| Year |
Citation |
Score |
| 2023 |
Elziny S, Sran S, Yoon H, Corrigan RR, Page J, Ringland A, Lanier A, Lapidus S, Foreman J, Heinzen EL, Iffland P, Crino PB, Bedrosian TA. Loss of alters development of the mouse cerebral cortex. Biorxiv : the Preprint Server For Biology. PMID 38077069 DOI: 10.1101/2023.11.29.569243 |
0.318 |
|
| 2022 |
Iffland PH, Everett ME, Cobb-Pitstick KM, Bowser LE, Barnes AE, Babus JK, Romanowski AJ, Baybis M, Elziny S, Puffenberger EG, Gonzaga-Jauregui C, Poulopoulos A, Carson VJ, Crino PB. NPRL3 loss alters neuronal morphology, mTOR localization, cortical lamination, and seizure threshold. Brain : a Journal of Neurology. PMID 35136953 DOI: 10.1093/brain/awac044 |
0.322 |
|
| 2022 |
Terry BK, Park R, Cho SH, Crino PB, Kim S. Abnormal activation of yap/Taz contributes to the pathogenesis of tuberous sclerosis complex. Human Molecular Genetics. PMID 34999833 DOI: 10.1093/hmg/ddab374 |
0.305 |
|
| 2021 |
Dang LT, Vaid S, Lin G, Swaminathan P, Safran J, Loughman A, Lee M, Glenn T, Majolo F, Crino PB, Parent JM. STRADA-mutant human cortical organoids model megalencephaly and exhibit delayed neuronal differentiation. Developmental Neurobiology. PMID 33619909 DOI: 10.1002/dneu.22816 |
0.312 |
|
| 2020 |
Dang LT, Glanowska KM, Iffland Ii PH, Barnes AE, Baybis M, Liu Y, Patino G, Vaid S, Streicher AM, Parker WE, Kim S, Moon UY, Henry FE, Murphy GG, Sutton M, ... ... Crino PB, et al. Multimodal Analysis of STRADA Function in Brain Development. Frontiers in Cellular Neuroscience. 14: 122. PMID 32457579 DOI: 10.3389/Fncel.2020.00122 |
0.658 |
|
| 2018 |
Iffland PH, Baybis M, Barnes AE, Leventer RJ, Lockhart PJ, Crino PB. DEPDC5 and NPRL3 modulate cell size, filopodial outgrowth, and localization of mTOR in neural progenitor cells and neurons. Neurobiology of Disease. PMID 29481864 DOI: 10.1016/j.nbd.2018.02.013 |
0.341 |
|
| 2017 |
Iffland PH, Crino PB. Focal Cortical Dysplasia: Gene Mutations, Cell Signaling, and Therapeutic Implications. Annual Review of Pathology. 12: 547-571. PMID 28135561 DOI: 10.1146/annurev-pathol-052016-100138 |
0.31 |
|
| 2016 |
Liu C, Russin J, Heck C, Kawata K, Adiga R, Yen W, Lambert J, Stear B, Law M, Marquez Y, Crino P, Millett D, Langford D. Dysregulation of PINCH signaling in mesial temporal epilepsy. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. PMID 27838154 DOI: 10.1016/j.jocn.2016.10.012 |
0.385 |
|
| 2016 |
Crino PB. The mTOR signalling cascade: paving new roads to cure neurological disease. Nature Reviews. Neurology. PMID 27340022 DOI: 10.1038/nrneurol.2016.81 |
0.308 |
|
| 2016 |
Bhoj EJ, Li D, Harr M, Edvardson S, Elpeleg O, Chisholm E, Juusola J, Douglas G, Guillen Sacoto MJ, Siquier-Pernet K, Saadi A, Bole-Feysot C, Nitschke P, Narravula A, Walke M, ... ... Crino P, et al. Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia. American Journal of Human Genetics. PMID 27040691 DOI: 10.1016/J.Ajhg.2016.03.016 |
0.374 |
|
| 2015 |
Jinks RN, Puffenberger EG, Baple E, Harding B, Crino P, Fogo AB, Wenger O, Xin B, Koehler AE, McGlincy MH, Provencher MM, Smith JD, Tran L, Al Turki S, Chioza BA, et al. Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73. Brain : a Journal of Neurology. 138: 2173-90. PMID 26070982 DOI: 10.1093/Brain/Awv153 |
0.333 |
|
| 2015 |
Crino PB. mTOR signaling in epilepsy: insights from malformations of cortical development. Cold Spring Harbor Perspectives in Medicine. 5. PMID 25833943 DOI: 10.1101/cshperspect.a022442 |
0.336 |
|
| 2014 |
Tsai V, Parker WE, Orlova KA, Baybis M, Chi AW, Berg BD, Birnbaum JF, Estevez J, Okochi K, Sarnat HB, Flores-Sarnat L, Aronica E, Crino PB. Fetal brain mTOR signaling activation in tuberous sclerosis complex. Cerebral Cortex (New York, N.Y. : 1991). 24: 315-27. PMID 23081885 DOI: 10.1093/Cercor/Bhs310 |
