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Journal Abstract Search


273 related items for PubMed ID: 9761305

  • 1. Tuberous sclerosis-related gene expression in normal and dysplastic brain.
    Vinters HV, Kerfoot C, Catania M, Emelin JK, Roper SN, DeClue JE.
    Epilepsy Res; 1998 Sep; 32(1-2):12-23. PubMed ID: 9761305
    [Abstract] [Full Text] [Related]

  • 2. Localization of tuberous sclerosis 2 mRNA and its protein product tuberin in normal human brain and in cerebral lesions of patients with tuberous sclerosis.
    Kerfoot C, Wienecke R, Menchine M, Emelin J, Maize JC, Welsh CT, Norman MG, DeClue JE, Vinters HV.
    Brain Pathol; 1996 Oct; 6(4):367-75. PubMed ID: 8944308
    [Abstract] [Full Text] [Related]

  • 3. Tuberous sclerosis as an underlying basis for infantile spasm.
    Yeung RS.
    Int Rev Neurobiol; 2002 Oct; 49():315-32. PubMed ID: 12040899
    [Abstract] [Full Text] [Related]

  • 4. Tuberous sclerosis-like lesions in epileptogenic human neocortex lack allelic loss at the TSC1 and TSC2 regions.
    Wolf HK, Normann S, Green AJ, von Bakel I, Blümcke I, Pietsch T, Wiestler OD, von Deimling A.
    Acta Neuropathol; 1997 Jan; 93(1):93-6. PubMed ID: 9006662
    [Abstract] [Full Text] [Related]

  • 5. Co-localization of TSC1 and TSC2 gene products in tubers of patients with tuberous sclerosis.
    Johnson MW, Emelin JK, Park SH, Vinters HV.
    Brain Pathol; 1999 Jan; 9(1):45-54. PubMed ID: 9989450
    [Abstract] [Full Text] [Related]

  • 6. Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.
    van Slegtenhorst M, de Hoogt R, Hermans C, Nellist M, Janssen B, Verhoef S, Lindhout D, van den Ouweland A, Halley D, Young J, Burley M, Jeremiah S, Woodward K, Nahmias J, Fox M, Ekong R, Osborne J, Wolfe J, Povey S, Snell RG, Cheadle JP, Jones AC, Tachataki M, Ravine D, Sampson JR, Reeve MP, Richardson P, Wilmer F, Munro C, Hawkins TL, Sepp T, Ali JB, Ward S, Green AJ, Yates JR, Kwiatkowska J, Henske EP, Short MP, Haines JH, Jozwiak S, Kwiatkowski DJ.
    Science; 1997 Aug 08; 277(5327):805-8. PubMed ID: 9242607
    [Abstract] [Full Text] [Related]

  • 7. Tuberous sclerosis complex: genetics to pathogenesis.
    Narayanan V.
    Pediatr Neurol; 2003 Nov 08; 29(5):404-9. PubMed ID: 14684235
    [Abstract] [Full Text] [Related]

  • 8. Evidence for separable functions of tuberous sclerosis gene products in mammalian cell cycle regulation.
    Miloloza A, Kubista M, Rosner M, Hengstschläger M.
    J Neuropathol Exp Neurol; 2002 Feb 08; 61(2):154-63. PubMed ID: 11853018
    [Abstract] [Full Text] [Related]

  • 9. Cell-specific alterations of glutamate receptor expression in tuberous sclerosis complex cortical tubers.
    Talos DM, Kwiatkowski DJ, Cordero K, Black PM, Jensen FE.
    Ann Neurol; 2008 Apr 08; 63(4):454-65. PubMed ID: 18350576
    [Abstract] [Full Text] [Related]

