These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 17606885)

  • 1. Clinical and neuropathologic study of a French family with a mutation in the neuroserpin gene.
    Gourfinkel-An I; Duyckaerts C; Camuzat A; Meyrignac C; Sonderegger P; Baulac M; Brice A
    Neurology; 2007 Jul; 69(1):79-83. PubMed ID: 17606885
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial dementia caused by polymerization of mutant neuroserpin.
    Davis RL; Shrimpton AE; Holohan PD; Bradshaw C; Feiglin D; Collins GH; Sonderegger P; Kinter J; Becker LM; Lacbawan F; Krasnewich D; Muenke M; Lawrence DA; Yerby MS; Shaw CM; Gooptu B; Elliott PR; Finch JT; Carrell RW; Lomas DA
    Nature; 1999 Sep; 401(6751):376-9. PubMed ID: 10517635
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the neuroserpin gene are rare in familial dementia. French Alzheimer's Disease and Fronto-Temporal Dementia Genetics Study Groups.
    Ann Neurol; 2000 May; 47(5):688. PubMed ID: 10805351
    [No Abstract]   [Full Text] [Related]  

  • 4. Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy.
    Takao M; Benson MD; Murrell JR; Yazaki M; Piccardo P; Unverzagt FW; Davis RL; Holohan PD; Lawrence DA; Richardson R; Farlow MR; Ghetti B
    J Neuropathol Exp Neurol; 2000 Dec; 59(12):1070-86. PubMed ID: 11138927
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Accumulation of mutant neuroserpin precedes development of clinical symptoms in familial encephalopathy with neuroserpin inclusion bodies.
    Galliciotti G; Glatzel M; Kinter J; Kozlov SV; Cinelli P; Rülicke T; Sonderegger P
    Am J Pathol; 2007 Apr; 170(4):1305-13. PubMed ID: 17392169
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association between conformational mutations in neuroserpin and onset and severity of dementia.
    Davis RL; Shrimpton AE; Carrell RW; Lomas DA; Gerhard L; Baumann B; Lawrence DA; Yepes M; Kim TS; Ghetti B; Piccardo P; Takao M; Lacbawan F; Muenke M; Sifers RN; Bradshaw CB; Kent PF; Collins GH; Larocca D; Holohan PD
    Lancet; 2002 Jun; 359(9325):2242-7. PubMed ID: 12103288
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cognitive deficits associated with a recently reported familial neurodegenerative disease: familial encephalopathy with neuroserpin inclusion bodies.
    Bradshaw CB; Davis RL; Shrimpton AE; Holohan PD; Rea CB; Fieglin D; Kent P; Collins GH
    Arch Neurol; 2001 Sep; 58(9):1429-34. PubMed ID: 11559315
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial conformational diseases and dementias.
    Crowther DC
    Hum Mutat; 2002 Jul; 20(1):1-14. PubMed ID: 12112652
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SERPINI1 pathogenic variants: An emerging cause of childhood-onset progressive myoclonic epilepsy.
    Ranza E; Garcia-Tarodo S; Varvagiannis K; Guipponi M; Lobrinus JA; Bottani A; Kern I; Kurian M; Pittet MP; Antonarakis SE; Fluss J; Korff CM
    Am J Med Genet A; 2017 Sep; 173(9):2456-2460. PubMed ID: 28631894
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neuroserpin Portland (Ser52Arg) is trapped as an inactive intermediate that rapidly forms polymers: implications for the epilepsy seen in the dementia FENIB.
    Belorgey D; Sharp LK; Crowther DC; Onda M; Johansson J; Lomas DA
    Eur J Biochem; 2004 Aug; 271(16):3360-7. PubMed ID: 15291813
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Encephalopathy with neuroserpin inclusion bodies presenting as progressive myoclonus epilepsy and associated with a novel mutation in the Proteinase Inhibitor 12 gene.
    Hagen MC; Murrell JR; Delisle MB; Andermann E; Andermann F; Guiot MC; Ghetti B
    Brain Pathol; 2011 Sep; 21(5):575-82. PubMed ID: 21435071
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neuroserpin: a selective inhibitor of tissue-type plasminogen activator in the central nervous system.
    Yepes M; Lawrence DA
    Thromb Haemost; 2004 Mar; 91(3):457-64. PubMed ID: 14983220
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Familial non-Alzheimer dementia].
    Tabira T
    Rinsho Shinkeigaku; 2003 Nov; 43(11):775-8. PubMed ID: 15152461
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep.
    Coutelier M; Andries S; Ghariani S; Dan B; Duyckaerts C; van Rijckevorsel K; Raftopoulos C; Deconinck N; Sonderegger P; Scaravilli F; Vikkula M; Godfraind C
    Neurology; 2008 Jul; 71(1):64-6. PubMed ID: 18591508
    [No Abstract]   [Full Text] [Related]  

  • 15. Familial encephalopathy with neuroserpin inclusion bodies.
    Davis RL; Holohan PD; Shrimpton AE; Tatum AH; Daucher J; Collins GH; Todd R; Bradshaw C; Kent P; Feiglin D; Rosenbaum A; Yerby MS; Shaw CM; Lacbawan F; Lawrence DA
    Am J Pathol; 1999 Dec; 155(6):1901-13. PubMed ID: 10595921
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutation-, aging-, and gene dosage-dependent accumulation of neuroserpin (G392E) in endoplasmic reticula and lysosomes of neurons in transgenic mice.
    Takasawa A; Kato I; Takasawa K; Ishii Y; Yoshida T; Shehata MH; Kawaguchi H; Mohafez OM; Sasahara M; Hiraga K
    J Biol Chem; 2008 Dec; 283(51):35606-13. PubMed ID: 18940798
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Japanese family with mutation in the proteinase inhibitor 12 L47P gene: A case report.
    Amano-Takeshige H; Oyama G; Kanai K; Miyagawa T; Mitsui J; Ugawa Y; Tsuji S; Hattori N
    J Neurol Sci; 2018 Jan; 384():126-128. PubMed ID: 29249370
    [No Abstract]   [Full Text] [Related]  

  • 18. A novel PSEN2 mutation associated with a peculiar phenotype.
    Piscopo P; Marcon G; Piras MR; Crestini A; Campeggi LM; Deiana E; Cherchi R; Tanda F; Deplano A; Vanacore N; Tagliavini F; Pocchiari M; Giaccone G; Confaloni A
    Neurology; 2008 Apr; 70(17):1549-54. PubMed ID: 18427071
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lectin OS-9 delivers mutant neuroserpin to endoplasmic reticulum associated degradation in familial encephalopathy with neuroserpin inclusion bodies.
    Schipanski A; Oberhauser F; Neumann M; Lange S; Szalay B; Krasemann S; van Leeuwen FW; Galliciotti G; Glatzel M
    Neurobiol Aging; 2014 Oct; 35(10):2394-403. PubMed ID: 24795221
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Latent S49P neuroserpin forms polymers in the dementia familial encephalopathy with neuroserpin inclusion bodies.
    Onda M; Belorgey D; Sharp LK; Lomas DA
    J Biol Chem; 2005 Apr; 280(14):13735-41. PubMed ID: 15664988
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.