-
1
-
-
0034007548
-
An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA)
-
Wirth, B. (2000) An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA). Hum. Mutat., 15, 228-237.
-
(2000)
Hum. Mutat.
, vol.15
, pp. 228-237
-
-
Wirth, B.1
-
2
-
-
1542350314
-
Progressive and selective degeneration of motoneurons in a mouse model of SMA
-
Ferri, A., Melki, J. and Kato, A.C. (2004) Progressive and selective degeneration of motoneurons in a mouse model of SMA. Neuroreport, 15, 275-280.
-
(2004)
Neuroreport
, vol.15
, pp. 275-280
-
-
Ferri, A.1
Melki, J.2
Kato, A.C.3
-
3
-
-
18244407748
-
Natural history of denervation in SMA: relation to age, SMN2 copy number, and function
-
Swoboda, K.J., Prior, T.W., Scott, C.B., McNaught, T.P., Wride, M.C., Reyna, S.P. and Bromberg, M.B. (2005) Natural history of denervation in SMA: relation to age, SMN2 copy number, and function. Ann. Neurol., 57, 704-712.
-
(2005)
Ann. Neurol.
, vol.57
, pp. 704-712
-
-
Swoboda, K.J.1
Prior, T.W.2
Scott, C.B.3
McNaught, T.P.4
Wride, M.C.5
Reyna, S.P.6
Bromberg, M.B.7
-
4
-
-
77949909934
-
Neuromuscular synaptic vulnerability in motor neurone disease: amyotrophic lateral sclerosis and spinal muscular atrophy
-
Murray, L.M., Talbot, K. and Gillingwater, T.H. (2010) Neuromuscular synaptic vulnerability in motor neurone disease: amyotrophic lateral sclerosis and spinal muscular atrophy. Neuropathol. Appl. Neurobiol., 36, 133-156.
-
(2010)
Neuropathol. Appl. Neurobiol.
, vol.36
, pp. 133-156
-
-
Murray, L.M.1
Talbot, K.2
Gillingwater, T.H.3
-
5
-
-
45249106162
-
Spinal muscular atrophy
-
Lunn, M.R. and Wang, C.H. (2008) Spinal muscular atrophy. Lancet, 371, 2120-2133.
-
(2008)
Lancet
, vol.371
, pp. 2120-2133
-
-
Lunn, M.R.1
Wang, C.H.2
-
6
-
-
46749124653
-
Diagnosis and clinical management of spinal muscular atrophy
-
Han, J.J. and McDonald, C.M. (2008) Diagnosis and clinical management of spinal muscular atrophy. Phys. Med. Rehabil. Clin. N. Am., 19, 661-680.
-
(2008)
Phys. Med. Rehabil. Clin. N. Am.
, vol.19
, pp. 661-680
-
-
Han, J.J.1
McDonald, C.M.2
-
7
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophydetermining gene
-
Lefebvre, S., Bürglen, L., Reboullet, S., Clermont, O., Burlet, P., Viollet, L., Benichou, B., Cruaud, C., Millasseau, P., Zeviani, M. et al. (1995) Identification and characterization of a spinal muscular atrophydetermining gene. Cell, 80, 155-165.
-
(1995)
Cell
, vol.80
, pp. 155-165
-
-
Lefebvre, S.1
Bürglen, L.2
Reboullet, S.3
Clermont, O.4
Burlet, P.5
Viollet, L.6
Benichou, B.7
Cruaud, C.8
Millasseau, P.9
Zeviani, M.10
-
8
-
-
29144463310
-
Spinal muscular atrophy: a deficiency in a ubiquitous protein; a motor neuron-specific disease
-
Monani, U.R. (2005) Spinal muscular atrophy: a deficiency in a ubiquitous protein; a motor neuron-specific disease. Neuron, 48, 885-896.
-
(2005)
Neuron
, vol.48
, pp. 885-896
-
-
Monani, U.R.1
-
9
-
-
67651083390
-
Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?
