-
1
-
-
0033416032
-
Stimulation of glucose transport by hypoxia: Signals and mechanisms
-
Behrooz A. and Ismail-Beigi F. (1999) Stimulation of glucose transport by hypoxia: signals and mechanisms. News Physiol. Sci. 14, 105-110.
-
(1999)
News Physiol. Sci.
, vol.14
, pp. 105-110
-
-
Behrooz, A.1
Ismail-Beigi, F.2
-
2
-
-
0034161419
-
Exonic splicing enhancers: Mechanism of action, diversity and role in human genetic diseases
-
Blencowe B. J. (2000) Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases. Trends Biochem. Sci. 25, 106-110.
-
(2000)
Trends Biochem. Sci.
, vol.25
, pp. 106-110
-
-
Blencowe, B.J.1
-
3
-
-
0036207384
-
Listening to silence and understanding nonsense: Exonic mutations that affect splicing
-
Cartegni L., Chew S. L. and Krainer A. R. (2002) Listening to silence and understanding nonsense: exonic mutations that affect splicing. Nat. Rev. Genet. 3, 285-298.
-
(2002)
Nat. Rev. Genet.
, vol.3
, pp. 285-298
-
-
Cartegni, L.1
Chew, S.L.2
Krainer, A.R.3
-
4
-
-
0028352313
-
Isolation of genes from complex sources of mammalian genomic DNA using exon amplification
-
Church D. M., Stotler C. J., Rutter J. L., Murrell J. R., Trofatter J. A. and Buckler A. J. (1994) Isolation of genes from complex sources of mammalian genomic DNA using exon amplification. Nat. Genet. 6, 98-105.
-
(1994)
Nat. Genet.
, vol.6
, pp. 98-105
-
-
Church, D.M.1
Stotler, C.J.2
Rutter, J.L.3
Murrell, J.R.4
Trofatter, J.A.5
Buckler, A.J.6
-
5
-
-
0032854745
-
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion
-
De Jonghe C., Cruts M., Rogaeva E. A. et al. (1999) Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion. Hum. Molec. Genet. 8, 1529-1540.
-
(1999)
Hum. Molec. Genet.
, vol.8
, pp. 1529-1540
-
-
De Jonghe, C.1
Cruts, M.2
Rogaeva, E.A.3
-
6
-
-
0032496159
-
Intracellular signaling by reactive oxygen species during hypoxia in cardiomyocytes
-
Duranteau J., Chandel N. S., Kulisz A., Shao Z. and Schumacker P. T. (1998) Intracellular signaling by reactive oxygen species during hypoxia in cardiomyocytes. J. Biol. Chem. 273, 11 619-11 624.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 11619-11624
-
-
Duranteau, J.1
Chandel, N.S.2
Kulisz, A.3
Shao, Z.4
Schumacker, P.T.5
-
7
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M., Lendon C. L., Rizzu P. et al. (1998) Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 393, 702-705.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
-
8
-
-
0032032013
-
Aberrant RNA processing in a neurodegenerative disease: The cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis
-
Lin C. L., Bristol L. A., Jin L., Dykes-Hoberg M., Crawford T., Clawson L. and Rothstein J. D. (1998) Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis. Neuron 20, 589-602.
-
(1998)
Neuron
, vol.20
, pp. 589-602
-
-
Lin, C.L.1
Bristol, L.A.2
Jin, L.3
Dykes-Hoberg, M.4
Crawford, T.5
Clawson, L.6
Rothstein, J.D.7
-
9
-
-
0037047440
-
The cytosolic inclusion bodies that consist of splice variants that lack exon 5 of the presenilin-2 gene differ obviously from Hirano bodies observed in the brain from sporadic cases of Alzheimer's disease patients
-
Manabe T., Katayama T., Sato N., Kudo T., Matsuzaki S., Imaizumi K. and Tohyama M. (2002) The cytosolic inclusion bodies that consist of splice variants that lack exon 5 of the presenilin-2 gene differ obviously from Hirano bodies observed in the brain from sporadic cases of Alzheimer's disease patients. Neurosci. Lett. 328, 198-200.
-
(2002)
Neurosci. Lett.
, vol.328
, pp. 198-200
-
-
Manabe, T.1
Katayama, T.2
Sato, N.3
Kudo, T.4
Matsuzaki, S.5
Imaizumi, K.6
Tohyama, M.7
-
10
-
-
0037636434
-
Induced HMGA1a expression causes aberrant splicing of Presenilin-2 pre-mRNA in sporadic Alzheimer's disease
-
Manabe T., Katayama T., Sato N. et al. (2003) Induced HMGA1a expression causes aberrant splicing of Presenilin-2 pre-mRNA in sporadic Alzheimer's disease. Cell Death Differ. 10, 698-708.
-
(2003)
Cell Death Differ.