0.747 |
|
| 2013 |
Parker WE, Orlova KA, Parker WH, Birnbaum JF, Krymskaya VP, Goncharov DA, Baybis M, Helfferich J, Okochi K, Strauss KA, Crino PB. Rapamycin prevents seizures after depletion of STRADA in a rare neurodevelopmental disorder. Science Translational Medicine. 5: 182ra53. PMID 23616120 DOI: 10.1126/Scitranslmed.3005271 |
0.757 |
|
| 2012 |
Sarnat H, Flores-Sarnat L, Crino P, Hader W, Bello-Espinosa L. Hemimegalencephaly: foetal tauopathy with mTOR hyperactivation and neuronal lipidosis. Folia Neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences. 50: 330-45. PMID 23319189 DOI: 10.5114/fn.2012.32363 |
0.411 |
|
| 2012 |
Chen J, Tsai V, Parker WE, Aronica E, Baybis M, Crino PB. Detection of human papillomavirus in human focal cortical dysplasia type IIB. Annals of Neurology. 72: 881-92. PMID 23280839 DOI: 10.1002/Ana.23795 |
0.732 |
|
| 2012 |
Marcotte L, Aronica E, Baybis M, Crino PB. Cytoarchitectural alterations are widespread in cerebral cortex in tuberous sclerosis complex. Acta Neuropathologica. 123: 685-93. PMID 22327361 DOI: 10.1007/s00401-012-0950-3 |
0.341 |
|
| 2011 |
Parker WE, Orlova KA, Heuer GG, Baybis M, Aronica E, Frost M, Wong M, Crino PB. Enhanced epidermal growth factor, hepatocyte growth factor, and vascular endothelial growth factor expression in tuberous sclerosis complex. The American Journal of Pathology. 178: 296-305. PMID 21224066 DOI: 10.1016/J.Ajpath.2010.11.031 |
0.736 |
|
| 2011 |
Blümcke I, Thom M, Aronica E, Armstrong DD, Vinters HV, Palmini A, Jacques TS, Avanzini G, Barkovich AJ, Battaglia G, Becker A, Cepeda C, Cendes F, Colombo N, Crino P, et al. The clinicopathologic spectrum of focal cortical dysplasias: a consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission. Epilepsia. 52: 158-74. PMID 21219302 DOI: 10.1111/J.1528-1167.2010.02777.X |
0.316 |
|
| 2010 |
Orlova KA, Tsai V, Baybis M, Heuer GG, Sisodiya S, Thom M, Strauss K, Aronica E, Storm PB, Crino PB. Early progenitor cell marker expression distinguishes type II from type I focal cortical dysplasias. Journal of Neuropathology and Experimental Neurology. 69: 850-63. PMID 20613634 DOI: 10.1097/Nen.0B013E3181Eac1F5 |
0.748 |
|
| 2010 |
Orlova KA, Parker WE, Heuer GG, Tsai V, Yoon J, Baybis M, Fenning RS, Strauss K, Crino PB. STRADalpha deficiency results in aberrant mTORC1 signaling during corticogenesis in humans and mice. The Journal of Clinical Investigation. 120: 1591-602. PMID 20424326 DOI: 10.1172/Jci41592 |
0.759 |
|
| 2010 |
Orlova KA, Crino PB. The tuberous sclerosis complex. Annals of the New York Academy of Sciences. 1184: 87-105. PMID 20146692 DOI: 10.1111/J.1749-6632.2009.05117.X |
0.749 |
|
| 2008 |
Boer K, Troost D, Jansen F, Nellist M, van den Ouweland AM, Geurts JJ, Spliet WG, Crino P, Aronica E. Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 28: 577-90. PMID 18410267 DOI: 10.1111/J.1440-1789.2008.00920.X |
0.391 |
|
| 2007 |
Crino PB. Focal brain malformations: a spectrum of disorders along the mTOR cascade. Novartis Foundation Symposium. 288: 260-72; discussion 2. PMID 18494264 DOI: 10.1002/9780470994030.ch18 |
0.321 |
|
| 2007 |
Gilby KL, Crino P, McIntyre DC. Neurodevelopment in seizure-prone and seizure-resistant rat strains: recognizing conflicts in management. Epilepsia. 48: 114-8. PMID 17910590 DOI: 10.1111/j.1528-1167.2007.01298.x |
0.326 |
|
| 2007 |
Lamparello P, Baybis M, Pollard J, Hol EM, Eisenstat DD, Aronica E, Crino PB. Developmental lineage of cell types in cortical dysplasia with balloon cells. Brain : a Journal of Neurology. 130: 2267-76. PMID 17711980 DOI: 10.1093/brain/awm175 |