-
Burghes, A.H. and Beattie, C.E. (2009) Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? Nat. Rev. Neurosci., 10, 597-609.
-
(2009)
Nat. Rev. Neurosci.
, vol.10
, pp. 597-609
-
-
Burghes, A.H.1
Beattie, C.E.2
-
10
-
-
43049168361
-
SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing
-
Zhang, Z., Lotti, F., Dittmar, K., Younis, I., Wan, L., Kasim, M. and Dreyfuss, G. (2008) SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing. Cell, 133, 585-600.
-
(2008)
Cell
, vol.133
, pp. 585-600
-
-
Zhang, Z.1
Lotti, F.2
Dittmar, K.3
Younis, I.4
Wan, L.5
Kasim, M.6
Dreyfuss, G.7
-
11
-
-
74249094999
-
Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy
-
Bäumer, D., Lee, S., Nicholson, G., Davies, J.L., Parkinson, N.J., Murray, L.M., Gillingwater, T.H., Ansorge, O., Davies, K.E. and Talbot, K. (2009) Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy. PLoS Genet., 5, e1000773.
-
(2009)
PLoS Genet.
, vol.5
-
-
Bäumer, D.1
Lee, S.2
Nicholson, G.3
Davies, J.L.4
Parkinson, N.J.5
Murray, L.M.6
Gillingwater, T.H.7
Ansorge, O.8
Davies, K.E.9
Talbot, K.10
-
12
-
-
0030776040
-
Expression of the SMN gene, the spinal muscular atrophy determining gene, in the mammalian central nervous system
-
Battaglia, G., Princivalle, A., Forti, F., Lizier, C. and Zeviani, M. (1997) Expression of the SMN gene, the spinal muscular atrophy determining gene, in the mammalian central nervous system. Hum. Mol. Genet., 6, 1961-1971.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1961-1971
-
-
Battaglia, G.1
Princivalle, A.2
Forti, F.3
Lizier, C.4
Zeviani, M.5
-
13
-
-
33745597622
-
SMN, the product of the spinal muscular atrophy-determining gene, is expressed widely but selectively in the developing human forebrain
-
Briese, M., Richter, D.U., Sattelle, D.B. and Ulfig, N. (2006) SMN, the product of the spinal muscular atrophy-determining gene, is expressed widely but selectively in the developing human forebrain. J. Comp. Neurol., 497, 808-816.
-
(2006)
J. Comp. Neurol.
, vol.497
, pp. 808-816
-
-
Briese, M.1
Richter, D.U.2
Sattelle, D.B.3
Ulfig, N.4
-
14
-
-
0034639645
-
The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy
-
Monani, U.R., Sendtner, M., Coovert, D.D., Parsons, D.W., Andreassi, C., Le, T.T., Jablonka, S., Schrank, B., Rossoll, W., Prior, T.W. et al. (2000) The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy. Hum. Mol. Genet., 9, 333-339.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 333-339
-
-
Monani, U.R.1
Sendtner, M.2
Coovert, D.D.3
Parsons, D.W.4
Andreassi, C.5
Le, T.T.6
Jablonka, S.7
Schrank, B.8
Rossoll, W.9
Prior, T.W.10
-
15
-
-
0033827353
-
Genetically confirmed spinal muscular atrophy type III with epilepsy, cerebral hypoperfusion, and parahippocampal gyrus atrophy
-
Higashi, K., Nakagawa, M., Higuchi, I., Saito, K. and Osame, M. (2000) Genetically confirmed spinal muscular atrophy type III with epilepsy, cerebral hypoperfusion, and parahippocampal gyrus atrophy. Rinsho Shinkeigaku, 40, 334-338.
-
(2000)
Rinsho Shinkeigaku
, vol.40
, pp. 334-338
-
-
Higashi, K.1
Nakagawa, M.2
Higuchi, I.3
Saito, K.4
Osame, M.5
-
16
-
-
0031789814
-
Neurogenesis in the adult human hippocampus
-
Eriksson, P.S., Perfilieva, E., Björk-Eriksson, T., Alborn, A.M., Nordborg, C., Peterson, D.A. and Gage, F.H. (1998) Neurogenesis in the adult human hippocampus. Nat. Med., 4, 1313-1317.
