-
1
-
-
0030983011
-
Chromosome 17 and hereditary dementia: Linkage studies in three non-Alzheimer families and kindreds with late-onset FAD
-
Bird, T.D., Wijsman, E.M., Nochlin, D., et al. (1997) Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD. Neurology 48, 949-954.
-
(1997)
Neurology
, vol.48
, pp. 949-954
-
-
Bird, T.D.1
Wijsman, E.M.2
Nochlin, D.3
-
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. & Krainer, A.R. (2002) Listening to silence and understanding nonsense: exonic mutations that affect splicing. Nature Rev. Genet. 3, 285-298.
-
(2002)
Nature Rev. Genet.
, vol.3
, pp. 285-298
-
-
Cartegni, L.1
Chew, S.L.2
Krainer, A.R.3
-
4
-
-
0036544654
-
Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1
-
Cartegni, L. & Krainer, A.R. (2002) Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1. Nature Genet. 30, 377-384.
-
(2002)
Nature Genet.
, vol.30
, pp. 377-384
-
-
Cartegni, L.1
Krainer, A.R.2
-
5
-
-
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. & Buckler, A.J. (1994) Isolation of genes from complex sources of mammalian genomic DNA using exon amplification. Nature Genet. 6, 98-105.
-
(1994)
Nature 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
-
6
-
-
0032573083
-
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
-
Clark, L.N., Poorkaj, P. & Wszolek, Z. (1998) Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. Proc. Natl. Acad. Sci. USA 95, 13103-13107.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 13103-13107
-
-
Clark, L.N.1
Poorkaj, P.2
Wszolek, Z.3
-
7
-
-
0033545946
-
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
-
D'Souza, I., Poorkaj, P., Hong, M., et al. (1999) Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements. Proc. Natl. Acad. Sci. USA 96, 5598-5603.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 5598-5603
-
-
D'Souza, I.1
Poorkaj, P.2
Hong, M.3
-
8
-
-
0032854745
-
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Aβ42 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 Aβ42 secretion. Hum. Mol. Genet. 8, 1529-1540.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1529-1540
-
-
De Jonghe, C.1
Cruts, M.2
Rogaeva, E.A.3
-
9
-
-
0035865268
-
The adenovirus E4-ORF4 splicing enhancer protein interacts with a subset of phosphorylated SR proteins
-
Estmer Nilsson, C., Petersen-Mahrt, S., Durot, C., et al. (2001) The adenovirus E4-ORF4 splicing enhancer protein interacts with a subset of phosphorylated SR proteins. EMBO J. 20, 864-871.
-
(2001)
EMBO J.
, vol.20
, pp. 864-871
-
-
Estmer Nilsson, C.1
Petersen-Mahrt, S.2
Durot, C.3
-
10
-
-
0030977392
-
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference
-
Conference Participants
-
Foster, N.L., Wilhelmsen, K., Sima, A.A., Jones, M.Z., D'Amato, C.J. & Gilman, S. (1997) Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants. Ann, Neurol. 41, 706-715.
-
(1997)
Ann. Neurol.
, vol.41
, pp. 706-715
-
-
Foster, N.L.1
Wilhelmsen, K.2
Sima, A.A.3
Jones, M.Z.4
D'Amato, C.J.5
Gilman, S.6
-
11
-
-
0032191105
-
Filamentous nerve cell inclusions in neurodegenerative diseases
-
Goedert, M., Spillantini, M.G. & Davies, S.W. (1998) Filamentous nerve cell inclusions in neurodegenerative diseases. Curr. Opin. Neurobiol. 8, 619-632.
-
(1998)
Curr. Opin. Neurobiol.
, vol.8
, pp. 619-632
-
-
Goedert, M.1
Spillantini, M.G.2
Davies, S.W.3
-
12
-
-
0034624014
-
Structural and functional differences between 3-repeat and 4-repeat tau isoforms. Implications for normal tau function and the onset of neurodegenetative disease
-
Goode, B.L., Chau, M., Denis, P.E. & Feinstein, S.C. (2000) Structural and functional differences between 3-repeat and 4-repeat tau isoforms. Implications for normal tau function and the onset of neurodegenetative disease. J. Biol. Chem. 275, 38182-38189.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 38182-38189
-
-
Goode, B.L.1
Chau, M.2
Denis, P.E.3
Feinstein, S.C.4
-
13
-
-
0033835333
-
Sorting out the complexity of SR protein functions
-
Graveley, B.R. (2000) Sorting out the complexity of SR protein functions. RNA 6, 1197-1211.
