-
1
-
-
30344475206
-
SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2
-
Cagnoli C, et al. SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2. Brain. 2006;129(pt 1):235-242.
-
(2006)
Brain.
, vol.129
, pp. 235-242
-
-
Cagnoli, C.1
-
2
-
-
77950298030
-
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28
-
Di Bella D, et al. Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. Nat Genet. 2010;42(4):313-321.
-
(2010)
Nat Genet.
, vol.42
, Issue.4
, pp. 313-321
-
-
Di Bella, D.1
-
3
-
-
78751600248
-
Missense mutations in the AFG3L2 proteolytic domain account for approximately 1.5% of European autosomal dominant cerebellar ataxias
-
Cagnoli C, et al. Missense mutations in the AFG3L2 proteolytic domain account for approximately 1.5% of European autosomal dominant cerebellar ataxias. Hum Mutat. 2010;31(10):1117-1124.
-
(2010)
Hum Mutat.
, vol.31
, Issue.10
, pp. 1117-1124
-
-
Cagnoli, C.1
-
4
-
-
77954916656
-
Early onset and slow progres-sion of SCA28, a rare dominant ataxia in a large four-generation family with a novel AFG3L2 mutation
-
Edener U, et al. Early onset and slow progres-sion of SCA28, a rare dominant ataxia in a large four-generation family with a novel AFG3L2 mutation. Eur J Hum Genet. 2010;18(8):965-968.
-
(2010)
Eur J Hum Genet.
, vol.18
, Issue.8
, pp. 965-968
-
-
Edener, U.1
-
5
-
-
80055087830
-
Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases
-
Pierson TM, et al. Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases. PLoS Genet. 2011;7(10):e1002325.
-
(2011)
PLoS Genet.
, vol.7
, Issue.10
, pp. e1002325
-
-
Pierson, T.M.1
-
6
-
-
34250369119
-
Protein degradation within mitochondria: Versatile activities of AAA proteases and other peptidases
-
Koppen M, Langer T. Protein degradation within mitochondria: versatile activities of AAA proteases and other peptidases. Crit Rev Biochem Mol Biol. 2007;42(3):221-242.
-
(2007)
Crit Rev Biochem Mol Biol.
, vol.42
, Issue.3
, pp. 221-242
-
-
Koppen, M.1
Langer, T.2
-
7
-
-
0032541406
-
The formation of respiratory chain complexes in mitochondria is under the proteolytic control of the m-AAA protease
-
Arlt H, Steglich G, Perryman R, Guiard B, Neu-pert W, Langer T. The formation of respiratory chain complexes in mitochondria is under the proteolytic control of the m-AAA protease. EMBO J. 1998;17(16):4837-4847.
-
(1998)
EMBO J.
, vol.17
, Issue.16
, pp. 4837-4847
-
-
Arlt, H.1
Steglich, G.2
Perryman, R.3
Guiard, B.4
Neu-Pert, W.5
Langer, T.6
-
8
-
-
0344736798
-
Loss of m-AAA protease in mitochondria causes complex i deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia
-
Atorino L, et al. Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. J Cell Biol. 2003;163(4):777-787.
-
(2003)
J Cell Biol.
, vol.163
, Issue.4
, pp. 777-787
-
-
Atorino, L.1
-
9
-
-
40849142484
-
The mitochondrial protease AFG3L2 is essential for axonal development
-
Maltecca F, et al. The mitochondrial protease AFG3L2 is essential for axonal development. J Neurosci. 2008;28(11):2827-2836.
-
(2008)
J Neurosci.
, vol.28
, Issue.11
, pp. 2827-2836
-
-
Maltecca, F.1
-
10
-
-
33746299692
-
Regulation of mitochondrial morphology through proteolytic cleavage of OPA1
-
Ishihara N, Fujita Y, Oka T, Mihara K. Regulation of mitochondrial morphology through proteolytic cleavage of OPA1. EMBO J. 2006;25(13):2966-2977.
-
(2006)
EMBO J.