-
(1998)
Nat. Med.
, vol.4
, pp. 1313-1317
-
-
Eriksson, P.S.1
Perfilieva, E.2
Björk-Eriksson, T.3
Alborn, A.M.4
Nordborg, C.5
Peterson, D.A.6
Gage, F.H.7
-
17
-
-
0035833068
-
Adult neurogenesis produces a large pool of new granule cells in the dentate gyrus
-
Cameron, H.A. and McKay, R.D. (2001) Adult neurogenesis produces a large pool of new granule cells in the dentate gyrus. J. Comp. Neurol., 435, 406-417.
-
(2001)
J. Comp. Neurol.
, vol.435
, pp. 406-417
-
-
Cameron, H.A.1
McKay, R.D.2
-
18
-
-
0346458659
-
Increased hippocampal neurogenesis in Alzheimer's disease
-
Jin, K., Peel, A.L., Mao, X.O., Xie, L., Cottrell, B.A., Henshall, D.C. and Greenberg, D.A. (2004) Increased hippocampal neurogenesis in Alzheimer's disease. Proc. Natl Acad. Sci. USA, 101, 343-347.
-
(2004)
Proc. Natl Acad. Sci. USA
, vol.101
, pp. 343-347
-
-
Jin, K.1
Peel, A.L.2
Mao, X.O.3
Xie, L.4
Cottrell, B.A.5
Henshall, D.C.6
Greenberg, D.A.7
-
19
-
-
0034194444
-
The relationship between SMN, the spinal muscular atrophy protein, and nuclear coiled bodies in differentiated tissues and cultured cells
-
Young, P.J., Le, T.T., thi Man, N., Burghes, A.H. and Morris, G.E. (2000) The relationship between SMN, the spinal muscular atrophy protein, and nuclear coiled bodies in differentiated tissues and cultured cells. Exp. Cell Res., 256, 365-374.
-
(2000)
Exp. Cell Res.
, vol.256
, pp. 365-374
-
-
Young, P.J.1
Le, T.T.2
thi Man, N.3
Burghes, A.H.4
Morris, G.E.5
-
20
-
-
39749168988
-
Abnormal motoneuron migration, differentiation, and axon outgrowth in spinal muscular atrophy
-
Simic, G., Mladinov, M., Seso Simic, D., Jovanov Milosevic, N., Islam, A., Pajtak, A., Barisic, N., Sertic, J., Lucassen, P.J., Hof, P.R. et al. (2008) Abnormal motoneuron migration, differentiation, and axon outgrowth in spinal muscular atrophy. Acta Neuropathol., 115, 313-326.
-
(2008)
Acta Neuropathol.
, vol.115
, pp. 313-326
-
-
Simic, G.1
Mladinov, M.2
Seso Simic, D.3
Jovanov Milosevic, N.4
Islam, A.5
Pajtak, A.6
Barisic, N.7
Sertic, J.8
Lucassen, P.J.9
Hof, P.R.10
-
21
-
-
49049091331
-
Pathogenesis of proximal autosomal recessive spinal muscular atrophy
-
Simic, G. (2008) Pathogenesis of proximal autosomal recessive spinal muscular atrophy. Acta Neuropathol., 116, 223-234.
-
(2008)
Acta Neuropathol.
, vol.116
, pp. 223-234
-
-
Simic, G.1
-
22
-
-
77949889554
-
Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy
-
Murray, L.M., Lee, S., Bäumer, D., Parson, S.H., Talbot, K. and Gillingwater, T.H. (2010) Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy. Hum. Mol. Genet., 19, 420-433.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 420-433
-
-
Murray, L.M.1
Lee, S.2
Bäumer, D.3
Parson, S.H.4
Talbot, K.5
Gillingwater, T.H.6
-
23
-
-
34548157263
-
Congenital bone fractures in spinal muscular atrophy: functional role for SMN protein in bone remodeling
-
Shanmugarajan, S., Swoboda, K.J., Iannaccone, S.T., Ries, W.L., Maria, B.L. and Reddy, S.V. (2007) Congenital bone fractures in spinal muscular atrophy: functional role for SMN protein in bone remodeling. J. Child Neurol., 22, 967-973.