-
(2000)
RNA
, vol.6
, pp. 1197-1211
-
-
Graveley, B.R.1
-
14
-
-
0032538791
-
A systematic analysis of the factors that determine the strength of pre-mRNA splicing enhancers
-
Graveley, B.R., Hertel, K.J. & Maniatis, T. (1998) A systematic analysis of the factors that determine the strength of pre-mRNA splicing enhancers. EMBO J. 17, 6747-6756.
-
(1998)
EMBO J.
, vol.17
, pp. 6747-6756
-
-
Graveley, B.R.1
Hertel, K.J.2
Maniatis, T.3
-
15
-
-
0033591225
-
5′ splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10
-
Grover, A., Houlden, H., Baker, M., et al. (1999) 5′ splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10. J. Biol. Chem. 274, 15134-15143.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 15134-15143
-
-
Grover, A.1
Houlden, H.2
Baker, M.3
-
16
-
-
0032561415
-
Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly
-
Hasegawa, M., Smith, M.J. & Goedert, M. (1998) Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly. FEBS Lett. 437, 207-210.
-
(1998)
FEBS Lett.
, vol.437
, pp. 207-210
-
-
Hasegawa, M.1
Smith, M.J.2
Goedert, M.3
-
17
-
-
0033060662
-
FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10
-
Hasegawa, M., Smith, M.J., Iijima, M., Tabira, T. & Goedert, M. (1999) FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10. FEBS Lett. 443, 93-96.
-
(1999)
FEBS Lett.
, vol.443
, pp. 93-96
-
-
Hasegawa, M.1
Smith, M.J.2
Iijima, M.3
Tabira, T.4
Goedert, M.5
-
18
-
-
0031045491
-
Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: A genetic and clinicopathological study of three Dutch families
-
Heutink, P., Stevens, M., Rizzu, P., et al. (1997) Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families. Ann. Neurol. 41, 150-159.
-
(1997)
Ann. Neurol.
, vol.41
, pp. 150-159
-
-
Heutink, P.1
Stevens, M.2
Rizzu, P.3
-
19
-
-
0032484089
-
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17
-
Hong, M., Zhukareva, V., Vogelsberg-Ragaglia, V., et al. (1998) Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. Science 282, 1914-1917.
-
(1998)
Science
, vol.282
, pp. 1914-1917
-
-
Hong, M.1
Zhukareva, V.2
Vogelsberg-Ragaglia, V.3
-
20
-
-
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
-
21
-
-
0034877085
-
Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells
-
Iseki, E., Matsumura, T., Marui, W., et al. (2001) Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells. Acta Neuropathol. 102, 285-292.
-
(2001)
Acta Neuropathol.
, vol.102
, pp. 285-292
-
-
Iseki, E.1
Matsumura, T.2
Marui, W.3
-
22
-
-
0034073995
-
Aberrant splicing of tau pre-mRNA caused by intronic mutations associated with the inherited dementia frontotemporal dementia with parkinsonism linked to chromosome 17
-
Jiang, Z., Cote, J., Kwon, J.M., Goate, A.M. & Wu, J.Y. (2000) Aberrant splicing of tau pre-mRNA caused by intronic mutations associated with the inherited dementia frontotemporal dementia with parkinsonism linked to chromosome 17. Mol. Cell. Biol. 20, 4036-4048.
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 4036-4048
-
-
Jiang, Z.1
Cote, J.2
Kwon, J.M.3
Goate, A.M.4
Wu, J.Y.5
-
23
-
-
0038819945
-
Mutations in tau gene exon 10 associated with FTDP-17 alter the activity of an exonic splicing enhancer to interact with Tra2 β
-
Jiang, Z., Tang, H., Havlioglu, N., et al. (2003) Mutations in tau gene exon 10 associated with FTDP-17 alter the activity of an exonic splicing enhancer to interact with Tra2 β. J. Biol. Chem. 278, 18997-19007.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 18997-19007
-
-
Jiang, Z.1
Tang, H.2
Havlioglu, N.3
-
24
-
-
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., et al. (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
-
25
-
-
0035158730
-
A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes
-
Liu, H.X., Cartegni, L., Zhang, M.Q. & Krainer, A.R. (2001) A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes. Nature Genet. 27, 55-58.
-
(2001)
Nature Genet.
, vol.27
, pp. 55-58
-
-
Liu, H.X.1
Cartegni, L.2
Zhang, M.Q.3
Krainer, A.R.4
-
26
-
-
0027948959
-
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex
-
Lynch, T., Sano, M., Marder, K.S., et al. (1994) Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. Neurology 44, 1878-1884.
