224 related articles for article (PubMed ID: 19914360)
21. A novel mutation at position +11 in the intron following exon 10 of the tau gene in FTDP-17.
Kowalska A; Hasegawa M; Miyamoto K; Akiguchi I; Ikemoto A; Takahashi K; Araki W; Tabira T
J Appl Genet; 2002; 43(4):535-43. PubMed ID: 12441638
[TBL] [Abstract][Full Text] [Related]
22. Complex regulation of tau exon 10, whose missplicing causes frontotemporal dementia.
Gao QS; Memmott J; Lafyatis R; Stamm S; Screaton G; Andreadis A
J Neurochem; 2000 Feb; 74(2):490-500. PubMed ID: 10646499
[TBL] [Abstract][Full Text] [Related]
23. A new case of frontotemporal dementia and parkinsonism resulting from an intron 10 +3-splice site mutation in the tau gene: clinical and pathological features.
Tolnay M; Grazia Spillantini M; Rizzini C; Eccles D; Lowe J; Ellison D
Neuropathol Appl Neurobiol; 2000 Aug; 26(4):368-78. PubMed ID: 10931371
[TBL] [Abstract][Full Text] [Related]
24. tau Exon 10 expression involves a bipartite intron 10 regulatory sequence and weak 5' and 3' splice sites.
D'Souza I; Schellenberg GD
J Biol Chem; 2002 Jul; 277(29):26587-99. PubMed ID: 12000767
[TBL] [Abstract][Full Text] [Related]
25. Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).
Spillantini MG; Van Swieten JC; Goedert M
Neurogenetics; 2000 Mar; 2(4):193-205. PubMed ID: 10983715
[TBL] [Abstract][Full Text] [Related]
26. FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10.
Hasegawa M; Smith MJ; Iijima M; Tabira T; Goedert M
FEBS Lett; 1999 Jan; 443(2):93-6. PubMed ID: 9989582
[TBL] [Abstract][Full Text] [Related]
27. Arginine/serine-rich protein interaction domain-dependent modulation of a tau exon 10 splicing enhancer: altered interactions and mechanisms for functionally antagonistic FTDP-17 mutations Delta280K AND N279K.
D'Souza I; Schellenberg GD
J Biol Chem; 2006 Feb; 281(5):2460-9. PubMed ID: 16308321
[TBL] [Abstract][Full Text] [Related]
28. Dual-specificity tyrosine phosphorylation-regulated kinase 1A (Dyrk1A) modulates serine/arginine-rich protein 55 (SRp55)-promoted Tau exon 10 inclusion.
Yin X; Jin N; Gu J; Shi J; Zhou J; Gong CX; Iqbal K; Grundke-Iqbal I; Liu F
J Biol Chem; 2012 Aug; 287(36):30497-506. PubMed ID: 22767602
[TBL] [Abstract][Full Text] [Related]
29. Tau alternative splicing in familial and sporadic tauopathies.
Niblock M; Gallo JM
Biochem Soc Trans; 2012 Aug; 40(4):677-80. PubMed ID: 22817715
[TBL] [Abstract][Full Text] [Related]
30. Tra2 beta, SF2/ASF and SRp30c modulate the function of an exonic splicing enhancer in exon 10 of tau pre-mRNA.
Kondo S; Yamamoto N; Murakami T; Okumura M; Mayeda A; Imaizumi K
Genes Cells; 2004 Feb; 9(2):121-30. PubMed ID: 15009090
[TBL] [Abstract][Full Text] [Related]
31. RBM4 interacts with an intronic element and stimulates tau exon 10 inclusion.
Kar A; Havlioglu N; Tarn WY; Wu JY
J Biol Chem; 2006 Aug; 281(34):24479-88. PubMed ID: 16777844
[TBL] [Abstract][Full Text] [Related]
32. Developmental regulation of tau splicing is disrupted in stem cell-derived neurons from frontotemporal dementia patients with the 10 + 16 splice-site mutation in MAPT.
Sposito T; Preza E; Mahoney CJ; Setó-Salvia N; Ryan NS; Morris HR; Arber C; Devine MJ; Houlden H; Warner TT; Bushell TJ; Zagnoni M; Kunath T; Livesey FJ; Fox NC; Rossor MN; Hardy J; Wray S
Hum Mol Genet; 2015 Sep; 24(18):5260-9. PubMed ID: 26136155
[TBL] [Abstract][Full Text] [Related]
33. Cyclic AMP-dependent protein kinase regulates the alternative splicing of tau exon 10: a mechanism involved in tau pathology of Alzheimer disease.
Shi J; Qian W; Yin X; Iqbal K; Grundke-Iqbal I; Gu X; Ding F; Gong CX; Liu F
J Biol Chem; 2011 Apr; 286(16):14639-48. PubMed ID: 21367856
[TBL] [Abstract][Full Text] [Related]
34. Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17.
Varani L; Hasegawa M; Spillantini MG; Smith MJ; Murrell JR; Ghetti B; Klug A; Goedert M; Varani G
Proc Natl Acad Sci U S A; 1999 Jul; 96(14):8229-34. PubMed ID: 10393977
[TBL] [Abstract][Full Text] [Related]
35. A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto).
Yasuda M; Takamatsu J; D'Souza I; Crowther RA; Kawamata T; Hasegawa M; Hasegawa H; Spillantini MG; Tanimukai S; Poorkaj P; Varani L; Varani G; Iwatsubo T; Goedert M; Schellenberg DG; Tanaka C
Ann Neurol; 2000 Apr; 47(4):422-9. PubMed ID: 10762152
[TBL] [Abstract][Full Text] [Related]
36. [The genetics of dementias. Part 1: Molecular basis of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)].
Kowalska A
Postepy Hig Med Dosw (Online); 2009 Jun; 63():278-86. PubMed ID: 19535823
[TBL] [Abstract][Full Text] [Related]
37. Mutations in tau gene exon 10 associated with FTDP-17 alter the activity of an exonic splicing enhancer to interact with Tra2 beta.
Jiang Z; Tang H; Havlioglu N; Zhang X; Stamm S; Yan R; Wu JY
J Biol Chem; 2003 May; 278(21):18997-9007. PubMed ID: 12649279
[TBL] [Abstract][Full Text] [Related]
38. Tau Isoforms: Gaining Insight into
Corsi A; Bombieri C; Valenti MT; Romanelli MG
Int J Mol Sci; 2022 Dec; 23(23):. PubMed ID: 36499709
[TBL] [Abstract][Full Text] [Related]
39. SRp54 (SFRS11), a regulator for tau exon 10 alternative splicing identified by an expression cloning strategy.
Wu JY; Kar A; Kuo D; Yu B; Havlioglu N
Mol Cell Biol; 2006 Sep; 26(18):6739-47. PubMed ID: 16943417
[TBL] [Abstract][Full Text] [Related]
40. Tau exon 10 alternative splicing and tauopathies.
Liu F; Gong CX
Mol Neurodegener; 2008 Jul; 3():8. PubMed ID: 18616804
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