-
(2007)
J. Child Neurol.
, vol.22
, pp. 967-973
-
-
Shanmugarajan, S.1
Swoboda, K.J.2
Iannaccone, S.T.3
Ries, W.L.4
Maria, B.L.5
Reddy, S.V.6
-
24
-
-
54049121013
-
Congenital heart disease is a feature of severe infantile spinal muscular atrophy
-
Rudnik-Schöneborn, S., Heller, R., Berg, C., Betzler, C., Grimm, T., Eggermann, T., Eggermann, K., Wirth, R., Wirth, B. and Zerres, K. (2008) Congenital heart disease is a feature of severe infantile spinal muscular atrophy. J. Med. Genet., 45, 635-638.
-
(2008)
J. Med. Genet.
, vol.45
, pp. 635-638
-
-
Rudnik-Schöneborn, S.1
Heller, R.2
Berg, C.3
Betzler, C.4
Grimm, T.5
Eggermann, T.6
Eggermann, K.7
Wirth, R.8
Wirth, B.9
Zerres, K.10
-
25
-
-
27344454223
-
Hypomorphic Smn knockdown C2C12 myoblasts reveal intrinsic defects in myoblast fusion and myotube morphology
-
Shafey, D., Côté, P.D. and Kothary, R. (2005) Hypomorphic Smn knockdown C2C12 myoblasts reveal intrinsic defects in myoblast fusion and myotube morphology. Exp. Cell Res., 311, 49-61.
-
(2005)
Exp. Cell Res.
, vol.311
, pp. 49-61
-
-
Shafey, D.1
Côté, P.D.2
Kothary, R.3
-
26
-
-
0037465776
-
Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy
-
Rudnik-Schöneborn, S., Goebel, H.H., Schlote, W., Molaian, S., Omran, H., Ketelsen, U., Korinthenberg, R., Wenzel, D., Lauffer, H., Kreiss-Nachtsheim, M. et al. (2003) Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy. Neurology, 60, 983-987.
-
(2003)
Neurology
, vol.60
, pp. 983-987
-
-
Rudnik-Schöneborn, S.1
Goebel, H.H.2
Schlote, W.3
Molaian, S.4
Omran, H.5
Ketelsen, U.6
Korinthenberg, R.7
Wenzel, D.8
Lauffer, H.9
Kreiss-Nachtsheim, M.10
-
27
-
-
31544437449
-
Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy
-
Jablonka, S., Karle, K., Sandner, B., Andreassi, C., von Au, K. and Sendtner, M. (2006) Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy. Hum. Mol. Genet., 15, 511-518.
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 511-518
-
-
Jablonka, S.1
Karle, K.2
Sandner, B.3
Andreassi, C.4
von Au, K.5
Sendtner, M.6
-
28
-
-
0034639745
-
Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III
-
Jablonka, S., Schrank, B., Kralewski, M., Rossoll, W. and Sendtner, M. (2000) Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III. Hum. Mol. Genet., 9, 341-346.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 341-346
-
-
Jablonka, S.1
Schrank, B.2
Kralewski, M.3
Rossoll, W.4
Sendtner, M.5
-
29
-
-
0142029138
-
Neuropathological analysis in spinal muscular atrophy type II
-
Araki, S., Hayashi, M., Tamagawa, K., Saito, M., Kato, S., Komori, T., Sakakihara, Y., Mizutani, T. and Oda, M. (2003) Neuropathological analysis in spinal muscular atrophy type II. Acta Neuropathol., 106, 441-448.
-
(2003)
Acta Neuropathol.