-
(1994)
Neurology
, vol.44
, pp. 1878-1884
-
-
Lynch, T.1
Sano, M.2
Marder, K.S.3
-
27
-
-
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
-
28
-
-
0032648206
-
Preparation of HeLa cell nuclear and cytosolic S100 extracts for in vitro splicing
-
Mayeda, A. & Krainer, A.R. (1999) Preparation of HeLa cell nuclear and cytosolic S100 extracts for in vitro splicing. Methods Mol. Biol. 118, 309-314.
-
(1999)
Methods Mol. Biol.
, vol.118
, pp. 309-314
-
-
Mayeda, A.1
Krainer, A.R.2
-
29
-
-
0037189483
-
Identification of a cis-acting element for the regulation of SMN exon 7 splicing
-
Miyajima, H., Miyaso, H., Okumura, M., Kurisu, J. & Imaizumi, K. (2002) Identification of a cis-acting element for the regulation of SMN exon 7 splicing. J. Biol. Chem. 277, 23271-23277.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 23271-23277
-
-
Miyajima, H.1
Miyaso, H.2
Okumura, M.3
Kurisu, J.4
Imaizumi, K.5
-
30
-
-
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
-
31
-
-
0030826625
-
Autosomal dominant dementia with widespread neurofibrillary tangles
-
Reed, L.A., Grabowski, T.J., Schmidt, M.L., et al. (1997) Autosomal dominant dementia with widespread neurofibrillary tangles. Ann. Neurol. 42, 564-572.
-
(1997)
Ann. Neurol.
, vol.42
, pp. 564-572
-
-
Reed, L.A.1
Grabowski, T.J.2
Schmidt, M.L.3
-
32
-
-
0028831527
-
Identification and characterization of three members of the human SR family of pre-mRNA
-
Screaton, G.R., Caceres, J.F., Mayeda, A., et al. (1995) Identification and characterization of three members of the human SR family of pre-mRNA. EMBO J. 14, 4336-4349.
-
(1995)
EMBO J.
, vol.14
, pp. 4336-4349
-
-
Screaton, G.R.1
Caceres, J.F.2
Mayeda, A.3
-
33
-
-
0024829844
-
Alternative splicing in the control of gene expression
-
Smith, C.W., Patton, J.G. & Nadal-Ginard, B. (1989) Alternative splicing in the control of gene expression. Annu. Rev. Genet. 23, 973-977.
-
(1989)
Annu. Rev. Genet.
, vol.23
, pp. 973-977
-
-
Smith, C.W.1
Patton, J.G.2
Nadal-Ginard, B.3
-
34
-
-
0030000867
-
Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles
-
Spillantini, M.G., Crowther, R.A. & Goedert, M. (1996) Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles. Acta Neuropathol (Berl). 92, 42-48.
-
(1996)
Acta Neuropathol. (Berl)
, vol.92
, pp. 42-48
-
-
Spillantini, M.G.1
Crowther, R.A.2
Goedert, M.3
-
35
-
-
0030887854
-
Familial multiple system tauopathy with presenile dementia: A disease with abundant neuronal and glial tau filaments
-
Spillantini, M.G., Goedert, M., Crowther, R.A., Murrell, J.R., Farlow, M.R. & Ghetti, B. (1997) Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments. Proc. Natl. Acad. Sci. USA 94, 4113-4118.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 4113-4118
-
-
Spillantini, M.G.1
Goedert, M.2
Crowther, R.A.3
Murrell, J.R.4
Farlow, M.R.5
Ghetti, B.6
-
36
-
-
0032560487
-
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
-
Spillantini, M.G., Murrell, J.R., Goedert, M., Farlow, M.R., Klug, A. & Ghetti, B. (1998) Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc. Natl. Acad. Sci. USA 95, 7737-7741.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 7737-7741
-
-
Spillantini, M.G.1
Murrell, J.R.2
Goedert, M.3
Farlow, M.R.4
Klug, A.5
Ghetti, B.6
-
37
-
-
0033663879
-
A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies
-
Spillantini, M.G., Yoshida, H., Rizzini, C., et al. (2000) A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies. Ann. Neurol. 48, 939-943.
-
(2000)
Ann. Neurol.
, vol.48
, pp. 939-943
-
-
Spillantini, M.G.1
Yoshida, H.2
Rizzini, C.3
-
38
-
-
0033574409
-
Alternative splicing determines the intracellular localization of the novel nuclear protein Nop30 and its interaction with the splicing factor SRp30c
-
Stoss, O., Schwaiger, F.W., Cooper, T.A. & Stamm, S. (1999) Alternative splicing determines the intracellular localization of the novel nuclear protein Nop30 and its interaction with the splicing factor SRp30c. J. Biol. Chem. 274, 10951-10962.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 10951-10962
-
-
Stoss, O.1
Schwaiger, F.W.2
Cooper, T.A.3
Stamm, S.4
-
39
-
-
0032478506
-
Human Tra2 proteins are sequence-specific activators of pre-mRNA splicing
-
Tacke, R., Tohyama, M., Ogawa, S. & Manley, J.L. (1998) Human Tra2 proteins are sequence-specific activators of pre-mRNA splicing. Cell 93, 139-148.
