| Year |
Citation |
Score |
| 2020 |
Franco A, Dang X, Walton EK, Ho JN, Zablocka B, Ly C, Miller TM, Baloh RH, Shy ME, Yoo AS, Dorn Ii GW. Burst mitofusin activation reverses neuromuscular dysfunction in murine CMT2A. Elife. 9. PMID 33074106 DOI: 10.7554/eLife.61119 |
0.325 |
|
| 2020 |
McCauley ME, O'Rourke JG, Yáñez A, Markman JL, Ho R, Wang X, Chen S, Lall D, Jin M, Muhammad AKMG, Bell S, Landeros J, Valencia V, Harms M, Arditi M, ... ... Baloh RH, et al. C9orf72 in myeloid cells suppresses STING-induced inflammation. Nature. PMID 32814898 DOI: 10.1038/S41586-020-2625-X |
0.351 |
|
| 2019 |
Mukherjee-Clavin B, Mi R, Kern B, Choi IY, Lim H, Oh Y, Lannon B, Kim KJ, Bell S, Hur JK, Hwang W, Che YH, Habib O, Baloh RH, Eggan K, et al. Comparison of three congruent patient-specific cell types for the modelling of a human genetic Schwann-cell disorder. Nature Biomedical Engineering. PMID 30962586 DOI: 10.1038/S41551-019-0381-8 |
0.309 |
|
| 2019 |
Zhou Y, Carmona S, Muhammad AKMG, Bell S, Landeros J, Vazquez M, Ho R, Franco A, Lu B, Dorn GW, Wang S, Lutz CM, Baloh RH. Restoring mitofusin balance prevents axonal degeneration in a Charcot-Marie-Tooth type 2A model. The Journal of Clinical Investigation. 130. PMID 30882371 DOI: 10.1172/Jci124194 |
0.32 |
|
| 2018 |
McCauley ME, Baloh RH. Inflammation in ALS/FTD pathogenesis. Acta Neuropathologica. PMID 30465257 DOI: 10.1007/S00401-018-1933-9 |
0.326 |
|
| 2018 |
Rocha AG, Franco A, Krezel AM, Rumsey JM, Alberti JM, Knight WC, Biris N, Zacharioudakis E, Janetka JW, Baloh RH, Kitsis RN, Mochly-Rosen D, Townsend RR, Gavathiotis E, Dorn GW. MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A. Science (New York, N.Y.). 360: 336-341. PMID 29674596 DOI: 10.1126/Science.Aao1785 |
0.373 |
|
| 2018 |
Muhammad AKMG, Kim K, Epifantseva I, Aghamaleky-Sarvestany A, Simpkinson ME, Carmona S, Landeros J, Bell S, Svaren J, Baloh RH. Cell transplantation strategies for acquired and inherited disorders of peripheral myelin. Annals of Clinical and Translational Neurology. 5: 186-200. PMID 29468179 DOI: 10.1002/Acn3.517 |
0.316 |
|
| 2017 |
Lall D, Baloh RH. Microglia and C9orf72 in neuroinflammation and ALS and frontotemporal dementia. The Journal of Clinical Investigation. PMID 28737506 DOI: 10.1172/Jci90607 |
0.354 |
|
| 2016 |
Ho R, Sances S, Gowing G, Amoroso MW, O'Rourke JG, Sahabian A, Wichterle H, Baloh RH, Sareen D, Svendsen CN. ALS disrupts spinal motor neuron maturation and aging pathways within gene co-expression networks. Nature Neuroscience. PMID 27428653 DOI: 10.1038/Nn.4345 |
0.324 |
|
| 2016 |
O'Rourke JG, Bogdanik L, Yáñez A, Lall D, Wolf AJ, Muhammad AK, Ho R, Carmona S, Vit JP, Zarrow J, Kim KJ, Bell S, Harms MB, Miller TM, Dangler CA, ... ... Baloh RH, et al. C9orf72 is required for proper macrophage and microglial function in mice. Science (New York, N.Y.). 351: 1324-9. PMID 26989253 DOI: 10.1126/Science.Aaf1064 |
0.381 |
|
| 2015 |
Albulym OM, Kennerson ML, Harms MB, Drew AP, Siddell AH, Auer-Grumbach M, Pestronk A, Connolly A, Baloh RH, Zuchner S, Reddel SW, Nicholson GA. MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs. Annals of Neurology. PMID 26659848 DOI: 10.1002/Ana.24575 |