, vol.25
, Issue.13
, pp. 2966-2977
-
-
Ishihara, N.1
Fujita, Y.2
Oka, T.3
Mihara, K.4
-
11
-
-
34548349869
-
OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria
-
Duvezin-Caubet S, et al. OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria. Mol Biol Cell. 2007;18(9):3582-3590.
-
(2007)
Mol Biol Cell.
, vol.18
, Issue.9
, pp. 3582-3590
-
-
Duvezin-Caubet, S.1
-
12
-
-
76149140917
-
Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1
-
Ehses S, et al. Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1. J Cell Biol. 2009;187(7):1023-1036.
-
(2009)
J Cell Biol.
, vol.187
, Issue.7
, pp. 1023-1036
-
-
Ehses, S.1
-
13
-
-
84865080562
-
Respiratory dysfunction by AFG3L2 deficiency causes decreased mitochondrial calcium uptake via organel-lar network fragmentation
-
Maltecca F, et al. Respiratory dysfunction by AFG3L2 deficiency causes decreased mitochondrial calcium uptake via organel-lar network fragmentation. Hum Mol Genet. 2012;21(17):3858-3870.
-
(2012)
Hum Mol Genet.
, vol.21
, Issue.17
, pp. 3858-3870
-
-
Maltecca, F.1
-
14
-
-
26844484821
-
The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria
-
Nolden M, Ehses S, Koppen M, Bernacchia A, Rugarli EI, Langer T. The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria. Cell. 2005;123(2):277-289.
-
(2005)
Cell.
, vol.123
, Issue.2
, pp. 277-289
-
-
Nolden, M.1
Ehses, S.2
Koppen, M.3
Bernacchia, A.4
Rugarli, E.I.5
Langer, T.6
-
15
-
-
84903976125
-
Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28
-
Smets K, et al. Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28. Neurology. 2014;82(23):2092-2100.
-
(2014)
Neurology.
, vol.82
, Issue.23
, pp. 2092-2100
-
-
Smets, K.1
-
16
-
-
67651154308
-
Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration
-
Maltecca F, Magnoni R, Cerri F, Cox GA, Quat-trini A, Casari G. Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration. J Neurosci. 2009;29(29):9244-9254.
-
(2009)
J Neurosci.
, vol.29
, Issue.29
, pp. 9244-9254
-
-
Maltecca, F.1
Magnoni, R.2
Cerri, F.3
Cox, G.A.4
Quat-Trini, A.5
Casari, G.6
-
17
-
-
0035433420
-
Four deaths and a funeral: From caspases to alternative mechanisms
-
Leist M, Jaattela M. Four deaths and a funeral: from caspases to alternative mechanisms. Nat Rev Mol Cell Biol. 2001;2(8):589-598.
-
(2001)
Nat Rev Mol Cell Biol.
, vol.2
, Issue.8
, pp. 589-598
-
-
Leist, M.1
Jaattela, M.2
-
18
-
-
31744441984
-
Spectrin mutations cause spinocerebellar ataxia type 5
-
Ikeda Y, et al. Spectrin mutations cause spinocerebellar ataxia type 5. Nat Genet. 2006;38(2):184-190.
-
(2006)
Nat Genet.
, vol.38
, Issue.2
, pp. 184-190
-
-
Ikeda, Y.1
-
19
-
-
33749010065
-
Bergmann glia expression of polyglutamine-expanded ataxin-7 produces neu-rodegeneration by impairing glutamate transport
-
Custer SK, et al. Bergmann glia expression of polyglutamine-expanded ataxin-7 produces neu-rodegeneration by impairing glutamate transport. Nat Neurosci. 2006;9(10):1302-1311.
-
(2006)
Nat Neurosci.
, vol.9
, Issue.10
, pp. 1302-1311
-
-
Custer, S.K.1
-
20
-
-
84856282307
-
Deranged calcium signaling in Purkinje cells and pathogenesis in spinocerebellar ataxia 2 (SCA2) and other atax-ias
-
Kasumu A, Bezprozvanny I. Deranged calcium signaling in Purkinje cells and pathogenesis in spinocerebellar ataxia 2 (SCA2) and other atax-ias. Cerebellum. 2012;11(3):630-639.