, vol.106
, pp. 441-448
-
-
Araki, S.1
Hayashi, M.2
Tamagawa, K.3
Saito, M.4
Kato, S.5
Komori, T.6
Sakakihara, Y.7
Mizutani, T.8
Oda, M.9
-
30
-
-
0031886390
-
A study of cell death in Werdnig Hoffmann disease brain
-
Hayashi, M., Arai, N., Murakami, T., Yoshio, M., Oda, M. and Matsuyama, H. (1998) A study of cell death in Werdnig Hoffmann disease brain. Neurosci. Lett., 243, 117-120.
-
(1998)
Neurosci. Lett.
, vol.243
, pp. 117-120
-
-
Hayashi, M.1
Arai, N.2
Murakami, T.3
Yoshio, M.4
Oda, M.5
Matsuyama, H.6
-
31
-
-
0032231880
-
MR findings of Werdnig-Hoffmann disease in two infants
-
Hsu, C.F., Chen, C.Y., Yuh, Y.S., Chen, Y.H., Hsu, Y.T. and Zimmerman, R.A. (1998) MR findings of Werdnig-Hoffmann disease in two infants. AJNR Am. J. Neuroradiol., 19, 550-552.
-
(1998)
AJNR Am. J. Neuroradiol.
, vol.19
, pp. 550-552
-
-
Hsu, C.F.1
Chen, C.Y.2
Yuh, Y.S.3
Chen, Y.H.4
Hsu, Y.T.5
Zimmerman, R.A.6
-
32
-
-
0347091768
-
Thalamic lesions in a long-surviving child with spinal muscular atrophy type I: MRI and EEG findings
-
Ito, Y., Kumada, S., Uchiyama, A., Saito, K., Osawa, M., Yagishita, A., Kurata, K. and Hayashi, M. (2004) Thalamic lesions in a long-surviving child with spinal muscular atrophy type I: MRI and EEG findings. Brain Dev., 26, 53-56.
-
(2004)
Brain Dev.
, vol.26
, pp. 53-56
-
-
Ito, Y.1
Kumada, S.2
Uchiyama, A.3
Saito, K.4
Osawa, M.5
Yagishita, A.6
Kurata, K.7
Hayashi, M.8
-
33
-
-
0029023481
-
Spinal muscular atrophy with oculomotor palsy, epilepsy, and cerebellar hypoperfusion
-
Oka, A., Matsushita, Y., Sakakihara, Y., Momose, T. and Yanaginasawa, M. (1995) Spinal muscular atrophy with oculomotor palsy, epilepsy, and cerebellar hypoperfusion. Pediatr. Neurol., 12, 365-369.
-
(1995)
Pediatr. Neurol.
, vol.12
, pp. 365-369
-
-
Oka, A.1
Matsushita, Y.2
Sakakihara, Y.3
Momose, T.4
Yanaginasawa, M.5
-
34
-
-
0020609035
-
A neuropathologic study of Werdnig-Hoffmann disease with special reference to the thalamus and posterior roots
-
Shishikura, K., Hara, M., Sasaki, Y. and Misugi, K. (1983) A neuropathologic study of Werdnig-Hoffmann disease with special reference to the thalamus and posterior roots. Acta Neuropathol., 60, 99-106.
-
(1983)
Acta Neuropathol
, vol.60
, pp. 99-106
-
-
Shishikura, K.1
Hara, M.2
Sasaki, Y.3
Misugi, K.4
-
35
-
-
0021931762
-
Is Werdnig-Hoffmann disease a pure lower motor neuron disorder?
-
Towfighi, J., Young, R.S. and Ward, R.M. (1985) Is Werdnig-Hoffmann disease a pure lower motor neuron disorder? Acta Neuropathol., 65, 270-280.
-
(1985)
Acta Neuropathol.
, vol.65
, pp. 270-280
-
-
Towfighi, J.1
Young, R.S.2
Ward, R.M.3
-
36
-
-
0026006911
-
Brain atrophy in Werdnig-Hoffmann disease
-
Yohannan, M., Patel, P., Kolawole, T., Malabarey, T. and Mahdi, A. (1991) Brain atrophy in Werdnig-Hoffmann disease. Acta Neurol. Scand., 84, 426-428.