0.374 |
|
| 2015 |
O'Rourke JG, Bogdanik L, Muhammad AK, Gendron TF, Kim KJ, Austin A, Cady J, Liu EY, Zarrow J, Grant S, Ho R, Bell S, Carmona S, Simpkinson M, Lall D, ... ... Baloh RH, et al. C9orf72 BAC Transgenic Mice Display Typical Pathologic Features of ALS/FTD. Neuron. 88: 892-901. PMID 26637796 DOI: 10.1016/J.Neuron.2015.10.027 |
0.327 |
|
| 2015 |
Gan JJ, Garcia V, Tian J, Tagliati M, Parisi JE, Chung JM, Lewis R, Baloh R, Levade T, Pierson TM. Acid ceramidase deficiency associated with spinal muscular atrophy with progressive myoclonic epilepsy. Neuromuscular Disorders : Nmd. PMID 26526000 DOI: 10.1016/J.Nmd.2015.09.007 |
0.339 |
|
| 2015 |
Zhao W, Beers DR, Bell S, Wang J, Wen S, Baloh RH, Appel SH. TDP-43 activates microglia through NF-κB and NLRP3 inflammasome. Experimental Neurology. 273: 24-35. PMID 26222336 DOI: 10.1016/J.Expneurol.2015.07.019 |
0.355 |
|
| 2015 |
Cirulli ET, Lasseigne BN, Petrovski S, Sapp PC, Dion PA, Leblond CS, Couthouis J, Lu YF, Wang Q, Krueger BJ, Ren Z, Keebler J, Han Y, Levy SE, Boone BE, ... ... Baloh RH, et al. Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways. Science (New York, N.Y.). 347: 1436-41. PMID 25700176 DOI: 10.1126/Science.Aaa3650 |
0.311 |
|
| 2015 |
Weihl CC, Baloh RH, Lee Y, Chou TF, Pittman SK, Lopate G, Allred P, Jockel-Balsarotti J, Pestronk A, Harms MB. Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis. Neuromuscular Disorders : Nmd. 25: 289-96. PMID 25617006 DOI: 10.1016/J.Nmd.2014.12.009 |
0.339 |
|
| 2015 |
Scoto M, Rossor AM, Harms MB, Cirak S, Calissano M, Robb S, Manzur AY, MartÃnez Arroyo A, Rodriguez Sanz A, Mansour S, Fallon P, Hadjikoumi I, Klein A, Yang M, De Visser M, ... ... Baloh RH, et al. Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy. Neurology. 84: 668-79. PMID 25609763 DOI: 10.1212/Wnl.0000000000001269 |
0.305 |
|
| 2015 |
Weihl CC, Iyadurai S, Baloh RH, Pittman SK, Schmidt RE, Lopate G, Pestronk A, Harms MB. Autophagic vacuolar pathology in desminopathies. Neuromuscular Disorders : Nmd. 25: 199-206. PMID 25557463 DOI: 10.1016/J.Nmd.2014.12.002 |
0.362 |
|
| 2014 |
Johnson JO, Pioro EP, Boehringer A, Chia R, Feit H, Renton AE, Pliner HA, Abramzon Y, Marangi G, Winborn BJ, Gibbs JR, Nalls MA, Morgan S, Shoai M, Hardy J, ... ... Baloh RH, et al. Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. Nature Neuroscience. 17: 664-6. PMID 24686783 DOI: 10.1038/Nn.3688 |
0.374 |
|
| 2013 |
Sumner CJ, d'Ydewalle C, Wooley J, Fawcett KA, Hernandez D, Gardiner AR, Kalmar B, Baloh RH, Gonzalez M, Züchner S, Stanescu HC, Kleta R, Mankodi A, Cornblath DR, Boylan KB, et al. A dominant mutation in FBXO38 causes distal spinal muscular atrophy with calf predominance. American Journal of Human Genetics. 93: 976-83. PMID 24207122 DOI: 10.1016/J.Ajhg.2013.10.006 |
0.442 |
|
| 2013 |
Harms MB, Baloh RH. Clinical neurogenetics: amyotrophic lateral sclerosis. Neurologic Clinics. 31: 929-50. PMID 24176417 DOI: 10.1016/J.Ncl.2013.05.003 |
0.313 |
|
| 2013 |