, vol.10
, pp. 698-708
-
-
Manabe, T.1
Katayama, T.2
Sato, N.3
-
11
-
-
0026034658
-
Mechanisms of alternative pre-mRNA splicing
-
Maniatis T. (1991) Mechanisms of alternative pre-mRNA splicing. Science 251, 33-34.
-
(1991)
Science
, vol.251
, pp. 33-34
-
-
Maniatis, T.1
-
12
-
-
12144288051
-
Metals accelerate production of the aberrant splicing isoform of the presenilin-2
-
Matsuzaki S., Manabe T., Katayama T., Nishikawa A., Yanagita T., Okuda H., Yasuda Y., Miyata S., Meshitsuka S. and Tohyama M. (2004) Metals accelerate production of the aberrant splicing isoform of the presenilin-2. J. Neurochem. 88, 1345-1351.
-
(2004)
J. Neurochem.
, vol.88
, pp. 1345-1351
-
-
Matsuzaki, S.1
Manabe, T.2
Katayama, T.3
Nishikawa, A.4
Yanagita, T.5
Okuda, H.6
Yasuda, Y.7
Miyata, S.8
Meshitsuka, S.9
Tohyama, M.10
-
13
-
-
0037189483
-
Identification of a cis-acting element for the regulation of SMN exon 7 splicing
-
Miyajima H., Miyaso H., Okumura M., Kurisu J. and Imaizumi K. (2002) Identification of a cis-acting element for the regulation of SMN exon 7 splicing. J. Biol. Chem. 277, 23 271-23 277.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 23271-23277
-
-
Miyajima, H.1
Miyaso, H.2
Okumura, M.3
Kurisu, J.4
Imaizumi, K.5
-
14
-
-
0029554875
-
A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 gene
-
Perez-Tur J., Froelich S., Prihar G. et al. (1995) A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 gene. Neuroreport 7, 297-301.
-
(1995)
Neuroreport
, vol.7
, pp. 297-301
-
-
Perez-Tur, J.1
Froelich, S.2
Prihar, G.3
-
15
-
-
10144264560
-
Structure and alternative splicing of the presenilin-2 gene
-
Prihar G., Fuldner R. A., Perez-Tur J. et al. (1996) Structure and alternative splicing of the presenilin-2 gene. Neuroreport 7, 1680-1684.
-
(1996)
Neuroreport
, vol.7
, pp. 1680-1684
-
-
Prihar, G.1
Fuldner, R.A.2
Perez-Tur, J.3
-
16
-
-
0032973469
-
A novel presenilin-2 splice variant in human Alzheimer's disease brain tissue
-
Sato N., Hori O., Yamaguchi A. et al. (1999) A novel presenilin-2 splice variant in human Alzheimer's disease brain tissue. J. Neurochem. 72, 2498-2505.
-
(1999)
J. Neurochem.
, vol.72
, pp. 2498-2505
-
-
Sato, N.1
Hori, O.2
Yamaguchi, A.3
-
17
-
-
0035910471
-
Increased production of beta-amyloid and vulnerability to endoplasmic reticulum stress by an aberrant spliced form of presenilin 2
-
Sato N., Imaizumi K., Manabe T. et al. (2001) Increased production of beta-amyloid and vulnerability to endoplasmic reticulum stress by an aberrant spliced form of presenilin 2. J. Biol. Chem. 276, 2108-2114.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 2108-2114
-
-
Sato, N.1
Imaizumi, K.2
Manabe, T.3
-
18
-
-
0024829844
-
Alternative splicing in the control of gene expression
-
Smith C. W., Patton J. G. and Nadal-Ginard B. (1989) Alternative splicing in the control of gene expression. Ann. Rev. Genet. 23, 527-577.
-
(1989)
Ann. Rev. Genet.
, vol.23
, pp. 527-577
-
-
Smith, C.W.1
Patton, J.G.2
Nadal-Ginard, B.3
-
19
-
-
0031893609
-
A presenilin-1 truncating mutation is present in two cases with autopsy-confirmed early-onset Alzheimer disease
-
Tysoe C., Whittaker J., Xuereb J., Cairns N. J., Cruts M., Van-Broeckhoven C., Wilcock G. and Rubinsztein D. C. (1998) A presenilin-1 truncating mutation is present in two cases with autopsy-confirmed early-onset Alzheimer disease. Am. J. Hum. Genet. 62, 70-76.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 70-76
-
-
Tysoe, C.1
Whittaker, J.2
Xuereb, J.3
Cairns, N.J.4
Cruts, M.5
Van-Broeckhoven, C.6
Wilcock, G.7
Rubinsztein, D.C.8
-
20
-
-
0024477261
-
On finding all suboptimal foldings of an RNA molecule
-
Zuker M. (1989) On finding all suboptimal foldings of an RNA molecule. Science 244, 48-52.
-
(1989)
Science
, vol.244
, pp. 48-52
-
-
Zuker, M.1
|