0.327 |
|
| 2007 |
Boer K, Troost D, Spliet WG, Redeker S, Crino PB, Aronica E. A neuropathological study of two autopsy cases of syndromic hemimegalencephaly. Neuropathology and Applied Neurobiology. 33: 455-70. PMID 17617874 DOI: 10.1111/J.1365-2990.2006.00818.X |
0.302 |
|
| 2007 |
Aronica E, Boer K, Baybis M, Yu J, Crino P. Co-expression of cyclin D1 and phosphorylated ribosomal S6 proteins in hemimegalencephaly. Acta Neuropathologica. 114: 287-93. PMID 17483958 DOI: 10.1007/s00401-007-0225-6 |
0.382 |
|
| 2006 |
Marcotte L, Crino PB. The neurobiology of the tuberous sclerosis complex. Neuromolecular Medicine. 8: 531-46. PMID 17028374 DOI: 10.1385/NMM:8:4:531 |
0.329 |
|
| 2004 |
Crino PB. Molecular pathogenesis of tuber formation in tuberous sclerosis complex. Journal of Child Neurology. 19: 716-25. PMID 15563019 |
0.346 |
|
| 2004 |
Ess KC, Uhlmann EJ, Li W, Li H, Declue JE, Crino PB, Gutmann DH. Expression profiling in tuberous sclerosis complex (TSC) knockout mouse astrocytes to characterize human TSC brain pathology. Glia. 46: 28-40. PMID 14999811 DOI: 10.1002/Glia.10324 |
0.334 |
|
| 2003 |
Hua Y, Crino PB. Single cell lineage analysis in human focal cortical dysplasia. Cerebral Cortex (New York, N.Y. : 1991). 13: 693-9. PMID 12764046 DOI: 10.1093/cercor/13.6.693 |
0.302 |
|
| 2002 |
Onda H, Crino PB, Zhang H, Murphey RD, Rastelli L, Gould Rothberg BE, Kwiatkowski DJ. Tsc2 null murine neuroepithelial cells are a model for human tuber giant cells, and show activation of an mTOR pathway. Molecular and Cellular Neurosciences. 21: 561-74. PMID 12504590 DOI: 10.1006/mcne.2002.1184 |
0.343 |
|
| 2001 |
Eberwine J, Crino P. Analysis of mRNA populations from single live and fixed cells of the central nervous system. Current Protocols in Neuroscience / Editorial Board, Jacqueline N. Crawley ... [Et Al.]. Unit 5.3. PMID 18428502 DOI: 10.1002/0471142301.ns0503s00 |
0.566 |
|
| 2001 |
Taylor JP, Sater R, French J, Baltuch G, Crino PB. Transcription of intermediate filament genes is enhanced in focal cortical dysplasia. Acta Neuropathologica. 102: 141-8. PMID 11563628 |
0.307 |
|
| 2000 |
Kacharmina JE, Job C, Crino P, Eberwine J. Stimulation of glutamate receptor protein synthesis and membrane insertion within isolated neuronal dendrites. Proceedings of the National Academy of Sciences of the United States of America. 97: 11545-50. PMID 11027353 DOI: 10.1073/pnas.97.21.11545 |
0.573 |
|
| 2000 |
O'Dell DM, Raghupathi R, Crino PB, Eberwine JH, McIntosh TK. Traumatic brain injury alters the molecular fingerprint of TUNEL-positive cortical neurons In vivo: A single-cell analysis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 20: 4821-8. PMID 10864939 DOI: 10.1523/Jneurosci.20-13-04821.2000 |
0.574 |
|
| 1999 |
Kacharmina JE, Crino PB, Eberwine J. Preparation of cDNA from single cells and subcellular regions. Methods in Enzymology. 303: 3-18. PMID 10349635 DOI: 10.1016/S0076-6879(99)03003-7 |
0.568 |
|
| 1999 |
Ginsberg SD, Crino PB, Hemby SE, Weingarten JA, Lee VM, Eberwine JH, Trojanowski JQ. Predominance of neuronal mRNAs in individual Alzheimer's disease senile plaques. Annals of Neurology. 45: 174-81. PMID 9989619 DOI: 10.1002/1531-8249(199902)45:2<174::Aid-Ana7>3.0.Co;2-E |
0.686 |
|
| 1998 |
O'Dell DM, Raghupathi R, Crino PB, Morrison B, Eberwine JH, McIntosh TK. Amplification of mRNAs from single, fixed, TUNEL-positive cells. Biotechniques. 25: 566-8, 570. PMID 9793634 DOI: 10.2144/98254Bm04 |
0.507 |
|
| 1998 |