-
(1991)
Acta Neurol. Scand.
, vol.84
, pp. 426-428
-
-
Yohannan, M.1
Patel, P.2
Kolawole, T.3
Malabarey, T.4
Mahdi, A.5
-
37
-
-
41149113045
-
Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy
-
Murray, L.M., Comley, L.H., Thomson, D., Parkinson, N., Talbot, K. and Gillingwater, T.H. (2008) Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy. Hum. Mol. Genet., 17, 949-962.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 949-962
-
-
Murray, L.M.1
Comley, L.H.2
Thomson, D.3
Parkinson, N.4
Talbot, K.5
Gillingwater, T.H.6
-
38
-
-
70349997680
-
Molecular correlates of axonal and synaptic pathology in mouse models of Batten disease
-
Kielar, C., Wishart, T.M., Palmer, A., Dihanich, S., Wong, A.M., Macauley, S.L., Chan, C.H., Sands, M.S., Pearce, D.A., Cooper, J.D. et al. (2009) Molecular correlates of axonal and synaptic pathology in mouse models of Batten disease. Hum. Mol. Genet., 18, 4066-4680.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 4066-4680
-
-
Kielar, C.1
Wishart, T.M.2
Palmer, A.3
Dihanich, S.4
Wong, A.M.5
Macauley, S.L.6
Chan, C.H.7
Sands, M.S.8
Pearce, D.A.9
Cooper, J.D.10
-
39
-
-
57249084636
-
Loss of translation elongation factor (eEF1A2) expression in vivo differentiates between Wallerian degeneration and dying-back neuronal pathology
-
Murray, L.M., Thomson, D., Conklin, A., Wishart, T.M. and Gillingwater, T.H. (2008) Loss of translation elongation factor (eEF1A2) expression in vivo differentiates between Wallerian degeneration and dying-back neuronal pathology. J. Anat., 213, 633-645.
-
(2008)
J. Anat.
, vol.213
, pp. 633-645
-
-
Murray, L.M.1
Thomson, D.2
Conklin, A.3
Wishart, T.M.4
Gillingwater, T.H.5
-
40
-
-
34548386721
-
Differential proteomics analysis of synaptic proteins identifies potential cellular targets and protein mediators of synaptic neuroprotection conferred by the slow Wallerian degeneration (Wlds) gene
-
Wishart, T.M., Paterson, J.M., Short, D.M., Meredith, S., Robertson, K.A., Sutherland, C., Cousin, M.A., Dutia, M.B. and Gillingwater, T.H. (2007) Differential proteomics analysis of synaptic proteins identifies potential cellular targets and protein mediators of synaptic neuroprotection conferred by the slow Wallerian degeneration (Wlds) gene. Mol. Cell. Proteomics, 6, 1318-1330.
-
(2007)
Mol. Cell. Proteomics
, vol.6
, pp. 1318-1330
-
-
Wishart, T.M.1
Paterson, J.M.2
Short, D.M.3
Meredith, S.4
Robertson, K.A.5
Sutherland, C.6
Cousin, M.A.7
Dutia, M.B.8
Gillingwater, T.H.9
-
41
-
-
34249062964
-
The minimum information about a proteomics experiment (MIAPE)
-
Taylor, C.F., Paton, N.W., Lilley, K.S., Binz, P.A., Julian, R.K. Jr, Jones, A.R., Zhu, W., Apweiler, R., Aebersold, R., Deutsch, E.W. et al. (2007) The minimum information about a proteomics experiment (MIAPE). Nat. Biotechnol., 25, 887-893.
-
(2007)
Nat. Biotechnol.
, vol.25
, pp. 887-893
-
-
Taylor, C.F.1
Paton, N.W.2
Lilley, K.S.3
Binz, P.A.4
Julian R.K., Jr.5
Jones, A.R.6
Zhu, W.7
Apweiler, R.8
Aebersold, R.9
Deutsch, E.W.10
|