  • 10. Pathogenesis of multifocal micronodular pneumocyte hyperplasia and lymphangioleiomyomatosis in tuberous sclerosis and association with tuberous sclerosis genes TSC1 and TSC2.
    Maruyama H, Ohbayashi C, Hino O, Tsutsumi M, Konishi Y.
    Pathol Int; 2001 Aug 08; 51(8):585-94. PubMed ID: 11564212
    [Abstract] [Full Text] [Related]

  • 11. The expression of hamartin, the product of the TSC1 gene, in normal human tissues and in TSC1- and TSC2-linked angiomyolipomas.
    Plank TL, Logginidou H, Klein-Szanto A, Henske EP.
    Mod Pathol; 1999 May 08; 12(5):539-45. PubMed ID: 10349994
    [Abstract] [Full Text] [Related]

  • 12. Tuberous sclerosis: immunohistochemistry expression of tuberin and hamartin in a 31-week gestational fetus.
    Vinaitheerthan M, Wei J, Mizuguchi M, Greco A, Barness EG.
    Fetal Pediatr Pathol; 2004 May 08; 23(4):241-9. PubMed ID: 16095035
    [Abstract] [Full Text] [Related]

  • 13. Distinct allelic variants of TSC1 and TSC2 in epilepsy-associated cortical malformations without balloon cells.
    Majores M, Blümcke I, Urbach H, Meroni A, Hans V, Holthausen H, Elger CE, Schramm J, Galli C, Spreafico R, Wiestler OD, Becker AJ.
    J Neuropathol Exp Neurol; 2005 Jul 08; 64(7):629-37. PubMed ID: 16042315
    [Abstract] [Full Text] [Related]

  • 14. Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band 16p13 occurs in sporadic as well as TSC-associated renal angiomyolipomas.
    Henske EP, Neumann HP, Scheithauer BW, Herbst EW, Short MP, Kwiatkowski DJ.
    Genes Chromosomes Cancer; 1995 Aug 08; 13(4):295-8. PubMed ID: 7547639
    [Abstract] [Full Text] [Related]

  • 15. The cell cycle and tuberous sclerosis.
    Hengstschläger M, Rosner M.
    Prog Cell Cycle Res; 2003 Aug 08; 5():43-8. PubMed ID: 14593699
    [Abstract] [Full Text] [Related]

  • 16. Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex.
    Boer K, Troost D, Jansen F, Nellist M, van den Ouweland AM, Geurts JJ, Spliet WG, Crino P, Aronica E.
    Neuropathology; 2008 Dec 08; 28(6):577-90. PubMed ID: 18410267
    [Abstract] [Full Text] [Related]

  • 17. Cyst-like tubers are associated with TSC2 and epilepsy in tuberous sclerosis complex.
    Chu-Shore CJ, Major P, Montenegro M, Thiele E.
    Neurology; 2009 Mar 31; 72(13):1165-9. PubMed ID: 19332694
    [Abstract] [Full Text] [Related]

  • 18. Interaction between hamartin and tuberin, the TSC1 and TSC2 gene products.
    van Slegtenhorst M, Nellist M, Nagelkerken B, Cheadle J, Snell R, van den Ouweland A, Reuser A, Sampson J, Halley D, van der Sluijs P.
    Hum Mol Genet; 1998 Jun 31; 7(6):1053-7. PubMed ID: 9580671
    [Abstract] [Full Text] [Related]

  • 19. Cortical dysplasia, genetic abnormalities and neurocutaneous syndromes.
    Vinters HV, Park SH, Johnson MW, Mischel PS, Catania M, Kerfoot C.
    Dev Neurosci; 1999 Nov 31; 21(3-5):248-59. PubMed ID: 10575248
    [Abstract] [Full Text] [Related]

  • 20. Tuberous sclerosis gene products in proliferation control.
    Hengstschläger M, Rodman DM, Miloloza A, Hengstschläger-Ottnad E, Rosner M, Kubista M.
    Mutat Res; 2001 Jul 31; 488(3):233-9. PubMed ID: 11397651
    [Abstract] [Full Text] [Related]


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