Sareen D, O'Rourke JG, Meera P, Muhammad AK, Grant S, Simpkinson M, Bell S, Carmona S, Ornelas L, Sahabian A, Gendron T, Petrucelli L, Baughn M, Ravits J, Harms MB, ... ... Baloh RH, et al. Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion. Science Translational Medicine. 5: 208ra149. PMID 24154603 DOI: 10.1126/Scitranslmed.3007529 |
0.35 |
|
| 2013 |
Eschbach J, Sinniger J, Bouitbir J, Fergani A, Schlagowski AI, Zoll J, Geny B, René F, Larmet Y, Marion V, Baloh RH, Harms MB, Shy ME, Messadeq N, Weydt P, et al. Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age. Neurobiology of Disease. 58: 220-30. PMID 23742762 DOI: 10.1016/J.Nbd.2013.05.015 |
0.377 |
|
| 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 |
0.383 |
|
| 2013 |
Harms MB, Cady J, Zaidman C, Cooper P, Bali T, Allred P, Cruchaga C, Baughn M, Libby RT, Pestronk A, Goate A, Ravits J, Baloh RH. Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis. Neurobiology of Aging. 34: 2234.e13-9. PMID 23597494 DOI: 10.1016/J.Neurobiolaging.2013.03.006 |
0.334 |
|
| 2013 |
Scoto M, Rossor A, Harms MB, Calissano M, Cirak S, Foley AR, Sewry C, Hafezparast M, Robb S, Manzur AY, Baloh RH, Reilly MM, Muntoni F. P.6.7 Wide phenotypic spectrum of SMA with lower limbs predominance due to mutations in the tail domain of DYNC1H1 gene: A case series Neuromuscular Disorders. 23: 772. DOI: 10.1016/J.Nmd.2013.06.478 |
0.35 |
|
| 2013 |
Bengoechea R, Tuck EP, Stein KC, Pittman SK, Baloh RH, True HL, Harms MB, Weihl CC. P.5.11 LGMD1D mutations in DNAJB6 disrupt disaggregation of TDP-43 Neuromuscular Disorders. 23: 767. DOI: 10.1016/J.Nmd.2013.06.463 |
0.327 |
|
| 2013 |
Harms MB, Kakkis E, Allred P, Hilliard JK, Cooper P, Florence J, Baloh RH, Pestronk A, Weihl CC. P.3.5 Identification of rare variants in GNE and other sialic biosynthetic genes in HIBM2 and sIBM Neuromuscular Disorders. 23: 756-757. DOI: 10.1016/J.Nmd.2013.06.430 |
0.323 |
|
| 2012 |
Harms MB, Ori-McKenney KM, Scoto M, Tuck EP, Bell S, Ma D, Masi S, Allred P, Al-Lozi M, Reilly MM, Miller LJ, Jani-Acsadi A, Pestronk A, Shy ME, Muntoni F, ... ... Baloh RH, et al. Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy. Neurology. 78: 1714-20. PMID 22459677 DOI: 10.1212/Wnl.0B013E3182556C05 |
0.354 |
|
| 2012 |
Misko AL, Sasaki Y, Tuck E, Milbrandt J, Baloh RH. Mitofusin2 mutations disrupt axonal mitochondrial positioning and promote axon degeneration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 4145-55. PMID 22442078 DOI: 10.1523/Jneurosci.6338-11.2012 |
0.564 |
|
| 2011 |
Beirowski B, Gustin J, Armour SM, Yamamoto H, Viader A, North BJ, Michán S, Baloh RH, Golden JP, Schmidt RE, Sinclair DA, Auwerx J, Milbrandt J. Sir-two-homolog 2 (Sirt2) modulates peripheral myelination through polarity protein Par-3/atypical protein kinase C (aPKC) signaling. Proceedings of the National Academy of Sciences of the United States of America. 108: E952-61. PMID 21949390 DOI: 10.1073/Pnas.1104969108 |
0.746 |
|
| 2011 |