-
(2012)
Cerebellum.
, vol.11
, Issue.3
, pp. 630-639
-
-
Kasumu, A.1
Bezprozvanny, I.2
-
21
-
-
0036831284
-
The molecular organization of cer-ebellar long-term depression
-
Ito M. The molecular organization of cer-ebellar long-term depression. Nat Rev. 2002;3(11):896-902.
-
(2002)
Nat Rev.
, vol.3
, Issue.11
, pp. 896-902
-
-
Ito, M.1
-
22
-
-
84864666047
-
Ca2+ signaling in cerebellar Purkinje neurons - Editorial
-
Gruol D, Manto M, Haines D. Ca2+ signaling in cerebellar Purkinje neurons - editorial. Cerebellum. 2012;11(3):605-608.
-
(2012)
Cerebellum.
, vol.11
, Issue.3
, pp. 605-608
-
-
Gruol, D.1
Manto, M.2
Haines, D.3
-
23
-
-
84863518019
-
Mitochondrial Ca(2)(+) homeostasis: Mechanism, role, and tissue specificities
-
Pizzo P, Drago I, Filadi R, Pozzan T. Mitochondrial Ca(2)(+) homeostasis: mechanism, role, and tissue specificities. Pflugers Arch. 2012;464(1):3-17.
-
(2012)
Pflugers Arch.
, vol.464
, Issue.1
, pp. 3-17
-
-
Pizzo, P.1
Drago, I.2
Filadi, R.3
Pozzan, T.4
-
24
-
-
0034145480
-
Dissection of mitochondrial Ca2+ uptake and release fluxes in situ after depolarization-evoked [Ca2+](i) elevations in sympathetic neurons
-
Colegrove SL, Albrecht MA, Friel DD. Dissection of mitochondrial Ca2+ uptake and release fluxes in situ after depolarization-evoked [Ca2+](i) elevations in sympathetic neurons. J Gen Physiol. 2000;115(3):351-370.
-
(2000)
J Gen Physiol.
, vol.115
, Issue.3
, pp. 351-370
-
-
Colegrove, S.L.1
Albrecht, M.A.2
Friel, D.D.3
-
25
-
-
0034307469
-
Stimulation-evoked increases in cytosolic [Ca(2+)] in mouse motor nerve terminals are limited by mitochondrial uptake and are temperature-dependent
-
David G, Barrett EF. Stimulation-evoked increases in cytosolic [Ca(2+)] in mouse motor nerve terminals are limited by mitochondrial uptake and are temperature-dependent. J Neuro-sci. 2000;20(19):7290-7296.
-
(2000)
J Neuro-sci.
, vol.20
, Issue.19
, pp. 7290-7296
-
-
David, G.1
Barrett, E.F.2
-
26
-
-
0034912995
-
Control of secretion by mitochondria depends on the size of the local [Ca2+] after chromaffin cell stimulation
-
Montero M, et al. Control of secretion by mitochondria depends on the size of the local [Ca2+] after chromaffin cell stimulation. Eur J Neurosci. 2001;13(12):2247-2254.
-
(2001)
Eur J Neurosci.
, vol.13
, Issue.12
, pp. 2247-2254
-
-
Montero, M.1
-
27
-
-
84863522994
-
Mitochondria, calcium-dependent neuronal death and neurodegenerative disease
-
Duchen MR. Mitochondria, calcium-dependent neuronal death and neurodegenerative disease. Pflugers Arch. 2012;464(1):111-121.
-
(2012)
Pflugers Arch.
, vol.464
, Issue.1
, pp. 111-121
-
-
Duchen, M.R.1
-
28
-
-
84864954362
-
Mitochon-drial dynamics in cancer and neurodegenerative and neuroinflammatory diseases
-
Corrado M, Scorrano L, Campello S. Mitochon-drial dynamics in cancer and neurodegenerative and neuroinflammatory diseases. Int J Cell Biol. 2012;2012:729290.
-
(2012)
Int J Cell Biol.