Crino P, Khodakhah K, Becker K, Ginsberg S, Hemby S, Eberwine J. Presence and phosphorylation of transcription factors in developing dendrites. Proceedings of the National Academy of Sciences of the United States of America. 95: 2313-8. PMID 9482882 DOI: 10.1073/pnas.95.5.2313 |
0.715 |
|
| 1997 |
Crino PB, Eberwine J. Cellular and molecular basis of cerebral dysgenesis. Journal of Neuroscience Research. 50: 907-16. PMID 9452005 DOI: 10.1002/(SICI)1097-4547(19971215)50:6<907::AID-JNR1>3.0.CO;2-H |
0.505 |
|
| 1997 |
Crino PB, Trojanowski JQ, Eberwine J. Internexin, MAP1B, and nestin in cortical dysplasia as markers of developmental maturity. Acta Neuropathologica. 93: 619-27. PMID 9194902 DOI: 10.1007/S004010050660 |
0.563 |
|
| 1997 |
Ginsberg SD, Crino PB, Lee VM, Eberwine JH, Trojanowski JQ. Sequestration of RNA in Alzheimer's disease neurofibrillary tangles and senile plaques. Annals of Neurology. 41: 200-9. PMID 9029069 DOI: 10.1002/Ana.410410211 |
0.521 |
|
| 1996 |
Crino PB, Trojanowski JQ, Dichter MA, Eberwine J. Embryonic neuronal markers in tuberous sclerosis: single-cell molecular pathology. Proceedings of the National Academy of Sciences of the United States of America. 93: 14152-7. PMID 8943076 DOI: 10.1073/pnas.93.24.14152 |
0.6 |
|
| 1996 |
Crino P, Hemby S, Eberwine J. Utility of in situ transcription, single-cell nucleic acid amplification and expression profiling in the study of the central nervous system development Cell Vision - Journal of Analytical Morphology. 3: 203-206. |
0.594 |
|
| 1995 |
Eberwine J, Crino P, Dichter M. Review : Single-Cell mRNA Amplification: Implications for Basic and Clinical Neuroscience The Neuroscientist. 1: 200-211. DOI: 10.1177/107385849500100404 |
0.585 |
|
| 1991 |
Vogt BA, Crino PB, Volicer L. Laminar alterations in gamma-aminobutyric acidA, muscarinic, and beta adrenoceptors and neuron degeneration in cingulate cortex in Alzheimer's disease. Journal of Neurochemistry. 57: 282-90. PMID 1675662 DOI: 10.1111/j.1471-4159.1991.tb02126.x |
0.436 |
|
| 1990 |
Volicer L, Crino PB. Involvement of free radicals in dementia of the Alzheimer type: a hypothesis. Neurobiology of Aging. 11: 567-71. PMID 2146522 DOI: 10.1016/0197-4580(90)90119-K |
0.415 |
|
| 1990 |
Crino PB, Vogt BA, Volicer L, Wiley RG. Cellular localization of serotonin 1A, 1B and uptake sites in cingulate cortex of the rat. The Journal of Pharmacology and Experimental Therapeutics. 252: 651-6. PMID 2138221 |
0.434 |
|
| 1989 |
Crino PB, Ullman MD, Vogt BA, Bird ED, Volicer L. Brain gangliosides in dementia of the Alzheimer type. Archives of Neurology. 46: 398-401. PMID 2705899 DOI: 10.1001/archneur.1989.00520400054019 |
0.466 |
|
| 1989 |
Crino PB, Vogt BA, Chen JC, Volicer L. Neurotoxic effects of partially oxidized serotonin: tryptamine-4,5-dione. Brain Research. 504: 247-57. PMID 2598027 DOI: 10.1016/0006-8993(89)91364-4 |
0.582 |
|
| 1989 |
Volicer L, Seltzer B, Rheaume Y, Karner J, Glennon M, Riley ME, Crino P. Eating difficulties in patients with probable dementia of the Alzheimer type. Journal of Geriatric Psychiatry and Neurology. 2: 188-95. PMID 2483945 DOI: 10.1177/089198878900200404 |
0.45 |
|
| 1989 |
Volicer L, Chen JC, Crino PB, Vogt BA, Fishman J, Rubins J, Schenepper PW, Wolfe N. Neurotoxic properties of a serotonin oxidation product: possible role in Alzheimer's disease. Progress in Clinical and Biological Research. 317: 453-65. PMID 2481322 DOI: 10.1097/00002093-198802030-00090 |
0.564 |
|
| 1989 |
Chen JC, Crino PB, Schnepper PW, To AC, Volicer L. Increased serotonin efflux by a partially oxidized serotonin: tryptamine-4,5-dione. The Journal of Pharmacology and Experimental Therapeutics. 250: 141-8. PMID 2473186 |
0.519 |
|
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