Ritz D, Vuk M, Kirchner P, Bug M, Schütz S, Hayer A, Bremer S, Lusk C, Baloh RH, Lee H, Glatter T, Gstaiger M, Aebersold R, Weihl CC, Meyer H. Endolysosomal sorting of ubiquitylated caveolin-1 is regulated by VCP and UBXD1 and impaired by VCP disease mutations. Nature Cell Biology. 13: 1116-23. PMID 21822278 DOI: 10.1038/Ncb2301 |
0.366 |
|
| 2011 |
Baloh RH. TDP-43: the relationship between protein aggregation and neurodegeneration in amyotrophic lateral sclerosis and frontotemporal lobar degeneration. The Febs Journal. 278: 3539-49. PMID 21777387 DOI: 10.1111/J.1742-4658.2011.08256.X |
0.356 |
|
| 2011 |
Viader A, Golden JP, Baloh RH, Schmidt RE, Hunter DA, Milbrandt J. Schwann cell mitochondrial metabolism supports long-term axonal survival and peripheral nerve function. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 10128-40. PMID 21752989 DOI: 10.1523/Jneurosci.0884-11.2011 |
0.75 |
|
| 2011 |
Udan M, Baloh RH. Implications of the prion-related Q/N domains in TDP-43 and FUS. Prion. 5: 1-5. PMID 21135580 DOI: 10.4161/Pri.5.1.14265 |
0.361 |
|
| 2011 |
Weihl CC, Miller SE, Zaidman CM, Pestronk A, Baloh RH, Al-Lozi M. Novel GNE mutations in two phenotypically distinct HIBM2 patients. Neuromuscular Disorders : Nmd. 21: 102-5. PMID 21131200 DOI: 10.1016/J.Nmd.2010.11.002 |
0.315 |
|
| 2011 |
Wegorzewska I, Baloh RH. TDP-43-based animal models of neurodegeneration: new insights into ALS pathology and pathophysiology. Neuro-Degenerative Diseases. 8: 262-74. PMID 21124004 DOI: 10.1159/000321547 |
0.347 |
|
| 2010 |
Harms MB, Allred P, Gardner R, Fernandes Filho JA, Florence J, Pestronk A, Al-Lozi M, Baloh RH. Dominant spinal muscular atrophy with lower extremity predominance: linkage to 14q32. Neurology. 75: 539-46. PMID 20697106 DOI: 10.1212/Wnl.0B013E3181Ec800C |
0.309 |
|
| 2010 |
Fuentealba RA, Udan M, Bell S, Wegorzewska I, Shao J, Diamond MI, Weihl CC, Baloh RH. Interaction with polyglutamine aggregates reveals a Q/N-rich domain in TDP-43. The Journal of Biological Chemistry. 285: 26304-14. PMID 20554523 DOI: 10.1074/Jbc.M110.125039 |
0.315 |
|
| 2010 |
Misko A, Jiang S, Wegorzewska I, Milbrandt J, Baloh RH. Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 4232-40. PMID 20335458 DOI: 10.1523/Jneurosci.6248-09.2010 |
0.556 |
|
| 2010 |
Lopate G, Baloh RH, Al-Lozi MT, Miller TM, Fernandes Filho JA, Ni O, Leston A, Florence J, Schierbecker J, Allred P. Familial ALS with extreme phenotypic variability due to the I113T SOD1 mutation. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 11: 232-6. PMID 20184521 DOI: 10.3109/17482960902898069 |
0.325 |
|
| 2009 |
Ju JS, Fuentealba RA, Miller SE, Jackson E, Piwnica-Worms D, Baloh RH, Weihl CC. Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease. The Journal of Cell Biology. 187: 875-88. PMID 20008565 DOI: 10.1083/Jcb.200908115 |
0.341 |
|
| 2009 |
Wegorzewska I, Bell S, Cairns NJ, Miller TM, Baloh RH. TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration. Proceedings of the National Academy of Sciences of the United States of America. 106: 18809-14. PMID 19833869 DOI: 10.1073/Pnas.0908767106 |
0.389 |
|
| 2009 |