, vol.2012
, pp. 729290
-
-
Corrado, M.1
Scorrano, L.2
Campello, S.3
-
29
-
-
77951096150
-
Mitochondrial dynamics - Fusion, fission, movement, and mitophagy - In neurodegenerative diseases
-
Chen H, Chan DC. Mitochondrial dynamics - fusion, fission, movement, and mitophagy - in neurodegenerative diseases. Hum Mol Genet. 2009;18(R2):R169-R176.
-
(2009)
Hum Mol Genet.
, vol.18
, Issue.R2
, pp. R169-R176
-
-
Chen, H.1
Chan, D.C.2
-
30
-
-
0029045611
-
Induction of calpain-mediated spectrin fragments by pathogenic treatments in long-term hippocampal slices
-
Bahr BA, Tiriveedhi S, Park GY, Lynch G. Induction of calpain-mediated spectrin fragments by pathogenic treatments in long-term hippocampal slices. J Pharmacol Exp Ther. 1995;273(2):902-908.
-
(1995)
J Pharmacol Exp Ther.
, vol.273
, Issue.2
, pp. 902-908
-
-
Bahr, B.A.1
Tiriveedhi, S.2
Park, G.Y.3
Lynch, G.4
-
31
-
-
0036118684
-
Survival signaling and selective neuroprotection through glutamatergic transmission
-
Bahr BA, et al. Survival signaling and selective neuroprotection through glutamatergic transmission. Exp Neurol. 2002;174(1):37-47.
-
(2002)
Exp Neurol.
, vol.174
, Issue.1
, pp. 37-47
-
-
Bahr, B.A.1
-
32
-
-
33846575665
-
Involvement of calpain in AMPA-induced toxicity to rat cerebellar Purkinje neurons
-
Mansouri B, et al. Involvement of calpain in AMPA-induced toxicity to rat cerebellar Purkinje neurons. Eur J Pharmacol. 2007;557(2-3):106-114.
-
(2007)
Eur J Pharmacol.
, vol.557
, Issue.2-3
, pp. 106-114
-
-
Mansouri, B.1
-
33
-
-
24344501808
-
Spectrin and calpain: A 'target' and a 'sniper' in the pathology of neuronal cells
-
Czogalla A, Sikorski AF. Spectrin and calpain: a 'target' and a 'sniper' in the pathology of neuronal cells. Cell Mol Life Sci. 2005;62(17):1913-1924.
-
(2005)
Cell Mol Life Sci.
, vol.62
, Issue.17
, pp. 1913-1924
-
-
Czogalla, A.1
Sikorski, A.F.2
-
34
-
-
0030581296
-
Diazoxide and cyclothiazide convert AMPA-induced dark cell degeneration of Purkinje cells to edematous damage in the cerebellar slice
-
Strahlendorf JC, Acosta S, Strahlendorf HK. Diazoxide and cyclothiazide convert AMPA-induced dark cell degeneration of Purkinje cells to edematous damage in the cerebellar slice. Brain Res. 1996;729(2):197-204.
-
(1996)
Brain Res.
, vol.729
, Issue.2
, pp. 197-204
-
-
Strahlendorf, J.C.1
Acosta, S.2
Strahlendorf, H.K.3
-
35
-
-
0028346797
-
Cell-cell interactions influence survival and differentiation of purified Purkinje cells in vitro
-
Baptista CA, Hatten ME, Blazeski R, Mason CA. Cell-cell interactions influence survival and differentiation of purified Purkinje cells in vitro. Neuron. 1994;12(2):243-260.
-
(1994)
Neuron.
, vol.12
, Issue.2
, pp. 243-260
-
-
Baptista, C.A.1
Hatten, M.E.2
Blazeski, R.3
Mason, C.A.4
-
36
-
-
33646570865
-
Ca2+ indicators based on computationally redesigned calmodulin-peptide pairs
-
Palmer AE, et al. Ca2+ indicators based on computationally redesigned calmodulin-peptide pairs. Chem Biol. 2006;13(5):521-530.
-
(2006)
Chem Biol.
, vol.13
, Issue.5
, pp. 521-530
-
-
Palmer, A.E.1
-
37
-
-
36248934609
-
Crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1)
-
Conti V, et al. crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1). Int J Mol Med. 2006;18(4):593-600.