-
(1998)
Cell
, vol.93
, pp. 139-148
-
-
Tacke, R.1
Tohyama, M.2
Ogawa, S.3
Manley, J.L.4
-
40
-
-
0028118641
-
Polypurine sequences within a downstream exon function as a splicing enhancer
-
Tanaka, K., Watakabe, A. & Shimura, Y. (1994) Polypurine sequences within a downstream exon function as a splicing enhancer. Mol. Cell. Biol. 14, 1347-1354.
-
(1994)
Mol. Cell. Biol.
, vol.14
, pp. 1347-1354
-
-
Tanaka, K.1
Watakabe, A.2
Shimura, Y.3
-
41
-
-
0026579802
-
Positive control of pre-mRNA splicing in vitro
-
Tian, M. & Maniatis, T. (1992) Positive control of pre-mRNA splicing in vitro. Science 256, 237-240.
-
(1992)
Science
, vol.256
, pp. 237-240
-
-
Tian, M.1
Maniatis, T.2
-
42
-
-
0028025033
-
A splicing enhancer exhibits both constitutive and regulated activities
-
Tian, M. & Maniatis, T. (1994) A splicing enhancer exhibits both constitutive and regulated activities. Genes Dev. 8, 1703-1712.
-
(1994)
Genes Dev.
, vol.8
, pp. 1703-1712
-
-
Tian, M.1
Maniatis, T.2
-
43
-
-
0031893609
-
A presenilin-1 truncating mutation is present in two cases with autopsy-confirmed early-onset Alzheimer disease
-
Tysoe, C., Whittaker, J., Xuereb, J., et al. (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
-
44
-
-
0034141513
-
Structural basis for recognition of the RNA major groove in the tau exon 10 splicing regulatory element by aminoglycoside antibiotics
-
Varani, L., Spillantini, M.G., Goedert, M. & Varani, G. (2000) Structural basis for recognition of the RNA major groove in the tau exon 10 splicing regulatory element by aminoglycoside antibiotics. Nucl. Acids Res. 28, 710-719.
-
(2000)
Nucl. Acids Res.
, vol.28
, pp. 710-719
-
-
Varani, L.1
Spillantini, M.G.2
Goedert, M.3
Varani, G.4
-
45
-
-
9044220964
-
Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21
-
Wijker, M., Wszolek, Z.K., Wolters, E.C., et al. (1996) Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21. Hum. Mol. Genet. 5, 151-154.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 151-154
-
-
Wijker, M.1
Wszolek, Z.K.2
Wolters, E.C.3
-
46
-
-
0028073692
-
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22
-
Wilhelmsen, K.C., Lynch, T., Pavlou, E., Higgins, M. & Nygaard, T.G. (1994) Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. Am. J. Hum. Genet. 55, 1159-1165.
-
(1994)
Am. J. Hum. Genet.
, vol.55
, pp. 1159-1165
-
-
Wilhelmsen, K.C.1
Lynch, T.2
Pavlou, E.3
Higgins, M.4
Nygaard, T.G.5
-
47
-
-
19244362853
-
Linkage of frontotemporal dementia to chromosome 17: Clinical and neuropathological characterization of phenotype
-
Yamaoka, L.H., Welsh-Bohmer, K.A., Hulette, C.M., et al. (1996) Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype. Am. J. Hum. Genet. 59, 1306-1312.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 1306-1312
-
-
Yamaoka, L.H.1
Welsh-Bohmer, K.A.2
Hulette, C.M.3
-
48
-
-
0036501065
-
SRp30c-dependent stimulation of survival motor neuron (SMN) exon 7 inclusion is facilitated by a direct interaction with hTr+a2 β 1
-
Young, P.J., DiDonato, C.J., Hu, D., Kothary, R., Androphy, E.J. & Lorson, C.L. (2002) SRp30c-dependent stimulation of survival motor neuron (SMN) exon 7 inclusion is facilitated by a direct interaction with hTr+a2 β 1. Hum. Mol. Genet. 11, 577-587.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 577-587
-
-
Young, P.J.1
DiDonato, C.J.2
Hu, D.3
Kothary, R.4
Androphy, E.J.5
Lorson, C.L.6
|