, Kamholz J, Jakowlew SB. Axons modulate the expression of transforming growth factor-betas in Schwann cells. Glia. 8: 265-76. PMID 8406683 DOI: 10.1002/glia.440080407  0.72
1993 Grinspan J, Wrabetz L, Kamholz J. Oligodendrocyte maturation and myelin gene expression in PDGF-treated cultures from rat cerebral white matter Journal of Neurocytology. 22: 322-333. PMID 7686214 DOI: 10.1007/BF01195556  0.72
1993 Baron P, Kamholz J, Scherer S, Honda H, Shy M, Scarpini E, Scarlato G, Pleasure D. Appearance of PLP mRNA in Specific Regions of the Developing Rat Lumbosacral Spinal Cord as Revealed by in Situ Hybridization Experimental Neurology. 121: 139-147. PMID 7684334 DOI: 10.1006/exnr.1993.1080  0.72
1993 Wrabetz L, Shumas S, Grinspan J, Feltri ML, Bozyczko D, McMorris FA, Pleasure D, Kamholz J. Analysis of the human MBP promoter in primary cultures of oligodendrocytes: positive and negative cis-acting elements in the proximal MBP promoter mediate oligodendrocyte-specific expression of MBP. Journal of Neuroscience Research. 36: 455-71. PMID 7505842 DOI: 10.1002/jnr.490360412  0.72
1992 Scherer SS, Vogelbacker HH, Kamholz J. Axons modulate the expression of proteolipid protein in the CNS. Journal of Neuroscience Research. 32: 138-48. PMID 1383558 DOI: 10.1002/jnr.490320203  0.72
1992 Kamholz J, Sessa M, Scherer S, Vogelbacker H, Mokuno K, Baron P, Wrabetz L, Shy M, Pleasure D. Structure and expression of proteolipid protein in the peripheral nervous system Journal of Neuroscience Research. 31: 231-244. PMID 1374129 DOI: 10.1002/jnr.490310204  0.72
1992 Feltri ML, Scherer SS, Wrabetz L, Kamholz J, Shy ME. Mitogen-expanded Schwann cells retain the capacity to myelinate regenerating axons after transplantation into rat sciatic nerve. Proceedings of the National Academy of Sciences of the United States of America. 89: 8827-31. PMID 1326765 DOI: 10.1073/PNAS.89.18.8827  0.72
1991 Burns FR, von Kannen S, Guy L, Raper JA, Kamholz J, Chang S. DM-GRASP, a novel immunoglobulin superfamily axonal surface protein that supports neurite extension. Neuron. 7: 209-20. PMID 1873027 DOI: 10.1016/0896-6273(91)90259-3  0.72
1991 Weiss BJ, Kamholz J, Ritter A, Zackai EH, McDonald-McGinn DM, Emanuel B, Fischbeck KH. Segmental spinal muscular atrophy and dermatological findings in a patient with chromosome 18q deletion. Annals of Neurology. 30: 419-23. PMID 1719916 DOI: 10.1002/ana.410300316  0.72
1991 Gutmann DH, Zackai EH, McDonald-McGinn DM, Fischbeck KH, Kamholz J. Oculodentodigital dysplasia syndrome associated with abnormal cerebral white matter. American Journal of Medical Genetics. 41: 18-20. PMID 1659191 DOI: 10.1002/ajmg.1320410106  0.72
1990 Wagner RW, Yoo C, Wrabetz L, Kamholz J, Buchhalter J, Hassan NF, Khalili K, Kim SU, Perussia B, McMorris FA. Double-stranded RNA unwinding and modifying activity is detected ubiquitously in primary tissues and cell lines. Molecular and Cellular Biology. 10: 5586-90. PMID 2398905  0.72
1990 Gutmann DH, Fischbeck KH, Kamholz J. Complicated hereditary spastic paraparesis with cerebral white matter lesions. American Journal of Medical Genetics. 36: 251-7. PMID 2368815 DOI: 10.1002/ajmg.1320360222  0.72
1990 Wrabetz LG, Kia-Noury D, Shumas S, Grinspan J, Pleasure D, Kamholz J. Transcriptional regulation of the human myelin basic protein gene Annals of the New York Academy of Sciences. 605: 354-357.  0.72
1990 Baron P, Shy M, Honda H, Sessa M, Conti G, Feltri ML, Pleasure D, Kamholz J. Distribution of PLP and P0 mRNA during rat peripheral nerve development Annals of the New York Academy of Sciences. 605: 375-376.  0.72
1989 Mokuno K, Kamholz J, Behrman T, Black C, Sessa M, Feinstein D, Lee V, Pleasure D. Neuronal modulation of Schwann cell glial fibrillary acidic protein (GFAP) Journal of Neuroscience Research. 23: 396-405. PMID 2769798  0.72
1989 Tiedeman AA, Keyhani J, Kamholz J, Daum HA, Gots JS, Smith JM. Nucleotide sequence analysis of the purEK operon encoding 5'-phosphoribosyl-5-aminoimidazole carboxylase of Escherichia coli K-12. Journal of Bacteriology. 171: 205-12. PMID 2464576  0.72
1988 Van Obberghen E, Kamholz J, Bishop JG, Zomzely-Neurath C, Lazzarini RA, Lazzarini RA. Human gamma enolase: isolation of a cDNA clone and expression in normal and tumor tissues of human origin. Journal of Neuroscience Research. 19: 450-6. PMID 3385803 DOI: 10.1002/jnr.490190409  0.72
1988 Kamholz J, Toffenetti J, Lazzarini RA. Organization and expression of the human myelin basic protein gene. Journal of Neuroscience Research. 21: 62-70. PMID 2464072 DOI: 10.1002/jnr.490210110  0.72
1987 Bray P, Carter A, Guo V, Puckett C, Kamholz J, Spiegel A, Nirenberg M. Human cDNA clones for an alpha subunit of Gi signal-transduction protein. Proceedings of the National Academy of Sciences of the United States of America. 84: 5115-9. PMID 3110783  0.72
1987 Kamholz J, Spielman R, Gogolin K, Modi W, O'Brien S, Lazzarini R. The human myelin-basic-protein gene: Chromosomal localization and RFLP analysis American Journal of Human Genetics. 40: 365-373. PMID 2437795  0.72
1986 Bray P, Carter A, Simons C, Guo V, Puckett C, Kamholz J, Spiegel A, Nirenberg M. Human cDNA clones for four species of G alpha s signal transduction protein. Proceedings of the National Academy of Sciences of the United States of America. 83: 8893-7. PMID 3024154  0.72
1986 Kamholz J, Keyhani J, Gots JS. Molecular cloning and characterization of the purE operon of Escherichia coli. Gene. 44: 55-62. PMID 3021590 DOI: 10.1016/0378-1119(86)90042-9  0.72
1986 Kamholz J, De Ferra F, Puckett C, Lazzarini R. Identification of three forms of human myelin basic protein by cDNA cloning Proceedings of the National Academy of Sciences of the United States of America. 83: 4962-4966. PMID 2425357  0.72
1985 Kamholz J, Tremblay G. Chickenpox with delayed contralateral hemiparesis caused by cerebral angiitis Annals of Neurology. 18: 358-360. PMID 4051463 DOI: 10.1002/ana.410180317  0.72
1985 de Ferra F, Engh H, Hudson L, Kamholz J, Puckett C, Molineaux S, Lazzarini RA. Alternative splicing accounts for the four forms of myelin basic protein. Cell. 43: 721-7. PMID 2416470 DOI: 10.1016/0092-8674(85)90245-4  0.72
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