-
(2006)
Int J Mol Med.
, vol.18
, Issue.4
, pp. 593-600
-
-
Conti, V.1
-
38
-
-
19944428649
-
β-Lactam antibiotics offer neuroprotection by increasing glutamate transporter expression
-
Rothstein JD, et al. β-Lactam antibiotics offer neuroprotection by increasing glutamate transporter expression. Nature. 2005;433(7021):73-77.
-
(2005)
Nature.
, vol.433
, Issue.7021
, pp. 73-77
-
-
Rothstein, J.D.1
-
39
-
-
0014244380
-
One trial learning in the mouse. I. Its characteristics and modification by experimental-seasonal variables
-
Irwin S, Banuazizi A, Kalsner S, Curtis A. One trial learning in the mouse. I. Its characteristics and modification by experimental-seasonal variables. Psychopharmacologia. 1968;12(4):286-302.
-
(1968)
Psychopharmacologia.
, vol.12
, Issue.4
, pp. 286-302
-
-
Irwin, S.1
Banuazizi, A.2
Kalsner, S.3
Curtis, A.4
-
40
-
-
4544235673
-
Calcium, ATP, and ROS: A mitochon-drial love-hate triangle
-
Brookes PS, Yoon Y, Robotham JL, Anders MW, Sheu SS. Calcium, ATP, and ROS: a mitochon-drial love-hate triangle. Am J Physiol Cell Physiol. 2004;287(4):C817-C833.
-
(2004)
Am J Physiol Cell Physiol.
, vol.287
, Issue.4
, pp. C817-C833
-
-
Brookes, P.S.1
Yoon, Y.2
Robotham, J.L.3
Anders, M.W.4
Sheu, S.S.5
-
41
-
-
84857055792
-
Mitochondria in motor nerve terminals: Function in health and in mutant superoxide dismutase 1 mouse models of familial ALS
-
Barrett EF, Barrett JN, David G. Mitochondria in motor nerve terminals: function in health and in mutant superoxide dismutase 1 mouse models of familial ALS. J Bioenerg Biomembr. 2011;43(6):581-586.
-
(2011)
J Bioenerg Biomembr.
, vol.43
, Issue.6
, pp. 581-586
-
-
Barrett, E.F.1
Barrett, J.N.2
David, G.3
-
42
-
-
2542487188
-
Ca(2+) homeostasis during mitochondrial fragmentation and peri-nuclear clustering induced by hFis1
-
Frieden M, James D, Castelbou C, Danckaert A, Martinou JC, Demaurex N. Ca(2+) homeostasis during mitochondrial fragmentation and peri-nuclear clustering induced by hFis1. J Biol Chem. 2004;279(21):22704-22714.
-
(2004)
J Biol Chem.
, vol.279
, Issue.21
, pp. 22704-22714
-
-
Frieden, M.1
James, D.2
Castelbou, C.3
Danckaert, A.4
Martinou, J.C.5
Demaurex, N.6
-
43
-
-
4944222095
-
Drp-1-dependent division of the mitochondrial network blocks intra-organellar Ca2+ waves and protects against Ca2+-mediated apoptosis
-
Szabadkai G, Simoni AM, Chami M, Wieckowski MR, Youle RJ, Rizzuto R. Drp-1-dependent division of the mitochondrial network blocks intra-organellar Ca2+ waves and protects against Ca2+-mediated apoptosis. Mol Cell. 2004;16(1):59-68.
-
(2004)
Mol Cell.
, vol.16
, Issue.1
, pp. 59-68
-
-
Szabadkai, G.1
Simoni, A.M.2
Chami, M.3
Wieckowski, M.R.4
Youle, R.J.5
Rizzuto, R.6
-
44
-
-
34547601410
-
Mitochondrial fusion protects against neurodegeneration in the cerebellum
-
Chen H, McCaffery JM, Chan DC. Mitochondrial fusion protects against neurodegeneration in the cerebellum. Cell. 2007;130(3):548-562.
-
(2007)
Cell.