Chang J, Baloh RH, Milbrandt J. The NIMA-family kinase Nek3 regulates microtubule acetylation in neurons. Journal of Cell Science. 122: 2274-82. PMID 19509051 DOI: 10.1242/Jcs.048975 |
0.536 |
|
| 2009 |
Sasaki Y, Vohra BP, Baloh RH, Milbrandt J. Transgenic mice expressing the Nmnat1 protein manifest robust delay in axonal degeneration in vivo. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 6526-34. PMID 19458223 DOI: 10.1523/Jneurosci.1429-09.2009 |
0.577 |
|
| 2009 |
Baloh RH, Strickland A, Ryu E, Le N, Fahrner T, Yang M, Nagarajan R, Milbrandt J. Congenital hypomyelinating neuropathy with lethal conduction failure in mice carrying the Egr2 I268N mutation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 2312-21. PMID 19244508 DOI: 10.1523/Jneurosci.2168-08.2009 |
0.75 |
|
| 2008 |
Gitcho MA, Baloh RH, Chakraverty S, Mayo K, Norton JB, Levitch D, Hatanpaa KJ, White CL, Bigio EH, Caselli R, Baker M, Al-Lozi MT, Morris JC, Pestronk A, Rademakers R, et al. TDP-43 A315T mutation in familial motor neuron disease. Annals of Neurology. 63: 535-8. PMID 18288693 DOI: 10.1002/Ana.21344 |
0.371 |
|
| 2008 |
Baloh RH. Mitochondrial dynamics and peripheral neuropathy. The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry. 14: 12-8. PMID 17911220 DOI: 10.1177/1073858407307354 |
0.396 |
|
| 2008 |
Gitcho MA, Baloh RH, Chakraverty S, Mayo K, Norton JB, Levitch D, Hatanpaa KJ, White CH, Bigio EH, Caselli R, Baker M, Al-Lozi MT, Morris JC, Pestronk A, Rademakers R, et al. P3-287: TDP-43 A315T mutation in familial motor neuron disease Alzheimer's & Dementia. 4: T606-T607. DOI: 10.1016/J.Jalz.2008.05.1855 |
0.341 |
|
| 2007 |
Ryu EJ, Wang JY, Le N, Baloh RH, Gustin JA, Schmidt RE, Milbrandt J. Misexpression of Pou3f1 results in peripheral nerve hypomyelination and axonal loss. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 11552-9. PMID 17959798 DOI: 10.1523/Jneurosci.5497-06.2007 |
0.724 |
|
| 2007 |
Baloh RH, Salavaggione E, Milbrandt J, Pestronk A. Familial parkinsonism and ophthalmoplegia from a mutation in the mitochondrial DNA helicase twinkle. Archives of Neurology. 64: 998-1000. PMID 17620490 DOI: 10.1001/Archneur.64.7.998 |
0.531 |
|
| 2007 |
Baloh RH, Rakowicz W, Gardner R, Pestronk A. Frequent atrophic groups with mixed-type myofibers is distinctive to motor neuron syndromes. Muscle & Nerve. 36: 107-10. PMID 17299742 DOI: 10.1002/Mus.20755 |
0.305 |
|
| 2007 |
Baloh RH, Schmidt RE, Pestronk A, Milbrandt J. Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 422-30. PMID 17215403 DOI: 10.1523/Jneurosci.4798-06.2007 |
0.598 |
|
| 2006 |
Wang X, Baloh RH, Milbrandt J, Garcia KC. Structure of artemin complexed with its receptor GFRalpha3: convergent recognition of glial cell line-derived neurotrophic factors. Structure (London, England : 1993). 14: 1083-92. PMID 16765900 DOI: 10.1016/J.Str.2006.05.010 |
0.52 |
|
| 2006 |
Baloh R, Milbrandt J, Pestronk A. N.P.3 06 In vitro analysis of MFN2 mutations associated with Charcot-Marie-Tooth disease Neuromuscular Disorders. 16: 666. DOI: 10.1016/J.Nmd.2006.05.082 |
0.431 |
|
| 2004 |