, vol.130
, Issue.3
, pp. 548-562
-
-
Chen, H.1
McCaffery, J.M.2
Chan, D.C.3
-
45
-
-
0034625542
-
MGluR1 in cerebellar Purkinje cells essential for long-term depression, synapse elimination, and motor coordination
-
Ichise T, et al. mGluR1 in cerebellar Purkinje cells essential for long-term depression, synapse elimination, and motor coordination. Science. 2000;288(5472):1832-1835.
-
(2000)
Science.
, vol.288
, Issue.5472
, pp. 1832-1835
-
-
Ichise, T.1
-
46
-
-
84866055384
-
Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1
-
Guergueltcheva V, et al. Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1. Am J Hum Genet. 2012;91(3):553-564.
-
(2012)
Am J Hum Genet.
, vol.91
, Issue.3
, pp. 553-564
-
-
Guergueltcheva, V.1
-
47
-
-
84859485229
-
Machado-Joseph disease and other rare spinocerebellar ataxias
-
Matilla-Duenas A. Machado-Joseph disease and other rare spinocerebellar ataxias. Adv Exp Med Biol. 2012;724:172-188.
-
(2012)
Adv Exp Med Biol.
, vol.724
, pp. 172-188
-
-
Matilla-Duenas, A.1
-
48
-
-
0034671149
-
A reliable method for culture of dissociated mouse cerebellar cells enriched for Purkinje neurons
-
Tabata T, Sawada S, Araki K, Bono Y, Furuya S, Kano M. A reliable method for culture of dissociated mouse cerebellar cells enriched for Purkinje neurons. J Neurosci Methods. 2000;104(1):45-53.
-
(2000)
J Neurosci Methods.
, vol.104
, Issue.1
, pp. 45-53
-
-
Tabata, T.1
Sawada, S.2
Araki, K.3
Bono, Y.4
Furuya, S.5
Kano, M.6
-
49
-
-
83055165915
-
PUNISHER: A high-level expression cassette for use with recombinant viral vectors for rapid and long term in vivo neuronal expression in the CNS
-
Montesinos MS, Chen Z, Young SM Jr. pUNISHER: a high-level expression cassette for use with recombinant viral vectors for rapid and long term in vivo neuronal expression in the CNS. J Neurophysiol. 2011;106(6):3230-3244.
-
(2011)
J Neurophysiol.
, vol.106
, Issue.6
, pp. 3230-3244
-
-
Montesinos, M.S.1
Chen, Z.2
Young, Jr.S.M.3
-
50
-
-
0034734772
-
A new vector system with inducible E2a cell line for production of higher titer and safer adenoviral vectors
-
Zhou H, Beaudet AL. A new vector system with inducible E2a cell line for production of higher titer and safer adenoviral vectors. Virology. 2000;275(2):348-357.
-
(2000)
Virology.
, vol.275
, Issue.2
, pp. 348-357
-
-
Zhou, H.1
Beaudet, A.L.2
-
51
-
-
0035988785
-
Construction of first-generation adenoviral vectors
-
Ng P, Graham FL. Construction of first-generation adenoviral vectors. Methods Mol Med. 2002;69:389-414.
-
(2002)
Methods Mol Med.
, vol.69
, pp. 389-414
-
-
Ng, P.1
Graham, F.L.2
-
52
-
-
33645457226
-
Synergistic control of protein kinase Cgamma activity by ionotropic and metab-otropic glutamate receptor inputs in hippocampal neurons
-
Codazzi F, et al. Synergistic control of protein kinase Cgamma activity by ionotropic and metab-otropic glutamate receptor inputs in hippocampal neurons. J Neurosci. 2006;26(13):3404-3411.
-
(2006)
J Neurosci.
, vol.26
, Issue.13
, pp. 3404-3411
-
-
Codazzi, F.1
-
53
-
-
0002294347
-
A simple sequentially rejective multiple test procedure
-
Holm S. A simple sequentially rejective multiple test procedure. Scand J Statist. 1979;6:65-70.
-
(1979)
Scand J Statist.
, vol.6
, pp. 65-70
-
-
Holm, S.1
|