Enomoto H, Hughes I, Golden J, Baloh RH, Yonemura S, Heuckeroth RO, Johnson EM, Milbrandt J. GFRalpha1 expression in cells lacking RET is dispensable for organogenesis and nerve regeneration. Neuron. 44: 623-36. PMID 15541311 DOI: 10.1016/J.Neuron.2004.10.032 |
0.567 |
|
| 2000 |
Tansey MG, Baloh RH, Milbrandt J, Johnson EM. GFRalpha-mediated localization of RET to lipid rafts is required for effective downstream signaling, differentiation, and neuronal survival. Neuron. 25: 611-23. PMID 10774729 DOI: 10.1016/S0896-6273(00)81064-8 |
0.504 |
|
| 2000 |
Baloh RH, Enomoto H, Johnson EM, Milbrandt J. The GDNF family ligands and receptors - implications for neural development. Current Opinion in Neurobiology. 10: 103-10. PMID 10679429 DOI: 10.1016/S0959-4388(99)00048-3 |
0.544 |
|
| 2000 |
Baloh RH, Tansey MG, Johnson EM, Milbrandt J. Functional mapping of receptor specificity domains of glial cell line-derived neurotrophic factor (GDNF) family ligands and production of GFRalpha1 RET-specific agonists. The Journal of Biological Chemistry. 275: 3412-20. PMID 10652334 DOI: 10.1074/Jbc.275.5.3412 |
0.54 |
|
| 1998 |
Baloh RH, Tansey MG, Lampe PA, Fahrner TJ, Enomoto H, Simburger KS, Leitner ML, Araki T, Johnson EM, Milbrandt J. Artemin, a novel member of the GDNF ligand family, supports peripheral and central neurons and signals through the GFRalpha3-RET receptor complex. Neuron. 21: 1291-302. PMID 9883723 DOI: 10.1016/S0896-6273(00)80649-2 |
0.543 |
|
| 1998 |
Golden JP, Baloh RH, Kotzbauer PT, Lampe PA, Osborne PA, Milbrandt J, Johnson EM. Expression of neurturin, GDNF, and their receptors in the adult mouse CNS. The Journal of Comparative Neurology. 398: 139-50. PMID 9703032 DOI: 10.1002/(Sici)1096-9861(19980817)398:1<139::Aid-Cne9>3.0.Co;2-2 |
0.542 |
|
| 1998 |
Baloh RH, Gorodinsky A, Golden JP, Tansey MG, Keck CL, Popescu NC, Johnson EM, Milbrandt J. GFRalpha3 is an orphan member of the GDNF/neurturin/persephin receptor family. Proceedings of the National Academy of Sciences of the United States of America. 95: 5801-6. PMID 9576965 DOI: 10.1073/Pnas.95.10.5801 |
0.545 |
|
| 1998 |
Milbrandt J, de Sauvage FJ, Fahrner TJ, Baloh RH, Leitner ML, Tansey MG, Lampe PA, Heuckeroth RO, Kotzbauer PT, Simburger KS, Golden JP, Davies JA, Vejsada R, Kato AC, Hynes M, et al. Persephin, a novel neurotrophic factor related to GDNF and neurturin. Neuron. 20: 245-53. PMID 9491986 DOI: 10.1016/S0896-6273(00)80453-5 |
0.549 |
|
| 1997 |
Creedon DJ, Tansey MG, Baloh RH, Osborne PA, Lampe PA, Fahrner TJ, Heuckeroth RO, Milbrandt J, Johnson EM. Neurturin shares receptors and signal transduction pathways with glial cell line-derived neurotrophic factor in sympathetic neurons. Proceedings of the National Academy of Sciences of the United States of America. 94: 7018-23. PMID 9192684 DOI: 10.1073/Pnas.94.13.7018 |
0.535 |
|
| 1997 |
Baloh RH, Tansey MG, Golden JP, Creedon DJ, Heuckeroth RO, Keck CL, Zimonjic DB, Popescu NC, Johnson EM, Milbrandt J. TrnR2, a novel receptor that mediates neurturin and GDNF signaling through Ret. Neuron. 18: 793-802. PMID 9182803 DOI: 10.1016/S0896-6273(00)80318-9 |
0.536 |
|
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